A racemic mixture of acetyl-D-carnitine and acetyl-L-carnitine
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Acetyl-DL-carnitine (chloride)

Item No. 31015

Technical Information
Formal Name
2-(acetyloxy)-3-carboxy-N,N,N-trimethyl-1-propanaminium, monochloride
CAS Number
2504-11-2
Synonyms
  • (±)-Acetylcarnitine
  • DL-Acetylcarnitine
  • CAR 2:0
  • C2:0 Carnitine
  • DL-Carnitine acetyl ester
Molecular Formula
C9H18NO4 • Cl
Formula Weight
Purity
≥98%
A solid
Acetonitrile: Slightly SolubleMethanol: SolubleWater: Soluble
SMILES
OC(CC(OC(C)=O)C[N+](C)(C)C)=O.[Cl-]
InChi Code
InChI=1S/C9H17NO4.ClH/c1-7(11)14-8(5-9(12)13)6-10(2,3)4;/h8H,5-6H2,1-4H3;1H
InChi Key
JATPLOXBFFRHDN-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    Acetyl-DL-carnitine is a racemic mixture of the short-chain acylcarnitine acetyl-D-carnitine and the mitochondrial metabolite acetyl-L-carnitine (Item No. 16948). It increases the oxidation rate of the branched-chain 2-oxo acid 3-methyl-2-butanoate in isolated rat muscle mitochondria in the absence of carnitine when used at a concentration of 1 mM.1 Acetyl-DL-carnitine decreases the hind limb vasculature blood flow rate in rats in a dose-dependent manner.2 It decreases the levels of palmitic acid (Item No. 10006627) and oleic acid (Item Nos. 90260 | 24659) in the cerebral cortex during the recovery period in a dog model of hypoglycemic brain injury induced by insulin.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Veerkamp, J.H., van Moerkerk, H.T.B., and Wagenmakers, A.J.M. Interaction of short-chain and branched-chain fatty acids and their carnitine and CoA esters and of various metabolites and agents with branced-chain 2-oxo acid oxidation in rat muscle and liver mitochondria. Int. J. Biochem. 17(9), 967-974 (1985).

    2. Louis-Ferdinand, R.T., Cutroneo, K.R., Kosegarten, D.C., et alFlow decrease through rat hind limb vasculature by (plus or minus)-carnitine, (plus or minus)-acetylcarnitine and (plus or minss)-chloroacetylcarnitine chlorides. J. Pharm. Pharmacol. 22(9), 704-705 (1970).

    3. Benzi, G., Gorini, A., Dossena, M., et alRecovery after hypoglycemic brain injury. Action of some biological substances on the cerebral metabolism. Biochem. Pharmacol. 32(6), 1083-1091 (1983).