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CAS No 360-68-9 , Cholestan-3-ol, (3b,5b)-

  • Name: Cholestan-3-ol, (3b,5b)-
  • Synonyms: Coprostanol; NSC 5060; Stercorin; NSC 18175; Koprosterol;5b-Cholestan-3b-ol (8CI);Cholestan-3-ol, (3b,5b)-; Coprostan-3b-ol;Koprosterin; 5b-Coprostanol; 3b-Hydroxy-5b-cholestanol; Coprosterol;
  • CAS Registry Number:
  • Melting Point: 101-103ºC
  • Flash Point: 190.7ºC
  • Boiling Point: 455.5ºC at 760 mmHg
  • Density: 0.956 g/cm3
  • Refractive index: 1.504
  • Water Solubility: chloroform, ethyl ether, warm methanol,CLEAR COLORLESS SOLUTION AT 50MG/ML IN CHLOROFORM
  • Safety Statements: Questionable carcinogen with experimental neoplastigenic data. When heated to decomposition it emits acrid smoke and irritating fumes.
  • Flash Point: 190.7ºC
  • EINECS: 206-638-8
  • Molecular Weight: 388.75
  • InChI: InChI=1/C27H48O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h18-25,28H,6-17H2,1-5H3/t19-,20-,21-,22-,23-,24-,25-,26-,27+/m0/s1
  • Molecular Formula: C27H48 O
  • Molecular Structure:CAS No:360-68-9 Cholestan-3-ol, (3b,5b)-
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360-68-9 2351.27-10MG 5BETA(H)-CHOLESTAN-3BETA-OL

  • Germany Campro Scientific GmbH [Manufacturer]
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360-68-9 5SS(H)-CHOLESTAN-3SS-OL

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360-68-9 Coprostanol

  • Coprostanol
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360-68-9 COPROSTAN-3B-OL

  • COPROSTAN-3B-OL
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360-68-9 COPROSTEROL

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References of Cholestan-3-ol, (3b,5b)-
Title: Coprosterol
CAS Registry Number: 360-68-9
CAS Name: (3b,5b)-Cholestan-3-ol
Synonyms: 3b-coprostanol; stercorin
Molecular Formula: C27H48O
Molecular Weight: 388.67
Percent Composition: C 83.44%, H 12.45%, O 4.12%
Literature References: Found in feces of man and of carnivorous animals: Bondzynski, Humnicki, Z. Physiol. Chem. 22, 396 (1896); Wells et al., Arch. Biochem. Biophys. 57, 437 (1955); Samuel et al., J. Chromatogr. 14, 508 (1964). Prepn from coprostenone: Ruzicka et al., Helv. Chim. Acta 17, 1407 (1934); Shoppee, Summers, J. Chem. Soc. 1950, 687. From coprostenol: Sch?nheimer, Evans, J. Biol. Chem. 114, 567 (1936); Ruzicka et al., Helv. Chim. Acta 21, 498 (1938); Agashe, Summers, J. Chem. Soc. 1957, 3107; Dart, Henbest, ibid. 1960, 3563. Prepn from cholesterol: Rosenfeld, Gallagher, Steroids 4, 515 (1964).
Properties: Needles from methanol, mp 101°. [a]D18 +28° (c = 1.8 in CHCl3). Freely sol in ether, chloroform, benzene; slightly sol in methanol (one gram dissolves in 145 ml MeOH). Insol in water.
Melting point: mp 101°
Optical Rotation: [a]D18 +28° (c = 1.8 in CHCl3)