N,N-Dimethyl-L-proline
N,N-Dimethyl-L-proline Basic information
- Product Name:
- N,N-Dimethyl-L-proline
- Synonyms:
-
- (2s)-1,1-dimethylpyrrolidinium-2-carboxylate
- (Pyrrolidinium, 2-carboxy-1,1-dimethyl-, innersalt, (2S)-
- Methyl hygrate betaine
- (S)-2-Carboxy-1,1-dimethylpyrrolidinium hydroxide inner salt
- 1-Methylproline methylbetaine
- Cadabine
- (2S)-1,1-Dimethyl-2-carboxylatopyrrolidin-1-ium
- (2S)-2-Carboxylato-1,1-dimethylpyrrolidin-1-ium
- CAS:
- 471-87-4
- MF:
- C7H14NO2
- MW:
- 144.19
- EINECS:
- 207-445-1
- Product Categories:
-
- Alkaloids
- Natural Plant Extract
- Mol File:
- 471-87-4.mol
N,N-Dimethyl-L-proline Chemical Properties
- Melting point:
- 235°C
- Boiling point:
- 261.28°C (rough estimate)
- Density
- 1.1095 (rough estimate)
- refractive index
- 1.4150 (estimate)
- storage temp.
- 2-8°C
- solubility
- Water: 100 mg/mL (698.42 mM); DMSO: 100 mg/mL (698.42 mM)
- form
- Solid
- color
- White to off-white
MSDS
- Language:English Provider:L-Proline betaine
N,N-Dimethyl-L-proline Usage And Synthesis
Description
This alkaloid, which has been isolated from the leaves of Cadaba fruticosa, has been shown, by comparison of its hydrochloride and the NMR spectrum, to be stachydrine.
Uses
Stachydrine 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.
Definition
ChEBI: L-proline betaine is an amino acid betaine that is L-proline zwitterion in which both of the hydrogens attached to the nitrogen are replaced by methyl groups. It has a role as a food component, a plant metabolite and a human blood serum metabolite. It is a N-methyl-L-alpha-amino acid, an alkaloid and an amino-acid betaine. It is functionally related to a L-prolinium. It is a conjugate base of a N,N-dimethyl-L-prolinium. It is an enantiomer of a D-proline betaine.
References
Ahmad, Basha, Atta-ur-Rahman, Pak. J. Sci. Ind. Res., 17, 109 (1975)
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