CAS 25767-20-8

Coproporphyrin I tetramethyl ester

Description:

Coproporphyrin I tetramethyl ester is a synthetic derivative of coproporphyrin, which is a type of porphyrin, a class of organic compounds characterized by their large, cyclic structures composed of four pyrrole rings interconnected by methine bridges. This compound is notable for its role in biological systems, particularly in relation to heme synthesis and its potential applications in photodynamic therapy and as a fluorescent marker. The tetramethyl ester form indicates that the carboxylic acid groups of coproporphyrin I have been esterified with methyl groups, enhancing its solubility and stability in various solvents. Coproporphyrin I tetramethyl ester exhibits strong absorption in the visible region of the electromagnetic spectrum, making it useful in various spectroscopic applications. Its chemical properties include the ability to form complexes with metal ions, which can influence its reactivity and functionality in biological and chemical processes. Overall, this compound serves as an important model for studying porphyrin chemistry and its applications in medicine and biochemistry.

Formula: C₄₀H₄₆N₄O₈

InChI: InChI=1/C40H46N4O8/c1-21-25(9-13-37(45)49-5)33-18-30-23(3)27(11-15-39(47)51-7)35(43-30)20-32-24(4)28(12-16-40(48)52-8)36(44-32)19-31-22(2)26(10-14-38(46)50-6)34(42-31)17-29(21)41-33/h17-20,41,44H,9-16H2,1-8H3/b29-17-,30-18-,31-19-,32-20-,33-18-,34-17-,35-20-,36-19-

InChI key: InChIKey=OVYASYKFNWTMII-OGHNNYICSA-N

SMILES: C(CC(OC)=O)C1=C2C=C3C(C)=C(CCC(OC)=O)C(=N3)C=C4C(C)=C(CCC(OC)=O)C(N4)=CC5=NC(=CC(N2)=C1C)C(CCC(OC)=O)=C5C

Synonyms:

• 2,7,12,17-Porphinetetrapropionic acid, 3,8,13,18-tetramethyl-, tetramethyl ester
• 21H,23H-Porphine-2,7,12,17-tetrapropanoic acid, 3,8,13,18-tetramethyl-, 2,7,12,17-tetramethyl ester
• 21H,23H-Porphine-2,7,12,17-tetrapropanoic acid, 3,8,13,18-tetramethyl-, tetramethyl ester
• Coproporphyrin I tetramethyl ester
• CoproporphyrinItetramethylestersyntheticpurplextl
• Coproporphyrin�I tetramethyl ester
• NSC 89196
• Tetramethyl 3,3',3'',3'''-(3,8,13,18-Tetramethylporphyrin-2,7,12,17-Tetrayl)Tetrapropanoate
• 2,7,12,17-Tetramethyl-21H,23H-porphyrin-3,8,13,18-tetrakis(propanoic acid methyl) ester
• TETRAMETHYL 3,8,13,18-TETRAMETHYL-21H,23H-PORPHINE-2,7,12,17-TETRAPROPIONATE
• COPROPORPHYRIN I TETRAMETHYL ESTER (SYNTHETIC)
• 32,82,132,182-Tetra(methoxycarbonyl)etioporphyrin I
• Coproporphyrin tetramethyl ester i
• coproporphyrin I n-propyl ester
• 23h-porphine-2,7,12,17-tetrapropanoicacid,3,8,13,18-tetramethyl-21tetrame
• COPROPORPHYRIN I TETRAMETHYL ESTER, 98%, SYNTHETIC
• Nsc89196

Coproporphyrin I tetramethyl ester

CAS: 25767-20-8

Formula: C₄₀H₄₆N₄O₈

Color and Shape: Solid

Molecular weight: 710.8152

Ref: IN-DA003P2E

Coproporphyrin I tetramethyl ester

CAS: 25767-20-8

Formula: C₄₀H₄₆N₄O₈

Molecular weight: 710.82

Ref: 7W-GT5807

Coproporphyrin I tetramethyl ester

CAS: 25767-20-8

Purity: >97%

Molecular weight: 710.83

Ref: FT-C710-1

Coproporphyrin I Tetramethyl Ester

Controlled Product

CAS: 25767-20-8

Applications Coproporphyrin I Tetramethyl Ester is a methyl ester derivative of Coproporphyrin I (C685400). Coproporphyrin I Tetramethyl Ester is a nutritional requirement for the development of N. brasiliensis egg to third stage larvae. Coproporphyrin I Tetramethyl Ester is a tetrapyrrole compound excreted by Rhodobacter sphaeroides. Dyes and metabolites.
References Lida, K. et al.: Chem. Pharm. Bull., 55, 1067 (2007); Bolla, R. et al.: Comp. Biochem. Physiol. Part B, 48, 147 (1974)

Formula: C₄₀H₄₆N₄O₈

Color and Shape: Neat

Molecular weight: 710.82

Ref: TR-C685405

Coproporphyrin-d8 I Tetramethyl Ester

Controlled Product

CAS: 25767-20-8

Formula: C₄₀D₈H₃₈N₄O₈

Color and Shape: Neat

Molecular weight: 718.865

Ref: TR-C685407