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Merck

10896

Vinyl laurate

Wacker Chemie AG, ≥98% (GC)

Synonym(s):

VL

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1 KG

CZK 2,360.00

167 KG

CZK 94,100.00

CZK 2,360.00


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About This Item

Linear Formula:
CH3(CH2)10COOCH=CH2
CAS Number:
Molecular Weight:
226.36
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-414-7
Beilstein/REAXYS Number:
1778369
MDL number:

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Product Name

Vinyl laurate, Wacker Chemie AG, ≥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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This Item
6172549682048486
assay

≥98% (GC)

assay

≥99.0% (GC)

assay

99%

assay

-

solubility

H2O: slightly soluble 1 g/L at 20 °C

solubility

-

solubility

-

solubility

-

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

density

0.871 g/mL at 20 °C (lit.)

density

0.871 g/mL at 20 °C (lit.)

density

1.188 g/mL at 25 °C (lit.)

density

0.934 g/mL at 25 °C (lit.)

bp

254 °C/1013 hPa (lit.)

bp

254 °C/1013 hPa (lit.)

bp

237 °C/733 mmHg (lit.)

bp

72-73 °C (lit.)

grade

produced by Wacker Chemie AG, Burghausen, Germany

grade

-

grade

-

grade

analytical standard

Application

Vinyl laurate was used in the synthesis of laurate and stearate esters of corn starch[1]. It was used as the acyl donor during synthesis of sucrose laurate esters catalyzed by Bacillus pseudofirmus AL-89 [2]. Vinyl laurate was also used in the preparation of chirally deuterated benzyl chlorides[3].

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[4]. The enzymatic acylation of Avicel cellulose with vinyl laurate, a solvent free reaction system, was studied[5].

Other Notes

prices for bulk quantities on request

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

257.0 °F

flash_point_c

125 °C

ppe

Eyeshields, Gloves


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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)
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
Sophie Cohen et al.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 60(7), 1111-1119 (2014-12-18)
Despite the declining incidence of severe neurological complications such as HIV encephalopathy, human immunodeficiency virus (HIV) infection in children is still associated with a range of cognitive problems. Although most HIV-infected children in industrialized countries are immigrants with a relatively

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