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COBALT meso-TETRAPHENYLPORPHINE | ||
PRODUCT IDENTIFICATION |
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CAS NO. | 14172-90-8 | |
EINECS NO. | 238-018-8 | |
FORMULA | C44H28CoN4 | |
MOL WT. | 671.67 | |
H.S. CODE |
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TOXICITY |
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SYNONYMS | ||
Cobalt(II) meso-Tetraphenylporphine; Cobalt TPP; 5,10,15,20-tetraphenyl-21H,23H- Porphine, Cobalt complex; | ||
[5,10,15,20-tetraphenyl-21H,23H-porphinato(2-)-N(21)-,N(22)-,N(23)-,N(24)-]-, (SP-4-1)-Cobalt; [5,10,15,20-tetraphenylporphinato(2-)]-Cobalt; Cobalt(II) alpha,beta,gamma,delta-tetraphenylporphine; Cobalt tetraphenylporphine; [5,10,15,20-tetraphenyl-21H,23H-porphinato (2-)-N21,N22,N23),N24]-(SP-4-1) Cobalt; (Tetraphenylporphinato)cobalt; | ||
CLASSIFICATION |
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PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE | brown crystalline powder | |
MELTING POINT | ||
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SOLUBILITY IN WATER | ||
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STABILITY |
Stable under ordinary conditions |
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GENERAL DESCRIPTION & APPLICATIONS |
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Porphyrin is a class of cyclic tetrapyrrolic ring structure compounds joined by four methene bridges (=C-) through alpha-carbon atoms of four pyrroles. Porphyrins are water-soluble biological pigments occuring widely in animal and plant tissues to take part in important biological functions such as metal-binding cofactors in hemoglobins in the blood of animals, chlorophyll in plants for photosynthesis, and certain enzymes for cell respiration. Numerous types of porphyrins can be obtained through the modification of a natural porphyrins and total synthesis. Not only their chemical transformations through nucleophilic and electrophilic substitution, substituent modification, reduction, oxidation but also thier metalation and demetalation properties with iron, zinc, copper, nickel, and cobalt give valuable biological applications in molecular biology, fluoroimmunoassay and new pharmaceutical developments. | ||
SALES SPECIFICATION | ||
APPEARANCE |
brown crystalline powder | |
ASSAY (HPLC) |
98.0% min |
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ABSORBANCE | 410 - 525 nm | |
TRANSPORTATION | ||
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OTHER INFORMATION | ||
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