O-Acetyl-L-carnitine hydrochloride

• Catalog No.: A6706
• CAS Number: 5080-50-2
• M. F.: C9H18ClNO4
• M. W.: 239.69652
• Purity: ≥99% (titration)

SYNONYMS

• IUPAC name: [(2R)-2-(acetyloxy)-3-carboxypropyl]trimethylazanium chloride
• IUPAC Traditional name: O-acetylcarnitinium chloride
• Synonyms: (R)-3-Acetoxy-4-(trimethylammonio)butyrate hydrochloride; R-(-)-2-Acetyloxy-3-carboxy-N,N,N-trimethyl-1-propanaminium chloride; ALC; ALCAR

DATABASE IDS

• MDL Number: MFCD00082230
• CAS Number: 5080-50-2
• Beilstein Number: 4340103
• PubChem SID: 24891132

PROPERTIES

• Purity: ≥99% (titration)
• Quality Level: PREMIUM
• Apperance: white to off-white powder
• Optical Rotation: [α]25/D -28°, c = 2 in H2O(lit.)
• Solubility: H2O: soluble100 mg/mL
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26-36
• Storage Temperature: 2-8°C
• German water hazard class: 3

DETAILS

Description (简体中文)

包装
1, 5 g in poly bottle
Biochem/physiol Actions
Endogenous mitochondrial metabolite that transports acetyl groups across the mitochondrial membrane. Exogenous acetylcarnitine enhances mitochondrial function in aged rats. As an acetate donor to coenzyme A, it increases the central and peripheral acetylcholine synthesis and function. Acetylcarnitine has antinociceptive activity that may be mediated by enhanced activity of muscarinic cholinergic receptors or mGlu2 glutamate receptors.