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.

1291.62

C₈₀H₉₀N₈O₈

105528-25-4

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

Room temperature in continental US; may vary elsewhere.

Please store the product under the recommended conditions in the Certificate of Analysis.

• [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