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258784

Sigma-Aldrich

Coproporphyrin I dihydrochloride

synthetic

Sinônimo(s):

3,8,13,18-Tetramethyl-21H,23H-porphine-2,7,12,17-tetrapropionic acid dihydrochloride

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About This Item

Fórmula empírica (Notação de Hill):
C36H38N4O8 · 2HCl
Número CAS:
69477-27-6
Peso molecular:
727.63
Número MDL:
MFCD00013469
Código UNSPSC:
12161600
ID de substância PubChem:
24855660
NACRES:
NA.22

Nível de qualidade

100

forma

solid

adequação da reação

core: porphyrin
reagent type: catalyst

λmax

395 nm

cadeia de caracteres SMILES

Cl.Cl.Cc1c(CCC(O)=O)c2cc3[nH]c(cc4nc(cc5[nH]c(cc1n2)c(CCC(O)=O)c5C)c(CCC(O)=O)c4C)c(CCC(O)=O)c3C

InChI

1S/C36H38N4O8.2ClH/c1-17-21(5-9-33(41)42)29-14-26-19(3)23(7-11-35(45)46)31(39-26)16-28-20(4)24(8-12-36(47)48)32(40-28)15-27-18(2)22(6-10-34(43)44)30(38-27)13-25(17)37-29;;/h13-16,37,40H,5-12H2,1-4H3,(H,41,42)(H,43,44)(H,45,46)(H,47,48);2*1H/b25-13-,26-14-,27-15-,28-16-,29-14-,30-13-,31-16-,32-15-;;

chave InChI

XROPZSRTTZKNQB-ARSPAUKVSA-N

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Descrição geral

Coproporphyrin I dihydrochloride belongs to the porphyrin group, and it is used as a starting material to synthesize monofunctional and phosphorescent metalloporphyrin labeling reagents.

Aplicação

Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
MKCQ0035
MKCL0559
MKCJ4919
MKCG5578
MKCF0601

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5,10,15,20-Tetra(4-pyridyl)-21H,23H-porphine 97%

Sigma-Aldrich

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Rita Giovannetti et al.
Talanta, 63(4), 857-864 (2008-10-31)
The reaction of 3,8,13,18-tetramethyl-21H,23H-porphine-2,7,12,17-tetrapropionic acid or coproporphyrin-I (CPI) with the elements of 11 group have been studied. CPI is an anionic porphyrin that slowly reacts with copper ion to form Cu(II)CPI and with silver ions to form Ag(II)CPI, Ag(III)CPI complexes
Krzysztof Kilian et al.
Talanta, 60(4), 669-678 (2008-10-31)
The reaction of 5,10,15,20-tetrakis(4-carboxylphenyl)porphyrin (TCPP) with Cd(II), Pb(II), Hg(II) and Zn(II) was studied spectrophotometrically and kinetics, equilibrium constants as well as photodecomposition of complexes were determined. It was verified that these metal ions with large radius accelerate the incorporation reaction
R Giovannetti et al.
Talanta, 46(5), 977-984 (2008-10-31)
The reaction of 3,8,13,18-tetramethyl-21H,23H-porphine-2,7,12,17-tetrapropionic acid or coproporphyrin-I (CPI) with mercury(II) was studied spectrophotometrically, and kinetic and equilibrium constants were determined; the influence of temperature on the reaction rate was also studied. It was verified that mercury(II) accelerates the incorporation reaction
R Giovannetti et al.
Talanta, 42(12), 1913-1918 (1995-12-01)
The reagent 3,8,13,18-tetramethyl-21H,23H-porphine-2,7,12,17-tetrapropionic acid or coproporphyrin-I (CPI) was used for the spectrophotometric determination of copper(II) and cobalt(II) in the presence of pyridine and imidazole catalysts. Optimum conditions were investigated and the methods were applied to the determination of parts per

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