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CAS No 478-61-5 , Berbamine

  • Name: Berbamine
  • Synonyms: Berbamine Dihydrochloride;Berbamine;
  • CAS Registry Number:
  • Flash Point: 381.4 ºC
  • Boiling Point: 707 ºC at 760 mmHg
  • Density: 1.204 g/cm3
  • Refractive index: 1.601
  • Flash Point: 381.4 ºC
  • EINECS: 207-523-5
  • Molecular Weight: 608.72
  • InChI: InChI=1/C37H40N2O6/c1-38-14-12-24-19-32(41-3)33-21-27(24)28(38)16-22-6-9-26(10-7-22)44-31-18-23(8-11-30(31)40)17-29-35-25(13-15-39(29)2)20-34(42-4)36(43-5)37(35)45-33/h6-11,18-21,28-29,40H,12-17H2,1-5H3
  • Molecular Formula: C37H40N2O6
  • Molecular Structure:CAS No:478-61-5 Berbamine

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478-61-5 berbamine, 95% 98%

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478-61-5 Berbamine dihydrochloride

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478-61-5 Berbamine Dihydrochloride

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478-61-5 BERBAMINE DIHYDROCHLORIDE

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References of Berbamine
Title: Berbamine
CAS Registry Number: 478-61-5
CAS Name: (4aS,16aR)-3,4,4a,5,16a,17,18,19-Octahydro-21,22,26-trimethoxy-4,17-dimethyl-16H-1,24:6,9-dietheno-11,15-metheno-2H-pyrido[2￠,3￠:17,18][1,11]dioxacycloeicosino[2,3,4-ij]isoquinolin-12-ol
Synonyms: 6,6￠,7-trimethoxy-2,2￠-dimethylberbaman-12-ol; berbenine
Molecular Formula: C37H40N2O6
Molecular Weight: 608.72
Percent Composition: C 73.00%, H 6.62%, N 4.60%, O 15.77%
Literature References: Alkaloid found in various members of Berberis family. Used as a traditional medicine in China as antipyretic, antidiarrheoa and as a tonic. Identification in Berberis vulgaris: C. Rüdel, Arch. Pharm. 229, 631 (1895); isoln from Atherosperma moschatum Labill., Monimiaceae: I. R. C. Bick et al., Aust. J. Chem. 9, 111 (1956). Structure: F. von Bruchhausen et al., Ann. 507, 144 (1933); configuration: Y. Inubishi, J. Pharm. Soc. Jpn. 72, 220 (1952), C.A. 47, 6429e (1953). Immunopharmacology and toxicology: C. W. Wong et al., Int. J. Immunopharmacol. 13, 579 (1991). Brief review: C.-X. Liu et al., Phytother. Res. 5, 228-230 (1991).
Properties: Colorless plates from aq ethanol as the monohydrate, sinters 147°. pKa (20°): 7.33 in aq methanol. [a]D20 +114.6° (c = 1.0 in chloroform). uv max (ethanol): 282 nm (log e 3.89; E 1cm1% 126).
pKa: pKa (20°): 7.33 in aq methanol
Optical Rotation: [a]D20 +114.6° (c = 1.0 in chloroform)
Absorption maximum: uv max (ethanol): 282 nm (log e 3.89; E 1cm1% 126)