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Carlson LM. Provisional Peer-Reviewed Toxicity Values for Perylene (CASRN 198-55-0). Cincinnati (OH): U.S. Environmental Protection Agency; 2023 Feb.

Cover of Provisional Peer-Reviewed Toxicity Values for Perylene (CASRN 198-55-0)

Provisional Peer-Reviewed Toxicity Values for Perylene (CASRN 198-55-0).

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3DERIVATION OF PROVISIONAL VALUES

3.1. DERIVATION OF PROVISIONAL REFERENCE DOSES

No studies were located regarding toxicity of perylene to humans or animals via oral exposure. Due to the lack of oral toxicity data for perylene, subchronic and chronic provisional reference doses (p-RfDs) were not derived directly. Instead, screening subchronic and chronic p-RfDs are derived in Appendix A using an alternative analogue approach. Based on the overall analogue approach presented in Appendix A, BaP was selected as the most appropriate analogue for perylene for deriving screening subchronic and chronic p-RfDs (see Table 5).

Table 5. Summary of Noncancer Reference Values for Perylene (CASRN 198-55-0).

Table 5

Summary of Noncancer Reference Values for Perylene (CASRN 198-55-0).

3.2. DERIVATION OF PROVISIONAL REFERENCE CONCENTRATIONS

No studies were located regarding toxicity of perylene to humans or animals via inhalation exposure. Due to the lack of inhalation toxicity data for perylene, subchronic and chronic provisional reference concentrations (p-RfCs) were not derived directly. Instead, screening subchronic and chronic p-RfCs are derived in Appendix A using an alternative analogue approach. Based on the overall analogue approach presented in Appendix A, BaP was selected as the most appropriate analogue for perylene for deriving screening subchronic and chronic p-RfCs (see Table 5).

3.3. SUMMARY OF NONCANCER SCREENING PROVISIONAL REFERENCE VALUES

The noncancer screening provisional reference values for perylene are summarized in Table 5.

3.4. CANCER WEIGHT-OF-EVIDENCE DESCRIPTOR

Although the scientific literature provides limited information on the mutagenicity and genotoxicity of perylene, no oral or inhalation studies have been conducted to assess its carcinogenicity. Available dermal studies and a single i.p. carcinogenicity study provide limited evidence of carcinogenic potential; the relevance of these findings to oral or inhalation exposure is unclear. Under the U.S. EPA Cancer Guidelines (U.S. EPA, 2005), there is “Inadequate Information to Assess Carcinogenic Potential” of perylene by oral or inhalation exposure (see Table 6).

Table 6. Cancer WOE Descriptor for Perylene (CASRN 198-55-0).

Table 6

Cancer WOE Descriptor for Perylene (CASRN 198-55-0).

3.5. DERIVATION OF PROVISIONAL CANCER RISK ESTIMATES

Due to inadequate information to assess carcinogenic potential, quantitative cancer risk estimates could not be derived for perylene (see Table 7).

Table 7. Summary of Cancer Risk Estimates for Perylene (CASRN 198-55-0).

Table 7

Summary of Cancer Risk Estimates for Perylene (CASRN 198-55-0).

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