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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Ecotoxicological information

Toxicity to microorganisms

Currently viewing:

Administrative data

Link to relevant study record(s)

Reference
Endpoint:
activated sludge respiration inhibition testing
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1996-08-30
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
guideline study with acceptable restrictions
Qualifier:
according to guideline
Guideline:
other: EG-Richtlinie L 133/118 vom 30.5.1988
GLP compliance:
yes
Analytical monitoring:
no
Vehicle:
no
Details on test solutions:
PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: The test substance was directly given into the test vessels in five different concentrations, the test vessels were 3 h incubated and stirred under permanent ventilation with clean, oil-free air in a water-filled pan
Controls: two replicates blank control, reference control (3,5-Dichlorophenol) in three different concentrations
- Evidence of undissolved material (e.g. precipitate, surface film, etc): no data
Test organisms (species):
activated sludge of a predominantly domestic sewage
Details on inoculum:
- Method of cultivation: not applicable
- Preparation of inoculum for exposure: approximately 5 l activated sludge of the sewage "Marl-Ost" was one-time sedimentated, three-times centrifuged each for 5 minutes 2000 min-1 and washed with 500 - 600 mL drinking water. The activated sludge was taken into 3.5 L drinking water and had a concentration of 3.603 g TS/L, that means for 500 mL test and 200 mL inoculum 1.44 g TS/L..
Test type:
flow-through
Water media type:
freshwater
Limit test:
no
Total exposure duration:
3 h
Post exposure observation period:
none
Hardness:
no data
Test temperature:
18 - 22 °C
pH:
7.6-7.8
Dissolved oxygen:
>= 2,5 mg/L
Nominal and measured concentrations:
57.4; 92.8; 189.4; 290.8; 380 mg/L
Details on test conditions:
TEST SYSTEM
- Test vessel: flasks
- Material, fill volume: glass, 500 ml fill volume
- Aeration: continuous
- Renewal rate of test solution (frequency/flow rate): not applicable
- No. of organisms per vessel: not applicable
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 2
- No. of vessels per vehicle control (replicates): not applicable
- Biomass loading rate: 200 mL inoculum; 1.44 g dry weight/L

EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : Oxygen consumption, pH

Reference substance (positive control):
yes
Remarks:
3,5-Dichlorophenol
Key result
Duration:
3 h
Dose descriptor:
EC50
Effect conc.:
> 370 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate
Results with reference substance (positive control):
- Results with reference substance valid: yes
- Relevant effect levels: EC50 = 5.1 mg/L
Validity criteria fulfilled:
yes
Executive summary:

Marlowet 4753 (Coconut oil, reaction products with polyethylene glycol and trimethylolpropane) was tested in Activated Sludge Respiration Inhibition Test according to EC guideline 88/302/EC. Within the tested concentration of 57.4; 92.8; 189.4; 290.8 and 380 mg/L there was no significant toxic effect. The determined positive effects were not proportional to increasing concentration. The EC50 was > 370 mg/L rounded up to two significant places. The test substance contents 98.4 % active substance.

Description of key information

Marlowet 4753 (Coconut oil, reaction products with polyethylene glycol and trimethylolpropane) was tested in Activated Sludge Respiration Inhibition Test according to EC guideline 88/302/EC. Within the tested concentration of 57.4; 92.8; 189.4; 290.8 and 380 mg/L there was no significant toxic effect. The determined positive effects were not proportional to increasing concentration. The EC50 was > 370 mg/L rounded up to two significant places. The test substance contents 98.4 % active substance.

Key value for chemical safety assessment

EC50 for microorganisms:
370 mg/L

Additional information