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Bile acid


DATA No : BBA0623 INFORMANT : Takashi Iida

NAME : 3b,5a,6b-Trihydroxycholan-24-oic Acid

COMMON NAME:
SYMBOL:
FORMULA: C24H40O5 MOL.WT (average) : 408.571


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BIOLOGICAL ACTIVITY

PHYSICAL AND CHEMICAL PROPERTIES
MELTING POINT:242-243degC, (Me ester ; mp, 203-205degC)(Ref. 0112/0237)

BOILING POINT:

REFRACTIVE INDEX:

OPTICAL ROTATION:[a]d-21: -10.3pm2deg (C=0.987, pyridine)(Ref. 0112/0237)
[a]d-20: -7.6pm2deg (C=0.996, pyridine) (Me ester)(Ref. 0112/0237)

DENSITY:

SOLUBILITY:
SPECTRAL DATA
UV SPECTRA:

IR SPECTRA:Me ester: nmaxmcm-1: 1710, 1692, 1674(C=O), 3575, 3433, 3000(OH)(Ref. 0112)

NMR SPECTRA:

MASS SPECTRA:

OTHER SPECTRA:
CHROMATOGRAM DATA

SOURCE

CHEMICAL SYNTHESIS

METABOLISM

GENETIC INFORMATION

NOTE

REFERENCES
[0112]
AUTHOR:Kawanami, J.
TITLE:Bile Acids and Steroids. XX. Steroids on the Hog Bile Acids (part 4). Synthesis of 3b,6b-Dihydroxy-5b-cholanoic Acid and 3b,6a-Dihydroxy-5a-cholanoic Acid.
JOURNAL:Bull. Chem. Soc. Jpn.
VOL:34 PAGE : 509 -513 (1961)
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[0237]
AUTHOR:Elliott, W. H. (1971) Allo Bile Acids, in The Bile Acids-Chemistry, Physiology, and Metabolism (Vol. 1: Chemistry) (Nair, P. P., and Kritchevsky, D. eds), pp47-93, Plenum Press, New York.
TITLE:
JOURNAL:
VOL: PAGE : - ()
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Last updated June 19, 2007. Copyright © 1989-2007 Japanese Conference on the Biochemistry of Lipids (JCBL). All rights reserved.