azoxynaphthalene

(organic chemistry) Any azoxy derivative of naphthalene


benzoannelated

(organic chemistry) annelated with one or more fused benzene rings


benzofulvene

(organic chemistry) Any benzo derivative of a fulvene


benzoxylation

(organic chemistry) Any reaction that introduces a benzoxyl group into a molecule


benzoylacetate

(organic chemistry) Any benzoyl derivative of an acetate group or ion


benzoyldiamidite

(organic chemistry) Any benzoyl derivative of a diamidite


benzoyloxy

(organic chemistry) The benzoate group when used as a substituent


benzoylphenyl

(organic chemistry, especially in combination) Any benzoyl derivative of a phenyl group


benzylamide

(organic chemistry) Any N-benzyl derivative of an amide


benzylhydroxylamine

(organic chemistry) Any benzyl derivative of hydroxylamine


benzylideneaniline

(organic chemistry) Any benzylidene derivative of aniline


benzyloxymethyl

(organic chemistry, especially in combination) Any benzyloxy derivative of a methyl group


benzyloxyphthalimide

(organic chemistry) Any benzyloxy derivative of phthalimide


benzylquercetin

(organic chemistry) Any benzyl derivative of quercetin


benzylsulfinyl

(organic chemistry, especially in combination) Any benzyl derivative of a sulfinyl group


bicyclisation

en-noun

bicyclisation (countable and uncountable, plural bicyclisations)

(organic chemistry) Any reaction that produces a bicyclic product


bipyrazine

bipyrazine (countable and uncountable, plural bipyrazines)

(organic chemistry) A bicyclic aromatic heterocycle composed of two pyrazine rings linked by a direct single bond


bipyrazyl

(organic chemistry, especially in combination) A univalent radical derived from bipyrazine

(organic chemistry) Synonym of bipyrazine


bipyrrole

(organic chemistry) A bicyclic heterocycle composed of two pyrrole rings linked by a single bond


bisalkylation

(organic chemistry) Any reaction that introduces two alkyl groups into a molecule


bisazene

(organic chemistry) Any compound that has two azene groups


bisenolate

(organic chemistry) Any compound that has two enolate groups


diazoindacene

(organic chemistry) Any diazo compound derived from indacene


bora-

(organic chemistry) Describing any compound in which a carbon atom (or a >CH group) has been replaced by one of boron


borabenzene

borabenzene (countable and uncountable, plural borabenzenes)

(organic chemistry) A heteroaromatic compound in which a carbon atom of a benzene ring has been replaced by one of boron


borapyridine

borapyridine (countable and uncountable, plural borapyridines)

(organic chemistry) A heteroaromatic compound in which a carbon atom of a pyridine ring has been replaced by one of boron


borafluorene

borafluorene (countable and uncountable, plural borafluorenes)

(organic chemistry) A heteroaromatic compound in which a carbon atom of a fluorene has been replaced by one of boron


borylate

en-verb

borylate (third-person singular simple present borylates, present participle borylating, simple past and past participle borylated)

borylates (present singular third-person)
borylating (participle present)
borylated (participle past)
borylated (past)

From boryl + -ate, Back-formation of borylation.

(organic chemistry) To modify by means of borylation


bromobenzaldehyde

(organic chemistry) Any bromo derivative of benzaldehyde


bromobenzoic

(organic chemistry, especially in combination) Any bromo derivative of a benzoic group


bromocarboxylate

(organic chemistry) Any bromo derivative of a carboxylate group or ion


bromocholestane

(organic chemistry) Any bromo derivative of a cholestane


bromocinnoline

(organic chemistry) Any bromo derivative of cinnoline


bromocyclization

en-noun

bromocyclization (countable and uncountable, plural bromocyclizations)

(organic chemistry) Any reaction in which bromination is accompanied by cyclization


bromoethanol

(organic chemistry) Any bromo derivative of ethanol


bromoetherification

bromoetherification (countable and uncountable, plural bromoetherifications)

(organic chemistry) Any reaction in which bromination is accompanied by etherification


bromopropanol

(organic chemistry) Any bromo derivative of propanol


bromotetrahydrofuran

(organic chemistry) Any bromo derivative of tetrahydrofuran


butenedione

(organic chemistry) Any diketone derived from a butene


butylaniline

(organic chemistry) Any butyl derivative of aniline


butylcinnoline

(organic chemistry) Any butyl derivative of cinnoline


butylimidazolium

(organic chemistry, especially in combination) Any butyl derivative of an imidazolium ion


butylmorpholine

(organic chemistry) Any butyl derivative of morpholine


butylperoxyl

(organic chemistry, especially in combination) Any peroxyl radical derived from a butylperoxide


butylphenyl

(organic chemistry, especially in combination) A univalent radical derived from butylphenol


camphoryl

(organic chemistry, especially in combination) Any univalent radical derived from camphor


carboheterocyclic

(organic chemistry) Synonym of heterocyclic


carbonyloxy

(organic chemistry, especially in combination) A univalent radical formed by deprotonation of a carboxyl group


chinesin

Hypericum japonicum
Hypericum japonicum#Translingual

(organic chemistry) Any of a group of phloroglucinol derivatives isolated from Hypericum japonicum (syn. Hypericum chinense).


chipericumin

(organic chemistry) Any of a group of prenylated acylphloroglucinols isolated from Hypericum japonicum (syn. Hypericum chinense).


chlorocholestane

(organic chemistry) Any chloro derivative of cholestane


chlorodeoxyadenosine

(organic chemistry) Any chloro derivative of deoxyadenosine


chloroethanol

(organic chemistry) Any chloro derivative of ethanol


chloroethoxyamine

(organic chemistry) Any chloro derivative of ethoxyamine


ethoxyamine

(organic chemistry) The ethyl derivative of hydroxylamine CH₃CH₂ONH₂


chlorophosphite

(organic chemistry) Any compound containing the -O-PCl-O- radical


chlorophthalimide

(organic chemistry) Any chloro derivative of a phthalimide


chlorosilane

(organic chemistry) Any organic derivative of this compound


chlorosuccinimide

(organic chemistry) Any chloro derivative of succinimide


chlorotetrahydrofuran

(organic chemistry) Any chloro derivative of tetrahydrofuran


syringetin

(organic chemistry) An O-methylated flavonol, a type of flavonoid.


chromeno

(organic chemistry, especially in combination) A radical derived from chromene


cinnamamide

cinnamamide (countable and uncountable, plural cinnamamides)

(organic chemistry) The amide of cinnamic acid


crownophane

(organic chemistry) A cyclophane that has some similarities to a crown ether


cyanobenzoate

(organic chemistry) Any cyano derivative of a benzoate group


cyanoethoxy

(organic chemistry, especially in combination) Any cyano derivative of an ethoxy radical


cycloadd

en-verb

cycloadd (third-person singular simple present cycloadds, present participle cycloadding, simple past and past participle cycloadded)

cycloadds (present singular third-person)
cycloadding (participle present)
cycloadded (participle past)
cycloadded (past)

(organic chemistry) To add by means of cycloaddition


cycloaliphatic

(organic chemistry) Relating to a cycloalkane or a cycloalkyl radical


cycloalkanol

(organic chemistry) Any cycloalkyl alcohol


cycloalkylcarboxylic

(organic chemistry, especially in combination) Any cycloalkyl derivative of a carboxylic group


cycloallyl

(organic chemistry) Any cycloaliphatic radical or cation that has a single double bond in the ring


cyclocholestane

(organic chemistry) Any derivative of cholestane that has an extra ring, but especially 3,5-cyclocholestane in which ring-A is converted into a cyclopentane and a cyclopropane rings


cyclocondensation

condensation reaction
condensation reaction

(organic chemistry) Any condensation reaction that is also a cyclization


cyclofenchene

en-noun

cyclofenchene (countable and uncountable, plural cyclofenchenes)

(organic chemistry) The tricyclic hydrocarbon 5,5,6-trimethyl-2,3,4,7-tetrahydro-1H-tricyclo[2.2.1.0^{2,6}]heptane


fenchene

fenchene (countable and uncountable, plural fenchenes)

(organic chemistry) The bicyclic hydrocarbon 7,7-dimethyl-3-methylidenebicyclo[2.2.1]heptane


cyclosteroid

(organic chemistry) Any steroid that has an extra ring, typically a cyclopropane ring


dendralene

(organic chemistry) Any of a class of acyclic cross-conjugated polyenes


deoxyfluorination

(organic chemistry) Any reaction that replaces a hydroxyl (-OH) group with fluoride (-F)


diacetonide

(organic chemistry) Any compound (typically derived from a sugar) that has two acetonide groups


diacetoxylation

(organic chemistry) Any reaction in which two acetoxyl groups are added


diacetylation

(organic chemistry) Any reaction in which two acetyl groups are added


dialkoxide

(organic chemistry) Any compound that has two alkoxide groups


dialkylcarbodiimide

(organic chemistry) Any dialkyl carbodiimide


dialkylphenyl

(organic chemistry, especially in combination) Any dialkyl derivative of a phenyl radical


diallylated

(organic chemistry) Modified by the introduction of two allyl groups


diallylic

(organic chemistry, especially in combination) Having two allyl groups


diaminobenzoate

(organic chemistry) Any diamino derivative of a benzoate group or ion


diarylacetylene

(organic chemistry) Any diaryl derivative of acetylene


diarylmethane

(organic chemistry) Any diaryl derivative of methane


diarylmethyl

(organic chemistry, especially in combination) A univalent radical derived from a diarylmethane


diarylpropylene

(organic chemistry) Any diaryl derivative of propylene


diarylpropyne

(organic chemistry) Any diaryl derivative of propyne


diazafluorenone

(organic chemistry) Any diaza derivative of a fluorenone


diazahelicene

(organic chemistry) Any diaza derivative of a helicene


diazirino

(organic chemistry, especially in combination) Any univalent radical derived from diazirine


diazoacetoacetate

(organic chemistry) Any diazo derivative of a acetoacetate group or ion


diazoacetylacetone

(organic chemistry) Any diazo derivative of acetylacetone


diazoalkane

(organic chemistry) Any diazo derivative of an alkane


diazodiketone

(organic chemistry) Any diazo derivative of a diketone


diazohydrocarbon

(organic chemistry) Any diazo derivative of a hydrocarbon


diazoketoester

(organic chemistry) Any diazo derivative of a ketoester


diazoketone

(organic chemistry) Any diazo derivative of a ketone


diazomalonate

(organic chemistry) Any diazo derivative of a malonate group or ion


dibromocholestane

(organic chemistry) Any dibromo derivative of cholestane


dibromocinnoline

(organic chemistry) Any dibromo derivative of cinnoline


dicarbamate

(organic chemistry) Any compound that contains two carbamate groups or ions


dichlorosilylene

(organic chemistry, especially in combination) Any dichloro derivative of a silylene group


dichlorotoluene

(organic chemistry) Any dichloro derivative of toluene


dicholesteryl

(organic chemistry, especially in combination) Two cholesteryl groups in a molecule


dicyanobenzoquinone

(organic chemistry) Any dicyano derivative of benzoquinone


dicyanovinylene

(organic chemistry, especially in combination) Any dicyano derivative of a vinylene group


dienic

(organic chemistry) Related to, or derived from a diene


diethylaminomethyl

(organic chemistry, especially in combination) Any diethylamino derivative of a methyl group


diethylthioxanthone

(organic chemistry) Any diethyl derivative of thioxanthone


diethynylcinnoline

(organic chemistry) Any diethynyl derivative of cinnoline


dihaloalkane

(organic chemistry) Any dihalo derivative of an alkane


dihydroazepino

(organic chemistry, especially in combination) Any dihydro derivative of an azepino group; a univalent radical derived from dihydroazepine


dihydroazepine

(organic chemistry) Any dihydro derivative of azepine


dihydroazolo

(organic chemistry, especially in combination) Any dihydro derivative of an azolo group; a radical derived from dihydroazole


dihydroazole

(organic chemistry) Any dihydro derivative of azole


dihydrobenzo

(organic chemistry, especially in combination) Any dihydro derivative of a benzo group


dihydropyrazole

(organic chemistry) Any dihydro derivative of a pyrazole


dihydropyrazolo

(organic chemistry, especially in combination) Any dihydro derivative of a pyrazolo group; a radical derived from a dihydropyrazole


pyrazolo

(organic chemistry, especially in combination) A radical derived from a pyrazole


dihydroxybutane

(organic chemistry) Any dihydroxy derivative of butane; Synonym of butanediol


diindolic

(organic chemistry) Relating to a diindole


diiodoarene

(organic chemistry) Any diiodo derivative of an arene


diiodohydroquinone

(organic chemistry) Any diiodo derivative of hydroquinone


diisocyanato

(organic chemistry, especially in combination) Two isocyanato groups in a molecule; a diisocyanate group as a substituent


isocyanato

(organic chemistry, especially in combination) An isocyanate group as a substituent


diisopropanolamine

diisopropanolamine (countable and uncountable, plural diisopropanolamines)

(organic chemistry) The secondary amine N,N-bis(2-hydroxypropyl)amine


diisopropylamino

(organic chemistry, especially in combination) A univalent radical derived from diisopropylamine


dimethoxyarene

(organic chemistry) Any dimethoxy derivative of an arene


dimethoxybenzaldehyde

(organic chemistry) Any dimethoxy derivative of benzaldehyde


dimethylaminopropyl

(organic chemistry, especially in combination) Any dimethylamino derivative of a propyl group


dipivaloylketene

(organic chemistry) Any dipivaloyl derivative of a ketene


dipivaloyl

(organic chemistry, especially in combination) Two pivaloyl groups in a molecule


dipropynyl

(organic chemistry, especially in combination) Two propynyl groups in a molecule


propynyl

(organic chemistry, especially in combination) A univalent radical derived from propyne


dipyrrolo

(organic chemistry, especially in combination) Any radical derived from a dipyrrole


dipyrrolomethane

(organic chemistry) Any dipyrrolo derivative of methane


disteroidal

(organic chemistry) Relating to, or derived from two steroids


disubstituent

(organic chemistry) Two substituents in a molecule


gem-disubstituent effect

gem-disubstituent effect (plural gem-disubstituent effects)

(organic chemistry) The effect of geminal substituents on the reactivity of the carbon atom to which they are attached


dolabellatrienone

(organic chemistry) An unsaturated ketone derived from dolabellane


electrocopolymerization

(organic chemistry) electrochemical copolymerization


electroenzymatic

(organic chemistry) Describing any electrochemical reaction that is catalyzed by an enzyme


enaminoester

(organic chemistry) Alternative form of enamino ester


enamino ester

(organic chemistry) Any ester of an enamino acid


enamino acid

(organic chemistry) Any amino acid in which the amino group is attached to the carbon atom of a double bond (R¹-NH-C(R²)=CHCOOH)


enedioate

(organic chemistry) Any salt or ester of an enedioic acid


enedioic acid

(organic chemistry) Any dioic acid in which the carboxylate groups are separated by a double bond


dioic acid

dicarboxylic acid
dicarboxylic acid#English

(organic chemistry) Synonym of dicarboxylic acid


enedione

(organic chemistry) Any dione (diketone) in which the two carbonyl groups are separated by a double bond


epoxyazepino

(organic chemistry, especially in combination) Any epoxy derivative of an azepino radical


ethoxymethylidene

(organic chemistry, especially in combination) Any ethoxy derivative of a methylidene group


ethoxytoluene

(organic chemistry) Any ethoxy derivative of toluene


ethylarene

(organic chemistry) Any ethyl derivative of an arene


fencholate

(organic chemistry) An alkoxide of fenchol


fenchyl

(organic chemistry, especially in combination) A univalent radical derived from fenchol


fluoroalkylamine

(organic chemistry) Any fluoro derivative of an alkylamine


furopyrimidine

furopyrimidine (countable and uncountable, plural furopyrimidines)

(organic chemistry) A bicyclic heterocycle composed of a furan ring fused to a pyrimidine ring


galloyl

(organic chemistry, especially in combination) A radical derived from gallic acid by removal of hydroxyl groups


glucopyranosidic

(organic chemistry) Derived from, or consisting of glucopyranosides


haloacene

(organic chemistry) Any halogenated acene


haloalkoxy

(organic chemistry, especially in combination) Any halogenated alkoxy group


haloanhydride

(organic chemistry) Any halogenated anhydride


haloketone

(organic chemistry) Any halogenated ketone


halopyrazine

(organic chemistry) Any halogenated derivative of pyrazine


hemisynthesis

(organic chemistry) The synthesis of a new compound derived from an existing natural product


hemisynthetic

(organic chemistry) Related to, or produced by hemisynthesis


heptynoic acid

(organic chemistry) Any of several isomeric carboxylic acids, derived from heptanoic acid, having a triple bond


hetaryl

(organic chemistry) Synonym of heteroaryl


heteroanalogue

(organic chemistry) Any compound, related to an existing one, in which one or more carbon atoms have been replaced by a heteroatom


hexahydroxy

(organic chemistry, in combination) Six hydroxy groups in a molecule


hexylamino

(organic chemistry, especially in combination) A univalent radical derived from hexylamine


hexylurea

(organic chemistry) Any N-hexyl derivative of urea


hydroamidation

(organic chemistry) The addition reaction of (the N-H group of) an amide across a double bond


hydrophosphinylation

hydrophosphinylation (usually uncountable, plural hydrophosphinylations)

(organic chemistry) The addition reaction of a phosphinic acid across a double bond


hydrophosphonylation

hydrophosphonylation (usually uncountable, plural hydrophosphonylations)

(organic chemistry) The addition reaction of a phosphonic acid across a double bond


hydroquinidine

(organic chemistry) The alkaloid (9S)-10,11-dihydro-6′-methoxycinchonan-9-ol derived from quinidine


hydrovinylation

hydrovinylation (countable and uncountable, plural hydrovinylations)

(organic chemistry) The addition reaction of ethylene (or similar alkene) across a double bond


hydroxyalkylation

(organic chemistry) An addition reaction that results in a hydroxyalkyl product


hydroxybenzyl

(organic chemistry, especially in combination) Any hydroxy derivative of a benzyl radical


hydroxycarbamate

(organic chemistry) Any hydroxy derivative of a carbamate


hydroxyester

(organic chemistry) Alternative form of hydroxy ester


hydroxy ester

(organic chemistry) The ester of a hydroxy acid


hydroxyimide

(organic chemistry) Any hydroxy derivative of an imide


hydroxyketone

hydroxyketones (plural)
hydroxy ketone (alternative)

(organic chemistry) Any hydroxy derivative of a ketone; a ketone with hydroxy group bonded to it.


hydroxypyrazole

(organic chemistry) Any hydroxy derivative of a pyrazole


hydroxythioxanthone

(organic chemistry) Any hydroxy derivative of a thioxanthone


iminoketene

(organic chemistry) Any imino derivative of a ketene (>N=C=C=O)


indanylidene

(organic chemistry, especially in combination) A divalent radical derived from the cyclopentane ring of an indane


indazolo

(organic chemistry, especially in combination) Any univalent radical derived from indazole


indenophane

(organic chemistry) A cyclophane based on indene


indenyl

(organic chemistry, especially in combination) A univalent radical derived from indene


integramycin

(organic chemistry) A particular hexacyclic natural product isolated from Actinoplanes that inhibits the action of integrase


iodoalkoxylate

en-verb

iodoalkoxylate (third-person singular simple present iodoalkoxylates, present participle iodoalkoxylating, simple past and past participle iodoalkoxylated)

iodoalkoxylates (present singular third-person)
iodoalkoxylating (participle present)
iodoalkoxylated (participle past)
iodoalkoxylated (past)

(organic chemistry) To add an iodine atom and an alkoxylate group across a double bond


iodoalkoxylation

en-noun

iodoalkoxylation (usually uncountable, plural iodoalkoxylations)

(organic chemistry) The addition reaction of an iodine atom and an alkoxyl group across a double bond


iodohydroquinone

(organic chemistry) Any iodo derivative of a hydroquinone


iodoketone

(organic chemistry) Any iodo derivative of a ketone


iodopyrazine

(organic chemistry) Any iodo derivative of pyrazine


iodosuccinimide

(organic chemistry) Any iodo derivative of succinimide


edunol

(organic chemistry) A prenylated pterocarpan found in the roots of Brongniartia snakeweeds


nicouline

From French, from the former taxonomic name Robinia nicou.


isopropylarene

(organic chemistry) Any isopropyl derivative of an arene


isopropylethylene

(organic chemistry) Any isopropyl derivative of ethylene


isopropylthioxanthone

isopropylthioxanthone (countable and uncountable, plural isopropylthioxanthones)

(organic chemistry) Any isopropyl derivative of a thioxanthone.


isosteviol

(organic chemistry) The isomer of steviol (4α,8β,13β)-13-methyl-16-oxo-17-norkauran-18-oic acid


isoxazolidinyl

(organic chemistry, especially in combination) A radical derived from isoxazolidine


julocrotine

suf

translingual <i class="Latn mention" lang="mul">Julocrot(on)</i>

(organic chemistry) A glutarimide alkaloid, N-[2,6-dioxo-1-(2-phenylethyl)-3-piperidinyl]-2-methylbutanamide, present in Julocroton montevidensis and Croton membranaceus.


glutarimide

en-noun

glutarimide (countable and uncountable, plural glutarimides)

(organic chemistry) The cyclic imide of glutaric acid


kadangustin

kadangustin (countable and uncountable, plural kadangustins)

From the plant species Kadsura angustifolia, + -in.

(organic chemistry) The lignan (2S,3R)-4,4-bis(3,4-dimethoxyphenyl)-2,3-dimethylbutan-1-ol.


ketoimine

(organic chemistry) Alternative form of ketimine

(organic chemistry) Any compound that is both a ketone and an imine


lactonize

en-verb

lactonize (third-person singular simple present lactonizes, present participle lactonizing, simple past and past participle lactonized)

lactonizes (present singular third-person)
lactonizing (participle present)
lactonized (participle past)
lactonized (past)

(organic chemistry) To convert (a hydroxy acid) into a lactone


mackinazolinone

(organic chemistry) The alkaloid 2,3,4,10-tetrahydro-1 H-pyrido[2,1-b]quinazolin-10-one


macrobicyclization

en-noun

macrobicyclization (countable and uncountable, plural macrobicyclizations)

(organic chemistry) The formation of a macrobicycle


macrobicycle

(organic chemistry, especially in combination) Any bicyclic macrocycle


macromulticycle

(organic chemistry, especially in combination) Any multicyclic macrocycle


malonitrile

malonitrile (countable and uncountable, plural malonitriles)

(organic chemistry) The nitrile of malonic acid


mandipropamid

(organic chemistry) The mandelamide fungicide 2-(4-chlorophenyl)-N-[2-(3-methoxy-4-prop-2-ynoxyphenyl)ethyl]-2-prop-2-ynoxyacetamide


mandelamide

mandelamide (countable and uncountable, plural mandelamides)

(organic chemistry) The amide of mandelic acid


menthylamine

menthylamine (countable and uncountable, plural menthylamines)

(organic chemistry) A cyclic monoterpene amine 5-methyl-2-propan-2-ylcyclohexan-1-amine


mercaptobenzaldehyde

(organic chemistry) Any mercapto derivative of benzaldehyde, especially 2-mercaptobenzaldehyde


methoxyarene

(organic chemistry) Any methoxy derivative of an arene


methoxybenzamide

(organic chemistry) Any methoxy derivative of benzamide


methoxyimino

(organic chemistry, especially in combination) Any methoxy derivative of an imino group


methylaniline

(organic chemistry) Any methyl derivative of aniline


methylanilino

(organic chemistry, especially in combination) A univalent radical derived from a methylaniline


methylarene

(organic chemistry) Any methyl derivative of an arene


methylbenzylamine

(organic chemistry) Any methyl derivative of benzylamine


methylcinnoline

(organic chemistry) Any methyl derivative of cinnoline


methylcyclohexanone

(organic chemistry) Any methyl derivative of cyclohexanone


methylenate

en-verb

methylenate (third-person singular simple present methylenates, present participle methylenating, simple past and past participle methylenated)

methylenates (present singular third-person)
methylenating (participle present)
methylenated (participle past)
methylenated (past)

(organic chemistry) To produce or to undergo methylenation


methylkaempferol

(organic chemistry) Any methyl derivative of kaempferol


methylmaleimide

(organic chemistry) Any methyl derivative of maleimide


methylpyridinium

(organic chemistry) Any methyl derivative of a pyridinium ion


methylthiourea

(organic chemistry) Any methyl derivative of thiourea.


monoacetoxylation

(organic chemistry) The addition of a single acetoxyl group


monoalkoxylated

(organic chemistry) Modified by the addition of a single alkoxy group


monoallylated

(organic chemistry) Modified by the addition of a single allyl group


monoazido

(organic chemistry, especially in combination) A single azido group in a molecule


monophenyl

(organic chemistry, especially in combination) A single phenyl group in a molecule


naphthonitrile

(organic chemistry) The nitrile of a naphthoic acid


naphthylmethyl

(organic chemistry, especially in combination) Any naphthyl derivative of a methyl group


neohexene

(organic chemistry) The aliphatic alkene 3,3-dimethyl-1-butene


nitroethylene

(organic chemistry) Any nitro derivative of ethylene


nitronaphthalene

(organic chemistry) Any nitro derivative of naphthalene


nitrosoalkene

(organic chemistry) Any nitroso derivative of an alkene


nonadiene

(organic chemistry) Any of several isomeric unsaturated hydrocarbons having nine carbon atoms and two double bonds


nucleosidation

(organic chemistry) Reaction with, or conversion to, a nucleoside


nucleosyl

(organic chemistry, especially in combination) Any univalent radical derived from a nucleoside


octafluoro

(organic chemistry, in combination) Eight fluorine atoms in a compound.


oxathiirane

en-noun

oxathiirane (countable and uncountable, plural oxathiiranes)

(organic chemistry) A saturated three-membered heterocycle containing one carbon, one sulfur and one oxygen atoms


oxaza-

(organic chemistry) Used to name compounds in which two carbon atoms have been replaced by one of oxygen and one of nitrogen


oxazaphospholidine

oxazaphospholidine (countable and uncountable, plural oxazaphospholidines)

(organic chemistry) A saturated five-membered heterocycle having two carbon atoms, and one each of oxygen, nitrogen and phosphorus


oxazinium

(organic chemistry) A cation derived from an oxazine or related compound


oxazolium

(organic chemistry) A cation derived from a oxazole


oxobutanoate

(organic chemistry) Any derivative of a butanoate in which a methylene group has been replaced by a carbonyl group


oxocarboxylate

(organic chemistry) Any derivative of a carboxylate in which a methylene group has been replaced by a carbonyl group


oxocarboxylic

(organic chemistry) Relating to a carboxylic acid in which a methylene group has been replaced by a carbonyl group


oxocholesterol

(organic chemistry) Any derivative of cholesterol in which a methylene group has been replaced by a carbonyl group


oxoindolizidine

(organic chemistry) Any derivative of indolizidine in which a methylene group has been replaced by a carbonyl group


palominol

(organic chemistry) A particular marine diterpenoid related to dolabellane


parylene

(organic chemistry) A polymer of p-xylene


pegamine

(organic chemistry) An amine derived from polyethylene glycol (PEG)


pentaacetylated

(organic chemistry) Modified by the addition of five acetyl groups


pentaacetylation

(organic chemistry) Modification by the addition of five acetyl groups


pentacetate

(organic chemistry) Alternative form of pentaacetate


pentafluoroethyl

(organic chemistry, especially in combination) Any pentafluoro derivative of an ethyl group


pentynyl

(organic chemistry, especially in combination) A univalent radical derived from a pentyne


peracetylation

(organic chemistry) acetylation in which all available sites are acetylated


perbromo

(organic chemistry, especially in combination) Describing a derivative in which all hydrogen atoms have been replaced by bromine


perchloro

(organic chemistry, especially in combination) Describing a derivative in which all hydrogen atoms have been replaced by chlorine


parasafranine

(organic chemistry) The compound C₂₀H₁₈N₄, obtainable from mauveine.


carbocupration

(organic chemistry) A carbometallation reaction involving copper.


perester

(organic chemistry) The ester of a peracid


persubstituted

(organic chemistry) substituted at all available positions


pervilleine

(organic chemistry) Any of a group of alkaloids related to tropane


phenoxenium

(organic chemistry) An unstable cation resulting from loss of a hydride ion from the hydroxyl group of a phenol


phenylation

(organic chemistry) Any reaction in which phenyl groups are added to a molecule


phenylazirine

(organic chemistry, especially in combination) Any phenyl derivative of an azirine


phenyloxy

(organic chemistry, especially in combination) Synonym of phenoxy


phenylsulfinyl

(organic chemistry, especially in combination) Any phenyl derivative of a sulfinyl group


phenylsulfonyl

(organic chemistry, especially in combination) Any phenyl derivative of a sulfonyl group


phosphitylated

(organic chemistry) Modified by phosphitylation


phosphitylation

(organic chemistry) The addition reaction of a phosphite


azidoazide azide

From azido- + azide + azide.
Coined by blogger Derek Lowe as a joke when referring to "1-diazidocarbamoyl-5-azidotetrazole"

Next up, we have the most explosive compound ever produced, the extremely fun to say azidoazide azide.

2016 January 20, Bec Crew, “WATCH: 5 of The World's Most Dangerous Chemicals”, in Science Alert:

Azidoazide azide, known by its chemical formula C₂N₁₄ or as N-amino azidotetrazole, was created by the US Army and a team of German scientists in 2010.

2016 September 28, Marlese Lessing, “Weird Wednesdays: The world's most volatile substance”, in UConn Daily Campus:

Azidoazide azide is a member of this group and is composed predominantly of nitrogen atoms.

2017 April 3, Orla Sherwood, “Do Not Try This At Home”, in University Observer:

(informal, organic chemistry) A very hazardous explosive inorganic heterocyclic molecule, namely 1-diazidocarbamoyl-5-azidotetrazole


phosphonodithioate

(organic chemistry) Any sulfur derivative of a phosphonate that has the form R-O-PH(=S)S⁻


phosphonoformate

phosphonoformic acid
phosphonoformic acid

(organic chemistry) Any salt of phosphonoformic acid


phosphonoselenoate

(organic chemistry) Any anion of the form R-O-PH(=O)-Se⁻


phosphonothioate

(organic chemistry) Any anion of the form R-O-PH(=O)-S⁻ (or similar forms having the negative charge on the oxygen atom)


phosphonyl

(organic chemistry, especially in combination) Any radical derived from a phosphonic acid


phthalaldehyde

phthalaldehyde (countable and uncountable, plural phthalaldehydes)

(organic chemistry) Any of three isomers of the dialdehyde C₆H₄(CHO)₂ derived from a phthalic acid (but especially the "ortho" isomer)


pinacolato

(organic chemistry, especially in combination) A pinacolate ester as a substituent


pivalic

Blend of pinacolin + valeric acid indicating that the eponymous acid is the isomer of valeric acid produced by oxidizing pinacolin.

(organic chemistry) Relating to pivalic acid or its derivatives.


polyethercarbonate

polyethercarbonates (plural)
poly(ethercarbonate) (alternative)

(organic chemistry) Any polymer, or the form [-R-O-CO-O-CH₂-O-]ₙ that has both ether and carbonate groups


polyfluoroalkyl

polyfluoroalkyls (plural)
polyfluoralkyl (alternative)

From polyfluoro + alkyl, equivalent to poly- + fluoro- + alkyl.

After research into foam at the Belgian seaside showing a concentration of per- and polyfluoroalkyl substances (PFAS) – widely used for their waterproofing qualities but difficult to destroy – the Dutch public health institute RIVM measured the coast in Zeeland, north and south Holland in April and August.

2023 December 13, Senay Boztas, “Netherlands warns children not to swallow sea foam over PFAS concerns”, in The Guardian, →ISSN:

(organic chemistry, especially in combination) Any polyfluoro derivative of an alkyl group.


polyfluoroalkylated

(organic chemistry) Modified by the addition of one or more polyfluoroalkyl grops


polyfused

(organic chemistry) Having multiple rings fused together (with at least one atom that is each part of several rings)


polyprenylated

(organic chemistry) Modified by the addition of multiple isoprenoid groups


polypyridyl

(organic chemistry, especially in combination) Multiple pyridyl groups in a molecule


polyserine

(organic chemistry) A polypeptide composed of only serine amino acids

(organic chemistry) A sequence of a protein composed of only serine amino acids


polytyrosine

(organic chemistry) A polypeptide composed of only tyrosine amino acids

(organic chemistry) A sequence of a protein composed of only tyrosine amino acids


prolineamide

(organic chemistry) The amide of the amino acid proline


pyrazino

(organic chemistry, especially in combination) A pyrazinyl radical as a substituent


pyrido

(organic chemistry, especially in combination) A pyridyl radical as a substituent


pyridylsulfoximine

(organic chemistry) Any pyridyl sulfoximine


pyrrolinone

(organic chemistry) A cyclic ketone formally derived from 2-pyrroline


quinazolino

(organic chemistry, especially in combination) A radical derived from a quinazoline


quinoidization

Our hypothesis is similar for these dications: dication formation provokes the quinoidization of the thienyl core, but this quinoidal structure is not indefinitely stable and there is an oligomer length at which it experiences instability, turning into an aromatic-like structure with a biradicaloid nature.

2011, Sandra R. González, “The frontiers of quinoidal stability in long oligothiophenes: raman spectra of dicationic polaron pairs”, in Journal of the American Chemical Society, volume 133, number 41, page 16350:

(organic chemistry) Modification by addition of, or conversion to a quinone.


rhamnocitrin

(organic chemistry) The cyclic ketone 3,5-dihydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one


salicylaldimine

(organic chemistry) The aldimine of salicylaldehyde


selenoalkoxylation

selenoalkoxylation (countable and uncountable, plural selenoalkoxylations)

(organic chemistry) The addition reaction of a selenium atom and an alkoxyl group across a double bond


selenoether

(organic chemistry) Any compound, of the form R-Se-R', formally derived from an ether by replacing the oxygen atom by one of selenium


silatropy

rearrangement reaction
rearrangement reaction

(organic chemistry) A rearrangement reaction in which a silyl group (typically a trimethylsilyl group) is moved from one place to another in a molecukr


silylbenzyl

(organic chemistry, especially in combination) Any silyl derivative of a benzyl group


silylketene

(organic chemistry) Any silyl derivative of a ketene


spiroazirine

(organic chemistry) A spiro compound, one of whose rings is an azirine


squaramide

(organic chemistry) The amide of squaric acid


sulfanylphenol

(organic chemistry) Any sulfanyl derivative of a phenol


sulfonimine

(organic chemistry) The imine of a sulfonic acid


terpyridyl

(organic chemistry, especially in combination) A radical derived from terpyridine


tetrahydroquinoline

(organic chemistry) An aromatic heterocyclic amine composed of a benzene ring fused to one of piperidine


tetraoctanoate

(organic chemistry) Any compound that has four octanoate groups or ions


tetrazolo

(organic chemistry, especially in combination) A radical derived from a tetrazole


tetrazolopyrimidine

(organic chemistry) Any tetrazolo derivative of pyrimidine


thiobenzophenone

thiobenzophenone (countable and uncountable, plural thiobenzophenones)

(organic chemistry) The thioketone analogous to benzophenone


thiochromane

thiochromane (countable and uncountable, plural thiochromanes)

(organic chemistry) The bicyclic heterocycle formally derived from chromane by replacing the oxygen atom by one of sulfur


thiochromene

thiochromene (countable and uncountable, plural thiochromenes)

(organic chemistry) The bicyclic heterocycle formally derived from chromene by replacing the oxygen atom by one of sulfur


thioglycosylation

(organic chemistry) The reaction, analogous to a glycosylation, that forms a thioglycoside


thiotetracene

(organic chemistry) A polycyclic aromatic compound consisting of a thiophene ring fused to tetracene


thymidyl

(organic chemistry, especially in combination) A univalent radical derived from thymidine by loss of a hydroxy group


toluidinyl

(organic chemistry, especially in combination) A radical derived from toluidine


tosylazetidine

(organic chemistry) Any tosyl derivative of azetidine


tosylaziridine

(organic chemistry) Any tosyl derivative of aziridine


tosylnucleoside

(organic chemistry) Any tosyl derivative of a nucleoside


tosylthymidine

(organic chemistry) Any tosyl derivative of thymidine


triazolium

(organic chemistry) A cation produced by protonation of a triazole


triazolo

(organic chemistry, especially in combination) A triazole moiety as a substituent


trifluoroacetoxy

(organic chemistry, especially in combination) Any trifluoro derivative of an acetoxy group


trifluoroacetoxylation

(organic chemistry) The addition reaction of a trifluoroacetoxy group


trifluoroethylamine

(organic chemistry) Any trifluoro derivative of ethylamine


trihydroxybenzene

(organic chemistry) Any trihydroxy derivative of benzene


trihydroxycholesterol

(organic chemistry) Any trihydroxy derivative of cholesterol, but especially (3β)-cholest-5-ene-1,1,2,3-tetrol


trimethoxy

(organic chemistry, especially in combination) Three methoxy groups in a molecule


trimethylaluminium

(organic chemistry) The organometallic compound (CH₃)₃Al


trimethylaniline

(organic chemistry) Any trimethyl derivative of aniline


trimethylphenol

(organic chemistry) Any trimethyl derivative of phenol


triphenylaluminium

(organic chemistry) The organometallic compound (C₆H₅)₃Al


triphosphole

(organic chemistry) Either of two isomeric unsaturated organic heterocycles that have two carbon atoms, three phosphorus atoms and two double bonds


tripropargylamine

(organic chemistry) The tertiary amine (HC≡C-CH₂)₃N


trispirane

(organic chemistry) Any compound having four rings linked spirocyclically via three carbon atoms


tetraspirane

(organic chemistry) Any compound having five rings linked spirocyclically via four carbon atoms


tritylate

(organic chemistry) The anion of triphenylmethanol


trivinylphosphine

trivinylphosphine (countable and uncountable, plural trivinylphosphines)

(organic chemistry) The organic phosphine (CH₂=CH)₃P


truxinate

(organic chemistry) Any salt or ester of truxinic acid


truxinic acid

(organic chemistry) The dicarboxylic acid 3,4-diphenyl-1,2-cyclobutanedicarboxylic acid


arophatic

The cyclic re-structuring of arophatic a-C(:H) nano-particles appears to be a viable route to formation of H2 for low to moderate radiation field intensities (1 < G_0 < 10^2), even when the dust is warm (T ~ 50 - 100 K)..

2015, A.P. Jones, E. Habart, “H2 formation via the UV photo-processing of a-C:H nano-particles”, in arXiv:

(informal, organic chemistry) Having both aliphatic and aromatic properties


perfluorohexacene

Here we investigated the physisorption of long-chain acenes, namely, hexacene and its fluorinated derivative perfluorohexacene, on bilayer graphene for tunable graphene devices using first principles methods.

2015, Yuefeng Yin, Jiri Cervenka, Nikhil V. Medhekar, “Tunable Hybridization Between Electronic States of Graphene and Physisorbed Hexacene”, in arXiv:

(organic chemistry) Any perfluoro derivative of a hexacene


beinséin

head

beinséin f (genitive singular beinséine)

beinséine (genitive singular)
nominative (indefinite)
beinséin (indefinite singular)
vocative (indefinite)
a bheinséin (indefinite singular)
genitive (indefinite)
beinséine (indefinite singular)
dative (indefinite)
nominative (definite)
an bheinséin (definite singular)
genitive (definite)
na beinséine (definite singular)
dative (definite)
leis an mbeinséin (definite singular)
don bheinséin (definite singular)
beinséin
bheinséin
mbeinséin
beinsín (alternative)


hexathiol

Using first-principle calculations, we propose the first demonstration of electron doping induced multiple quantum phase transition in a single material of the organometallic framework, HTT-Pt, which has been synthesized by reacting triphenylene hexathiol molecules (HTT) with PtCl2.

2015, Xiaoming Zhang, Mingwen Zhao, Feng Liu, “Tunable Topological States in Electron-Doped HTT-Pt”, in arXiv:

(organic chemistry) Any compound that has six thiol groups


內酯

/neɪ̯⁵¹ ʈ͡ʂʐ̩²¹⁴⁻²¹⁽⁴⁾/

/nɔːi̯²² t͡siː³⁵/

/neɪ̯⁵¹ ʈ͡ʂʐ̩²¹⁴⁻²¹⁽⁴⁾/

/nɔːi̯²² t͡siː³⁵/


甲醇

/t͡ɕi̯ä²¹⁴⁻²¹ ʈ͡ʂʰu̯ən³⁵/

/t͡ɕi̯ä²¹⁴⁻²¹ ʈ͡ʂʰu̯ən³⁵/


甲酸

/t͡ɕi̯ä²¹⁴⁻²¹ su̯än⁵⁵/

/t͡ɕi̯ä²¹⁴⁻²¹ su̯än⁵⁵/

(organic chemistry) methanoic acid; formic acid


硝化甘油

ㄒㄧㄠ ㄏㄨㄚˋ ㄍㄢ ㄧㄡˊ

/ɕi̯ɑʊ̯⁵⁵ xu̯ä⁵¹ kän⁵⁵ joʊ̯³⁵/

/siːu̯⁵⁵ faː³³ kɐm⁵⁵ jɐu̯²¹/

/ɕi̯ɑʊ̯⁵⁵ xu̯ä⁵¹ kän⁵⁵ joʊ̯³⁵/

/siːu̯⁵⁵ faː³³ kɐm⁵⁵ jɐu̯²¹/

(organic chemistry) nitroglycerine; glyceryl trinitrate (GTN)


taxiphyllin

(organic chemistry) A chemical produced in many plants, belonging to cyanogenic glycosides, having the formula C₁₄H₁₇NO₇.


dhurrin

From Arabic ذُرَة (ḏura, “sorghum”) + -in.


dimyristoylphosphatidylcholine

As an example, we applied the method for mixed monolayers with different proportions of distearoylphosphatidylcholine (DSPC) and dimyristoylphosphatidylcholine (DMPC) and obtained the excess dipolar density, which were in agreement with those obtained from surface potential measurements.

2015, Elena Rufeil Fiori, Natalia Wilke, Adolfo J. Banchio, “Inter-domain dipolar repulsion in lipid monolayers with phase coexistence”, in arXiv:

(organic chemistry) A form of lecithin (phosphatidylcholine) in which both acyl groups are myristoyls


distearoylphosphatidylcholine

(organic chemistry) A form of lecithin (phosphatidylcholine) in which both acyl groups are stearoyls


丙醇

/piŋ²¹⁴⁻²¹ ʈ͡ʂʰu̯ən³⁵/

/pɪŋ³⁵ sɵn²¹/

/piŋ²¹⁴⁻²¹ ʈ͡ʂʰu̯ən³⁵/

/pɪŋ³⁵ sɵn²¹/


polyanhydride

(organic chemistry) The acid anhydride of a polycarboxylic acid


αιθίνιο

aithínio (romanization)
αιθίνιο (nominative singular)
αιθινίου (genitive singular)
αιθίνιο (accusative singular)
αιθίνιο (singular vocative)

(organic chemistry) ethyne (IUPAC name), acetylene


αιθυλένιο

αιθυλένιο • (aithylénio) n (uncountable)

aithylénio (romanization)
αιθυλένιο (nominative singular)
αιθυλενίου (genitive singular)
αιθυλένιου (genitive singular)
αιθυλένιο (accusative singular)
αιθυλένιο (singular vocative)

(organic chemistry) ethylene, ethene (IUPAC name)


αιθένιο

aithénio (romanization)
αιθένιο (nominative singular)
αιθενίου (genitive singular)
αιθένιο (accusative singular)
αιθένιο (singular vocative)

(organic chemistry) ethene (IUPAC name), ethylene


ασετυλίνη

asetylíni (romanization)
ασετυλίνη (nominative singular)
ασετυλίνης (genitive singular)
ασετυλίνη (accusative singular)
ασετυλίνη (singular vocative)
ασετιλίνη (alternative)

(organic chemistry) acetylene, ethyne (IUPAC name)


tert-butylhydroquinone

tert-butylhydroquinones (plural)
tertbutylhydroquinone (alternative)
tertbutyl hydroquinone (alternative)
tert-butyl hydroquinone (alternative)

(organic chemistry) A preservative of fats and oils, used in food. An aromatic organic compound that is a type of phenol. It is a derivative of hydroquinone, substituted with a tertbutyl group.


胺基

/ˀän⁵¹ t͡ɕi⁵⁵/

/ˀän⁵⁵ t͡ɕi⁵⁵/

/ɔːn⁵⁵ kei̯⁵⁵/

/ˀän⁵¹ t͡ɕi⁵⁵/

/ˀän⁵⁵ t͡ɕi⁵⁵/

/ɔːn⁵⁵ kei̯⁵⁵/

(Taiwan, organic chemistry) amino; amino group


antóiciainin

antóiciainin f (genitive singular antóiciainine, nominative plural antóiciaininí)

antóiciainine (genitive singular)
antóiciaininí (nominative plural)
nominative (indefinite)
antóiciainin (indefinite singular)
antóiciaininí (indefinite plural)
vocative (indefinite)
a antóiciainin (indefinite singular)
a antóiciaininí (indefinite plural)
genitive (indefinite)
antóiciainine (indefinite singular)
dative (indefinite)
nominative (definite)
an antóiciainin (definite singular)
na hantóiciaininí (definite plural)
genitive (definite)
na hantóiciainine (definite singular)
na n-antóiciaininí (definite plural)
dative (definite)
leis an antóiciainin (definite singular)
don antóiciainin (definite singular)
leis na hantóiciaininí (definite plural)
antóiciainin
n-antóiciainin
hantóiciainin


dioctylbenzothienobenzothiophene

Here, we fabricate hybrid 2D heterostructures with p-type dioctylbenzothienobenzothiophene (C8-BTBT) and n-type MoS2.

183103 (2015), Daowei He, Yiming Pan, Haiyan Nan, Shuai Gu, Ziyi Yang, Bing Wu, Xiaoguang Luo, Bingchen Xu, Yuhan Zhang, Yun Li, Zhenhua Ni, Baigeng Wang, Jia Zhu, Yang Chai, Yi Shi, Xinran Wang, “A van der Waals pn heterojunction with organic/inorganic semiconductors”, in Applied Physics Letters, volume 183103:

(organic chemistry) The dioctyl derivative of benzothienobenzothiophene


benzothienobenzothiophene

en-noun

benzothienobenzothiophene (countable and uncountable, plural benzothienobenzothiophenes)

(organic chemistry) Any of a family of tetracyclic organic heterocycles composed of two fused benzothiophene groups, especially [1]benzothieno[3,2-b][1]benzothiophene, the basis of organic conductors of electricity


diphenylbutadiene

diphenylbutadiene (countable and uncountable, plural diphenylbutadienes)

A first prototype has been developed relying on the low density and high light yield of the diphenylbutadiene doped para-therphenyl organic scintillator.

2015, Elena Solfaroli Camillocci, Fabio Bellini, Valerio Bocci, Francesco Collamati, Erika De Lucia, Riccardo Faccini, Michela Marafini, Ilaria Mattei, Silvio Morganti, Riccardo Paramatti, Vincenzo Patera, Davide Pinci, Luigi Recchia, Andrea Russomando, Alessio Sarti, Adalberto Sciubba, Martina Senzacqua, Cecilia Voena, “Polycrystalline para-terphenyl scintillator adopted in a β⁻ detecting probe for radio-guided surgery”, in Journal of Physics: Conference Series, volume 620:

(organic chemistry) Any diphenyl derivative of butadiene, but especially trans,trans-1,4-diphenyl-1,3-butadiene


cyclodehydrogenation

Here, we describe the successful bottom-up synthesis of ZGNRs, which are fabricated by the surface-assisted colligation and cyclodehydrogenation of specifically designed precursor monomers including carbon groups that yield atomically precise zigzag edges.

2015, Pascal Ruffieux, Shiyong Wang, Bo Yang, Carlos Sanchez, Jia Liu, Thomas Dienel, Leopold Talirz, Prashant Shinde, Carlo A. Pignedoli, Daniele Passerone, Tim Dumslaff, Xinliang Feng, Klaus Muellen, Roman Fasel, “On-surface synthesis of graphene nanoribbons with zigzag edge topology”, in arXiv:

(organic chemistry) Any reaction in which cyclization is accompanied by dehydrogenation


bicyclohexane

bicyclohexane (countable and uncountable, plural bicyclohexanes)

We study both 5CB and a binary mixture of bicyclohexane derivatives (CCN-47 and CCN-55).

2016, Lisa Tran, Maxim O. Lavrentovich, Daniel A. Beller, Ningwei Li, Kathleen J. Stebe, Randall D. Kamien, “Lassoing Saddle-Splay: Topological Control of Topological Defects”, in arXiv:

(organic chemistry) The bicyclic alicyclic hydrocarbon cyclohexylcyclohexane


glycoanalyst

(organic chemistry) A scientist who analyzes carbohydrates


polyperylene

polyperylene (countable and uncountable, plural polyperylenes)

Bond order studies show that zigzag fused naphthalene does not have tendency to distort while armchair fused naphthalene and polyperylene have a tendency to distort along the edges.

2016, V. M. L. Durga Prasad Goli, Suryoday Prodhan, Sumit Mazumdar, S. Ramasesha, “Correlated Electronic Properties of Some Graphene Nanoribbons: A DMRG Study”, in arXiv:

(organic chemistry) Any polymer composed of perylene moieties either fused together or joined by single bonds


butenone

butenone (countable and uncountable, plural butenones)

The code was then used to study a Diels-Alder reaction of cyclopentadiene and butenone by ab initio string method.

2016, Sergi Ruiz-Barragan, Kazuya Ishimura, Motoyuki Shiga, “On the hierarchical parallelization of ab initio simulations”, in arXiv:

(organic chemistry) The unsaturated aliphatic ketone but-3-en-2-one CH₂=CH-CO-CH₃


亞碸

/jä⁵¹ fɤŋ⁵⁵/

/jä²¹⁴⁻²¹ fɤŋ⁵⁵/

/aː³³ fʊŋ⁵⁵/

/jä⁵¹ fɤŋ⁵⁵/

/jä²¹⁴⁻²¹ fɤŋ⁵⁵/

/aː³³ fʊŋ⁵⁵/


Baldwin's rules

(organic chemistry) A series of guidelines outlining the relative favorabilities of ring closure reactions in alicyclic compounds.


diphenylethyne

diphenylethyne (countable and uncountable, plural diphenylethynes)

A combination of classical molecular dynamics (MM/MD) and quantum chemical calculations based on the density functional theory (DFT) was performed to describe conformational properties of diphenylethyne (DPE), methylated-DPE and poly para phenylene ethynylene (PPE).

2016, Behnaz Bagheri, Björn Baumeier, Mikko Karttunen, “Getting excited: Challenges in quantum-classical studies of excitons in polymeric systems”, in arXiv:

(organic chemistry) Synonym of diphenylacetylene


methanimine

methanimine (countable and uncountable, plural methanimines)

We conducted survey observations of a glycine precursor, methanimine or methylenimine (CH#95;2NH), with the NRO 45 m telescope and the SMT telescope towards 12 high-mass and two low-mass star-forming regions in order to increase number of CH#95;2NH sources and to better understand the characteristics of CH2NH sources.

2016, Taiki Suzuki, Masatoshi Ohishi, Tomoya Hirota, Masao Saito, Liton Majumdar, Valentine Wakelam, “Survey Observations of a Possible Glycine Precursor, Methanimine (CH₂NH)”, in arXiv:

(organic chemistry) Synonym of azomethine


methylenimine

methylenimine (countable and uncountable, plural methylenimines)


isopentanol

isopentanol (countable and uncountable, plural isopentanols)

As a demonstration, we first establish the correctness of the Jacobian matrices for kinetic models of hydrogen, methane, ethylene, and isopentanol oxidation, then demonstrate the performance achievable on CPUs and GPUs using pyJac via matrix evaluation timing comparisons..

2016, Kyle E. Niemeyer, Nicholas J. Curtis, Chih-Jen Sung, “pyJac: analytical Jacobian generator for chemical kinetics”, in arXiv:

(organic chemistry) Any isomer of n-pentanol, but especially amyl alcohol


cyanoacrylic

An asymmetric A-{\pi}-D-{\pi}-D-{\pi}-A' tribranched organic dye (dye1) with a cyanoacrylic acid and an indolinum carboxyl acid as electron acceptors and a triphenylamine as an electron donor was designed and theoretically investigated for dye-sensitized solar cells (DSSCs).

2016, Geon Hyeong Lee, Young Sik Kim, “Theoretical study of asymmetric A-π-D-π-D-π-A' tribranched organic sensitizer for Dye-sensitized solar cells”, in arXiv:

(organic chemistry) Relating to cyanoacrylic acid or its derivatives

cianacrilico

relating to cyanoacrylic acid or its derivatives


cyanoacrylic acid

cyanoacrylic acid (countable and uncountable, plural cyanoacrylic acids)

(organic chemistry) Any cyano derivative of acrylic acid, but especially 2-cyanoacrylic CH₂=C(CN)COOH


indolinium

quaternary ammonium compound
quaternary ammonium compound

(organic chemistry) A cation or quaternary ammonium compound formed from indole


VX

(organic chemistry) The nerve agent O-ethyl S-[2-(diisopropylamino)ethyl] methylphosphonothioate.


sulfacetic acid

(organic chemistry) The sulfonic acid analogous to acetic acid CH₃SO₂OH


sulfacetic

(organic chemistry) Relating to sulfacetic acid or its derivatives


reazione di Cannizzaro

it-noun

reazione di Cannizzaro f (plural reazioni di Cannizzaro)

Named after Italian chemist Stanislao Cannizzaro (1826–1910), who discovered it.

named-after

(organic chemistry) Cannizzaro reaction (disproportionation of an aldehyde into an alcohol and a carboxylic acid)


нафталин

naftalin (romanization)
нафталин (nominative singular)
нафталиндер (nominative plural)
нафталиннің (genitive singular)
нафталиндердің (genitive plural)
нафталинге (dative singular)
нафталиндерге (dative plural)
нафталинді (accusative singular)
нафталиндерді (accusative plural)
нафталинде (locative singular)
нафталиндерде (locative plural)
нафталиннен (ablative singular)
нафталиндерден (ablative plural)
нафталинмен (instrumental singular)
нафталиндермен (instrumental plural)

kk-decl-noun

нафталиндердің

нафталиндерге

нафталиндерді

нафталиндерде

нафталиндерден

нафталиндермен

Borrowed from Russian нафтали́н (naftalín), ultimately from Ancient Greek νάφθα (náphtha) + -ηνός (-ēnós).

bor+

Kazakh alphabets#Arabic script
Kazakh alphabets#Cyrillic script
Kazakh alphabets#Latin script


нафталин

naftalin (romanization)
нафталин (indefinite singular)
нафталинот (definite singular unspecified)
нафталинов (definite proximal singular)
нафталинон (definite distal singular)
нафталину (singular vocative)


нафталин

ru-noun+

нафтали́новый

нафтали́нный

нафтали́н • (naftalín) m inan (genitive нафтали́на, nominative plural нафтали́ны, genitive plural нафтали́нов, relational adjective нафтали́новый or нафтали́нный)

нафтали́н (canonical)
naftalín (romanization)
нафтали́на (genitive)
нафтали́ны (nominative plural)
нафтали́нов (genitive plural)
нафтали́новый (adjective relational)
нафтали́нный (adjective relational)
нафтали́н (nominative singular)
нафтали́ны (nominative plural)
нафтали́на (genitive singular)
нафтали́нов (genitive plural)
нафтали́ну (dative singular)
нафтали́нам (dative plural)
нафтали́н (accusative singular)
нафтали́ны (accusative plural)
нафтали́ном (instrumental singular)
нафтали́нами (instrumental plural)
нафтали́не (prepositional singular)
нафтали́нах (plural prepositional)


anailín

anailín (genitive singular)
nominative (indefinite)
anailín (indefinite singular)
vocative (indefinite)
a anailín (indefinite singular)
genitive (indefinite)
dative (indefinite)
nominative (definite)
an t-anailín (definite singular)
genitive (definite)
an anailín (definite singular)
dative (definite)
leis an anailín (definite singular)
don anailín (definite singular)
anailín
n-anailín
hanailín
t-anailín

From German Anilin, from Portuguese anil (“indigo”) + -in (“-ine (organic compounds)”).


cocontinuous

Further, this structure is retained even during melt processing without loss of the interpenetrating cocontinuous structure.

1986, Donald R. Paul, Leslie Howard Sperling, Multicomponent polymer materials, page 43:

An example of cocontinuous phases in three dimensions is an air filter and the air that flows through it.

1987, Herman Francis Mark, Jacqueline I. Kroschwitz, Encyclopedia of Polymer Science and Engineering:

Chapter 4 relates photomicrographs of thermoplastics/thermoplastics, thermoplastics/thermosets, and some selected thermoplastic vulcanizates in which the phase morphology is not particularly cocontinuous.

2009, Charef Harrats, Multiphase Polymer- Based Materials, →ISBN:

(organic chemistry) Blending two linear, amorphous polymers such that the phases interpenetrate.


acetilè

acetilens (plural)
acetilé (alternative)


triangulene

en-noun

triangulene (countable and uncountable, plural triangulenes)

From triangular + -ene (“benzenoid/graphene”). From being a triangle composed of benzene rings.

suffix

(organic chemistry) A flat hydrocarbon graphene fragment, C₂₂H₁₂, composed of 6 fused benzene rings in a triangular configuration; being a radical having two unpaired electrons.


青蒿素

/t͡ɕʰiŋ⁵⁵ xɑʊ̯⁵⁵ su⁵¹/

/t͡sʰɪŋ⁵⁵ hou̯⁵⁵ sou̯³³/

/t͡ɕʰiŋ⁵⁵ xɑʊ̯⁵⁵ su⁵¹/

/t͡sʰɪŋ⁵⁵ hou̯⁵⁵ sou̯³³/

(organic chemistry) artemisinin; qinghaosu


tectomer

(organic chemistry) Any of a class of self-assembling compounds composed of two, three or four oligoglycine residues surrounding a central hydrocarbon chain


oligoglycine

(organic chemistry) An oligopeptide composed of glycine residues


PVF

en-noun

PVF (countable and uncountable, plural PVFs)

polyvinyl fluoride
polyvinyl fluoride#English

(organic chemistry) Initialism of polyvinyl fluoride.


PVOH

From polyvinyl (“PV”) and the hydroxyl group -OH found in alcohol.

polyvinyl alcohol
polyvinyl alcohol#English

(organic chemistry) Abbreviation of polyvinyl alcohol.


ακρυλικό οξύ

head

ακρυλικό οξύ • (akrylikó oxý) n (uncountable)

(organic chemistry) acrylic acid, propenoic acid


ακρυλικός

ακρυλικός • (akrylikós) m (feminine ακρυλική, neuter ακρυλικό)

akrylikós (romanization)
ακρυλική (feminine)
ακρυλικό (neuter)
ακρυλικός (masculine nominative singular)
ακρυλική (feminine nominative singular)
ακρυλικό (neuter nominative singular)
ακρυλικοί (masculine nominative)
ακρυλικές (feminine nominative plural)
ακρυλικά (neuter nominative plural)
ακρυλικού (genitive masculine singular)
ακρυλικής (feminine genitive singular)
ακρυλικού (genitive neuter singular)
ακρυλικών (genitive masculine)
ακρυλικών (feminine genitive plural)
ακρυλικών (genitive neuter plural)
ακρυλικό (accusative masculine singular)
ακρυλική (accusative feminine singular)
ακρυλικό (accusative neuter singular)
ακρυλικούς (accusative masculine)
ακρυλικές (accusative feminine plural)
ακρυλικά (accusative neuter plural)
ακρυλικέ (masculine singular vocative)
ακρυλική (feminine singular vocative)
ακρυλικό (neuter singular vocative)
ακρυλικοί (masculine vocative)
ακρυλικές (feminine plural vocative)
ακρυλικά (neuter plural vocative)

el-decl-adj-table

ακρυλικός (akrylikós)

ακρυλική (akrylikí)

ακρυλικό (akrylikó)

ακρυλικοί (akrylikoí)

ακρυλικές (akrylikés)

ακρυλικά (akryliká)

ακρυλικού (akrylikoú)

ακρυλικής (akrylikís)

ακρυλικού (akrylikoú)

ακρυλικών (akrylikón)

ακρυλικών (akrylikón)

ακρυλικών (akrylikón)

ακρυλικό (akrylikó)

ακρυλική (akrylikí)

ακρυλικό (akrylikó)

ακρυλικούς (akrylikoús)

ακρυλικές (akrylikés)

ακρυλικά (akryliká)

ακρυλικέ (akryliké)

ακρυλική (akrylikí)

ακρυλικό (akrylikó)

ακρυλικοί (akrylikoí)

ακρυλικές (akrylikés)

ακρυλικά (akryliká)


προπενικό οξύ

head

προπενικό οξύ • (propenikó oxý) n (uncountable)

(organic chemistry) Synonym of acrylic acid


Citronensäure

de-noun

Citronensäure f (genitive Citronensäure, no plural)

Citronensäure (genitive)
Citronensäure (nominative singular)
Citronensäure (genitive singular)
Citronensäure (dative singular)
Citronensäure (accusative singular)

(organic chemistry) citric acid; alternative form of Zitronensäure


acylhomoserine

(organic chemistry) The N-acyl derivative of homoserine, whose lactone is active in quorum sensing


pentanedione

(organic chemistry) Either of two isomeric aliphatic diketones (2,3-pentanedione, 2,4-pentanedione) derived from pentane


laureth

(organic chemistry) An ethoxylated form of the lauryl radical


bituminosulfonate

ammonium bituminosulfonate
ammonium bituminosulfonate

(organic chemistry, petrochemistry) An anion found in ammonium bituminosulfonate (ichthammol), obtained by dry distillation of oil shale and subsequent sulfonation.


antraicéin

head

antraicéin f (genitive singular antraicéine)

antraicéine (genitive singular)
nominative (indefinite)
antraicéin (indefinite singular)
vocative (indefinite)
a antraicéin (indefinite singular)
genitive (indefinite)
antraicéine (indefinite singular)
dative (indefinite)
nominative (definite)
an antraicéin (definite singular)
genitive (definite)
na hantraicéine (definite singular)
dative (definite)
leis an antraicéin (definite singular)
don antraicéin (definite singular)
antraicéin
n-antraicéin
hantraicéin

From Ancient Greek ἄνθραξ (ánthrax, “coal”) + -éin (“-ene”).


myresyre

myresyre (indefinite nominative singular)
myresyren (definite nominative singular)
myresyres (genitive indefinite singular)
myresyrens (definite genitive singular)


linoxyn

en-noun

linoxyn (usually uncountable, plural linoxyns)

(organic chemistry) Alternative form of linoxin


(organic chemistry) An amphetamine that produces entactogenic and stimulant effects, used recreationally.


葉酸

/jɛ⁵¹ su̯än⁵⁵/

/jɛ⁵¹ su̯än⁵⁵/

(organic chemistry, biochemistry) folic acid


葉酸

葉酸 (canonical)
yōsan (romanization)
efusan (romanization)
えふさん (hiragana historical)


alloaromadendrene

(organic chemistry) The tricyclic hydrocarbon (4aS,7R,7aR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene


bergamotene

bergamotene (countable and uncountable, plural bergamotenes)

(organic chemistry) The unsaturated bicyclic hydrocarbon 4,6-dimethyl-6-(4-methylpent-3-enyl)bicyclo[3.1.1]hept-3-ene found in bergamot


cannabidiolic

(organic chemistry) Relating to cannabidiolic acid or its derivatives


cannabidiolic acid

(organic chemistry) The carboxylic acid 2,4-dihydroxy-3-[(1R,6R)-3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-yl]-6-pentylbenzoic acid found in cannabis.


cannabigerolic

(organic chemistry) Relating to cannabigerolic acid or its derivatives


cannabigerolic acid

(organic chemistry) The carboxylic acid 3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxy-6-pentylbenzoic acid found in cannabis


hydroxyacyl

(organic chemistry) Any hydroxy derivative of an acyl radical


olivetolic

(organic chemistry) Relating to olivetolic acid or its derivatives


olivetolic acid

(organic chemistry) The carboxylic acid 2,4-dihydroxy-6-pentylbenzoic acid related to olivetol


カプサイシン

[ka̠pɯ̟̊sa̠iɕĩɴ]


Isobutan

de-noun

Isobutan n (strong, genitive Isobutans, no plural)

Isobutans (genitive)
Isobutan (nominative singular)
Isobutans (genitive singular)
Isobutan (dative singular)
Isobutan (accusative singular)


蘋果酸

ㄆㄧㄥˊ ㄍㄨㄛˇ ㄙㄨㄢ

/pʰiŋ³⁵ ku̯ɔ²¹⁴⁻²¹ su̯än⁵⁵/

/pʰɪŋ²¹ kʷɔː³⁵ syːn⁵⁵/

/pʰiŋ³⁵ ku̯ɔ²¹⁴⁻²¹ su̯än⁵⁵/

/pʰɪŋ²¹ kʷɔː³⁵ syːn⁵⁵/


clupein

(organic chemistry) A protamine found in herring.


salmine

(organic chemistry) A protamine found in salmon.


亞士匹靈

/aː³³ siː²² pʰɐt̚⁵ lɪŋ²¹/

/aː³³ siː²² pʰɐt̚⁵ lɪŋ²¹/

(Cantonese, organic chemistry, pharmacology) aspirin


哥羅芳

/kɤ⁵⁵ lu̯ɔ³⁵ fɑŋ⁵⁵/

/kɔː⁵⁵ lɔː²¹ fɔːŋ⁵⁵/

/kɤ⁵⁵ lu̯ɔ³⁵ fɑŋ⁵⁵/

/kɔː⁵⁵ lɔː²¹ fɔːŋ⁵⁵/

(chiefly Cantonese, organic chemistry) chloroform


阿斯匹靈

ㄚ ㄙ ㄆㄧˇ ㄌㄧㄥˊ

/ˀä⁵⁵ sz̩⁵⁵ pʰi²¹⁴⁻²¹ liŋ³⁵/

/ˀä⁵⁵ sz̩⁵⁵ pʰi⁵⁵ liŋ³⁵/

/aː³³ siː⁵⁵ pʰɐt̚⁵ lɪŋ²¹/

/a¹¹ sɨ⁵⁵ pʰi⁵⁵ lin³¹/

/a⁴⁴⁻³³ su⁵³⁻⁴⁴ pʰi⁵³⁻⁴⁴ lin⁵³/

/a⁴⁴⁻³³ su⁴¹⁻⁴⁴ pʰi⁴¹⁻⁴⁴ lin⁴¹/

/ˀä⁵⁵ sz̩⁵⁵ pʰi²¹⁴⁻²¹ liŋ³⁵/

/ˀä⁵⁵ sz̩⁵⁵ pʰi⁵⁵ liŋ³⁵/

/aː³³ siː⁵⁵ pʰɐt̚⁵ lɪŋ²¹/

/a¹¹ sɨ⁵⁵ pʰi⁵⁵ lin³¹/

/a⁴⁴⁻³³ su⁵³⁻⁴⁴ pʰi⁵³⁻⁴⁴ lin⁵³/

/a⁴⁴⁻³³ su⁴¹⁻⁴⁴ pʰi⁴¹⁻⁴⁴ lin⁴¹/

Phono-semantic matching of English aspirin.

psm

(chiefly Taiwan, organic chemistry, pharmacology) aspirin


阿斯巴甜

/ˀä⁵⁵ sz̩⁵⁵ pä⁵⁵ tʰi̯ɛn³⁵/

/aː³³ siː⁵⁵ paː⁵⁵ tʰiːm²¹/

/ˀä⁵⁵ sz̩⁵⁵ pä⁵⁵ tʰi̯ɛn³⁵/

/aː³³ siː⁵⁵ paː⁵⁵ tʰiːm²¹/

Phono-semantic matching of English aspartame.


雙酚A

/ʂu̯ɑŋ⁵⁵ fən⁵⁵ ˀeɪ̯⁵⁵/

/ʂu̯ɑŋ⁵⁵ fən⁵⁵ ˀeɪ̯⁵⁵/


海藻酸

хайцзаосуань

/xaɪ̯²¹⁴⁻³⁵ t͡sɑʊ̯²¹⁴⁻²¹ su̯än⁵⁵/

/xaɪ̯²¹⁴⁻³⁵ t͡sɑʊ̯²¹⁴⁻²¹ su̯än⁵⁵/

(organic chemistry, biochemistry) alginic acid


烏洛托品

ㄨ ㄌㄨㄛˋ ㄊㄨㄛ ㄆㄧㄣˇ

/u⁵⁵ lu̯ɔ⁵¹ tʰu̯ɔ⁵⁵ pʰin²¹⁴⁻²¹⁽⁴⁾/

/u⁵⁵ lu̯ɔ⁵¹ tʰu̯ɔ⁵⁵ pʰin²¹⁴⁻²¹⁽⁴⁾/

(organic chemistry) urotropine; hexamethylenetetramine; methenamine


福爾馬林

ㄈㄨˊ ㄦˇ ㄇㄚˇ ㄌㄧㄣˊ

/fu³⁵ ˀɤɻ²¹⁴⁻³⁵ mä²¹⁴⁻²¹ lin³⁵/

/fu³⁵ ˀɤɻ²¹⁴⁻³⁵ mä²¹⁴⁻²¹ lin³⁵/

(organic chemistry, colloquial) formalin


氟利昂

/fu³⁵ li⁵¹ ˀɑŋ³⁵/

/fu³⁵ li⁵¹ ˀɑŋ³⁵/

(organic chemistry, refrigeration) freon


雷酸

/leɪ̯³⁵ su̯än⁵⁵/

/leɪ̯³⁵ su̯än⁵⁵/


立方烷

/li⁵¹ fɑŋ⁵⁵ wän³⁵/

/li⁵¹ fɑŋ⁵⁵ wän³⁵/


金剛烷

цзиньганвань

/t͡ɕin⁵⁵ kɑŋ⁵⁵ wän³⁵/

/kɐm⁵⁵ kɔːŋ⁵⁵ jyːn²¹⁻³⁵/

/t͡ɕin⁵⁵ kɑ̃³³ ɦuø²¹/

/t͡ɕin⁵⁵ kɑŋ⁵⁵ wän³⁵/

/kɐm⁵⁵ kɔːŋ⁵⁵ jyːn²¹⁻³⁵/

/t͡ɕin⁵⁵ kɑ̃³³ ɦuø²¹/


卡賓

/kʰä²¹⁴⁻²¹ pin⁵⁵/

/kʰä²¹⁴⁻²¹ pin⁵⁵/

(organic chemistry) carbene (highly reactive molecule)


硬脂酸

/iŋ⁵¹ ʈ͡ʂʐ̩⁵⁵ su̯än⁵⁵/

/iŋ⁵¹ ʈ͡ʂʐ̩²¹⁴⁻²¹ su̯än⁵⁵/

/ŋaːŋ²² t͡siː⁵⁵ syːn⁵⁵/

/iŋ⁵¹ ʈ͡ʂʐ̩⁵⁵ su̯än⁵⁵/

/iŋ⁵¹ ʈ͡ʂʐ̩²¹⁴⁻²¹ su̯än⁵⁵/

/ŋaːŋ²² t͡siː⁵⁵ syːn⁵⁵/


軟脂酸

жуаньчжисуань

/ʐu̯än²¹⁴⁻²¹ ʈ͡ʂʐ̩⁵⁵ su̯än⁵⁵/

/ʐu̯än²¹⁴⁻³⁵ ʈ͡ʂʐ̩²¹⁴⁻²¹ su̯än⁵⁵/

/ʐu̯än²¹⁴⁻²¹ ʈ͡ʂʐ̩⁵⁵ su̯än⁵⁵/

/ʐu̯än²¹⁴⁻³⁵ ʈ͡ʂʐ̩²¹⁴⁻²¹ su̯än⁵⁵/


月桂酸

ㄩㄝˋ ㄍㄨㄟˋ ㄙㄨㄢ

/ɥɛ⁵¹⁻⁵³ ku̯eɪ̯⁵¹ su̯än⁵⁵/

/ɥɛ⁵¹⁻⁵³ ku̯eɪ̯⁵¹ su̯än⁵⁵/


煙酸

/jɛn⁵⁵ su̯än⁵⁵/

/jɛn⁵⁵ su̯än⁵⁵/

(organic chemistry, biochemistry) niacin


抗壞血酸

ㄎㄤˋ ㄏㄨㄞˋ ㄒㄩㄝˋ ㄙㄨㄢ

ㄎㄤˋ ㄏㄨㄞˋ ㄒㄩㄝˇ ㄙㄨㄢ

ㄎㄤˋ ㄏㄨㄞˋ ㄒㄧㄝˇ ㄙㄨㄢ

канхуайсюэсуань

/kʰɑŋ⁵¹⁻⁵³ xu̯aɪ̯⁵¹⁻⁵³ ɕy̯ɛ⁵¹ su̯än⁵⁵/

/kʰɑŋ⁵¹⁻⁵³ xu̯aɪ̯⁵¹ ɕy̯ɛ²¹⁴⁻²¹ su̯än⁵⁵/

канхуайсесуань

/kʰɑŋ⁵¹⁻⁵³ xu̯aɪ̯⁵¹ ɕi̯ɛ²¹⁴⁻²¹ su̯än⁵⁵/

/kʰɑŋ⁵¹⁻⁵³ xu̯aɪ̯⁵¹⁻⁵³ ɕy̯ɛ⁵¹ su̯än⁵⁵/

/kʰɑŋ⁵¹⁻⁵³ xu̯aɪ̯⁵¹ ɕy̯ɛ²¹⁴⁻²¹ su̯än⁵⁵/

/kʰɑŋ⁵¹⁻⁵³ xu̯aɪ̯⁵¹ ɕi̯ɛ²¹⁴⁻²¹ su̯än⁵⁵/

(organic chemistry, biochemistry) ascorbic acid


視黃醇

ㄕˋ ㄏㄨㄤˊ ㄔㄨㄣˊ

/ʂʐ̩⁵¹ xu̯ɑŋ³⁵ ʈ͡ʂʰu̯ən³⁵/

/ʂʐ̩⁵¹ xu̯ɑŋ³⁵ ʈ͡ʂʰu̯ən³⁵/

(organic chemistry, biochemistry) retinol


非那西汀

ㄈㄟ ㄋㄚˋ ㄒㄧ ㄊㄧㄥ

/feɪ̯⁵⁵ nä⁵¹ ɕi⁵⁵ tʰiŋ⁵⁵/

/feɪ̯⁵⁵ nä⁵¹ ɕi⁵⁵ tʰiŋ⁵⁵/

(organic chemistry, pharmacology) phenacetin


布洛芬

/pu⁵¹⁻⁵³ lu̯ɔ⁵¹ fən⁵⁵/

/pou̯³³ lɔːk̚² fɐn⁵⁵/

/pu²¹³⁻⁵⁵ lok̚⁴⁻² huŋ³³/

/pu⁵¹⁻⁵³ lu̯ɔ⁵¹ fən⁵⁵/

/pou̯³³ lɔːk̚² fɐn⁵⁵/

/pu²¹³⁻⁵⁵ lok̚⁴⁻² huŋ³³/

(organic chemistry, pharmacology) ibuprofen


美沙酮

/meɪ̯²¹⁴⁻²¹ ʂä⁵⁵ tʰʊŋ³⁵/

/mei̯¹³ saː⁵⁵ tʰʊŋ²¹/

/meɪ̯²¹⁴⁻²¹ ʂä⁵⁵ tʰʊŋ³⁵/

/mei̯¹³ saː⁵⁵ tʰʊŋ²¹/

(organic chemistry, pharmacology) methadone


阿托品

/ˀä⁵⁵ tʰu̯ɔ⁵⁵ pʰin²¹⁴⁻²¹⁽⁴⁾/

/aː³³ tʰɔːk̚³ pɐn³⁵/

/ˀä⁵⁵ tʰu̯ɔ⁵⁵ pʰin²¹⁴⁻²¹⁽⁴⁾/

/aː³³ tʰɔːk̚³ pɐn³⁵/


蘇丹紅

/su⁵⁵ tän⁵⁵ xʊŋ³⁵/

/su⁵⁵ tän⁵⁵ xʊŋ³⁵/


硫醇

/li̯oʊ̯³⁵ ʈ͡ʂʰu̯ən³⁵/

/li̯oʊ̯³⁵ ʈ͡ʂʰu̯ən³⁵/


二噁英

/ˀɤɻ⁵¹⁻⁵³ ˀɤ⁵¹ iŋ⁵⁵/

/jiː²² ɔːk̚³ jɪŋ⁵⁵/

/ɦəl²² oʔ⁵⁵ in²¹/

/ˀɤɻ⁵¹⁻⁵³ ˀɤ⁵¹ iŋ⁵⁵/

/jiː²² ɔːk̚³ jɪŋ⁵⁵/

/ɦəl²² oʔ⁵⁵ in²¹/

2019, 王渊超 (Wang Yuanchao) (lyrics and music), 《垃圾分类再垃圾倒》

二噁英 二噁英 邪氣惡形 / 所以 濕-垃圾脫乾-垃圾要分分清

二𫫇英 二𫫇英 邪气恶形 / 所以 湿-垃圾脱干-垃圾要分分清

(Mainland China, Hong Kong, organic chemistry) dioxin


戴奧辛

/taɪ̯⁵¹⁻⁵³ ˀɑʊ̯⁵¹ ɕin⁵⁵/

/taɪ̯⁵¹⁻⁵³ ˀɑʊ̯⁵¹ ɕin⁵⁵/


地塞米松

ㄉㄧˋ ㄙㄞˋ ㄇㄧˇ ㄙㄨㄥ

/ti⁵¹⁻⁵³ saɪ̯⁵¹ mi²¹⁴⁻²¹ sʊŋ⁵⁵/

/ti⁵¹⁻⁵³ saɪ̯⁵¹ mi²¹⁴⁻²¹ sʊŋ⁵⁵/

(organic chemistry, pharmacology) dexamethasone


阿莫西林

ㄚ ㄇㄛˋ ㄒㄧ ㄌㄧㄣˊ

/ˀä⁵⁵ mu̯ɔ⁵¹ ɕi⁵⁵ lin³⁵/

/ˀä⁵⁵ mu̯ɔ⁵¹ ɕi⁵⁵ lin³⁵/

(organic chemistry, pharmacology) amoxicillin


泛酸

/fän⁵¹ su̯än⁵⁵/

/fän⁵¹ su̯än⁵⁵/

(organic chemistry, biochemistry) pantothenic acid


番茄紅素

ㄈㄢ ㄑㄧㄝˊ ㄏㄨㄥˊ ㄙㄨˋ

/fän⁵⁵ t͡ɕʰi̯ɛ³⁵ xʊŋ³⁵ su⁵¹/

/faːn⁵⁵ kʰɛː²¹⁻³⁵ hʊŋ²¹ sou̯³³/

/fän⁵⁵ t͡ɕʰi̯ɛ³⁵ xʊŋ³⁵ su⁵¹/

/faːn⁵⁵ kʰɛː²¹⁻³⁵ hʊŋ²¹ sou̯³³/


富馬酸

/fu⁵¹ mä²¹⁴⁻²¹ su̯än⁵⁵/

/fu⁵¹ mä²¹⁴⁻²¹ su̯än⁵⁵/

延胡索酸 延胡索酸#Chinese

(organic chemistry) Alternative name for 延胡索酸 (yánhúsuǒsuān, “fumaric acid”).


胡椒醛

ㄏㄨˊ ㄐㄧㄠ ㄑㄩㄢˊ

/xu³⁵ t͡ɕi̯ɑʊ̯⁵⁵ t͡ɕʰy̯ɛn³⁵/

/xu³⁵ t͡ɕi̯ɑʊ̯⁵⁵ t͡ɕʰy̯ɛn³⁵/


黃麴黴素

ㄏㄨㄤˊ ㄑㄩ ㄇㄟˊ ㄙㄨˋ

ㄏㄨㄤˊ ㄑㄩˊ ㄇㄟˊ ㄙㄨˋ

хуанцюймэйсу

/xu̯ɑŋ³⁵ t͡ɕʰy⁵⁵ meɪ̯³⁵ su⁵¹/

/xu̯ɑŋ³⁵ t͡ɕʰy³⁵ meɪ̯³⁵ su⁵¹/

/xu̯ɑŋ³⁵ t͡ɕʰy⁵⁵ meɪ̯³⁵ su⁵¹/

/xu̯ɑŋ³⁵ t͡ɕʰy³⁵ meɪ̯³⁵ su⁵¹/


孔雀石綠

ㄎㄨㄥˇ ㄑㄩㄝˋ ㄕˊ ㄌㄩˋ

/kʰʊŋ²¹⁴⁻²¹ t͡ɕʰy̯ɛ⁵¹ ʂʐ̩³⁵ ly⁵¹/

/hʊŋ³⁵ t͡sœːk̚³ sɛːk̚² lʊk̚²/

/kʰʊŋ²¹⁴⁻²¹ t͡ɕʰy̯ɛ⁵¹ ʂʐ̩³⁵ ly⁵¹/

/hʊŋ³⁵ t͡sœːk̚³ sɛːk̚² lʊk̚²/


魯米諾

ㄌㄨˇ ㄇㄧˇ ㄋㄨㄛˋ

/lu²¹⁴⁻³⁵ mi²¹⁴⁻²¹ nu̯ɔ⁵¹/

/lu²¹⁴⁻³⁵ mi²¹⁴⁻²¹ nu̯ɔ⁵¹/


檸檬醛

ㄋㄧㄥˊ ㄇㄥˊ ㄑㄩㄢˊ

/niŋ³⁵ mɤŋ³⁵ t͡ɕʰy̯ɛn³⁵/

/niŋ³⁵ mɤŋ³⁵ t͡ɕʰy̯ɛn³⁵/


茜素

/t͡ɕʰi̯ɛn⁵¹⁻⁵³ su⁵¹/

/t͡ɕʰi̯ɛn⁵¹⁻⁵³ su⁵¹/


秋水仙素

ㄑㄧㄡ ㄕㄨㄟˇ ㄒㄧㄢ ㄙㄨˋ

/t͡ɕʰi̯oʊ̯⁵⁵ ʂu̯eɪ̯²¹⁴⁻²¹ ɕi̯ɛn⁵⁵ su⁵¹/

/t͡ɕʰi̯oʊ̯⁵⁵ ʂu̯eɪ̯²¹⁴⁻²¹ ɕi̯ɛn⁵⁵ su⁵¹/


麴酸

/t͡ɕʰy⁵⁵ su̯än⁵⁵/

/t͡ɕʰy³⁵ su̯än⁵⁵/

/t͡ɕʰy⁵⁵ su̯än⁵⁵/

/t͡ɕʰy³⁵ su̯än⁵⁵/


屍胺

/ʂʐ̩⁵⁵ ˀän⁵¹/

/ʂʐ̩⁵⁵ ˀän⁵⁵/

/ʂʐ̩⁵⁵ ˀän⁵¹/

/ʂʐ̩⁵⁵ ˀän⁵⁵/


塔崩

/tʰä²¹⁴⁻²¹ pɤŋ⁵⁵/

/tʰaːp̚³ pɐŋ⁵⁵/

/tʰä²¹⁴⁻²¹ pɤŋ⁵⁵/

/tʰaːp̚³ pɐŋ⁵⁵/


甜菜鹼

ㄊㄧㄢˊ ㄘㄞˋ ㄐㄧㄢˇ

тяньцайцзянь

/tʰi̯ɛn³⁵ t͡sʰaɪ̯⁵¹ t͡ɕi̯ɛn²¹⁴⁻²¹⁽⁴⁾/

/tʰi̯ɛn³⁵ t͡sʰaɪ̯⁵¹ t͡ɕi̯ɛn²¹⁴⁻²¹⁽⁴⁾/

(organic chemistry) betaine; trimethylglycine


香豆素

/ɕi̯ɑŋ⁵⁵ toʊ̯⁵¹⁻⁵³ su⁵¹/

/ɕi̯ɑŋ⁵⁵ toʊ̯⁵¹⁻⁵³ su⁵¹/


亞麻酸

/jä⁵¹ mä³⁵ su̯än⁵⁵/

/jä²¹⁴⁻²¹ mä³⁵ su̯än⁵⁵/

/jä⁵¹ mä³⁵ su̯än⁵⁵/

/jä²¹⁴⁻²¹ mä³⁵ su̯än⁵⁵/


亞油酸

/jä⁵¹ joʊ̯³⁵ su̯än⁵⁵/

/jä²¹⁴⁻²¹ joʊ̯³⁵ su̯än⁵⁵/

/jä⁵¹ joʊ̯³⁵ su̯än⁵⁵/

/jä²¹⁴⁻²¹ joʊ̯³⁵ su̯än⁵⁵/


油酸

/joʊ̯³⁵ su̯än⁵⁵/

/jɐu̯²¹ syːn⁵⁵/

/joʊ̯³⁵ su̯än⁵⁵/

/jɐu̯²¹ syːn⁵⁵/


植酸

/ʈ͡ʂʐ̩³⁵ su̯än⁵⁵/

/ʈ͡ʂʐ̩³⁵ su̯än⁵⁵/


三唑侖

ㄙㄢ ㄗㄨㄛˋ ㄌㄨㄣˊ

/sän⁵⁵ t͡su̯ɔ⁵¹ lu̯ən³⁵/

/saːm⁵⁵ t͡sɔː²² lɵn²¹/

/sän⁵⁵ t͡su̯ɔ⁵¹ lu̯ən³⁵/

/saːm⁵⁵ t͡sɔː²² lɵn²¹/

(organic chemistry, pharmacology) triazolam


氯乙烯

/ly⁵¹ i²¹⁴⁻²¹ ɕi⁵⁵/

/ly⁵¹ i²¹⁴⁻²¹ ɕi⁵⁵/

(organic chemistry) vinyl chloride; chloroethene


顛茄鹼

ㄉㄧㄢ ㄑㄧㄝˊ ㄐㄧㄢˇ

/ti̯ɛn⁵⁵ t͡ɕʰi̯ɛ³⁵ t͡ɕi̯ɛn²¹⁴⁻²¹⁽⁴⁾/

/ti̯ɛn⁵⁵ t͡ɕʰi̯ɛ³⁵ t͡ɕi̯ɛn²¹⁴⁻²¹⁽⁴⁾/


雙酚

/ʂu̯ɑŋ⁵⁵ fən⁵⁵/

/ʂu̯ɑŋ⁵⁵ fən⁵⁵/


花生四烯酸

ㄏㄨㄚ ㄕㄥ ㄙˋ ㄒㄧ ㄙㄨㄢ

хуашэнсысисуань

/xu̯ä⁵⁵ ʂɤŋ⁵⁵ sz̩⁵¹ ɕi⁵⁵ su̯än⁵⁵/

/faː⁵⁵ sɐŋ⁵⁵ sei̯²¹ hei̯⁵⁵ syːn⁵⁵/

/xu̯ä⁵⁵ ʂɤŋ⁵⁵ sz̩⁵¹ ɕi⁵⁵ su̯än⁵⁵/

/faː⁵⁵ sɐŋ⁵⁵ sei̯²¹ hei̯⁵⁵ syːn⁵⁵/


六六六

ㄌㄧㄡˋ ㄌㄧㄡˋ ㄌㄧㄡˋ

/li̯oʊ̯⁵¹⁻⁵³ li̯oʊ̯⁵¹⁻⁵³ li̯oʊ̯⁵¹/

/lʊk̚² lʊk̚² lʊk̚²/

/li̯oʊ̯⁵¹⁻⁵³ li̯oʊ̯⁵¹⁻⁵³ li̯oʊ̯⁵¹/

/lʊk̚² lʊk̚² lʊk̚²/

Thus called for its chemical formula being C₆H₆Cl₆.

(scientific name)

(organic chemistry) gammexane; (1,2,3,4,5,6-)hexachlorocyclohexane; benzene hexachloride (BHC)


滴滴涕

/tiː⁵⁵ tiː⁵⁵ tʰiː⁵⁵/

/tiː⁵⁵ tiː⁵⁵ tʰiː⁵⁵/

(organic chemistry) DDT (dichlorodiphenyltrichloroethane)


樂果

/lɤ⁵¹ ku̯ɔ²¹⁴⁻²¹⁽⁴⁾/

/lɤ⁵¹ ku̯ɔ²¹⁴⁻²¹⁽⁴⁾/

Phono-semantic matching of English Rogor, the trade name of the insecticide.


延胡索酸

ㄧㄢˊ ㄏㄨˊ ㄙㄨㄛˇ ㄙㄨㄢ

яньхусосуань

/jɛn³⁵ xu³⁵ su̯ɔ²¹⁴⁻²¹ su̯än⁵⁵/

/jɛn³⁵ xu³⁵ su̯ɔ²¹⁴⁻²¹ su̯än⁵⁵/


羥胺

/t͡ɕʰi̯ɑŋ²¹⁴⁻²¹ ˀän⁵¹/

/t͡ɕʰi̯ɑŋ²¹⁴⁻²¹ ˀän⁵⁵/

/kʰœːŋ¹³ ɔːn⁵⁵/

/t͡ɕʰi̯ɑŋ²¹⁴⁻²¹ ˀän⁵¹/

/t͡ɕʰi̯ɑŋ²¹⁴⁻²¹ ˀän⁵⁵/

/kʰœːŋ¹³ ɔːn⁵⁵/

(organic chemistry) hydroxylamine (derivative)


二氮䓬

/ˀɤɻ⁵¹⁻⁵³ tän⁵¹ ʈ͡ʂu̯ɔ³⁵/

/ˀɤɻ⁵¹⁻⁵³ tän⁵¹ ʈ͡ʂu̯ɔ³⁵/


肌酸酐

цзисуаньгань

/t͡ɕi⁵⁵ su̯än⁵⁵ kän⁵⁵/

/t͡ɕi⁵⁵ su̯än⁵⁵ kän⁵⁵/

(organic chemistry, biochemistry) creatinine


肌酐

/t͡ɕi⁵⁵ kän⁵⁵/

/t͡ɕi⁵⁵ kän⁵⁵/

(organic chemistry, biochemistry) Short for 肌酸酐 (jīsuāngān, “creatinine”).


鞣酸

/ʐoʊ̯³⁵ su̯än⁵⁵/

/ʐoʊ̯³⁵ su̯än⁵⁵/


鞣質

/ʐoʊ̯³⁵ ʈ͡ʂʐ̩⁵¹/

/ʐoʊ̯³⁵ ʈ͡ʂʐ̩³⁵/

/ʐoʊ̯³⁵ ʈ͡ʂʐ̩⁵¹/

/ʐoʊ̯³⁵ ʈ͡ʂʐ̩³⁵/


單寧

/tän⁵⁵ niŋ³⁵/

/tän⁵⁵ niŋ³⁵/

(organic chemistry) Alternative name for 鞣質／鞣质 (róuzhì, “tannin”).


丹寧

/tän⁵⁵ niŋ³⁵/

/tän⁵⁵ niŋ³⁵/


梯恩梯

/tʰi⁵⁵ ˀən⁵⁵ tʰi⁵⁵/

/tʰɐi̯⁵⁵ jɐn⁵⁵ tʰɐi̯⁵⁵/

/tʰi⁵⁵ ˀən⁵⁵ tʰi⁵⁵/

/tʰɐi̯⁵⁵ jɐn⁵⁵ tʰɐi̯⁵⁵/


阿尼林

/ˀä⁵⁵ ni³⁵ lin³⁵/

/ˀä⁵⁵ ni³⁵ lin³⁵/

(organic chemistry) Alternative name for 苯胺 (běn'àn, “aniline”).


苯胺

/pən²¹⁴⁻²¹ ˀän⁵¹/

/pən²¹⁴⁻²¹ ˀän⁵⁵/

/puːn³⁵ ɔːn⁵⁵/

/pən²¹⁴⁻²¹ ˀän⁵¹/

/pən²¹⁴⁻²¹ ˀän⁵⁵/

/puːn³⁵ ɔːn⁵⁵/


山道年

/ʂän⁵⁵ tɑʊ̯⁵¹ ni̯ɛn³⁵/

/ʂän⁵⁵ tɑʊ̯⁵¹ ni̯ɛn³⁵/


фурфурол

ru-noun+

фурфуро́л • (furfuról) m inan (genitive фурфуро́ла, nominative plural фурфуро́лы, genitive plural фурфуро́лов)

фурфуро́л (canonical)
furfuról (romanization)
фурфуро́ла (genitive)
фурфуро́лы (nominative plural)
фурфуро́лов (genitive plural)
фурфуро́л (nominative singular)
фурфуро́лы (nominative plural)
фурфуро́ла (genitive singular)
фурфуро́лов (genitive plural)
фурфуро́лу (dative singular)
фурфуро́лам (dative plural)
фурфуро́л (accusative singular)
фурфуро́лы (accusative plural)
фурфуро́лом (instrumental singular)
фурфуро́лами (instrumental plural)
фурфуро́ле (prepositional singular)
фурфуро́лах (plural prepositional)


氮烯

/tän⁵¹ ɕi⁵⁵/

/tän⁵¹ ɕi⁵⁵/


乃春

/naɪ̯²¹⁴⁻²¹ ʈ͡ʂʰu̯ən⁵⁵/

/naɪ̯²¹⁴⁻²¹ ʈ͡ʂʰu̯ən⁵⁵/

(organic chemistry) Alternative name for 氮烯 (dànxī, “nitrene”).


DCDP

(organic chemistry) Abbreviation of deoxycytidine diphosphate.


苯環

/pən²¹⁴⁻²¹ xu̯än³⁵/

/pən²¹⁴⁻²¹ xu̯ɑɻ³⁵/

/pən²¹⁴⁻²¹ xu̯än³⁵/

/pən²¹⁴⁻²¹ xu̯ɑɻ³⁵/


芳香烴

/fɑŋ⁵⁵ ɕi̯ɑŋ⁵⁵ tʰiŋ⁵⁵/

/fɑŋ⁵⁵ ɕi̯ɑŋ⁵⁵ tʰiŋ⁵⁵/

(organic chemistry) aromatic hydrocarbon


花青素

/xu̯ä⁵⁵ t͡ɕʰiŋ⁵⁵ su⁵¹/

/xu̯ä⁵⁵ t͡ɕʰiŋ⁵⁵ su⁵¹/


陰丹士林

ㄧㄣ ㄉㄢ ㄕˋ ㄌㄧㄣˊ

иньданьшилинь

/in⁵⁵ tän⁵⁵ ʂʐ̩⁵¹ lin³⁵/

/in⁵⁵ tän⁵⁵ ʂʐ̩⁵¹ lin³⁵/


硝酸甘油

ㄒㄧㄠ ㄙㄨㄢ ㄍㄢ ㄧㄡˊ

сяосуань ганью

/ɕi̯ɑʊ̯⁵⁵ su̯än⁵⁵ kän⁵⁵ joʊ̯³⁵/

ㄒㄧㄠ ㄙㄨㄢ ㄍㄢ ㄧㄡˊㄦ

сяосуаньганьюр

/ɕi̯ɑʊ̯⁵⁵ su̯än⁵⁵ kän⁵⁵ jɤʊ̯ɻʷ³⁵/

/ɕi̯ɑʊ̯⁵⁵ su̯än⁵⁵ kän⁵⁵ joʊ̯³⁵/

/ɕi̯ɑʊ̯⁵⁵ su̯än⁵⁵ kän⁵⁵ jɤʊ̯ɻʷ³⁵/


火棉

/xu̯ɔ²¹⁴⁻²¹ mi̯ɛn³⁵/

/xu̯ɔ²¹⁴⁻²¹ mi̯ɛn³⁵/

(organic chemistry) nitrocellulose (containing relatively much nitrogen)


膠棉

/t͡ɕi̯ɑʊ̯⁵⁵ mi̯ɛn³⁵/

/t͡ɕi̯ɑʊ̯⁵⁵ mi̯ɛn³⁵/

(organic chemistry) nitrocellulose (containing relatively little nitrogen)


冰醋酸

/piŋ⁵⁵ t͡sʰu⁵¹ su̯än⁵⁵/

/pɪŋ⁵⁵ t͡sʰou̯³³ syːn⁵⁵/

/piŋ⁵⁵ t͡sʰu⁵¹ su̯än⁵⁵/

/pɪŋ⁵⁵ t͡sʰou̯³³ syːn⁵⁵/


SPPS

(organic chemistry) Initialism of solid-phase peptide synthesis.


芳烴

/fɑŋ⁵⁵ tʰiŋ⁵⁵/

/fɑŋ⁵⁵ tʰiŋ⁵⁵/

(organic chemistry) Short for 芳香烴／芳香烃 (fāngxiāngtīng, “aromatic hydrocarbon”).


丁醇

/tiŋ⁵⁵ ʈ͡ʂʰu̯ən³⁵/

/tɪŋ⁵⁵ sɵn²¹/

/tiŋ⁵⁵ ʈ͡ʂʰu̯ən³⁵/

/tɪŋ⁵⁵ sɵn²¹/


苯並芘

ㄅㄣˇ ㄅㄧㄥˋ ㄅㄧˇ

/pən²¹⁴⁻²¹ piŋ⁵¹ pi²¹⁴⁻²¹⁽⁴⁾/

/pən²¹⁴⁻²¹ piŋ⁵¹ pi²¹⁴⁻²¹⁽⁴⁾/


敵敵畏

/ti³⁵ ti³⁵ weɪ̯⁵¹/

/ti³⁵ ti³⁵ weɪ̯⁵¹/

Phono-semantic matching of English DDVP.


carane

(organic chemistry) The bicyclic hydrocarbon 3,7,7-trimethylbicyclo[4.1.0]heptane


沒食子酸

ㄇㄛˋ ㄕˊ ㄗˇ ㄙㄨㄢ

мошицзысуань

/mu̯ɔ⁵¹ ʂʐ̩³⁵ t͡sz̩²¹⁴⁻²¹ su̯än⁵⁵/

/muːt̚² sɪk̚² t͡siː³⁵ syːn⁵⁵/

/mu̯ɔ⁵¹ ʂʐ̩³⁵ t͡sz̩²¹⁴⁻²¹ su̯än⁵⁵/

/muːt̚² sɪk̚² t͡siː³⁵ syːn⁵⁵/


illudin

(organic chemistry) Any of a family of sesquiterpenes with antitumor antibiotic properties produced by some mushrooms.


gladiolin

Gladiolin is structurally related to etnangien, a highly unstable antibiotic from Sorangium cellulosum that is also active against Mycobacteria.

2017, Lijiang Song et al., “Discovery and biosynthesis of gladiolin: a Burkholderia gladioli antibiotic with promising activity against Mycobacterium tuberculosis”, in Journal of the American Chemical Society, →DOI, page 7974:

The configuration of all but one of the stereogenic centers of gladiolin has previously been elucidated using a combination of NOESY NMR experiments and predictive sequence analysis of the polyketide synthase responsible for its assembly.

2018, Christopher Perry, Jacob R. Sargeant, Lijiang Song, Gregory L. Challis, “Relative stereochemical assignment of C-33 and C-35 in the antibiotic gladiolin”, in Tetrahedron, →DOI, page 5150:

In this study, a previously uncharacterised trans-AT PKS subunit interface between a ketoreductase and a methyltransferase domain (KR/MT junction) is examined from the gladiolin trans-AT PKS.

2020, Helen Smith, Lona Alkhalaf, Józef Lewandowski, Greg Challis, Matthew Jenner, “Reconstitution of a split C-methylating module from the gladiolin trans-AT polyketide synthase”, in 3rd International Conference on Natural Products Discovery and Development in the Genomic Era:

(medicine, organic chemistry) An antibiotic produced by the bacterium Burkholderia gladioli, with potential applications in treating tuberculosis.


actinidiolide

(organic chemistry) A particular chemical compound that attracts cats: 4,4,7a-trimethyl-4,5-dihydrobenzofuran-2(7aH)-one.


boschnialactone

(organic chemistry) A cat attractant found in Boschniakia species.


onikulactone

From Japanese oniku (the name for the plant) + lactone.

(organic chemistry) A cat attractant found in Boschniakia rossica.


mitsugashiwalactone

From Japanese 三槲 (mitsugashiwa, “buckbean (Menyanthes trifoliata)”) + lactone.

der

Menyanthes trifoliata
Menyanthes trifoliata#Translingual

(organic chemistry) A cat attractant found in the buckbean (Menyanthes trifoliata).


phyllophyllin

(organic chemistry) A monocarboxylic acid derivative of chlorophyll.


methyl ethyl ketone peroxide

en-noun

methyl ethyl ketone peroxide (uncountable)

(organic chemistry) The peroxide of methyl ethyl ketone, 2,2'-peroxydi(butane-2-peroxol)


mercaptobenzothiazole

mercaptobenzothiazole (countable and uncountable, plural mercaptobenzothiazoles)

(organic chemistry) An organosulfur compound, C₆H₄(NH)SC=S, used in the sulfur vulcanization of rubber.


methylenediphenol

methylenediphenol (countable and uncountable, plural methylenediphenols)

(organic chemistry) The phenolic compound CH₂(C₆H₄OH)₂ or any derivative of this compound


烏頭鹼

/u⁵⁵ tʰoʊ̯³⁵ t͡ɕi̯ɛn²¹⁴⁻²¹⁽⁴⁾/

/u⁵⁵ tʰoʊ̯³⁵ t͡ɕi̯ɛn²¹⁴⁻²¹⁽⁴⁾/


亞胺

/jä⁵¹⁻⁵³ ˀän⁵¹/

/jä⁵¹ ˀän⁵⁵/

/jä⁵¹⁻⁵³ ˀän⁵¹/

/jä⁵¹ ˀän⁵⁵/


水硫基

[sɨiɾʲɨːkʲi]

水 (sui, “hydrogen”) + 硫 (ryū, “sulfur”) + 基 (ki, “radical”)


ヒドロキシル基

ヒドロキシル基 (canonical)
hidorokishiru-ki (romanization)

English hydroxyl (English hydroxyl) + 基 (ki, “radical”)

compound

English <i class="Latn mention" lang="en">hydroxyl</i>


ベンゾール

[bẽ̞nd͡zo̞ːɾɯ̟]


inulol

Inula helenium
Inula helenium#Translingual

(organic chemistry) A yellow-coloured organic compound with the formula of C₁₀H₁₆O, obtained by distillation from the root of elecampane (Inula helenium).


蒎烯

/pʰaɪ̯⁵¹ ɕi⁵⁵/

/pʰaːi̯³³ hei̯⁵⁵/

/pʰaɪ̯⁵¹ ɕi⁵⁵/

/pʰaːi̯³³ hei̯⁵⁵/


pyranocoumarin

(organic chemistry) Any of a class of organic compound in which a pyran ring is fused to that of a coumarin


葉立德

/jɛ⁵¹⁻⁵³ li⁵¹ tɤ³⁵/

/jɛ⁵¹⁻⁵³ li⁵¹ tɤ³⁵/

(organic chemistry) Synonym of 鎓內鹽 /𬭩内盐 (wēngnèiyán, “ylide”)


鎓內鹽

/wəŋ⁵⁵ neɪ̯⁵¹ jɛn³⁵/

/wəŋ⁵⁵ neɪ̯⁵¹ jɛn³⁵/


thaumetopoein

(organic chemistry) An urticating toxin found in the defensive bristles of certain moths.


cochinelic acid

These have been termed cochinic acid C₉H₈O₅, a body very soluble in alcohol, but nearly insoluble in water, melting at 293° with decomposition : and cochinelic acid, C₁₀H₈O₇, which forms crystalline needles melting at 224° to 225°.

1902, Ernest John Parry, John Henry Coste, The Chemistry of Pigments, page 202:

When heated with sulphuric acid, this dicarboxylic acid forms cochinelic acid and carbon dioxide.

1909, Journal of the Chemical Society, page 486:

...on heating with concentrated H₂SO₄, decomposes into CO and the so-called cochinelic acid , C₁₀H₈O₇.

1922, Victor von Richter, Richard Anschütz, Georg Schroeter, Organic Chemistry: Or, Chemistry of the Carbon Compounds:

(organic chemistry) An organic compound: C₁₀H₈O₇, derived from phenylhydrazone.


zooxanthine

(organic chemistry) A carotenoid pigment, of uncertain composition, obtained from some feathers


薴烯

/niŋ³⁵ ɕi⁵⁵/

/nɪŋ²¹ hei̯⁵⁵/

/niŋ³⁵ ɕi⁵⁵/

/nɪŋ²¹ hei̯⁵⁵/


リモネン

[ɾʲimo̞nẽ̞ɴ]


ナフタレン

[na̠ɸɯ̟ta̠ɾẽ̞ɴ]


ナフタリン

[na̠ɸɯ̟ta̠ɾʲĩɴ]


ホスフィン

(inorganic chemistry) phosphine (PH₃)
(organic chemistry) phosphine (PR₃)


莰烷

/kʰän²¹⁴⁻²¹ wän³⁵/

/hɐm³⁵ jyːn²¹⁻³⁵/

/kʰän²¹⁴⁻²¹ wän³⁵/

/hɐm³⁵ jyːn²¹⁻³⁵/


莰烯

/kʰän²¹⁴⁻²¹ ɕi⁵⁵/

/kʰän²¹⁴⁻²¹ ɕi⁵⁵/


polyuretan

polyuretan (nominative singular)
polyuretany (nominative plural)
polyuretanu (genitive singular)
polyuretanů (genitive plural)
polyuretanu (dative singular)
polyuretanům (dative plural)
polyuretan (accusative singular)
polyuretany (accusative plural)
polyuretane (singular vocative)
polyuretany (plural vocative)
polyuretanu (locative singular)
polyuretanech (locative plural)
polyuretanem (instrumental singular)
polyuretany (instrumental plural)


異腈

/i⁵¹ t͡ɕiŋ⁵⁵/

/jiː²² t͡sʰɪŋ⁵⁵/

/i⁵¹ t͡ɕiŋ⁵⁵/

/jiː²² t͡sʰɪŋ⁵⁵/


イソニトリル

[iso̞ɲ̟ito̞ɾʲiɾɯ̟]

(obsolete, organic chemistry) isocyanide


カルビルアミン

[ka̠ɾɯ̟bʲiɾɯ̟a̠mʲĩɴ]


ヒドラジン

[çido̞ɾa̠ʑĩɴ]

(organic chemistry) hydrazine (derivative)


ニトリル

[ɲ̟ito̞ɾʲiɾɯ̟]


磺酰基

/xu̯ɑŋ³⁵ ɕi̯ɛn⁵⁵ t͡ɕi⁵⁵/

/wɔːŋ²¹ siːn⁵⁵ kei̯⁵⁵/

/xu̯ɑŋ³⁵ ɕi̯ɛn⁵⁵ t͡ɕi⁵⁵/

/wɔːŋ²¹ siːn⁵⁵ kei̯⁵⁵/

(organic chemistry) sulfonyl (any univalent radical derived from a sulfonic acid)


スルホニル基

スルホニル基 (canonical)
suruhoniru-ki (romanization)

[sɨɾɯ̟ho̞ɲ̟iɾɯ̟kʲi]

English sulfonyl (English sulfonyl) + 基 (ki, “radical”)

English <i class="Latn mention" lang="en">sulfonyl</i>


苄基

/pi̯ɛn⁵¹ t͡ɕi⁵⁵/

/pi̯ɛn⁵¹ t͡ɕi⁵⁵/


ベンジル基

ベンジル基 (canonical)
benjiru-ki (romanization)

[bẽ̞ɲ̟d͡ʑiɾɯ̟kʲi]

English benzyl (English benzyl) + 基 (ki, “radical”)

English <i class="Latn mention" lang="en">benzyl</i>


アセナフテン

[a̠se̞na̠ɸɯ̟tẽ̞ɴ]


アントラセン

[ã̠nto̞ɾa̠sẽ̞ɴ]


ヒドロキシルアミン

[çido̞ɾo̞kʲiɕiɾɯ̟a̠mʲĩɴ]

(organic chemistry) hydroxylamine (derivative)


グアニジン

[ɡɯ̟a̠ɲ̟iʑĩɴ]


糖苷

/tʰɑŋ³⁵ kän⁵⁵/

/tʰɔːŋ²¹ kɐm⁵⁵/

/tʰɑŋ³⁵ kän⁵⁵/

/tʰɔːŋ²¹ kɐm⁵⁵/


配糖物

/pʰeɪ̯⁵¹ tʰɑŋ³⁵ u⁵¹/

/pʰuːi̯³³ tʰɔːŋ²¹ mɐt̚²/

/pʰeɪ̯⁵¹ tʰɑŋ³⁵ u⁵¹/

/pʰuːi̯³³ tʰɔːŋ²¹ mɐt̚²/


フェノール

ja-noun

フェノール • (fenōru)

[ɸe̞no̞ːɾɯ̟]

(organic chemistry) phenol (caustic compound derived from benzene)

(organic chemistry) phenol (any of a class of aromatic organic compounds having at least one hydroxyl group attached directly to the benzene ring)


アセチレン系炭化水素

アセチレン-けい たんか すいそ

アセチレンけいたんくわすいそ

アセチレン系(けい)炭(たん)化(か)水(すい)素(そ) • (asechiren-kei tanka suiso) ^(←アセチレンけいたんくわすいそ (asetirenkeitankwasuiso)?)

アセチレン系炭化水素 (canonical)
asechiren-kei tanka suiso (romanization)
asetirenkeitankwasuiso (romanization)
アセチレンけいたんくわすいそ (historical katakana)

アセチレンけーたんかすいそ

[a̠se̞t͡ɕiɾẽ̞ŋke̞ː tã̠ŋka̠ sɨiso̞]

アセチレン (asechiren, “acetylene”) + 系 (-kei, “family”) + 炭化水素 (tanka suiso, “hydrocarbon”)

suffix

あせちれんけいたんかすいそ

compound

あせちれんけいたんかすいそ


メタン系炭化水素

ja-noun

メタン-けい たんか すいそ

メタンけいたんくわすいそ

メタン系(けい)炭(たん)化(か)水(すい)素(そ) • (metan-kei tanka suiso) ^(←メタンけいたんくわすいそ (metankeitankwasuiso)?)

メタン系炭化水素 (canonical)
metan-kei tanka suiso (romanization)
metankeitankwasuiso (romanization)
メタンけいたんくわすいそ (historical katakana)

メタン (metan, “methane”) + 系 (-kei, “family”) + 炭化水素 (tanka suiso, “hydrocarbon”)


エチレン系炭化水素

ja-noun

エチレン-けい たんか すいそ

エチレンけいたんくわすいそ

エチレン系(けい)炭(たん)化(か)水(すい)素(そ) • (echiren-kei tanka suiso) ^(←エチレンけいたんくわすいそ (etirenkeitankwasuiso)?)

エチレン系炭化水素 (canonical)
echiren-kei tanka suiso (romanization)
etirenkeitankwasuiso (romanization)
エチレンけいたんくわすいそ (historical katakana)

エチレンけーたんかすいそ

[e̞t͡ɕiɾẽ̞ŋke̞ː tã̠ŋka̠ sɨiso̞]

エチレン (echiren, “ethylene”) + 系 (-kei, “family”) + 炭化水素 (tanka suiso, “hydrocarbon”)

suffix

えちれんけいたんかすいそ

compound

えちれんけいたんかすいそ


オレフィン系炭化水素

ja-noun

オレフィン-けい たんか すいそ

オレフィンけいたんくわすいそ

オレフィン系(けい)炭(たん)化(か)水(すい)素(そ) • (orefin-kei tanka suiso) ^(←オレフィンけいたんくわすいそ (orefinkeitankwasuiso)?)

オレフィン系炭化水素 (canonical)
orefin-kei tanka suiso (romanization)
orefinkeitankwasuiso (romanization)
オレフィンけいたんくわすいそ (historical katakana)

オレフィンけーたんかすいそ

[o̞ɾe̞ɸʲĩŋke̞ː tã̠ŋka̠ sɨiso̞]

オレフィン (orefin, “olefin”) + 系 (-kei, “family”) + 炭化水素 (tanka suiso, “hydrocarbon”)

suffix

おれふぃんけいたんかすいそ

compound

おれふぃんけいたんかすいそ


磺酰胺

/xu̯ɑŋ³⁵ ɕi̯ɛn⁵⁵ ˀän⁵¹/

/xu̯ɑŋ³⁵ ɕi̯ɛn⁵⁵ ˀän⁵⁵/

/xu̯ɑŋ³⁵ ɕi̯ɛn⁵⁵ ˀän⁵¹/

/xu̯ɑŋ³⁵ ɕi̯ɛn⁵⁵ ˀän⁵⁵/

(Mainland China, Hong Kong, organic chemistry) sulfonamide


磺胺

/xu̯ɑŋ³⁵ ˀän⁵¹/

/xu̯ɑŋ³⁵ ˀän⁵⁵/

/wɔːŋ²¹ ɔːn⁵⁵/

/hɔŋ²⁴⁻²² an⁴⁴/

/xu̯ɑŋ³⁵ ˀän⁵¹/

/xu̯ɑŋ³⁵ ˀän⁵⁵/

/wɔːŋ²¹ ɔːn⁵⁵/

/hɔŋ²⁴⁻²² an⁴⁴/

磺胺類藥物

磺胺类药物


苯甲酸

ㄅㄣˇ ㄐㄧㄚˇ ㄙㄨㄢ

бэньцзясуань

/pən²¹⁴⁻³⁵ t͡ɕi̯ä²¹⁴⁻²¹ su̯än⁵⁵/

/pən²¹⁴⁻³⁵ t͡ɕi̯ä²¹⁴⁻²¹ su̯än⁵⁵/


エチレン

[e̞t͡ɕiɾẽ̞ɴ]


エテン

(organic chemistry) Synonym of エチレン (echiren, “ethylene”); ethene


オレイン酸

オレイン酸 (canonical)
orein-san (romanization)

[o̞ɾẽ̞ːɰ̃sã̠ɴ]


xylophene

(organic chemistry) pentachlorophenol (when used to preserve wood from boring insects).


heptanoid

(organic chemistry) Any organic compound in which substituents are attached to each end of a heptanone chain


indolylalkylamine

(organic chemistry) Any indolyl derivative of an alkylamine


noraporphine

(organic chemistry) Any compound formally derived from an aporphine by the addition of a methylene group


蟻醛

/i²¹⁴⁻²¹ t͡ɕʰy̯ɛn³⁵/

/i²¹⁴⁻²¹ t͡ɕʰy̯ɛn³⁵/

(organic chemistry, informal) formaldehyde


phenylalkylamine

(organic chemistry) Any phenyl derivative of an alkylamine


ethylpyrimidine

(organic chemistry) Any ethyl derivative of pyrimidine


enolize

en-verb

enolize (third-person singular simple present enolizes, present participle enolizing, simple past and past participle enolized)

enolizes (present singular third-person)
enolizing (participle present)
enolized (participle past)
enolized (past)
enolise (alternative)

As in base-catalyzed reactions, crossed reactions between two carbonyl compounds each of which can enolize are likely to result in a mixture of four products.

1993, Richard O.C. Norman, James M. Coxon, Principles of Organic Synthesis, 3rd Edition, CRC Press, →ISBN, page 258:

These differences have been attributed to the ability of free saccharides to enolize in basic media and to the resistance of hydrazones to do so, as detailed next.

2000, Derek Horton, Advances in Carbohydrate Chemistry and Biochemistry, Gulf Professional Publishing, →ISBN, page 185:

The phosphorus tribromide is then formed in situ. Carboxylic acids that enolize easily will also react without a catalyst present.

2005, Thomas Laue, Andreas Plagens, Named Organic Reactions, John Wiley & Sons, →ISBN, page 160:

If we condense two species where one cannot enolize, then this principle reduces our number of primary products to two.

2014, Penny Chaloner, Organic Chemistry: A Mechanistic Approach, CRC Press, →ISBN, page 798:

Pyruvate is known to enolize rapidly under the conditions employed by Oshima and Tamiya; in contrast, the a-keto analogs of a number of other amino acids enolize at much slower rates.

2016, Paul D. Boyer, Henry Lardy, Karl Myrbäck, Group Transfer Syntheses Coupled to ATP Cleavage, Elsevier, →ISBN, page 217:

(organic chemistry, intransitive) To become an enol or enolate, often through isomerization.

It was thus proposed that the matched pK values of the dienolate and of Tyr-14 permitted the hydrogen bond between them to become a very strong one, thus providing the energy to enolize the substrate and form the unstable intermediate.

1999, Enzyme Kinetics and Mechanisms, Part E, Energetics of Enzyme Catalysis, Academic Press, →ISBN, page 23:

(organic chemistry, transitive) To convert into an enol or enolate.


anthraco-

classical compound
international scientific vocabulary

From international scientific vocabulary, reflecting a New Latin combining form, from New Latin anthracites, from Ancient Greek ἄνθραξ (ánthrax), whence also Latin anthrax, whence English anthrax (because the black eschars of that disease are named for their resemblance to coals).

anthrax

etymologically related but semantically never overlapping; no anthraco-derived English terms have reference to anthrax

(organic chemistry) Alternative form of anthra- (for derivatives of anthracene).


脂肪族

/ʈ͡ʂʐ̩⁵⁵ fɑŋ³⁵ t͡su³⁵/

/t͡siː⁵⁵ fɔːŋ⁵⁵ t͡sʊk̚²/

/ʈ͡ʂʐ̩⁵⁵ fɑŋ³⁵ t͡su³⁵/

/t͡siː⁵⁵ fɔːŋ⁵⁵ t͡sʊk̚²/


脂肪族

脂肪族 (canonical)
shibōzoku (romanization)


パルミチン酸

パルミチン酸 (canonical)
parumichin-san (romanization)

[pa̠ɾɯ̟mʲit͡ɕĩɰ̃sã̠ɴ]


棕櫚酸

цзунлюйсуань

/t͡sʊŋ⁵⁵ ly³⁵ su̯än⁵⁵/

/t͡sʊŋ⁵⁵ ly²¹⁴⁻²¹ su̯än⁵⁵/

/t͡sʊŋ⁵⁵ lɵy̯¹³ syːn⁵⁵/

/t͡sʊŋ⁵⁵ lɵy̯²¹ syːn⁵⁵/

/t͡sʊŋ⁵⁵ lɵy̯³³ syːn⁵⁵/

/t͡sʊŋ⁵⁵ ly³⁵ su̯än⁵⁵/

/t͡sʊŋ⁵⁵ ly²¹⁴⁻²¹ su̯än⁵⁵/

/t͡sʊŋ⁵⁵ lɵy̯¹³ syːn⁵⁵/

/t͡sʊŋ⁵⁵ lɵy̯²¹ syːn⁵⁵/

/t͡sʊŋ⁵⁵ lɵy̯³³ syːn⁵⁵/


ステアリン酸

ステアリン酸 (canonical)
sutearin-san (romanization)

[sɨte̞a̠ɾʲĩɰ̃sã̠ɴ]

ステアリン (sutearin, “stearin”) + 酸 (san, “acid”)


オクタデカン酸

オクタデカン酸 (canonical)
okutadekan-san (romanization)

[o̞kɯ̟ta̠de̞kã̠ɰ̃sã̠ɴ]

オクタデカン (okutadekan, “octadecane”) + 酸 (san, “acid”)


스테아르산

[sʰɯtʰe̞a̠ɾɯsʰa̠n]


ステアリン

[sɨte̞a̠ɾʲĩɴ]


硬脂精

/iŋ⁵¹ ʈ͡ʂʐ̩⁵⁵ t͡ɕiŋ⁵⁵/

/ŋaːŋ²² t͡siː⁵⁵ t͡sɪŋ⁵⁵/

/iŋ⁵¹ ʈ͡ʂʐ̩⁵⁵ t͡ɕiŋ⁵⁵/

/ŋaːŋ²² t͡siː⁵⁵ t͡sɪŋ⁵⁵/


十八烷

/ʂʐ̩³⁵ pä⁵⁵ wän³⁵/

/sɐp̚² paːt̚³ jyːn²¹⁻³⁵/

/ʂʐ̩³⁵ pä⁵⁵ wän³⁵/

/sɐp̚² paːt̚³ jyːn²¹⁻³⁵/


グリセロール

[ɡɯ̟ɾʲise̞ɾo̞ːɾɯ̟]


グリセリン

[ɡɯ̟ɾʲise̞ɾʲĩɴ]


글리세롤

[kɯʎʎisʰe̞ɾo̞ɭ]


프로필렌

[pʰɯɾo̞pʰiɭɭe̞n]


albuminone

(organic chemistry, dated) A principle derived from certain albuminoids; it is soluble in alcohol and is not coagulable by heat.


dinitrodiphenylamine

From di- + nitro- + di- + phenyl + amine.

(organic chemistry) A chemical compound obtained from the reaction of aniline, dinitrochlorobenzene, and soda ash, and used in producing hexanitrodiphenylamine.


벤졸

[pe̞ɲd͡ʑo̞ɭ]

From German Benzol via Japanese ベンゾール (benzōru).


フェニル基

フェニル基 (canonical)
feniru-ki (romanization)

[ɸe̞ɲ̟iɾɯ̟kʲi]


苯基

/pən²¹⁴⁻²¹ t͡ɕi⁵⁵/

/pən²¹⁴⁻²¹ t͡ɕi⁵⁵/


설폰

[sʰʌ̹ɭpʰo̞n]


하이드록실아민

(organic chemistry) hydroxylamine (NH₂OH)

(organic chemistry) hydroxylamine (derivative)


설포닐기

[sʰʌ̹ɭpʰo̞niɭɡi]

(organic chemistry) sulfonyl (any univalent radical derived from a sulfonic acid)


하이드라진

(organic chemistry) hydrazine (derivative)


이소니트릴

(obsolete, organic chemistry) isocyanide


ピリミジン

[pʲiɾʲimʲiʑĩɴ]


설프히드릴기

[sʰʌ̹ɭpʰɯʝidɯɾiɭɡi]


카르복실기

[kʰa̠ɾɯbo̞kɕ͈iɭɡi]


カルボキシル基

カルボキシル基 (canonical)
karubokishiru-ki (romanization)

[ka̠ɾɯ̟bo̞kʲiɕiɾɯ̟kʲi]


플루오렌

[pʰɯɭɭuo̞ɾe̞n]


アシル基

アシル基 (canonical)
ashiru-ki (romanization)

[a̠ɕiɾɯ̟kʲi]

アシル (ashiru, “acyl”) + 基 (ki, “radical”)


烯丙基

/ɕi⁵⁵ piŋ²¹⁴⁻²¹ t͡ɕi⁵⁵/

/hei̯⁵⁵ pɪŋ³⁵ kei̯⁵⁵/

/ɕi⁵⁵ piŋ²¹⁴⁻²¹ t͡ɕi⁵⁵/

/hei̯⁵⁵ pɪŋ³⁵ kei̯⁵⁵/


炔丙基

/t͡ɕʰy̯ɛ⁵⁵ piŋ²¹⁴⁻²¹ t͡ɕi⁵⁵/

/kʰyːt̚³ pɪŋ³⁵ kei̯⁵⁵/

/t͡ɕʰy̯ɛ⁵⁵ piŋ²¹⁴⁻²¹ t͡ɕi⁵⁵/

/kʰyːt̚³ pɪŋ³⁵ kei̯⁵⁵/


アリル基

アリル基 (canonical)
ariru-ki (romanization)

[a̠ɾʲiɾɯ̟kʲi]

アリル (ariru, “allyl”) + 基 (ki, “radical”)


プロパルギル基

プロパルギル基 (canonical)
puroparugiru-ki (romanization)

[pɯ̟ɾo̞pa̠ɾɯ̟ɡʲiɾɯ̟kʲi]

プロパルギル (puroparugiru, “propargyl”) + 基 (ki, “radical”)


프로파길

[pʰɯɾo̞pʰa̠ɡiɭ]


피라졸

[pʰiɾa̠d͡ʑo̞ɭ]


喹喔啉

/kʰu̯eɪ̯³⁵ ˀɔ⁵⁵ lin³⁵/

/fuːi̯⁵⁵ ɔː⁵⁵ lɐm²¹/

/kʰu̯eɪ̯³⁵ ˀɔ⁵⁵ lin³⁵/

/fuːi̯⁵⁵ ɔː⁵⁵ lɐm²¹/


蝶呤

/ti̯ɛ³⁵ liŋ⁵¹/

/ti̯ɛ³⁵ liŋ³⁵/

/tiːp̚² lɪŋ²¹/

/ti̯ɛ³⁵ liŋ⁵¹/

/ti̯ɛ³⁵ liŋ³⁵/

/tiːp̚² lɪŋ²¹/


プテリン

[pɯ̟te̞ɾʲĩɴ]


蝶啶

/ti̯ɛ³⁵ tiŋ⁵¹/

/tiːp̚² tɪŋ²²/

/ti̯ɛ³⁵ tiŋ⁵¹/

/tiːp̚² tɪŋ²²/


プテリジン

[pɯ̟te̞ɾʲiʑĩɴ]


喹唑啉

ㄎㄨㄟˊ ㄗㄨㄛˋ ㄌㄧㄣˊ

/kʰu̯eɪ̯³⁵ t͡su̯ɔ⁵¹ lin³⁵/

/fuːi̯⁵⁵ t͡sɔː²² lɐm²¹/

/kʰu̯eɪ̯³⁵ t͡su̯ɔ⁵¹ lin³⁵/

/fuːi̯⁵⁵ t͡sɔː²² lɐm²¹/


萘啶

/naɪ̯⁵¹⁻⁵³ tiŋ⁵¹/

/nɔːi̯²² tɪŋ²²/

/naɪ̯⁵¹⁻⁵³ tiŋ⁵¹/

/nɔːi̯²² tɪŋ²²/


酞嗪

/tʰaɪ̯⁵¹ t͡ɕʰin³⁵/

/tʰaːi̯³³ t͡sʰɵn²¹/

/tʰaɪ̯⁵¹ t͡ɕʰin³⁵/

/tʰaːi̯³³ t͡sʰɵn²¹/


フタラジン

[ɸɯ̟ta̠ɾa̠ʑĩɴ]


프탈라진

[pʰɯtʰa̠ɭɭa̠d͡ʑin]


ナフチリジン

[na̠ɸɯ̟t͡ɕiɾʲiʑĩɴ]


marmesin

Named after the species Aegle marmelos, in which it was discovered in 1949, + -in.

(organic chemistry) A particular furocoumarin.


daphnoretin

(organic chemistry) A particular hydroxycoumarin.


acetopropylic

(organic chemistry) That contains the CH₃CO(CH₂)₃- group


acétylaminophénol

fr-noun

acétylaminophénol m (plural acétylaminophénols)


acetylaminophenol

(organic chemistry) Any of three isomeric acetylamino derivatives of phenol


alcoyler

alcoyler (infinitive)
avoir + past participle (infinitive multiword-construction)
alcoylant (gerund participle present)
ayant + past participle (gerund multiword-construction participle present)
alcoylé (participle past)
alcoyle (first-person indicative present singular)
alcoyles (indicative present second-person singular)
alcoyle (indicative present singular third-person)
alcoylons (first-person indicative plural present)
alcoylez (indicative plural present second-person)
alcoylent (indicative plural present third-person)
alcoylais (first-person imperfect indicative singular)
alcoylais (imperfect indicative second-person singular)
alcoylait (imperfect indicative singular third-person)
alcoylions (first-person imperfect indicative plural)
alcoyliez (imperfect indicative plural second-person)
alcoylaient (imperfect indicative plural third-person)
alcoylai (first-person historic indicative past singular)
alcoylas (historic indicative past second-person singular)
alcoyla (historic indicative past singular third-person)
alcoylâmes (first-person historic indicative past plural)
alcoylâtes (historic indicative past plural second-person)
alcoylèrent (historic indicative past plural third-person)
alcoylerai (first-person future indicative singular)
alcoyleras (future indicative second-person singular)
alcoylera (future indicative singular third-person)
alcoylerons (first-person future indicative plural)
alcoylerez (future indicative plural second-person)
alcoyleront (future indicative plural third-person)
alcoylerais (conditional first-person singular)
alcoylerais (conditional second-person singular)
alcoylerait (conditional singular third-person)
alcoylerions (conditional first-person plural)
alcoyleriez (conditional plural second-person)
alcoyleraient (conditional plural third-person)
future of avoir + past participle (future indicative multiword-construction perfect)
conditional of avoir + past participle (conditional multiword-construction perfect)
alcoyle (first-person present singular subjunctive)
alcoyles (present second-person singular subjunctive)
alcoyle (present singular subjunctive third-person)
alcoylions (first-person plural present subjunctive)
alcoyliez (plural present second-person subjunctive)
alcoylent (plural present subjunctive third-person)
alcoylasse (first-person imperfect singular subjunctive)
alcoylasses (imperfect second-person singular subjunctive)
alcoylât (imperfect singular subjunctive third-person)
alcoylassions (first-person imperfect plural subjunctive)
alcoylassiez (imperfect plural second-person subjunctive)
alcoylassent (imperfect plural subjunctive third-person)
alcoyle (imperative second-person singular)
alcoylons (first-person imperative plural)
alcoylez (imperative plural second-person)


allyler

allyler (infinitive)
avoir + past participle (infinitive multiword-construction)
allylant (gerund participle present)
ayant + past participle (gerund multiword-construction participle present)
allylé (participle past)
allyle (first-person indicative present singular)
allyles (indicative present second-person singular)
allyle (indicative present singular third-person)
allylons (first-person indicative plural present)
allylez (indicative plural present second-person)
allylent (indicative plural present third-person)
allylais (first-person imperfect indicative singular)
allylais (imperfect indicative second-person singular)
allylait (imperfect indicative singular third-person)
allylions (first-person imperfect indicative plural)
allyliez (imperfect indicative plural second-person)
allylaient (imperfect indicative plural third-person)
allylai (first-person historic indicative past singular)
allylas (historic indicative past second-person singular)
allyla (historic indicative past singular third-person)
allylâmes (first-person historic indicative past plural)
allylâtes (historic indicative past plural second-person)
allylèrent (historic indicative past plural third-person)
allylerai (first-person future indicative singular)
allyleras (future indicative second-person singular)
allylera (future indicative singular third-person)
allylerons (first-person future indicative plural)
allylerez (future indicative plural second-person)
allyleront (future indicative plural third-person)
allylerais (conditional first-person singular)
allylerais (conditional second-person singular)
allylerait (conditional singular third-person)
allylerions (conditional first-person plural)
allyleriez (conditional plural second-person)
allyleraient (conditional plural third-person)
future of avoir + past participle (future indicative multiword-construction perfect)
conditional of avoir + past participle (conditional multiword-construction perfect)
allyle (first-person present singular subjunctive)
allyles (present second-person singular subjunctive)
allyle (present singular subjunctive third-person)
allylions (first-person plural present subjunctive)
allyliez (plural present second-person subjunctive)
allylent (plural present subjunctive third-person)
allylasse (first-person imperfect singular subjunctive)
allylasses (imperfect second-person singular subjunctive)
allylât (imperfect singular subjunctive third-person)
allylassions (first-person imperfect plural subjunctive)
allylassiez (imperfect plural second-person subjunctive)
allylassent (imperfect plural subjunctive third-person)
allyle (imperative second-person singular)
allylons (first-person imperative plural)
allylez (imperative plural second-person)


amidé

fr-adj

amidé (feminine amidée, masculine plural amidés, feminine plural amidées)

amidée (feminine)
amidés (masculine plural)
amidées (feminine plural)


aminobenzène

(organic chemistry, singular only) aniline


anthemol

(organic chemistry) A monoterpene alcohol, [4-(propan-2-yl)cyclohexa-1,3-dien-1-yl]methanol, found in the oil of camomile as esters of tiglic and angelic acids


arachin

(organic chemistry) The triglyceride of arachidic acid


avornin

(organic chemistry) Synonym of frangulin


azalein

(organic chemistry) A flavonol 2-(3,4-dihydroxyphenyl)-7-hydroxy-5-methoxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one


azobenzène

(organic chemistry) azobenzene (an aromatic azo compound, diphenyl diazene, the basis of many dyes)


benzopinacol

en-noun

benzopinacol (countable and uncountable, plural benzopinacols)

(organic chemistry) A pinacol in which each of the four substituents is a phenyl group


benzopinacone

(organic chemistry) Synonym of benzopinacol


bombycic acid

(organic chemistry) A constituent of the fluid used by silkworms to dissolve the gum that binds the silk threads of a cocoon


brassic acid

docosadienoic acid
docosadienoic acid#English

(organic chemistry) Synonym of docosadienoic acid


calendic

(organic chemistry) Relating to calendic acid or its derivatives


calendic acid

octadecatrienoic acid
octadecatrienoic acid

(organic chemistry) 8,10,12-octadecatrienoic acid


camphorin

(organic chemistry) The triglyceride of camphoric acid


carbazotique

(obsolete, organic chemistry) carbazotic


carbomeric

(organic chemistry) Relating to a carbomer


carboxylsyre

carboxylsyre (indefinite nominative singular)
carboxylsyren (definite nominative singular)
carboxylsyrer (indefinite nominative plural)
carboxylsyrerne (definite nominative plural)
carboxylsyres (genitive indefinite singular)
carboxylsyrens (definite genitive singular)
carboxylsyrers (genitive indefinite plural)
carboxylsyrernes (definite genitive plural)


syregruppe

syregruppe (indefinite nominative singular)
syregruppen (definite nominative singular)
syregrupper (indefinite nominative plural)
syregrupperne (definite nominative plural)
syregruppes (genitive indefinite singular)
syregruppens (definite genitive singular)
syregruppers (genitive indefinite plural)
syregruppernes (definite genitive plural)


carbovinate

(obsolete, organic chemistry) Any of a class of poorly-characterized salts derived from ethanol


cascaroside

(organic chemistry) Any of a group of hydroxyanthracene glycosides, found in cascara, that act as laxatives


catalpic acid

(organic chemistry) A particular isomer of octadecatrienoic acid


catalpic

(organic chemistry) Relating to catalpic acid or its derivatives


chlorofluorocarbone

fr-noun

chlorofluorocarbone m (plural chlorofluorocarbones)


chloroformic

(organic chemistry) Relating to chloroformic acid or its derivatives


cholesterate

(organic chemistry) Any salt or ester of cholesteric acid


acide cholique

acide cholique m (plural acides choliques)


choleate

(organic chemistry) Any salt or ester of choleic acid


chrysanthémate

chrysanthémate m (plural chrysanthémates)


chrysanthemate

(organic chemistry) Any salt or ester of chrysanthemic acid


cycloartane

en-noun

cycloartane (countable and uncountable, plural cycloartanes)

(organic chemistry) A derivative of lanostane, 4,4,14-trimethyl-9,19-cyclo-5alpha,9beta-cholestane, having a methylene bridge between the 5- and 9- positions