Acid Violet 43

Acid Violet 43

Acid Violet 43

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  • Purity: 99
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Keywords

Chrome Violet Anthraquinone CovasolViolet W 5002 Egacid Violet 3B

Quick Details

  • Appearance:
  • Application:The Acid Violet 43, with the CAS register number 4430-18-6, has other names as solway purple; solway purple r; quinizarin blue r; ext.d&cvioletno.2; monosidiumsaltof2-[(9,10-dihydro-4-hydroxy-9,10-dio
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  • Transportation:The Acid Violet 43, with the CAS register number 4430-18-6, has other names as solway purple; solway purple r; quinizarin blue r; ext.d&cvioletno.2; monosidiumsaltof2-[(9,10-dihydro-4-hydroxy-9,10-dio

Superiority:

The Acid Violet 43, with the CAS register number 4430-18-6, has other names as solway purple; solway purple r; quinizarin blue r; ext.d&cvioletno.2; monosidiumsaltof2-[(9,10-dihydro-4-hydroxy-9,10-dioxo-1-anteracenyl)amino]-5-methyl-benzenesulfonicacid; jarocol violet 43; anthraquinone iris r; ci no 60730.

Some physical characteristics of this chemical are as the following: (1)ACD/LogP: 4.93; (2)ACD/LogD (pH 5.5): 1.43; (3)ACD/LogD (pH 7.4): 1.32; (4)ACD/BCF (pH 5.5): 1.03; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 3.61; (7)ACD/KOC (pH 7.4): 2.84; (8)#H bond acceptors: 7; (9)#H bond donors: 3; (10)#Freely Rotating Bonds: 4; (11)Polar Surface Area: 109.36.

This is soluble in ethanol. And it is blue in concentrated sulfuric acid and turns into Olive brown after diluting, with the appearance of purple sediment. This is irritant, so avoid contact with skin and eyes while dealing with it. Its product categories are various, including dyes and pigments; organics; aminoanthraquinones; anthraquinones; hydroxyanthraquinones. And its raw material is 1,4-Dihydroxyanthraquinone.

As to its usage, it is usually used in dyeing of wool and other wool products. Besides, it could also be used in dyeing and printing of silk, nylon, leater and other wool fabric. When comes to its making method, it is below: prepare the material of 1,4-Dihydroxyanthraquinone and Para Toluene, and then restore the 1,4-Dihydroxyanthraquinone to its leuco body; Then condense with Para Toluene and then go through the oxidation. Finally, sulfonate with fuming sulphuric acid and then neutralize, salting out, filtering, drying, and you could get the Acid Violet 43.

In addition, you could refer to the following data information to get the molecular structure:
(1)SMILES:[Na+].[O-]S(=O)(=O)c1cc(ccc1Nc4c3C(=O)c2ccccc2C(=O)c3c(O)cc4)C
(2)InChI:InChI=1/C21H15NO6S.Na/c1-11-6-7-14(17(10-11)29(26,27)28)22-15-8-9-16(23)19-18(15)20(24)12-4-2-3-5-13(12)21(19)25;/h2-10,22-23H,1H3,(H,26,27,28);/q;+1/p-1 
(3)InChIKey:GTKIEPUIFBBXJQ-REWHXWOFAA

 

Details:

The Acid Violet 43, with the CAS register number 4430-18-6, has other names as solway purple; solway purple r; quinizarin blue r; ext.d&cvioletno.2; monosidiumsaltof2-[(9,10-dihydro-4-hydroxy-9,10-dioxo-1-anteracenyl)amino]-5-methyl-benzenesulfonicacid; jarocol violet 43; anthraquinone iris r; ci no 60730.

Some physical characteristics of this chemical are as the following: (1)ACD/LogP: 4.93; (2)ACD/LogD (pH 5.5): 1.43; (3)ACD/LogD (pH 7.4): 1.32; (4)ACD/BCF (pH 5.5): 1.03; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 3.61; (7)ACD/KOC (pH 7.4): 2.84; (8)#H bond acceptors: 7; (9)#H bond donors: 3; (10)#Freely Rotating Bonds: 4; (11)Polar Surface Area: 109.36.

This is soluble in ethanol. And it is blue in concentrated sulfuric acid and turns into Olive brown after diluting, with the appearance of purple sediment. This is irritant, so avoid contact with skin and eyes while dealing with it. Its product categories are various, including dyes and pigments; organics; aminoanthraquinones; anthraquinones; hydroxyanthraquinones. And its raw material is 1,4-Dihydroxyanthraquinone.

As to its usage, it is usually used in dyeing of wool and other wool products. Besides, it could also be used in dyeing and printing of silk, nylon, leater and other wool fabric. When comes to its making method, it is below: prepare the material of 1,4-Dihydroxyanthraquinone and Para Toluene, and then restore the 1,4-Dihydroxyanthraquinone to its leuco body; Then condense with Para Toluene and then go through the oxidation. Finally, sulfonate with fuming sulphuric acid and then neutralize, salting out, filtering, drying, and you could get the Acid Violet 43.

In addition, you could refer to the following data information to get the molecular structure:
(1)SMILES:[Na+].[O-]S(=O)(=O)c1cc(ccc1Nc4c3C(=O)c2ccccc2C(=O)c3c(O)cc4)C
(2)InChI:InChI=1/C21H15NO6S.Na/c1-11-6-7-14(17(10-11)29(26,27)28)22-15-8-9-16(23)19-18(15)20(24)12-4-2-3-5-13(12)21(19)25;/h2-10,22-23H,1H3,(H,26,27,28);/q;+1/p-1 
(3)InChIKey:GTKIEPUIFBBXJQ-REWHXWOFAA

 

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