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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

No skin/eye irritation/corrosion studies of registered substance were available. The registered substance is a complex reaction mixture, containing N,N'-bis(3-aminopropyl)ethylenediamine (CAS No. 10563-26-5) and N-(2-aminoethyl)-1,3-propanediamine (CAS No. 13531-52-7) among others as majors components. These two components were used as surrogate to evaluate the skin/eye irritation/corrosion potential of the registered substance. For read across justification please refer to IUCLID chapter 13.

Key value for chemical safety assessment

Skin irritation / corrosion

Endpoint conclusion
Endpoint conclusion:
adverse effect observed (corrosive)

Eye irritation

Endpoint conclusion
Endpoint conclusion:
adverse effect observed (irritating)

Respiratory irritation

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Skin irritation:

Two skin irritation/corrosion studies are available for surrogates of the registered substance, both of validity 2 (BASF- XXVI/99 and BASFAG.XXVI/100). In the two studies, the test substance was shown to be corrosive to the rabbit skin/caused severe skin irritation.

 

In the BASF study with N-(2-aminoethyl)-1,3-propanediamine (CAS No. 13531-52-7), the a primary skin irritation evaluated in rabbits with undiluted test substance (exposure times of 1, 5 and 15 min and 20 hours) in a study design similar to the OECD guideline 404. Necrosis was observed irrespective of the exposure duration and both animals tested died within two days.

 

Eye irritation:

In a primary eye irritation study in rabbits conducted with the same surrogate as above, 50 µL of the test substance were applied to the conjunctival sac of one eye in 2 animals. Necrosis, staphyloma were also observable and not completely reversible at the end of the 8 days observation period.

Respiratory irritation:

No data

 

Effects on skin irritation/corrosion: corrosive

Effects on eye irritation: corrosive

Justification for classification or non-classification

Based on the above described studies and considering the worst case assumption that the test substance contains 100% of its most toxic surrogate the test substance should be classified according to the EU Classification, Labelling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 1272/2008 as follows:

corrosive to skin and eyes (GHS cat. 1A)