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Merck
CN

148997

戊酸甲酯

99%

别名:

甲基戊酸酯

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线性分子式:
CH3(CH2)3CO2CH3
化学文摘社编号:
分子量:
116.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-838-0
Beilstein/REAXYS Number:
1741905
MDL number:
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assay

99%

form

liquid

InChI key

HNBDRPTVWVGKBR-UHFFFAOYSA-N

InChI

1S/C6H12O2/c1-3-4-5-6(7)8-2/h3-5H2,1-2H3

SMILES string

CCCCC(=O)OC

refractive index

n20/D 1.397 (lit.)

bp

128 °C (lit.)

density

0.875 g/mL at 25 °C (lit.)

Quality Level

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Application

Methyl valerate can be used:
  • In the preparation of lankacidin C 8-valerate.
  • As a reactant to synthesize bis(2,2,2-trifluoroethyl) 2-oxoalkylphosphonates.
  • As a substrate in the fluorination reactions of unactivated C(sp3)H bonds using decatungstate photocatalyst and N-fluorobenzenesulfonimide.

General description

Methyl valerate is a methyl ester of valeric acid, generally used as a fragrance in the manufacture of soaps and laundry detergents. It is also used as a plasticizer and surrogate component for biodiesel.

pictograms

FlameExclamation mark

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3 - Skin Sens. 1B

存储类别

3 - Flammable liquids

wgk

WGK 2

flash_point_f

84.2 °F

flash_point_c

29 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Design and control of reactive distillation process for the production of methyl valerate
Chen C-L, et al.
Industrial & Engineering Chemistry Research, 55(5), 1347-1360 (2016)
A Convenient Photocatalytic Fluorination of Unactivated C-H Bonds
Halperin SD, et al.
Angewandte Chemie (International Edition in English), 126(18), 4778-4781 (2014)
K Nakahama et al.
The Journal of antibiotics, 28(5), 390-394 (1975-05-01)
Lankacidin C, a component of lankacidin-group (T-2636) antibiotics, was esterified to lankacidin C 8-butyrate in the presence of methyl butyrate by culture broth and by cell-free extract of Bacillus megaterium IFO 12108. In addition, methyl isobutyrate, methyl valerate and methyl
A practical process for the preparation of bis (2, 2, 2-trifluoroethyl) 2-oxoalkylphosphonates by acylation with carboxylic esters
Molnar K, et al.
Tetrahedron Letters, 56(34), 4877-4879 (2015)
Studies on lankacidin-group (T-2636) antibiotics. X
Nakahama K, et al.
The Journal of Antibiotics, 28(5), 390-394 (1975)

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