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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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 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. 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. The critical health effect is aspiration toxicity (potential lung damage following accidental swallowing), although this applies only for lower viscosity products (3.0 and 4.0 cSt at 100°C). It is not possible to determine quantitative dose descriptors for this effect. Qualitative risk characterisation is required based on the aspiration hazard.

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. 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. The critical health effect is aspiration toxicity (potential lung damage following accidental swallowing), although this applies only for lower viscosity products (3.0 and 4.0 cSt at 100°C). It is not possible to determine quantitative dose descriptors for this effect. Qualitative risk characterisation is required based on the aspiration hazard.