Basic information Safety Supplier Related

Sodium ketoisocaproate

Basic information Safety Supplier Related

Sodium ketoisocaproate Basic information

Product Name:
Sodium ketoisocaproate
Synonyms:
  • Sodium ketoisocaproate
  • SODIUM 4-METHYL-2-OXOVALERATE
  • SODIUM ALPHA-KETOISOCAPRATE
  • 2-KETOISOCAPROIC ACID SODIUM SALT
  • 2-KETOISOHEXANOIC ACID SODIUM SALT
  • A-KETOISOCAPROIC ACID, SODIUM SALT
  • ALPHA-KETOISOCAPROIC ACID SODIUM SALT
  • 4-Methyl-2-oxopentanoic acid monosodium salt
CAS:
4502-00-5
MF:
C6H9NaO3
MW:
152.12
EINECS:
224-816-3
Product Categories:
  • pharmacetical
Mol File:
4502-00-5.mol
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Sodium ketoisocaproate Chemical Properties

Melting point:
275 °C (dec.)(lit.)
storage temp. 
2-8°C
solubility 
Water (Slightly)
form 
Solid
color 
White to Off-White
Odor
at 100.00 %. butyric valeric buttery
Odor Type
buttery
JECFA Number
633.1
BRN 
4239297
Stability:
Hygroscopic
LogP
0.17
CAS DataBase Reference
4502-00-5(CAS DataBase Reference)
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Safety Information

Safety Statements 
24/25-22
WGK Germany 
3

MSDS

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Sodium ketoisocaproate Usage And Synthesis

Occurrence

Reported found in banana, asparagus, cheese, white wine, cocoa, blue cheese and provolone cheese.

Uses

Sodium 4-methyl-2-oxovalerate has been used for quantifying branched-chain keto acids from cell extracts by HPLC-fluorescence method.

Uses

4-Methyl-2-oxovaleric Acid is an α-ketomonocarboxylic acid that triggers insulin release by acting upon receptor sites which differ from those occupied by amino acids. 4-Methyl-2-oxovaleric Acid is an intermediate in the metabolism of Leucine.

Biochem/physiol Actions

α-Ketoisocaproic acid is a leucine metabolite that is known to induce insulin secretion from the βcells of pancreas. Enteral infusion of aα-Ketoisocaproate is found to ameliorate, endotoxemic condition. The resulting ketone bodies obtained from its conversion, might serve as an energy source. Accumulation of α-Ketoisocaproic acid is characterized in branched chain ketoaciduria, which is caused due to the lack of branched chain L-2-keto acid dehydrogenase activity. α-Ketoisocaproic acid causes dissociation in the oxidative phosphorylation reaction and acts as a metabolic inhibitor of α-ketoglutarate dehydrogenase. Thus, leads to a defect in the mitochondrial homeostasis, observed in branched chain ketoaciduria.

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