Registration Dossier
Registration Dossier
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EC number: 807-112-6 | CAS number: 1393708-17-2
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 014
- Report date:
- 2014
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 420 (Acute Oral Toxicity - Fixed Dose Method)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.1 bis (Acute Oral Toxicity - Fixed Dose Procedure)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- Frey-Tox GmbH, Osteroda 38, 04916 Herzberg (Elster)
- Test type:
- fixed dose procedure
- Limit test:
- no
Test material
- Reference substance name:
- 3-(diethylcarbamoyl)-1-(3-sulfonatopropyl)pyridin-1-ium
- EC Number:
- 807-112-6
- Cas Number:
- 1393708-17-2
- Molecular formula:
- C13H20N2O4S
- IUPAC Name:
- 3-(diethylcarbamoyl)-1-(3-sulfonatopropyl)pyridin-1-ium
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
- Details on test material:
- - Name of test material (as cited in study report): PYRIDINIUMSULFONATE
- Substance type: white powder
- Analytical purity: 99.8 % (HPLC)
- Lot/batch No.: CHZT000001
- Expiration date of the lot/batch: Feb. 2016
- Storage condition of test material: min. - 5 °C - max. +40 °C
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- female
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- water
- Doses:
- 2000 mg/kg bw, selected based on the results of preliminary tests with doses of 300 and 2000 mg/kg bw using one female rat
- No. of animals per sex per dose:
- 4
- Control animals:
- no
Results and discussion
Effect levels
- Sex:
- female
- Dose descriptor:
- LD50
- Effect level:
- > 2 000 mg/kg bw
- Based on:
- test mat.
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- No classifcation required according to EU CLP regulation EU No 1272/2008
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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