Coproporphyrin III dihydrochloride

C654-3 Coproporphyrin III Technical Data Sheet

SDS

Product Number: C654-3; CAS Number: 14643-66-4

  • Fast Global Shipping
  • Guaranteed Purity
  • Need smaller sizes or bulk? Contact us!
$126.00
$926.00
SKU: C654-3 Category:

Coproporphyrin III dihydrochloride 3,8,13,17-Tetramethyl-21H,23H-porphine-2,7,12,18-tetrapropionic acid dihydrochloride CAS: 14643-66-4 MDL: MFCD00058927

Field of Interest: Heme Metabolism, Rare Diseases, Porphyrias, Mitochondria

 Background: Coproporphyrin a porphyrin based metabolic product of heme catabolism implicated in porphyria diseases and  in heavy metal exposure1,2   This specialty chemical has photosensitizing properties and has shown to form ordered micelles and aggregates under aqueous conditions.3,4 Copropoprhyrin I and III can be analyzed by HPLC and LCMS.5,6

Molecular weight: 727.63 g/mol

Molecular Formula: C36H38N4O8 • 2HCl       

 CAS Number:  14643-66-4

Storage: Store at room temperature, protect from light

Synonyms:  Coproporphyrin III,  14643-66-4,  Zincphyrin,  21H,23H-Porphine-2,7,12,18-tetrapropanoic acid, 3,8,13,17-tetramethyl-, Zinc coproporphyrin III,  3,8,13,17-tetramethylporphyrin-2,7,12,18-tetrapropanoic acid,  Koproporphyrin,  Koproporphyrin III

References: 

 1.)  B Cribier, D Rey, G Uhl, C Le Coz, C Hirth, E Libbrecht, D Vetter, J M Lang, F Stoll-Keller, Abnormal urinary coproporphyrin levels in patients infected by hepatitis C virus with or without human immunodeficiency virus. A study of 177 patients, Arch Dermatol, 1996 Dec;132(12):1448-52. 

2.)  Mahaffey, Kathryn R.; Capar, Stephen G.; Gladen, Beth C.; Fowler, Bruce A., Concurrent exposure to lead, cadmium, and arsenic. Effects on toxicity and tissue metal concentrations in the rat, Journal of Laboratory and Clinical Medicine (1981), 98(4), 463-81.

3.)  Finlay, Jarod C.; Conover, David L.; Hull, Edward L.; Foster, Thomas H., Porphyrin bleaching and PDT-induced spectral changes are irradiance dependent in ALA-sensitized normal rat skin in vivo, Photochemistry and Photobiology (2001), 73(1), 54-63.

4.)  Brown, Stanley B.; Shillcock, Margaret; Jones, Peter, Equilibrium and kinetic studies of the aggregation of porphyrins in aqueous solution, Biochemical Journal (1976), 153(2), 279-85. Language: English, Database: CAPLUS

5.) High-performance liquid chromatography of uroporphyrin and coproporphyrin isomers. Lim ,et al. Methods in Enzymology Volume 123, 1986, Pages 383-389. https://doi.org/10.1016/S0076-6879(86)23046-3

6.) A fully automated and validated human plasma LC–MS/MS assay for endogenous OATP biomarkers coproporphyrin-I and coproporphyrin-III. King-Ahmad, et al. BIOANALYSIS VOL. 10, NO. 9. https://doi.org/10.4155/bio-2017-0270

SDS

Categories

Porphyrins

Scaffold/Subcategory

Natural Porphyrins and Derivatives

CAS #

[14643-66-4]

Purity %

>97%

Smiles

[Cl-].[Cl-].CC1=C(CCC(O)=O)/C2=C/C3=[NH+]/C(=CC4=C(CCC(O)=O)C(C)=C(N4)/C=C4[NH+]=C(C=C1N2)C(C)=C4CCC(O)=O)/C(C)=C3CCC(O)=O

Molecular Weight

727.64

Molecular Formula

C36H40Cl2N4O8

Porphyrin Family

Free Base Porphyrins, Protoporphyrin Derivatives

Porphyrin Substitution

Alkyl Substituted Porphyrins, Beta Substituted Porphyrins, Carboxy Substituted Porphyrins

You may also like…

Shopping Cart
Scroll to Top