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381896

Sigma-Aldrich

2,3-Naphthalocyanine

Dye content 95 %

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About This Item

Empirical Formula (Hill Notation):
C48H26N8
CAS Number:
23627-89-6
Molecular Weight:
714.77
Beilstein:
4345876
MDL number:
MFCD00134560
UNSPSC Code:
12352103
PubChem Substance ID:
57649813
NACRES:
NA.23

composition

Dye content, 95%

λmax

712 nm

SMILES string

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)

InChI key

LKKPNUDVOYAOBB-UHFFFAOYSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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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