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toluene - National Park Service

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UN1294 (DOT) [607]<br />

CP 25 [609]<br />

Molecular Formula:<br />

C7-H8 [609]<br />

Associated Chemicals or Topics (Includes Transformation Products):<br />

See also individual BTEX entries:<br />

Ethylbenzene<br />

Benzene<br />

Xylenes, Total<br />

BTEX<br />

See also individual combination product entries:<br />

Gasoline, General<br />

Petroleum, General<br />

There are many alkyl benzenes and alkyl <strong>toluene</strong>s (for example<br />

p-isopropyl <strong>toluene</strong>) and often information may be found by<br />

searching for information on the individual compounds (Roy Irwin,<br />

<strong>National</strong> <strong>Park</strong> <strong>Service</strong>, personal communication, 1996).<br />

Industrial grade <strong>toluene</strong> is 98% pure and may contain up to 2%<br />

xylenes and benzene [866].<br />

Other associated chemicals are cymene (p-isopropyl <strong>toluene</strong>)<br />

[366] and xylene (methyl <strong>toluene</strong>).<br />

Some of the metabolites of <strong>toluene</strong> in humans are hippuric<br />

acid, o-cresol, and p-cresol in humans [904].<br />

Metabolism/Metabolites [609]:<br />

Following inhalation, <strong>toluene</strong> is oxidized to benzoic acid and<br />

then conjugated with either glycine to form hippuric acid or<br />

with glucuronic acid to give benzoyl glucuronates. Both<br />

hippuric acid and benzoyl glucuronic acid are excreted in the<br />

urine. [Haddad, L.M. and Winchester, J.F. Clinical Management<br />

of Poisoning and Drug Overdosage. Philadelphia, PA: W.B.<br />

Saunders Co., 1983. 790].<br />

In rats, approx 0.5%-1.1% of the dose is converted to o-cresol<br />

and p-cresol and is excreted as glucuronide and sulfate<br />

conjugates. [Bakke OM, Scheline RR; Tox Appl Pharm 16: 691-<br />

700 (1970) as cited in NRC; Alkyl Benzenes p.221 (1981)].<br />

In printers exposed to air containing <strong>toluene</strong> (avg concn 23<br />

ppm), urinary excretion of o-cresol, which is not a normal<br />

constituent of urine, was observed. Apparently, <strong>toluene</strong> was<br />

oxidized at aromatic nucleus forming cresols, besides hippuric<br />

acid. [Angerer J; Int Arch Occup Environ Health 43 (1): 63<br />

(1979).

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