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381896

Sigma-Aldrich

2,3-Naphthalocyanine

Dye content 95 %

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About This Item

Fórmula empírica (Notação de Hill):
C48H26N8
Número CAS:
23627-89-6
Peso molecular:
714.77
Beilstein:
4345876
Número MDL:
MFCD00134560
Código UNSPSC:
12352103
ID de substância PubChem:
57649813
NACRES:
NA.23

composição

Dye content, 95%

λmax

712 nm

cadeia de caracteres SMILES

c1ccc2cc3c4nc(nc5[nH]c(nc6nc(nc7[nH]c(n4)c8cc9ccccc9cc78)c%10cc%11ccccc%11cc6%10)c%12cc%13ccccc%13cc5%12)c3cc2c1

InChI

1S/C48H26N8/c1-2-10-26-18-34-33(17-25(26)9-1)41-49-42(34)54-44-37-21-29-13-5-6-14-30(29)22-38(37)46(51-44)56-48-40-24-32-16-8-7-15-31(32)23-39(40)47(52-48)55-45-36-20-28-12-4-3-11-27(28)19-35(36)43(50-45)53-41/h1-24H,(H2,49,50,51,52,53,54,55,56)

chave InChI

LKKPNUDVOYAOBB-UHFFFAOYSA-N

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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)

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Certificados de análise (COA)

Lot/Batch Number
MKCL6418
MKCJ2505
MKBH4066V
16323LD
10614JD

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Copper(II) 5,9,14,18,23,27,32,36-octabutoxy-2,3-naphthalocyanine Dye content 90 %

Sigma-Aldrich

415286

Copper(II) 5,9,14,18,23,27,32,36-octabutoxy-2,3-naphthalocyanine

Q Huan et al.
The Journal of chemical physics, 135(1), 014705-014705 (2011-07-13)
Selective excitations of specific vibronic modes in position space are realized in single naphthalocyanine molecules adsorbed on an ultrathin alumina film by a scanning tunneling microscope at low temperature. Distinct spatial distributions are imaged for the different vibronic modes, which
Wen-Jun Wang et al.
Guang pu xue yu guang pu fen xi = Guang pu, 25(1), 149-152 (2005-04-28)
Deposition of Langmuir-Blodgett films and the aggregative properties of three centrosymmetric naphthalocyanine derivatives were investigated by using linear absorption spectra. Good LB films could be formed for all the three compounds. In dilute solution,the monomers are the main formation for
V Mantareva et al.
Journal of photochemistry and photobiology. B, Biology, 40(3), 258-262 (1998-02-12)
A Si(IV)-naphthalocyanine bearing two methoxyethylenglycol axial ligands to the centrally coordinated metal ion (SiNc) was prepared by chemical synthesis and assayed for the phototherapeutic activity after administration in a Cremophor formulation to C57BI/6 mice bearing a subcutaneously transplanted Lewis lung
N Michailov et al.
Journal of photochemistry and photobiology. B, Biology, 37(1-2), 154-157 (1997-01-01)
In vivo experiments were performed to evaluate the effect of fluence rate on the efficiency of Zn(II)-2,3 naphthalocyanine (ZnNc) photosensitization of B16 pigmented melanoma subcutaneously transplanted in C57B1/6 mice. The tumour was irradiated with 774 nm light at 24 h
S Müller et al.
Journal of photochemistry and photobiology. B, Biology, 35(3), 167-174 (1996-09-01)
The aim of this study is to report the synthesis and photochemical and phototherapeutic activities of tetraamido-substituted 2,3-naphthalocyanine zinc(II) complexes (ZnNcs 5-8). Four naphthalocyanine complexes, tetrabenzamido- (ZnNc 5), tetramethoxybenzamido- (ZnNc 6), tetrahexylamido- (ZnNc 7) and tetradodecylamido- (ZnNc 8) naphthalocyanine zinc
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