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EC number: 442-300-8
CAS number: -
Acute oral toxicity: LD50 > 2000 mg/kg bw; OECD Guideline Study, 2002Acute dermal toxicity: LD50 > 2000 mg/kg bw; OECD Guideline Study, 2002
In a GLP-compliant acute oral toxicity study (OECD 423), groups of
fasted 8 week old rats (3/sex) were given a single oral dose of the
unchanged test item at 2000 mg/kg body weight and observed for 14 days.
No mortality occurred and normal body weight gains were found in this
study. There were no signs of systemic toxicity and no abnormalities
were noted at necropsy.
In a GLP-compliant acute dermal toxicity study (OECD 402), groups of 8
week old rats (5/sex) were dermally exposed to undiluted test item for
24 hours to 10% of body surface area at 2000 mg/kg body weight. Animals
then were observed for 14 days. No mortality occurred and normal body
weight gains were found in this study. There were no signs of systemic
toxicity or dermal irritation and no abnormalities were noted at
Classification, Labeling, and
Packaging Regulation (EC) No. 1272/2008
The available experimental test data are
reliable and suitable for the purpose of classification under Regulation
(EC) No 1272/2008. Based on the data, classification for acute toxicity
is not warranted under Regulation (EC) No 1272/2008, as
amended for the eighth time in Regulation (EU) No 2016/218.
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