Registration Dossier
Registration Dossier
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 205-391-3 | CAS number: 140-01-2
Acute Toxicity: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: early study report; only orientating results regarding inhalation toxicity
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 968
- Report date:
- 1968
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- BASF-internal standard. Exposure to air saturated with vapour from DTPA solution.
- GLP compliance:
- no
- Test type:
- other:
- Limit test:
- no
Test material
- Reference substance name:
- Diethylenetriaminepentaacetic acid sodium salt
- IUPAC Name:
- Diethylenetriaminepentaacetic acid sodium salt
- Reference substance name:
- Pentasodium (carboxylatomethyl)iminobis(ethylenenitrilo)tetraacetate
- EC Number:
- 205-391-3
- EC Name:
- Pentasodium (carboxylatomethyl)iminobis(ethylenenitrilo)tetraacetate
- Cas Number:
- 140-01-2
- Molecular formula:
- C14H23N3O10.5Na
- IUPAC Name:
- .
- Details on test material:
- Name of test substance: Trilon C fluessig
Chemical name:
Diethylenetriaminepentaacetic acid sodium salt
CAS No.: 140-01-2
Content: 40 % test substance,
60 % water
Constituent 1
Constituent 2
Test animals
- Species:
- rat
- Strain:
- not specified
- Sex:
- male/female
Administration / exposure
- Route of administration:
- inhalation: vapour
- Vehicle:
- other: unchanged (no vehicle)
- Analytical verification of test atmosphere concentrations:
- no
- Duration of exposure:
- 8 h
- No. of animals per sex per dose:
- 12
- Control animals:
- not specified
Results and discussion
- Mortality:
- No mortalities.
- Clinical signs:
- other: Nothing abnormal detected.
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
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.
