N,N-Dimethyl-1-naphthylamine
From Self-sufficiency
| N,N-Dimethyl-1-naphthylamine | |
|---|---|
| skeletal formula | |
| Other names N,N-dimethylnaphthalen-1-amine | |
| style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
| CAS number | 86-56-6 
|
| PubChem | 24893807 |
| ChemSpider | 6587 |
| SMILES | Script error: No such module "collapsible list". |
| InChI | Script error: No such module "collapsible list". |
| InChI key | AJUXDFHPVZQOGF-UHFFFAOYAQ |
| style="background: #F8EABA; text-align: center;" colspan="2" | Properties[1][2] | |
| Molecular formula | C12H13N |
| Molar mass | 171.24 g mol−1 |
| Density | 1.042 g/cm³ at 25 °C |
| Melting point |
°C |
| Boiling point |
139-140 °C at 13 mmHg |
| style="background: #F8EABA; text-align: center;" colspan="2" | Related compounds | |
| Related compounds | 1-naphthylamine 1-naphthol naphthalene aniline dimethylaniline Proton Sponge |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 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
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<references />, or <references group="..." />| 30px | This article about an organic compound is a stub. You can help ssf by expanding it. |
- ↑ "N,N-dimethylnaphthalen-1-amine". ChemSpider. Retrieved 15 April 2010.
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
- ↑ "73426 (Fluka) Nitrate Reduction Test". Sigma-Aldrich. Retrieved 15 April 2010.
