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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 400-100-8 | CAS number: 84057-97-6 BLEU N-RM 2114; BLEU NYLOSAN N-BLN; BLUE N-RM 2114; NYLOSAN BLAU N-BLN; NYLOSAN BLEU N-BLN; NYLOSAN BLUE N-BLN
Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Only data summary seen from SNIF docs
Data source
Reference
- Reference Type:
- other: ECHA
- Title:
- Unnamed
- Report date:
- 1983
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- GLP compliance:
- yes
Test material
- Reference substance name:
- Sodium 1-amino-4-[2-methyl-5-(4-methylphenylsulfonylamino)phenylamino]anthraquinone-2-sulfonate
- EC Number:
- 400-100-8
- EC Name:
- Sodium 1-amino-4-[2-methyl-5-(4-methylphenylsulfonylamino)phenylamino]anthraquinone-2-sulfonate
- Cas Number:
- 84057-97-6
- Molecular formula:
- C28H22N3NaO7S2
- IUPAC Name:
- sodium 1-amino-4-[2-methyl-5-(4-methylphenylsulfonylamino)phenylamino]anthraquinone-2-sulfonate
- Details on test material:
- Not defined in record seen - SNIF
Constituent 1
Results and discussion
In vivo
Results
- Remarks on result:
- other: Other: not classified
Any other information on results incl. tables
4106 EYE IRR RESULT: Clear irritation noted immediately on application due, in part, to the physical state of the material. Moderate conjunctival and corneal irritation persisted for up to 48 hours post-dose, but cleared by 72 hours. The substance is not classified as an eye irritant.
Applicant's summary and conclusion
- Conclusions:
- Data obtained through ECHA Inquiry under the 12 year rule.
- Executive summary:
Data obtained through ECHA Inquiry under the 12 year rule.
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.
