335654-28-9

Basic information

• Product Name: N-n-butyl-1,6,7,12-tetra(4-tert-butylphenoxy)perylene-3,4-dicarboxylate anhydride-9,10-dicarboxylate imide
• Synonyms: N-n-butyl-1,6,7,12-tetra(4-tert-butylphenoxy)perylene-3,4-dicarboxylate anhydride-9,10-dicarboxylate imide
• CAS NO: 335654-28-9
• Molecular Weight: 1040.27
• Mol File: 335654-28-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-n-butyl-1,6,7,12-tetra(4-tert-butylphenoxy)perylene-3,4-dicarboxylate anhydride-9,10-dicarboxylate imide(CAS DataBase Reference)
• NIST Chemistry Reference: N-n-butyl-1,6,7,12-tetra(4-tert-butylphenoxy)perylene-3,4-dicarboxylate anhydride-9,10-dicarboxylate imide(335654-28-9)
• EPA Substance Registry System: N-n-butyl-1,6,7,12-tetra(4-tert-butylphenoxy)perylene-3,4-dicarboxylate anhydride-9,10-dicarboxylate imide(335654-28-9)

Safety Data

• Hazardous Substances Data: 335654-28-9(Hazardous Substances Data)

Upstream product

• 109-73-9 N-butylamine 
• 156028-30-7 1,6,7,12-tetrakis(4-tert-butylphenoxy)perylene-3,4:9,10-tetracarboxylic acid dianhydride 
• 335654-34-7 N,N'-dibutyl-1,6,7,12-tetra(4-tert-butylphenoxy)perylene-3,4:9,10-tetracarboxylic acid bisimide 

Downstream Products

• 1411700-49-6 N-butyl-tetra(tert-butylphenoxy)methoxybenzo[c,d]perylenone 
• 1574527-41-5 C₈₂H₈₁N₅O₈ 
• 1400874-45-4 N-n-butyl-N-p-phenylenediamine-1,6,7,12-tetra(4-tert-butylphenoxy)perylene-3,4:9,10-tetracarboxylic diimide 
• 1400874-43-2 C₁₀₆H₉₁N₅O₁₃ 
• 478491-50-8 2-butyl-5,6,12,13-tetrakis-(4-tert-butyl-phenoxy)-9-(4-[2,2';6',2'']terpyridin-4'-yl-phenyl)-anthra[2,1,9-def;6,5,10-d'e'f']diisoquinoline-1,3,8,10-tetraone 
• 1259371-46-4 C₇₄H₇₀BF₂N₃O₇ 
• 1196670-76-4 C₉₀H₁₀₀N₂O₈S₈ 

Relevant articles and documents

Synthesis and properties of a covalently linked angular perylene imide dimer

Utilizing the unexplored chemistry of a monocarbon analog to perylene bisimide, a covalently linked angular perylene dimer was synthesized. On the basis of measured optical properties and molecular modeling, the spectral changes relative to a monomeric reference perylene can be explained by an angle-dependent oblique exciton coupling model. With a roughly trigonal interchromophore arrangement, the dimer building block is promising for larger, cyclic assemblies to mimic naturally occurring light harvesting complexes.

Novel fluorescent dyes with fused perylene tetracarboxlic diimide and BODIPY analogue structures

(Chemical Equation) Two novel fluorescent dyes based on perylene tetracarboxylic diimides and BODIPY were designed and synthesized. Significant features, such as longer wavelength absorption and emission, high fluorescence quantum yields, and strong elect