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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 214-317-9 | CAS number: 1120-71-4
Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation
- Remarks:
- other: Assessment of existing data and expert judgemnt
- Type of information:
- other: Assessment and expert judgement
- Adequacy of study:
- key study
- Study period:
- 2011
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Expert judgement. Basic data given. Reliable source
Data source
Reference
- Reference Type:
- other company data
- Title:
- Unnamed
- Year:
- 2 011
- Report date:
- 2011
Materials and methods
- Principles of method if other than guideline:
- According to Annex VII "Standard Information Requirements for Substances Manufactured or Imported in Quantities of one Tonne or More" of the "Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), establishing a European Chemicals Agency, amending Directive 1999/45/EC and repealing Council Regulation (EEC) No 793/93 and Commission Regulation (EC) No 1488/94 as well as Council Directive 76/769/EEC and Commission Directives 91/155/EEC, 93/67/EEC, 93/105/EC and 2000/21/EC” (as amended) (OJ L 396, 30.12.2006, p.1) 8.3, the "assessment of this endpoint shall comprise the following consecutive steps:
(1) an assessment of the available human, animal and alternative data,
(2) In vivo testing" - GLP compliance:
- no
- Type of study:
- other: Expert judgement
Test material
- Reference substance name:
- 1,3-propanesultone
- EC Number:
- 214-317-9
- EC Name:
- 1,3-propanesultone
- Cas Number:
- 1120-71-4
- Molecular formula:
- C3H6O3S
- IUPAC Name:
- 1,2-oxathiolane 2,2-dioxide
- Details on test material:
- not applicable
Constituent 1
In vivo test system
Test animals
- Species:
- other: not applicable
Results and discussion
Any other information on results incl. tables
According to Annex VII "Standard Information Requirements for Substances Manufactured or Imported in Quantities of one Tonne or More" of the "Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), establishing a European Chemicals Agency, amending Directive 1999/45/EC and repealing Council Regulation (EEC) No 793/93 and Commission Regulation (EC) No 1488/94 as well as Council Directive 76/769/EEC and Commission Directives 91/155/EEC, 93/67/EEC, 93/105/EC and 2000/21/EC” (as amended) (OJ L 396, 30.12.2006, p.1) 8.3, the assessment of this endpoint comprised the following consecutive steps:
(1) an assessment of the available human, animal and alternative data: no reports on adverse effects identified
(2) In vivo testing had not to be performed because
— the available information indicates that the substance should be classified for skin corrosivity.
No in vitro study had to be performed because the available information indicates that a extremely high level of protection is reached.
Corrosive substances are exempted from testing because - in general - they not unawarely in contact with the skin or eye. As the substance is classified as a CMR substance, at least, the same level level of protection is reached and no test is required.
Applicant's summary and conclusion
- Interpretation of results:
- other: not relevant
- Remarks:
- Criteria used for interpretation of results: EU
- Conclusions:
- Required level of Protection reached if substance is handled under strictly controlled conditions.
- Executive summary:
No in vitro study had to be performed because the available information indicates that a extremely high level of protection is reached.
Corrosive substances are exempted from testing because - in general - they not unawarely in contact with the skin or eye. As the substance is classified as a CMR substance, at least, the same level level of protection is reached and no test is required.
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.
