Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Workers - Hazard via inhalation route

Systemic effects

Long term exposure
Hazard assessment conclusion:
no hazard identified
Acute/short term exposure
Hazard assessment conclusion:
no hazard identified
DNEL related information

Local effects

Long term exposure
Hazard assessment conclusion:
no hazard identified
Acute/short term exposure
Hazard assessment conclusion:
no hazard identified
DNEL related information

Workers - Hazard via dermal route

Systemic effects

Long term exposure
Hazard assessment conclusion:
no hazard identified
Acute/short term exposure
Hazard assessment conclusion:
no hazard identified
DNEL related information

Local effects

Long term exposure
Hazard assessment conclusion:
no hazard identified
Acute/short term exposure
Hazard assessment conclusion:
no hazard identified

Workers - Hazard for the eyes

Local effects

Hazard assessment conclusion:
no hazard identified

Additional information - workers

A DNEL for acute toxicity should be derived if an acute hazard leading to acute toxicity (e.g. C&L) has been identified and there is a potential for high peak exposures. This is not the case with propene.

Systemic effects: None at the highest dose level tested in chronic toxicity study.

Local effects: The weight of evidence indicates that the nasal effects in rodents, which unlike man are obligate nasal breathers, superimposed on a high background of spontaneous nasal pathology and with no obvious dose-response relationships, are likely to be of little relevance in extrapolation of risk to humans and considered an inappropriate finding from which to derive a DNEL. In addition, the concentrations at which these effects were reported in the animal experiments are very high compared to the actual human exposure levels in practice.

Dermal and oral studies with propene are not technically feasible as the substance is a gas at room temperature.

General Population - Hazard via inhalation route

Systemic effects

Long term exposure
Hazard assessment conclusion:
no hazard identified
Acute/short term exposure
Hazard assessment conclusion:
no hazard identified
DNEL related information

Local effects

Long term exposure
Hazard assessment conclusion:
no hazard identified
Acute/short term exposure
Hazard assessment conclusion:
no hazard identified
DNEL related information

General Population - Hazard via dermal route

Systemic effects

Long term exposure
Hazard assessment conclusion:
no hazard identified
Acute/short term exposure
Hazard assessment conclusion:
no hazard identified
DNEL related information

Local effects

Long term exposure
Hazard assessment conclusion:
no hazard identified
Acute/short term exposure
Hazard assessment conclusion:
no hazard identified

General Population - Hazard via oral route

Systemic effects

Long term exposure
Hazard assessment conclusion:
no hazard identified
Acute/short term exposure
Hazard assessment conclusion:
no hazard identified
DNEL related information

General Population - Hazard for the eyes

Local effects

Hazard assessment conclusion:
no hazard identified

Additional information - General Population

A DNEL for acute toxicity should be derived if an acute hazard leading to acute toxicity (e.g. C&L) has been identified and there is a potential for high peak exposures. This is not the case with propene.

Systemic effects: None at the highest dose level tested in chronic toxicity study.

Local effects: The weight of evidence indicates that the nasal effects in rodents, which unlike man are obligate nasal breathers, superimposed on a high background of spontaneous nasal pathology and with no obvious dose-response relationships, are likely to be of little relevance in extrapolation of risk to humans and considered an inappropriate finding from which to derive a DNEL. In addition, the concentrations at which these effects were reported in the animal experiments are very high compared to the actual human exposure levels in practice.

Dermal and oral studies with propene are not technically feasible as the substance is a gas at room temperature.