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ACRYLAMIDE<br />

CAS No: 79-06-1<br />

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

Molecular weight 71.08<br />

Boiling point<br />

125°C at 25 mm Hg<br />

Melting point 84.5<br />

Vapor pressure 0.007 mm Hg at 25°C<br />

Air concentration conversion 1 ppm = 2.91 mg/m 3<br />

II.<br />

HEALTH ASSESSMENT VALUES<br />

Unit Risk Factor: 1.3 E-3 (µg/m 3 ) -1<br />

Slope Factor: 4.5 E+0 (mg/kg-day) -1<br />

[Calculated by US EPA/IRIS (1988, 1993) from female Fischer 344 rat tumor data (central<br />

nervous system, mammary and thyroid glands, uterus, oral cavity) (Johnson et al., 1986) using a<br />

linearized multistage procedure, extra risk; adopted by CDHS/RCHAS (1990).]<br />

III.<br />

CARCINOGENIC EFFECTS<br />

Human Studies<br />

US EPA (1993) reviewed a study of cancer mortality in workers exposed to acrylamide by Collins<br />

(1984). Data from a long duration exposure group (10 individuals) and a short duration/intermittent<br />

exposure group (52 individuals) was analyzed using a standardized proportional mortality ratio (SPMR)<br />

procedure. No excess mortality for all types of cancer combined was noted in either group. Mortality<br />

from lung and central nervous system cancer appeared to be slightly elevated. However, the SPMRs<br />

were not significantly different from expected values, due to small group size. US EPA (1993) also<br />

noted additional study limitations including underrepresentation of the potential at-risk worker<br />

population, incomplete cause of death ascertainment, and incomplete exposure data.<br />

Sobel et al. (1986) studied the mortality experience of 371 workers (365 white males, 6 white females)<br />

employed in acrylamide monomer production and polymerization operations at the Michigan Division of<br />

the Dow Chemical Company from 1955 through 1979. Vital status followup was performed from the<br />

date of the first potential exposure to December 31, 1982. Mortality comparisons were made between<br />

the cohort and United States white male mortality rates; comparisons were made with a subcohort of<br />

workers previously exposed to organic dyes both included and excluded. Slight excesses of mortality<br />

from all cancers (11 observed/7.9 expected), digestive tract cancer (4 observed/1.9 expected) and<br />

respiratory tract cancer (4 observed/2.9 expected) were observed in the total cohort; these excesses<br />

were not observed when the organic dye exposure subcohort was excluded. The authors concluded<br />

that the study did not support a relationship between acrylamide exposure and general or specific<br />

31

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