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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Weight of evidence: 
Oral acute toxicity: data obtained from single administration in rats. LD50 = 580 mg/kg bw in rats.
Oral acute toxicity: data obtained in rats. LD50 = 540 ± 34 mg/kg bw in rats and 600 ± 21 mg/kg bw in mice.

Key value for chemical safety assessment

Additional information

Weight of evidence:

Acute toxicity: oral:

In a test on albino rats with a single intragastric introduction of para-phenetidine the LD50 for the substance was found to be 580 mg/kg bw. The substance showed no cumulative properties. Poisoning with this substance is characterized by the development of methemoglobinemia.

The toxic properties of p-phenetidine were studied after oral administration. The LD50 for white rats and mice correspond to 540 ± 34 and 600 ± 21 mg/kg bw respectively.The results are processed by probit analysis of Prozorovsky.

 

Justification for classification or non-classification

The substance is included in Table 3 of Annex VI of CLP Regulation (harmonised classification and labelling) and classified as:

Acute Oral Toxicity Category 4* (minimum classification)

Acute Dermal Toxicity Category 4* (minimum classification)

Acute Inhalation Toxicity Category 4* (minimum classification)

The available information on acute oral toxicity supports the classification as Acute Oral Toxicity Category 4.