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Acrylamide Quickview (CASRN 79-06-1)

Health assessment information on a chemical substance is included in IRIS only after a comprehensive review of toxicity data by U.S. EPA health scientists from several Program Offices, Regional Offices, and the Office of Research and Development.

Disclaimer: This QuickView represents a snapshot of key information. We suggest that you read the IRIS Summary to put this information into complete context.

For definitions of terms in the IRIS Web site, refer to the IRIS Glossary.

Status of Data for Acrylamide

File First On-Line: 09/26/1988; Last Significant Revision: 01/01/1991

Category (section)
Status
Last Revised
Oral RfD Assessment On-line 03/01/1991
Inhalation RfC Assessment Message 11/01/1990
Carcinogenicity Assessment On-line 07/01/1993
Under Re-Assessment
Synonyms
  • 79-06-1
  • Acrylamide
  • Acrylic amide
  • Akrylamid
  • Amid kyseliny akrylove
  • Ethylenecarboxamide
  • Propenamide
  • 2-Propenamide
  • RCRA Waste Number u007
  • UN 2074
Acrylamide Source Documents
Revision History
Date Section Description
04/01/1997 III., IV., V. Drinking Water Health Advisories, EPA Regulatory Actions, and Supplementary Data were removed from IRIS on or before April 1997. IRIS users were directed to the appropriate EPA Program Offices for this information.
Chronic Health Hazard Assessments for Noncarcinogenic Effects

Reference Dose for Chronic Oral Exposure (RfD)

Critical Effect
Point of Departure*
UF MF RfD
Nerve damage NOEL : 0.2 mg/kg-day 1000 1 2 x10-4 mg/kg-day

* The Point of Departure listed serves as a basis from which the Oral RfD was derived. See Discussion of Conversion Factors and Assumptions for more details.

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Reference Concentration for Chronic Inhalation Exposure (RfC)

Information reviewed but value not estimated. See IRIS Summary.

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Carcinogenicity Assessment for Lifetime Exposure
  • Weight-of-Evidence Characterization
    • B2 (Probable human carcinogen - based on sufficient evidence of carcinogenicity in animals)
  • Weight-of-Evidence Narrative:
    • Based on inadequate human data and sufficient evidence of carcinogenicity in animals; significantly increased incidences of benign and/or malignant tumors at multiple sites in both sexes of rats, and carcinogenic effects in a series of one-year limited bioassays in mice by several routes of exposures. The classification is supported by positive genotoxicity data, adduct formation activity, and structure-activity relationships to vinyl carbamate and acrylonitrile.
    • This may be a synopsis of the full weight-of-evidence narrative. See IRIS Summary.

Quantitative Estimate of Carcinogenic Risk from Oral Exposure

Oral Slope Factor(s)
Extrapolation Method
4.5 per mg/kg-day Linearized multistage procedure, extra risk
Drinking Water Unit Risks
1.3x10-4 per ug/L
Risk Level
Concentration
E-4 (1 in 10,000) 8x10-1 ug/L
E-5 (1 in 100,000) 8x10-2 ug/L
E-6 (1 in 1,000,000) 8x10-3 ug/L

Quantitative Estimate of Carcinogenic Risk from Inhalation Exposure

Inhalation Unit Risk(s)
Extrapolation Method
1.3 x10-3 per ug/m3 Linearized multistage procedure, extra risk

Inhalation Concentrations at Specified Risk Levels

Risk Level
Concentration
E-4 (1 in 10,000) 8x10-2 ug/m3
E-5 (1 in 100,000) 8x10-3 ug/m3
E-6 (1 in 1,000,000) 8x10-4 ug/m3

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