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| | 5,9,14,18,23,27,32,36-Octabutoxy- 2,3-naphthalocyanine Basic information |
| Product 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- | | CAS: | 105528-25-4 | | MF: | C80H90N8O8 | | MW: | 1291.62 | | EINECS: | | | Product Categories: | Infrared (IR) DyesPhotonic and Optical Materials;Organic Electronics and Photonics;Photonic and Optical Materials;Phthalocyanine and Porphyrin Dyes;Phthalocyanines | | Mol File: | 105528-25-4.mol |  |
| | 5,9,14,18,23,27,32,36-Octabutoxy- 2,3-naphthalocyanine Chemical Properties |
| Melting point | 303 °C | | density | 1+-.0.06 g/cm3(Predicted) | | λmax | 867 nm | | BRN | 4949121 | | InChIKey | BFXKASLQHBYWIJ-UHFFFAOYSA-N |
| Safety Statements | 22-24/25 | | WGK Germany | 3 | | Storage Class | 11 - Combustible Solids |
| | 5,9,14,18,23,27,32,36-Octabutoxy- 2,3-naphthalocyanine Usage And Synthesis |
| 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 |
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