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Description

Neurology 1984, 34: 1128-1129

The components act synergistically to facilitate lipotropic activity in research settings, with applications including hepatic lipid transport and fat mobilization, methionine and choline roles in methylation and phospholipid synthesis, carnitine-mediated beta-oxidation of fatty acids, and liver function marker studies in metabolic stress or steatosis models

2010;(2):Cd007280

The specific rotation of acetyl L-carnitine hydrochloride is as follows: [64] Specific rotation [] 25 = -28 (C=I, H O) [65] Industrial Applicability [66] As can be seen from Examples 1 through 5, a process for preparing L-carnitine or acetyl L-carnitine hydrochloride in accordance with the present invention employs a very inexpensive material as a starting material and involves a simplified reaction process in conjunction with a capability to prepare an intermediate having a high optical purity at a low production cost