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Coproporphyrin III tetramethyl ester (CAS 5522-63-4)

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Alternate Names:
Tetramethyl 3,8,13,17-tetramethyl-21H,23H-porphine-2,7,12,18-tetrapropionate
Application:
Coproporphyrin III tetramethyl ester is a tetrapyrrole secreted by Rhodobacter sphaeroides
CAS Number:
5522-63-4
Molecular Weight:
710.82
Molecular Formula:
C40H46N4O8
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Coproporphyrin III tetramethyl ester is a chemically synthesized porphyrin derivative, characterized by the methylation of the carboxyl groups at the propionic acid side chains in coproporphyrin III, resulting in esterified forms. This modification enhances its lipophilicity, facilitating its incorporation into various experimental systems. As a component of the vast porphyrin family, it plays a pivotal role in the study of photodynamic processes and the mimicry of biological systems, particularly in the context of photosynthesis and the electron transfer chain mechanisms. The tetramethyl ester modification allows researchers to probe the structure-function relationships within porphyrin complexes, aiding in the elucidation of the roles these compounds play in natural and artificial light-harvesting systems. Its unique properties make it an indispensable tool in the synthesis of porphyrin-based materials for applications in photovoltaics, sensor technology, and the development of novel photoresponsive compounds, serving as a key substance in the exploration of light-mediated chemical reactions and energy conversion processes.


Coproporphyrin III tetramethyl ester (CAS 5522-63-4) References

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  2. Spectral-absorption coefficients of some porphyrins in the Soret-band region.  |  Rimington, C. 1960. Biochem J. 75: 620-3. PMID: 16748818
  3. Identification of tetrapyrrole compounds excreted by Rhodobacter sphaeroides and sources of the methyl hydrogens of bacteriochlorophyll a biosynthesized by R. sphaeroides, based on 13C-NMR spectral analysis of coproporphyrin III tetramethyl ester.  |  Iida, K., et al. 2007. Chem Pharm Bull (Tokyo). 55: 1067-9. PMID: 17603203
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  6. In vitro nutritional requirements of Nippostrongylus brasiliensis. II. Effects of heme compounds, porphyrins and bile pigments on the free-living stages.  |  Bolla, RI., et al. 1974. Comp Biochem Physiol B. 48: 147-57. PMID: 4598741
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  11. Dealkylation during electron impact mass spectrometric analysis of N- monoalkylated porphyrin methyl esters  |   and Andrew G. Smith, Peter B. Farmer. 1982. Biological Mass Spectrometry. 9, 3: 111-114.
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Coproporphyrin III tetramethyl ester, 1 mg

sc-214758
1 mg
$103.00

Coproporphyrin III tetramethyl ester, 5 mg

sc-214758A
5 mg
$348.00