''N'',''N''-Dimethyl-1-naphthylamine
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| Names | |
|---|---|
| Other names
N,N-dimethylnaphthalen-1-amine | |
| Identifiers | |
| 3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.001.530 |
| PubChem CID |
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| Properties[1][2] | |
| C12H13N | |
| Molar mass | 171.24 g·mol−1 |
| Density | 1.042 g/cm3 at 25 °C |
| Boiling point | 139 to 140 °C (282 to 284 °F; 412 to 413 K) at 13 mmHg |
| Related compounds | |
| Related compounds |
1-naphthylamine 1-naphthol naphthalene aniline dimethylaniline Proton Sponge |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
N,N-Dimethyl-1-naphthylamine is an aromatic amine. It is formally derived from 1-naphthylamine by replacing the hydrogen atoms on the amino group with methyl groups. N,N-Dimethyl-1-naphthylamine is used in the nitrate reductase test to form a red precipitate of Prontosil by reacting with a nitrite-sulfanilic acid complex.[3]
References
- ↑ "N,N-dimethylnaphthalen-1-amine". ChemSpider. Retrieved 15 April 2010.
- ↑ "D4011 N,N-Dimethyl-1-naphthylamine, ≥98.0% (GC)". Sigma-Aldrich. Retrieved 15 April 2010.
- ↑ "73426 (Fluka) Nitrate Reduction Test". Sigma-Aldrich. Retrieved 15 April 2010.
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