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3,7,13,17-tetramethyl-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid

Base Information Edit
  • Chemical Name:3,7,13,17-tetramethyl-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid
  • CAS No.:3082-03-9
  • Molecular Formula:C36H38 N4 O8
  • Molecular Weight:654.72
  • Hs Code.:
  • Mol file:3082-03-9.mol
3,7,13,17-tetramethyl-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid

Synonyms:2,8,12,18-Porphinetetrapropionicacid, 3,7,13,17-tetramethyl- (8CI); Coproporphyrin II (7CI)

Suppliers and Price of 3,7,13,17-tetramethyl-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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Total 1 raw suppliers
Chemical Property of 3,7,13,17-tetramethyl-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid Edit
Chemical Property:
  • Boiling Point:1264.7°Cat760mmHg 
  • Flash Point:718.7°C 
  • PSA:205.50000 
  • Density:1.366g/cm3 
  • LogP:2.98470 
Purity/Quality:

98.5% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 3,7,13,17-tetramethyl-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid

There total 1 articles about 3,7,13,17-tetramethyl-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid 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 hydrogenchloride; phosphate buffer; deaminase-cosynthetase from Euglena gracilis; Mechanism; Product distribution; multistep reaction; 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
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