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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
medium hazard (no threshold derived)

Additional information - workers

The substance is not acutely toxic by either the oral or dermal routes of exposure (LD50 > 2000 mg/kg). A 28 -day repeat dose study by the oral route in rats gave an NOAEL > 1000 mg/kg bw/day. The substance is not a skin irritant or skin sensitiser but read-across to a close analog substance indicates the potential to be a severe eye irritant. The substance shows no potential for mutagenicity in in vitro studies. In the absence of systemic or local effects by the oral or dermal route a DNEL could not be derived.

Workers will wear appropriate protective equipment, goggles, to prevent exposure to the eyes.

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

The substance is not acutely toxic by either the oral or dermal routes of exposure (LD50 > 2000 mg/kg). A 28 -day repeat dose study by the oral route in rats gave an NOAEL > 1000 mg/kg bw/day. The substance is not a skin irritant or skin sensitiser but read-across to a close analog substance indicates the potential to be a severe eye irritant. The substance shows no potential for mutagenicity in in vitro studies. In the absence of systemic or local effects by the oral or dermal route a DNEL could not be derived.

The concentration of the substance in the final end-use product is 0.5% and below the concentration limit for classification of a mixture in respect to eye irritation.