3-Nitroaniline
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| Names | |||
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| Preferred IUPAC name 3-Nitroaniline | |||
| Systematic IUPAC name 3-Nitrobenzenamine | |||
| Other names meta-Nitroaniline m-Nitroaniline | |||
| Identifiers | |||
3D model (JSmol) | |||
| ChEMBL | |||
| ChemSpider | |||
| ECHA InfoCard | 100.002.481 | ||
| EC Number |
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PubChem CID | |||
| RTECS number |
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| UNII | |||
| UN number | 1661 | ||
CompTox Dashboard (EPA) | |||
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| Properties | |||
| C6H6N2O2 | |||
| Molar mass | 138.126 g·mol−1 | ||
| Appearance | Yellow solid | ||
| Density | 0.9011 | ||
| Melting point | 114 °C (237 °F; 387 K) | ||
| Boiling point | 306 °C (583 °F; 579 K) | ||
| 0.1 g/100 ml (20 °C) | |||
| Acidity (pKa) | 2.47 | ||
| −70.09·10−6 cm3/mol | |||
| Hazards | |||
| GHS labelling: | |||
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| Danger | |||
| H301, H311, H331, H373, H412 | |||
| P260, P261, P264, P270, P271, P273, P280, P301+P310, P302+P352, P304+P340, P311, P312, P314, P321, P322, P330, P361, P363, P403+P233, P405, P501 | |||
| Related compounds | |||
Related compounds | 2-Nitroaniline, 4-Nitroaniline | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |||
3-Nitroaniline is an organic compound with the formula H2NC6H4NO2. A yellow solid, it is a derivative of aniline, carrying a nitro functional group in position 3. It is an isomer of 2-nitroaniline and 4-nitroaniline. It is used as a precursor to dyes.[1]
Synthesis and applications

3-Nitroaniline is produced on a commercial scale by reduction of 1,3-dinitrobenzene with hydrogen sulfide,[1] or sodium sulfide (a Zinin reaction).
It is used as a chemical intermediate for azo coupling component and the dyes disperse yellow 5 and acid blue 29.
References
- ^ a b Gerald Booth (2007). "Nitro Compounds, Aromatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_411. ISBN 978-3-527-30673-2.



