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Names | |||
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Preferred IUPAC name
3-Methylbenzoic acid | |||
Other names
meta-Toluic acid
m-Methylbenzoic acid meta-Methylbenzoic acid | |||
Identifiers | |||
3D model (
JSmol)
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ChEBI | |||
ChemSpider | |||
ECHA InfoCard | 100.002.476 | ||
EC Number |
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KEGG | |||
PubChem
CID
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UNII | |||
CompTox Dashboard (
EPA)
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Properties | |||
C8H8O2 | |||
Molar mass | 136.15 g/mol | ||
Density | 1.05 g/cm3, solid | ||
Melting point | 111 to 113 °C (232 to 235 °F; 384 to 386 K) | ||
Boiling point | 263 °C (505 °F; 536 K) | ||
Acidity (pKa) | 4.27 (in water) [2] | ||
Hazards | |||
Safety data sheet (SDS) | External MSDS | ||
Related compounds | |||
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
m-Toluic acid, ( IUPAC: 3-methylbenzoic acid), is an aromatic carboxylic acid, with formula (CH3)C6H4(COOH). It is an isomer of p-toluic acid and o-toluic acid.
m-toluic acid is often prepared in the laboratory by refluxing m-xylene with either nitric acid or potassium permanganate, oxidizing one of the methyl groups to COOH.
It serves, among other purposes, as a precursor to DEET (N,N-diethyl-m-toluamide), the well-known insect repellent. [3] [4]
| |||
Names | |||
---|---|---|---|
Preferred IUPAC name
3-Methylbenzoic acid | |||
Other names
meta-Toluic acid
m-Methylbenzoic acid meta-Methylbenzoic acid | |||
Identifiers | |||
3D model (
JSmol)
|
|||
ChEBI | |||
ChemSpider | |||
ECHA InfoCard | 100.002.476 | ||
EC Number |
| ||
KEGG | |||
PubChem
CID
|
|||
UNII | |||
CompTox Dashboard (
EPA)
|
|||
| |||
| |||
Properties | |||
C8H8O2 | |||
Molar mass | 136.15 g/mol | ||
Density | 1.05 g/cm3, solid | ||
Melting point | 111 to 113 °C (232 to 235 °F; 384 to 386 K) | ||
Boiling point | 263 °C (505 °F; 536 K) | ||
Acidity (pKa) | 4.27 (in water) [2] | ||
Hazards | |||
Safety data sheet (SDS) | External MSDS | ||
Related compounds | |||
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
m-Toluic acid, ( IUPAC: 3-methylbenzoic acid), is an aromatic carboxylic acid, with formula (CH3)C6H4(COOH). It is an isomer of p-toluic acid and o-toluic acid.
m-toluic acid is often prepared in the laboratory by refluxing m-xylene with either nitric acid or potassium permanganate, oxidizing one of the methyl groups to COOH.
It serves, among other purposes, as a precursor to DEET (N,N-diethyl-m-toluamide), the well-known insect repellent. [3] [4]