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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
biodegradation in water: ready biodegradability
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2001
Report date:
2001

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 301 A (Ready Biodegradability: DOC Die Away Test)
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
(R)-1-hydroxy-1-phenylacetone
EC Number:
217-285-4
EC Name:
(R)-1-hydroxy-1-phenylacetone
Cas Number:
1798-60-3
Molecular formula:
C9H10O2
IUPAC Name:
(1R)-1-hydroxy-1-phenylpropan-2-one
Details on test material:
- Name of test material (as cited in study report): (-)-Phenylacetylcarbinol, roh
- Analytical purity: 65.5 %
- Impurities (identity and concentrations): Benzylalcohol 27.95 %; Phenylmethylglycol 5.95 %
- Lot/batch No.: P. 222/26

Study design

Oxygen conditions:
aerobic
Inoculum or test system:
activated sludge, domestic (adaptation not specified)
Details on inoculum:
- Source of inoculum/activated sludge (e.g. location, sampling depth, contamination history, procedure): Activated sludge from laboratory wastewater treatment plants fed with municipal sewage.
- Concentration of sludge: 30 mg/l
Duration of test (contact time):
15 d
Initial test substance concentrationopen allclose all
Initial conc.:
20 mg/L
Based on:
DOC
Initial conc.:
30 mg/L
Based on:
test mat.
Parameter followed for biodegradation estimation
Parameter followed for biodegradation estimation:
DOC removal
Details on study design:
TEST CONDITIONS
- Test temperature: 22 ± 2 °C
- pH: 7.4 - 7.7
Reference substance
Reference substance:
aniline

Results and discussion

% Degradationopen allclose all
Parameter:
% degradation (DOC removal)
Value:
< 10
Sampling time:
1 d
Parameter:
% degradation (DOC removal)
Value:
20 - 30
Sampling time:
2 d
Parameter:
% degradation (DOC removal)
Value:
60 - 70
Sampling time:
4 d
Parameter:
% degradation (DOC removal)
Value:
90 - 100
Sampling time:
15 d
Details on results:
Kinetic of test substance (in %):
= 29 after 1 day(s)
= 43 after 3 day(s)
= 97 after 5 day(s)
Kinetic of control substance (in %):
= 1 after 1 day(s)
= 95 after 5 day(s)

Applicant's summary and conclusion

Interpretation of results:
readily biodegradable