| Weight | 104.105 g/mol |
|---|---|
| Formula | C4H8O3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
3-hydroxybutyric acid
beta Hydroxybutyric Acid · beta Hydroxybutyrate · 3 Hydroxybutyrate
625-71-8, 300-85-6, 26063-00-3
Score:
#994 in Biochemistry
,
#2610 in Biology
,
#3262 in Chemistry
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- Sigma-Aldrich - 3-hydroxybutyric acid46.80 - 138.50 USD
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- Cloning of the Alcaligenes eutrophus genes for synthesis of poly-beta-hydroxybutyric acid (PHB) and synthesis of PHB in Escherichia coli. (Journal of Bacteriology, 1988)
- Nile blue A as a fluorescent stain for poly-beta-hydroxybutyrate. (Applied and Environmental Microbiology, 1982)
- Poly-beta-hydroxybutyrate (PHB) biosynthesis in Alcaligenes eutrophus H16. Identification and characterization of the PHB polymerase gene (phbC). (Journal of Biological Chemistry, 1989)
- D-beta-hydroxybutyrate protects neurons in models of Alzheimer's and Parkinson's disease. (Proceedings of the National Academy of Sciences of the United States of America, 2000)
- Cloning and expression in Escherichia coli of the Alcaligenes eutrophus H16 poly-beta-hydroxybutyrate biosynthetic pathway (Journal of Bacteriology, 1988)
- Free fatty acids, beta-hydroxybutyrate, and ischaemic heart-disease. (The Lancet, 1970)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - beta Hydroxybutyric Acid
- beta Hydroxybutyrate
- 3 Hydroxybutyrate
- beta-Hydroxybutyrate
- beta-Hydroxybutyric Acid
- (+ -)-3-Hydroxybutyric Acid
- 3 Hydroxybutyric Acid
- 3-Hydroxybutyrate
-
SMILESCC(CC(=O)O)O
-
InChIKeyWHBMMWSBFZVSSR-UHFFFAOYSA-N
- Pubchem - 3-hydroxybutyric acid
- Wikipedia - (+/-)3-hydroxybutyric acid
-Hydroxybutyric acid, also known as 3-hydroxybutyric acid, is an organic compound and a beta hydroxy acid with the formula CH3CH(OH)CH2CO2H; its conjugate base is -hydroxybutyrate, also known as 3-hydroxybutyrate. -Hydroxybutyric acid is a chiral compound having two enantiomers, D--hydroxybutyric acid and L--hydroxybutyric acid. Its oxidized and polymeric derivatives occur widely in nature.
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Similar Compounds
beta-Hydroxyisovaleric acid
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3-HYDROXYNONANOIC ACID
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Ethyl 3-hydroxybutyrate
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4-PENTYNOIC ACID
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D-12-Hydroxystearic acid
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4-CHLOROBUTYRIC ACID
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3-Cyanopropanoic acid
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3,3-DIMETHYLBUTYRIC ACID
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(5469-16-9)
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NONANOIC ACID
(68937-75-7, 67762-36-1, 112-05-0)
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NONADECANOIC ACID
(68002-88-0, 646-30-0)
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Arachidic acid
(506-30-9)
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7-Hydroxyheptanoic acid
(3710-42-7)
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Octadecanedioic acid
(871-70-5)
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8-Hydroxyoctanoic acid
(764-89-6)
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Octanedioic acid
(68937-72-4, 505-48-6)
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Pentadecanedioic acid
(1460-18-0)
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Docosanedioic acid
(505-56-6)
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UNDECANOIC ACID
(112-37-8)
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HEXADECANEDIOIC ACID
(505-54-4)
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HEPTADECANOIC ACID
(63399-94-0, 506-12-7, 68424-37-3, 67701-03-5)
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UNDECANEDIOIC ACID
(1852-04-6)
9 alternate names
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10-Hydroxydecanoic acid
(1679-53-4)
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15-Hydroxypentadecanoic acid
(4617-33-8)
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(3788-56-5)
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HEXACOSANOIC ACID
(506-46-7)
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(7617-31-4, 660-60-6)
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TRIDECANEDIOIC ACID
(505-52-2)
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(3669-80-5)
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(1002-89-7)
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(1002-84-2)
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(72864-23-4)
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(55682-83-2)
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(62675-82-5)
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Methyl 3-hydroxyoctanoate
(7367-87-5)
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4-Methoxybutanoic acid
(29006-02-8)
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CYCLOPROPANECARBOXYLIC ACID
(1759-53-1)
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Ethyl 3-hydroxy-3-methylbutanoate
(18267-36-2)
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7-OXOOCTANOIC ACID
(14112-98-2)
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5-Acetylvaleric Acid
(3128-07-2)
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tert-Butyl 3-hydroxybutanoate
(90435-23-7)
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(6149-41-3)
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4,4-dimethylpentanoic acid
(95823-36-2, 1118-47-4)
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5-Chlorovaleric acid
(1119-46-6)
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5-METHYLHEXANOIC ACID
(1330-19-4, 628-46-6)
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5-Aminovaleric acid
(660-88-8)
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5-HEXENOIC ACID
(1577-22-6)
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5-Hexynoic acid
(53293-00-8)
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3-Ethoxypropanoic acid
(1331-11-9, 4324-38-3)
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4-Acetylbutyric acid
(3128-06-1)
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461-05-2
(461-05-2)
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10017-44-4
(10017-44-4)
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2-Hydroxyvaleric acid
(6450-97-1, 617-31-2)
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5-methoxypentanoic Acid
(70160-05-3)
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4-CYANOBUTANOIC ACID
(39201-33-7)
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5-Bromovaleric acid
(2067-33-6)
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3-MERCAPTOPROPIONIC ACID
(107-96-0)
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METHYL ACETOACETATE
(105-45-3)
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3-hydroxybutyric acid
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