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EC number: 242-359-8 | CAS number: 18479-51-1
- 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
- Study period:
- 04/05/2000 - 03/08/2000
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Study according to international guideline (ISO Standard 6341) under GLP, validity criteria met.
Cross-referenceopen allclose all
- Reason / purpose for cross-reference:
- reference to same study
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 000
- Report date:
- 2000
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- ISO 6341 (Water quality - Determination of the Inhibition of the Mobility of Daphnia magna Straus (Cladocera, Crustacea))
- Deviations:
- yes
- Remarks:
- protected from light
- Principles of method if other than guideline:
- Not relevant
- GLP compliance:
- yes
- Remarks:
- Statement of Compliance
Test material
- Reference substance name:
- 3,7-dimethyloct-1-en-3-ol
- EC Number:
- 242-358-2
- EC Name:
- 3,7-dimethyloct-1-en-3-ol
- Cas Number:
- 18479-49-7
- Molecular formula:
- C10H20O
- IUPAC Name:
- 3,7-dimethyloct-6-en-3-ol
- Details on test material:
- - Name of test material (as cited in study report): Dihydrolinalool
- Physical state: Liquid
- Storage condition of test material: In refrigerator, protected from light
Constituent 1
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material (migrated information):
Not relevant
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: Nominal: 5.6, 10, 18, 32 and 56 mg/l
- Sampling method: 10 ml from the approximate centre of the test vessel from freshly prepared solutions of 5.6, 18 and 56 mg/l and from 24h-old
solutions of 5.6, 18 and 56 mg/l. Additionally, reserve samples of 10 ml were taken. These samples were stored in a deep-freeze for possible analysis until delivery of the final report with a maximum of three months.
- Sample storage conditions before analysis: Not applicable, samples were analysed on the day of
sampling.
Test solutions
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: Preparation of test solutions started with a solution of 100 mg/l (range-finding test) or a stock solution of 1000 mg/I (final test). Magnetic stirring was sufficient to achieve complete dissolution of the test substance in the test medium. The lower concentrations tested were prepared by
subsequent dilutions in test medium.
- Controls: yes, test medium without test substance or other additives.
- Evidence of undissolved material (e.g. precipitate, surface film, etc): The batch of DIHYDROLINALOOL tested was a clear and colourless liquid and
was completely soluble in test medium at the concentrations tested.
Test organisms
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: Daphnia magna
- Strain: Straus 1820
- Age at study initiation (mean and range, SD): <24 hours
- Method of breeding: Breeding starts with new-born animals, less than 3 days old, placing about 250 of them into 10 liters of medium in an all-glass culture vessel. After 7 days of cultivation half of the medium is renewed twice a week. Cultures are kept at 18 - 22 degrees Celsius.
- Feeding during test: No
ACCLIMATION
- Acclimation period: 24 hours
- Acclimation conditions (same as test or not): Yes
Study design
- Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Post exposure observation period:
- Not relevant
Test conditions
- Hardness:
- 250 mg/l CaCO3
- Test temperature:
- 20.5 - 21.2 °C in blank control.
- pH:
- 7.8 - 8.0
- Dissolved oxygen:
- 8.0 - 9.3 mg/l
- Salinity:
- Not relevant
- Nominal and measured concentrations:
- Nominal: 5.6, 10, 18, 32 and 56 mg/l
Measured (0 h): 6.30, 20.2 and 57.8 mg/l
Measured (24 h, old): 5.56, 17.9 and 54.7 mg/l
Measured (24 h, old): 5.68, 17.8 and 57.9 mg/l
Concentrations were only measured in test vessels with nominal concentrations of 5.6, 18 and 56 mg/l. - Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Type (delete if not applicable): open
- Material, size, headspace, fill volume: all-glass 100 ml, filled with 80 ml medium
- Aeration: None
- No. of organisms per vessel: 10
- No. of vessels per concentration (replicates): 2
- No. of vessels per control (replicates): 2
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Milli-RO water containing: 293.8 mg/l CaCl2.2H2O, 123.3 mg/l MgSO4.7H2O, 64.8 mg/l NaHCO3, 5.8 mg/l
KCl, 0.125 mg/l B, 0.05 mg/l Fe, 0.025 mg/l Mn, 0.0125 mg/l Li, Rb and Sr, 0.0063 mg/l Mo, 0.0025 mg/l Br, 0.0016 mg/l Cu, 0.0063 mg/l Zn, 0.0025 mg/l Co and J, 0.0010 mg/l Se, 0.0003 mg/l V, 2.5 mg/l Na2EDTA.2H2O, 10.0 mg/l Na2SiO3.9H2O, 0.27 mg/l NaNO3, 0.14 mg/l KH2PO4, 0.18 mg/l K2HPO4, 75.0 ug/l Thiamine, 1.0 mg/l B12 and 0.75 ug/l Biotin.
- Culture medium different from test medium: No
- Intervals of water quality measurement: 24 hours
OTHER TEST CONDITIONS
- Photoperiod: Continuous dark
- Light intensity: 12 lux
EFFECT PARAMETERS MEASURED (with observation intervals if applicable): immobilization
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 1.8 - Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 32 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 95%CL: 29 - 37 mg/l
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 56 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 18 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- - Mortality of control: no immobilisations in the control treatments
- Effect concentrations exceeding solubility of substance in test medium: DIHYDROLINALOOL was completely soluble in test medium at the
concentrations tested. - Results with reference substance (positive control):
- - Results with reference substance valid? Yes
- Mortality: 0% in control, 100% at 1 mg/l after 48 hours.
- EC50/LC50: the 48h-EC50 was 0.60 mg/l with 95% fiducial limits of 0.52 - 0.79 mg/l. - Reported statistics and error estimates:
- The EC50-value was calculated at 48 hours of exposure from the probits of the percentages of affected daphnia and the logarithms of the
corresponding test substance concentrations using the maximum likelihood estimation method (Finney, D.J 1971: Probit analysis, Cambridge University Press, Cambridge, U.K., 3rd edition).
Any other information on results incl. tables
not relevant
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Remarks:
- Control immobilisation <10%; oxygen contentration remained > 2 mg/l, 24h-EC50 of potassium dichromate within range
- Conclusions:
- The 48h-EC50 of Dihydrolinalool to Daphnia magna is 32 mg/l.
- Executive summary:
The toxicity of Dihydrolinalool towards Daphnia magna was investigated according to ISO Guideline 6341. The 48h-EC50 was found to be 32 mg/l (29 - 37 mg/l), the 24h EC50 was found to be 56 mg/l. The 48h NOEC is 18 mg/l.
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