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Ecotoxicological information

Short-term toxicity to aquatic invertebrates

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Endpoint:
short-term toxicity to aquatic invertebrates
Type of information:
experimental study
Adequacy of study:
disregarded due to major methodological deficiencies
Study period:
From 04 February 2013 to 04 March 2013
Reliability:
3 (not reliable)
Rationale for reliability incl. deficiencies:
significant methodological deficiencies
Remarks:
This study was performed according to OECD Guideline 202 and EU Method C.2 with GLP statement. All validity criteria were fulfilled. However, the measured concentration of the 100% v/v saturated solution used to prepare the different test concentrations was determined at 28 mg/L, which is well greater than the real water solubility value. The saturated solution was prepared by dispersing an amount of test substance is reconstituted water with the aid of propeller stirring for 24 hours. After 24 hours, the stirring was stopped and any undissolved test substance was removed by filtration to give the saturated solution. An hypothesis of this high measured concentration (28 mg/L) whould be that 24 hours of stirring is not sufficient to dissolve this test substance and even if clear colorless solutions were reported, stable emulsions are suspected to be formed, which can explain possible physical effects. Due to this significant methodological deficiencies (tested concentrations greater than the water solubility value), this study is not reliable.
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
Principles of method if other than guideline:
Not applicable
GLP compliance:
yes (incl. QA statement)
Remarks:
2012-11-30
Analytical monitoring:
yes
Details on sampling:
Water samples were taken from the control and each test group (replicates R1 – R4 pooled) at 0 and 24 hours (old media) and from the control and each surviving test group at 24 (fresh media) and 48 hours (old media) for quantitative analysis. Samples were stored at approximately -20 °C prior to analysis.
Vehicle:
no
Details on test solutions:
Preliminary solubility work conducted indicated that the test item was practically insoluble in water using traditional methods of preparation e.g. ultrasonication and high shear mixing.
Based on this information, a media preparation trial was conducted in order to determine the solubility of the test item under test conditions. The test item was prepared using a rapid stir saturated solution method of preparation, stirred for a period of 24 hours prior to the removal of any undissolved test item by filtration through a 0.2 μm Sartorius Sartopore filter (first approximate 2 liters discarded) to give a nominal test concentration of approximately 32 mg/L.

PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
An amount of test item (1100 mg) was dispersed in 11 liters of reconstituted water with the aid of propeller stirring at approximately 1500 rpm for 24 hours. After 24 hours the stirring was stopped and any undissolved test item was removed by filtration through a 0.2 μm Sartorius Sartopore filter (first approximate 2 liters discarded in order to pre-condition the filter) to give a 100% v/v saturated solution with a mean measured concentration of 28 mg/L. A series of dilutions was made from the saturated solution to give further test concentrations of 56, 32, 18 and 10% v/v saturated solution (equivalent to mean measured test concentrations of 15, 8.7, 4.7 and 3.7 mg/L).
Each prepared concentration was inverted several times to ensure adequate mixing and homogeneity.
Test organisms (species):
Daphnia magna
Details on test organisms:
TEST ORGANISM
- Common name: Daphnia magna
- Strain: no data
- Source: in-house laboratory cultures
- Age at study initiation (mean and range, SD): 1st instar (less than 24 hours old)
- Weight at study initiation (mean and range, SD): no data
- Length at study initiation (length definition, mean, range and SD): no data
- Valve height at study initiation, for shell deposition study (mean and range, SD): no data
- Peripheral shell growth removed prior to test initiation: no data
- Method of breeding: no data
- Feeding during test: no

ACCLIMATION
Adult Daphnia were maintained in 150 mL glass beakers containing Elendt M7 medium in a temperature controlled room at approximately 20 °C. The lighting cycle was controlled to give a 16 hours light and 8 hours darkness cycle with 20 minute dawn and dusk transition periods. Each culture was fed daily with a mixture of algal suspension (Desmodesmus subspicatus) and Tetramin® flake food suspension. Culture conditions ensured that reproduction was by parthenogenesis. Gravid adults were isolated the day before initiation of the test.
Test type:
semi-static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
48 h
Remarks on exposure duration:
none
Post exposure observation period:
None
Hardness:
250 mg/L as CaCO3
Test temperature:
20 to 21°C
pH:
7.8 to 8.1
Dissolved oxygen:
8.7 to 9.5 mg O2/L (96 to 106% of Air Saturation Value)
Salinity:
Not applicable
Nominal and measured concentrations:
- Nominal concentrations: Control, 10, 18, 32, 56 and 100% v/v saturation solution
- Measured concentrations: See table 6.1.3/1 and 6.1.3/2 in "Any other information on results incl. tables".
Details on test conditions:
TEST SYSTEM
- Test vessel: 100 mL ground glass stoppered conical flasks
- Aeration: no
- Renewal rate of test solution (frequency/flow rate): daily renewal of the test preparations
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
- No. of vessels per vehicle control (replicates): not applicable

TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Reconstituted water
- Stock Solutions:
a) CaCl2.2H2O = 11.76 g/L;
b) MgSO4.7H2O = 4.93 g/L;
c) NaHCO3 = 2.59 g/L;
d) KCl = 0.23 g/L.
- Preparation: An aliquot (25 mL) of each of solutions (a) to d)) was added to each liter (final volume) of deionized water with a conductivity of <5 μS cm-1. The reconstituted water had a pH of 7.8 ± 0.2 and was aerated until the dissolved oxygen concentration was approximately air-saturation value. The reconstituted water had an approximate theoretical total hardness of 250 mg/L as CaCO3.

OTHER TEST CONDITIONS
- Adjustment of pH: no
- Photoperiod: 16h light and 8h darkness with 20 minute dawn and dusk transition periods
- Light intensity: 638 to 663 lux

EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : Any immobilization or adverse reactions to exposure were recorded at 24 and 48 hours after the start of exposure. The criterion of effect used was that Daphnia were considered to be immobilized if they were unable to swim for approximately 15 seconds after gentle agitation.

TEST CONCENTRATIONS
- Range finding study: yes (0.10, 1.0, 10 and 100% v/v saturation solution).
- Results used to determine the conditions for the definitive study: No immobilization was observed at the test concentrations of 0.10, 1.0 and 10% v/v saturated solution. However, 100% immobilization was observed at 100% v/v saturated solution. Based on this information test concentrations of 10, 18, 32, 56 and 100% v/v saturated solution were selected for the definitive test. Chemical analysis of the 10 and 100% v/v saturated solution test preparations at 0 hours showed measured test concentrations of 3.0 and 27 mg/L respectively were obtained. A decline in measured test concentration was observed at 48 hours to 1.9 and 19 mg/L for the 10 and 100% v/v saturated solution test preparations respectively. These results indicated that the test item was possibly unstable under test conditions and therefore it was considered appropriate to perform the definitive test using semi-static conditions in order to try and maintain near nominal test concentrations.
Reference substance (positive control):
yes
Remarks:
Potassium dichromate
Key result
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
5.3 mg/L
Nominal / measured:
meas. (arithm. mean)
Conc. based on:
test mat.
Basis for effect:
mobility
Remarks on result:
other: 95% CL: 4.8-6.5 mg/L
Duration:
48 h
Dose descriptor:
other: The highest concentration without observed effect
Effect conc.:
3.7 mg/L
Nominal / measured:
meas. (arithm. mean)
Conc. based on:
test mat.
Basis for effect:
mobility
Details on results:
See table 6.1.3/3 in "Any other information on results incl. tables".
- Behavioural abnormalities: not reported
- Observations on body length and weight: not reported
- Other biological observations: not reported
- Mortality of control: none (0%)
- Other adverse effects control: none
- Abnormal responses: not reported
- Any observations (e.g. precipitation) that might cause a difference between measured and nominal values: none
- Effect concentrations exceeding solubility of substance in test medium: No. Throughout the duration of the test all control and test preparations were observed to be clear colorless solutions.
Results with reference substance (positive control):
- Results with reference substance valid? yes
- 24h EC50 = 0.75 mg/L (95% CL: 0.56-1.0 mg/L); 24h NOEC = 0.56 mg/L.
- 48h EC50 = 0.45 mg/L (95% CL: 0.42-0.48 mg/L); 48h NOEC = 0.32 mg/L.
Reported statistics and error estimates:
The slope and the standard error of the response curve at 48 hours was 12 (SE = 3.3).

Table 6.1.3/1: Measured concentrations during the test

Time point (hours)

Nominal concentrations (% v/v saturation solution)

Measured concentrations (mg/L)

% to initial concentrations

0 - fresh

Control

10

18

32

56

100

<LOQ

4.85

5.02

9.21

15.3

29.3

-

24 - old

Control

10

18

32

56

100

<LOQ

3.83

4.19

7.83

14.0

27.1

-

79

83

85

92

92

24 - fresh

Control

10

18

32

<LOQ

3.17

5.19

8.92

-

-

-

-

48 - old

Control

10

18

32

<LOQ

2.79

4.57

8.98

-

88

88

101

Table 6.1.3/2: Mean measured concentrations

Nominal concentrations (% v/v saturation solution)

Mean measured concentrations (mg/L)

Control

10

18

32

56

100

<LOQ

3.7

4.7

8.7

15

28

Table 6.1.3/3: Cumulative immobilization data in the definitive test

Mean measured concentrations (mg/L)

Cumulative immobilized Daphnia (initial population: 5 per replicate)

24 hours

48 hours

R1

R2

R3

R4

Total

%

R1

R2

R3

R4

Total

%

Control

0

0

0

0

0

0

0

0

0

0

0

0

3.7

0

0

0

0

0

0

0

0

1

0

1*

5

4.7

0

2

0

0

2

10

0

2

2

1

5

25

8.7

4

4

3

3

14

70

5

5

5

5

20

100

15

5

5

5

5

20

100

5

5

5

5

20

100

28

5

5

5

5

20

100

5

5

5

5

20

100

* Single immobilized daphnid considered to be due to natural causes rather than a true toxic effect given that less than 10% immobilization occurred.

Validity criteria fulfilled:
yes
Conclusions:
The 48h-EC50 based on mean measured test concentrations was 5.3 mg/L (95% confidence limits: 4.8 – 6.5 mg/L). This value is greater than the real water solubility value.
Executive summary:

This study was performed, according to OECD Guideline 202 and EU Method C.2 with GLP statement, to assess the acute toxicity of the substance to Daphnia magna.

Pre-study solubility work conducted indicated that it was not possible to obtain a testable solution of the test item using traditional methods of preparation e.g. ultrasonication and high shear mixing.

A pre-study media preparation trial indicated that a dissolved test item concentration of approximately 32 mg/L was obtained from a saturated solution method of preparation indicating this to be the limit of water solubility of this item under test conditions.

Following a preliminary range-finding tests, twenty daphnids (4 replicates of 5 animals) were exposed to an aqueous solution of the substance at mean measured concentrations of 3.7, 4.7, 8.7, 15 and 28 mg/L for 48 hours at a temperature of 20 °C to 21 °C under semi-static test conditions. The test item solution was prepared by stirring an excess (100 mg/L) of test item in test medium using a propeller stirrer at approximately 1500 rpm for 24 hours. After the stirring period any undissolved test item was removed by filtration (0.2 μm Sartorius Sartopore filter, first approximate 2 liters discarded in order to pre-condition the filter) to produce a 100% v/v saturated solution of the test item with a mean measured concentration of 28 mg/L. A series of dilutions was made from this saturated solution to further give test concentrations of 56, 32, 18 and 10% v/v saturated solution (equivalent to mean measured test concentrations of 15, 8.7, 4.7 and 3.7 mg/L). The number of immobilized Daphnia were recorded after 24 and 48 hours.

Due to the potentially volatile nature of the substance, the test was conducted in completely filled and sealed test vessels.

Exposure of Daphnia magna to the substance gave a 48-Hour EC50 value based on the mean measured test concentrations of 5.3 mg/L (95% confidence limits: 4.8 – 6.5 mg/L). The highest concentration without observed effect was 3.7 mg/L.

Even if all validity criteria were fulfilled, this study is not realiable due to significant methodological deficiencies (tested concentrations greater than the water solubility value). The measured concentration of the 100% v/v saturated solution used to prepare the different test concentrations was determined at 28 mg/L, which is well greater than the real water solubility value. The saturated solution was prepared by dispersing an amount of test substance is reconstituted water with the aid of propeller stirring for 24 hours. After 24 hours, the stirring was stopped and any undissolved test substance was removed by filtration to give the saturated solution. An hypothesis of this high measured concentration (28 mg/L) whould be that 24 hours of stirring is not sufficient to dissolve this test substance and even if clear colorless solutions were reported, stable emulsions are suspected to be formed, which can explain possible physical effects.

Endpoint:
short-term toxicity to aquatic invertebrates
Type of information:
(Q)SAR
Adequacy of study:
key study
Study period:
From March 20th, 2020 to March 23rd, 2020
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
results derived from a valid (Q)SAR model and falling into its applicability domain, with adequate and reliable documentation / justification
Justification for type of information:
1. SOFTWARE
iSafeRat® HA-QSAR toolbox v2.5

2. MODEL (incl. version number)
iSafeRat® daphEC50 v1.9

3. SMILES OR OTHER IDENTIFIERS USED AS INPUT FOR THE MODEL
CC(=O)O[C@@H]1CC[C@@H](CC1)C(C)(C)C
Input for the prediction: Subcooled Liquid Water Solubility (SLWS) of the test item. For liquids at 25°C, the SLWS is directly equal to the value of the Water Solubility of the test item. Water Solubility of the test item was predicted to be 4.16 mg/L or -4.678 in log10 (mol/L) at 25°C (KREATiS, 2020) using the measured log KOW value as the input. Log KOW of the test item was experimentally measured to be 4.8 at 25°C (Givaudan, 1996).

4. SCIENTIFIC VALIDITY OF THE (Q)SAR MODEL
See attached QMRF

5. APPLICABILITY DOMAIN
See attached QPRF

6. ADEQUACY OF THE RESULT
See attached QPRF
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
Deviations:
not applicable
Remarks:
QSAR model
Principles of method if other than guideline:
The purpose of this QSAR model is to accurately predict the acute toxicity to daphnids as would be expected in a laboratory experiment following OECD Guideline 202 and EC method C.2 for specific, named mechanisms of action. The model provides an in silico prediction for the 48-hour EC50 value that can effectively be used in place of an experimentally derived 48-hour EC50 value. The regression based method used to achieve this has been fully validated following the OECD recommendations (OECD, 2004).
GLP compliance:
no
Remarks:
QSAR model
Specific details on test material used for the study:
- log KOW = 4.8 (experimental study performed on a read-across substance, Givaudan, 1996)
- Water Solubility = 4.16 mg/L (KREATiS, 2020)
- Mechanism of action: MechoA 2.1: mono-/poly-esters whose hydrolysis products are narcotics (Bauer et al., 2018)
Analytical monitoring:
no
Details on sampling:
not applicable
Vehicle:
no
Details on test solutions:
not applicable
Test organisms (species):
other: Daphnia magna, Daphnia pulex
Details on test organisms:
No difference in terms of toxic mechanism of action between invertebrate (or indeed other) aquatic species is expected. Any observed differences may be attributed to lifestyle related parameters (e.g. shell closing in molluscs) and relative duration of study versus bodysize rather than to a specific toxic mechanism causing species differences.
Test type:
other: QSAR model
Water media type:
freshwater
Limit test:
no
Total exposure duration:
48 h
Remarks on exposure duration:
Results from a test duration of 48 hours only were used for daphnid species.
Post exposure observation period:
not applicable
Hardness:
The QSAR is based on data from studies performed at acceptable hardness to ensure control survival.
Test temperature:
The temperatures varied from approximately 20 to 23 °C depending on the species used to construct the algorithm. This small difference is not expected to contribute to the variability of the EC50 values found in experimental data.
pH:
Test results were taken from studies with measured pHs between 6 - 9.
Dissolved oxygen:
The model is based on data from studies performed at acceptable oxygen concentrations (generally >60%).
Salinity:
Not applicable
Conductivity:
Not applicable
Nominal and measured concentrations:
Studies were used only where sufficient evidence was presented to determine that the substance was stable under test conditions (i.e. maintained within ± 20 % of the nominal) or, if not, the result was based on measured concentrations as geometric mean.
Details on test conditions:
Preferentially results from semi-static studies were used. However, substances tested using a static design were accepted (preferably accompanied by analytical measurements over the study period). For suspected volatile substances only tests performed in closed vessels were accepted unless accompanying analytical monitoring proved such a design was not necessary.
Reference substance (positive control):
no
Remarks:
QSAR model
Key result
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
4.2 mg/L
Nominal / measured:
meas. (not specified)
Conc. based on:
test mat.
Basis for effect:
mobility
Remarks on result:
other: 95%CL: 3.2 - 5.5 mg/L
Remarks:
The toxicity value is greater than the limit of solubility within the exposure period of the test.
Details on results:
The test item falls within the applicability domain of the model and can therefore be considered as a reliable prediction for ACUTE TOXICITY TO DAPHNIDS (48-HOUR EC50). Therefore, this endpoint value can be considered valid for use in risk assessment and classification and labelling.
The 48h-EC50 of the test item to daphnids was predicted as 4.2 mg/L. Therefore, the toxicity value is greater than the limit of solubility within the exposure period of the test.
Results with reference substance (positive control):
not applicable
Reported statistics and error estimates:
95% confidence interval (α = 0.05): 3.2 - 5.5 mg/L.
QSAR statistical parameters are given in the QMRF and the QPRF

Applicability Domain of the model

Descriptor domain:

The Subcooled Liquid Water Solubility value (4.16 mg/L or -4.678 in log10 (mol/L)) given as the input to the iSafeRat® daphEC50 model falls within the descriptor domain of the model between a Subcooled Liquid Water Solubility of -4.79 to 0.93 in log10 (mol/L).

Structural fragment domain:

All chemical groups within the molecular structure are taken into account by the model.

Mechanistic domain:

Currently, the ecotoxicity module of the iSafeRat® Holistic HA-QSAR can reliably predict the aquatic toxicity for chemicals with the following mechanisms of action of toxicity (MechoA):

• non-polar narcosis (MechoA 1.1)

• polar narcosis of alkyl-/alkoxy-phenols (MechoA 1.2)

• polar narcosis of aliphatic amines (MechoA 1.2)

• cationic narcosis of quaternary ammoniums (MechoA 1.3)

• mono-/poly-esters whose hydrolysis products are narcotics (MechoA 2.1)

• hard electrophile reactivity (MechoA 3.1)

• RedOx cycling of primary thiols (MechoA 4.4)

• Proton release of carboxylic acids (MechoA 5.2)

The MechoA of molecules is predicted directly from the structure. The test item as an ester is expected to exert a MechoA 2.1 and can be taken into account by the model (Bauer et al., 2018).

See QMRF in "attached background material".

Validity criteria fulfilled:
yes
Conclusions:
The test item falls within the applicability domain of the model and was therefore reliably predicted for its acute toxicity (48h-EC50) to daphnids. Therefore, this endpoint value can be considered valid for use in risk assessment and classification and labelling.
The 48h-EC50 of the test item to daphnids was predicted as 4.2 mg/L. Therefore, the toxicity value is greater than the limit of solubility within the exposure period of the test.
95% confidence interval (α = 0.05): 3.2 – 5.5 mg/L.
Executive summary:

A Quantitative Structure-Activity Relationship (QSAR) model was used to calculate the acute toxicity of the test item to daphnid. This QSAR model has been validated to be compliant with the OECD recommendations for QSAR modeling (OECD, 2004a) and predicts the endpoint value which would be expected when testing the substance under experimental conditions in a laboratory following the Guideline for Testing of Chemicals No. 202, "Daphnia sp., Acute Immobilisation Test" (OECD, 2004b), referenced as Method C.2 of Commission Regulation No. 440/2008 (European Commission, 2008). The criterion predicted was the EC50 (Median Effective Concentration), a statistically derived concentration which is expected to cause immobility in 50% of test animals within a period of 48 hours.

The immobility of the daphnids was determined using a validated QSAR model for the Mechanism of Action (MechoA) in question (MechoA 2.1, i.e. mono-/poly-esters whose hydrolysis products are narcotics) (Bauer et al., 2018). The QSAR model is based on validated data for a training set of 41 chemicals derived from 48-hour test on daphnids, for which the concentrations of the test item had been determined by chemical analyses over the test period.

The 48h-EC50 of the test item to daphnids was predicted as 4.2 mg/L. Therefore, the toxicity value is greater than the limit of solubility within the exposure period of the test.

95% confidence interval (α = 0.05): 3.2 – 5.5 mg/L.

Description of key information

iSafeRat® HA-QSAR toolbox v2.5, KREATiS, 2020:

48h-EC50 > solubility limit

Key value for chemical safety assessment

Additional information

One experimental study and one QSAR prediction are available to assess the short-term toxicity of the registered substance to aquatic invertebrates.

The experimental study (Harlan, 2013), performed on the registered substance according to OECD Guideline 202 and EU Method C.2 with GLP statement was considered as not reliable and was disregarded due to major methodological deficiencies. Exposure of Daphnia magna to the test substance gave a 48h-EC50 value based on the mean measured test concentrations of 5.3 mg/L (95% CL: 4.8 - 6.5 mg/L). Even if all validity criteria were fulfilled, the measured concentration of the 100% v/v saturated solution used to prepare the different test concentrations was determined at 28 mg/L, which is well greater than the real water solubility value (determined at 4.16 mg/L (KREATiS, 2020)). The saturated solution was prepared by dispersing an amount of test substance is reconstituted water with the aid of propeller stirring for 24 hours. After 24 hours, the stirring was stopped and any undissolved test substance was removed by filtration to give the saturated solution. An hypothesis of this high measured concentration (28 mg/L) whould be that 24 hours of stirring is not sufficient to dissolve this test substance and even if clear colorless solutions were reported, stable emulsions are suspected to be formed, which can explain possible physical effects at this saturated solution and other tested concentrations.

The QSAR prediction (KREATiS, 2020) was considered as reliable. The QSAR model has been validated to be compliant with the OECD recommendations for QSAR modelling (OECD, 2004) and predicts the endpoint value which would be expected when testing the substance under experimental conditions in a laboratory following OECD Guideline 202.The immobility of the daphnids was determined using a validated QSAR model for the Mechanism of Action (MechoA) in question (MechoA 2.1, i.e. mono-/poly-esters whose hydrolysis products are narcotics) (Bauer et al., 2018). The QSAR model is based on validated data for a training set of 41 chemicals derived from 48 -hour test on daphnids, for which the concentrations of the test item had been determined by chemical analyses over the test period. The test item falls within the applicability domain of the model and was therefore reliably predicted for its acute toxicity (48h-EC50) to daphnids. Therefore, this endpoint value can be considered valid for use in risk assessment and classification and labelling.

The 48-h EC50 of the registered substance to daphnids was predicted at 4.2 mg/L (95% CI: 3.2 - 5.5 mg/L). The toxicity value is greater than the limit of solubility (determined at 4.16 mg/L) within the exposure period of the test.