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EC number: 479-310-7
CAS number: -
The following Acute toxicity studies are available:Acute Oral toxicity study (rat)Acute dermal toxicity study (rabbit)Acute inhalation toxicity (rats)
Acute oral (male and female rats), acute dermal (male and female
rabbits) and acute inhalation (male and female rats) toxicity studies
were performed with Fyrolflex SOL-DP.
Following either oral or dermal administration no mortalities were
observed in either sex at 5000 mg/kg, no signs of systemic toxicity were
noted during clinical observations and no abnormalities were noted
Following the 4 hours inhalation exposure to 5.23 mg/l aerosol SOL-DP,
no exposure related findings were shown in clinical signs of both sexes
and only a minor effect on bodyweight profile was noted. Limited
necropsy findings were observed in the lungs and mandibular lymph nodes
of some animals, and the lung: body weight ratios were considered to be
The above results triggered no classification under the EEC criteria for
classification and labelling requirements for Dangerous Substances and
Preparations (67/548/EEC) and the CLP Regulation (EC No 1272/2008).
Therefore, Fyrolflex SOL-DP is not classified for acute toxicity.
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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