5,9,14,18,23,27,32,36-OCTABUTOXY- 2,3-NAPHTHALOCYANINE
- Product Name
- 5,9,14,18,23,27,32,36-OCTABUTOXY- 2,3-NAPHTHALOCYANINE
- CAS No.
- 105528-25-4
- Chemical Name
- 5,9,14,18,23,27,32,36-OCTABUTOXY- 2,3-NAPHTHALOCYANINE
- 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-
- CBNumber
- CB2502801
- Molecular Formula
- C80H90N8O8
- Formula Weight
- 1291.62
- MOL File
- 105528-25-4.mol
5,9,14,18,23,27,32,36-OCTABUTOXY- 2,3-NAPHTHALOCYANINE Property
- Melting point:
- 303 °C
- Density
- 1?+-.0.06 g/cm3(Predicted)
- λmax
- 867 nm
- BRN
- 4949121
Safety
- Safety Statements
- 22-24/25
- WGK Germany
- 3
N-Bromosuccinimide Price
- Product number
- 412074
- Product name
- 5,9,14,18,23,27,32,36-Octabutoxy-2,3-naphthalocyanine
- Purity
- Dye content 95 %
- Packaging
- 100mg
- Price
- $191
- Updated
- 2025/07/31
5,9,14,18,23,27,32,36-OCTABUTOXY- 2,3-NAPHTHALOCYANINE Chemical Properties,Usage,Production
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
5,9,14,18,23,27,32,36-OCTABUTOXY- 2,3-NAPHTHALOCYANINE Preparation Products And Raw materials
Raw materials
Preparation Products
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