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Key Documents

219819

Sigma-Aldrich

2-Hydroxyisocaproic acid

99%

Synonym(s):

2-Hydroxy-4-methylvaleric acid, DL-leucic acid

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About This Item

Linear Formula:
(CH3)2CHCH2CH(OH)CO2H
CAS Number:
Molecular Weight:
132.16
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

mp

78-80 °C (lit.)

SMILES string

CC(C)CC(O)C(O)=O

InChI

1S/C6H12O3/c1-4(2)3-5(7)6(8)9/h4-5,7H,3H2,1-2H3,(H,8,9)

InChI key

LVRFTAZAXQPQHI-UHFFFAOYSA-N

Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Extraction-spectrophotometric determination of antimony (V) with 2-hydroxyisocaproic acid and citrate, with application to differential determination of antimony (V) and antimony (III).
SATO S and UCHIKAWA S.
Analytical Sciences, 2, 47-47 (1986)
Polymer, Assisted Solution Phase Synthesis of tr, Ketoamides.
Parlow JJ, et al.
High-Throughput Synthesis: Principles and Practices, 143-143 (2001)
K D Webster et al.
Archives of biochemistry and biophysics, 273(2), 562-571 (1989-09-01)
L-Thiomorpholine-3-carboxylic acid (L-TMC) is a cyclized analog of S-(2-chloroethyl)-L-cysteine, which is cytotoxic in vitro and nephrotoxic in vivo. To determine whether L-TMC may play a role in S-(2-chloroethyl)-L-cysteine-induced toxicity, the cytotoxicity of L-TMC was studied in isolated rat kidney cells.
L J Spaapen et al.
Journal of inherited metabolic disease, 10(4), 383-390 (1987-01-01)
Analysis of urinary organic acids in patients admitted for screening for inborn errors of metabolism incidentally revealed the presence of abnormal amounts of 4-hydroxyphenyllactate (4-HPLA) and phenyllactate (PLA). These compounds are found in tyrosinaemia and phenylketonuria but in our patients
Continuous enzymatically catalyzed production of L-leucine from the corresponding racemic hydroxy acid.
B Bossow et al.
Annals of the New York Academy of Sciences, 506, 325-336 (1987-01-01)

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