Registration Dossier
Registration Dossier
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EC number: 701-246-8 | CAS number: -
Endpoint summary
Administrative data
Description of key information
Due to international regulatory requirements for agricultural spray adjuvants, more than one acute toxicity study report is available for each route of administration (oral, inhalation, dermal). All reported no significant toxicity (and certainly no mortalities) at the maximum tested exposure level.
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Dose descriptor:
- LD50
- Value:
- 16 000 mg/kg bw
Acute toxicity: via inhalation route
Endpoint conclusion
- Dose descriptor:
- LC50
- Value:
- 4 430 mg/m³ air
Acute toxicity: via dermal route
Endpoint conclusion
- Dose descriptor:
- LD50
- Value:
- 4 000 mg/kg bw
Additional information
LD50/LC50 values cited represent maximum test exposures, at which no evident toxicity was seen and so are actually acute NOAELs.
Justification for classification or non-classification
Acute toxicity studies using all three routes of administration found no evident toxicity at very high dosages/test concentrations (in excess of the limit values for classification and labelling).
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.
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