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Merck
CN

277827

4-Methylvaleric acid

99%

Synonym(s):

4-Methylpentanoic acid, Isocaproic acid

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About This Item

Linear Formula:
(CH3)2CHCH2CH2CO2H
CAS Number:
646-07-1
Molecular Weight:
116.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24856788
EC Number:
211-464-0
Beilstein/REAXYS Number:
1741912
MDL number:
MFCD00002803
Assay:
99%
Form:
liquid

Key Documents

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Product Name

4-Methylvaleric acid, 99%

InChI key

FGKJLKRYENPLQH-UHFFFAOYSA-N

InChI

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

SMILES string

CC(C)CCC(O)=O

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.)

functional group

carboxylic acid

Quality Level

100

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Application

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

General description

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

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1C

Storage Class

8A - Combustible corrosive hazardous materials

wgk

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

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Certificates of Analysis (COA)

Lot/Batch Number
SHBS9360
SHBR7492
SHBR3272
SHBQ1414
SHBN7601

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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)
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
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
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
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