78151-55-0

Basic information

• Product Name: N-hexylperylene-3,4:9,10-tetracarboxylic acid 3,4-anhydride 9,10-imide
• Synonyms: N-hexylperylene-3,4:9,10-tetracarboxylic acid 3,4-anhydride 9,10-imide
• CAS NO: 78151-55-0
• Molecular Weight: 475.5
• Mol File: 78151-55-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-hexylperylene-3,4:9,10-tetracarboxylic acid 3,4-anhydride 9,10-imide(CAS DataBase Reference)
• NIST Chemistry Reference: N-hexylperylene-3,4:9,10-tetracarboxylic acid 3,4-anhydride 9,10-imide(78151-55-0)
• EPA Substance Registry System: N-hexylperylene-3,4:9,10-tetracarboxylic acid 3,4-anhydride 9,10-imide(78151-55-0)

Safety Data

• Hazardous Substances Data: 78151-55-0(Hazardous Substances Data)

Upstream product

• 111-26-2 hexan-1-amine 
• 128-69-8 perylene-3,4,9,10-tetracarboxylic acid 3,4:9,10-dianhydride 

Relevant articles and documents

Synthesis and Reactions of Perylenecarboxylic Acid Derivatives. VIII. Synthesis of N-Alkyl-3,4:9,10-Perylenetetracarboxylic Monoanhydride Monoimide

The condensations of 3,4:9,10-perylenetetracarboxylic dianhydride with alkylamines (isobutyl-, pentyl-, hexyl-, and octylamines) were spectroscopically determined.Under all of the reaction conditions employed, N-alkyl-3,4:9,10-perylenetetracarboxylic monoanhydride monoimide (2a-d) (alkyl=a; isobutyl, b; pentyl, c; hexyl, d; octyl) were obtained.As the reaction proceeded, the yield of 2a-d increased at an initial stage but decreased gradually after reaching a maximum.This maximum yield of 2a-d was: 2a; 85-88percent, 2b; 85-89percent, 2c; 78-84percent, 2d; 79-85percent.The kinetics of the reaction were also examined.