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19390

Sigma-Aldrich

Vinyl butyrate

contains 20 ppm 4-methoxyphenol as stabilizer, ≥99.0% (GC)

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About This Item

Fórmula lineal:
CH3CH2CH2COOCH=CH2
Número de CAS:
123-20-6
Peso molecular:
114.14
Beilstein/REAXYS Number:
1744933
EC Number:
204-609-4
MDL number:
MFCD00059410
UNSPSC Code:
12352100
PubChem Substance ID:
57647792
NACRES:
NA.22

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

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

Categorías relacionadas

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.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

hcodes

H225,H332

Hazard Classifications

Acute Tox. 4 Inhalation - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

V1503

Vinyl acetate

Vinyl 4-tert-butylbenzoate 99%

Sigma-Aldrich

380806

Vinyl 4-tert-butylbenzoate

Umar Akbar et al.
Tetrahedron letters, 51(8), 1220-1220 (2010-02-23)
The natural flavonoid bergenin was directly immobilized onto carboxylic acid functionalized controlled pore glass (carboxy-CPG) at 95% yield. Immobilized bergenin was brominated via chloroperoxidase in aqueous solution and then transesterified with vinyl butyrate in diisopropyl ether by subtilisin carslberg (SC)
Betzaida Castillo et al.
BMC biotechnology, 6, 51-51 (2006-12-26)
Enzymes have been extensively used in organic solvents to catalyze a variety of transformations of biological and industrial significance. It has been generally accepted that in dry aprotic organic solvents, enzymes are kinetically trapped in their conformation due to the
Ming Jian Liu et al.
Drug delivery, 23(9), 3444-3451 (2016-05-21)
The butyryl galactose ester-modified coix component microemulsions (But-Gal-CMEs) was developed for enhanced liver tumor-specific targeting. The study was aimed to evaluate the hepatoma-targeting potential of But-Gal-CMEs in vitro and in vivo. But-Gal-CMEs with a uniform spherical shape exhibited a small
Mozaffar Shakeri et al.
Journal of biotechnology, 145(3), 281-283 (2009-12-02)
We examined the activity of free Rhizopus oryzae lipase (ROL) and ROL immobilized on mesoporous materials in transesterification reactions in various dialkylimidazolium-cation based ionic liquids. For free ROL, the highest activity (0.39 U/mg protein) was obtained in [OMIm][PF(6)] followed by
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
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