16153-75-6

Usage

InChI:InChI=1/C9H14N2/c1-7(2)11-9-5-3-8(10)4-6-9/h3-7,11H,10H2,1-2H3

Upstream product

• 25186-43-0 N-isopropyl-p-nitroaniline 
• 100-01-6 4-nitro-aniline 
• 75-29-6 isopropyl chloride 
• 122-80-5 N-acetyl-p-phenylenediamine 

Downstream Products

• 79094-62-5 N-isopropyl-N'-(1-methyl-4-butylselenobutyl)-p-phenylenediamine 
• 731026-35-0 2,6-di-tert-butyl-4-[(4-isopropylamino-phenylamino)-methyl]-phenol 
• 856010-28-1 2-benzotriazol-2-yl-4-[(4-isopropylamino-phenylamino)-methyl]-phenol 

Relevant academic research and scientific papers

Process for dyeing keratinous fibers with 2,4-diamino-1,3-dimethoxybenzene at an acid ph and compositions employed

Process for dyeing keratinous fibres, especially human keratinous fibres such as the hair, characterised in that a composition containing, in a medium suitable for dyeing, at least 2,4-diamino-1,3-dimethoxybenzene as a coupler; an oxidation dye precursor; and an oxidising agent; is applied to these fibres, the pH of the composition applied to the fibres being less than 7.

Non-staining and slightly-staining antiozonants

There is disclosed compounds having, within their structural formulae, a trivalent moiety: STR1 which exhibit antiozonant activity when added to rubber compositions at antiozonant effective levels and which exhibit synergistic antiozonant activity when used with conventional antiozonants in rubber compositions. There is also disclosed novel compounds which can be used as antiozonants.

Process for making N-mono-substituted p-phenylenediamines

A process for preparing an N-mono-substituted-p-phenylenediamine by reacting the corresponding p-nitroso-N-mono-substituted aniline compound with a primary or secondary alcohol in the presence of a base.

Synthesis of Selenium-containing para-Phenylenediamines: Novel Antidegradants for Natural Rubber

The synthesis of novel N,N'-substituted para-phenylenediamines bearing side-chains containing one or two monoselenide linkages is described.Reductive alkylation of para-phenylenediamines with oxoselenides using sodium cyanoborohydride in methanol gives good to high yields of these compounds.Compounds containing one selenide linkage react with 3 mol equivalents of ozone, and those containing two selenide linkages react with 4 mol equivalents of ozone, compared to only 2 mol equivalents of ozone in the case of N-isopropyl-N'-phenyl-p-phenylenediamine.Synthetic routes to the oxoselenides required as precursors are described.