Substance
ID:181100
Names and Identifiers
Synonyms
R-(-)-2-Acetyloxy-3-carboxy-N,N,N-trimethyl-1-propanaminium chlorideO-Acetyl-L-carnitine hydrochlorideALC(R)-3-Acetoxy-4-(trimethylammonio)butyrate hydrochlorideALCAR
IUPAC name
[(2R)-2-(acetyloxy)-3-carboxypropyl]trimethylazanium chloride
IUPAC Traditional name
O-acetylcarnitinium chloride
Registration numbers
Beilstein Number
MDL Number
CAS Number
PubChem SID
Properties
Product Information
Quality Level
PREMIUM
Purity
≥99% (titration)
Physical Property
Optical Rotation
[α]25/D -28°, c = 2 in H2O(lit.)
Apperance
white to off-white powder
Solubility
H2O: soluble100 mg/mL
Safety Information
GHS Hazard statements
H315-H319-H335
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements
P261-P305+P351+P338
GHS Signal Word
Warning
Risk Statements
36/37/38
European Hazard Symbols
Irritant (Xi)Safety Statements
26-36
Storage Temperature
2-8°C
German water hazard class
3
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Molecule Details
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.
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.
Molecular Spectra
No Data Available
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References
No Data Available
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