Identification | Back Directory | [Name]
L-Carnitine hydrochloride | [CAS]
10017-44-4 | [Synonyms]
d-Carnitine chloride S-Cartininehydrochloride L-Carnitine hydrochloride (S)-Carnitine hydrochloride (+)-Carnitine hydrochloride (S)-3-Carboxy-2-hydroxy-N,N,N-triMethylpropan-1-aMiniuM chloride 3-carboxy-2-hydroxy-n,n,n-trimethyl-, chloride, (s)-1-propanaminiu 1-Propanaminium, 3-carboxy-2-hydroxy-N,N,N-trimethyl-, chloride, (S)- 1-Propanaminium, 3-carboxy-2-hydroxy-N,N,N-trimethyl-, chloride, (2S)- 1-Propanaminium, 3-carboxy-2-hydroxy-N,N,N-trimethyl-, chloride, (2S)- (9CI) | [EINECS(EC#)]
207-309-1 | [Molecular Formula]
C7H15NO3HCl | [MDL Number]
MFCD00064131 | [MOL File]
10017-44-4.mol | [Molecular Weight]
197.66 |
Chemical Properties | Back Directory | [Melting point ]
135-137 °C | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Methanol (Slightly), Water (Slightly) | [form ]
Solid | [color ]
White to Off-White |
Hazard Information | Back Directory | [Chemical Properties]
White crystalline powder, easily soluble in water, slightly soluble in ethanol, insoluble in acetone, easy to deliquescence and turn yellow. | [Uses]
L-Carnitine hydrochloride can be used in medicine, nutritional food additives, feed additives, etc. | [Biological Activity]
L-Carnitine hydrochloride is biosynthesized from lysine, which may be involved in the energy production of branched-chain amino acids. | [in vitro]
When expressed in human embryonic kidney (HEK)293 cells, hOCTN2 (SLC22A5) shows low but significant stereospecific transport activity: D-carnitine is transported with lower affinity (K m =10.9 μM) than the L-isomer (K m =4.3 μM). | [storage]
Store at -20°C |
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