| Chemical & Physical Properties | |
|---|---|
| CAS Number | 506-43-4 |
| Catalog No. | 2A-1169491 |
| Chinese Name | 亚麻醇 |
| Synonyms | (9Z,12Z)-9,12-Octadecadien-1-ol; EINECS 208-038-1; Linoleyl alcohol; (9Z,12Z)-Octadeca-9,12-dien-1-ol; cis,cis-9,12-Octadecadien-1-ol |
| Molecular Formula | C18H34O |
| Molecular Weight | 266.462 |
| Purity | 98 |
| Density | 0.9±0.1 g/cm3 |
| Boiling Point | 374.0±11.0 °C at 760 mmHg |
| Storage Condition | Sealed and stored at -20°C, placed in a ventilated |
| Application | Linoleic acid alcohol is a structural analog of linoleic acid without a-carboxyl group and is a fatty alcohol [1]. |
| HTC | 2905290000 |
| PubChem ID | 11655085 |
| SMILES | CCCCCC=CCC=CCCCCCCCCO |
| InChI | InChI=1S/C18H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h6-7,9-10,19H,2-5,8,11-18H2,1H3/b7-6-,10-9- |
| InChI Key | JXNPEDYJTDQORS-HZJYTTRNSA-N |
| Bioactivity | Linoleyl alcohol, a structural analog of Linoleic acid with no a-carboxyl group, is a fatty alcohol[1]. Related Catalog Signaling Pathways >> Others >> Others Research Areas >> Metabolic Disease In Vitro The dioxygenation of Linoleyl alcohol by potato tuber lipoxygenase leads to formation of two positional isomeric products-9- and 13-hydroperoxyoctadecadien-1-ols[1]. In Vivo Animal feeding experiments have revealed that esters made from Gallic acid (GA) and (-)-Epigallo-catechin (EGC) or Linoleyl alcohol are more effective in weight-loss promotion and metabolic syndrome management than are intact GA and EGC[2]. References [1]. I A Butovich, et al. Oxidation of linoleyl alcohol by potato tuber lipoxygenase: kinetics and positional, stereo, and geometrical (cis, trans) specificity of the reaction. Arch Biochem Biophys. 2000 Jun 1;378(1):65-77. [2]. Nagao Totani, et al. Gallic acid glycerol ester promotes weight-loss in rats. J Oleo Sci. 2011;60(9):457-62. Chemical & Physical Properties Density 0.9±0.1 g/cm3 Boiling Point 374.0±11.0 °C at 760 mmHg Molecular Formula C18H34O Molecular Weight 266.462 Flash Point 124.1±15.6 °C Exact Mass 266.260956 PSA 20.23000 LogP 7.28 Vapour Pressure 0.0±1.9 mmHg at 25°C Index of Refraction 1.473 InChIKey JXNPEDYJTDQORS-HZJYTTRNSA-N SMILES CCCCCC=CCC=CCCCCCCCCO Storage condition 2-8°C |
| Use of | Linoleyl alcohol, a structural analog of Linoleic acid with no a-carboxyl group, is a fatty alcohol[1]. Properties Name cis,cis-9,12-Octadecadien-1-ol Synonym More Synonyms (9Z,12Z)-Octadeca-9,12-dien-1-ol Biological Activity Description Linoleyl alcohol, a structural analog of Linoleic acid with no a-carboxyl group, is a fatty alcohol[1]. Related Catalog Signaling Pathways >> Others >> Others Research Areas >> Metabolic Disease In Vitro The dioxygenation of Linoleyl alcohol by potato tuber lipoxygenase leads to formation of two positional isomeric products-9- and 13-hydroperoxyoctadecadien-1-ols[1]. In Vivo Animal feeding experiments have revealed that esters made from Gallic acid (GA) and (-)-Epigallo-catechin (EGC) or Linoleyl alcohol are more effective in weight-loss promotion and metabolic syndrome management than are intact GA and EGC[2]. References [1]. I A Butovich, et al. Oxidation of linoleyl alcohol by potato tuber lipoxygenase: kinetics and positional, stereo, and geometrical (cis, trans) specificity of the reaction. Arch Biochem Biophys. 2000 Jun 1;378(1):65-77. [2]. Nagao Totani, et al. Gallic acid glycerol ester promotes weight-loss in rats. J Oleo Sci. 2011;60(9):457-62. Chemical & Physical Properties Molecular Formula C18H34O Exact Mass 266.260956 PSA 20.23000 Index of Refraction 1.473 InChIKey JXNPEDYJTDQORS-HZJYTTRNSA-N SMILES CCCCCC=CCC=CCCCCCCCCO |
| Tax Rebate | 9.0% |
| Supervision | none |
| Transport Info | Product name: Purity: 95.0% |
| MSDS Transport Info | Module 14. Shipping information United Nations classification: inconsistent with United Nations classification standards UN number: not specified |
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