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5,9,14,18,23,27,32,36-Octabutoxy-2,3-naphthalocyanine

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.

Product Specifications

CAS Number

105528-25-4

UNSPSC

12352005

Hazard Statement

H302-H315-H319-H335

Target

Biochemical Assay Reagents; Endogenous Metabolite

Type

Reference compound

Related Pathways

Metabolic Enzyme/Protease; Others

Applications

Metabolism-protein/nucleotide metabolism

Field of Research

Cancer

Assay Protocol

https://www.medchemexpress.com/5-9-14-18-23-27-32-36-octabutoxy-2-3-naphthalocyanine.html

Smiles

CCCCOC(C1=C2/C3=N/C(NC(NC(C4=C/5C(OCCCC)=C6C=CC=CC6=C4OCCCC)=NC5=N/C(C7=C/8C(OCCCC)=C9C=CC=CC9=C7OCCCC)=NC8=N/C1=N3)=C%10%11)=C%11C(OCCCC)=C%12C=CC=CC%12=C%10OCCCC)=C%13C=CC=CC%13=C2OCCCC

Molecular Formula

C80H90N8O8

Molecular Weight

1291.62

Precautions

P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

References & Citations

[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

Shipping Conditions

Room temperature

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Frequently Asked Questions

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