19390
Vinyl butyrate
contains 20 ppm 4-methoxyphenol as stabilizer, ≥99.0% (GC)
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About This Item
Linear Formula:
CH3CH2CH2COOCH=CH2
CAS Number:
Molecular Weight:
114.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-609-4
Beilstein/REAXYS Number:
1744933
MDL number:
Assay:
≥99.0% (GC)
Quality Level
assay
≥99.0% (GC)
contains
20 ppm 4-methoxyphenol as stabilizer
refractive index
n20/D 1.410
density
0.899 g/mL at 20 °C
functional group
ester
storage temp.
2-8°C
SMILES string
CCCC(=O)OC=C
InChI
1S/C6H10O2/c1-3-5-6(7)8-4-2/h4H,2-3,5H2,1H3
InChI key
MEGHWIAOTJPCHQ-UHFFFAOYSA-N
General description
Vinyl butyrate causes the transesterification of natural flavonoid bergenin immobilized onto carboxylic acid functionalized controlled pore glass.
Application
Vinyl butyrate was used as acyl donor in the synthesis of citronellyl esters (acetate, propionate, butyrate, caprate and laurate) using immobilized Candida antarctical ipase B.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
68.0 °F - closed cup
flash_point_c
20 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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M Holmquist et al.
Journal of protein chemistry, 14(4), 217-224 (1995-05-01)
To reveal the functional role of Glu87 and Trp89 in the lid of Humicola lanuginosa lipase, site-directed mutagenesis at Glu87 and Trp89 was carried out. The catalytic performance of wild-type and mutated lipases was studied in transesterification reactions in cyclohexane
Betzaida Castillo et al.
Biotechnology and bioengineering, 94(3), 565-574 (2006-02-24)
Enzymes are attractive catalysts for the production of optically active compounds in organic solvents. However, their often low catalytic activity in such applications hampers their practical use. To overcome this, we investigated the effectiveness of the covalent modification of alpha-chymotrypsin
Giulia Martelli et al.
Bioorganic chemistry, 88, 102975-102975 (2019-05-19)
Obtainment and testing of pure enantiomers are of great importance for bioactive compounds, because of the assessed implications of enantioselectivity in receptor-mediated responses. Herein we evaluated the use of biocatalysis to obtain enantiomerically pure β-lactam intermediates further exploited in the