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1-Amino-2-naphthol hydrochloride

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1-Amino-2-naphthol hydrochloride Basic information

Product Name:
1-Amino-2-naphthol hydrochloride
Synonyms:
  • 1-amino-2-naphthohydrochloride
  • 1-AMINO-2-HYDROXYNAPHTHALENE HYDROCHLORIDE
  • 1-AMINO-2-NAPHTHOL HCL
  • 1-AMINO-2-NAPHTHOL HYDROCHLORIDE
  • 2-HYDROXY-1-NAPHTHYLAMINE HYDROCHLORIDE
  • 2-HYDROXY-1-NAPHTHYLAMMONIUM CHLORIDE
  • TIMTEC-BB SBB000347
  • 1-AMINO-2-NAPHTHOL HYDROCHLORIDE, TECH., 90%
CAS:
1198-27-2
MF:
C10H10ClNO
MW:
195.65
EINECS:
214-830-8
Product Categories:
  • Aromatic Hydrocarbons (substituted) & Derivatives
  • Organic Building Blocks
  • Oxygen Compounds
  • Phenols
Mol File:
1198-27-2.mol
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1-Amino-2-naphthol hydrochloride Chemical Properties

Melting point:
250 °C (dec.)(lit.)
storage temp. 
Hygroscopic, Refrigerator, under inert atmosphere
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
color 
Purple
Water Solubility 
Soluble
Sensitive 
Light Sensitive
BRN 
3699817
InChIKey
DEKREBCFNLUULC-UHFFFAOYSA-N
CAS DataBase Reference
1198-27-2(CAS DataBase Reference)
EPA Substance Registry System
2-Naphthalenol, 1-amino-, hydrochloride (1198-27-2)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
20/21/22-36/37/38-40
Safety Statements 
26-27-36/37/39
WGK Germany 
3
RTECS 
QL3335000
Hazard Note 
Irritant
TSCA 
Yes
HS Code 
29222990

MSDS

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1-Amino-2-naphthol hydrochloride Usage And Synthesis

Chemical Properties

lilac to light grey fluffy powder

Uses

1-Amino-2-naphthol hydrochloride was used in a study on degradation of the azo dye Acid Orange 7 in batch anaerobic unstirred assay.

General Description

1-Amino-2-naphthol undergoes condensation with methylene-substituted azaheterocycles in presence of an oxidizing agent to yield photochromic spirooxazines.

Purification Methods

Crystallise the salt from the minimum volume of hot water containing a few drops of stannous chloride in an equal weight of hydrochloric acid (to reduce atmospheric oxidation). Filter the solution and add half its volume of conc HCl and set aside. The salt crystallises almost quantitatively. Dry it in a vacuum in the dark (m 260o). The salt is more stable than the free base which has m 150o (darkening at 130o) and its O-methyl ether has m 49o and b 159-159o/9mm. [Desai et al. J Chem Soc 324 1938, Beilstein 13 H 666, 13 I 268, 13 II 408, 13 III 1875, 13 IV 2080.]

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