Biliverdine

Title: Biliverdine
CAS Registry Number: 114-25-0
CAS Name: 3,18-Diethenyl-1,19,22,24-tetrahydro-2,7,13,17-tetramethyl-1,19-dioxo-21H-biline-8,12-dipropanoic acid
Additional Names: 1,19,22,24-tetrahydro-2,7,13,17-tetramethyl-1,19-dioxo-3,18-divinylbiline-8,12-dipropionic acid; 1,3,6,7-tetramethyl-4,5-dicarboxyethyl-2,8-divinylbilenone; 4,5-di(2-carboxyethyl)-1,3,6,7-tetramethyl-2,8-divinylbilatriene; dehydrobilirubin; uteroverdine; oöcyan
Molecular Formula: C33H34N4O6
Molecular Weight: 582.65
Percent Composition: C 68.03%, H 5.88%, N 9.62%, O 16.48%
Literature References: Precursor of bilirubin. Formed in the body from hemoglobin. The bile of amphibia and of birds contains biliverdine only. Does not occur in normal human bile or normal human serum, but regularly accompanies bilirubin in the serum of patients with carcinomatous obstruction of the bile duct, and frequently in that of patients with liver cirrhosis, catarrhal jaundice, and bile duct occlusion by gallstones. Can be obtained by autooxidation of bilirubin in alkaline soln but the yield is poor: Lemberg, Biochem. J. 28, 978 (1934); better yields by oxidation of bilirubin with ferric chloride in glacial acetic acid: Lemberg, Ann. 499, 25 (1932); by coupled oxidation of hemoglobin and ascorbic acid: Lemberg et al., Biochem. J. 35, 363 (1941); by oxidation of bilirubin with ferric chloride in methanol: Gray et al., J. Chem. Soc. 1961, 2264. Crystal and molecular structure: W. S. Sheldrick, J. Chem. Soc. Perkin Trans. 2 1976, 1457. Comprehensive reviews: Lemberg, Legge, Hematin Compounds and Bile Pigments (New York, 1949); With, Bile Pigments (Academic Press, New York, 1968).
Properties: Dark green plates or prisms with violet surface color from methanol. Does not melt, blackens and dec above 300°. Absorption spectrum: Gray et al., loc. cit. Soluble in methanol, ether, chloroform, carbon disulfide, benzene, soln of alkali hydroxides. Gives the later color changes of the Gmelin test starting with green.
Derivative Type: Dimethyl ester
Molecular Formula: C35H38N4O6
Molecular Weight: 610.70
Percent Composition: C 68.83%, H 6.27%, N 9.17%, O 15.72%
Properties: Green crystals from chloroform + petr ether. When produced from bilirubin, mp 215-223°; synthetic 206-209°; from hemin 208°; from hemoglobin 216°.
Melting point: mp 215-223°; synthetic 206-209°; from hemin 208°; from hemoglobin 216°
Derivative Type: Dimethyl ester ferrichloride
Molecular Formula: C35H39Cl4FeN4O6
Molecular Weight: 809.36
Percent Composition: C 51.94%, H 4.86%, Cl 17.52%, Fe 6.90%, N 6.92%, O 11.86%
Properties: (Green hemin ester), pleochroitic elongated platelets, no definite mp. Ferric chloride and HCl can be removed by washing the chloroform soln with water.
Bimosiamose Binapacryl Binedaline Binifibrate Binodenoson

Biliverdin
Biliverdin3.svg
Identifiers
CAS number 114-25-0 YesY
PubChem 251
ChemSpider 10628548 YesY
MeSH Biliverdin
ChEBI CHEBI:17033 YesY
ChEMBL CHEMBL455477 YesY
Jmol-3D images Image 1
Properties
Molecular formula C33H34N4O6
Molar mass 582.646
Melting point > 300 °C
Hazards
MSDS Sigma-Aldrich
Main hazards Irritant
 YesY (verify) (what is: YesY/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Biliverdin is a green tetrapyrrolic bile pigment, and is a product of heme catabolism.[1][2] It is the pigment responsible for a greenish color sometimes seen in bruises.[2]