5-(4-aminophenyl)-10,15,20-triphenyl porphine

Product Number: A40960; CAS Number: 67605-64-5

A40960 Technical Data Sheet 




5-(4-aminophenyl)-10,15,20-triphenyl porphine CAS: 67605-64-5 MDL: MFCD01074434

Molecular weight: 629.8  g/mol

Molecular Formula: C44H31N5  

CAS Number:  67605-64-5

Storage: Store at room temperature, protect from light.

Purity: >95%

Synonyms:   5-(4-aminophenyl)-10,15,20-triphenyl porphine, SCHEMBL3999312, CHEMBL3408510, C-0168, 5-(4-aminophenyl)-10,15,20-triphenylporphyrin, 5-(4-aminophenyl)-10,15,20-(triphenyl)porphyrin, 5-(4-aminophenyl)-10-15-20-(triphenyl)porphyrin, 5-(4-Aminophenyl)-10,15,20-tris(phenyl)porphyrin, 4-(5,10,20-Triphenyl-21H,23H-porphyrin-15-yl)aniline, 4-(10,15,20-Triphényl-5-porphyrineyl)aniline, 4-(10,15,20-Triphenyl-5-porphyrinyl)anilin, 4-(10,15,20-Triphenyl-5-porphyrinyl)aniline, Benzenamine, 4-(10,15,20-triphenyl-21H,23H-porphin-5-yl)- , 4-(7,12,17-TRIPHENYL-21,22,23,24-TETRAAZAPENTACYCLO[,6).1(8,11).1(13,16)]TETRACOSA-1(21),2,4,6,8(23),9,11,13,15,17,19-UNDECAEN-2-YL)ANILINE, 4-(7,12,17-triphenyl-21,22,23,24-tetraazapentacyclo[,6.18,11.113,16]tetracosa-1(21),2,4,6,8(23),9,11,13,15,17,19-undecaen-2-yl)aniline, 4-[(1Z,4Z,9Z,15Z)-10,15,20-triphenyl-21,23-dihydroporphyrin-5-yl]aniline, 5-(4-aminophenyl)-10,15,20-triphenyl porphine, 5-(4-Aminophenyl)-10,15,20-triphenylporphyrin, 5-(p-aminophenyl)-10,15,20-triphenylporphyrin, 5-(氨苯基)- 10,15,20-苯基卟啉, 67605-64-5, D01074434, MFCD01074434, TPP-p-NH2-PH2

Fields of Interest: Nanocomposites, Catalysis, Photocatalysis, Metal Organic Frameworks, Immunoassay, Porphyrin Functionalized Materials

Background: 5-(4-aminophenyl)-10,15,20-triphenyl porphine is a synthetic porphyrin specialty chemical manufactured by Frontier Specialty Chemicals. 5-(4-aminophenyl)-10,15,20-triphenyl porphine  was used to covalently functionalize graphene oxide.1 5-(4-aminophenyl)-10,15,20-triphenyl porphine was found to effectively chelate the radioisotope 64Cu and found to have favorable bio distribution in mice.2 Electropolymerization of 5-(4-aminophenyl)-10,15,20-triphenyl porphine and its Cu(II) adducts resulted in the precipitation of electro-conductive films.3 5-(4-aminophenyl)-10,15,20-triphenyl porphine was used to construct porphyrin containing light-responsive capsules for controlled drug release.4 5-(4-aminophenyl)-10,15,20-triphenyl porphine was used to synthesize an electrochemiluminescent porphyrin by coupling to a tetraphenylethylene derivative.5 5-(4-aminophenyl)-10,15,20-triphenyl porphine was used to synthesize porphyrin modified siloxanes.6


1.) Karousis, et al. Graphene oxide with covalently linked porphyrin antennae: Synthesis, characterization and photophysical properties. J. Mater. Chem., 2011, 21, 109-117. 10.1039/C0JM00991A

2.) Aguilar-Ortiz, et al. Synthesis, characterization and evaluation of a Cu-labeled macrocyclic-porphyrin as a potential chelator for 64Cu-based radiopharmaceuticals. Journal of Radioanalytical and Nuclear Chemistry volume 320, pages 79–86 (2019). https://doi.org/10.1007/s10967-019-06454-4

3.) Tesakova, et al. Electroconductive films based on amino-substituted tetraphenylporphyrins and their metal copper complexes. Journal of Porphyrins and Phthalocyanines. Vol. 20, No. 07, pp. 793-803 (2016). https://doi.org/10.1142/S1088424616500930

4.) Li, et al. Porphyrin containing light-responsive capsules for controlled drug release. J. Mater. Chem., 2012,22, 4623-4626. https://doi.org/10.1039/C2JM16702F

5.) Zhang, et al. Switching the Photoluminescence and Electrochemiluminescence of Liposoluble Porphyrin in Aqueous Phase by Molecular Regulation. Angew. Chemie. Int. Ed. Volume 59, Issue51 December 14, 2020 Pages 23261-23267. https://doi.org/10.1002/anie.202010216

6.) Almeida, et al. (Aminophenyl)porphyrins as precursors for the synthesis of porphyrin-modified siloxanes. Journal of Porphyrins and Phthalocyanines Vol. 23, No. 09, pp. 1001-1012 (2019). https://doi.org/10.1142/S1088424619500573

7.) Labels for fluorescence immunoassays and intermediates for their preparation, Schmidt, Dieter  Steffen, Hans, Eur. Pat. Appl. (1984), EP 127797 A1 19841212,

8.) Syntheses and characterization of molybdenum/zinc porphyrin dimers bridged by aromatic linkers­, Song, Sai-Nan  Li, Dong-Mei  Wu, Jun-Feng  Zhuang, Chang-Fu  Ding, Hong  Song, Wen-Bo  Cui, Li-Feng  Cao, Geng-Zhen  Liu, Guo-Fa, European Journal of Inorganic Chemistry (2007), (13), 1844-1853. DOI:10.1002/ejic.200600853




Porphyrin Substitution

Amino-Phenyl Substituted Porphyrins, Phenyl Substituted Porphyrins

Porphyrin Family

A3B Porphyrins, Amino Porphyrins, Free Base Porphyrins, Tetra-Phenyl Porphine Derivatives

Functional Groups


Purity %


Molecular Formula


Molecular Weight



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