Stachydrine

Stachydrine Basic information
Product Name:Stachydrine
Synonyms:Stachydrine;turicine;cis-4-hydroxy-D-proline betaine;Stachydrine USP/EP/BP;13C,2H3]-Cis-4-Hydroxy-D-proline betaine
CAS:515-24-2
MF:C7H13NO3
MW:159.18302
EINECS:
Product Categories:
Mol File:515-24-2.mol
Stachydrine Structure
Stachydrine Chemical Properties
Melting point 259-260°
alpha D20 +37.8° (c = 1 in water)
Safety Information
MSDS Information
Stachydrine Usage And Synthesis
DescriptionThis base occurs in the fruit of Capparis torrnentosa, Citrus grandis and in Stachys tubi/era Naudin. It normally crystallizes as the monohydrate which has m.p. 116-8°C. The specific rotation is [α]>D- 40.25° (c 4.0, H20). It is soluble in EtOH and H20, insoluble in CHC13 and Et20. The free base is unstable in air and decomposes quite rapidly. The hydrochloride yields colourless crystals from EtOH with m.p. 222°C; [α]20D - 28.1° (c 4.83, H20); aurichloride, m.p. 232°C; platinichloride, decomposing at 200°C; oxalate, colourless needles, m.p. 105- 7°C and the picrate, m.p. 199-2000 C. The structure is that of the methylbetaine of hygric acid.
UsesStachydrine is used for various ethnobotany and ethnomedicinal uses. It can also be used to promote healthy neural development in an unborn baby, as well as to determine the differential effects of post-weaning diet and maternal obesity on mouse liver and brain metabolomes.
DefinitionChEBI: An amino-acid betaine that is trans-4-hydroxy-D-proline zwitterion in which both of the hydrogens attached to the nitrogen have been replaced by methyl groups.
ReferencesSchultz, Trier., Z. physiol. Chern., 67, 59 (1910)
Steenbock., J. Bioi. Chern., 35, 1 (1918)
Kuhn, Brydowna., Ber., 70, 1333 (1937)
Henry, King.,J. Chern. Soc., 2866 (1950)
Cornforth, Henry., ibid, 601 (1952)
Paudler, Wagner., Chern. & Ind., 1693 (1963)




Stachydrine Preparation Products And Raw materials

Email:[email protected] [email protected]
Copyright © 2024 Mywellwork.com All rights reserved.