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CAS No 471-87-4 , Pyrrolidinium,2-carboxy-1,1-dimethyl-, inner salt, (2S)-

  • Name: Pyrrolidinium,2-carboxy-1,1-dimethyl-, inner salt, (2S)-
  • Synonyms: Hygric acid, methylbetaine;Stachydrin; S-(-)-Stachydrine;Pyrrolidinium,2-carboxy-1,1-dimethyl-, inner salt, (2S)-; (S)-2-Carboxy-1,1-dimethylpyrrolidinium hydroxide inner salt;(-)-Stachydrine; Stachydrine (6CI,8CI); Cadabine;Pyrrolidinium,2-carboxy-1,1-dimethyl-, hydroxide, inner salt, (S)-; Proline betaine; Methyl hygrate betaine;1-Methylproline methylbetaine;L-Stachydrine;
  • CAS Registry Number:
  • Flash Point: °C
  • Boiling Point: °Cat760mmHg
  • Density: g/cm3
  • Water Solubility: soluble in water, easily soluble in methanol, ethanol and chloroform; almost insoluble in ether
  • HS Code: 29214980
  • Flash Point: °C
  • EINECS: 207-445-1
  • Molecular Weight: 143.1836
  • InChI: InChI=1S/C7H13NO2/c1-8(2)5-3-4-6(8)7(9)10/h6H,3-5H2,1-2H3/t6-/m0/s1
  • Molecular Formula: C7H13 N O2
  • Molecular Structure:CAS No:471-87-4 Pyrrolidinium,2-carboxy-1,1-dimethyl-, inner salt, (2S)-

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471-87-4 Pyrrolidinium,2-carboxy-1,1-dimethyl-, inner salt, (2S)-

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471-87-4 Pyrrolidinium,2-carboxy-1,1-dimethyl-, inner salt, (2S)-

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References of Pyrrolidinium,2-carboxy-1,1-dimethyl-, inner salt, (2S)-
Title: Stachydrine
CAS Registry Number: 471-87-4
CAS Name: (2S)-2-Carboxy-1,1-dimethylpyrrolidinium inner salt
Synonyms: methyl hygrate betaine; hygric acid methylbetaine
Molecular Formula: C7H13NO2
Molecular Weight: 143.18
Percent Composition: C 58.72%, H 9.15%, N 9.78%, O 22.35%
Literature References: Occurs widely in nature, especially in alfalfa, chrysanthemum, citrus and stachys species. May be prepd by methylation of proline. Isoln: Planta, Schulze, Ber. 26, 939 (1893); Jahns, ibid. 29, 2065 (1896); Yoshimura, Z. Physiol. Chem. 88, 334 (1913); Vickery, J. Biol. Chem. 61, 117 (1924). Structure: Schulze, Trier, Z. Physiol. Chem. 67, 59 (1910). Synthesis: Karrer, Widmer, Helv. Chim. Acta 8, 364 (1925). Biosynthesis: Robertson, Marion, Can. J. Chem. 38, 396 (1960). Review: Marion in The Alkaloids vol. 1, R. H. F. Manske, H. L. Holmes, Eds. (Academic Press, New York, 1950) pp 101-103.
 
Derivative Type: Monohydrate
Properties: Deliquescent crystals, sweetish taste, mp 235° when anhydr. Isomerizes at the mp to methyl hygrate. Sol in water, alcohol, dil acids. Practically insol in ether, chloroform.
Melting point: mp 235° when anhydr
 
Derivative Type: Hydrochloride
Molecular Formula: C7H13NO2.HCl
Molecular Weight: 179.64
Percent Composition: C 46.80%, H 7.86%, N 7.80%, O 17.81%, Cl 19.74%
Properties: Large prisms from abs alcohol, dec 235°, very sol in water, sol in 13 parts alcohol.
 
Derivative Type: Acid oxalate
Molecular Formula: C7H13NO2.C2H2O4
Molecular Weight: 233.22
Percent Composition: C 46.35%, H 6.48%, N 6.01%, O 41.16%
Properties: Needles, mp 106°. Practically insol in abs alcohol.
Melting point: mp 106°
 
Derivative Type: Aurichloride
Molecular Formula: C7H13NO2.HAuCl4
Molecular Weight: 482.97
Percent Composition: C 17.41%, H 2.92%, N 2.90%, O 6.63%, Au 40.78%, Cl 29.36%
Properties: Yellow leaflets, mp 225° (rapid heating). Practically insol in cold water. Quite sol in hot water.
Melting point: mp 225° (rapid heating)
 
Derivative Type: Platinichloride tetrahydrate
Molecular Formula: (C7H13NO2)2.H2PtCl6.4H2O
Molecular Weight: 768.25
Percent Composition: C 21.89%, H 4.72%, N 3.65%, O 16.66%, Pt 25.39%, Cl 27.69%
Properties: Orange crystals, dec 210-220° (rapid heating), very sol in water and dil alc. Also obtained with 2 mols H2O of crystn.