Cu(II) Chlorin e6 Trisodium Salt

Catalog#: C40405; CAS Number: 11006-34-1

C40405 Technical Data Sheet 

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Cu(II) Chlorin e6 Trisodium Salt CAS: 11006-34-1 MDL: MFCD27981354

Molecular weight: 724.15      g/mol

Molecular Formula: C34H31CuN4Na3O6

CAS Number:  11006-34-1

Storage: Store at –20 °C, protect from light.

Synonyms: chlorophyllin, chlorophyllin a, chlorophyllin copper complex, chlorophyllin e4, chlorophyllin, copper complex, chlorophyllin, sodium cobalt complex, chlorophyllin, sodium copper complex, chlorophyllin, sodium iron complex, chlorophyllin, copper chlorophyll, copper chlorophyllin, [18-(2-CarboxyĂ©thyl)-20-(carboxymĂ©thyl)-7-Ă©thyl-3,8,13,17-tĂ©tramĂ©thyl-12-vinyl-2-porphyrinecarboxylato(5-)-κ2N,N’]cuprate(3-) de trisodium, Cuprate(3-), [18-carboxy-20-(carboxymethyl)-8-ethenyl-13-ethyl-3,7,12,17-tetramethyl-21H,23H-porphine-2-propanoato(5-)-κN21,κN23]-, sodium (1:3), Sodium copper chlorophyllin, Trinatrium-[18-(2-carboxyethyl)-20-(carboxymethyl)-7-ethyl-3,8,13,17-tetramethyl-12-vinyl-2-porphyrincarboxylato(5-)-κ2N,N’]cuprat(3-), Trisodium [18-(2-carboxyethyl)-20-(carboxymethyl)-7-ethyl-3,8,13,17-tetramethyl-12-vinyl-2-porphyrincarboxylato(5-)-κ2N,N’]cuprate(3-), 234-242-5, 97659-67-, Chlorophyllin sodium copper salt, Chlorophyllin, coppered trisodium salt, MFCD00012149, MFCD28016032

Uses: Photosynthesis, Photodynamic Therapy, Photovoltaics, Solar Cells, Antiinflammation/Antioxidant agent

Copper Chlorin e6, trisodium salt, is a natural product derived from plants and studied in photosynthesis, and has numerous uses in photodynamic therapy, as a food additive,  interactions in the inflammasome, and has been used in solar cell construction. 1-5

References:

1.) Artificial photosynthesis.   Photosensitization of titania solar cells with chlorophyll derivatives and related natural porphyrin, Kay, Andreas; Graetzel, Michael, Journal of Physical Chemistry (1993), 97(23), 6272-7, DOI:10.1021/j100125a02

2.) Primary mutagenicity screening of food additives currently used in Japan, Ishidate, M., Jr.; Sofuni, T.; Yoshikawa, K.; Hayashi, M.; Nohmi, T.; Sawada, M.; Matsuoka, A., Food and Chemical Toxicology (1984), 22(8), 623-36 DOI:10.1016/0278-6915(84)90271-0

3.) Antioxidant activity of chlorophylls and their derivatives, Lanfer-Marquez, Ursula M.; Barros, Rosa M. C.; Sinnecker, Patricia, Food Research International (2005), 38(8-9), 885-891DOI:10.1016/j.foodres.2005.02.012

4.) Copper chlorophyllin: A food colorant with bioactive properties?, Tumolo, Tathyana; Lanfer-Marquez, Ursula Maria, Food Research International (2012), 46(2), 451-459. Language: English, DOI:10.1016/j.foodres.2011.10.031

5.) Artificial Photosynthesis. 2. Investigations on the Mechanism of Photosensitization of Nanocrystalline TiO2 Solar Cells by Chlorophyll Derivatives, Kay, Andreas; Humphry-Baker, Robin; Graetzel, Michael, Journal of Physical Chemistry (1994), 98(3), 952-9. DOI:10.1021/j100054a035

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Categories

Porphyrins

Scaffold/Subcategory

Natural Porphyrins & Derivatives

CAS #

[11006-34-1]

Purity %

>95%

Smiles

CCC1=C(C)C2=NC1=C/C1=C(C)C(C(=O)O[Na])=C3N1[Cu]N1C(=CC4=NC([C@@H](CCC(=O)O[Na])[C@@H]4C)=C/3CC(=O)O[Na])/C(C)=C(C=C)C1=C2

Molecular Weight

724.148

Molecular Formula

C34H31CuN4Na3O6

Porphyrin Family

Chlorophyll Derivatives, Metallo Porphyrins

Porphyrin Substitution

Alkyl Substituted Porphyrins, Beta Substituted Porphyrins, Carboxy Substituted Porphyrins

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