Skip to Content
Merck
CN

19390

Vinyl butyrate

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

Sign In to View Organizational & Contract Pricing.

Select a Size


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)
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

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

InChI key

MEGHWIAOTJPCHQ-UHFFFAOYSA-N

InChI

1S/C6H10O2/c1-3-5-6(7)8-4-2/h4H,2-3,5H2,1H3

SMILES string

CCCC(=O)OC=C

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

Quality Level

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.

General description

Vinyl butyrate causes the transesterification of natural flavonoid bergenin immobilized onto carboxylic acid functionalized controlled pore glass.

pictograms

FlameExclamation mark

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

Regulatory Information

危险化学品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
Ionic liquids improve citronellyl ester synthesis catalyzed by immobilized Candida antarctica lipase B in solvent-free media.
Lozano P, et al.
Green Chemistry, 9(7), 780-784 (2007)
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
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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service