256660-16-9

Basic information

• Product Name: (2-Ethyl-6-methylphenyl)diphenylamine
• Synonyms: (2-Ethyl-6-methylphenyl)diphenylamine
• CAS NO: 256660-16-9
• Molecular Formula: C₂₁H₂₁N
• Molecular Weight: 287.4
• Mol File: 256660-16-9.mol

Chemical Properties

• Boiling Point: 406 °C at 760 mmHg
• Flash Point: 177.9 °C
• Appearance: /
• Density: 1.065
• PKA: -2.04±0.36(Predicted)
• CAS DataBase Reference: (2-Ethyl-6-methylphenyl)diphenylamine(CAS DataBase Reference)
• NIST Chemistry Reference: (2-Ethyl-6-methylphenyl)diphenylamine(256660-16-9)
• EPA Substance Registry System: (2-Ethyl-6-methylphenyl)diphenylamine(256660-16-9)

Safety Data

• Hazardous Substances Data: 256660-16-9(Hazardous Substances Data)

Usage

Uses

Used in Rubber and Plastics Industry:
(2-Ethyl-6-methylphenyl)diphenylamine is used as a stabilizer for [its antioxidant properties] to prevent and slow down the oxidative degradation of rubbers and plastics, thereby prolonging their service life.
Used in High-Temperature Applications:
(2-Ethyl-6-methylphenyl)diphenylamine is used as a stabilizer for [its low volatility and high thermal stability] in applications that require high-temperature processing.
Safety Considerations:
It is important to handle (2-Ethyl-6-methylphenyl)diphenylamine with care and follow proper safety measures during its use, as it can be harmful or toxic if improperly handled or ingested.

Upstream product

• 591-50-4 iodobenzene 
• 24549-06-2 6-ethyl-o-toluidine 
• 108-86-1 bromobenzene 

Downstream Products

• 256660-20-5 2-ethyl-6-methyl-4'-formyltriphenylamine 

Relevant articles and documents

Novel method for synthesizing triphenylamine compound

The invention discloses a novel method for synthesizing a triphenylamine compound. The novel method comprises the steps of with aniline and bromobenzene with different substituents as raw materials in a high-pressure kettle, adding alkali powder, and heat

STILBENE DERIVATIVE, METHOD FOR PRODUCING THE SAME AND ELECTROPHOTOGRAPHIC PHOTORECEPTOR

PROBLEM TO BE SOLVED: To obtain a stilbene derivative that is hardly crystallized, has excellent compatibility with a binder resin and predetermined sensitivity not only at the early stage but also for many hours by having a triphenylamine structure containing a diphenylethenyl group in the molecule of a stilbene derivative, to provide a method for producing the same and to obtain an electrophotographic photoreceptor containing the stilbene derivative. SOLUTION: The stilbene derivative has a triphenylamine structure containing a diphenylethenyl group. The stilbene derivative is represented by formula (1) (R1, R2, R4-R10 and R12-R16 are each independently a 1-20C substituted or nonsubstituted alkyl group or the like; R3 and R11 are each a 1-20C substituted or nonsubstituted alkyl group or a 14-30C substituted or nonsubstituted diphenylethenyl group or the like; a repeating number A is an integer of 2-6). The electrophotographic photoreceptor comprises the stilbene derivative.

Stilbene derivative and method for producing the same

The present invention provides a novel stilbene derivative represented by the general formula (1): STR1 wherein R1 and R3 represent an alkyl group, an aryl group, an aralkyl group or an alkoxy group which are optionally substituted; and R2 and R4 represent a hydrogen atom, an alkyl group or an alkoxy group which are optionally substituted, provided that when the substitution position of R2 and R4 is the 4-(para) position, R2 and R4 are hydrogen atoms, a method for producing the same and use thereof. The above stilbene derivative (1) is useful as an electric charge transferring material, particularly hole transferring material.