PRODUCT IDENTIFICATION

58-85-5

H.S. CODE

TOXICITY

Coenzyme R; Vitamin H; Biotin; beta-Biotin;

(3aS-(3aalpha,4b,6aalpha))-Hexahydro-2-oxo-1H-thieno(3,4-d)imidaz- ole-4-pentanoic acid;  (3aS,4S,6aR)-Hexahydro-2-oxo-1H-thieno(3,4-d)imidazole-4-valeric acid; 2'-Keto-3,4-imidazolido-2-tetrahydrothiophene-N-valeric acid; Bioepiderm; Biotina; Biotine; Biotinum; D-Biotin; Factor S; Injacom H; Medebiotin; Vitamin B7; Vitamin Bw; cis-Hexahydro-2-oxo-1H-thieno(3,4)imidazole-4-valeric acid; cis-Tetrahydro-2-oxothieno(3,4-d)imidazoline-4-valeric acid; Other RN: 3672-05-7, 15720-24-8, 22879-79-4, 58073-87-3

SMILES

N1[C@@H]2[C@@H](NC1=O)CS[C@@H]2CCCCC(O)=O

CLASSIFICATION

EXTRA NOTES

PHYSICAL AND CHEMICAL PROPERTIES

AUTOIGNITION

NFPA RATINGS

REFRACTIVE INDEX

EXTERNAL LINKS & GENERAL DESCRIPTION

Wikipedia Linking

Google Scholar Search

Drug Information Portal (U.S. National Library of Medicine) - Biotin

PubChem Compound Summary - Biotin

Drug Bank -  Biotin

KEGG (Kyoto Encyclopedia of Genes and Genomes) -  Biotin

http://www.ebi.ac.uk/chebi/ -  Biotin

http://www.ncbi.nlm.nih.gov/ -  Biotin

Human Metabolome Database - Biotin

Material Safety Data Sheet

Local:
Vitamin B complex. Biotin functions as a coenzyme important in the catalysis of essential metabolic reactions to synthesize fatty acids, carbohydrates, and amino acids.

EXAMPLES OF NATURALLY OCCURRING CARBOXYLIC ACIDS
(excluding fatty acids)

IDENTITY

Pass

APPEARANCE

97.5 - 101.5%

OPTICAL ROTATION

+89° ~ 93° 

ORGANIC VOLATILES