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1,3-PROPANE SULTONE<br />

CAS No: 1120-71-4<br />

I. PHYSICAL AND CHEMICAL PROPERTIES (From HSDB, 1994)<br />

Molecular weight 122.1<br />

Boiling point<br />

180°C at 30 mm Hg<br />

Melting point 31°C<br />

Vapor pressure<br />

not available<br />

Air concentration conversion 1 ppm = 5.01 mg/m 3<br />

II.<br />

HEALTH ASSESSMENT VALUES<br />

Unit Risk Factor: 6.9 E-4 (µg/m 3 ) -1<br />

Slope Factor: 2.4 E+0 (mg/kg-day) -1<br />

[Male rat cerebellar malignant glioma tumor data (Ulland et al., 1971; Weisburger et al.,<br />

1981), contained in Gold et al. database (1984), expedited Proposition 65 methodology<br />

(Cal/EPA, 1992)]<br />

III.<br />

CARCINOGENIC EFFECTS<br />

Human Studies<br />

No studies on the potential carcinogenic effects of 1,3-propane sultone on humans are known to exist.<br />

Animal Studies<br />

Several studies exist on the potential carcinogenic effects of 1,3-propane sultone in animals. These<br />

studies have been reviewed by IARC (1974).<br />

BD rats (12/group, sex unspecified) were given 30 mg/kg body weight 1,3-propane sultone as a 3%<br />

aqueous solution weekly by gavage (Druckrey et al., 1970). Four of 10 survivors developed tumors<br />

between days 248 and 377; tumors noted were 1 glial-mesodermal mixed tumor, 1 advential cell<br />

sarcoma of the brain, 1 nephroblastoma and 1 subcutaneous spindle cell sarcoma.<br />

Local sarcomas resulting in mortality were induced in all of 18 BD rats given weekly subcutaneous<br />

injections of 15 mg/kg 1,3-propane sultone in water (total dose 225 mg/kg) between 208 and 387<br />

days. Additionally, single subcutaneous injections of 30 or 100 mg/kg produced local sarcomas at the<br />

injection site resulting in mortality in 12/18 animals and 18/18 animals, respectively (Druckrey et al.,<br />

1970). In the same study, BD rats were given 1,3-propane sultone as a 1% solution in arachis oil by<br />

subcutaneous injection weekly at doses of 15 or 30 mg/kg. Mortality resulted from local sarcomas<br />

which developed (myosarcomas and fibrosarcomas) at the site of injection (7/12 and 11/11 rats in the<br />

500

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