Catalog |
name |
Description |
price |
R-C-5960 |
5,10,15,20-Tetrakis-(4-bromophenyl)-porphine-Ni(II) cas:112592-50-4 |
5,10,15,20-Tetrakis(4-bromophenyl)porphine-Ni(II) is a metalloporphyrin complex featuring a central nickel (Ni(II)) ion.Porphyrin compounds are widely studied due to their importance in biological systems (such as in hemoglobin and chlorophyll) and their applications in various fields including catalysis, photodynamic therapy,sensors,and materials science. |
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R-C-5964 |
TPP-DOX |
TPP-DOX,Tetraphenylporphyrin-doxorubicin is a conjugate of the anticancer drug doxorubicin with tetraphenylporphyrin,a synthetic organic compound with potential photodynamic therapy properties.This conjugate is being studied as a potential treatment for cancer,as it may have improved tumor-targeting and reduced systemic toxicity compared to doxorubicin alone. |
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R-C-5495 |
2,3,7,8,12,13,17,18-Octaethylporphyrin CAS:2683-82-1 |
Octaethylporphyrin and its derivatives have various applications due to their unique properties. They exhibit strong absorbance of light in the visible region, making them useful in photovoltaic devices and photocatalysis. Octaethylporphyrin can also form complexes with metal ions, leading to enhanced properties such as light absorption, emission, and catalytic activity. |
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R-C-5497 |
5,15-Diphenylporphyrin cas:22112-89-6 |
5,15-Diphenylporphyrin can form complexes with metal ions, resulting in modified properties such as altered electronic structures and improved catalytic activity. Metalloporphyrin complexes are extensively investigated for applications in catalysis, sensing, and electron transfer processes due to their versatile nature. |
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R-C-5782 |
TCPP-Cu(2+) CAS:41699-93-8 |
Cu(II) meso-Tetra(4-carboxyphenyl)porphine is a synthetic porphyrin.CU(II) Meso-tetra(4-carboxyphenyl)porphine has has been studied for its versatile applications across various fields,including catalysis,electrochemistry, photochemistry, and biochemistry.In catalysis,this compound has exhibited exceptional efficacy as a catalyst,facilitating diverse organic reactions like alcohol oxidation and nitro compound reduction. |
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R-C-5785 |
5-(4-aminophenyl)-10,15,20-triphenyl porphine CAS:67605-64-5 |
4-(10,15,20-Triphenylporphyrin-5-yl)phenylamine,CAS:67605-64-5 ,5-(4-aminophenyl)-10,15,20-triphenyl porphine is a porphyrin used in proteomics research.This product is only used for scientific research experiments and not for human or clinical experiments. |
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R-C-5788 |
5,10,15,20-Tetra(4-dihydroxyborylphenyl)porphyrin CAS:97654-08-5 |
5,10,15,20-Tetra(4-dihydroxyborylphenyl)porphyrin,Synonymous:H2TBPP:TDHB;Boronic acid, B,B,B,B-(21H,23H-porphine-5,10,15,20-tetrayltetra-4,1-phenylene)tetrakis-
CAS:97654-08-5. |
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R-C-5791 |
5,10,15,20-Tetrakis(4-aminophenyl)porphyrin CAS:22112-84-1 |
5,10,15,20-Tetrakis(4-aminophenyl)porphyrin is a porphyrin compound substituted with four 4-aminophenyl moieties.This porphyrin has been described as a useful ligand for the design of catalysts, and was used to prepare a manganese(III)complex for catalyzing oxidative decarboxylations of carboxylic acids with sodium periodate.It functions by absorbing light in the visible range and converting it into energy. |
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R-C-5810 |
TPP-Cur |
TPP-curcumin,Tetraphenylporphyrin (TPP)is a well-known porphyrin derivative that exhibits interesting photophysical and photochemical properties, while curcumin is a natural compound found in turmeric with numerous biological activities.The combination of TPP and curcumin in TPP-Cur leads to the formation of a hybrid molecule with enhanced properties.TPP provides TPP-Cur with fluorescence and photosensitization capabilities,making it useful in fluorescence imaging and photodynamic therapy(PDT). Curcumin,on the other hand,contributes its antioxidant, anti-inflammatory,and anticancer properties to TPP-Cur. |
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R-C-5845 |
5,10,15,20-Tetra-p-tolyl-21H,23H-porphine CAS:14527-51-6 |
5,10,15,20-Tetra-p-tolyl-21H,23H-porphine is a specific chemical compound that belongs to the class of porphyrin derivatives. Porphyrins are heterocyclic compounds consisting of four pyrrole rings connected through methine bridges. They are commonly found in many biological molecules, such as chlorophyll and heme. |
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