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277827

Sigma-Aldrich

Ácido 4-metilvalérico

99%

Sinónimos:

Ácido 4-metilpentanoico, Ácido isocaproico

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About This Item

Fórmula lineal:
(CH3)2CHCH2CH2CO2H
Número de CAS:
646-07-1
Peso molecular:
116.16
Beilstein/REAXYS Number:
1741912
EC Number:
211-464-0
MDL number:
MFCD00002803
UNSPSC Code:
12352100
PubChem Substance ID:
24856788
NACRES:
NA.22

assay

99%

form

liquid

refractive index

n20/D 1.414 (lit.)

bp

199-201 °C (lit.)

density

0.923 g/mL at 25 °C (lit.)

SMILES string

CC(C)CCC(O)=O

InChI

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

InChI key

FGKJLKRYENPLQH-UHFFFAOYSA-N

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General description

Conductimetric detection of 4-methylvaleric acid on unfunctionized polymethacrylate resin (TSKgel G3000PWXL) columns has been reported.

Application

4-Methylvaleric acid has been used in asymmetric synthesis of (4S)-4-isopropyl-3-[(2′S)-2′,4′-dimethyl-valeryl)]-2-oxazolidinone.

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 3

flash_point_f

206.6 °F - closed cup

flash_point_c

97 °C - closed cup

ppe

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

Certificados de análisis (COA)

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Kazutoku Ohta et al.
Journal of chromatography. A, 1039(1-2), 171-177 (2004-07-15)
The application of unfunctionized polymethacrylate resin (TSKgel G3000PWXL) as a stationary phase in liquid chromatography with conductimetric detection for C1-C7 aliphatic monocarboxylic acids (formic acid, acetic acid, propionic acid, butyric acid, isovaleric acid, valeric acid, 3,3-dimethylbutyric acid, 4-methylvaleric acid, hexanoic
G E Mortimore et al.
The Journal of biological chemistry, 262(34), 16322-16327 (1987-12-05)
Previous studies with livers from fed rats perfused in the single-pass mode have shown that regulatory amino acids (Leu, Tyr, Gln, Pro, Met, His, and Trp) as a group as well as leucine alone inhibit deprivation-induced protein degradation optimally at
S C Ling et al.
Journal of applied microbiology, 111(3), 559-571 (2011-06-22)
Polyhydroxyalkanoate (PHA) with enhanced physicochemical properties will be ideal for a wide range of practical applications. The incorporation of 3-hydroxy-4-methylvalerate (3H4MV) into the polymer backbone is known to improve the overall properties of the resulting polymer. However, the most suitable
Viridiana Tejada-Ortigoza et al.
Molecules (Basel, Switzerland), 24(4) (2019-02-17)
Fruit by-products are being investigated as non-conventional alternative sources of dietary fiber (DF). High hydrostatic pressure (HHP) treatments have been used to modify DF content as well as its technological and physiological functionality. Orange, mango and prickly pear peels untreated
Progress towards the total synthesis of callipeltin A. Asymmetric synthesis of (2R, 3R, 4S)-3-hydroxy-2, 4, 6-trimethylheptanoic acid.
Guerlavais V, et al.
Tetrahedron Asymmetry, 13(7), 675-680 (2002)
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