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ACID BLUE 40

Cost-effective and customizable ACID BLUE 40 6424-85-7 for sale

  • Molecular Formula: C22H17N3O6S·Na
  • Molecular Weight: 473.441
  • Appearance/Colour: Brownish blue wder 
  • Melting Point: 129-132°C(lit.) 
  • PSA: 166.87000 
  • LogP: 4.45830 

ACID BLUE 40(Cas 6424-85-7) Usage

Preparation

1-Amino-4-bromo-9,10-dioxo-9,10-dihydroanthracene-2-sulfonic acid and N-(4-aminophenyl)acetamide in copper salt and tied the presence of acid agents condensation, and then into sodium salt.

Properties and Applications

green light blue. Dark blue powder, soluble in water, solubility in water (80 ℃) 100 g/L, water solution is blue. Soluble in acetone and ethanol, slightly soluble in nitrobenzene, insoluble in benzene and dimethyl benzene, encounter the dark brown color of sulfuric acid, a product after diluted red; In the hydrochloric acid and sodium hydroxide solution discoloration. Mainly used for wool, polyamide fiber and silk dyeing and printing, also can be used for leather color. Standard Light Fastness Soaping Persperation Fastness Oxygen bleaching Fastness to seawater Fading Stain Fading Stain Fading Stain ISO 6 2 2 3 1-2 1-2 3 1-2 AATCC 5 1-2 1-2 2 1 1 2-3 2-3

Standard

Light Fastness

Fading

Stain

ISO

6

AATCC

5

InChI:InChI=1/C22H17N3O6S.Na/c1-11(26)24-12-6-8-13(9-7-12)25-16-10-17(32(29,30)31)20(23)19-18(16)21(27)14-4-2-3-5-15(14)22(19)28;/h2-10,25H,23H2,1H3,(H,24,26)(H,29,30,31);/q;+1/p-1

6424-85-7 Relevant articles

High-affinity, non-nucleotide-derived competitive antagonists of platelet P2Y12 receptors

Baqi, Younis,Atzler, Kerstin,K?se, Meryem,Gl?nzel, Markus,Müller, Christa E.

supporting information; experimental part, p. 3784 - 3793 (2010/04/24)

Anthraquinone derivatives related to the...

Combinatorial synthesis of anilinoanthraquinone derivatives and evaluation as non-nucleotide-derived P2Y2 receptor antagonists

Weyler, Stefanie,Baqi, Younis,Hillmann, Petra,Kaulich, Marko,Hunder, Andrea M.,Mueller, Ingrid A.,Mueller, Christa E.

, p. 223 - 227 (2008/09/19)

A library of anilinoanthraquinone deriva...

6424-85-7 Process route

1-amino-4-bromo-9,10-dioxoanthracene-2-sulphonic acid
116-81-4

1-amino-4-bromo-9,10-dioxoanthracene-2-sulphonic acid

N-acetyl-p-phenylenediamine
122-80-5

N-acetyl-p-phenylenediamine

acid blue 40 sodium salt
6424-85-7

acid blue 40 sodium salt

Conditions
Conditions Yield
With copper; at 120 ℃; for 0.0833333h; under 7500.75 Torr; aq. phosphate buffer; Microwave irradiation;
90%
sodium 1-amino-4-bromoanthraquinone-2-sulfonate
6258-06-6

sodium 1-amino-4-bromoanthraquinone-2-sulfonate

N-acetyl-p-phenylenediamine
122-80-5

N-acetyl-p-phenylenediamine

1-amino-4-hydroxy-9,10-dioxo-9,10-dihydroanthracene-2-sulfonic acid
24929-02-0

1-amino-4-hydroxy-9,10-dioxo-9,10-dihydroanthracene-2-sulfonic acid

acid blue 40 sodium salt
6424-85-7

acid blue 40 sodium salt

Conditions
Conditions Yield
With sodium carbonate; copper(II) sulfate; at 90 ℃; for 48h;
90%

6424-85-7 Upstream products

  • 6258-06-6
    6258-06-6

    sodium 1-amino-4-bromoanthraquinone-2-sulfonate

  • 122-80-5
    122-80-5

    N-acetyl-p-phenylenediamine

  • 116-81-4
    116-81-4

    1-amino-4-bromo-9,10-dioxoanthracene-2-sulphonic acid

6424-85-7 Downstream products

  • 753411-75-5
    753411-75-5

    4-[4-(acetamino)phenylamino]-9,10-dioxo-9,10-dihydroanthracene-2-sulfonic acid