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Environmental fate & pathways

Biodegradation in water: screening tests

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Administrative data

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

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1996
Report date:
1996

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 301 D (Ready Biodegradability: Closed Bottle Test)
Deviations:
not specified
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Hexakis[μ-(acetato-O:O')]-μ3-oxo-triangulo-triruthenium acetate
EC Number:
259-653-7
EC Name:
Hexakis[μ-(acetato-O:O')]-μ3-oxo-triangulo-triruthenium acetate
Cas Number:
55466-76-7
Molecular formula:
C12H18O13Ru3.C2H3O2
IUPAC Name:
hexamethyl-2λ³-oxa-4λ³-oxa-6λ³-oxa-8λ³-oxa-10λ³-oxa-12λ³-oxa-13λ³-oxa-15λ³-oxa-16λ³-oxa-18λ³-oxa-19λ³-oxa-21λ³,22λ¹-dioxa-1,5,9-triruthenahexacyclo[7.3.3.3¹,⁵.3⁵,⁹.1¹,⁵.0⁹,²²]docosa-3,7,11,14,17,20-hexaene-1,1,1,5,5,5,9,9,9-nonakis(ylium)-2,6,10,13,16,19-hexaide-22,22-diuide acetate
Details on test material:
ruthenium acetate

Study design

Oxygen conditions:
aerobic
Inoculum or test system:
sewage, domestic (adaptation not specified)
Details on inoculum:
Mixed population of sewage treatment microorganisms from second stage sewage treatment at Belper, Derbyshire.
The effluent was allowed to settle for approximately 1 hour, the supernatant removed and maintained on continuous aeration at a temperature of
21°C prior to use.
Duration of test (contact time):
28 d
Initial test substance concentration
Initial conc.:
12 mg/L
Based on:
test mat.
Parameter followed for biodegradation estimation
Parameter followed for biodegradation estimation:
O2 consumption
Details on study design:
Stock solution concentration was 200 mg/l. Test concentration was 12 mg/l.
BOD bottles were set up as follows:
- Control (in duplicate)
- Reference material (in duplicate)
- Test material (in duplicate)
- Toxicity control (in duplicate)

Media was inoculated with sewage treatment micro-organisms at a rate of 1 drop of inoculum per litre.

BOD bottles were incubated in a water bath at 21°C.

Sampling for dissolved oxygen was performed on days 0, 3, 6, 9, 12, 15, 18, 21, 24 and 28.

Reference substance
Reference substance:
other: sodium benzoate

Results and discussion

% Degradation
Parameter:
% degradation (O2 consumption)
Value:
59
Sampling time:
28 d
Details on results:
Toxicity control containing both Ruthenium acetate and sodium benzoate, attained 51% degradation after 28 days thereby confirm that the test material was not toxic to the sewage treatment micro-organisms used in the study

BOD5 / COD results

Results with reference substance:
Sodium benzoate (3mg/l) with inoculum attained 81% degradation in 28 days

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Interpretation of results:
not readily biodegradable
Conclusions:
Ruthenium acetate attained 59% degradation after 28 days and therefore cannot be considered as readily biodegradable under guideline 301D.
Executive summary:

This is a GLP compliant study following OECD guideline 301D. A control, toxicity control and reference item were all included in the study set up. The toxicity control containing both ruthenium acetate and sodium benzoate, attained 51% degradation after 28 days thereby confirms that the test material was not toxic to the sewage treatment micro-organisms used in the study The study is considered to be suitable for use as the key study for this endpoint. Ruthenium acetate attained 59% degradation after 28 days and therefore cannot be considered as readily biodegradable under guideline 301D.