90133-93-0

Basic information

• Product Name: N,N-BIS(N-BUTYL)-4-IODOANILINE
• Synonyms: N,N-BIS(N-BUTYL)-4-IODOANILINE;N,N-DIBUTYL-4-IODOANILINE;N,N-DIBUTYL-4-IODOBENZENEAMINE;N,N-dibutyl-4-iodobenzenamine
• CAS NO: 90133-93-0
• Molecular Formula: C₁₄H₂₂IN
• Molecular Weight: 331.24
• Mol File: 90133-93-0.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N,N-BIS(N-BUTYL)-4-IODOANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-BIS(N-BUTYL)-4-IODOANILINE(90133-93-0)
• EPA Substance Registry System: N,N-BIS(N-BUTYL)-4-IODOANILINE(90133-93-0)

Safety Data

• Hazardous Substances Data: 90133-93-0(Hazardous Substances Data)

Upstream product

• 109-65-9 1-bromo-butane 
• 540-37-4 p-aminoiodobenzene 
• 53358-54-6 1-bromo-4-(N,N-dibutyl)aniline 
• 613-29-6 N-Dibutylaniline 
• 542-69-8 1-iodo-butane 

Downstream Products

• 834856-07-4 2,5-bis[(4'-N,N-dibutylaminophenyl)ethynyl]-1,4-bis[(triisopropylsilyl)ethynyl]benzene 
• 667865-56-7 1,2-bis[(4'-N,N-dibutylaminophenyl)ethynyl]-4,5-bis[(triisopropylsilyl)ethynyl]benzene 
• 834856-05-2 2,4-bis[(4'-N,N-dibutylaminophenyl)ethynyl]-1,5-bis[(triisopropylsilyl)ethynyl]benzene 
• 667865-53-4 N,N-dibutyl-4-[(trimethylsilyl)ethynyl]aniline 
• 435268-50-1 4-{{4-{[4-(dibutylamino)phenyl]ethynyl}-2,5-bis(octyloxy)phenyl}ethynyl}-2,5-bis(octyloxy)benzaldehyde 
• 435268-51-2 4-{{4-{{4-{[4-(dibutylamino)phenyl]ethynyl}-2,5-bis(octyloxy)phenyl}ethynyl}-2,5-bis(octyloxy)phenyl}ethynyl}-2,5-bis(ocyloxy)benzaldehyde 
• 1044502-87-5 C₂₃H₂₉N 
• 1261246-72-3 (4-methoxyphenyl)(4-N,N-dibutylaminophenyl)diethylsilane 
• 1325219-57-5 bis(4-((4-(dibutylamino)phenyl)ethynyl)phenyl)methanone 
• 1325219-58-6 2,7-bis((4-(dibutylamino)phenyl)ethynyl)-9H-fluoren-9-one 
• 1325219-59-7 3,6-bis((4-(dibutylamino)phenyl)ethynyl)-9H-fluoren-9-one 
• 1325219-60-0 2,6-bis((4-(dibutylamino)phenyl)ethynyl)anthracene-9,10-dione 
• 1185275-28-8 4-(4-(N,N-dibutylamino)phenyl)-2-methylbut-3-yn-2-ol 
• 1236567-85-3 N,N-dibutyl-4-(5-(pyridin-4-yl)thiophene-2-yl)benzenamine 

Relevant articles and documents

New Aggregation-Induced Emitters: Tetraphenyldistyrylbenzenes

The synthesis of five novel distyrylbenzene (DSB) derivatives, featuring a central tetraphenylbenzene core, is reported. The targets show aggregation-induced emission (AIE), which, however, is substituent-dependent. For the pure hydrocarbon and derivative

In vitro imaging of β-cells using fluorescent cubic bicontinuous liquid crystalline nanoparticles

To evaluate the potential of monoolein-based cubic bicontinuous liquid crystalline nanoparticles (cubosomes) as diagnostic tools in diabetes and pancreatic β-cell transplantation, fluorescent cubosomes were formulated, entrapping within the lipid bilayer a newly synthesized, potent, hydrophobic dye. Cryo-TEM, SAXS, and DLS were performed to assess the morphological and structural aspects of this formulation. Rat pancreatic β-cells (INS-1E) readily took up the cubosome nanoparticles, as revealed by in vitro internalization tests, and flow-cytometric analyses confirmed the persistence of the fluorescence for up to 24 hours. The cytotoxicity of cubosomes at various concentrations, evaluated with a real-time analysis of proliferation, revealed that the proliferation curves relative to the less concentrated formulation (5 μM in terms of monoolein content) were comparable to the untreated cultures. INS-1E cell cycle and apoptosis supported such results. In conclusion, this formulation, with dye content in the nanomolar range, seems to be useful for β-cell imaging.

Nonlinear optical and energy-level modulation of organic alkynes by click chemistry

A series of novel donor–acceptor chromophores have been successfully synthesized in excellent yield by metal-free [2+2] click chemistry, which was effective in the energy-level modulation of organic the π-conjugation aniline derivatives. Meanwhile, struct