Coproporphyrinogen I

Base Information

Chemical Name:Coproporphyrinogen I
CAS No.:31110-56-2
Molecular Formula:C36H44 N4 O8
Molecular Weight:660.767
Hs Code.:
DSSTox Substance ID:DTXSID60331524
Nikkaji Number:J357.100I
Wikipedia:Coproporphyrinogen_I
Wikidata:Q2468963
Metabolomics Workbench ID:38049
Mol file:31110-56-2.mol

Synonyms:Coproporphyrinogen I;31110-56-2;3,8,13,18-tetramethyl-5,10,15,20,22,24-hexahydroporphyrin-2,7,12,17-tetrapropanoic acid;3,8,13,18-tetramethyl-5,10,15,20,22,24-hexahydroporphyrin-2,7,12,17-tetrapropanoate;SCHEMBL574777;CHEBI:28607;DTXSID60331524;C05768;Q2468963;3,8,13,18-tetramethyl-5,10,15,20,22,24-hexahydroporphyrin-2,7,12,17-tetrapropionic acid;3-[9,14,19-tris(2-carboxyethyl)-5,10,15,20-tetramethyl-21,22,23,24-tetraazapentacyclo[16.2.1.1^{3,6}.1^{8,11}.1^{13,16}]tetracosa-1(20),3,5,8,10,13,15,18-octaen-4-yl]propanoic acid

Suppliers and Price of Coproporphyrinogen I

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 1 raw suppliers

Chemical Property of Coproporphyrinogen I

Chemical Property:

Boiling Point:961°Cat760mmHg
PKA:4.09±0.10(Predicted)
Flash Point:535°C
PSA：212.36000
Density:1.358g/cm³
LogP:4.97800
XLogP3:3.6
Hydrogen Bond Donor Count:8
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:12
Exact Mass:660.31591437
Heavy Atom Count:48
Complexity:995

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C2CC3=C(C(=C(N3)CC4=C(C(=C(N4)CC5=C(C(=C(N5)CC(=C1CCC(=O)O)N2)C)CCC(=O)O)C)CCC(=O)O)C)CCC(=O)O

Technology Process of Coproporphyrinogen I

There total 4 articles about Coproporphyrinogen I 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-[(4Z,10Z,15Z,19Z)-7,12,17-Tris-(2-carboxy-ethyl)-3,8,13,18-tetramethyl-1,21,22,24-tetrahydro-porphin-2-yl]-propionic acid

: 31110-56-2
coproporphyrinogen I

Guidance literature:: With sodium amalgam; In water; at 20 ℃; for 2h; pH=8 - 9;
DOI:10.1016/j.bmc.2006.01.041

Reference yield:

: 72698-25-0
pentacarboxylic acid porphyrinogen I

: 31110-56-2
coproporphyrinogen I

Guidance literature:: With ethylenediaminetetraacetic acid; DL-dithiothreitol; uroporphyrinogen decarboxylase; In phosphate buffer; water; at 37 ℃; for 0.5h; pH=6.8;
DOI:10.1021/ac702130n

Reference yield:

: 3-[(4Z,10Z,15Z,19Z)-7,12,17-Tris-(2-methoxycarbonyl-ethyl)-3,8,13,18-tetramethyl-1,21,22,24-tetrahydro-porphin-2-yl]-propionic acid methyl ester

: 31110-56-2
coproporphyrinogen I

Guidance literature:: Multi-step reaction with 2 steps

1: KOH / tetrahydrofuran; H₂O / 20 °C

2: sodium amalgam / H₂O / 2 h / 20 °C / pH 8 - 9

With potassium hydroxide; sodium amalgam; In tetrahydrofuran; water;
DOI:10.1016/j.bmc.2006.01.041