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Merck

H7396

Sigma-Aldrich

(±)-2-Hydroxyoctanoic acid

Sinónimos:

2-Hydroxycaprylic acid, (±)-2-Hydroxycaprylic acid

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About This Item

Fórmula lineal:
CH3(CH2)5CH(OH)COOH
Número de CAS:
Peso molecular:
160.21
Beilstein:
1760638
Número CE:
Número MDL:
Código UNSPSC:
12352211
ID de la sustancia en PubChem:
NACRES:
NA.25

Formulario

powder

Nivel de calidad

grupo funcional

carboxylic acid

tipo de lípido

saturated FAs

Condiciones de envío

ambient

temp. de almacenamiento

room temp

cadena SMILES

CCCCCCC(O)C(O)=O

InChI

1S/C8H16O3/c1-2-3-4-5-6-7(9)8(10)11/h7,9H,2-6H2,1H3,(H,10,11)

Clave InChI

JKRDADVRIYVCCY-UHFFFAOYSA-N

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Acciones bioquímicas o fisiológicas

(±)-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).

Aplicación

Pictogramas

Exclamation mark

Palabra de señalización

Warning

Frases de peligro

Clasificaciones de peligro

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órganos de actuación

Respiratory system

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Gloves


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Stéphane Grison et al.
Metabolomics : Official journal of the Metabolomic Society, 12(10), 154-154 (2016-10-13)
Data are sparse about the potential health risks of chronic low-dose contamination of humans by uranium (natural or anthropogenic) in drinking water. Previous studies report some molecular imbalances but no clinical signs due to uranium intake. In a proof-of-principle study
Yang Zhang et al.
Drug metabolism and pharmacokinetics, 34(3), 187-193 (2019-03-17)
Mandelic acid (MA) is generally used as a biomarker of the exposure of styrene, which is classified as a class of hazardous environmental pollutants, and also used as an important chiral intermediate in pharmaceutical industry. The previous studies have found
M Duran et al.
European journal of pediatrics, 150(3), 190-195 (1991-01-01)
Two siblings were found to be affected by long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency, one of which died suddenly and unexpectedly on the 3rd day of life suffering from extreme hypoketotic hypoglycaemia. The younger sibling started to have feeding problems, lowered consciousness
Worapan Pormsila et al.
Electrophoresis, 31(12), 2044-2048 (2010-05-25)
The enantiomers of the anions of five alpha-hydroxy acids, namely lactic acid, alpha-hydroxybutyric acid, 2-hydroxycaproic acid, 2-hydroxyoctanoic acid and 2-hydroxydecanoic acid, as well as the two alpha-amino acids aspartic acid and glutamic acid, were baseline separated and detected by CE
Ying Li et al.
Plant physiology, 180(4), 1860-1876 (2019-05-30)
Mobilization of seed storage compounds, such as starch and oil, is required to provide energy and metabolic building blocks during seedling development. Over 50% of fatty acids in Arabidopsis (Arabidopsis thaliana) seed oil have a cis-double bond on an even-numbered

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