2-Hydroxycaprylic acid
2-Hydroxycaprylic acid Basic information
- Product Name:
- 2-Hydroxycaprylic acid
- Synonyms:
-
- A-HYDROXYCAPRYLIC ACID
- Octanoic acid, 2-hydroxy-
- Hydroxyoctanoic acid
- ALPHA-HYDROXYCAPRYLIC ACID
- ALPHA HYDROXY OCTANOIC ACID
- 2-Hydroxyoctanoicacid,98+%
- DL-2-HYDROXYOCTANOIC ACID
- DL-ALPHA-HYDROXYCAPRYLIC ACID
- CAS:
- 617-73-2
- MF:
- C8H16O3
- MW:
- 160.21
- EINECS:
- 210-524-3
- Product Categories:
-
- Hydroxy Fatty Acids
- Biochemicals and Reagents
- Building Blocks
- C8
- Carbonyl Compounds
- Carboxylic Acids
- Chemical Synthesis
- Fatty Acids and conjugates
- Fatty Acyls
- Lipids
- Organic Building Blocks
- Mol File:
- 617-73-2.mol
2-Hydroxycaprylic acid Chemical Properties
- Melting point:
- 66-68 °C
- Boiling point:
- 226.12°C (rough estimate)
- Density
- 1.0227 (rough estimate)
- refractive index
- 1.4310 (estimate)
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- Chloroform (Sparingly), Methanol (Slightly)
- form
- Solid
- pka
- 3.86±0.21(Predicted)
- color
- White to Off-White
- BRN
- 1760638
- LogP
- 1.960 (est)
- CAS DataBase Reference
- 617-73-2(CAS DataBase Reference)
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
2-Hydroxycaprylic acid Usage And Synthesis
Uses
2-Hydroxyoctanoic acid is a medium chain acyl-CoA synthetase inhibitor with a Ki of 500 μM[1].
Definition
ChEBI: A hydroxy fatty acid that is caprylic (octanoic) acid substituted by a hydroxy group at position 2.
Biological Activity
(±)-2-Hydroxyoctanoic acid inhibits purified medium-chain acyl-CoA synthetase from bovine liver mitochondria (Ki, 500 uM) with hexanoic acid as a substrate .', '(±)-2-Hydroxyoctanoic acid is a mixture of the D and L-2-hydroxyoctanoic acid enantiomers. (±)-2-Hydroxyoctanoic acid may be used in the development of medium-chain hydroxy-fatty acid enantiomer separation and detection systems. 2-Hydroxyoctanoic acid may be used as an inhibitor to study the kinteics of medium chain acyl-CoA synthetase(s).
Purification Methods
Crystallise the acid from EtOH/pet ether or ether/ligroin. [Beilstein 3 IV 873.]
References
[1] F Kasuya, et al. Inhibition of a medium chain acyl-CoA synthetase involved in glycine conjugation by carboxylic acids. Biochem Pharmacol. 1996 Nov 22;52(10):1643-6. DOI:10.1016/s0006-2952(96)00563-1
2-Hydroxycaprylic acid Preparation Products And Raw materials
Preparation Products
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