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ChemicalBook--->CAS DataBase List--->25243-95-2

25243-95-2

25243-95-2 Structure

25243-95-2 Structure
IdentificationBack Directory
[Name]

(3S)-3-octanoyloxy-4-trimethylazaniumylbutanoate
[CAS]

25243-95-2
[Synonyms]

L-Octanoylcarnitine
OCTANOYL-L-CARNITINE
O-octanoyl-L-carnitine
Octanoyl-L-carnitine >=97.0% (TLC)
(3S)-3-octanoyloxy-4-trimethylazaniumylbutanoate
[Molecular Formula]

C15H29NO4
[MDL Number]

MFCD28580111
[MOL File]

25243-95-2.mol
[Molecular Weight]

287.4
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[color ]

White to off-white
[optical activity]

[α]/D -17±2°, c = 1 in H2O
[BRN ]

5955761
Hazard InformationBack Directory
[Uses]

Octanoyl-L-carnitine may be used as an analytical standard in the following:
  • Separation and identification of underivatized octanoyl-L-carnitine in human plasma samples using high-performance liquid chromatography coupled to tandem mass spectrometry (HPLC-MS/MS).
  • Quantification of the analyte in biological samples of patients treated with continuous ambulatory peritoneal dialysis (CAPD) or automated peritoneal dialysis (APD) using high-performance liquid chromatography/tandem quadrupole mass spectrometry (HPLC-TQMS). The feasibility of adding L-carnitine to the peritoneal dialysis (PD) solution in APD-treated end-stage renal disease patients is investigated.

It may be used as a test material for investigating its rate of oxidation by mitochondria, isolated from the livers of fed, starved and glucagon treated virgin and lactating rats.
[Definition]

ChEBI: The L-enantiomer of an O-octanoylcarnitine.
[General Description]

Octanoyl-L-carnitine is a medium-chain endogenous ester of L-carnitine, obtained via acylcarnitine family transferase.
[Biochem/physiol Actions]

L-Octanoylcarnitine is the physiologically active form of octanoylcarnitine and is detected in medium-chain acyl-CoA dehydrogenase (MCAD) deficiency. MCAD is characterized by intolerance to prolonged fasting, recurrent episodes of hypoglycemic coma with medium-chain dicarboxylic aciduria, impaired ketogenesis, and low plasma and tissue carnitine levels.
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