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EC number: 618-233-7 | CAS number: 890707-28-5
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
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- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
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- Solubility in organic solvents / fat solubility
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- Flash point
- Auto flammability
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- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
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- Nanomaterial crystallite and grain size
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- Nanomaterial specific surface area
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- Endpoint summary
- Stability
- Biodegradation
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- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
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- Specific investigations
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- Additional toxicological data

Short-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 16 March 2020 to 6 April 2020
- 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)
- Version / remarks:
- 2004
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- Test item: 2-Amino-5-Chloro-N,3-Dimethylbenzamide (M198)
Batch: 628-042-00
CAS number: [890707-28-5]
Test item content: 983.7 ± 2.8 g/kg
Analysis date: 16 October 2019
Expiry date: 16 October 2021
Supplier: ADAMA Makhteshim Ltd.
Appearance: Beige powder
Packaging: White opaque plastic bag
Quantity: received 1 kg
Date of receipt: 12 November 2019
Storage: In darkness at room temperature - Analytical monitoring:
- yes
- Details on sampling:
- Concentration/control:
A semi-static concentration-response test was conducted at 6.25 - 12.50 - 25.00 - 50.00 - 100.00 mg/L of test item in ISO medium containing 0.01 % of the solvent DMSO, plus two untreated control groups (with and without solvent).
Sampling method:
20 daphnids, divided in 4 replicates of 5 daphnids, were used for each group.
The test organisms were exposed to the test solutions for 48 hours, with renewal of the test solutions after 24 hours. The number of mobile and immobile daphnids was counted at 24 and 48 hours after the beginning of the test.
Sample analysis:
The samples to be analysed were collected as follows: at the start of the test from fresh test solutions (T0), at the renewal from the freshly prepared and the spent test solutions (T24), as well as at the end of the test from the spent test solutions (T48); the spent samples were taken after the pooling of the replicates. The samples were stored deep-frozen at ≤ -18°C prior to analysis. Analysis was performed within one week after termination of the biological part of the experiment.
The samples to be analysed were collected as follows:
- 7 samples at 0 hours, from the fresh solutions: 2 untreated controls, 5 concentrations of test item;
- 7 samples at 24 hours, from the aged solutions: 2 untreated controls, 5 concentrations of test item;
- 7 samples at 24 hours, from the fresh solutions: 2 untreated controls, 5 concentrations of test item;
- 7 samples at 48 hours, from the aged solutions: 2 untreated controls, 5 concentrations of test item.
The samples were diluted to the calibration range with Diluent before the analysis.
Each sample was measured by double injection and the content of active ingredient in the test samples was calculated on the basis of the calibration curve equation obtained in the same chromatographic session. - Vehicle:
- no
- Details on test solutions:
- All stock and test solutions were prepared in ISO medium containing 100 μL/L solvent (DMSO, 0.01%).
At the start of the test, a stock solution of 100 mg test item/L was prepared as follows: 100.0 mg test item were added to a 1 L volumetric flask containing test medium. C1: 6.25 Nominal test item concentration [mg/L] ; C2: 12.50 Nominal test item concentration [mg/L]; C3: 25.00 Nominal test item concentration [mg/L]; C4: 50.00 Nominal test item concentration [mg/L]; C5: 100.00 Nominal test item concentration [mg/L] - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
Species: Daphnia magna
- code of the culture: Dm 29/02/20
- Age: < 24 hours old
- Diet: No feeding during the test
- Housing (before the test): Under breeding conditions, the test organisms were fed with algae suspension (Pseudokirchneriella subcapitata) and were maintained in reconstituted water.
- pH of medium: 6 - 9
- dissolved oxygen: ≥ 3 mg/L
- maintained in thermostatic chamber at the temperature range of 20±2°C, with a photoperiod of 16 hours light and 8 hours dark. - Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Hardness:
- between 140 and 250 mg/L (as CaCO3)
- Test temperature:
- in the range of 20.0 - 20.5 °C
- pH:
- in the range of 6-9
- Dissolved oxygen:
- ≥ 3 mg/L
- Nominal and measured concentrations:
- Nominal test item concentration [mg/L]: 6.25 - 12.50 - 25.00 - 50.00 - 100.00 mg/L
- Details on test conditions:
- The test was conducted in a thermostatic chamber designed to maintain the test conditions specified in the protocol and in agreement with OECD 202 (2004). The temperature and light intensity values in the chamber were measured continuously during the test using a data-logger system.
During the exposure period, the temperature measured in the medium was in the range of 20.0 - 20.5 °C, the temperature measured in the thermostatic chamber was in the range of 19.4 - 20.3 °C, the light intensity was at maximum 862 Lux and a photoperiod of 16 hours light and 8 hours dark was applied.
Dissolved oxygen concentration and pH values were measured in the treated and untreated solutions, at the beginning and at the end of the test and at the test solutions renewal. The hardness of the medium was measured at the start of the test. The test solutions were not aerated and the daphnids have not been fed during the test.
During the test, the vessel position was modified daily and recorded in the study notebook; the vessels were positioned without a predetermined order, in order to minimise the influence of spatial differences of incubation conditions. - Reference substance (positive control):
- no
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC10
- Effect conc.:
- 54.93 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 76.5 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Key result
- Duration:
- 48 h
- Dose descriptor:
- LOEC
- Effect conc.:
- 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Key result
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 50 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- No other effects (e.g. behavioural effects, discoloration or trapping) were observed on the exposed organisms.
- Reported statistics and error estimates:
- There were no significant statistical differences between control and solvent control, therefore the treated groups were compared with the solvent control.
The assessment of the effects was based on the nominal concentrations of test item. - Validity criteria fulfilled:
- yes
- Conclusions:
- For 2-Amino-5-Chloro-N,3-Dimethylbenzamide the water hazard on Daphnia magna after 48 hours of exposure was determined with the following results:
- EC10 54.93 mg/L; EC20 61.54 mg/L; EC50 76.50 mg/L;
- Corresponding LOEC 100.00 mg/L;
- Corresponding NOEC 50.00 mg/L.
Additionally no other effects were observed on the exposed organisms.
No classification as hazardous according to EU regulation 1272/2008 (CLP) is required. - Executive summary:
The acute immobilisation test was performed, under semi-static conditions, to assess the effects of test item 2-Amino-5-Chloro-N,3-Dimethylbenzamide on Daphnia magna after 48 hours of exposure.
20 daphnids, less than 24 hours old, were exposed to 6.25 - 12.50 - 25.00 - 50.00 - 100.00 mg/L of test item in ISO medium containing 0.01 % of the solvent DMSO, plus two untreated control groups (with and without solvent).
The analytical determination of the active ingredient content showed a mean recovery of 92.15% in the fresh samples and 92.51% in the aged samples. Accordingly, the assessment of the effects was based on the nominal concentrations of the test item.
After 48 hours, the endpoints based on the test item nominal concentrations were estimated to be the following:
- EC10:54.93 mg/L; EC20:61.54 mg/L; EC50:76.50 mg/L;
- Corresponding LOEC: 100.00 mg/L;
- Corresponding NOEC: 50.00 mg/L.
No other effects were observed on the exposed organisms.
The validity criteria of OECD 202 (2004) were fulfilled.
Reference
Percent immobilisation after 24 and 48 hours of exposure of Daphnia magna to the test item:
Code |
Nominal test item conc. [mg/L] |
Number of exposed daphnids |
Response at 24 h |
Response at 48 h |
||
Number of immobilised |
%I |
Number of immobilised |
%I |
|||
CTRL |
0.00 |
20 |
0 |
0 |
0 |
0 |
CT SOLV |
0.00 |
20 |
0 |
0 |
0 |
0 |
C1 |
6.25 |
20 |
0 |
0 |
0 |
0 |
C2 |
12.50 |
20 |
0 |
0 |
0 |
0 |
C3 |
25.00 |
20 |
0 |
0 |
0 |
0 |
C4 |
50.00 |
20 |
0 |
0 |
1 |
5 |
C5 |
100.00 |
20 |
7 |
35 |
17 |
85 |
According to OECD 202 (2004), the validity criteria were evaluated: Validity criteria results of the immobilisation test with Daphnia magna:
Validity criteria |
Threshold |
Observed |
Immobilised daphnids in the untreated group, at the end of the test: |
< 10% |
0% |
Dissolved oxygen concentration at the end of the test in treated and untreated groups: |
≥ 3 mg/L |
7.51 - 7.88 mg/L |
Accordingly, all validity criteria are met.
Summary of the analytical results for fresh and aged media samples from the biological part of the study with Daphnia magna:
Code |
Nominal conc. [mg test item/L] |
Mean of measured conc. [mg test item/L] |
Mean Recovery (%) |
CTRL |
0.00 |
< LOD * |
n.d. |
CT SOLV |
0.00 |
< LOD * |
n.d. |
C1 |
6.15 |
5.56 |
90.44 |
C2 |
12.30 |
11.59 |
94.26 |
C3 |
24.59 |
21.98 |
89.38 |
C4 |
49.19 |
46.40 |
94.32 |
C5 |
98.37 |
91.71 |
93.23 |
* Parameter from the validated analytical method: LOD 0.0546 μg/L; LOQ 0.1 μg/L;
n.d. = not determinable.
The analytical determination of the content of test item in the test solutions showed recovery values within the range 80-120% of the nominal values (with a mean recovery of 92.15% in the fresh samples and 92.51% in the aged samples), therefore the data evaluation was performed using the nominal concentrations.
Effect on Daphnia magna after 48 h-exposure to the Test item, in relation to the control:
Code |
Test item concentration [mg/L] |
%I |
C1 |
6.25 |
0 |
C2 |
12.50 |
0 |
C3 |
25.00 |
0 |
C4 |
50.00 |
5 |
C5 |
100.00 |
85 + |
+ indicates a significant difference compared to the untreated control (Step-down Cochran-Armitage Test Procedure (α = 0.050; one-sided greater
Effect concentrations as calculated by Probit analysis are presented in the following table.
Effect concentrations of the Test item on Daphnia magna after 48 h exposure:
Endpoint (48 hours) |
Test item concentration [mg/L] |
Confidence limits |
|
Lower |
Upper |
||
EC10 |
54.93 |
39.76 |
64.69 |
EC20 |
61.54 |
47.64 |
71.27 |
EC50 |
76.50 |
65.03 |
88.84 |
LOEC |
100.00 |
- |
- |
NOEC |
50.00 |
- |
- |
|
Description of key information
After 48 hours, the endpoints based on the test item nominal concentrations were estimated to be the following:
- EC10:54.93 mg/L; EC20:61.54 mg/L; EC50:76.50 mg/L;
- Corresponding LOEC: 100.00 mg/L;
- Corresponding NOEC: 50.00 mg/L.
No other effects were observed on the exposed organisms.
The validity criteria of OECD 202 (2004) were fulfilled.
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 76.5 mg/L
Additional information
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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