m-Cresol is a precursor to numerous compounds. Important applications include: pesticides such as fenitrothion and fenthion; synthetic vitamin E by methylation to give 2,3,6-trimethylphenol [3] antiseptics, such as amylmetacresol; a solvent for polymers.

3-Cresol, meta-Cresol, m-Cresylic acid, 1-Hydroxy-3-methylbenzene, 3-Hydroxytoluene, 3-Methyl phenol. Colorless to yellowish liquid with a sweet, tarry odor. [Note: A solid below 54°F.] Class IIIA Combustible Liquid: Fl.P. at or above 140°F and below 200°F. Strong oxidizers, acids.

M-Cresol | CH3C6H4OH or C7H8O | CID 342 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

In its chemical structure, a molecule of cresol has a methyl group substituted onto the ring of phenol. There are three forms of cresol: ortho-cresol (o-cresol), meta-cresol (m-cresol), and para-cresol (p-cresol). These forms occur separately or as a mixture, which can also be called cresol or more specifically, tricresol.

Three types (or isomers) of cresols exist: ortho-cresol, meta-cresol, and para-cresol; abbreviated as o-cresol, m-cresol, and p-cresol. Pure cresols are solid, while mixtures tend to be liquid. Cresols have a medicinal smell.

There are three forms of cresols that differ slightly in their chemical structure: ortho-cresol (o-cresol), meta-cresol (m-cresol, and para-cresol (p-cresol). These forms occur separately or as a mixture.

M-CRESOL is sensitive to air, light and heat. It is also hygroscopic. This chemical can react vigorously with strong oxidizers and strong bases. It reacts violently with nitric acid, oleum, chlorosulfonic acid, metals and strong acids.