23894-12-4

Basic information

• Product Name: 6-AMINO-1-NAPHTHOL
• Synonyms: 6-AMINO-1-NAPHTHOL;6-Amino-1-naphtol;6-aminonaphthol;6-AMINO-1-NAPHTHOL 97+%;2-Amino-5-naphthol;6-Aminonaphthalene-1-ol;6-aminonaphthalen-1-ol;6-azanylnaphthalen-1-ol
• CAS NO: 23894-12-4
• Molecular Formula: C₁₀H₉NO
• Molecular Weight: 159.18
• EINECS: 245-933-6
• Mol File: 23894-12-4.mol
• Article Data: 1

Chemical Properties

• Melting Point: 206 °C
• Boiling Point: 385.6°Cat760mmHg
• Flash Point: 187°C
• Appearance: /
• Density: 1.281g/cm³
• Vapor Pressure: 1.69E-06mmHg at 25°C
• Refractive Index: 1.741
• Solubility: soluble in Methanol
• PKA: 9.59±0.40(Predicted)
• CAS DataBase Reference: 6-AMINO-1-NAPHTHOL(CAS DataBase Reference)
• NIST Chemistry Reference: 6-AMINO-1-NAPHTHOL(23894-12-4)
• EPA Substance Registry System: 6-AMINO-1-NAPHTHOL(23894-12-4)

Safety Data

• Statements: 41
• Safety Statements: 26-39
• Hazardous Substances Data: 23894-12-4(Hazardous Substances Data)

Usage

Uses

6-Amino-1-naphthol is used in the preparation of naphthalene base autocatalytic polyphenylene nitrile resin.

InChI:InChI=1/C10H9NO/c11-8-4-5-9-7(6-8)2-1-3-10(9)12/h1-6,12H,11H2

Upstream product

• 87-02-5 7-amino-4-hydroxy-2-naphthalenesulfonic acid 
• 871887-69-3 2-amino-5-hydroxy-naphthalene-1-sulfonic acid 
• 81-05-0 6-aminonaphthalene-1-sulfonic acid 
• 117-62-4 2-amino-1,5-naphthalenedisulfonic acid 
• 81-16-3 2-aminonaphthalenesulfonic acid 
• 623-11-0 1-methyl-4-nitrosobenzene 
• 38397-06-7 6-nitro-1-naphthalenol 

Downstream Products

• 214628-92-9 2-(5-hydroxynaphthalen-2-yl)isoindoline-1,3-dione 
• 503832-26-6 6-amino-1,2,3,4-tetrahydronaphthalen-1-ol 
• 13772-94-6 5-methoxynaphthalen-2-ylamine 
• 1439931-83-5 5-methoxy-2-(dimethylamino)naphthalene 

Relevant articles and documents

Method for preparing adduct of butadiene polymer or copolymer and α, β-ethylenically unsaturated dicarboxylic acid compound

In a method for preparing an adduct of (A) a butadiene lower polymer or butadiene lower copolymer and (B) a α,β-ethylenically unsaturated dicarboxylic acid compound, said method is characterized in that said (A) and (B) are caused to react in the presence of one or more compounds selected from (C) p-phenylenediamine derivatives, catechol derivatives, pyrogallol derivatives, N-nitrosamines, quinoline derivatives and naphthol derivatives, thus serious increase of the viscosity of said adduct in the addition reaction can be prevented.