E4762
甲基反油酸
≥99% (capillary GC)
别名:
反-9-十八碳烯酸甲酯, 反油酸甲酯
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线性分子式:
CH3(CH2)7CH=CH(CH2)7COOCH3
化学文摘社编号:
分子量:
296.49
MDL number:
UNSPSC Code:
12352211
NACRES:
NA.25
PubChem Substance ID:
EC Number:
217-712-4
Beilstein/REAXYS Number:
1727038
产品名称
甲基反油酸, ≥99% (capillary GC)
InChI key
QYDYPVFESGNLHU-ZHACJKMWSA-N
InChI
1S/C19H36O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h10-11H,3-9,12-18H2,1-2H3/b11-10+
SMILES string
CCCCCCCC\C=C\CCCCCCCC(=O)OC
assay
≥99% (capillary GC)
form
liquid
density
0.871 g/mL at 20 °C (lit.)
functional group
ester
lipid type
unsaturated FAs
shipped in
ambient
storage temp.
−20°C
Quality Level
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Packaging
密封安瓿包装。
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Atanu Biswas et al.
Journal of agricultural and food chemistry, 56(14), 5611-5616 (2008-06-19)
An environmentally friendly water-based pathway to form the azide derivatives of soybean oil and fatty esters is reported. This entails first the formation of epoxides and then the azidization of the epoxides. The azidization reaction is carried out at high
Farshad Darvishi et al.
New biotechnology, 28(6), 756-760 (2011-02-18)
The yeast Yarrowia lipolytica degrades efficiently low-cost hydrophobic substrates for the production of various added-value products such as lipases. To obtain yeast strains producing high levels of extracellular lipase, Y. lipolytica DSM3286 was subjected to mutation using ethyl methanesulfonate (EMS)
Renee M Thomas et al.
Journal of the American Chemical Society, 133(19), 7490-7496 (2011-04-23)
N-Aryl,N-alkyl N-heterocyclic carbene (NHC) ruthenium metathesis catalysts are highly selective toward the ethenolysis of methyl oleate, giving selectivity as high as 95% for the kinetic ethenolysis products over the thermodynamic self-metathesis products. The examples described herein represent some of the
Ursula Biermann et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(26), 8201-8207 (2012-05-18)
A kinetic study of the dodecanethiol-catalyzed cis/trans isomerization of methyl oleate (cis-2) without added initiator was performed by focusing on the initiation of the radical chain reaction. The reaction orders of the rate of isomerization were 2 and 0.5 for
Cyril Thurier et al.
ChemSusChem, 1(1-2), 118-122 (2008-07-09)
Unsaturated vegetable oils are an attractive renewable feedstock, and the selective cleavage of unsaturated fatty esters is an important transformation in this respect. The efficient and selective cross-metathesis of methyl oleate with ethylene was achieved under mild conditions with ruthenium-alkylidene
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