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Merck

10896

Sigma-Aldrich

月桂酸乙烯酯

Wacker Chemie AG, ≥98% (GC)

别名:

VL

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1 KG
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About This Item

线性分子式:
CH3(CH2)10COOCH=CH2
CAS号:
分子量:
226.36
Beilstein:
1778369
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

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方案

≥98% (GC)

制造商/商品名称

Wacker Chemie AG

沸点

254 °C/1013 hPa (lit.)

溶解性

H2O: slightly soluble 1 g/L at 20 °C

密度

0.871 g/mL at 20 °C (lit.)

官能团

ester

SMILES字符串

CCCCCCCCCCCC(=O)OC=C

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

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一般描述

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[1]. The enzymatic acylation of Avicel cellulose with vinyl laurate, a solvent free reaction system, was studied[2].

应用

Vinyl laurate was used in the synthesis of laurate and stearate esters of corn starch[3]. It was used as the acyl donor during synthesis of sucrose laurate esters catalyzed by Bacillus pseudofirmus AL-89 [4]. Vinyl laurate was also used in the preparation of chirally deuterated benzyl chlorides[5].

其他说明

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储存分类代码

10 - Combustible liquids

WGK

WGK 1

闪点(°F)

257.0 °F

闪点(°C)

125 °C

个人防护装备

Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Slide 1 of 1

1 of 1

Synthesis of sucrose laurate using a new alkaline protease.
Pedersen NR, et al.
Tetrahedron Asymmetry, 14(6), 667-673 (2003)
Novel gelling behavior of poly (N-isopropylacrylamide-co-vinyl laurate) microgel dispersions.
Benee LS, et al.
Langmuir, 18(16), 6025-6030 (2002)
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)
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
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

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