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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

Short-term toxicity to aquatic invertebrates

Administrative data

Endpoint:
short-term toxicity to aquatic invertebrates
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2014
Report date:
2014

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
EPA OPPTS 850.1010 (Aquatic Invertebrate Acute Toxicity Test, Freshwater Daphnids)
Deviations:
no
Qualifier:
according to guideline
Guideline:
OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
Deviations:
no
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
3-hydroxy-4-methoxypyridine-2-carboxylic acid
Cas Number:
210300-09-7
Molecular formula:
C7H7NO4
IUPAC Name:
3-hydroxy-4-methoxypyridine-2-carboxylic acid
Specific details on test material used for the study:
Substance name: X696476
Lot #: XS9-109113-80 (TSN300901)
Purity: 100%

Sampling and analysis

Analytical monitoring:
yes

Test solutions

Vehicle:
no

Test organisms

Test organisms (species):
Daphnia magna

Study design

Test type:
other: Static-renewal
Water media type:
freshwater
Total exposure duration:
48 h

Test conditions

Hardness:
150 mg CaCO3/L
Test temperature:
19.3 to 20.9°C
pH:
8.3 to 8.5
Dissolved oxygen:
Dissolved Oxygen (new): 8.1 to 9.0 mg/L (95 to 103% sat.)
Dissolved Oxygen (old): 8.5 to 9.1 mg/L (96 to 105% sat.)
Salinity:
Alkalinity: 160 mg CaCO3/L
Conductivity:
349 μS
Nominal and measured concentrations:
Nominal: 0 (control), 0.63, 1.3, 2.5, 5.0, and 10 mg/L
Mean measured:

Results and discussion

Effect concentrationsopen allclose all
Key result
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
> 9.53 mg/L
Nominal / measured:
meas. (arithm. mean)
Conc. based on:
test mat.
Basis for effect:
other: immobility
Remarks on result:
other: highest concentration tested
Duration:
48 h
Dose descriptor:
NOEC
Effect conc.:
9.53 mg/L
Nominal / measured:
meas. (arithm. mean)
Conc. based on:
test mat.
Basis for effect:
other: immobility and sublethal effects
Remarks on result:
other: highest concentration tested

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Conclusions:
48 h EC50 (Daphnia): >9.53 mg/L
48 h NOEC (Daphnia): 9.53 mg/L
Executive summary:

A definitive test was performed at nominal concentrations 0 (control), 0.63, 1.3, 2.5, 5.0, and 10 mg/L. Five neonates (<24-hours old) were added to each of four test chambers per treatment at the start of the test. The daphnids were observed for immobility and sublethal effects at approximately 24 and 48 hours after test initiation.


Total hardness, total alkalinity, and conductivity were measured in the dilution water at test initiation. Temperature, dissolved oxygen concentration, and pH were measured in all treatment replicates daily. A thermistor probe was located in a surrogate test chamber to continuously record temperature.


All test acceptability criteria were met for this study. Immobilization among control daphnids was 0%, which is below the acceptability limit of 10% as stated in the protocol and the OECD 202 test guideline. The dissolved oxygen concentration at the end of the test was ≥ 8.5 mg/L in control and test substance treatments, higher than the acceptability minimum of 3 mg/L. This study is classified as acceptable and satisfies the guideline requirement for an acute toxicity test with Daphnia magna.


Based on arithmetic and geometric mean measured concentrations, the 24-hour and 48-hour EC50 values were >9.53 and >9.50 mg/L, respectively, the highest concentration tested. The 48 hour NOEC, based on arithmetic and geometric mean measured concentrations, was 9.53 and 9.50 mg/L, respectively, based on the absence of statistically significant immobility and sublethal effects at this, and all lower test substance concentrations.