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Diss Factsheets

Ecotoxicological information

Short-term toxicity to aquatic invertebrates

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Administrative data

Link to relevant study record(s)

Reference
Endpoint:
short-term toxicity to aquatic invertebrates
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2020-07-16 - 2021-04-26
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
GLP compliance:
yes (incl. QA statement)
Specific details on test material used for the study:
200116MA1 liquid
Analytical monitoring:
yes
Details on sampling:
concentrations and the control were taken at the start of the test and at day 1.
For the determination of the stability of the test item under the test conditions and of the maintenance of the test item concentrations during the test period, four samples from the aged test media of all test concentrations and the control were collected at day 1 (after 24 hours of exposure) and at the end of the test by pouring together the contents of the test beakers of each treatment.
One set of duplicate samples of each sampling point was used for the analysis of DCD and Hydantoic acid.
The other set of duplicate samples of each sampling point was used for the determination of total organic carbon (TOC).
All samples remained undiluted.
Vehicle:
no
Test organisms (species):
Daphnia magna
Test type:
semi-static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
48 h
Hardness:
2.5 mmol/L (= 250 mg/L) as CaCO3
Test temperature:
20.1 to 20.8 °C in the freshly prepared media;
20.2 to 20.8°C in the aged test media
pH:
7.7 to 8.0 in the freshly prepared media;
7.9 in the aged test media; and thus the pH-value did not vary by more than 1.5 units
Dissolved oxygen:
8.7 to 9.1 mg/L in the freshly prepared media;
7.9 to 8.7 mg/L in the aged test media
Nominal and measured concentrations:
Nomnal concentrations:
889, 404, 184, 83.5 and 37.9 mg test item/L
equivalent to 160, 72.7, 33.1, 15.0 and 6.83 mg total dissolved solids/L
equivalent to 24.003, 10.908, 4.968, 2.255, 1.023 mg DCD/L

Measured concentrations (% of nominal):

24.003 mg/L: 105
10.908 mg/L: 99
4.968 mg/L: 97
2.255 mg/L: 101
1.023 mg/L: 100
Reference substance (positive control):
yes
Remarks:
Potassium dichromate
Key result
Duration:
48 h
Dose descriptor:
NOEC
Effect conc.:
> 160 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Remarks:
mg dissolved solids/L
Basis for effect:
mortality
Validity criteria fulfilled:
yes
Conclusions:
The toxic effect of the test item "Solution of By-product from Guanidinoacetic acid manufacturing" to Daphnia magna was assessed in a semi-static concentration-response test. The 48-hour NOEC was determined to be ≥ 889 mg test item/L / ≥ 160 mg dissolved solids/L (based on immobility). The 48-hour LOEC was determined to be > 889 mg test item/L / > 160 mg dissolved solids/L (based on immobility) and the 48-hour EC50 value was determined to be > 889 mg test item/L / > 160 mg dissolved solids/L.
Executive summary:

The toxic effect of the test item "Solution of By-product from Guanidinoacetic acid manufacturing" to Daphnia magna was assessed in a semi-static concentration-response test. The 48-hour NOEC was determined to be ≥ 889 mg test item/L / ≥ 160 mg dissolved solids/L (based on immobility). The 48-hour LOEC was determined to be > 889 mg test item/L / > 160 mg dissolved solids/L (based on immobility) and the 48-hour EC50 value was determined to be > 889 mg test item/L / > 160 mg dissolved solids/L.
The initial concentrations and the maintenance of the exposure concentrations during the test were determined in the analytical part.
Correct dosage was confirmed by the analysis of the component DCD of the test item because DCD is the component with the highest content in the test item. This component is stable under the experimental conditions and does not undergo any reaction with any other component of the test item. Furthermore, a reference substance is commercially available.
All reported results refer to nominal values since the concentrations of DCD in the test item were within ± 20% of the nominal concentrations during the test and “Solution of By-product from Guanidinoacetic acid manufacturing” is an UVCB substance (Unknown or Variable composition, Complex reaction products or Biological material).

Description of key information

Key value for chemical safety assessment

Fresh water invertebrates

Fresh water invertebrates
Dose descriptor:
EC50
Remarks:
mg dissolved solids / mL
Effect concentration:
> 160 mg/L

Additional information