CAS 2909-84-4

Benzenamine, 2,4-bis(1,1-dimethylethyl)-

Description:

Benzenamine, 2,4-bis(1,1-dimethylethyl)-, also known as 2,4-di-tert-butylaniline, is an organic compound characterized by its amine functional group attached to a benzene ring, which is further substituted at the 2 and 4 positions by tert-butyl groups. This structure imparts significant steric hindrance, influencing its reactivity and physical properties. The compound is typically a colorless to pale yellow liquid or solid, depending on temperature and purity. It is known for its low solubility in water but good solubility in organic solvents, making it useful in various chemical applications. Benzenamine derivatives are often employed as intermediates in the synthesis of dyes, pharmaceuticals, and agrochemicals. Additionally, the presence of the tert-butyl groups enhances its thermal stability and resistance to oxidation. Safety considerations include handling it with care due to potential irritant properties and the need for appropriate personal protective equipment during use.

Formula: C₁₄H₂₃N

Synonyms:

• 2,4-Di-tert-butyl aniline

2,4-Di-tert-butylaniline

CAS: 2909-84-4

Formula: C₁₄H₂₃N

Purity: 98%

Color and Shape: Liquid

Molecular weight: 205.3391

Ref: IN-DA007LVG

2,4-Di-Tert-Butylaniline

CAS: 2909-84-4

2,4-Di-Tert-Butylaniline

Purity: 98%

Molecular weight: 205.34g/mol

Ref: 54-OR1026485

2,4-di-tert-Butylaniline hydrochloride

CAS: 2909-84-4

The reaction mechanism of 2,4-di-tert-butylaniline hydrochloride is the alkylation of anilines with protonated tert-butyl chloride. This reaction proceeds by a substitution process in which one or more hydrogen atoms are replaced by the substituent. The selectivity of this reaction depends on the parameters and conditions used to carry it out. The reaction can be carried out under autogenous conditions or with the addition of a catalyst such as nickel (Ni), palladium (Pd) or platinum (Pt). The product obtained can be modified by changing the catalyst, solvent, temperature, pressure and other parameters. Reaction kinetics is affected by additives such as water, alcohols and acids that may be added during the reaction process. The size and shape of nanoparticles can also affect kinetic properties.
2,4-di-tert-Butylaniline hydrochloride has been shown to have high activity for organic synthesis in hom

Formula: C₁₄H₂₄ClN

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 241.8 g/mol

Ref: 3D-FD67134

2,4-Di-tert-butylaniline

CAS: 2909-84-4

Purity: 98%

Molecular weight: 205.3450012

Ref: 10-F626420