| Identification | Back Directory | [Name]
3,8,13,18-tetramethyl-21H,23H-porphine-2,7,12,17-tetrapropionic acid | [CAS]
531-14-6 | [Synonyms]
NSC 267073
Coproporphyrin I-d8
Coproporphyrin I, 85%(contains 13% Coproporphyrin lll)
3,8,13,18-TetraMethyl- 2,7,12,17-porphinetetrapropionic Acid
3,8,13,18-tetramethyl-21H,23H-porphine-2,7,12,17-tetrapropionic acid
3,8,13,18-tetramethyl-21H,23H-Porphine-2,7,12,17-tetrapropanoic acid
3,8,13,18-Tetramethyl-21H,23H-porphyrin-2,7,12,17-tetrapropionic acid
21H,23H-Porphine-2,7,12,17-tetrapropanoic acid, 3,8,13,18-tetramethyl-
3,8,13,18-Tetramethyl-21H,23H-porphyrin-2,7,12,17-tetrakispropanoic acid
3,8,13,18-Tetramethyl-21H,23H-porphyrin-2,7,12,17-tetrakispropionic acid
3,8,13,18-Tetramethyl-21H,23H-porphyrin-2,7,12,17-tetrakis(propionic acid)
3,3',3'',3'''-(3,8,13,18-Tetramethyl-21H,23H-porphyrin-2,7,12,17-tetryl)tetrakispropionic acid
3-[7,12,17-tris(2-carboxyethyl)-3,8,13,18-tetramethyl-21,24-dihydroporphin-2-yl]propionic acid
3-[7,12,17-tris(2-carboxyethyl)-3,8,13,18-tetramethyl-21,24-dihydroporphyrin-2-yl]propanoic acid | [EINECS(EC#)]
208-502-3 | [Molecular Formula]
C36H38N4O8 | [MOL File]
531-14-6.mol | [Molecular Weight]
654.71 |
| Chemical Properties | Back Directory | [Boiling point ]
1258.0±65.0 °C(Predicted) | [density ]
1.366±0.06 g/cm3(Predicted) | [storage temp. ]
Refrigerator | [solubility ]
DMSO (Slightly), Methanol (Slightly, Heated) | [form ]
Solid | [color ]
Black | [EPA Substance Registry System]
21H,23H-Porphine-2,7,12,17-tetrapropanoic acid, 3,8,13,18-tetramethyl- (531-14-6) |
| Hazard Information | Back Directory | [Uses]
Coproporphyrin I is a porphyrin, a naturally occuring aromatic heterocyclic marcomolecule. The ratio of Coproporphyrin I and Coproporphyrin III provides a useful biochemical marker for distinguishing familial and sporadic porphyria cutanea tarda. Coproporphyrin I also serve as a biomarker of environmental toxicity and susceptibility in autism. | [Definition]
ChEBI: Coproporphyrin I is a coproporphyrin. It has a role as a human metabolite. It is a conjugate acid of a coproporphyrin I(4-). | [Purification Methods]
It crystallises from pyridine/glacial acetic acid. The dihydrochloride has M 727.7 and at 395nm in water. [Beilstein 26 III/IV 3094.] |
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