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EC number: 297-025-4
CAS number: 93281-13-1
X = sign observed
- = observation performed, sign not
(G) = max. grade
The substance was assessed for its acute
toxicity to rats in a limit test, according to the OECD guideline 401
and the EU Method B.1. The acqueous solution of the substance was
administrated by oral gavage to five female and five male Wistar rats in
a concentration of 2000 mg/kg bw. The rats were observed for mortality,
clinical signs, macroscopic changes and vitality four times during test
day 1 (at 1, 2, 3 and 5 hrs) and daily during days 2 - 15. The animals
were weighed on test day 1 (pre-administration), day 8 and 15.
During the observation period, no
mortality was observed and no macroscopical findings were noted. The
body weight was increased. Clinical signs observed in some animals were
sedated behaviour and hunched posture, while ruffled fur and diarrhea
was observed in all animals until day 10 and day 2 respectively. No
obvious macroscopical organ findings were seen in any animal.
LD50 (males and female) > 2000 mg/kg bw
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.Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
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