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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Classification & Labelling & PBT assessment

PBT assessment

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Administrative data

PBT assessment: overall result

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Name:
Zinc, bis(O,O-diisodecyl phosphorodithioato-.kappa.S,.kappa.S') - Boundary composition
Type of composition:
boundary composition of the substance
State / form:
liquid
Reference substance:
Zinc, bis(O,O-diisodecyl phosphorodithioato-.kappa.S,.kappa.S') - Boundary composition
Reference substance:
Zinc, bis(O,O-diisodecyl phosphorodithioato-.kappa.S,.kappa.S') - Boundary composition
Reference substance:
Zinc, bis(O,O-diisodecyl phosphorodithioato-.kappa.S,.kappa.S') - Boundary composition
Reference substance:
Zinc, bis(O,O-diisodecyl phosphorodithioato-.kappa.S,.kappa.S') - Boundary composition
Name:
Zinc, bis(O,O-diisodecyl phosphorodithioato-.kappa.S,.kappa.S') - Legal entity composition
Type of composition:
legal entity composition of the substance
State / form:
liquid
Reference substance:
Zinc, bis(O,O-diisodecyl phosphorodithioato-.kappa.S,.kappa.S') - Legal entity composition
Reference substance:
Zinc, bis(O,O-diisodecyl phosphorodithioato-.kappa.S,.kappa.S') - Legal entity composition
Reference substance:
Zinc, bis(O,O-diisodecyl phosphorodithioato-.kappa.S,.kappa.S') - Legal entity composition
Reference substance:
Zinc, bis(O,O-diisodecyl phosphorodithioato-.kappa.S,.kappa.S') - Legal entity composition
PBT status:
the substance is not PBT / vPvB
Justification:

Only 1% degradation was demonstrated after 28 days in a ready biodegradation study with the test item and therefore it is considered to be persistent or very persistent.

For bioaccumulation a weight of evidence assessment based on the physico-chemical properties of the substance, QSAR predictions and previous regulatory reviews is considered to demonstrate that the substance is not bioaccumulative or very bioaccumulative.

The test item does not meet the screening criteria for toxicity based on ecotoxicological results, and is not classified for human health endpoints, therefore it is not considered to be toxic.

As the substance is not bioaccumulative or toxic it is not PBT or vPvB.