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105528-25-4

105528-25-4 Structure

105528-25-4 Structure
IdentificationBack Directory
[Name]

5,9,14,18,23,27,32,36-OCTABUTOXY- 2,3-NAPHTHALOCYANINE
[CAS]

105528-25-4
[Synonyms]

5 9 14 18 23 27 32 36-OCTABUTOXY-2 3- &
5,9,14,18,23,27,32,36-Octabutoxy-2,3-naphthalocyanine
5,9,14,18,23,27,32,36-Octabutoxy-2,3-naphthalocyanine Dye content 95 %
37H,39H-Tetranaphtho[2,3-b:2',3'-g:2'',3''-l:2''',3'''-q]porphyrazine, 5,9,14,18,23,27,32,36-octabutoxy-
[Molecular Formula]

C80H90N8O8
[MDL Number]

MFCD00192363
[MOL File]

105528-25-4.mol
[Molecular Weight]

1291.62
Chemical PropertiesBack Directory
[Melting point ]

303 °C
[density ]

1?+-.0.06 g/cm3(Predicted)
[λmax]

867 nm
[BRN ]

4949121
Safety DataBack Directory
[Safety Statements ]

22-24/25
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

5,9,14,18,23,27,32,36-Octabutoxy-2,3-naphthalocyanine is a photosensitive material with excellent light absorption and electron conduction activity. 5,9,14,18,23,27,32,36-Octabutoxy-2,3-naphthalocyanine is widely used in optoelectronic devices and is considered to be an effective photocatalyst. 5,9,14,18,23,27,32,36-Octabutoxy-2,3-naphthalocyanine can be used to improve the performance of solar cells and increase the photoelectric conversion efficiency. 5,9,14,18,23,27,32,36-Octabutoxy-2,3-naphthalocyanine also has potential anti-tumor activity and can inhibit the proliferation of certain cancer cells. 5,9,14,18,23,27,32,36-Octabutoxy-2,3-naphthalocyanine exhibits excellent fluorescence properties in medical imaging, which helps to improve the clarity and accuracy of imaging. 5,9,14,18,23,27,32,36-Octabutoxy-2,3-naphthalocyanine is studied as a component of a novel compound delivery system to improve the targeting and release effect of the compound.
[References]

[1] Multiple catalytic functions of brain nitric oxide synthase
[2] The inhibition of arginase by N-hydroxy-L-arginine controls the growth of Leishmania inside macrophages
[3] Hydrogen peroxide-supported oxidation of NG-hydroxy-L-arginine by nitric oxide synthase
[4] Characteristics of the nitric oxide synthase-catalyzed conversion of arginine to N-hydroxyarginine, the first oxygenation step in the enzymic synthesis of nitric oxide
Spectrum DetailBack Directory
[Spectrum Detail]

5,9,14,18,23,27,32,36-OCTABUTOXY- 2,3-NAPHTHALOCYANINE(105528-25-4)FT-IR
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