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109878

Sigma-Aldrich

2-Methylvaleric acid

98%

Sinónimos:

(±)-2-Methylvaleric acid, 2-Methylpentanoic acid

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About This Item

Fórmula lineal:
CH3CH2CH2CH(CH3)CO2H
Número de CAS:
97-61-0
Peso molecular:
116.16
Beilstein/REAXYS Number:
1720658
EC Number:
202-594-9
MDL number:
MFCD00002671
UNSPSC Code:
12352100
eCl@ss:
39021337
PubChem Substance ID:
24846943
NACRES:
NA.22

assay

98%

refractive index

n20/D 1.414 (lit.)

bp

196-197 °C (lit.)

density

0.931 g/mL at 25 °C (lit.)

SMILES string

CCCC(C)C(O)=O

InChI

1S/C6H12O2/c1-3-4-5(2)6(7)8/h5H,3-4H2,1-2H3,(H,7,8)

InChI key

OVBFMEVBMNZIBR-UHFFFAOYSA-N

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Application

2-Methylpentanoic acid (2-Methylvaleric acid) was used as an internal standard for gas chromatographic analysis of microbial end products.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1C

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 2

flash_point_f

199.4 °F - closed cup

flash_point_c

93 °C - closed cup

ppe

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

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J W Mayhew et al.
Applied and environmental microbiology, 33(4), 1002-1003 (1977-04-01)
2-Methylpentanoic acid and benzoic acid are suggested for use as routine internal standards for gas chromatographic analysis of microbial end products.
Xiaoqing Cai et al.
Bioorganic & medicinal chemistry, 19(12), 3831-3844 (2011-05-27)
Previous studies have indicated that the methylvalerate subunit of bleomycin (BLM) plays an important role in facilitating DNA cleavage by BLM and deglycoBLM. Eleven methylvalerate analogues have been synthesized and incorporated into deglycoBLM congeners by the use of solid-phase synthesis.
D A Dawson
Teratology, 44(5), 531-546 (1991-11-01)
A modified FETAX (Frog Embryo Teratogenesis Assay: Xenopus) protocol was used to assess the joint action of ten aliphatic carboxylic acids on Xenopus embryo development. Stock solutions of each acid alone, made up at twice the EC50 of the individual
Z Suarez de Mata et al.
Archives of biochemistry and biophysics, 285(1), 158-165 (1991-02-15)
The condensation of two propionyl-CoA units or a propionyl-CoA with acetyl-CoA is required for the synthesis of 2-methylvalerate or 2-methylbutyrate, respectively, two of the major fermentation products of Ascaris anaerobic muscle metabolism. An enzyme that preferentially catalyzes the condensation of
R Komuniecki et al.
The Journal of parasitology, 67(6), 841-846 (1981-12-01)
Disrupted Ascaris mitochondria formed 2-methylbutyrate (2-MB) and 2-methylvalerate (2-MV) when incubated anaerobically with acetyl CoA, propionyl CoA and NADH. However, when mitochondrial membranes were removed by high speed centrifugation and the mitochondrial soluble fraction was incubated with the same substrates
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