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| Names | |||
|---|---|---|---|
| Preferred IUPAC name
1-Methyl-2-nitrobenzene | |||
| Other names
o-Nitrotoluene, o-Methylnitrobenzene, 2-Methylnitrobenzene, ortho-Nitrotoluene
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| Identifiers | |||
3D model (JSmol)
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| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
| ECHA InfoCard | 100.001.685 | ||
| EC Number |
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| KEGG | |||
PubChem CID
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| RTECS number |
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| UNII | |||
| UN number | 1664 | ||
CompTox Dashboard (EPA)
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| Properties | |||
| C7H7NO2 | |||
| Molar mass | 137.138 g·mol−1 | ||
| Appearance | yellow liquid[1] | ||
| Odor | weak, aromatic[1] | ||
| Density | 1.1611 g·cm−3 @ 19°C [2] | ||
| Melting point | −10.4 °C (13.3 °F; 262.8 K)[2] | ||
| Boiling point | 222 °C (432 °F; 495 K)[2] | ||
| 0.07% (20°C)[1] | |||
| Vapor pressure | 0.1 mmHg (20°C)[1] | ||
| -72.28·10−6 cm3/mol | |||
| Hazards | |||
| GHS labelling: | |||
  
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| Danger | |||
| H302, H340, H350, H361, H411 | |||
| P201, P202, P264, P270, P273, P281, P301+P312, P308+P313, P330, P391, P405, P501 | |||
| NFPA 704 (fire diamond) | |||
| Flash point | 106 °C; 223 °F; 379 K[1] | ||
| Explosive limits | 2.2%-?[1] | ||
| Lethal dose or concentration (LD, LC): | |||
LD50 (median dose)
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891 mg/kg (oral, rat) 970 mg/kg (oral, mouse) 1750 mg/kg (oral, rabbit)[3] | ||
| 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)
|
200 ppm[1] | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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2-Nitrotoluene or ortho-nitrotoluene is an organic compound with the formula CH3C6H4NO2. It is pale yellow liquid that crystallizes in two forms, called α (−9.27 °C) and β (−3.17 °C). It is mainly a precursor to o-toluidine, which is an intermediate in the production of various dyes.[4]
YouTube Encyclopedic
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Nitration of Toluene, Chlorobenzene, and Benzoic Acid Reaction Mechanism
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NitroBenzene to Aniline - Nitro to Amine Reduction Mechanism - Proposed Mechanism
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Benzene to Toluene - CH3Cl + AlCl3 - Friedel Crafts Alkylation Mechanism
Transcription
Synthesis and reactions
It is made by nitrating toluene at above -10 °C. This reaction affords a 2:1 mixture of 2-nitro and 4-nitro isomers.[4]
Chlorination of 2-nitrotoluene gives two isomers of the chloronitrotoluenes. Similarly nitration gives two isomers of dinitrotoluene.
2-Nitrotoluene is mainly consumed in the production of o-toluidine, a precursor to dyes.[4]
References
- ^ a b c d e f g h i NIOSH Pocket Guide to Chemical Hazards. "#0462". National Institute for Occupational Safety and Health (NIOSH).
- ^ a b c 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.
- ^ "Nitrotoluene (o-, m-, p-isomers)". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
- ^ a b c Gerald Booth (2007). "Nitro Compounds, Aromatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_411. ISBN 978-3527306732.
External links
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This page was last edited on 9 January 2024, at 02:58