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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Ecotoxicological information

Toxicity to microorganisms

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Administrative data

Link to relevant study record(s)

Reference
Endpoint:
activated sludge respiration inhibition testing
Type of information:
read-across from supporting substance (structural analogue or surrogate)
Remarks:
See Justification of Read Across
Adequacy of study:
supporting study
Study period:
1992
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
test procedure in accordance with national standard methods with acceptable restrictions
Justification for type of information:
See the Read Across justification document
Reason / purpose for cross-reference:
read-across: supporting information
Reason / purpose for cross-reference:
read-across source
Qualifier:
according to guideline
Guideline:
DIN 38412-27 (Pseudomonas putida Zellvermehrungshemmtest)
Deviations:
no
GLP compliance:
yes
Specific details on test material used for the study:
Name: Phosphoric acid, mixed decyl and octyl esters, compds. with diethanolamine (Phosphorsaeure (C8-C10-Alkyl)-ester, DEA-Salz)
CAS No.: 68425-57-0 (68186-45-8)
Physical state: white solid at 20 °C (turbid, non-pourable paste)
Analytical monitoring:
no
Vehicle:
no
Details on test solutions:
Culture media: H5-Water, Glucose
Test organisms (species):
Pseudomonas putida
Details on inoculum:
Pseudomonas putida MIGULA, Stamm Berlin 33/2 (DSM 50026)
Test type:
static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
3 h
Details on test conditions:
Age of susension at beginning of the test: 2 d
Test volume: 100 mL
Conentrations: 300, 100, 3000 mg test item / L
Reference substance (positive control):
not specified
Key result
Duration:
3 h
Dose descriptor:
EC0
Effect conc.:
1 000 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat. (total fraction)
Basis for effect:
inhibition of total respiration
Key result
Duration:
3 h
Dose descriptor:
EC10
Effect conc.:
1 030 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Validity criteria fulfilled:
yes
Conclusions:
The test item had no inhibitory effect on the total oxygen uptake of activated sludge microorganisms after 3 hours at 1000 mg/l. The EC0 is therefore determined to be 1000 mg/L. The EC10 for total oxygen uptake was calculated at a test item concentration of 1030 mg/L.
Executive summary:

The objectives of this study were to determine the effects of test item on microorganisms respiration under laboratory conditions. The oxygen uptake rate was measured after 3 hours of exposure. The total oxygen uptake rate of the same microorganisms in the presence of various concentrations of the test item under otherwise identical conditions was also measured. The GLP study was performed according to DIN 38412, Part 27. The test item had no inhibitory effect on the total oxygen uptake of microorganisms after 3 hours at a concentration of 1000 mg/l. The EC0 is therefore determined to be 1000 mg/L. The EC10 for total oxygen uptake was calculated at a  test item concentration of 1030 mg/L.

Description of key information

The toxicity to microorganisms was evaluated with results of a similar substance, tested according to DIN 38412-27 (Pseudomonas putida Zellvermehrungshemmtest). See the Justification of the Read Across.

Key value for chemical safety assessment

EC10 or NOEC for microorganisms:
1 030 mg/L

Additional information