151237-05-7

Basic information

• Product Name: Benzenamine, 3,4,5-tris(dodecyloxy)-
• CAS NO: 151237-05-7
• Molecular Formula: C42H79NO3
• Molecular Weight: 646.094
• Mol File: 151237-05-7.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: Benzenamine, 3,4,5-tris(dodecyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 3,4,5-tris(dodecyloxy)-(151237-05-7)
• EPA Substance Registry System: Benzenamine, 3,4,5-tris(dodecyloxy)-(151237-05-7)

Safety Data

• Hazardous Substances Data: 151237-05-7(Hazardous Substances Data)

Usage

General Description

Benzenamine, 3,4,5-tris(dodecyloxy)- is an organic compound with the molecular formula C33H57NO. It is an aromatic amine with three dodecyloxy (C12H25O-) groups attached to the benzene ring at positions 3, 4, and 5. This chemical is commonly used as a surfactant or emulsifier in various industrial and consumer products, such as detergents, cleaners, and cosmetics. Its long carbon chain allows it to effectively reduce the surface tension of liquids and improve their ability to mix with other substances. Additionally, its hydrophobic nature makes it useful for creating stable emulsions and suspensions. However, it is important to handle this chemical with caution as it may cause skin and eye irritation, and it should be stored and used in accordance with safety procedures.

Upstream product

• 117241-33-5 3,4,5-tris(dodecanyloxy)benzoyl chloride 
• 123126-44-3 3,4,5-tris(dodecyloxy)benzoyl azide 
• 10157-76-3 dodecyl 4-methylbenzenesulphonate 
• 123126-39-6 methyl [3,4,5-tris(n-dodecan-1-yloxy)]benzoate 
• 99-24-1 methyl galloate 
• 117241-31-3 3,4,5-tridodecyloxy benzoic acid 
• 6307-90-0 3,4,5-trimethoxy-1-nitrobenzene 
• 14416-24-1 3,4,5-trihydroxy-1-nitrobenzene 
• 87-66-1 2-hydroxyresorcinol 
• 151237-08-0 1,2,3-tris(n-dodecan-1-yloxy)benzene 
• 143-15-7 1-dodecylbromide 
• 151237-01-3 3,4,5-tris(n-dodecan-1-yloxy)-1-nitrobenzene 

Downstream Products

• 851608-71-4 3,4,5-tris(n-dodecan-1-yloxy)-1-iodobenzene 
• 1223560-07-3 2,6-bis(trimethylsilyl)-4-(3,4,5-tris(dodecyloxy)phenyl)-4H-diselenopheno[3,2-b:2',3'-d]pyrrole 
• 1223560-05-1 2,6-bis(trimethylsilyl)-4-(3,4,5-tris(dodecyloxy)phenyl)-4H-dithieno[3,2-b:2’,3’-d]pyrrole 
• 1222450-39-6 C₅₀H₇₉I₂NO₃S₂ 
• 1393742-47-6 bis[3,4,5-tris(dodecyloxy)phenyl]amine 

Relevant articles and documents

An electron-deficient tris(triazole)-based discotic liquid crystal that exhibits fast electron transport

In this study, a C3-symmetric star-shaped discotic mesogen has been reported based on an electron-deficient tris(triazole) central rigid core functionalized with three peripheral trialkoxyphenyl units. The mesogen exhibits an enantiotropic columnar hexagonal (Colh) phase that can sustain over a significant temperature range. When used in space-charge limited current (SCLC) devices, it showed ambipolar charge transport behavior with high electron mobility (μe) of 1.61 × 10-2 cm2 V-1 s-1 at ambient temperature. The finding is sufficiently significant to warrant their use in organic electronic devices.

High Hole Mobility and Efficient Ambipolar Charge Transport in Heterocoronene-Based Ordered Columnar Discotics

Heterocoronene, a new redox-active core fragment, is utilized for the synthesis of room-temperature columnar discotic liquid crystals (DLCs). Three wedge-shaped side chains having different lengths of alkyl tails are introduced at the periphery of the het

Generation of liquid crystallinity from a Td-symmetry central unit

A series of new columnar liquid crystals containing an adamantane central unit with its four bridgehead positions partially or fully decorated with different numbers (1-4) of 3,4,5-tris(dodecyloxy)phenyl carbamoyl groups were designed and investigated carefully to explore the structure-property correlations. The molecular structures and mesomorphic properties of the DLCs were characterized by 1H-NMR, 13C-NMR, IR, UV-vis, POM, DSC and XRD. It was found that the mesophase symmetry and thermal stability were extremely dependent on the structures of the adamantane derivatives. No mesophase was observed for the 1-adamantanecarboxylic acid derivative ADLC1, while two different mesophases were observed for ADLC2, a 1,3-disubstituted derivative functionalized with two 3,4,5-tris(dodecyloxy)phenyl carbamoyl groups at two symmetric bridgehead positions. At lower temperature ADLC2 exhibited a rectangular columnar phase, which switched to a square columnar phase possessing a wide temperature range. Similarly, a hexagonal columnar mesophase was observed for the bridgehead trisubstituted adamantane molecule ADLC3. Interestingly, the fully bridgehead-functionalized 1,3,5,7-tetrasubstituted adamantane compound ADLC4 completely lost liquid crystallinity.