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Vinyl chloride (CASRN 75-01-4)

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Toxicological Review (PDF) Available

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 Full 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 Vinyl chloride


File First On-Line: 08/07/2000
Last Significant Revision: 08/07/2000
 
 Category Status Last Revised
Oral RfD Assessment On-line 08/07/2000
Inhalation RfC Assessment On-line 08/07/2000
Carcinogenicity Assessment On-line 08/07/2000


Chronic Health Hazard Assessments for Noncarcinogenic Effects

Reference Dose for Chronic Oral Exposure (RfD)


Critical Effect Experimental Dose
Liver cell polymorphism NOAEL (HED): 0.09 mg/kg-day 30
1
3 x10-3 mg/kg-day
 

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

Principal Study

Rat chronic feeding study, Til et al., 1983, 1991

Confidence in the Oral RfD

Study -- High
Database -- Medium/High
RfD -- Medium

Reference Concentration for Chronic Inhalation Exposure (RfC)


Critical Effect Experimental Dose
Liver cell polymorphism NOAEL (HEC): 2.5 mg/m3 30
1
1x10-1 mg/m3
 

The Experimental Dose listed serves as a basis from which the Inhalation RfC was derived. See Discussion of Conversion Factors and Assumptions for more details.

Principal Study

Rat chronic feeding study, Til et al., 1983, 1991

Confidence in the Inhalation RfC

Study -- High
Database -- Medium/High
RfC -- Medium


Carcinogenicity Assessment for Lifetime Exposure

Weight of Evidence Characterization


Weight of Evidence (1986 US EPA Guidelines):
A (Human carcinogen)

Weight of Evidence Narrative:
Under the Proposed Guidelines for Carcinogen Risk Assessment (U.S. EPA, 1996), it is concluded that VC is a known human carcinogen by the inhalation route of exposure, based on human epidemiological data, and by analogy the oral route because of positive animal bioassay data as well as pharmacokinetic data allowing dose extrapolation across routes. VC is also considered highly likely to be carcinogenic by the dermal route because it is well absorbed and acts systemically.

This may be a synopsis of the full weight-of-evidence narrative. See Full IRIS Summary.


Quantitative Estimate of Carcinogenic Risk from Oral Exposure


Oral Slope Factor(s) Extrapolation Method
7.2x10-1 per mg/kg-day 1
(Continuous lifetime exposure during adulthood)
LMS method
 
1.5 per mg/kg-day 1
(Continuous lifetime exposure from birth)
LED 10/ linear method
 

1 This represents the lowest/highest of multiple discrete slope factors for this substance. See Full IRIS Summary.

Drinking Water Unit Risk(s)
2.1x10-2 per mg/L 1
(Continuous lifetime exposure during adulthood)
4.2x10-2 per mg/L 1
(Continuous lifetime exposure from birth)
1 This represents the lowest/highest of drinking water unit risks for this substance. See Full IRIS Summary.

Drinking Water Concentrations at Specified Risk Levels
Risk Level Concentration
E-4 (1 in 10,000) 2.4x10-3 mg/L(Continuous lifetime exposure from birth)
E-5 (1 in 100,000) 2.4x10-4 mg/L(Continuous lifetime exposure from birth)
E-6 (1 in 1,000,000) 2.4x10-5 mg/L(Continuous lifetime exposure from birth)
 
E-4 (1 in 10,000) 4.8x10-3 mg/L(Continuous lifetime exposure during adulthood)
E-5 (1 in 100,000) 4.8x10-4 mg/L(Continuous lifetime exposure during adulthood)
E-6 (1 in 1,000,000) 4.8x10-5 mg/L(Continuous lifetime exposure during adulthood)

Dose-Response Data (Carcinogenicity, Oral Exposure)
Tumor Type: Total of liver angiosarcoma, hepatocellular carcinoma, and neoplastic nodules
Test Species: Female Wistar rats
Route: Oral, Diet
Reference: Feron et al., 1981


Quantitative Estimate of Carcinogenic Risk from Inhalation Exposure


Air Unit Risk(s) Extrapolation Method
4.4x10-3 per mg/m3
(Continuous lifetime exposure during adulthood)
LMS method
4.4x10-3 per mg/m3
(Continuous lifetime exposure during adulthood)
LED 10/ linear method
8.8x10-3 per mg/m3
(Continuous lifetime exposure from birth)
LMS method
8.8x10-3 per mg/m3
(Continuous lifetime exposure from birth)
LED 10/ linear method

Air Concentrations at Specified Risk Levels
Risk Level Concentration
E-4 (1 in 10,000) 2.3x10-2 mg/m3(Continuous lifetime exposure during adulthood)
E-5 (1 in 100,000) 2.3x10-3 mg/m3(Continuous lifetime exposure during adulthood)
E-6 (1 in 1,000,000) 2.3x10-4 mg/m3(Continuous lifetime exposure during adulthood)

2 This represents the lowest/highest of multiple discrete slope factors for this substance. See
Full IRIS Summary.

Dose-Response Data (Carcinogenicity, Inhalation Exposure)
Tumor Type: Liver angiosarcomas, angiomas, hepatomas, and neoplastic nodules
Test Species: Female Sprague-Dawley rats
Route: Inhalation
Reference: Maltoni et al. (1981, 1984)


Revision History


Review Full IRIS Summary for complete Revision History.


Synonyms


VCM
Chloroethene
VC
Chloroethylene
Vinyl chloride
Vinyl chloride monomer
75-01-4

 

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Last Updated on Wednesday, November 3, 2004