Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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.

Diss Factsheets

Environmental fate & pathways

Biodegradation in water: screening tests

Currently viewing:

Administrative data

Endpoint:
biodegradation in water: inherent biodegradability
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2007
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2007
Report date:
2008

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 302 B (Inherent biodegradability: Zahn-Wellens/EMPA Test)
Deviations:
no
Qualifier:
according to guideline
Guideline:
EU Method C.9 (Biodegradation: Zahn-Wellens Test)
Deviations:
no
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
604-144-0
EC Number:
604-144-0
Cas Number:
139525-77-2
Molecular formula:
C13H15NO.HCl
IUPAC Name:
604-144-0
Test material form:
solid: particulate/powder
Details on test material:
White powder
Specific details on test material used for the study:
Batch : 839411/006Purity : 100.9%Expiry date : 10 Feb 2009Storage : room temperature (20 +/- 5°C), dry

Study design

Oxygen conditions:
aerobic
Inoculum or test system:
activated sludge, domestic, adapted
Details on inoculum:
The sludge was taken from the activation basin of th ESN sewage treatment plant, Im Altenschemel, NW-Lachen-Speyerdord (date of collection : 8 nov 2007)The sludge was washed with tap water twice, then filtrated through a cloth and resuspended in test medium. It was then aerated. The dry matter was determined with 3960 mg suspended solids/L.
Duration of test (contact time):
ca. 28 d
Initial test substance concentration
Initial conc.:
ca. 200 mg/L
Based on:
DOC
Parameter followed for biodegradation estimation
Parameter followed for biodegradation estimation:
DOC removal
Details on study design:
Before sampling for DOC analysis, the pH was measured and adjusted, if necessary, evaporated water was replenished. From each flask; sample of 5 ml were taken on days 0.125 - 2 - 4 - 8 12 - 15 - 20 - 27 and 28. The samples were membrane filtrated and the DOC was measured.
Reference substance
Reference substance:
aniline

Results and discussion

Test performance:
All criteria were met : difference within replicates : 0,2% (target value <20%)Degradation of reference item : 7 days (target value < 14 days)Degradation in the toxicity control on day 14 : 42% (target value > 25%)
% Degradation
Key result
Parameter:
% degradation (DOC removal)
Value:
ca. 2
Sampling time:
28 d
Details on results:
As nearly no elimination or no degration occurend, no lag phase and no degradatio phase could be determined

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Interpretation of results:
not inherently biodegradable
Conclusions:
According the guideline 302B, Mephtamin HCL is not inherently biodegradable.
Executive summary:

Mephtamin HCL was tested using a concentration of nominally 200 mg organic carbon/L in test medium following OECD 302B.

Aniline was chosen as reference item. Activated sludge from a sewage treating plant was used as inoculum (concentration 600 mg dry matter/L). The test was left running for 28 days.

To measure the degradation of test and Mephtamin HCL, the content of dissolved organic carbon (DOC) in the test vessels was measured nine times during the test.

All validity criteria were met. Degradation of the reference item was 98% after 8 days and of the Mephtamin at the end of the test is 2%

Therefore Mephtamin HCL is not inherently biodegradable.