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2,2'-[[3-acetamido-4-[(4-nitrophenyl)azo]phenyl]imino]diethyl diacetate, with the chemical formula C26H27N5O8, is a yellow to red powder that serves as a dye in various industries and is utilized in biochemical and pharmaceutical research. This complex organic compound features two azo groups and two acetate groups, which contribute to its unique structure and reactivity. It is recognized for its capacity to form strong coordination complexes with metal ions and its azo groups enable color changes in response to specific chemical or environmental stimuli. 2,2'-[[3-acetamido-4-[(4-nitrophenyl)azo]phenyl]imino]diethyl diacetate's versatility and reactivity render it an invaluable asset for the development of vibrant colored products and the study of intricate biochemical interactions. However, its use is strictly regulated to mitigate potential environmental and health risks.

1533-74-0

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1533-74-0 Usage

Uses

Used in Dye Industry:
2,2'-[[3-acetamido-4-[(4-nitrophenyl)azo]phenyl]imino]diethyl diacetate is used as a dye for its ability to produce vibrant colors in various applications, such as textiles, plastics, and paints, due to its distinctive structure and reactivity.
Used in Biochemical Research:
In biochemical research, 2,2'-[[3-acetamido-4-[(4-nitrophenyl)azo]phenyl]imino]diethyl diacetate is used as a reagent for studying the interactions of metal ions with organic compounds, given its strong coordination complex-forming ability.
Used in Pharmaceutical Research:
2,2'-[[3-acetamido-4-[(4-nitrophenyl)azo]phenyl]imino]diethyl diacetate is used as a research tool in pharmaceutical research to explore its potential applications in drug development, taking advantage of its unique chemical properties and reactivity.
Used in Environmental and Health Studies:
2,2'-[[3-acetamido-4-[(4-nitrophenyl)azo]phenyl]imino]diethyl diacetate is also used in studies related to environmental and health impacts to understand its potential effects and develop strategies for safe handling and disposal.

Check Digit Verification of cas no

The CAS Registry Mumber 1533-74-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,3 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1533-74:
(6*1)+(5*5)+(4*3)+(3*3)+(2*7)+(1*4)=70
70 % 10 = 0
So 1533-74-0 is a valid CAS Registry Number.

1533-74-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names Disperse Red 74

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:1533-74-0 SDS

1533-74-0Downstream Products

1533-74-0Relevant academic research and scientific papers

Continuous coupling process for ester-based azo disperse dye

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Paragraph 0056-0059, (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.

Disperse dye composition, and preparation method and application thereof

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Paragraph 0107-0110, (2017/08/28)

Disclosed are a disperse dye composition, and a preparation method and application thereof. The disperse dye composition comprises a component A composed of one or more of compounds shown as a formula (1) (please see the specifications for the formula), a component B composed of one or more of compounds shown as a formula (2) (please see the specifications for the formula), forbidden aromatic amine compounds, chlorinated phenols, chlorobenzene and chlorotoluene, optional auxiliaries, and other unavoidable impurities. The total content of the forbidden aromatic amine compounds is 10 ppm or below, the respective content of the various chlorinated phenols is 0.5 ppm or below, and the total content of the chlorobenzene and chlorotoluene is 1 ppm or below. The various environment protection indexes of the disperse dye composition meet the requirements of Oeko-Tex Standard 100(2016). In addition, after fabric is dyed through the disperse dye composition, the dyed fabric meets the baby level requirements of Oeko-Tex Standard 100(2016).

Preparation method of ester group-containing azo disperse dye

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Paragraph 0042; 0043; 0044; 0045, (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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