Chemistry:3-Nitrotoluene
From HandWiki
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| Names | |
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| Preferred IUPAC name
1-Methyl-3-nitrobenzene | |
| Other names
m-Nitrotoluene
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| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChemSpider | |
PubChem CID
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| Properties | |
| C7H7NO2 | |
| Molar mass | 137.138 g·mol−1 |
| Appearance | yellow liquid[1] |
| Odor | mild, aromatic[1] |
| Density | 1.1581 g·cm−3 @ 20°C [2] |
| Melting point | 15.5 °C (59.9 °F; 288.6 K)[2] |
| Boiling point | 232 °C (450 °F; 505 K)[2] |
| 0.05% (20°C)[1] | |
| Vapor pressure | 0.1 mmHg (20°C)[1] |
| -72.71·10−6 cm3/mol | |
| Hazards | |
| Flash point | 106 °C; 223 °F; 379 K[1] |
| Explosive limits | 1.6%-?[1] |
| NIOSH (US health exposure limits): | |
PEL (Permissible)
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TWA 5 ppm (30 mg/m3) [skin][1] |
REL (Recommended)
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TWA 2 ppm (11 mg/m3) [skin][1] |
IDLH (Immediate danger)
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200 ppm[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Tracking categories (test):
3-Nitrotoluene or meta-nitrotoluene is an organic compound with the formula CH
3C
6H
4NO
2. It is one of three isomers of nitrotoluene. A yellow liquid, it is used in the manufacture of meta-toluidine, which is an intermediate in the production of various dyes.[3]
Synthesis and reactions
It is made by nitrating toluene. This reaction mainly affords a 2:1 mixture of 2-nitro and 4-nitro isomers, but after removal of the 2-isomer, the 3-nitrotoluene can be purified by distillation. It is a precursor to toluidine, which is used in producing azo dyes.[3]
References
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 NIOSH Pocket Guide to Chemical Hazards. "#0463". National Institute for Occupational Safety and Health (NIOSH). https://www.cdc.gov/niosh/npg/npgd0463.html.
- ↑ 2.0 2.1 2.2 Lide DR, ed (2004). CRC handbook of chemistry and physics: a ready-reference book of chemical and physical data (85 ed.). Boca Ratan Florida: CRC Press. ISBN 0-8493-0485-7. https://archive.org/details/crchandbookofche81lide.
- ↑ 3.0 3.1 Gerald Booth (2007). "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_411.
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