"octadecyl" meaning in All languages combined

{
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      "args": {
        "1": "en",
        "2": "octadecane",
        "3": "yl"
      },
      "expansion": "octadecane + -yl",
      "name": "suffix"
    }
  ],
  "etymology_text": "octadecane + -yl",
  "forms": [
    {
      "form": "octadecyls",
      "tags": [
        "plural"
      ]
    }
  ],
  "head_templates": [
    {
      "args": {},
      "expansion": "octadecyl (plural octadecyls)",
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  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
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          "kind": "other",
          "name": "English entries with incorrect language header",
          "parents": [
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          "source": "w"
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          "name": "English terms suffixed with -yl",
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        },
        {
          "kind": "topical",
          "langcode": "en",
          "name": "Organic chemistry",
          "orig": "en:Organic chemistry",
          "parents": [
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        {
          "ref": "2001 May 11, Xi Zuwei et al., “Reaction-Controlled Phase-Transfer Catalysis for Propylene Epoxidation to Propylene Oxide”, in Science, volume 292, number 5519, →DOI, pages 1139–1141",
          "text": "Although catalyst IV also has good catalytic performance, it was totally soluble in the reaction system during and after the epoxidation, because it contains a big octadecyl benzyl dimethyl ammonium ion.",
          "type": "quotation"
        },
        {
          "ref": "1997 May 9, H. T. Alborn et al., “An Elicitor of Plant Volatiles from Beet Armyworm Oral Secretion”, in Science, volume 276, number 5314, →DOI, pages 945–949",
          "text": "A 0.5-ml sample of the supernatant was put on a 6-ml activated, octadecyl solid-phase extraction cartridge (Bakerbond, J. T. Baker, Phillipsburg, NJ) and eluted with 2-ml volumes of H 2 O, 50% CH 3 CN (Low-UV HPLC grade, Burdick and Jackson) in H 2 O, and CH 3 CN. All fractions were concentrated to near dryness under vacuum (Speed Vac rotary concentrator, Savant Instruments, Farmingdale, NY) and redissolved in 0.5 ml of 50 mM pH 8 buffer, for bioassay.",
          "type": "quotation"
        }
      ],
      "glosses": [
        "Any of very many isomeric univalent hydrocarbon radicals, C₁₈H₃₇, formally derived from an octadecane by the loss of a hydrogen atom"
      ],
      "id": "en-octadecyl-en-noun-LOpcj5Pc",
      "links": [
        [
          "organic chemistry",
          "organic chemistry"
        ],
        [
          "isomeric",
          "isomeric"
        ],
        [
          "univalent",
          "univalent"
        ],
        [
          "hydrocarbon",
          "hydrocarbon"
        ],
        [
          "octadecane",
          "octadecane"
        ],
        [
          "hydrogen",
          "hydrogen"
        ]
      ],
      "raw_glosses": [
        "(organic chemistry) Any of very many isomeric univalent hydrocarbon radicals, C₁₈H₃₇, formally derived from an octadecane by the loss of a hydrogen atom"
      ],
      "related": [
        {
          "word": "octadecylic"
        },
        {
          "word": "octadecylic acid"
        }
      ],
      "topics": [
        "chemistry",
        "natural-sciences",
        "organic-chemistry",
        "physical-sciences"
      ]
    }
  ],
  "word": "octadecyl"
}

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        "2": "octadecane",
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  ],
  "etymology_text": "octadecane + -yl",
  "forms": [
    {
      "form": "octadecyls",
      "tags": [
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      ]
    }
  ],
  "head_templates": [
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      "args": {},
      "expansion": "octadecyl (plural octadecyls)",
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  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "related": [
    {
      "word": "octadecylic"
    },
    {
      "word": "octadecylic acid"
    }
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  "senses": [
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      "categories": [
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        {
          "ref": "2001 May 11, Xi Zuwei et al., “Reaction-Controlled Phase-Transfer Catalysis for Propylene Epoxidation to Propylene Oxide”, in Science, volume 292, number 5519, →DOI, pages 1139–1141",
          "text": "Although catalyst IV also has good catalytic performance, it was totally soluble in the reaction system during and after the epoxidation, because it contains a big octadecyl benzyl dimethyl ammonium ion.",
          "type": "quotation"
        },
        {
          "ref": "1997 May 9, H. T. Alborn et al., “An Elicitor of Plant Volatiles from Beet Armyworm Oral Secretion”, in Science, volume 276, number 5314, →DOI, pages 945–949",
          "text": "A 0.5-ml sample of the supernatant was put on a 6-ml activated, octadecyl solid-phase extraction cartridge (Bakerbond, J. T. Baker, Phillipsburg, NJ) and eluted with 2-ml volumes of H 2 O, 50% CH 3 CN (Low-UV HPLC grade, Burdick and Jackson) in H 2 O, and CH 3 CN. All fractions were concentrated to near dryness under vacuum (Speed Vac rotary concentrator, Savant Instruments, Farmingdale, NY) and redissolved in 0.5 ml of 50 mM pH 8 buffer, for bioassay.",
          "type": "quotation"
        }
      ],
      "glosses": [
        "Any of very many isomeric univalent hydrocarbon radicals, C₁₈H₃₇, formally derived from an octadecane by the loss of a hydrogen atom"
      ],
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          "organic chemistry",
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        ],
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          "octadecane",
          "octadecane"
        ],
        [
          "hydrogen",
          "hydrogen"
        ]
      ],
      "raw_glosses": [
        "(organic chemistry) Any of very many isomeric univalent hydrocarbon radicals, C₁₈H₃₇, formally derived from an octadecane by the loss of a hydrogen atom"
      ],
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  ],
  "word": "octadecyl"
}