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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 403-360-0 | CAS number: 42405-40-3 BONTRON E-84; E-84
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: GLP-Guideline study, only basic data available from SNIF (ECHA)
Data source
Reference
- Reference Type:
- other: Body responsible for the test
- Title:
- Unnamed
- Report date:
- 1990
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Version / remarks:
- Previous version, 1981. Conforms with method B4 of Annex V to Dir. 67/548/EEC. (OJ vol. 27, 19-9-84)
- GLP compliance:
- yes
Test material
- Reference substance name:
- 610-025-4
- EC Number:
- 610-025-4
- IUPAC Name:
- 610-025-4
- Reference substance name:
- Bis(3,5-bis(1,1-dimethylethyl)-2-hydroxybenzoato-O1,O2)zinc
- EC Number:
- 403-360-0
- EC Name:
- Bis(3,5-bis(1,1-dimethylethyl)-2-hydroxybenzoato-O1,O2)zinc
- Cas Number:
- 42405-40-3
- Molecular formula:
- C30H42O6Zn
- IUPAC Name:
- bis(3,5-bis(1,1-dimethylethyl)-2-hydroxybenzoato-O1,O2)zinc
Constituent 1
Constituent 2
Test animals
- Species:
- other: Albino rabbit New Zealand white
Test system
- Type of coverage:
- occlusive
- Vehicle:
- other: Distilled water
- Amount / concentration applied:
- 500 mg
- Duration of treatment / exposure:
- 4 h
- Number of animals:
- 3
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Remarks:
- Mean score 1
- Time point:
- other: Overall at 24, 48 and 72 h
- Score:
- ca. 3
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Remarks:
- Mean score 2
- Time point:
- other: Overall at 24, 48 and 72 h
- Score:
- ca. 0
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Remarks:
- Mean score 3
- Time point:
- other: Overall at 24, 48 and 72 h
- Score:
- 0
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Remarks:
- Mean score 1
- Time point:
- other: Overall at 24, 48 and 72 h
- Score:
- ca. 3
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Remarks:
- Mean score 2
- Time point:
- other: Overall at 24, 48 and 72 h
- Score:
- ca. 0
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Remarks:
- Mean score 3
- Time point:
- other: Overall at 24, 48 and 72 h
- Score:
- 0
- Other effects:
- Intensity and duration of effects:
No oedema and erythema were observed during this period. No dermal irritation was observed during the remainder of the observation period.
Applicant's summary and conclusion
- Interpretation of results:
- other: not classified
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.
