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

Safety Information

Safety Statements 

22-24/25

WGK Germany 

3

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(105528-25-4)Related Product Information

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