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The synthesis technology of L-carnitine in the present invention is : It is started from S-epichlorohydrin, which is firstly used to produce a L-quaternary ammonium salt (L-chloro-3-chloro-2-hydroxypropyl trimethylamine) by the amination of trimethylamine hydrochloride, the quaternary ammonium salt is then cyanided with NaCN to produce a L-cyanide (L-chloro-3-cyan-2-hydroxypropyl trimethylamine), the cyanide is then hydrolyzed with concentrated hydrochloric acid to produce L-carnitine hydrochloride, the L-carnitine hydrochloride is finally used to produce L-carnitine product by electrodialysis desalination, concentration and refine

The human equivalent dose of approximately 0.035 mg is extremely small, suggesting that even standard anti-aging doses could provide some degree of neurological benefit as a secondary effect

There is also an indication of some neuronal synthesis, yet the majority of insulin in the brain is of peripheral origin

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