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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Irritation data are based on structural analogues LiDNNSA, DNNSA and BaDNNSA

Skin irritation
Six rabbits were exposed to the test substance dermally for 24 hours under occlusion (PSL 1981 (1), PSL 1981 (2)). The test substance initiated irritation of the skin at 24 and 72 h observations. This irritation was not shown to be reversible. Therefore the test substance is classified as skin irritant category 2.
Eye irritation
Six rabbits were treated with the test substance in an eye irritation test (PSL 1981 (1), PSL 1981 (2)). During the observation period of 72 hours severe eye irritation was reported (including effects on cornea), which was not shown to be reversible within 72 hours. In view of the absence of effects on the iris and a mean maximum overall score of 1.3 for cornea, it was concluded that the test substance is a category 2 eye irritant.
Studies on skin and eye irritation toxicity are available on DNNSA and BaDNNSA. These studies are indicative of moderate to severe irritation and therefore show that both DNNSA and BaDNNSA are suitable candidates for read-across.

Key value for chemical safety assessment

Skin irritation / corrosion

Endpoint conclusion
Endpoint conclusion:
adverse effect observed (irritating)

Eye irritation

Endpoint conclusion
Endpoint conclusion:
adverse effect observed (irritating)

Respiratory irritation

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

The available studies contain sufficient information to be used for classification and labelling.


Justification for selection of skin irritation / corrosion endpoint:
Studies were conducted prior to GLP regulations but used methods generally consistent with accepted procedures. Two studies of equal quality are available. Both can be indicated as key-study. The results of both studies are comparable.

Justification for selection of eye irritation endpoint:
Studies were conducted prior to GLP regulations but used methods generally consistent with accepted procedures. Two studies of equal quality are available. Both can be indicated as key-study. The results of both studies are comparable

Effects on skin irritation/corrosion: irritating

Effects on eye irritation: moderately irritating

Justification for classification or non-classification

Based on the outcome of the available tests, the test substance needs to classified as skin irritant (CLP category 2, H315: Causes skin

irritation) and severe eye irritant (CLP category 2, H319: Causes serious eye irritation).