2-hydroxypentanoic acid

pentanoic acid, 2-hydroxy-

CAS: 617-31-2 C5 H10 O3 MW: 118.13230000

Identification

Name2-hydroxypentanoic acid
CAS Number617-31-2
EINECS210-509-1
FDA UNIISearch
Molecular FormulaC5 H10 O3
Molecular Weight118.13230000
MDL NumberMFCD00065002
Nikkaji NumberJ95.434I

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Melting Point 34.00 °C. @ 760.00 mm Hg
Boiling Point 248.00 °C. @ 760.00 mm Hg (est)
Flash Point 244.00 °F. TCC ( 118.00 °C. ) (est)
logP (o/w) 0.450
Soluble in water, 3.381e+005 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for 2-hydroxypentanoic acid usage levels up tonot for fragrance use.
Recommendation for 2-hydroxypentanoic acid flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

found in nature

Synonyms

2- hydroxyvaleric acid pentanoic acid, 2-hydroxy- PubMed: Metabolomics reveals amino acids contribute to variation in response to simvastatin treatment. PubMed: Chlorinated-solvent-free gas chromatographic analysis of biomass containing polyhydroxyalkanoates. PubMed: Routine analysis of short-chain fatty acids for anaerobic bacteria identification using capillary electrophoresis and indirect ultraviolet detection. PubMed: Total syntheses of (+/-)-anchinopeptolide D and (+/-)-cycloanchinopeptolide D. PubMed: Poststatin, a new inhibitor of prolyl endopeptidase. IV. The chemical synthesis of poststain. PubMed: Poststatin, a new inhibitor of prolyl endopeptidase. III. Optical resolution of 3-amino-2-hydroxyvaleric acid and absolute configuration of poststatin. PubMed: Facile synthesis of chiral 2-hydroxy acids catalyzed by a stable duck epsilon-crystallin with endogenous L-lactate dehydrogenase activity. PubMed: Hydroxylated analogues of 5-aminovaleric acid as 4-aminobutyric acidB receptor antagonists: stereostructure-activity relationships. PubMed: Analyses of fermentation products of Listeria species by frequency-pulsed electron-capture gas-liquid chromatography.