Cas no 67605-64-5 (5-(4-Aminophenyl)-10,15,20-triphenyl porphine)

5-(4-Aminophenyl)-10,15,20-triphenyl porphine is a functionalized porphyrin derivative characterized by its distinct structural and electronic properties. The presence of an aminophenyl group at the 5-position enhances its reactivity, making it a versatile intermediate for further chemical modifications, such as conjugation or metallation. This compound exhibits strong absorption in the visible region, rendering it useful in photodynamic therapy, catalysis, and materials science applications. Its triphenyl substitution pattern contributes to stability while maintaining solubility in organic solvents. The porphyrin core allows for coordination with various metal ions, enabling tailored applications in sensing, optoelectronics, and biomimetic systems. Its well-defined structure and synthetic accessibility make it a valuable tool in research and industrial contexts.

5-(4-Aminophenyl)-10,15,20-triphenyl porphine structure

67605-64-5 structure

Product Name:5-(4-Aminophenyl)-10,15,20-triphenyl porphine

CAS No:67605-64-5

MF:C₄₄H₃₁N₅

MW:629.750449419022

CID:2189430

PubChem ID:135423398

Update Time:2025-06-30

5-(4-Aminophenyl)-10,15,20-triphenyl porphine Chemical and Physical Properties

Names and Identifiers

- 4-(10,15,20-Triphenylporphyrin-5-yl)phenylamine
- 4-(10,15,20-triphenyl-21H,23H-porphin-5-yl)-Benzenamine
- 5-(4-aMinophenyl)-10,15,20-triphenyl porphine
- TPP-p-NH2-PH2
- 5-(4-Aminophenyl)-10,15,20-triphenyl-21H,23H-porphine
- 4-(10,15,20-Triphenyl-21H,23H-porphin-5-yl)benzenamine
- 4-(10,15,20-triphenylporphyrin-5-yl)aniline
- CS-0086506
- 5-(4-aminophenyl)-10,15,20-(triphenyl)porphyrin
- 5-(4-aminophenyl)-10,15,20-triphenylporphyrin
- 5-(4-Aminophenyl)-10,15,20-tris(phenyl)porphyrin
- CHEMBL3408510
- BS-47662
- DB-315634
- E85151
- 5-(4-aminophenyl)-10,15,20-triphenylporphine
- YSWG152
- SCHEMBL3999312
- 67605-64-5
- 4-(10,15,20-triphenyl-21,23-dihydroporphyrin-5-yl)aniline
- 5-(4-Aminophenyl)-10,15,20-triphenyl porphine
- Inchi： 1S/C44H31N5/c45-32-18-16-31(17-19-32)44-39-26-24-37(48-39)42(29-12-6-2-7-13-29)35-22-20-33(46-35)41(28-10-4-1-5-11-28)34-21-23-36(47-34)43(30-14-8-3-9-15-30)38-25-27-40(44)49-38/h1-27,46,49H,45H2/b41-33-,41-34-,42-35-,42-37-,43-36-,43-38-,44-39-,44-40-
- InChI Key： NSCOPASYOISSAC-LWQDQPMZSA-N
- SMILES： N1C2C=CC1=C(C1C=CC(=CC=1)N)C1C=CC(=C(C3C=CC=CC=3)C3=CC=C(C(C4C=CC=CC=4)=C4C=CC(C=2C2C=CC=CC=2)=N4)N3)N=1 |c:18,43,t:5,38|

Computed Properties

Exact Mass: 629.25794601g/mol
Monoisotopic Mass: 629.25794601g/mol
Isotope Atom Count: 0
Hydrogen Bond Donor Count: 3
Hydrogen Bond Acceptor Count: 3
Heavy Atom Count: 49
Rotatable Bond Count: 4
Complexity: 1040
Covalently-Bonded Unit Count: 1
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count : 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Topological Polar Surface Area: 83.4
XLogP3: 9.7

Experimental Properties

Density: 1.278

5-(4-Aminophenyl)-10,15,20-triphenyl porphine Pricemore >>

Related Categories	No.	Product Name	Cas No.	Purity	Specification	Price	update time
Frontier Specialty Chemicals	A40960-100 mg	5-(4-aminophenyl)-10,15,20-triphenyl porphine	67605-64-5		100mg	$ 111.00	2022-11-04
Frontier Specialty Chemicals	A40960-250 mg	5-(4-aminophenyl)-10,15,20-triphenyl porphine	67605-64-5		250mg	$ 201.00	2022-11-04
Frontier Specialty Chemicals	A40960-1 g	5-(4-aminophenyl)-10,15,20-triphenyl porphine	67605-64-5		1g	$ 660.00	2022-11-04
Frontier Specialty Chemicals	A40960-500 mg	5-(4-aminophenyl)-10,15,20-triphenyl porphine	67605-64-5		500mg	$ 368.00	2022-11-04
SHANG HAI XIAN DING Biotechnology Co., Ltd.	A40960-1g	5-(4-aminophenyl)-10,15,20-triphenyl porphine	67605-64-5		1g	14386.0CNY	2021-07-13
SHANG HAI XIAN DING Biotechnology Co., Ltd.	A40960-250mg	5-(4-aminophenyl)-10,15,20-triphenyl porphine	67605-64-5		250mg	4018.0CNY	2021-07-13
SHANG HAI XIAN DING Biotechnology Co., Ltd.	A40960-500mg	5-(4-aminophenyl)-10,15,20-triphenyl porphine	67605-64-5		500mg	7636.0CNY	2021-07-13
SHANG HAI XIAN DING Biotechnology Co., Ltd.	A40960-100mg	5-(4-aminophenyl)-10,15,20-triphenyl porphine	67605-64-5		100mg	1925.0CNY	2021-07-13
SU ZHOU XIN JIA YUAN HUA XUE Technology Co., Ltd.	lj1146-250mg	5-(4-Aminophenyl)-10,15,20-triphenyl porphine	67605-64-5	95%	250mg	￥3000.0	2024-07-19
SU ZHOU XIN JIA YUAN HUA XUE Technology Co., Ltd.	lj1146-100mg	5-(4-Aminophenyl)-10,15,20-triphenyl porphine	67605-64-5	95%	100mg	￥1500.0	2024-07-19

5-(4-Aminophenyl)-10,15,20-triphenyl porphine Suppliers

Suzhou Senfeida Chemical Co., Ltd

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(CAS:67605-64-5)4-(10,15,20-Triphenyl-21H,23H-porphin-5-yl)benzenamine

Order Number:sfd725

Stock Status:in Stock

Quantity:200kg

Purity:99.9%

Pricing Information Last Updated:Friday, 19 July 2024 14:32

Price ($):discuss personally

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Additional information on 5-(4-Aminophenyl)-10,15,20-triphenyl porphine

Comprehensive Overview of 5-(4-Aminophenyl)-10,15,20-triphenyl porphine (CAS No. 67605-64-5): Properties, Applications, and Research Insights

5-(4-Aminophenyl)-10,15,20-triphenyl porphine, identified by its CAS No. 67605-64-5, is a highly specialized porphyrin derivative that has garnered significant attention in both academic and industrial research. This compound belongs to the porphyrin family, a class of heterocyclic macrocycles known for their unique photophysical and electrochemical properties. The presence of the 4-aminophenyl group and three triphenyl substituents in its structure makes it a versatile building block for advanced materials, sensors, and biomedical applications.

In recent years, the demand for porphyrin-based compounds has surged due to their applications in photodynamic therapy (PDT), organic electronics, and catalysis. Researchers are particularly interested in 5-(4-Aminophenyl)-10,15,20-triphenyl porphine for its potential in light-harvesting systems and molecular recognition. Its ability to absorb light in the visible spectrum and transfer energy efficiently makes it a promising candidate for solar cell technologies and artificial photosynthesis.

The synthesis of 5-(4-Aminophenyl)-10,15,20-triphenyl porphine typically involves the condensation of pyrrole with appropriate aldehydes, followed by functionalization to introduce the aminophenyl group. This process requires precise control over reaction conditions to ensure high purity and yield. The compound's structural stability and solubility in organic solvents further enhance its utility in various experimental setups.

One of the most exciting applications of this compound is in the field of biomedical imaging. Its strong fluorescence emission and biocompatibility make it suitable for fluorescence labeling and diagnostic probes. Additionally, its metal-binding capacity allows for the creation of metalloporphyrins, which are widely used in oxygen sensing and drug delivery systems.

From an environmental perspective, 5-(4-Aminophenyl)-10,15,20-triphenyl porphine is being explored for its role in pollutant degradation and wastewater treatment. Its ability to generate reactive oxygen species (ROS) under light irradiation makes it effective in breaking down organic contaminants. This aligns with the growing global focus on sustainable chemistry and green technologies.

In the realm of nanotechnology, this porphyrin derivative is being integrated into nanostructured materials and supramolecular assemblies. Its planar structure and π-conjugated system facilitate interactions with carbon nanotubes and graphene, opening doors for innovations in nanoelectronics and quantum computing.

For researchers and industry professionals, understanding the spectroscopic properties of 5-(4-Aminophenyl)-10,15,20-triphenyl porphine is crucial. Techniques such as UV-Vis spectroscopy, NMR, and mass spectrometry are commonly employed to characterize its electronic and molecular structure. These analyses reveal insights into its absorption maxima, fluorescence quantum yield, and photostability.

As the scientific community continues to explore the potential of porphyrin derivatives, 5-(4-Aminophenyl)-10,15,20-triphenyl porphine stands out as a compound with multifaceted applications. Its relevance in emerging technologies and interdisciplinary research ensures its place as a subject of ongoing investigation. Future studies may focus on optimizing its synthesis, expanding its functionalization, and exploring novel applications in energy storage and smart materials.

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