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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

The test item is not hazardous for human health with respect to skin irritation, eye irritation, acute toxicity (lethality or specific target organ toxicity following a single exposure), sensitisation, specific target organ toxicity following repeated exposures, reproductive toxicity, developmental toxicity, carcinogenicity and genetic toxicity.

The critical health effects are aspiration hazard (potential lung damage following accidental swallowing) and potential skin dryness or cracking following repeated dermal exposures. It is not possible to determine quantitative dose descriptors for these effects.

In the absence of adverse effects in acute and long-term systemic and reproductive studies it is not possible to determine DNEL values for systemic effects and risk characterisation is not necessary.

Qualitative risk characterisation is required based on the aspiration hazard and potential skin dryness and cracking.

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 hazardous for human health with respect to skin irritation, eye irritation, acute toxicity (lethality or specific target organ toxicity following a single exposure), sensitisation, specific target organ toxicity following repeated exposures, reproductive toxicity, developmental toxicity, carcinogenicity and genetic toxicity.

The critical health effects are aspiration hazard (potential lung damage following accidental swallowing) and potential skin dryness or cracking following repeated dermal exposures. It is not possible to determine quantitative dose descriptors for these effects.

In the absence of adverse effects in acute and long-term systemic and reproductive studies it is not possible to determine DNEL values for systemic effects and risk characterisation is not necessary.

Qualitative risk characterisation is required based on the aspiration hazard and potential skin dryness and cracking.