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2-[[4-[[4-[(4-amino-6-chloro-1,3,5-triazin-2-yl)amino]-5-sulpho-1-naphthyl]azo]-2,5-dimethylphenyl]azo]benzene-1,4-disulphonic acid

  • CAS No.: 93892-90-1
  • Purity: 99%
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Manufacturer supply high quality 2-[[4-[[4-[(4-amino-6-chloro-1,3,5-triazin-2-yl)amino]-5-sulpho-1-naphthyl]azo]-2,5-dimethylphenyl]azo]benzene-1,4-disulphonic acid 93892-90-1 with ISO standards

  • Molecular Formula: C27H22ClN9O9S3
  • Molecular Weight: 748.178
  • PSA: 318.37000 
  • Density: 1.78g/cm3 
  • LogP: 8.78610 

2-[[4-[[4-[(4-amino-6-chloro-1,3,5-triazin-2-yl)amino]-5-sulpho-1-naphthyl]azo]-2,5-dimethylphenyl]azo]benzene-1,4-disulphonic acid(Cas 93892-90-1) Usage

Type

Synthetic organic compound
Category of the chemical substance

Usage

Yellow dye in the textile industry
Primary application of the compound

Structure

Complex with multiple azo and sulphonate groups
Composition and arrangement of atoms in the molecule

Binding ability

Can bind to a variety of fabrics and materials
Adhesion properties to different substrates

Water solubility

Water-soluble
Ability to dissolve in water

Stability

Stable under normal conditions
Chemical stability under typical environmental conditions

Environmental and health concerns

Potentially toxic and carcinogenic
Possible negative effects on the environment and human health

Regulation

Use regulated in some jurisdictions
Legal restrictions on the use of the compound in certain areas

General Description

2-[[4-[[4-[(4-amino-6-chloro-1,3,5-triazin-2-yl)amino]-5-sulpho-1-naphthyl]azo]-2,5-dimethylphenyl]azo]benzene-1,4-disulphonic acid, also known as Acid yellow 36, is a synthetic organic compound commonly used as a yellow dye in the textile industry. It has a complex structure with multiple azo and sulphonate groups, giving it the ability to bind to a variety of fabrics and materials. The compound is water-soluble and stable under normal conditions, making it a popular choice for dyeing processes. However, like many azo dyes, Acid yellow 36 has come under scrutiny for its potential environmental and health impacts, as some studies have suggested that it can be toxic and carcinogenic. Therefore, its use is regulated in some jurisdictions.

InChI:InChI=1/C27H22ClN9O9S3/c1-13-11-20(36-37-21-12-15(47(38,39)40)6-9-22(21)48(41,42)43)14(2)10-19(13)35-34-17-7-8-18(30-27-32-25(28)31-26(29)33-27)24-16(17)4-3-5-23(24)49(44,45)46/h3-12H,1-2H3,(H,38,39,40)(H,41,42,43)(H,44,45,46)(H3,29,30,31,32,33)/b35-34+,37-36+

93892-90-1 Relevant articles

Reactive dye

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Page/Page column 7; 8, (2018/04/14)

A reactive dye of the formula (I): where...

93892-90-1 Process route

C<sub>27</sub>H<sub>20</sub>Cl<sub>2</sub>N<sub>8</sub>O<sub>9</sub>S<sub>3</sub>
94021-17-7

C27 H20 Cl2 N8 O9 S3

C<sub>27</sub>H<sub>22</sub>ClN<sub>9</sub>O<sub>9</sub>S<sub>3</sub>
93892-90-1

C27 H22 ClN9 O9 S3

Conditions
Conditions Yield
With ammonium hydroxide; at 45 - 50 ℃; for 2h; pH=10 - 11;
amino-benzene-1,4-disulfonic acid
98-44-2

amino-benzene-1,4-disulfonic acid

C<sub>27</sub>H<sub>22</sub>ClN<sub>9</sub>O<sub>9</sub>S<sub>3</sub>
93892-90-1

C27 H22 ClN9 O9 S3

Conditions
Conditions Yield
Multi-step reaction with 3 steps
1.1: hydrogenchloride; sodium nitrite / water / 1 h / 0 - 5 °C / Cooling with ice
1.2: 4 h / 15 - 20 °C / pH 3
2.1: sodium hydrogencarbonate / 2 h / 5 - 10 °C / pH 6.5 - 7 / Cooling with ice
3.1: ammonium hydroxide / 2 h / 45 - 50 °C / pH 10 - 11
With hydrogenchloride; ammonium hydroxide; sodium hydrogencarbonate; sodium nitrite; In water;

93892-90-1 Upstream products

  • 94021-17-7
    94021-17-7

    C27 H20 Cl2 N8 O9 S3

  • 98-44-2
    98-44-2

    amino-benzene-1,4-disulfonic acid

  • 95-78-3
    95-78-3

    2,5-Dimethylaniline

  • 82-75-7
    82-75-7

    8-anilino-1-naphthalenesulfonate

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