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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Link to relevant study record(s)

Description of key information

Additional information

One study adressing the endpoint toxicity to other organisms is available. In this GLP study, the acute toxicity of the test item to Xenopus laevis was assessed in a 48-hour static test. The test design did not follow a specific guideline but methodologies from USEPA, OPPTS Guideline 850.1075, USEPA-FIFRA, 40 CFR, Part 158, Guideline No. 72 -1 and OECD Guideline 203 were considered. X laevis tadpoles were exposed to five concentrations of the test substance in the range between 6.25 and 100 mg a.i./L. The mean measured recovery of solutions analyzed on day 0 and day 2 was between 96 and 100 % of nominal. Throughout the exposure, organisms were healthy and appeared normal in the control, 6.25 and 12.5 mg a.i./L test levels. However, there was a single mortality in the control group. Toxicant related mortalities (26.7 %) only occurred in the 100 mg a.i./L level. The LC50 (48) was determined to be > 100 mg a.i./L (nominal).