83916
蓖麻油酸甲酯
analytical standard
别名:
(R)-12-羟基-顺式-9-十八烯酸甲酯, 12-羟基油酸甲酯, 蓖麻油酸甲酯
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关于此项目
经验公式（希尔记法）:
C19H36O3
化学文摘社编号:
分子量:
312.49
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
EC Number:
205-472-3
Beilstein/REAXYS Number:
6132055
MDL number:
产品名称
蓖麻油酸甲酯, analytical standard
InChI key
XKGDWZQXVZSXAO-ADYSOMBNSA-N
InChI
1S/C19H36O3/c1-3-4-5-12-15-18(20)16-13-10-8-6-7-9-11-14-17-19(21)22-2/h10,13,18,20H,3-9,11-12,14-17H2,1-2H3/b13-10-/t18-/m1/s1
SMILES string
O=C(OC)CCCCCCC/C=C\C[C@H](O)CCCCCC
grade
analytical standard
assay
≥99.0% (GC)
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
format
neat
functional group
ester
shipped in
ambient
storage temp.
−20°C
Quality Level
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Application
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General description
蓖麻油酸甲酯是一种对映体可再生的化合物，通过从蓖麻油中进行酯交换而商业获得，通常用于化妆品，增塑剂，润滑油和精细化学工业。
Packaging
无底玻璃瓶。内含物装在插入的融合锥内。
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Optimization of methyl ricinoleate synthesis with ionic liquids as catalysts using the response surface methodology.
Xu W, et al.
Chemical Engineering Journal, 275(11), 63-70 (2015)
Synthesis of Enantiomerically Pure 2, 3, 4, 6-Tetrasubstituted Tetrahydropyrans by Prins-Type Cyclization of Methyl Ricinoleate and Aldehydes.
Biermann U, et al.
European Journal of Organic Chemistry, 2006(11), 2631-2637 (2006)
A Endrizzi et al.
Journal of basic microbiology, 35(5), 285-292 (1995-01-01)
The capacity of several strains of yeasts to do the bioconversion of methyl ricinoleate into gamma-decalactone, was studied in a medium containing this methylic ester of fatty acid as sole carbon source. Amongst the strains which are able to do
David S Wunschel et al.
The Analyst, 137(9), 2077-2085 (2012-03-15)
The investigation of crimes involving chemical or biological agents is infrequent, but presents unique analytical challenges. The protein toxin ricin is encountered more frequently than other agents and is found in the seeds of Ricinus communis, commonly known as the
J T Lin et al.
Lipids, 35(5), 481-486 (2000-07-25)
We have examined the role of 2-oleoyl-PE (phosphatidylethanolamine) in the biosynthesis of triacylglycerols (TAG) by castor microsomes. In castor microsomal incubation, the label from 14C-oleate of 1-palmitoyl-2-[1-(14)C]oleoyl-sn-glycero-3-phosphoethanolamine is incorporated into TAG containing ricinoleate. The enzyme characteristics, such as optimal pH
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