10896
月桂酸乙烯酯
Wacker Chemie AG, ≥98% (GC)
别名:
VL
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线性分子式:
CH3(CH2)10COOCH=CH2
化学文摘社编号:
分子量:
226.36
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-414-7
Beilstein/REAXYS Number:
1778369
MDL number:
Assay:
≥98% (GC)
InChI
1S/C14H26O2/c1-3-5-6-7-8-9-10-11-12-13-14(15)16-4-2/h4H,2-3,5-13H2,1H3
InChI key
GLVVKKSPKXTQRB-UHFFFAOYSA-N
SMILES string
CCCCCCCCCCCC(=O)OC=C
assay
≥98% (GC)
manufacturer/tradename
Wacker Chemie AG
bp
254 °C/1013 hPa (lit.)
solubility
H2O: slightly soluble 1 g/L at 20 °C
density
0.871 g/mL at 20 °C (lit.)
functional group
ester
Quality Level
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General description
Vinyl laurate is a clear, colorless to light yellow colored liquid. The flash point is 125°C. It forms aqueous colloidal microgel by copolymerization with N-isopropylacrylamide. The enzymatic acylation of Avicel cellulose with vinyl laurate, a solvent free reaction system, was studied.
Application
Vinyl laurate was used in the synthesis of laurate and stearate esters of corn starch. It was used as the acyl donor during synthesis of sucrose laurate esters catalyzed by Bacillus pseudofirmus AL-89 . Vinyl laurate was also used in the preparation of chirally deuterated benzyl chlorides.
Other Notes
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存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
257.0 °F
flash_point_c
125 °C
ppe
Eyeshields, Gloves
Synthesis of sucrose laurate using a new alkaline protease.
Pedersen NR, et al.
Tetrahedron Asymmetry, 14(6), 667-673 (2003)
Stavros Gremos et al.
Bioresource technology, 102(2), 1378-1382 (2010-10-05)
Cellulose esters are an important class of functional biopolymers with great interest in the chemical industry. In this work the enzymatic acylation of Avicel cellulose with vinyl propionate, vinyl laurate and vinyl stearate, has been performed successfully in a solvent
Synthesis of higher fatty acid starch esters using vinyl laurate and stearate as reactants.
Junistia L, et al.
Starch/Staerke, 60(12), 667-675 (2008)
Novel gelling behavior of poly (N-isopropylacrylamide-co-vinyl laurate) microgel dispersions.
Benee LS, et al.
Langmuir, 18(16), 6025-6030 (2002)
Derek W Barnett et al.
Journal of labelled compounds & radiopharmaceuticals, 56(1), 6-11 (2013-11-29)
Chirally deuterated benzyl chlorides were prepared using novel, general hexachloroacetone/polymer-supported triphenylphosphine treatment of chirally deuterated benzyl alcohols. Doubly labeled protected tyrosine was obtained in 62% yield with 86% de at the α-carbon and 82% de at the β-carbon. Key in
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