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EC number: 201-901-3 | CAS number: 89-36-1
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- 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
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data

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
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: According to OECD 202 and GLP
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 010
- Report date:
- 2010
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- 4-(3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-1-yl)benzene-1-sulfonic acid
- EC Number:
- 201-901-3
- Cas Number:
- 89-36-1
- Molecular formula:
- C10H10N2O4S
- IUPAC Name:
- 4-(3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-1-yl)benzene-1-sulfonic acid
Constituent 1
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: 25.0 - 50.0 - 100 - 200 - 400 mg/L
- Sampling method: All concentration levels, the pH control and the control after 0 h (fresh media) and 48 h (old media) were analytically verified via HPLC. For the old media, separate replicates without test organisms were prepared and incubated under test conditions.
- Sample storage conditions before analysis:All samples were stored at 6 ± 2 °C until start of analysis if necessary.
Test solutions
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: A stock solution (400 mg/L) was freshly prepared, dispersion treatment was agitation.
- Eluate: Dilution water
- Differential loading: 25.0 - 50.0 - 100 - 200 - 400 mg/L
- Controls: Dilution water without test item tested under the same conditions as the test groups
Test organisms
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: Daphnia magna (STRAUS)
- Strain: Clone 5
- Source: Institut für Wasser-, Boden- Lufthygiene (WaBoLu), further own breeding
- Age at study initiation (mean and range, SD): 2 to 24 h
- Method of breeding: In 2-3 L glass vessels with appr. 1.8 L culture medium, at 20 +/- 2 °C, in an incubator, 16 h illumination, illumination strength max. 20 µExm-2 x s-1
- Feeding during test: No feeding
ACCLIMATION
- Acclimation period: 2 h
- Acclimation conditions (same as test or not): Same as test
- Type and amount of food: No feeding
- Health during acclimation (any mortality observed): Healthy, no mortality observed
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Post exposure observation period:
- No
Test conditions
- Hardness:
- Dilution water at test start: 274 (mg CaCO3/L)
- Test temperature:
- 21.8 °C
- pH:
- Water Quality Parameters at Test Start (0 hours, Fresh Media)
(measured in one additional replicate per concentration level, pH control and control)
Nominal
test item
concentration
mg/L] pH-Value
400 (pH-control)* 7.14
400 3.47
200 4.89
100 6.47
50.0 6.88
25.0 7.11
Control 7.77
Water Quality Parameters at Test End (48 hours, Old Media)
(measured in all replicates)
Nominal
test item
concentration
[mg/L] pH-Values
Replicates
1 2 3 4
400 (pH-control)* 7.03 7.11 7.06 7.13
400 3.38 3.36 3.29 3.29
200 5.51 5.33 5.49 5.88
100 7.20 6.95 6.92 6.89
50.0 7.27 7.14 7.21 7.21
25.0 7.38 7.35 7.31 7.30
Control 7.34 7.34 7.50 7.48 - Dissolved oxygen:
- Water Quality Parameters at Test Start (0 hours, Fresh Media)
(measured in one additional replicate per concentration level, pH control and control)
Nominal
test item
concentration
mg/L] O2-Concentration
[mg/L]
400 (pH-control)* 7.87
400 7.84
200 7.93
100 7.95
50.0 7.97
25.0 8.04
Control 8.16
Water Quality Parameters at Test End (48 hours, Old Media)
(measured in all replicates)
Nominal
test item
concentration
[mg/L] O2 -Concentration [mg/L]
Replicates
1 2 3 4
400 (pH-control)* 6.45 6.93 7.07 7.12
400 8.03 8.09 7.99 7.97
200 7.72 7.80 7.65 6.53
100 7.69 7.52 7.82 7.62
50.0 7.75 7.69 7.70 7.72
25.0 7.84 7.80 7.78 7.69
Control 7.93 8.01 8.00 7.93 - Salinity:
- Freshwater
- Nominal and measured concentrations:
- Concentrations and Recovery Rates of the Test Item Pyrazolsäure-4, trocken
Sampling date 2009-08-11
Test start (0 h) 2009-08-13
Test end (48 h)
Start of analysis 2009-08-11 2009-08-13
Pyrazolsäure-4, trocken
Nominal
test item
concentration
[mg/L] Measured
concentration1)
[mg/L] RR
[%] Measured
concentration1)
[mg/L] RR
[%]
400 (pH-control)* 399 100 381 95
400 400 100 407 102
200 205 103 205 103
100 99.4 99 97.7 98
50.0 49.6 99 42.9 86
25.0 24.8 99 16.22) 65
Control < LOQ -- < LOQ -- - Details on test conditions:
- TEST SYSTEM
- Test vessel: Glass beakers, 50 mL
- Type (delete if not applicable): closed with parafilm
- Material, size, headspace, fill volume: Glass beakers (4 cm ID x 7 cm H), 50 mL
- Aeration: No
- Renewal rate of test solution (frequency/flow rate): One application at test start, static test
- 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): None
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Acc. to Directive 92/69/EEC Method C.2, Annex 1
- Conductivity: Dilution water at test start: 640 µS/cm
- Culture medium different from test medium: Elendt M4 acc. to ELENDT (1990), modified to a total hardness of 160 to 180 mg CaCO3/L
- Intervals of water quality measurement: At test start and test end
OTHER TEST CONDITIONS
- Adjustment of pH: No
- Photoperiod: 16:8 light:dark cycle
- Light intensity: Diffuse light, illumination strength max. 20 µE x m-2 x s-1
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
TEST CONCENTRATIONS
- Range finding study
Immobilization Rates of the Preliminary Range Finding Test
(n = 20, divided into 2 replicates with 10 daphnids each)
Nominal
Test Item
Concentration
[mg/L] IMMOBILIZATION [%]
24 h 48 h
Replicates Replicates
1 2 MV 1 2 MV
800 100 100 100 100 100 100
400 100 100 100 100 100 100
50 0 0 0 0 0 0
Control 0 0 0 0 0 0
800 (pH-control)* 30 30 30 100 100 100
- Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate
Results and discussion
Effect concentrations
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 141 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: (100 - 200)
- Details on results:
- - Behavioural abnormalities: None
- Mortality of control: 0%
- Other adverse effects control: None
- Abnormal responses: None
- Any observations (e.g. precipitation) that might cause a difference between measured and nominal values: None - Results with reference substance (positive control):
- - Results with reference substance valid? Yes
- EC50/LC50: 1.50 (CI 1.39 - 1.63) mg/L - Reported statistics and error estimates:
- The EC10-values after 24 and 48 h, the EC50-value after 24 h and the EC50 for the of the reference test were calculated by sigmoidal dose -response regression. The confidence intervals for the EC50-values were calculated from the best-fit values, the standard error and the t-distribution with the software GraphPad prism.
Since only 0 % and 100 % immobilization occurred after 48 h, the EC50-value was determined by calculating the geometric mean of the highest concentration causing no immobilization and the lowest concentration causing 100 % immobilization. As confidence limits for the EC50 the highest concentration causing no immobility and the lowest concentration causing 100 % immobility were used, because only 0% and 100 % mortality occurred within the tested concentration range.
Any other information on results incl. tables
Percentage of Daphnids Incapable of Swimming after 24 and 48 h of Exposure
(n = 20, divided into 4 replicates with 5 daphnids each)
pyrazolic acid 4 |
IMMOBILIZATION [%] |
|||||||||
Nominal Test Item Concentration |
24 h |
48 h |
||||||||
Replicates |
Replicates |
|||||||||
[mg/L] |
1. |
2. |
3. |
4. |
MV |
1. |
2. |
3. |
4. |
MV |
400 (pH-control)* |
60 |
40 |
20 |
20 |
35 |
100 |
60 |
100 |
80 |
85 |
400 |
100 |
100 |
100 |
100 |
100 |
100 |
100 |
100 |
100 |
100 |
200 |
40 |
100 |
80 |
80 |
75 |
100 |
100 |
100 |
100 |
100 |
100 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
50.0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
25.0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
Control |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- In this study the test substance was found to be toxic to Daphnia magna after 48 h at concentrations of 200 mg/L (LOEC48 h) and higher. The NOEC after 48 hours was 100 mg/L. The EC50 (48 h) was determined to be 141 mg/L (CI: 100 - 200 mg/L). All effect values given are based on the nominal concentrations of the test item
- Executive summary:
In the acute immobilization test with Daphnia magna (STRAUS) the effects of the test item were determined according to OECD 202 (2004).
The study was conducted under static conditions with 5test item concentration levels ranging from 25.0 to 400 mg/L set up in a geometrical series with a dilution factor of 2over a period of 48 hours. 20 test organisms were exposed to each test concentration and the control.
All concentration levels and the control were analysed via HPLC after 0 h and 48 h.
The recoveries were in the range of 98 to 103 % of the nominal values at the biologically relevant test item concentrations of 100 to 400 mg/L, demonstrating that concentrations of the test substance were successfully maintained for the duration of the test. All effect values given are based on the nominal concentrations of the test item (Table 1).
The water quality parameters (pH-value and dissolved oxygen concentration), measured at 0 h and 48 h, were determined to be within the acceptable limits. The validity criteria of the test guideline were fulfilled.Table 1: EC10-, EC50- (with Confidence Interval), EC100 - Values, NOEC and LOEC
(based on the nominal concentrations of the test item)
Test Duration
[h]Nominal
Concentration of the Test Item
pyrazolic acid 4
[mg/L]Confidence Interval
p = 95%
[mg/L]EC10
24
162
---
48
127
---
EC50
24
187
178 – 196
48
141
100 – 200
EC100
24
400
---
48
200
---
NOEC
48
100
---
LOEC
48
200
---
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