Basic information Safety Supplier Related

ACID ALIZARIN VIOLET N

Basic information Safety Supplier Related

ACID ALIZARIN VIOLET N Basic information

Product Name:
ACID ALIZARIN VIOLET N
Synonyms:
  • ATLANTICHROME VIOLET B
  • Acid Alizarin Violet N, pure
  • Mordant violet 5 (C.I. 15760)
  • Acid Chrome Violet K, Mordant Violet 5
  • Eriochrome Violet Bb
  • Cromal Cviolet B
  • Duroch
  • Cromalviolet B
CAS:
2092-55-9
MF:
C16H11N2NaO5S
MW:
366.32
EINECS:
218-246-4
Product Categories:
  • Azo
Mol File:
2092-55-9.mol
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ACID ALIZARIN VIOLET N Chemical Properties

Melting point:
>300°C
solubility 
Solubility Soluble in water, ethanol
pka
4.35, 7.4, 9.35(at 25℃)
form 
crystals
color 
Reddish-violet
PH Range
Orange-red (6.5) to violet (9.0)
λmax
501nm
Stability:
Stable. Incompatible with strong oxidizing agents.
Major Application
inks, dye lasers, in manufacture of vinyl polymers, textiles determination of iron, calcium, aluminum, tantalum, monitoring hardness in industrial water, measuring chlorine dioxide in drinking water, hypoglycemic agents, nuclear fluorochrome
CAS DataBase Reference
2092-55-9
EPA Substance Registry System
Benzenesulfonic acid, 4-hydroxy-3-[(2-hydroxy-1-naphthalenyl)azo]-, monosodium salt (2092-55-9)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
24/25-37/39-26
RTECS 
DB7012000
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ACID ALIZARIN VIOLET N Usage And Synthesis

Chemical Properties

red powder

Preparation

3-Amino-4-hydroxybenzenesulfonic acid diazotization, and Naphthalen-2-ol coupling.

Properties and Applications

dark red light purple. Soluble in water for magenta, soluble in ethanol for red orange, slightly soluble in acetone. In concentrated sulfuric acid to red light purple, after dilution to orange; In concentrated nitric acid for yellow brown. Dye aqueous solution to join concentrated hydrochloric acid for orange; Join concentrated sodium hydroxide solution for brown light orange.

Standard Ironing Fastness Light Fastness Fulling Persperation Fastness Soaping Water
Alkali Acid
ISO 3-4 6 4 3-4 4-5 5 5
AATCC 4 6 4-5 5 4-5 5

Purification Methods

Convert the acid to the monosodium salt by precipitation with NaOAc/AcOH buffer of pH 4, then purify by precipitation of the free acid from aqueous solution with conc HCl, washing and extracting with EtOH in a Soxhlet extractor. The acid precipitates on evaporating the EtOH and is reconverted to the sodium salt as described for Chlorazole Sky Blue FF. Dry it at 110o. It is hygroscopic. [Coates & Rigg Trans Faraday Soc 57 1088 1961, Beilstein 16 II 127.]

ACID ALIZARIN VIOLET NSupplier

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