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10896

Sigma-Aldrich

Vinyl laurate

Wacker Chemie AG, ≥98% (GC)

Synonym(s):

VL

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About This Item

Linear Formula:
CH3(CH2)10COOCH=CH2
CAS Number:
2146-71-6
Molecular Weight:
226.36
Beilstein/REAXYS Number:
1778369
EC Number:
218-414-7
MDL number:
MFCD00048421
UNSPSC Code:
12352100
PubChem Substance ID:
57646832
NACRES:
NA.22

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Quality Level

100

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

SMILES string

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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1 of 4

This Item
6172549682048486
Vinyl laurate Wacker Chemie AG, ≥98% (GC)

Sigma-Aldrich

10896

Vinyl laurate

Vinyl laurate ≥99.0% (GC)

Sigma-Aldrich

61725

Vinyl laurate

4-Vinyl-1,3-dioxolan-2-one 99%

Sigma-Aldrich

496820

4-Vinyl-1,3-dioxolan-2-one

Vinyl acetate analytical standard

Supelco

48486

Vinyl acetate

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

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

Application

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].

Other Notes

prices for bulk quantities on request

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

257.0 °F

flash_point_c

125 °C

ppe

Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN7036
BCCM5579
BCCJ5044
BCCL4274
BCCL9125

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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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