Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Not skin irritant


Not eye irritant

Key value for chemical safety assessment

Skin irritation / corrosion

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (not irritating)

Eye irritation

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (not irritating)

Respiratory irritation

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Skin irritation/corrosion


The test item was applied to the skin of the flank of 6 rabbits, through occlusive coverage. The right flank was treated with the undiluted product, while the left flank was treated with the 10% dilution of the product in sesame oil. The exposure time was 24 hours; the observation period was up to 72 hs. The irritation index was calculated based on erythema and oedema scores after 24 and 72 hours and it was found to be 1.9 for the undiluted product and 0.4 for the dilution. 


Eye irritation/corrosion


The test item was instilled into the right eye of 6 rabbits, while the left eye served as control. 0.1 mL of undiluted product was instilled in the eye and washed after 72 hs. The observation period was up to 72 hs. Fluorescein was instilled after 48 hours and 72 hours to assess the scores. The irritation index was calculated based on effects on cornea, iris and conjunctiva after 1, 7, 24, 48 and 72 hours. The maximum score was 2 and it was observed after 7 hours. The effect was fully reversible after 24 hours.

Justification for classification or non-classification

No effects on the eyes after topic application of PCBTF in rabbits were seen. The scores assigned for iris, conjunctiva and cornea were 0. For this reason the test substance is not classified as irritant to the eye according to the CLP Regulation 1272/2008.


 


As per skin irritation, scores for oedema were not fully reversible after 72 hours. However, considering the very short observation period after application of the substance and the trend of the scores assigned after 24, 48 and 72 hours it is expected fully reversibility within a hypothetical 14 days obsarvation period.


In addition the substance shows no toxicity on the eyes, considered as a higher sensitive organ respect to the skin.


Overall, the test substance is considered to have no irritation potential for the skin and for this reason it is not classified as skin irritant according to the CLP Regulation 1272/2008.