m-Toluic acid 98% White crystalline Powder 98% OUCHEM

3-Methylbenzoic acid

Benzoic acid,3-methyl-;m-Toluic acid;3-Methylbenzoic acid;m-Methylbenzoic acid;β-Methylbenzoic acid;m-Toluic acid;NSC 2214

99-04-7

C8H8O2

InChIKey=GPSDUZXPYCFOSQ-UHFFFAOYSA-N

136.15

136.15

970526

202-723-9

1UA7K8EEXT

2214

DTXSID1021617

29163900

Bulk Drug Intermediates

37.3

2.4

Slightly yellow to beige-yellow Crystalline Solid

1.054 g/mL at 25 °C(lit.)

108.7 °C

148-150 °C @ Press: 15-16 Torr

150 °C

1.509

H2O: <0.1 g/100 mL at 19 ºC;soluble in alcohol and ether.

Store below +30°C.

1 mm Hg at 207° F (NTP, 1992)

LD50 orally in Rabbit: 7000 mg/kg

Fine dust dispensed in air in sufficient concentrations, and in the presence of an ignition source is a potential dust explosion hazard. (NTP, 1992). Insoluble in water.

Acids, Carboxylic

M-TOLUIC ACID is a carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in it to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions. This chemical is incompatible with strong oxidizers. (NTP, 1992)