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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
activated sludge respiration inhibition testing
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2002
Report date:
2002

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
Deviations:
no
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Reference substance name:
Creosote
EC Number:
232-287-5
EC Name:
Creosote
Cas Number:
8001-58-9
IUPAC Name:
8001-58-9
Constituent 2
Reference substance name:
EINECS No. 232-287-5
IUPAC Name:
EINECS No. 232-287-5
Constituent 3
Reference substance name:
A complex combination of monocyclic aromatic hydrocarbons, polycyclic aromatic hydrocarbons, tar acids and tar bases, obtained by the distillation of coal tars produced by the high-temperature destructive distillation of bituminous coal to form coke. It consists of hydrocarbons boiling in the range of approximately 200°C-355°C
IUPAC Name:
A complex combination of monocyclic aromatic hydrocarbons, polycyclic aromatic hydrocarbons, tar acids and tar bases, obtained by the distillation of coal tars produced by the high-temperature destructive distillation of bituminous coal to form coke. It consists of hydrocarbons boiling in the range of approximately 200°C-355°C
Details on test material:
- Name of test material (as cited in study report): Creosote
Creosote WEI-Type B, containing less than 50 ppm BaP
- Substance type: organic
- Physical state: liquid
- Composition

Name CAS-No. Concentration [w%]
RUETGERS Chemicals // Biochem. Inst.Grimmer
=================================================
Naphthalene 91-20-3 5.07 5.39
Fluorene 86-73-7 3.06 3.07
Acenaphthylene 208-96-8 -- 0.09
Acenaphthene 83-32-9 4.09 4.04
Phenanthrene 85-01-8 8.95 8.56
Anthracene 120-12-7 0.45 0.38
Fluoranthene 206-44-0 3.70 3.84
Pyrene 129-00-0 2.49 2.08
Benz[a]anthracene 56-55-3 0.04 0.04
Chrysene 218-01-9 0.03 0.03
Benzo(a)pyrene 50-32-8 <10 ppm ca. 6. ppm
----------------------------------------------------------------

Total of 5 remaining EPA-PAH: --- < 20 pp
----------------------------------------------------------------
(Benzo[b]fluoranthene 205-99-2
Benzo[k]fluoranthene 207-08-9
Indeno[1,2,3-cd]pyrene 193-39-5
Dibenzo[a,h]anthracene 53-70-3
Benzo[ghi]perylene) 191-24-2
===========================================

Sampling and analysis

Analytical monitoring:
no
Details on sampling:
--

Test solutions

Vehicle:
no
Details on test solutions:
PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: direct addition and agitation by aeration in the presence of inoculum
- Differential loading: yes

Test organisms

Test organisms (species):
activated sludge of a predominantly domestic sewage
Details on inoculum:
- Cultivation: Activated sludge from the effluent of the aeration tank of the municipal WWTP at Taunusstein-Biederstadt/Germany.
The isolated sludge mixture (MLSS) (approx. 4 g/l dry mass) was pre-incubated in synthetic medium for 2 d.
The culture medium contained 8 ml synthetic sewage feed (prepared from peptone (16 g/l), beef extract (11 g/l), urea (3 g/l),
mineral salts), 100 ml inoculum and tap water for a total volume of 250 ml.
- Initial biomass concentration: approx. 1.5 g/l (dry mass).

Study design

Test type:
static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
3 h
Remarks on exposure duration:
= incubation time of the test solutions (test substance + inoculum) under aeration prior to measuring
Post exposure observation period:
--

Test conditions

Hardness:
--
Test temperature:
18.0 - 18.1 °C
pH:
8.3 - 8.4
Dissolved oxygen:
parameter to be measured
Salinity:
--
Nominal and measured concentrations:
125, 250, 500, 1000, and 2000 mg/l (nominal, without separation of undissolved material) (derived from a pre-test).
Details on test conditions:
TEST SYSTEM
- Test vessel:
- Type (delete if not applicable): closed at measuring of O2 consumption
- Material, size, headspace, fill volume: 250-ml glass bottle with inlet for aeration
- Aeration: 3 h until start of determination of the respiration rate
- Measuring equipment: pH-Electrode: WTW portable; O2-Electrode WTW OXI 530
- No. of vessels per concentration (replicates): one
- No. of vessels per control (replicates): Two parallel trials without test substance / one abiotic control containing 2000 mg creosote/L
(without biomass)

TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: synthetic

EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : O2-consumption


TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2
Reference substance (positive control):
yes
Remarks:
3,5- dichlorophenol (5 - 30 mg/L)

Results and discussion

Effect concentrations
Duration:
3 h
Dose descriptor:
other: inhibitory loading EL50
Effect conc.:
670 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate
Remarks on result:
other: 95% C.I of the inhibition rate: approx. +- 12 %
Details on results:
- Any observations (e.g. precipitation) that might cause a difference between measured and nominal values: dispersion
- Effect concentrations exceeding solubility of substance in test medium: yes,
(At the EL50, the WAF is estimated to have been between 30 and 40 mg dissolved carbon/L, based on water solubility data.)

- Pre-test:
Test loadings: 10, 100, and 1000 mg/L
Results: No inhibition, but about >40-% stimulation (10 mg/L);
26-% inhibition (100 mg/L);
50-% inhibition (1000 mg/L)
Results with reference substance (positive control):
- Results with reference substance valid? yes, at 5, 15, 30 mg/L
- Relevant effect levels: EC50 approx. 10 mg/L

Any other information on results incl. tables

Summary of effects data: Inhibition in % versus loadings of test substance:

Test [mg/l, nominal]

Respiration Rate
[mg O2/(l*min), after 3-h incubation

Inhibition of Respiration [%]

Control
[mean of 2]

0.84
0.91
av. 0.88

0

Abiotic Control [2000 mg/l]

0

--

125

0.71

18.9

250

0.54

38.4

500

0.46

47.4

1000

0.48

45.1

2000

0.22

74.9

Applicant's summary and conclusion