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EC number: 701-241-0
CAS number: -
Unable to include all results data in this
See attached Tables 1 to 5 for information
study was performed to assess the acute dermal toxicity of the test
material in the Wistar strain rat. The method was designed to meet the
requirements of the following
OECD Guidelines for the Testing of
Chemicals No. 402 “Acute Dermal Toxicity” (adopted 24 February 1987)
Method B3 Acute Toxicity (Dermal) of
CommissionRegulation (EC) No. 440/2008
A group of ten animals (five males and
five females) was given a single, 24-hour, semi-occluded dermal
application of the undiluted test material to intact skin at a dose
level of 2000 mg/kg bodyweight. Clinical signs and bodyweight
development were monitored during the study. All animals were subjected
to gross necropsy.
There were no deaths.
There were no signs of systemic
There were no signs of dermal
Animals showed expected gains in
bodyweight over the study period except for one female which showed no
gain in bodyweight during the first week but expected gain in bodyweight
during the second week.
No abnormalities were noted at
acute dermal median lethal dose (LD50) of the test material
in the Wistar strain rat was found to be greater than 2000 mg/kg
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