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Key Documents

148997

Sigma-Aldrich

Methyl valerate

99%

Synonym(s):

Methyl pentanoate

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About This Item

Linear Formula:
CH3(CH2)3CO2CH3
CAS Number:
Molecular Weight:
116.16
Beilstein:
1741905
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

liquid

refractive index

n20/D 1.397 (lit.)

bp

128 °C (lit.)

density

0.875 g/mL at 25 °C (lit.)

SMILES string

CCCCC(=O)OC

InChI

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

InChI key

HNBDRPTVWVGKBR-UHFFFAOYSA-N

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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.

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.

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Flam. Liq. 3 - Skin Sens. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

84.2 °F

Flash Point(C)

29 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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)
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 Convenient Photocatalytic Fluorination of Unactivated C-H Bonds
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Studies on lankacidin-group (T-2636) antibiotics. X
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The Journal of Antibiotics, 28(5), 390-394 (1975)
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