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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Oral standard acute method, rats: LD50 710 mg/kg

Key value for chemical safety assessment

Acute toxicity: via oral route

Link to relevant study records
Reference
Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
data from handbook or collection of data
Guideline:
other: no data
GLP compliance:
not specified
Test type:
standard acute method
Species:
rat
Strain:
not specified
Sex:
male
Route of administration:
oral: unspecified
Vehicle:
not specified
Sex:
male
Dose descriptor:
LD50
Effect level:
710 mg/kg bw
Based on:
test mat.
95% CL:
>= 470 - <= 1 070
Clinical signs:
other:
Interpretation of results:
Category 4 based on GHS criteria
Remarks:
EU GHS
Conclusions:
The oral LD50 in rat was described as 710 mg/kg.
Executive summary:

The test item was assessed in an standard acute toxicity test in rats following national stndard methods. The oral LD50 in rats was determined to be 710 mg/kg.

Endpoint conclusion
Endpoint conclusion:
adverse effect observed
Dose descriptor:
LD50
Value:
710 mg/kg bw
Quality of whole database:
data collection of sufficient quality

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Justification for classification or non-classification

Based on the oral median lethal dose of an standard acute toxicity tests in rats, the substance would be classified as Acute toxic Cat. 4 (H302) according to Regulation (EC) No 1272/2008. As Xylidines have an entry in Annex VI of Regulation (EC) No 1272/2008, the harmonised classification is applied: Acute Tox. Cat. 3 (H301)