Cresol

In its chemical structure, a molecule of cresol has a methyl group substituted onto the ring of phenol. There are three forms (isomers) 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.^{[citation needed]} About half of the world's supply of cresols are extracted from coal tar. The rest is produced by hydrolysis of chlorotoluenes or the related sulfonates. Another method entails methylation of phenol with methanol over a solid acid catalyst, often comprising magnesium oxide or alumina. Temperatures above 300 °C are typical. Anisole converts to cresols under these conditions.^[5][6]

Another isomer of cresol is called Benzyl alcohol, or alpha-cresol (α-cresol). Benzyl alcohol has a hydroxy group inside a methyl group on the benzene ring.

Cresols are precursors or synthetic intermediates to other compounds and materials, including plastics, pesticides, pharmaceuticals, and dyes.^[6]

For cresol bactericides or disinfectants the mechanism of action is due to the destruction of bacterial cell membranes.^[7][8]

Most recently, cresols have been used to create a breakthrough in manufacturing carbon nanotubes at scale that are separated and not twisted, without additional chemicals that change the surface properties of the nanotubes.^[9][10]

• Creolin, a 19th-century disinfectant.
• Carbolic soap, 19th-century.
• The original Lysol formulation, essentially a water solution of carbolic soap.^[11] "Lysol" has been used as a generic trademark to refer to such a cresol soap solution and remains used as such in some professional settings. The CAS number is 12772-68-8.

Derivatives of p-cresol include:

• Butylated hydroxytoluene, a common antioxidant

Derivatives of o-cresol include:

• Indo-1, a popular calcium indicator
• MCPA, (4-chloro-2-methylphenoxy)acetic acid
• MCPB, 4-(4-chloro-2-methylphenoxy)butanoic acid
• Mecoprop, (RS)-2-(4-chloro-2-methylphenoxy)propanoic acid
• the amine atomoxetine, (3R)-N-methyl-3-(2-methylphenoxy)-3-phenylpropan-1-amine
• the diol mephenesin, 3-(2-methylphenoxy)propane-1,2-diol

Derivatives of m-cresol include:

• Amylmetacresol, an antiseptic
• Bevantolol, (RS)-[2-(3,4-dimethoxyphenyl)ethyl] [2-hydroxy-3-(3-methylphenoxy)propyl]amine
• Bromocresol green
• Bupranolol, a non-selective beta blocker
• Chloro-m-cresol which is used as a household disinfectant
• Tolimidone, 5-(3-methylphenoxy)pyrimidin-2(1H)-one

When cresols are inhaled, ingested, or applied to the skin, they can be very harmful. Effects observed in people include irritation and burning of skin, eyes, mouth, and throat; abdominal pain and vomiting; heart damage; anemia; liver and kidney damage; facial paralysis; coma; and death.

Breathing high levels of cresols for a short time results in irritation of the nose and throat. Aside from these effects, very little is known about the effects of breathing cresols, for example, at lower levels over longer times.

Ingesting high levels results in kidney problems, mouth and throat burns, abdominal pain, vomiting, and effects on the blood and nervous system.

Skin contact with high levels of cresols can burn the skin and damage the kidneys, liver, blood, brain, and lungs.

Short-term and long-term studies with animals have shown similar effects from exposure to cresols. No human or animal studies have shown harmful effects from cresols on reproduction.

It is not known what the effects are from long-term ingestion or skin contact with low levels of cresols.

The Occupational Safety and Health Administration has set a permissible exposure limit at 5 ppm (22 mg/m³) over an eight-hour time-weighted average, while the National Institute for Occupational Safety and Health recommends a limit of 2.3 ppm (10 mg/m³).^[12]

• Dihydroxytoluene
• Trihydroxytoluene