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Dichloromethane Quickview (CASRN 75-09-2)

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 Dichloromethane

File First On-Line: 01/31/1987; Last Significant Revision: 01/01/1991

Category (section)
Status
Last Revised
Oral RfD Assessment On-line 03/01/1988
Inhalation RfC Assessment No data 09/01/1991
Carcinogenicity Assessment On-line 02/01/1995
Synonyms
  • 75-09-2
  • Aerothene MM
  • Chlorure de methylene
  • DCM
  • Dichlormethan, uvasol
  • Dichloromethane
  • 1,1-Dichloromethane.
  • Freon 30
  • Methane dichloride
  • Methane, dichloro-
  • Methylene bichloride
  • more...
Dichloromethane Source Documents
Chronic Health Hazard Assessments for Noncarcinogenic Effects

Reference Dose for Chronic Oral Exposure (RfD)

Critical Effect
Point of Departure*
UF MF RfD
Liver toxicity NOAEL : 5.85 mg/kg-day 100 1 6 x10-2 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)

Not Assessed under the IRIS Program.

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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; increased incidence of hepatocellular neoplasms and alveolar/bronchiolar neoplasms in male and female mice, and increased incidence of benign mammary tumors in both sexes of rats, salivary gland sarcomas in male rats and leukemia in female rats. This classification is supported by some positive genotoxicity data, although results in mammalian systems are generally negative.
    • 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
7.5 x10-3 per mg/kg-day Linearized multistage procedure, extra risk
Drinking Water Unit Risks
2.1x10-7 per µg/L
Risk Level
Concentration
E-4 (1 in 10,000) 5x102 µg/L
E-5 (1 in 100,000) 5x101 µg/L
E-6 (1 in 1,000,000) 5 µg/L
  • Dose-Response Data (Carcinogenicity, Oral Exposure)
    • Tumor Type: Hepatocellular adenomas or carcinomas (NTP) and hepatocellular cancer and neoplastic nodules (NCA)
    • Test Species: Mouse/ B6C3F1 (female, NTP; male, NCA)
    • Route: Inhalation, (NTP); oral, drinking water (NCA)
    • Reference: NTP, 1986; National Coffee Association (NCA), 1983

Quantitative Estimate of Carcinogenic Risk from Inhalation Exposure

Inhalation Unit Risk(s)
Extrapolation Method
4.7 x10-7 per µg/m3 Linearized multistage procedure, extra risk

Inhalation Concentrations at Specified Risk Levels

Risk Level
Concentration
E-4 (1 in 10,000) 2x102 µg/m3
E-5 (1 in 100,000) 2x101 µg/m3
E-6 (1 in 1,000,000) 2 µg/m3

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