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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

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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 screening criteria given in the "Guidance on information requirements and chemical safety assessment, chapter R.11: PBT Assessment" (ECHA, 2014) are used as surrogate information to decide whether Fatty acids, vegetable-oil, esters with dipropylene glycol (CAS 95009-41-9) may potentially fulfil the PBT or vPvB criteria.

Persistence Assessment

Based on the available data, Fatty acids, vegetable-oil, esters with dipropylene glycol is considered to be readily biodegradable. Thus, the substance does not meet the screening criterion for persistence and it is not considered to be P or vP.

Bioaccumulation Assessment

The bioaccumulation potential of Fatty acids, vegetable-oil, esters with dipropylene glycol is expected to be low. This assumption is based on a low bioavailability of the substances due to its ready biodegradability, high adsorption potential and low water solubility. Furthermore, the substance is rapidly metabolised and excreted by organisms and thus significant accumulation is not expected. This is supported by calculated low BCF/BAF values of 2.07 - 19.26 and 2.45 - 19.33 L/kg (Arnot-Gobas estimate, upper trophic), respectively. Please refer to IUCLID Section 5.3 for a detailed overview on bioaccumulation of the substance. Thus, taking all information into account, the test substance is not considered to be B or vB.

Toxicity Assessment

Long-term toxicity testing with Desmodesmus subspicatus and Daphnia magna resulted in no effects up to the limit of water solubility. All available short-term toxicity data did not result in any toxicity up to the water solubility limit as well. Moreover, the substance is not classified according to Directive 67/548/EEC and Regulation (EC) No 1272/2008 and the Regulation (EU) No 944/2013 (5th ATP). Thus, the criteria set out in Annex XIII of Regulation (EC) No 1907/2006 are not met and the test substance is not considered to meet the T criterion.