Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
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
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 201-956-3 | CAS number: 89-98-5
- 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
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:
- 1986-08-05 - 1986-08-06
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: well performed study with some limitations in the experimental design (e.g. exposure period was 24h only)documentation (e.g oxygen concentrations in the vessels were not reported)
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- yes
- Remarks:
- Test duration 24h
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- ISO 6341 (Water quality - Determination of the Inhibition of the Mobility of Daphnia magna Straus (Cladocera, Crustacea))
- Deviations:
- yes
- Remarks:
- Test duration 24h
- Principles of method if other than guideline:
- The reevaluation/validation of older data from Hoechst (Report date 2008-09-04) is based on the raw data from 6.1.3/Hoechst_1986-08-27/W86-254. The test was performed according to DIN 38412, Part 11, a method related to OECD guideline 202 (I) but with a test duration of only 24 instead of 48 hours.
- GLP compliance:
- no
- Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- -Stock solution: saturated solution prepared by stirring a batch in water at room temperature and filtrating it through a folded paper filter;
- Concentration of stock solution: 630 mg DOC/L, correspoinding to 1053.3 mg/l 2-Chlorobenzaldehyde; - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Strain: Daphnia magna Straus
- Source: own laboratory breed
- Age at study initiation (mean and range, SD): >3h < 24h
- Method of breeding: Adult animals were cultivated in glass vessels (volume: 4 litres). The medium was changed once a week. Twice daily the animals were fed with algae (Scenedesmus supspicatus).
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 24 h
- Test temperature:
- 21°C
- pH:
- Measured in additional test vessels of each test concentration
- Dissolved oxygen:
- Measured in additional test vessels of each test concentration
- Nominal and measured concentrations:
- Nominal concentrations: Dilution of the stock solution with 630 mg DOC/L, correspoinding to 1053.3 mg/l 2-Chlorobenzaldehyde
1:20 corresponding to 53 mg/L test substance;
1:25 corresponding to 42 mg/L test substance;
1:35 corresponding to 30 mg/L test substance;
1:44 corresponding to 24 mg/L test substance;
1:50 corresponding to 21 mg/L test substance; - Details on test conditions:
- TEST SYSTEM
- Test vessel: 100 ml glass vessels;
- Test volume: 50 ml;
- No. of organisms per vessel: 10
- No. of vessels per concentration (replicates): 2
- No. of vessels per control (replicates): 4
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Synthetic water according to DIN 38 412 Part 11
- Culture medium identical to test medium;
OTHER TEST CONDITIONS
- Photoperiod: 24h dark
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : Immobilization after 24h
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 1.25 - Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate
- Duration:
- 24 h
- Dose descriptor:
- EC0
- Effect conc.:
- 21 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 24 h
- Dose descriptor:
- EC10
- Effect conc.:
- 24 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Key result
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 30 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 24 h
- Dose descriptor:
- EC100
- Effect conc.:
- 53 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Results with reference substance (positive control):
- After 24 hours the EC50 of potassium dichromate was between 0.9 mg/l to 1.9 mg/l which is in line with the range of 0.6 mg/l and 2.1 mg/l as required by OECD 2002 (2004).
- Reported statistics and error estimates:
- The EC0/EC10, EC50 and EC90/EC100 values were estimated graphically in a plot on the probability net.
- Validity criteria fulfilled:
- yes
- Conclusions:
- With the indicated test data the EC50 of 2-Chlorobenzaldehyde to Daphnia magna under the conditions of the test was estimated to be 30 mg/l. No immobilization was observed at the lowest test concentration of 21 mg/l.
- Executive summary:
A toxicity test for 2 -Chlorobenzaldehyde with Daphnia magna Straus was performed close to OECD-guideline 202, albeit with 24h instead of 48h duration. The application of a reference substance (potassium dichromate) resulted in 24h EC50 between 0.9 and 1.9 mg/L, which is in line with the range of 0.6 mg/L and 2.1 mg/L as required by OECD guideline 202 (2004). Not more than 10 % of the daphnids of the control had been immobilized (mean of 4 controls 0% immobilization after 24h) and the dissolved oxygen had been measured albeit data are not recorded. With the indicated test data the EC50 of 2-Chlorobenzaldehyde (tested batch) to Daphnia magna under the conditions of the test was estimated to be 30 mg/l. No immobilization was observed at the lowest test concentration of 21 mg/l.
Reference
Table 1: Immobilization rates of Daphnia magna exposed to 2-Chlorobenzaldehyde over a period of 24 hours
Dilution of |
Replicate |
Number |
Number of 24 h |
Percentage of |
Mean 24 h |
Control |
1 |
10 |
0 |
0 |
0 |
2 |
10 |
0 |
0 |
||
3 |
10 |
0 |
0 |
||
4 |
10 |
0 |
0 |
||
01:20 |
1 |
10 |
10 |
100 |
100 |
2 |
10 |
10 |
100 |
||
01:25 |
1 |
10 |
9 |
90 |
95 |
2 |
10 |
10 |
100 |
||
01:30 |
1 |
10 |
8 |
80 |
75 |
2 |
10 |
7 |
70 |
||
01:40 |
1 |
10 |
5 |
50 |
40 |
2 |
10 |
3 |
30 |
||
01:50 |
1 |
10 |
0 |
0 |
0 |
2 |
10 |
0 |
0 |
Table 2: Number and percentage of immobilization of Daphnia magna after 24 hours exposed to the reference substance Potassium dichromate
Nominal |
Replicate |
Number |
Number of |
Percentage of |
Mean |
0.9 |
1 |
10 |
3 |
30 |
30 |
|
2 |
10 |
3 |
30 |
|
1.9 |
1 |
10 |
8 |
80 |
75 |
|
2 |
10 |
7 |
70 |
−After 24 hours the EC50 of potassium dichromate was between 0.9 mg/l to 1.9 mg/l which is in line with the range of 0.6 mg/l and 2.1 mg/l as required by OECD 2002 (2004).
−The percentage of immobilized daphnids in the control was below 10%.
−Incubation time was only 24 hours, not 48 hours as required by OECD 2002 (2004).
The EC0/EC10, EC50 and EC90/EC100 values were estimated graphically in a plot on the probability net.
Results-Table 3: ECx values for the immobilization rate of Daphnia magna exposed to 2-Chlorobenzaldehyde over a period of 24 hours
Effect |
24 h, Dilution of the |
24 h, mg DOC/l |
24 h, mg/l |
EC0 |
01:50 |
12.6 |
21 |
EC10 |
01:44 |
14.3 |
24 |
EC50 |
01:35 |
18.0 |
30 |
EC90 |
01:25 |
25.2 |
42 |
EC100 |
01:20 |
31.5 |
53 |
Description of key information
Test organism: Daphnia magna;
Test guideline: close to OECD 202;
Test duration: 24h;
EC50 Daphnia 30 mg/L
Endpoint: immobilization;
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 30 mg/L
Additional information
The reliable (with restrictions, RL 2) experimental key study was performed close to guideline OECD 202. The test duration however is only 24h (according to OECD 202 part I (1984)) insead of 48 h. The validity criteria are fulfilled and a reference substance (potassium dichromate) confirms the reliability of the study. The values for acute toxicity of 2 -Chlorobenzaldehyde on Daphnia magna are
EC0 = 21 mg/L
EC10 = 24 mg/L
EC50 = 30 mg/L.
No other experimental studies are available. QSAR results are not assignable due to the missing information on validation criteria. The result from the Danish EPA QSAR Database is 39 mg/L and based on the MULTICASE ACUTE AQUATIC TOXICITY model for which substance and organism are confirmed to be inside the model domain. This is very close to the experimental result.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.