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Diss Factsheets

Ecotoxicological information

Short-term toxicity to aquatic invertebrates

Administrative data

Endpoint:
short-term toxicity to aquatic invertebrates
Type of information:
experimental study
Adequacy of study:
key study
Study period:
From September 2014 to February 2015
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Well described study performed according to OECD guideline and GLP

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2015
Report date:
2015

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
Deviations:
no
Qualifier:
according to guideline
Guideline:
EU Method C.2 (Acute Toxicity for Daphnia)
Deviations:
no
GLP compliance:
yes
Remarks:
Certificate available in the attached report.

Test material

Constituent 1
Chemical structure
Reference substance name:
2-({3-nitropyrazolo[1,5-a]pyridin-2-yl}oxy)ethan-1-ol
EC Number:
938-829-3
Cas Number:
936103-10-5
Molecular formula:
C9H9N3O4
IUPAC Name:
2-({3-nitropyrazolo[1,5-a]pyridin-2-yl}oxy)ethan-1-ol
Constituent 2
Reference substance name:
2-[(3-Nitropyrazolo[1,5-a]pyridin-2-yl)oxy] ethanol
IUPAC Name:
2-[(3-Nitropyrazolo[1,5-a]pyridin-2-yl)oxy] ethanol
Test material form:
solid: particulate/powder
Remarks:
migrated information: powder

Test solutions

Details on test solutions:
Test Concentrations:
100 mg test item/L and a control.

Test organisms

Test organisms (species):
Daphnia magna
Details on test organisms:
Female Daphnia magna, clone 5; 6.0 to 22.5 hours old.
Source: The daphnids introduced in the test were taken from IBACON's in-house laboratory culture.
The daphnids were bred in the laboratories of IBACON under similar temperature and light conditions as used in the test. The cultivation of the parental daphnids was performed in the same reconstituted water as the test water used in the test. The test organisms were not first brood progeny. The daphnids in the stock culture were fed at least on all working days with green algae (Desmodesmus subspicatus) freshly grown in the laboratories of IBACON.

Study design

Test type:
static
Water media type:
saltwater
Limit test:
yes
Total exposure duration:
48 h

Test conditions

Hardness:
Water Hardness: 2.5 mmol/L (= 250 mg/L) as CaCO3
Test temperature:
Test Environment: Controlled environment room
Water temperature: 20 °C
pH:
pH value: 7.7 – 8.2
Dissolved oxygen:
dissolved oxygen concentration: 7.7 – 8.8 mg/L
Details on test conditions:
This study encompassed two treatment groups (one test item concentration at nominal 100 mg/L and one control) each containing 20 individuals.
Photoperiod: 16 h light - 8 h dark.
Light intensity: 240 – 340 lux.

Results and discussion

Effect concentrationsopen allclose all
Duration:
24 h
Dose descriptor:
EC50
Effect conc.:
> 100 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
> 100 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Duration:
24 h
Dose descriptor:
NOEC
Effect conc.:
ca. 100 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Duration:
48 h
Dose descriptor:
NOEC
Effect conc.:
ca. 100 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Duration:
24 h
Dose descriptor:
LOEC
Effect conc.:
> 100 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Duration:
48 h
Dose descriptor:
LOEC
Effect conc.:
> 100 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Details on results:
See report attached.

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Conclusions:
The toxic effect of the test item R0056895A to Daphnia magna was assessed in a static limit test. The 48-hour NOEC was determined to be 100 mg test item/L. The 48-hour LOEC was determined to be > 100 mg test item/L and the 48-hour EC50 value was determined to be > 100 mg test item/L.