Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

The oral LD50 in Wister rats was >2000 mg/kg bw. 

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
discriminating dose
Quality of whole database:
GLP and guideline study

Additional information

Oral

The effect of the test item was determined in an acute oral toxicity study to Wistar rats according to OECD guideline 423, EU method B1 and EPA OPPTS 870.1100. A limit test was conducted with a dose of 2000 mg/kg bw. Olive oil was used as vehicle. The duration of observation following administration was at leat 14 days. The LD50 was determined to be >2000 mg/kg bw.

In a supporting study the acute oral toxicity of Bis-2,4-dimethylphenoxy-propan-1,3-ol-2 (read across) to Wistar rats was tested according to OECD guideline 423. The concentration tested was 2000 mg/kg bw. 5 females and 5 males were used. The LD50 determined was 2000 mg/kg bw.


Justification for selection of acute toxicity – oral endpoint
GLP and guideline study

Justification for classification or non-classification

Dangerous Substance Directive (67/548/EEC)

The available studies are considered reliable and suitable for classification purposes under 67/548/EEC. As a result the substance is not considered to be classified for acute oral toxicity under Directive 67/548/EEC, as amended for the 31st time in Directive 2009/2/EG.

Classification, Labelling, and Packaging Regulation (EC) No 1272/2008 The available experimental test data are reliable and suitable for classification purposes under Regulation (EC) No 1272/2008. As a result the substance is not considered to be classified for acute oral toxicity under Regulation (EC) No 1272/2008, as amended for the sixth time in Regulation No 605/2014.