61725
Vinyl laurate
≥99.0% (GC)
Sinónimos:
Dodecanoic acid vinyl ester, Vinyl dodecanoate
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Fórmula lineal:
CH3(CH2)10COOCH=CH2
Número CAS:
Peso molecular:
226.36
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-414-7
Beilstein/REAXYS Number:
1778369
MDL number:
Assay:
≥99.0% (GC)
Servicio técnico
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Permítanos ayudarleQuality Level
assay
≥99.0% (GC)
refractive index
n20/D 1.441
bp
254 °C/1013 hPa (lit.)
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
General description
Vinyl laurate acts as an acyl donor during the transeterification of L-α-glycerophosphorylcholine (GPC) in the presence of Candida antarctica lipase B as catalyst to form lysophosphatidylcholine (LPC).
Application
Vinyl laurate can be used to synthesize the following:
- sucrose laurate esters from sucrose in organic solvents
- poly(vinyl laurate) (PVL)latexes
- porous conducting ‘‘soft′′ polymer foams which can be used as gas sensors
Clase de almacenamiento
10 - Combustible liquids
wgk
WGK 3
flash_point_f
257.0 °F
flash_point_c
125 °C
ppe
Eyeshields, Gloves
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"Conducting Nanocomposite Polymer Foams from Ice-Crystal-Templated Assembly of Mixtures of Colloids"
Colard.L.AC, et al.
Advanced Mat., 21(28), 2894-2898 (2009)
Lysophosphatidylcholine synthesis with Candida antarctica lipase B (Novozym 435)
Virto C and Adlercreutz P
Enzyme and Microbial Technology, 26(08), 630-635 (2000)
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