10896
月桂酸乙烯酯
Wacker Chemie AG, ≥98% (GC)
别名:
VL
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线性分子式:
CH3(CH2)10COOCH=CH2
化学文摘社编号:
分子量:
226.36
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-414-7
Beilstein/REAXYS Number:
1778369
MDL number:
Assay:
≥98% (GC)
产品名称
月桂酸乙烯酯, 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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Other Notes
根据要求提供批量采购价
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.
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
257.0 °F
flash_point_c
125 °C
ppe
Eyeshields, Gloves
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.
The Journal of antimicrobial chemotherapy, 69(12), 3169-3180 (2014-07-31)
The efficacy of abacavir/lamivudine has been reported to be inferior to tenofovir/emtricitabine. Several randomized clinical trials (RCTs) investigated the effectiveness and safety of abacavir/lamivudine and tenofovir/emtricitabine combined antiretroviral treatment (cART) and we have reviewed the available evidence. Systematic review and
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