Difference between revisions of "2-Nitrotoluene"
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==Projects== | ==Projects== | ||
*Make indigo | *Make indigo | ||
+ | *Make di- and trinitrotoluene | ||
==Handling== | ==Handling== | ||
===Safety=== | ===Safety=== | ||
2-nitrotoluene is quite toxic and a suspected carcinogen. It must be handled with care, and should be used only in a fume hood. Care should be taken to avoid inhaling its vapors. | 2-nitrotoluene is quite toxic and a suspected carcinogen. It must be handled with care, and should be used only in a fume hood. Care should be taken to avoid inhaling its vapors. | ||
+ | |||
===Storage=== | ===Storage=== | ||
A glass bottle with a tight fitting, chemical resistant cap is sufficient for containing 2-nitrotoluene. | A glass bottle with a tight fitting, chemical resistant cap is sufficient for containing 2-nitrotoluene. | ||
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===Disposal=== | ===Disposal=== | ||
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<references/> | <references/> | ||
===Relevant Sciencemadness threads=== | ===Relevant Sciencemadness threads=== | ||
− | [https://www.sciencemadness.org/whisper/viewthread.php?tid=29111 Preparation of Mononitrotoluenes (o-, p-)] | + | *[https://www.sciencemadness.org/whisper/viewthread.php?tid=29111 Preparation of Mononitrotoluenes (o-, p-)] |
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+ | [[Category:Chemical compounds]] | ||
+ | [[Category:Organic compounds]] | ||
+ | [[Category:Nitrates]] | ||
+ | [[Category:Nitrated organic compounds]] | ||
+ | [[Category:Energetic materials]] | ||
+ | [[Category:Carcinogenic]] |
Revision as of 20:06, 19 November 2015
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200px | |
Names | |
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IUPAC name
1-methyl-2-nitro-benzene
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Systematic IUPAC name
1-methyl-2-nitro-benzene | |
Properties | |
C6H4CH3NO2 | |
Molar mass | 137.14 |
Melting point | −10.4 °C (13.3 °F; 262.8 K) |
Boiling point | 222 °C (432 °F; 495 K) |
Related compounds | |
Related compounds
|
3-nitrotoluene 4-nitrotoluene |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
2-nitrotoluene, also known as o-nitrotoluene, is an isomer of mononitrotoluene. It is a yellow, oily liquid that is slightly more dense than water.
Contents
Properties
Chemical
Through many different methods, 2-nitrotoluene is oxidized to 2-nitrobenzaldehyde which is a direct precursor to indigo dye.
The nitro group on 2-nitrotoluene may be reduced to yield 2-methylaniline.
Physical
2-nitrotoluene is a yellow, oily liquid. It has a strong, aromatic odor resembling almonds.
Availability
Nitrotoluenes are not available in any consumer products due to being toxic and possibly carcinogenic.
Preparation
A mixture of mononitrotoluene isomers can be prepared from the nitration of toluene between -10º and 30º C. Lower temperatures result in little or no reaction, while higher temperatures will result in double nitration forming dinitrotoluenes.
Relevant thread: Preparation of Mononitrotoluenes (o-, p-)
Projects
- Make indigo
- Make di- and trinitrotoluene
Handling
Safety
2-nitrotoluene is quite toxic and a suspected carcinogen. It must be handled with care, and should be used only in a fume hood. Care should be taken to avoid inhaling its vapors.
Storage
A glass bottle with a tight fitting, chemical resistant cap is sufficient for containing 2-nitrotoluene.