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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Key value for chemical safety assessment

Effects on fertility

Effect on fertility: via oral route
Dose descriptor:
NOAEL
1 000 mg/kg bw/day
Additional information

To determine toxicity to reproduction and prenatal development of ethylenediamine, +4PO, the test substance was administered to Wistar rats by gavage (dose levels: 0, 100, 300 and 1000 mg/kg bw; vehicle: water). Treatment started 14 days before mating. In total, males were treated for approximately 30 days and females for 49 days. Females and their pups were sacrificed 4 days post partum. Signs of developmental or reproductive toxicity were not reported at any dose level (BASF, 95R0628/04108, 2009).

Thus the NOAEL for developmental toxicity and toxicity to reproduction is 1000 mg/kg bw.

Short description of key information:

Reproduction / Developmental Toxicity Screening Test (GLP & OECD 422): NOAEL = 1000 mg/kg bw for developmental toxicity

Effects on developmental toxicity

Description of key information

Reproduction / Developmental Toxicity Screening Test (GLP & OECD 422): NOAEL = 1000 mg/kg bw for developmental toxicity

Effect on developmental toxicity: via oral route
Dose descriptor:
NOAEL
1 000 mg/kg bw/day
Additional information

For details see record "effects on fertility".

Justification for classification or non-classification

The available study is considered reliable and suitable for classification purposes under 67/548/EEC and 1272/2008/EEC. In conclusion, ethylendiamine, +4PO does not require classification for developmental toxicity and toxicity to reproduction.

Additional information