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Diss Factsheets
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EC number: 701-122-3 | CAS number: 106185-75-5
- 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
Long-term toxicity to fish
Administrative data
Link to relevant study record(s)
- Endpoint:
- fish early-life stage toxicity
- Type of information:
- (Q)SAR
- Adequacy of study:
- key study
- Study period:
- 7 October 2015 to 15 October 2015
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- accepted calculation method
- Remarks:
- Value obtained by QSAR method.
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 210 (Fish, Early-Life Stage Toxicity Test)
- Principles of method if other than guideline:
- The chronic toxicity to fish was determined using a validated QSAR for the Mode of Action in question, (MOA 1, non-polar narcosis). Use of this MOA for unsaturated alcohols has previously been demonstrated as acceptable in a position paper (Bauer et al., 2015) (2). The QSAR is based on validated data for a training set of 26 chemicals derived from 14 to 32-day 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
- Analytical monitoring:
- no
- Details on sampling:
- Not applicable
- Vehicle:
- no
- Details on test solutions:
- Not applicable
- Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- Also applicale: Pimephales promelas, Oryzias latipes, Leuciscus idus, Jordanella floridae, Cyprinus carpio
- Test type:
- other: Flow-through, semi-static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 28 d
- Remarks on exposure duration:
- median duration: 14 to 32 days
- 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 QSAR is based on data from studies performed between 21 and 27°C depending on species used.
- pH:
- The QSAR is based on data from studies performed between 6.0 and 8.5.
- Dissolved oxygen:
- The QSAR is based on data from studies performed at acceptable oxygen concentrations (generally >60%).
- Salinity:
- Not applicable
- Conductivity:
- Not applicable
- Nominal and measured concentrations:
- The QSAR is based on data from studies performed using measured concentrations or with acceptable stability.
- Details on test conditions:
- Not applicable
- Reference substance (positive control):
- not required
- Remarks:
- QSAR
- Key result
- Duration:
- 28 d
- Dose descriptor:
- NOEC
- Effect conc.:
- ca. 0.23 mg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- reproduction
- Remarks:
- or growth
- Remarks on result:
- other: 95%CL: 0.17-0.31
- Details on results:
- Not applicable
- Results with reference substance (positive control):
- Not applicable
- Reported statistics and error estimates:
- 95% confidence interval: 0.17 - 0.31 mg/L
Qsar statitical parameters are given in the QPRF - Validity criteria fulfilled:
- yes
- Remarks:
- The substance falls into applicability domains of the QSAR model.
- Conclusions:
- The 28d-NOEC value based on measured concentrations has been calculated as 0.23 mg/L.
95%CL: 0.17-0.31 mg/L - Executive summary:
A QSAR prediction was performed to assess the chronic toxicity of the test item to fish. This QSAR 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 Guideline for Testing of Chemicals No. 210, "Fish, Early-life Stage Toxicity Test" (1). The criterion predicted was the NOEC (No Observed Effect Concentration), a tested concentration which is observed to cause no effect on growth or reproducibility within a period of 28 days. The chronic toxicity to fish of the test item has been investigated using a QSAR model that predicts fish lethality in an OECD 210 study. The test item falls within the applicability domain of the model as demonstrated in the QPRF. The 28d-NOEC = 0.23 mg test item/L with 95%-Confidence Limit of 0.17 -0.31 mg test item/L. This toxicity study is acceptable and can be used for that endpoint.
Results Synopsis
Test Type: QSAR model
NOEC: 0.23 mg test material/L
95%-C.I.: 0.17 to 0.31 mg test material/L
Reference
No data
Description of key information
The 28d-NOEC has been calculated as 0.23 mg/L using a valid QSAR.
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Effect concentration:
- 0.23 mg/L
Additional information
One QSAR data is available to determine the long-term toxicity to fish.
A QSAR prediction was performed to assess the chronic toxicity of the test item 2-ethyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-(2E)-buten-1-ol to fish. This QSAR 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 Guideline for Testing of Chemicals No. 210, "Fish, Early-life Stage Toxicity Test" (1). The criterion predicted was the NOEC (No Observed Effect Concentration), a tested concentration which is observed to cause no effect on growth or reproducibility within a period of 28 days. The chronic toxicity to fish of 2-ethyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-en-1-ol has been investigated using a QSAR model that predicts fish lethality in an OECD 210 study. 2-ethyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-en-1-ol, falls within the applicability domain of the model as demonstrated in the QPRF. The 28d-NOEC = 0.23 mg test item/L with 95%-Confidence Limit of 0.17 -0.31 mg test item/L. This toxicity study is acceptable and can be used for that endpoint.
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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