Celliton Fast Pink B Property

Melting point:

207-209 °C

Boiling point:

381.88°C (rough estimate)

Density 

1.2326 (rough estimate)

refractive index 

1.4700 (estimate)

pka

7.38±0.20(Predicted)

form 

Crystalline Powder

color 

Deep purple to dark brown

Water Solubility 

Soluble in water, ethanol, acetone, benzene.

CAS DataBase Reference

116-85-8(CAS DataBase Reference)

NIST Chemistry Reference

1-Hydroxy-4-aminoanthraquinone(116-85-8)

EPA Substance Registry System

9,10-Anthracenedione, 1-amino-4-hydroxy- (116-85-8)

Safety

Hazard Codes 

Xn

Risk Statements 

68-65-40-33

Safety Statements 

36/37-24/25

RTECS 

CB5600000

TSCA 

Yes

HS Code 

29225000

Toxicity

mouse,LD50,intravenous,56mg/kg (56mg/kg),U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#00428,

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Hazard statements

H341Suspected of causing genetic defects

Precautionary statements

P201Obtain special instructions before use.

P202Do not handle until all safety precautions have been read and understood.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P308+P313IF exposed or concerned: Get medical advice/attention.

P405Store locked up.

Celliton Fast Pink B Chemical Properties,Usage,Production

Chemical Properties

deep purple to dark brown crystalline powder

Uses

The use of the inclusion complex of 1-amino-4-hydroxyanthraquinone (AHA) in the internal cavity of β-cyclodextrin confers increased sensitivity, selectivity and detection limit, and allows the determination of 10-70 ng ml-1 beryllium, compared to 60-500 ng ml-1 in the absence of the cyclodextrin.

Safety Profile

Poison by intravenous route. Moderately toxic by intraperitoneal route. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx,.

Synthesis

1-Amino-4-hydroxyanthraquinone is prepared from 1-amino-4-hydroxyanthraquinone- 3-sulfonic acid by splitting off the SO3H group , from 1-benzoylamino-4-chloroanthraquinone by treatment with boric–sulfuric acid, or from 1-nitroanthraquinone by reduction with FeCl2 in sulfuric acid and rearrangement of the hydroxylamine stage , from 1,4-diaminoanthraquinone with MnO2 in sulfuric acid , or from 1-hydroxyanthraquinone by nitration followed by reduction with Na2S

Properties and Applications

blue light pink to red blue light. Soluble in acetone, ethanol, benzene and linseed oil. The strong sulfuric acid to dark yellow, diluted for brown. Used in vinegar fiber, three vinegar, polyamide, polyester fiber, acrylic dyeing, also can be used for sheep and plastic color. Levelness and promote good rate.

Purification Methods

Purify it by TLC on SiO2 gel plates (0.75mm thick) using toluene/acetone (9:1) as eluent. The main band is scraped off and extracted with MeOH. The solvent is evaporated, and the dye is dried in a drying pistol [Land et al. J Chem Soc, Faraday Trans 1 72 2091 1976]. It has also been recrystallised from aqueous EtOH. [Beilstein 14 H 268, 14 I 503, 14 II 168, 14 III 652, 14 IV 891.]