toluene - National Park Service
toluene - National Park Service
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).