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Diss Factsheets

Environmental fate & pathways

Biodegradation in water: screening tests

Administrative data

Endpoint:
biodegradation in water: ready biodegradability
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2016
Report date:
2016

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 301 F (Ready Biodegradability: Manometric Respirometry Test)
Deviations:
no
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
o-(trifluoromethyl)benzamide
EC Number:
206-637-2
EC Name:
o-(trifluoromethyl)benzamide
Cas Number:
360-64-5
Molecular formula:
C8H6F3NO
IUPAC Name:
2-(trifluoromethyl)benzamide
Test material form:
solid: crystalline

Study design

Oxygen conditions:
aerobic
Inoculum or test system:
activated sludge, domestic, non-adapted
Details on inoculum:
Activated sludge from the municipal wastewater treatment plant Breisgauer Bucht was used as inoculum with a concentration corresponding to 30 mg dry solids per litre. The treatment plant clarifies predominantly domestic wastewater of the region of Freiburg and has a capacity of 600.000 inhabitant equivalents. Sampling date of activated sludge was 9 August 2016. Dry solid of the activated sludge was determined as 3.4 g/L by weight measurements after 2.0 h drying at 105°C (mean of triplicate measurements). The activated sludge was washed twice with tap water by settling the sludge, decanting the supernatant and re-suspending the sludge.
Duration of test (contact time):
28 d
Initial test substance concentration
Initial conc.:
54 mg/L
Based on:
test mat.
Parameter followed for biodegradation estimation
Parameter followed for biodegradation estimation:
O2 consumption
Reference substance
Reference substance:
acetic acid, sodium salt

Results and discussion

% Degradation
Key result
Parameter:
% degradation (O2 consumption)
Value:
4.7
Sampling time:
28 d

BOD5 / COD results

Results with reference substance:
The reference compound sodium acetate reached the pass level for ready biodegradability (60% ThOD and 10-day window) within 8 days. The pH in the test bottles at the end of the test was 8.8 - 9.0.

Any other information on results incl. tables

Test item:

The biodegradation of the test item was 4.7% within 28 days (mean value of three

replicates, see table 2). Therefore the criterion for ready biodegradability was not met (60%

ThOD and 10-day window).

The pH in the test bottles at the end of the test was 7.6.

Toxicity control:

The degradation in the toxicity control reached 26.7% within 8 days (see table 2) and was thus above the criterion for inhibition effects to the inoculum (<25% on day 14). The test item had no toxic effect to the inoculum according to the validity criteria of OECD 301. The pH in the vessel was 8.6.

Blank:

The oxygen consumption of the blanks was 18.7 mg O2/L in 28 days (mean of three replicates, see table 1). The pH in the vessels was 7.6.

Temperature:

The temperature range was 20.1 - 21.6 °C throughout the whole study.

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Interpretation of results:
not readily biodegradable
Conclusions:
The biodegradation of the test item was 4.7% within 28 days (mean value of three replicates, see table 2). Therefore the criterion for ready biodegradability was not met (60% ThOD and 10-day window).