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线性分子式:
CH3(CH2)3(CH2CH=CH)2(CH2)7COOC2H5
化学文摘社编号:
分子量:
308.50
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-868-4
Beilstein/REAXYS Number:
1727827
MDL number:
InChI key
FMMOOAYVCKXGMF-MURFETPASA-N
InChI
1S/C20H36O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22-4-2/h8-9,11-12H,3-7,10,13-19H2,1-2H3/b9-8-,12-11-
SMILES string
CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC
grade
technical
concentration
≥65% (GC)
Quality Level
bp
224 °C/17 mmHg (lit.)
density
0.876 g/mL at 25 °C (lit.)
functional group
ester
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General description
Ethyl linoleate can undergo auto-oxidation in the presence of the catalyst manganese(II)acetylacetonate.
Application
Ethyl linoleate can be used as a drying agent for alkyd paints. It can also form N2,3-ethenoguanine via reaction with deoxyguanosine.
Biochem/physiol Actions
从三角紫叶酢浆草中分离的亚油酸乙酯能够在小鼠B16黑素瘤细胞中抑制毛喉素诱导的黑色素生成和酪氨酸酶活性。这种抗黑色素生成作用是通过抑制cAMP产生来介导的。
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves
"4-Hydroxy-2-nonenal and ethyl linoleate form N 2, 3-ethenoguanine under peroxidizing conditions"
Ham.L J-A, et al.
Chemical Research in Toxicology, 1243-1250 (2000)
"Fast autoxidation of ethyl linoleate catalyzed by [Mn (acac) 3] and bipyridine: A possible drying catalyst for alkyd paints"
Gorkum VR, et al.
Inorganic Chemistry, 43(08), 2456-2458 (2004)
Yun Ding et al.
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Fatty acid ethyl esters: a novel biologic marker for heavy in utero ethanol exposure: a case report.
J Klein et al.
Therapeutic drug monitoring, 21(6), 644-646 (1999-12-22)
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