10896
Vinyl laurate
produced by Wacker Chemie AG, Burghausen, Germany, ≥98% (GC)
Synonym(s):
VL
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About This Item
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grade
produced by Wacker Chemie AG, Burghausen, Germany
Assay
≥98% (GC)
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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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
prices for bulk quantities on request
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
257.0 °F
Flash Point(C)
125 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis of sucrose laurate using a new alkaline protease.
Tetrahedron Asymmetry, 14(6), 667-673 (2003)
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.
Starch/Staerke, 60(12), 667-675 (2008)
Novel gelling behavior of poly (N-isopropylacrylamide-co-vinyl laurate) microgel dispersions.
Langmuir, 18(16), 6025-6030 (2002)
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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