62262
亚油酸乙酯
technical, ≥65% (GC)
别名:
亚麻油酸乙酯
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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
refractive index
n20/D 1.455
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
"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)
"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)
Yun Ding et al.
Current biology : CB, 29(7), 1089-1099 (2019-03-19)
It is unclear where in the nervous system evolutionary changes tend to occur. To localize the source of neural evolution that has generated divergent behaviors, we developed a new approach to label and functionally manipulate homologous neurons across Drosophila species.
D L Luthria et al.
Biochimica et biophysica acta, 1213(1), 1-4 (1994-06-23)
In order to determine how dietary linoleate is metabolized, rats were maintained on a chemically defined diet containing 1.6% ethyl linoleate. After 5 weeks the linoleate was replaced by an equal amount of ethyl 9,10,12,13-d4-linoleate. The animals were killed 3
A Murakami et al.
Oncology, 53(5), 386-391 (1996-09-01)
The anti-tumor-promoting activity of 1'-acetoxychavicol acetate (ACA) was examined in a two-stage carcinogenesis experiment in ICR mouse skin using 7,12-dimethylbenz[a]anthracene (0.19 mumol) and 12-O-tetradecanoylphorbol-13-acetate (TPA; 1.6 nmol). Topical application of ACA (160 nmol) markedly reduced the average number of tumors
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