67923-43-7

Basic information

• Product Name: Disperse Yellow 163
• Synonyms: 3,3'-[[4-[(2,6-dichloro-4-nitrophenyl)azo]phenyl]imino]bispropiononitrile;C.I. Disperse Yellow 163 press cake;3,3'-[[4-[(2,6-Dichloro-4-nitrophenyl)azo]phenyl]imino]bispropanenitrile;C.I. 111235;Disperse Yellow 163;Allilon Yellow S-BRL;Disperse Yellow BR;Hisperse Yellow C-BR
• CAS NO: 67923-43-7
• Molecular Formula: C₁₈H₁₄Cl₂N₆O₂
• Molecular Weight: 417.24876
• EINECS: 267-758-4
• Mol File: 67923-43-7.mol

Chemical Properties

• Boiling Point: 685.4 °C at 760 mmHg
• Flash Point: 368.3 °C
• Appearance: /
• Density: 1.37
• PKA: 0.86±0.50(Predicted)
• CAS DataBase Reference: Disperse Yellow 163(CAS DataBase Reference)
• NIST Chemistry Reference: Disperse Yellow 163(67923-43-7)
• EPA Substance Registry System: Disperse Yellow 163(67923-43-7)

Safety Data

• Hazardous Substances Data: 67923-43-7(Hazardous Substances Data)

Usage

Uses

Used in Textile Industry:
Disperse Yellow 163 is used as a dyeing agent for polyester and blended fabrics, providing a red light yellow hue to the material. It is particularly suitable for dyeing polyester super fine fibers, enhancing the aesthetic appeal and colorfastness of the fabric.
The dye also offers excellent fastness properties, such as:
Ironing Fastness: ISO 5
Light Fastness: ISO 5
Perspiration Fastness: ISO 5
Washing Fastness: ISO 5
These properties ensure that the dyed fabric maintains its color and quality even under various conditions, making Disperse Yellow 163 a reliable choice for the textile industry.

Preparation

2,6-Dichioro-4-nitroaniline diazo, and N,N-bis(2-cyanoethyl)benzenamine?coupling

Flammability and Explosibility

Notclassified

Standard

Ironing Fastness

Fading

Stain

ISO

5

Upstream product

• 99-30-9 4-nitro-2,6-dichloroaniline 
• 1555-66-4 N,N-bis(2-cyanoethyl)aniline 

Relevant articles and documents

Stable diazonium salts of weakly basic amines—Convenient reagents for synthesis of disperse azo dyes

A new synthetic strategy for industrially important deep-shade disperse azo dyes was presented in this study. The key procedure is to prepare stable solid diazonium salts of weakly basic amines in the absence of concentrated sulfuric acid. Diazotization by tert-butyl nitrite in ethyl acetate was allowed to proceed in the presence of equivalent 1,5-naphthalenedisulfonic acid as stabilizer of diazonium salts and donor of hydrogen ion for the reaction. The separated solid diazonium salts exhibited good thermal stability. The corresponding disperse azo dyes were subsequently synthesized through the azo-coupling of the prepared solid diazonium salts with a range of aromatic tertiary amines. The azo dyes were produced in short reaction time, excellent yields, mild reaction conditions, simple experimental procedure and low energy consumption.

Disperse dye composition, and preparation method and application thereof

The invention relates to a disperse dye composition, and a preparation method and application thereof. The disperse dye composition comprises a component A formed by one or more of compounds shown in formula (1), a forbidden aromatic amine compound, chlorinated phenol, chlorobenzene, chlorotoluene, any auxiliary materials and other unavoidable impurities. According to the disperse dye composition, not only are various environment-protective indexes conform to the requirements of Oeko-Tex-Standard 100(2016), but also the total content of the forbidden aromatic amine compound in a dye composition chemical product for dyeing is 10ppm or lower, the total content of each chlorinated phenol is 0.5ppm or lower, and the total content of chlorobenzene and chlorotoluene (COCs) is 1ppm or lower. The sewage after the dyeing also can meet the environmental protection requirement; and meanwhile, the use is more convenient and secure. (Shown in description).

Clean preparation method for weakly alkaline arylamine azo disperse dye

The present invention provides a clean preparation method for weakly alkaline arylamine azo disperse dye. The method is characterized in that when a weakly alkaline arylamine diazonium double salt solid is coupled with a coupling component, the coupling component is pretreated to obtain a fine particle dispersion to be coupled with the weakly alkaline arylamine diazonium double salt; and the generated disperse dye is precipitated from the coupling system and is filtered and dried, thereby obtaining the weakly alkaline arylamine azo disperse dye. According to the preparation method provided by the present invention, by using a stable double salt structure of a diazonium salt, during the coupling, the process of adding acid for dissolution can be omitted; the coupling is performed at the normal temperature, and extra cooling is not required; and the method has a broad application prospect.