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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 233-899-5 | CAS number: 10421-48-4
Dermal absorption
Administrative data
- Endpoint:
- dermal absorption
- Type of information:
- other: EFSA review conclusion
- Adequacy of study:
- weight of evidence
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: EFSA review conclusion for use of iron sulphate in plant protection products
Data source
Reference
- Reference Type:
- publication
- Title:
- EFSA CONCLUSION ON PESTICIDE PEER REVIEW, Conclusion on the peer review of the pesticide risk assessment of the active substance iron sulfate European Food Safety Authority
- Author:
- Anon.
- Bibliographic source:
- EFSA Journal 2012;10(1):2521
Materials and methods
- Principles of method if other than guideline:
- Not applicable
- GLP compliance:
- no
Test material
- Reference substance name:
- Iron sulphate
- EC Number:
- 231-753-5
- EC Name:
- Iron sulphate
- Cas Number:
- 7720-78-7
- IUPAC Name:
- iron(2+) sulfate
- Test material form:
- not specified
- Details on test material:
- No further information
Constituent 1
- Radiolabelling:
- not specified
Test animals
- Details on test animals or test system and environmental conditions:
- No detailed information presented in EFSA review conclusion
Administration / exposure
- Duration of exposure:
- No detailed information presented in EFSA review conclusion
- Doses:
- No detailed information presented in EFSA review conclusion
- No. of animals per group:
- No detailed information presented in EFSA review conclusion
- Details on study design:
- No detailed information presented in EFSA review conclusion
- Details on in vitro test system (if applicable):
- No detailed information presented in EFSA review conclusion
Results and discussion
- Signs and symptoms of toxicity:
- not specified
- Dermal irritation:
- not specified
- Absorption in different matrices:
- No detailed information presented in EFSA review conclusion
- Conversion factor human vs. animal skin:
- Not available
Applicant's summary and conclusion
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.
