3-methylbenzoic acid: Difference between revisions

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(Created page with "{{Compound|akam-toluic acid|chemf=C8H8O2 |mm=136.15|density= 1.05|mp=111|bp=263|sol_aq= |stp_p=|stp_q= }} ==Uses== {{Justify}} ===Other=== ==Natural occurrence== ==Hazards== ==Character== ==Production== ===Extraction=== ===Synthesis=== Reflux m-xylene with either nitric acid or potassium permanganate, oxidizing one of the methyl groups to COOH. ==Testing== ==Purification== ==Storage== ==Disposal== ==See Also== ==References== <references/>")
 
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===Extraction===
===Extraction===
===Synthesis===
===Synthesis===
Reflux [[m-xylene]] with either nitric acid or potassium permanganate, oxidizing one of the methyl groups to COOH.
Reflux [[1,3-dimethylbenzene]] with either nitric acid or potassium permanganate, oxidizing one of the methyl groups to COOH.


==Testing==
==Testing==

Revision as of 22:15, 4 December 2024

 
3-methylbenzoic acid
Chemical formula C8H8O2
Molar Mass(g/mol) 136.15 
Density(g/cc) 1.05 
Melting Point(°C) 111 
Boiling Point(°C) 263
NFPA 704
NFPA704.png
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Uses

Justification Questioned

Other

Natural occurrence

Hazards

Character

Production

Extraction

Synthesis

Reflux 1,3-dimethylbenzene with either nitric acid or potassium permanganate, oxidizing one of the methyl groups to COOH.

Testing

Purification

Storage

Disposal

See Also

References