67676-48-6

Basic information

• Product Name: 1,3-Benzenediamine, N,N,N',N'-tetrabutyl-
• CAS NO: 67676-48-6
• Molecular Formula: C22H40N2
• Molecular Weight: 332.573
• Mol File: 67676-48-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1,3-Benzenediamine, N,N,N',N'-tetrabutyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Benzenediamine, N,N,N',N'-tetrabutyl-(67676-48-6)
• EPA Substance Registry System: 1,3-Benzenediamine, N,N,N',N'-tetrabutyl-(67676-48-6)

Safety Data

• Hazardous Substances Data: 67676-48-6(Hazardous Substances Data)

Usage

General Description

1,3-Benzenediamine, N,N,N',N'-tetrabutyl- is a chemical compound with the molecular formula C18H36N2. It is commonly used as an antioxidant and an intermediate in the synthesis of dyes and pigments. 1,3-Benzenediamine, N,N,N',N'-tetrabutyl- is a derivative of 1,3-benzenediamine, and its four butyl groups make it highly lipophilic, meaning it has a strong affinity for fats and oils. This property makes it useful in products such as lubricants and plastics. However, it is also important to handle this chemical with care, as it can be toxic if ingested or inhaled and may cause skin and eye irritation upon contact.

Upstream product

• 109-65-9 1-bromo-butane 
• 108-45-2 m-phenylenediamine 
• 123-72-8 butyraldehyde 

Downstream Products

• 89331-94-2 2'-anilino-3'-methyl-6'-(dibutylamino)spiro[isobenzofuran-1(3H),9'-(9H)xanthen]-3-one 

Relevant articles and documents

Synthesis, characterization and comparative studies of nonlinear optical chromophores with rod-like, Y-shaped and X-shaped configurations

A series of highly polarizable nonlinear optical (NLO) chromophores ZJ1-4 with three different configurations, including rod-like, Y-shaped and X-shaped configurations, have been synthesized with facile routes and systematically studied. The resulted chro

Avenues into the Synthesis of Illusive Poly(m-phenylene-alt-squaraine)s: Polycondensation of m-Phenylenediamines with Squaric Acid Intercepted by Intermediate Semisquaraines of Exceptionally Low Reactivity

The synthesis and properties of a novel class of ortho-dialkylamino-substituted semisquaraines are described. The exceptionally low reactivity of the investigated compounds is caused by an intramolecular hydrogen bond as evidenced by experimental and computational studies. Although this constitutes the reason for our failed attempts to prepare poly(m-phenylene-alt-squaraine)s, the discovered influence of hydrogen bonding on the photophysical properties of these semisquaraines provides a promising new motif for sensor design.

Heteroarylphthalides

3-Aryl-3-indolylphthalides, 3-aryl-3-pyrrolylphthalides and 3-aryl-3-carbazolylphthalides prepared by interaction of the appropriate 2-(heteroaryl)carbonylbenzoic acid and the appropriate phenylamine, and 3,3-bis(indolyl)-phthalides prepared by the interaction of the appropriate 2-(indolyl)carbonylbenzoic acid and the appropriate indole are useful as color formers in pressure-sensitive carbonless duplicating systems, thermal marking systems and hectographic copying systems.