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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Additional information

Justification for classification or non-classification

The acute oral LD50 for Diethylene Glycol Diethyl Ether is 4970mg/kg bw in male rats and 3674.3mg/kg bw in female mice.

The acute dermal LD50 values for Diethylene Glycol Ethyl Ether and Diethylene Glycol Methyl Ethyl Ether are 6000 and 6420mg/kg bw in rats, respectively. These two substances are used as read across for the classification of acute dermal toxicity of DEGDEE (see Category Approach-Read across Bis(2 -ethoxyethyl)ether, 2013).

The acute inhalation LC50 of diethylene glycol dimethyl ether in rats after 7 h inhalation exposure is >11 mg/L (saturated atmosphere).The acute dermal LD50 value for Diethylene Glycol Ethyl Ether is >5.24 mg/L (mists) in rats. These two substances are used as read across for the classification of acute toxicity of DEGDEE by the inhalation route (see Category Approach-Read across Bis(2 -ethoxyethyl)ether, 2013).

Based on these results, DEGDEE is not classified as acutely toxic according to CLP criteria (Regulation (EC) No 1272/2008).