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Merck

K1750

Sigma-Aldrich

α-Ketoglutarsäure

≥98.5% (NaOH, titration)

Synonym(e):

2-Oxo-glutarsäure, 2-Oxopentandisäure

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100 G
CHF 152.00
1 KG
CHF 912.00

CHF 152.00


Voraussichtliches Versanddatum15. April 2025


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100 G
CHF 152.00
1 KG
CHF 912.00

About This Item

Lineare Formel:
HOOCCH2CH2COCOOH
CAS-Nummer:
Molekulargewicht:
146.10
Beilstein:
1705689
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352204
PubChem Substanz-ID:
NACRES:
NA.32

CHF 152.00


Voraussichtliches Versanddatum15. April 2025


Bulk-Bestellung anfordern

Qualitätsniveau

Assay

≥98.5% (NaOH, titration)

Form

powder

Löslichkeit

water: 100 mg/mL, clear to slightly hazy, colorless to faintly yellow

Lagertemp.

2-8°C

SMILES String

OC(=O)CCC(=O)C(O)=O

InChI

1S/C5H6O5/c6-3(5(9)10)1-2-4(7)8/h1-2H2,(H,7,8)(H,9,10)

InChIKey

KPGXRSRHYNQIFN-UHFFFAOYSA-N

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Verwandte Kategorien

Allgemeine Beschreibung

α-Ketoglutaric acid (α-KG) is produced in the tricarboxylic acid cycle.[1]

Anwendung

α-Ketoglutaric acid (α-KG) has been used:
  • to study its effects on swine fecal microflora in an in vitro fermentation system[2]
  • to study its effects on the activation of CD8+ T-cells[3]
  • as a substrate in glutamate oxaloacetate transaminase (GOT2) mitochondrial lysate assay[4]

Biochem./physiol. Wirkung

α-Ketoglutaric acid (α-KG) has a wide range of applications in the animal feed, food, pharmaceutical and fine chemistry industries.[1]

Piktogramme

Corrosion

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

Eye Dam. 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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Long Liu et al.
Journal of biotechnology, 164(1), 97-104 (2013-01-22)
Currently, α-ketoglutaric acid (α-KG) is industrially produced by multi-step chemical synthesis, which can cause heavy environmental pollution. Here we reported a simple one-step approach for the production of α-KG by transforming l-glutamic acid with an engineered l-amino acid deaminase (l-AAD)
G Biagi et al.
Journal of animal science, 85(5), 1184-1191 (2007-02-14)
Adding organic acids to piglet diets is known to be helpful in overcoming postweaning syndrome, and butyric acid is known to be the main energy source for the epithelial cells of the large intestine and the terminal ileum. This study
J Kitaura et al.
European journal of pediatrics, 158(5), 410-413 (1999-05-20)
Two cases of hyperinsulinaemic hypoglycaemia associated with persistent hyperammonaemia in unrelated infants of 7 days and 4 months of age are reported. Blood ammonia levels were 100-300 micromol/l (normal values <40 micromol/l). The hyperammonaemia was asymptomatic and not associated with
F Rocchiccioli et al.
Biomedical mass spectrometry, 11(1), 24-28 (1984-01-01)
Quantification of 2-ketoglutaric acid in plasma and cerebrospinal fluid as its O-trimethylsilyl++-quinoxalinol derivative by gas chromatography chemical ionization mass spectrometry is described with benzoylformic acid as internal standard. This technique, with ammonia as reactant gas, only detects the protonated molecular
Victoria I Bunik et al.
International journal of molecular sciences, 21(11) (2020-05-30)
Genetic up-regulation of mitochondrial 2-oxoglutarate dehydrogenase is known to increase reactive oxygen species, being detrimental for cancer cells. Thiamine diphosphate (ThDP, cocarboxylase) is an essential activator of the enzyme and inhibits p53-DNA binding in cancer cells. We hypothesize that the

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