8-Hydroxy-2-naphthylamine-3,6-disulfonic acid
- Product Name
- 8-Hydroxy-2-naphthylamine-3,6-disulfonic acid
- CAS No.
- 90-40-4
- Chemical Name
- 8-Hydroxy-2-naphthylamine-3,6-disulfonic acid
- Synonyms
- SULFO GAMMA ACID;VNWVMZDJPMCAKD-UHFFFAOYSA-N;2-Amino-8-naphthol-6-disulfonic acid;8-Hydroxy-2-naphthylamine-3,6-disulfonic acid;3-amino-5-hydroxynaphthalene-2,7-disulfonic acid;3-Amino-5-hydroxy-2,7-naphthalenedisulfonic acid;3-amino-5-hydroxynaphthalene-2,7-disulphonic acid;2,7-Naphthalenedisulfonicacid, 3-aMino-5-hydroxy-;3-azanyl-5-hydroxy-naphthalene-2,7-disulfonic acid;(2R)-2-amino-3-[[(2R)-2-amino-2-carboxypropyl]trisulfanyl]-2-methylpropanoic acid
- CBNumber
- CB6875787
- Molecular Formula
- C10H9NO7S2
- Formula Weight
- 319.31
- MOL File
- 90-40-4.mol
8-Hydroxy-2-naphthylamine-3,6-disulfonic acid Property
- Boiling point:
- 603.18℃[at 101 325 Pa]
- Density
- 1.88[at 20℃]
- vapor pressure
- 0Pa at 25℃
- Water Solubility
- 35.36g/L at 25℃
- LogP
- -2.334
- EPA Substance Registry System
- 2,7-Naphthalenedisulfonic acid, 3-amino-5-hydroxy- (90-40-4)
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H319Causes serious eye irritation
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- CHM0388965
- Product name
- 3-AMINO-5-HYDROXYNAPHTHALENE-2,7-DISULFONIC ACID
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $504.88
- Updated
- 2021/12/16
8-Hydroxy-2-naphthylamine-3,6-disulfonic acid Chemical Properties,Usage,Production
Chemical Properties
2-Amino-8-hydroxynaphthalene-3,6-disulfonic acid [90-40-4]. (3-amino-5-hydroxy2,7-disulfonic acid), RR acid, 2 R acid, Columbia acid, C10H9NO7S2, Mr 319.3, and its alkali salts are readily soluble in water. Coupling with diazo compounds takes place under alkaline conditions in the position ortho to the hydroxyl group.
Uses
The RR acid is used as a coupling component in azo dyes, e.g., C.I. Food Black 2 and C.I. Direct Brown 151.
Production Methods
2-Aminonaphthalene-3,6,8-trisulfonic acid liquor is concentrated by evaporation and heated with sodium hydroxide liquor in an autoclave [7]. The temperature is raised to 195℃ over 10 h and held at 195℃ for another 8 – 10 h until completion of the reaction is determined by working up a test sample and obtaining a strength by alkaline coupling equal to the diazotization titer. After dilution, acidification, and stirring while hot until all sulfur dioxide is expelled, the product is filtered off as its monosodium salt at 55℃ and washed with brine. Most of the isomeric 2-amino-3-hydroxynaphthalene-6,8-disulfonic acid impurity is removed in the filtrate. Crude RR acid is obtained in 65 % yield and is suitable for certain outlets. Further purification is necessary for critical derived dyes, and this is achieved by dissolving in dilute alkali, filtering at 80℃, and reprecipitating by addition of sodium chloride and hydrochloric acid. Filtration at 55℃ gives 90 % recovery of product.
Flammability and Explosibility
Not classified