Fe(III) Deuteroporphyrin IX chloride

Product Number: D40654; CAS Number: 21007-21-6

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Fe(III) Deuteroporphyrin IX chloride Deutero-hemin CAS: 21007-21-6 MDL: MFCD18070953

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Molecular weight: 599.866 g/mol

Molecular Formula: C30H26ClFeN4O4

CAS Number: 21007-21-6

Storage: Store at room temperature, protect from light

Synonyms: Eisen(3+)hydrogenchlorid-3,3′-(3,7,12,17-tetramethylporphin-21,24-diid-2,18-diyl)dipropanoat (1:2:1:1), 21007-21-6, 61160-34-7, Fe(III) Deuteroporphyrin IX chloride, Ferrate(2-), chloro(3,7,12,17-tetramethyl-21H,23H-porphine-2,18-dipropanoato(4-)-N21,N22,N23,N24)-, dihydrogen, (SP-5-13)-

Field of Interest: Chemistry of Heme derivatives, Coordination Chemistry, Malaria Pigment, Oxidation Chemistry, Cytochrome P450 models

Background: Fe(III) Deuteroporphyrin IX chloride is a natural porphyrin specialty chemical manufactured by Frontier Specialty Chemicals. Fe(III) Deuteroporphyrin IX chloride is useful for studying the chemistry of heme due to its higher stability, compared to heme.

References: 

1.) Wyllie, et al. NO Orientation and Tilting in (Nitrosyl)iron(II) Deuteroporphyrin IX. Inorg. Chem. 2003, 42, 14, 4259–4261. https://doi.org/10.1021/ic034364e

2.) Kelly, et al. Chlorite ion oxidation of the iron(III) complex of deuteroporphyrin IX. Inorg. Chem. 1981, 20, 4, 1086–1090. https://doi.org/10.1021/ic50218a026

3.) Teng, et al. Singlet Oxygen Generation in Ferriporphyrin-Polymer Dots Catalyzed Chemiluminescence System for Cancer Therapy. ACS Appl. Bio Mater. 2020, 3, 8, 5020–5029. https://doi.org/10.1021/acsabm.0c00522

4.) Kuter, et al. Hydrating the Bispropionate Notch in Malaria Pigment: A New Structural Motif in the Iron(III)(deuteroporphyrin) Dimer. Chemistry, a European Journal. Volume 25, Issue 17, March 21, 2019, Pages 4373-4378. https://doi.org/10.1002/chem.201805116

5.) Zhou, et al. Metallo-deuteroporphyrin as a novel catalyst for p-xylene oxidation using molecular oxygen. Inorganica Chimica Acta. Volume 382, 15 March 2012, Pages 167-170.

6.) Brault, et al. Reactions of iron(III) porphyrins with peroxyl radicals derived from halothane and halomethanes. J. Phys. Chem. 1984, 88, 13, 2857–2862. https://doi.org/10.1021/j150657a038

 

 

Categories

Porphyrins

Scaffold/Subcategory

Natural Porphyrins and Derivatives

CAS #

[21007-21-6]

Purity %

95%

Smiles

CC1=C/C2=C/C3=C(C)C=C4C=C5/N=C(/C=C6N([Fe](Cl)N34)C(=CC1=N2)/C(C)=C6CCC(O)=O)C(CCC(O)=O)=C/5C

Molecular Weight

599.866

Molecular Formula

C30H28ClFeN4O4

Porphyrin Family

Metallo Porphyrins, Protoporphyrin Derivatives

Porphyrin Substitution

Alkyl Substituted Porphyrins, Beta Substituted Porphyrins, Carboxy Substituted Porphyrins

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