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Disperse Red 167-1 is a synthetic organic chemical that functions as a dye and colorant, specifically classified as a disperse dye due to its insolubility in water. It is renowned for its vibrant red hue and is primarily utilized for coloring synthetic fibers such as polyester and acetate.
Used in Textile Industry:
Disperse Red 167-1 is used as a dye for synthetic fibers in the textile industry, providing a vibrant red color to textiles such as clothing, carpets, and upholstery. Its application enhances the visual appeal and aesthetic value of these products.
Used in Plastics Industry:
In the plastics industry, Disperse Red 167-1 is used as a colorant to impart a red hue to various plastic products. This enhances the appearance and design flexibility of plastic items, catering to diverse consumer preferences.
Used in Printing Industry:
Disperse Red 167-1 is utilized as a colorant in the printing industry, allowing for the creation of red ink and pigments for various printing applications. This contributes to the production of high-quality printed materials with a consistent and striking red color.
It is crucial to handle Disperse Red 167-1 with care, as it can be potentially harmful if it comes into direct contact with skin or is ingested, highlighting the importance of safety measures during its use in various applications.

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  • 79300-13-3 Structure
  • Basic information

    1. Product Name: Disperse Red 167-1
    2. Synonyms: C.I. Disperse Red 354;5'-(Bis(2-hydroxyethyl)amino)-2'-((2-chloro-4-nitrophenyl)azo)acetanilide, diacetate (ester);Acetamide, N-(5-(bis(2-(acetyloxy)ethyl)amino)-2-(2-(2-chloro-4-nitrophenyl)diazenyl)phenyl)-;Ccris 8991;Einecs 216-251-6
    3. CAS NO:79300-13-3
    4. Molecular Formula: C22H24ClN5O7
    5. Molecular Weight: 505.90826
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 79300-13-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Disperse Red 167-1(CAS DataBase Reference)
    10. NIST Chemistry Reference: Disperse Red 167-1(79300-13-3)
    11. EPA Substance Registry System: Disperse Red 167-1(79300-13-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 79300-13-3(Hazardous Substances Data)

79300-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79300-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,0 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79300-13:
(7*7)+(6*9)+(5*3)+(4*0)+(3*0)+(2*1)+(1*3)=123
123 % 10 = 3
So 79300-13-3 is a valid CAS Registry Number.

79300-13-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[3-acetamido-N-(2-acetyloxyethyl)-4-[(2-chloro-4-nitrophenyl)diazenyl]anilino]ethyl acetate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:79300-13-3 SDS

79300-13-3Downstream Products

79300-13-3Relevant articles and documents

Continuous coupling process for ester-based azo disperse dye

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Paragraph 0043-0045, (2018/07/06)

The invention belongs to the technical field of fine chemical preparation, and particularly relates to a continuous coupling process for an ester-based azo disperse dye. The process includes the stepsthat 1, a coupling component compound containing an ester group or a coupling component mixture containing a compound and an aqueous solution A are simultaneously and continuously added into a mixerfor mixing; 2, a diazonium salt solution and an aqueous solution B are simultaneously and continuously added into another mixer for mixing adjustment; 3, the two raw materials obtained above are mixedand subjected to a reaction at equal moles to obtain a coupling reaction product; 4, the coupling reaction product continuously enters another reactor, and continuous material discharging, suction filtration, washing to neutrality and drying are performed to obtain a disperse dye compound. Through continuous improvement of conventional intermittent coupling reaction processes in a step-by-step mode, the coupling temperature of an easily hydrolyzable coupling component compound under acidic conditions is increased, the dependency on a refrigerant is reduced, the coupling reaction time is greatly shortened at the same time, the hydrolysis of coupling components is reduced, the product yield is increased, the production efficiency is improved, and the COD of mother liquor wastewater is reduced.

Method for preparing diazonium salt

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Paragraph 0035; 0038; 0040, (2017/09/01)

The invention discloses a method for preparing diazonium salt. The method for preparing the diazonium salt includes the following step that the diazonium salt shown in the formula 2 is prepared through a diazotization reaction of a compound 4 and nitrosyl sulfuric acid in a sulfuric acid aqueous solution with the mass concentration of 60-80 wt%. The method is mild in reaction condition and environmental friendly. The formula can be seen in the description.

Preparation method of azo compounds

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, (2017/11/18)

The invention discloses a preparation method of azo compounds. The preparation method of the azo compounds comprises the following steps: (1) in a sulfuric acid aqueous solution with the mass concentration being 60 to 80 percent by weight, performing diazo-reaction on a compound 4 and nitrosyl sulfuric acid to prepare a mixture containing diazo salt as shown in a formula 2, and performing coupling reaction on the mixture and a compound 3 to obtain a compound 1. The method is mild in reaction condition and environmentally-friendly. (The formula is as shown in the description).

Disperse dye composition and preparation method and use thereof

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Paragraph 0043; 0044; 0045; 0046; 0051; 0052, (2017/07/19)

A disperse dye composition and a preparation method and use thereof are disclosed, the disperse dye composition comprises a component A, a banned aromatic amine compound, chlorinated phenol, chlorobenzene, chlorotoluene, optional accessories, and other inescapable impurities, the component A comprises one or more compounds of compounds shown as formula (1), the total content of the prohibited aromatic amine compound is 10ppm or below, the total content of various types of the chlorinated phenol is respectively 0.5ppm or below, and the total content of the chlorobenzene and the chlorotoluene is 1ppm or below. All environmentally-friendly indicators of the disperse dye composition meet the requirements of Oeko-Tex Standard 100 (2016). In addition, after a fabric is dyed with the disperse dye composition, and the dyed fabric meets the baby level requirements of the Oeko-Tex Standard 100 (2016).

Preparation method of ester group-containing azo disperse dye

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Paragraph 0038; 0039; 0040; 0041, (2016/10/10)

The invention discloses a preparation method of an ester group-containing azo disperse dye. The method comprises the following steps: carrying out a coupling reaction on a diazo salt and a coupling component, adding an alkali to the above obtained azo compound material system after the coupling reaction is completed in order to adjust the pH value of the system to 5-7, carrying out heating crystal transformation, and post-processing to obtain a dye filter cake. The pH value of the system is adjusted to 5-7 after the coupling reaction and before the crystal transformation, so hydrolysis of ester groups in the dye product is avoided, the yield of the dye product is improved, and the content of organic matters in wastewater is reduced, thereby the wastewater post-treatment difficulty is reduced.

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