Registration Dossier
Registration Dossier
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: 953-704-3 | CAS number: 2411191-47-2
- 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 fish
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to fish
- Type of information:
- (Q)SAR
- Adequacy of study:
- key study
- Study period:
- April 15, 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® holistic HA-QSAR v1.9
2. MODEL (incl. version number)
iSafeRat® fishLC50 v1.9
3. SMILES OR OTHER IDENTIFIERS USED AS INPUT FOR THE MODEL
CC1CC(=CCCC=O)CC1(C)C
Water solubility = 50.3 mg/L (LPL, 2020)
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 203 (Fish, Acute Toxicity Test)
- Deviations:
- not applicable
- Remarks:
- QSAR model
- Principles of method if other than guideline:
- The ACUTE TOXICITY TO FISH (96-HOUR LC50) was determined using the iSafeRat® fishLC50, a validated QSAR model for the Mechanism of Action (MechoA) in question (MechoA 3.1, i.e. hard electrophiles) (Bauer et al., 2018). The QSAR is based on validated data for a training set of 5 chemicals derived from 96-hour test on fish, for which the concentrations of the test item had been determined by chemical analyses over the test period.
- GLP compliance:
- no
- Remarks:
- Not applicable: QSAR model
- Specific details on test material used for the study:
- - Mechanism of action : MechoA 3.1: hard electrophiles (Bauer et al., 2018)
- Water solubility : 50.3 mg/L (LPL, 2020) - Analytical monitoring:
- not required
- Remarks:
- QSAR model
- Details on sampling:
- Not applicable
- Vehicle:
- no
- Details on test solutions:
- Not applicable
- Test organisms (species):
- other: Results from the following species were used in the regression: Danio rerio, Oncorhynchus mykiss, Lepomis macrochirus, Pimephales promelas, Oryzias latipes, Leuciscus idus
- Details on test organisms:
- No difference in terms of toxic mechanism of action between fish freshwater species is expected. Any observed differences may be attributed to lifestyle related parameters (e.g. relative differences in storage lipid content between species) 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:
- 96 h
- Remarks on exposure duration:
- Only results from a test duration of 96 hours were included.
- Post exposure observation period:
- Not applicable
- Hardness:
- Not applicable
- Test temperature:
- The temperatures varied from approximately 14 to 25 °C depending on the fish species used to construct the algorithm. While it is recognized that this may contribute to some extent to the variability of the LC50 values found in experimental data, KREATiS has not observed a clear trend suggesting that normalization to temperature would necessarily improve the algorithm (say for trout as opposed to warm water species like fathead minnow for example) for monoconstituents. Nevertheless, this is a recognized area for further research by KREATiS.
- pH:
- Test results were taken from studies with measured pHs between 6.0 - 8.5.
- Dissolved oxygen:
- The dissolved oxygen concentration was more than 60% of the air-saturation value throughout the duration of the test. In exceptional cases where studies with oxygen concentrations lower than 60% were used, all aspects of the study were thoroughly evaluated in order to satisfy the evaluator that the effects found were not due to reduced oxygen concentration (i.e. the study would correctly receive a Klimisch score of 2 under the REACH Regulation (REACH, 2006).
- Salinity:
- Not applicable
- Conductivity:
- Not applicable
- Nominal and measured concentrations:
- Studies were used only where sufficient evidence was presented to determine that the stubstance was stable under test conditions (i.e. maintened within ± 20 % of the nominal) or, if not, the result was based on measured concentrations as geometric mean.
- Details on test conditions:
- A variety of test designs were accepted: Preferentially results from semi-static experiments with daily renewal of test solutions and the control or from flow-through tests were used. However, for stable, low volatility substances a static design was 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):
- not required
- Remarks:
- QSAR model
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- 2.2 mg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: 95CI: [1.1 ; 4.5] mg/L
- Results with reference substance (positive control):
- Not applicable
- Reported statistics and error estimates:
- 95% confidence interval (α = 0.05): 1.1-4.5 mg/L. QSAR statistical parameters are precised in the QMRF, in the attached background material.
- Sublethal observations / clinical signs:
No additional information
- Validity criteria fulfilled:
- yes
- Remarks:
- The substance falls into the applicability domains of the QSAR model.
- Conclusions:
- The QSAR model used to achieve the study has been fully validated following the OECD recommendations (OECD, 2004). The test item falls within the applicability domain of the model and was therefore reliably predicted for its ACUTE TOXICITY TO FISH (96-HOUR LC50). Therefore, this endpoint value can be considered valid for use in risk assessment and classification and labelling.
The ACUTE TOXICITY TO FISH (96-HOUR LC50) of the test item was predicted as 2.2 mg/L.
95% confidence interval (α = 0.05): 1.1 – 4.5 mg/L. - Executive summary:
A Quantitative Structure Activity Realtionship (QSAR) model was used to calculate the ACUTE TOXICITY TO FISH (96-HOUR LC50) for the test item. This QSAR model has been validated to be compliant with the OECD recommendations for QSAR modeling (OECD, 2004) 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. 203, "Fish Acute Toxicity Test" (OECD, 2019), referenced as Method C.1 of Commission Regulation No. 440/2008 (European Commission, 2008). The criterion predicted was the LC50 (Median Lethal Concentration), a statistically derived concentration which is expected to cause mortality in 50% of test animals within a period of 96 hours.
The ACUTE TOXICITY TO FISH (96-HOUR LC50) was determined using the iSafeRat® fishLC50, a validated QSAR model for the Mechanism of Action (MechoA) in question (MechoA 3.1, i.e. hard electrophiles) (Bauer et al., 2018). The QSAR is based on validated data for a training set of 5 chemicals derived from 96-hour test on fish, 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 TO FISH (96-HOUR LC50). Therefore, this endpoint value can be considered valid for use in risk assessment and classification and labelling.
The ACUTE TOXICITY TO FISH (96-HOUR LC50) of the test item was predicted as 2.2 mg/L.
95% confidence interval (α = 0.05): 1.1 – 4.5 mg/L.
Reference
Description of key information
iSafeRat® High-Accuracy-Quantitative Structure-Activity Relationship, KREATIS, 2020 :
96h-LC50 = 2.2 mg/L (95% confidence interval: 1.1 – 4.5 mg/L)
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Effect concentration:
- 2.2 mg/L
Additional information
One QSAR prediction is available to assess the short-term toxicity of the registered substance to fish.
This QSAR prediction (KREATiS, 2020) was considered as reliable and was used as the key data. 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 203. The acute toxicity to fish (96h-LC50 value) was determined using a validated QSAR model for the Mechanism of Action (MechoA) in question (MechoA 3.1, i.e. hard electrophiles) (Bauer et al., 2018). The QSAR model is based on validated data for a training set of 5 chemicals derived from 96 -hour test on fish, 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 to fish. Therefore, this endpoint value can be considered valid for use in risk assessment and classification and labelling.
The 96h-LC50 of the registered substance to fish was predicted at 2.2 mg/L (95% CI: 1.1 - 4.5 mg/L).
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.

EU Privacy Disclaimer
This website uses cookies to ensure you get the best experience on our websites.