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ChemicalBook--->CAS DataBase List--->531-14-6

531-14-6

531-14-6 Structure

531-14-6 Structure
IdentificationBack 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 PropertiesBack 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 InformationBack 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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