| Weight | 104.105 g/mol |
|---|---|
| Formula | C4H8O3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
2-Hydroxybutyric acid (600-15-7, 565-70-8)
alpha-hydroxybutyrate · 2-hydroxybutyric acid, monosodium salt, (+-)-isomer · 2-hydroxybutyric acid, (+-)-isomer
Score:
#1100 in Biochemistry
,
#2824 in Biology
,
#3538 in Chemistry
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- The thermal degradation of poly(-(d)--hydroxybutyric acid): Part 2Changes in molecular weight (Polymer Degradation and Stability, 1984)
- An inherited disorder of isoleucine catabolism causing accumulation of alpha-methylacetoacetate and alpha-methyl-beta -hydroxybutyrate, and intermittent metabolic acidosis. (Pediatric Research, 1973)
- KINETICS OF IN VIVO CONVERSION OF -[3H]AMINOBUTYRIC ACID TO -[3H]HYDROXYBUTYRIC ACID BY RAT BRAIN1,2 (Journal of Neurochemistry, 1977)
- Effect of gamma-hydroxybutyrate on pain, fatigue, and the alpha sleep anomaly in patients with fibromyalgia. Preliminary report. (The Journal of Rheumatology, 1998)
- Accumulation of 3-hydroxyisobutyric acid, 2-methyl-3-hydroxybutyric acid and 3-hydroxyisovaleric acid in ketoacidosis. (Clinica Chimica Acta, 1975)
- Cellular glycogen, beta-1,2,-glucan, poly beta-hydroxybutyric acid and extracellular polysaccharides in fast-growing species of Rhizobium. (Antonie Van Leeuwenhoek International Journal of General and Molecular Microbiology, 1981)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - alpha-hydroxybutyrate
- 2-hydroxybutyric acid, monosodium salt, (+-)-isomer
- 2-hydroxybutyric acid, (+-)-isomer
- 2-hydroxybutyric acid, (R)-isomer
- 2-hydroxybutanoic acid
- 2-hydroxybutyric acid, monosodium salt
-
SMILESCCC(C(=O)O)O
-
InChIKeyAFENDNXGAFYKQO-UHFFFAOYSA-N
- Pubchem - 2-Hydroxybutyric acid
- Wikipedia - 2-hydroxybutyric acid
2-Hydroxybutyric acid, also known as alpha-hydroxybutyrate and -hydroxybutyrate, is a hydroxybutyric acid with the hydroxyl group on the carbon adjacent to the carboxyl. It is a chiral compound having two enantiomers, D-2-hydroxybutyric acid and L-2-hydroxybutyric acid. 2-Hydroxybutyrate, the conjugate base of 2-hydroxybutyric acid, is produced in mammalian tissues (principally hepatic) that catabolize L-threonine or synthesize glutathione.
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