Registration Dossier
Registration Dossier
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EC number: 227-876-9 | CAS number: 6021-61-0
Mode of degradation in actual use
Administrative data
- Endpoint:
- mode of degradation in actual use
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- documentation insufficient for assessment
Data source
Reference
- Reference Type:
- other company data
- Title:
- Unnamed
- Year:
- 1 980
- Report date:
- 1980
Materials and methods
- Principles of method if other than guideline:
- Static Method HOECHST No 4, November 1973
- GLP compliance:
- no
Test material
- Reference substance name:
- Disperse Red 054
- IUPAC Name:
- Disperse Red 054
Constituent 1
Results and discussion
Any other information on results incl. tables
Bioelimination
| Substance conc. | Days | Elimination | |||
| mg/l | mg DOC/l | After 3hrs | Mean | Dispersion | |
| 840 | 400 | 14 | 24 | 35 | 29 - 41 |
| 240 | 120 | 14 | 46 | 54 | 47 - 71 |
Applicant's summary and conclusion
- Conclusions:
- Bioelimination (14d): 35 - 54 %
Bioelimination (3h): 24 - 46 % - Executive summary:
The bioelimination potential of the test item was assessed, in accordance with the Static Method, HOECHST no. 4, November 1973. Unfortunately, no details about testing procedures and conditions are available. The elimination of the substance was estimated on the basis of the DOC elimination.
The elimination after 3 hours resulted to be 24 - 46 %, while after 14 days it was 35 - 54 %.
Conclusion
Bioelimination (14d): 35 - 54 %
Bioelimination (3h): 24 - 46 %
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