o-Cresol

In addition to the materials derived from these natural sources, about two thirds of the Western world's supply is produced by methylation of phenol using methanol.

Many other production methods have been examined, including oxidative decarboxylation of salicylic acid, oxygenation of toluene, and hydrolysis of 2-chlorotoluene.

Chlorination and etherification gives members of commercially important herbicides, such as 2-methyl-4-chlorophenoxyacetic acid (MCPA).

When cresols are inhaled, ingested, or applied to the skin at very high levels, they can be harmful.

Breathing high levels of cresols for a short time results in irritation of the nose and throat.

Kekulé, skeletal formula of o-cresol with some implicit hydrogens shown
Kekulé, skeletal formula of o -cresol with some implicit hydrogens shown
Spacefill model of o-cresol
Spacefill model of o -cresol
NFPA 704 four-colored diamond Health 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gas Flammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuel Instability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogen Special hazards (white): no code