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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

PBT status:
the substance is not PBT / vPvB
Justification:

The PBT Assessment is based on the criteria set out in the “Guidance on information requirements and chemical safety assessment, Chapter R.11: PBT Assessment” (ECHA, 2017).

 

Persistence (P) Assessment

 

Tefuryltrione is not readily biodegradable according to OECD criteria (4% after 28 d, OECD 301F). The mineralisation rate, determined in a sediment simulation test, was 0.7 – 1% after 101 days based on the measured CO2 elevation). In the available studies on the aerobic transformation in soil the substance attained 11.5 to 63.2% degradation (elevation of 14CO2) after 120 days. The substance was not significantly degraded in soil under anaerobic conditions in the dark in the laboratory. The calculated half-lives under anaerobic conditions were > 1000 days.

Based on the available data, Tefuryltrione is assessed as persistent (P).

 

Bioaccumulation (B) assessment

 

Tefuryltrione has a low potential for bioaccumulation based on the log Kow and log D values < 3 (determined for pH 4 ,7 and 9).

 

Toxicity (T) assessment

 

Tefuryltrioneis is classified for specific target organ toxicity as STOT RE 1 (oral route) and STOT RE 2 (dermal route). The criteria for “T” based on mammalian effects are therefore met. Thus, the criteria set out in Annex XIII of Regulation (EC) No. 1907/2006 are met and the substance is considered to be T.

 

Summary and overall conclusions on PBT or vPvB properties

 

In conclusion, the substance is not PBT/vPvB