Registration Dossier
Registration Dossier
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EC number: 700-627-6 | CAS number: 17270-01-8
Endpoint summary
Administrative data
Link to relevant study record(s)
Description of key information
Key value for chemical safety assessment
- Bioaccumulation potential:
- no bioaccumulation potential
Additional information
No specific study was performed on the absorption, distribution, metabolism and/or excretion (ADME) of ADK STAB FP-800. Its absorption and systemic availability after topical or oral administration is expected to be limited, because of its high molecular weight (650.6), low water solubility (< 0.01 mg/L at 20°C) and high lipohilicity (Log 10Pow = 5.5 at 25°C) and because of the absence of relevant toxicity findings in all available toxicity studies.
Quasi-inert behaviour of ADK STAB FP-800 in biological systems has been inferred from the absence of relevant toxicity in all available toxicology studies and the absence of adverse effects on algae, daphnia, fish or bacteria in ecotoxicology studies, and from ADK STAB FP-800 being not readily biodegradable in a standard laboratory test and not predicted as oxidising.
All available study results gave no indication regarding the metabolic pathway, distribution or excretion of ADK STAB FP-800. Bioaccumulation was not investigated in mammals, but in fish it was not evident.
Based on all available information it is concluded that ADK STAB FP-800 does not have an accumulation potential.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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