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5,10,15,20,22,24-Hexahydrouroporphyrin IV

Base Information
  • Chemical Name:5,10,15,20,22,24-Hexahydrouroporphyrin IV
  • CAS No.:53790-14-0
  • Molecular Formula:C40H44N4O16
  • Molecular Weight:836.7946
  • Hs Code.:
  • Mol file:53790-14-0.mol
5,10,15,20,22,24-Hexahydrouroporphyrin IV

Synonyms:Hexahydro-uroporphyrin IV (Uroporphyrinogen IV);Hexahydro-porphyrin-1,3,6,8-tetraessigsaeure-2,4,5,7-tetrapropionsaeure;3,3',3'',3'''-(3,8,12,17-tetrakis-carboxymethyl-5,10,15,20,22,24-hexahydro-21H,23H-porphine-2,7,13,18-tetrayl)-tetrakis-propionic acid;

Suppliers and Price of 5,10,15,20,22,24-Hexahydrouroporphyrin IV
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
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Total 5 raw suppliers
Chemical Property of 5,10,15,20,22,24-Hexahydrouroporphyrin IV
Chemical Property:
  • Boiling Point:1163.6°Cat760mmHg 
  • Flash Point:657.5°C 
  • PSA:361.56000 
  • Density:1.575g/cm3 
  • LogP:2.25280 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 5,10,15,20,22,24-Hexahydrouroporphyrin IV

There total 5 articles about 5,10,15,20,22,24-Hexahydrouroporphyrin IV 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:
Guidance literature:
With cosynthetase;
Guidance literature:
With phosphate buffer; deaminase-cosynthetase from Euglena gracilis; In water; at 16 ℃; for 16h; Mechanism; Product distribution; other products ratio with enzyme solution which had been heated (96 deg C, 5 min); labelling experiments; mechanism of biosynthesis of uroporphyrinogens;
DOI:10.1039/P19810002779
upstream raw materials:

C40H46N4O17

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