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Technology Process of I-Urobilin

I-Urobilin

Base Information
  • Chemical Name:I-Urobilin
  • CAS No.:1856-98-0
  • Molecular Formula:C33H42N4O6
  • Molecular Weight:590.72
  • Hs Code.:
  • European Community (EC) Number:217-456-3
  • DSSTox Substance ID:DTXSID30883762,DTXSID201334824,DTXSID601334826
  • Nikkaji Number:J31.894I
  • Wikipedia:Urobilin
I-Urobilin

Synonyms:Urobilin

Suppliers and Price of I-Urobilin
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 6 raw suppliers
Chemical Property of I-Urobilin
Chemical Property:
  • Vapor Pressure:4.84E-34mmHg at 25°C 
  • Refractive Index:1.639 
  • Boiling Point:890.5oC at 760 mmHg 
  • PKA:4.37±0.10(Predicted) 
  • Flash Point:492.4oC 
  • PSA：160.95000 
  • Density:1.32g/cm3 
  • LogP:4.79270 
  • XLogP3:1.6
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:13
  • Exact Mass:590.31043507
  • Heavy Atom Count:43
  • Complexity:1350
Purity/Quality:

98%,99%, *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC1=C(C(=O)NC1CC2=C(C(=C(N2)C=C3C(=C(C(=N3)CC4C(=C(C(=O)N4)CC)C)C)CCC(=O)O)CCC(=O)O)C)C
  • Isomeric SMILES:CCC1=C(C(=O)NC1CC2=C(C(=C(N2)/C=C\3/C(=C(C(=N3)CC4C(=C(C(=O)N4)CC)C)C)CCC(=O)O)CCC(=O)O)C)C
Technology Process of I-Urobilin

There total 1 articles about I-Urobilin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

3,3'-(2,17-diethyl-3,7,13,18-tetramethyl-1,19-dioxo-1,4,5,15,16,19,22,24-octahydro-21<i>H</i>-biline-8,12-diyl)-bis-propionic acid
1856-98-0,6921-61-5,24404-93-1,80735-65-5,80735-67-7,80735-69-9

3,3'-(2,17-diethyl-3,7,13,18-tetramethyl-1,19-dioxo-1,4,5,15,16,19,22,24-octahydro-21H-biline-8,12-diyl)-bis-propionic acid

Guidance literature:
Bilirubin, H2 in Chlf. + A. (Adams-Katalysator) -> Mesobilirubinogen ->(aethanol. I2 in Ae. + W. 1:1, dann 33percent HCl)-> I-Urobilin-hydrochlorid;
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Total 8 Pictures about this product