Chemistry:1-Naphthylamine

1-Naphthylamine

Names
Preferred IUPAC name Naphthalen-1-amine
Other names (Naphthalen-1-yl)amine 1-Naphthylamine α-Naphthylamine 1-Aminonaphthalene
Identifiers
CAS Number	134-32-7 Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:50450 Y
ChEMBL	ChEMBL57394 Y
ChemSpider	8319 Y
KEGG	C14790 Y
PubChem CID	8640
UNII	9753I242R5 Y
InChI InChI=1S/C10H9N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,11H2 Y Key: RUFPHBVGCFYCNW-UHFFFAOYSA-N Y InChI=1/C10H9N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,11H2 Key: RUFPHBVGCFYCNW-UHFFFAOYAD
SMILES Nc1c2ccccc2ccc1
Properties
Chemical formula	C10H9N
Molar mass	143.19 g/mol
Appearance	Colorless crystals (reddish-purple in air)
Odor	ammonia-like
Density	1.114 g/cm3
Melting point	47 to 50 °C (117 to 122 °F; 320 to 323 K)
Boiling point	301 °C (574 °F; 574 K)
Solubility in water	0.002% (20°C)
Vapor pressure	1 mmHg (104°C)
Magnetic susceptibility (χ)	-98.8·10−6 cm3/mol -127.6·10−6 cm3/mol (HCl salt)
Hazards
Safety data sheet	[1] [2]
Flash point	157 °C; 315 °F; 430 K
Related compounds
Related compounds	2-Naphthylamine 1-Naphthol Naphthalene Aniline 1,8-Bis(dimethylamino)naphthalene
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Tracking categories (test):

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1-Naphthylamine is an aromatic amine derived from naphthalene. It can cause bladder cancer (transitional cell carcinoma). It crystallizes in colorless needles which melt at 50 °C. It possesses a disagreeable odor, sublimes readily, and turns brown on exposure to air. It is the precursor to a variety of dyes.

Preparation and reactions

It can be prepared by reducing 1-nitronaphthalene with iron and hydrochloric acid followed by steam distillation.

Oxidizing agents, such as ferric chloride, give a blue precipitate with solutions of its salts. Chromic acid converts it into 1-naphthoquinone. Sodium in boiling amyl alcohol reduces the unsubstituted ring, giving tetrahydro-1-naphthylamine. This tetrahydro compound yields adipic acid when oxidized by potassium permanganate.

At 200 °C in sulfuric acid, it converts to 1-naphthol.

Use in dyes

The sulfonic acid derivatives of 1-naphthylamine are used for the preparation of azo dye. These compounds possess the important property of dyeing unmordanted cotton.

An important derivative is naphthionic acid (1-aminonaphthalene-4-sulfonic acid), which is produced by heating 1-naphthylamine and sulfuric acid to 170–180 °C in the presence of crystallized oxalic acid. It forms small needles, very sparingly soluble in water. Upon treatment with the bis(diazonium) derivative of benzidine, 1-aminonaphthalene-4-sulfonic acid gives Congo red.

Safety

It is listed as one of the 13 carcinogens covered by the OSHA General Industry Standards.

See also

• Used in preparation of aptiganel.