552-46-5

Basic information

• Product Name: 1-Naphthylamine hydrochloride
• Synonyms: 1-Naphthalenamine,hydrochloride;1-naphthalenaminehydrochloride;1-NAPHTHYLAMINE HCL 99%;1-NaphthylamineHCl;1-NAPHTHYLAMMONIUM CHLORIDE 98+%;Naphthalen-1-aMine hydrochloride;1-AMinonaphthalene HCl;1-Naphthaleneamine hydrochloride
• CAS NO: 552-46-5
• Molecular Formula: C₁₀H₁₀N*Cl
• Molecular Weight: 179.65
• EINECS: 209-014-3
• Mol File: 552-46-5.mol

Chemical Properties

• Melting Point: 272-275°C
• Flash Point: 152.1 °C
• Appearance: White to pale red/Crystalline
• Density: 1.137g/cm³
• Vapor Pressure: 0.00108mmHg at 25°C
• Storage Temp.: Store below +30°C.
• Solubility: 37.7g/l
• Water Solubility: Soluble in water, alcohol, ether
• Sensitive: Air Sensitive
• Merck: 14,6398
• CAS DataBase Reference: 1-Naphthylamine hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthylamine hydrochloride(552-46-5)
• EPA Substance Registry System: 1-Naphthylamine hydrochloride(552-46-5)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• RIDADR: 2811
• WGK Germany: WGK 2 water endangering
• RTECS: QM3150000
• TSCA: Yes
• HazardClass: 6.1
• PackingGroup: III
• Hazardous Substances Data: 552-46-5(Hazardous Substances Data)

Usage

Uses

Applied as a synthesis reagent.

Purification Methods

Crystallise the salt from water (charcoal). [Beilstein 12 III 2849, 12 IV 3009.]

InChI:InChI=1/C10H9N.ClH/c11-10-7-3-5-8-4-1-2-6-9(8)10;/h1-7H,11H2;1H

Upstream product

• 67-56-1 methanol 
• 31528-95-7 1-(1-naphthyl)-3-phenyl-2,2-dichloroaziridine 
• 35704-34-8 2,4-dichloro-3-naphthalen-1-yl-1,2,3,4-tetrahydro-naphtho[2,1-e][1,3,2,4]diazadiborinine 
• 134-32-7 1-amino-naphthalene 
• 91-20-3 naphthalene 

Downstream Products

• 116999-94-1 2,3-diphenyl-1H-benzo[g]indole 
• 4669-06-1 N-naphthyl-N-2-naphthylamine 
• 2835-61-2 4-(1-naphthalenylazo)-1-naphthalenamine 
• 86-84-0 1-Naphthyl isocyanate 
• 90-15-3 α-naphthol 
• 7469-77-4 2-methylnaphthalen-1-ol 
• 2216-68-4 N-methylnaphthalen-1-amine 
• 2216-69-5 1-Methoxynaphthalene 
• 4542-57-8 dilauryl ether 
• 3007-31-6 N,N-didodecylamine 
• 56799-95-2 N-(1-naphthyl)-4-chlorobenzenesulfonamide 
• 15309-82-7 N-(naphthalen-1-yl)benzenesulfonamide 

Relevant articles and documents

Removal of methylene blue and rose bengal dyes from aqueous solutions using 1-naphthylammonium tetrachloroferrate (III)

In this work, an ionic liquid (IL), 1-naphthylammonium tetrachloroferrate (III), was synthesized and characterized using different characterization techniques. The IL existed as solid at room temperature and hence it was explored as an adsorbent for the removal of methylene blue (MB) and rose bengal (RB) dyes from aqueous solutions. The adsorption capacity of the adsorbent at equilibrium was found to be 6.443 mg/g for MB and 20.70 mg/g for RB. Furthermore, the adsorption isotherms were fitted into Langmuir isotherm model indicating that the two dyes were homogenously adsorbed on the surface of the material and the adsorption kinetics followed pseudo-second-order kinetic model with R2 value above 0.99. In addition, density functional theory (DFT) calculation confirmed the experimental findings showing energy gap (ΔE) of 3.572 eV and 4.084 eV for MB and RB respectively, and after complexation, a shift of 1.261 eV was observed in MB compared to 0.484 eV in RB in basic medium, indicating higher tendency of MB adsorption. The adsorption energies exhibited a greater affinity for MB with 13.2 kcal/mol, while RB in acidic condition with a value of 20.2 kcal/mol and 2.806 ? binding distances for RB which is lower than the Van der Waals radii, 2.990 ? showing Lewis acid-base interaction.

New method for the direct electrophilic amination of aromatic compounds and its use in the annelation of the pyrimidine ring

A method has been developed for the synthesis of aromatic amines by the amination of the corresponding aromatic compounds using sodium azide in PPA. A method for the synthesis of quinazolines and benzo[h]quinazolines using this reaction and the subsequent reaction of the intermediates with 1,3,5-triazines has been developed.

Synthesis of primary amines by the electrophilic amination of Grignard reagents with 1,3-dioxolan-2-one O-sulfonyloxime

(Chemical equation presented) Primary amines are prepared by the electrophilic amination of Grignard reagents with 4,4,5,5-tetramethyl-1,3- dioxolan-2-one O-phenylsulfonyloxime and the acidic hydrolysis of the resulting imines.