10896
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:
Molecular Weight:
226.36
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-414-7
Beilstein/REAXYS Number:
1778369
MDL number:
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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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.
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.
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
Mario Cruciani et al.
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