Difference between revisions of "2-Nitrotoluene"

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| OtherCompounds = 3-nitrotoluene 4-nitrotoluene
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| OtherCompounds = 3-nitrotoluene<br>4-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.
 +
 
===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]]
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[[Category:Organic compounds]]
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[[Category:Nitrates]]
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[[Category:Nitrated organic compounds]]
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[[Category:Energetic materials]]
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[[Category:Carcinogenic]]

Revision as of 20:06, 19 November 2015

2-nitrotoluene
200px
Names
IUPAC name
1-methyl-2-nitro-benzene
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.

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.

Disposal

References

MSDS

Relevant Sciencemadness threads