Registration Dossier

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:
1980
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
Name:
Unnamed
Type:
Constituent

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 bioeliminationpotential 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 cestimated on the basis of the DOC elimination.

The elimination after 3 hours resulted to be 24 - 46 %, while after 14 days it reach the 35 - 54 %, respectively.

Conclusion

Bioelimination (14d): 35 - 54 %

Bioelimination (3h): 24 - 46 %