Cas no 57450-62-1 (5,10,15,20-Tetrakis(4-butoxyphenyl)-Porphine)

5,10,15,20-Tetrakis(4-butoxyphenyl)-porphine is a synthetic porphyrin derivative characterized by four butoxyphenyl substituents at the meso-positions of the porphine core. This modification enhances solubility in organic solvents while retaining the photophysical and coordination properties typical of porphyrins. The butoxy groups improve processability, making it suitable for applications in organic electronics, catalysis, and photodynamic therapy. Its extended conjugation and electron-donating substituents contribute to tunable optical properties, including absorption in the visible spectrum. The compound is often utilized in supramolecular chemistry and as a building block for advanced materials due to its structural stability and functional versatility.
5,10,15,20-Tetrakis(4-butoxyphenyl)-Porphine structure
57450-62-1 structure
Product Name:5,10,15,20-Tetrakis(4-butoxyphenyl)-Porphine
CAS No:57450-62-1
MF:C60H62N4O4
MW:903.158695697784
CID:1023610
PubChem ID:135411732
Update Time:2025-06-30

5,10,15,20-Tetrakis(4-butoxyphenyl)-Porphine Chemical and Physical Properties

Names and Identifiers

    • 5,10,15,20-Tetrakis(4-butoxyphenyl)-Porphine
    • 5,10,15,20-tetrakis(4-butoxyphenyl)-21,22-dihydroporphyrin
    • 5,10,15,20-tetrakis-(4-butoxy-phenyl)-21H,23H-porphine
    • 5,10,15,20-tetrakis-(4-butoxy-phenyl)-porphyrin
    • AC1NP3ZZ
    • AK102908
    • ANW-65289
    • CTK8C0797
    • meso-tetra(4-butoxyphenyl)porphyrin
    • 5,10,15,20-tetrakis(4-butoxyphenyl)-21,23-dihydroporphyrin
    • 57450-62-1
    • AKOS016005086
    • 5,10,15,20-tetra-(4-butoxyphenyl)porphine
    • AG-690/12764397
    • MDL： MFCD00302483
    • Inchi： 1S/C60H62N4O4/c1-5-9-37-65-45-21-13-41(14-22-45)57-49-29-31-51(61-49)58(42-15-23-46(24-16-42)66-38-10-6-2)53-33-35-55(63-53)60(44-19-27-48(28-20-44)68-40-12-8-4)56-36-34-54(64-56)59(52-32-30-50(57)62-52)43-17-25-47(26-18-43)67-39-11-7-3/h13-36,61,64H,5-12,37-40H2,1-4H3/b57-49-,57-50-,58-51-,58-53-,59-52-,59-54-,60-55-,60-56-
    • InChI Key： ALIFKTXKRLSRSL-NWQHMXIBSA-N
    • SMILES： O(CCCC)C1C=CC(=CC=1)C1C2C=CC(=C(C3C=CC(=CC=3)OCCCC)C3=CC=C(C(C4C=CC(=CC=4)OCCCC)=C4C=CC(C(C5C=CC(=CC=5)OCCCC)=C5C=CC=1N5)=N4)N3)N=2 |c:16,67,t:46,63|

Computed Properties

  • Exact Mass: 902.47746
  • Monoisotopic Mass: 902.47710647g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 8
  • Heavy Atom Count: 68
  • Rotatable Bond Count: 20
  • Complexity: 1200
  • 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
  • XLogP3: 15.3
  • Topological Polar Surface Area: 94.3?2

Experimental Properties

  • Density: 1.151
  • Refractive Index: 1.608
  • PSA: 89.46

5,10,15,20-Tetrakis(4-butoxyphenyl)-Porphine Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Alichem
A019112531-1g
5,10,15,20-Tetrakis(4-butoxyphenyl)-Porphine
 57450-62-1 95%
1g
 $373.12 2023-09-01

5,10,15,20-Tetrakis(4-butoxyphenyl)-Porphine Related Literature

Additional information on 5,10,15,20-Tetrakis(4-butoxyphenyl)-Porphine

Recent Advances in the Study of 5,10,15,20-Tetrakis(4-butoxyphenyl)-Porphine (CAS: 57450-62-1)

The compound 5,10,15,20-Tetrakis(4-butoxyphenyl)-Porphine (CAS: 57450-62-1) has garnered significant attention in the field of chemical biology and pharmaceutical research due to its unique photophysical properties and potential applications in photodynamic therapy (PDT), catalysis, and materials science. Recent studies have explored its synthesis, characterization, and functional applications, shedding light on its versatility and efficacy in various biomedical and industrial contexts.

One of the most notable advancements in the study of this porphyrin derivative is its role in photodynamic therapy. Researchers have demonstrated that 5,10,15,20-Tetrakis(4-butoxyphenyl)-Porphine exhibits strong absorption in the visible spectrum, making it an excellent candidate for PDT applications. Its ability to generate reactive oxygen species (ROS) upon light irradiation has been leveraged to target and destroy cancer cells with high precision. Recent in vitro and in vivo studies have shown promising results, with minimal side effects and high therapeutic efficacy.

In addition to its biomedical applications, this porphyrin derivative has also been investigated for its catalytic properties. Studies have revealed its potential as a catalyst in organic transformations, including oxidation and reduction reactions. The butoxyphenyl substituents enhance its solubility in organic solvents, facilitating its use in homogeneous catalytic systems. Recent work has focused on optimizing its catalytic performance and exploring its mechanistic pathways, providing valuable insights for future applications in green chemistry.

Another area of interest is the use of 5,10,15,20-Tetrakis(4-butoxyphenyl)-Porphine in materials science. Its ability to form stable complexes with metal ions has been exploited to develop novel materials with tailored optical and electronic properties. Recent research has highlighted its potential in the fabrication of organic light-emitting diodes (OLEDs) and photovoltaic devices, where its high quantum yield and tunable emission spectra offer significant advantages.

Despite these advancements, challenges remain in the large-scale synthesis and commercialization of this compound. Researchers are actively working to address issues related to cost, scalability, and stability under various environmental conditions. Collaborative efforts between academia and industry are expected to drive further innovations and expand the range of applications for this versatile porphyrin derivative.

In conclusion, 5,10,15,20-Tetrakis(4-butoxyphenyl)-Porphine (CAS: 57450-62-1) represents a promising candidate for a wide range of applications in chemical biology and pharmaceutical research. Its unique properties and multifunctional capabilities continue to inspire new studies and technological developments. Future research should focus on overcoming existing limitations and exploring novel applications to fully realize its potential in addressing current and emerging challenges in the field.

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