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EC number: 229-861-2 | CAS number: 6790-58-5
- 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

Hydrolysis
Administrative data
- Endpoint:
- hydrolysis
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- No data
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
- Remarks:
- This study was not performed according to international guideline and is not GLP. However, this study is well documented and is considered reliable with restrictions.
Data source
Reference
- Reference Type:
- other company data
- Title:
- Unnamed
- Year:
- 2 011
- Report date:
- 2011
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 111 (Hydrolysis as a Function of pH)
- Principles of method if other than guideline:
- This study was not performed according to international guideline. The aim of the study is to assess the stability of the substance in a series of simple media simulating perfumery applications. The test media are standard aqueous buffers at pH 2, pH 5, pH 7, pH 8.5 and pH 12 containing 1% of non ionic surfactant. The tests are done in accelerated conditions at 40°C during ca. one month.
- GLP compliance:
- no
Test material
- Reference substance name:
- [3aR-(3aα,5aβ,9aα,9bβ)]-dodecahydro-3a,6,6,9a-tetramethylnaphtho[2,1-b]furan
- EC Number:
- 229-861-2
- EC Name:
- [3aR-(3aα,5aβ,9aα,9bβ)]-dodecahydro-3a,6,6,9a-tetramethylnaphtho[2,1-b]furan
- Cas Number:
- 6790-58-5
- Molecular formula:
- C16H28O
- IUPAC Name:
- (3aR,5aS,9aS,9bR)-3a,6,6,9a-tetramethyl-dodecahydronaphtho[2,1-b]furan
- Test material form:
- not specified
Constituent 1
- Radiolabelling:
- not specified
Study design
- Analytical monitoring:
- yes
- Estimation method (if used):
- Not applicable
Duration of testopen allclose all
- Duration:
- 28 d
- pH:
- 12
- Temp.:
- 40 °C
- Initial conc. measured:
- > 200 - < 300 other: ppm
- Duration:
- 28 d
- pH:
- 8.5
- Temp.:
- 40 °C
- Initial conc. measured:
- > 200 - < 300 other: ppm
- Duration:
- 28 d
- pH:
- 7
- Temp.:
- 40 °C
- Initial conc. measured:
- > 200 - < 300 other: ppm
- Duration:
- 28 d
- pH:
- 5
- Temp.:
- 40 °C
- Initial conc. measured:
- > 200 - < 300 other: ppm
- Duration:
- 28 d
- pH:
- 2
- Temp.:
- 40 °C
- Initial conc. measured:
- > 200 - < 300 other: ppm
Results and discussion
- Transformation products:
- not measured
Total recovery of test substance (in %)open allclose all
- % Recovery:
- > 90
- pH:
- 2
- Temp.:
- 40 °C
- Duration:
- 28 d
- % Recovery:
- > 90
- pH:
- 5
- Temp.:
- 40 °C
- Duration:
- 28 d
- % Recovery:
- > 90
- pH:
- 7
- Temp.:
- 40 °C
- Duration:
- 28 d
- % Recovery:
- > 90
- pH:
- 8.5
- Temp.:
- 40 °C
- Duration:
- 28 d
- % Recovery:
- > 90
- pH:
- 12
- Temp.:
- 40 °C
- Duration:
- 28 d
Any other information on results incl. tables
No additional information
Applicant's summary and conclusion
- Validity criteria fulfilled:
- not applicable
- Conclusions:
- The disappearance of the parent compound after 5 days as well as after 28d is less than 10% at any pH (from 2 to 12) at 40°C. Therefore, it can be concluded that the substance is hydrolytically stable under the conditions of the test.
- Executive summary:
This study was not performed according to international guideline and is not GLP. The aim of the study is to assess the stability of the substance in a series of simple media simulating perfumery applications. The test media are standard aqueous buffers at pH 2, pH 5, pH 7, pH 8.5 and pH 12 containing 1% of non ionic surfactant (Arkopal N 150). The tests are done in accelerated conditions at 40°C during ca. one month. This study is well documented and is considered reliable with restrictions.
200 – 300 ppm of raw material are dissolved in the pH buffer containing the surfactant and put into storage in an oven at 40°C. Small aliquots of the test solution are extracted with an organic solvent (typically cyclohexane or ethyl acetate) containing a hydrocarbon standard (typically C12, C17 or C20) on a regular basis throughout the test (typically at time = 0, 0.25, 1, 2, 4, 7, 15, 21 and 28 days). The extracts are analyzed by GC-FID and the results are plotted as (Area/Area Std) expressed in [%]. The measurement at time = 0 is set at 100% and the succeeding measurements are calculated relatively to the time = 0 measurement. Therefore the curves represent the percentage of product remaining in the test solution at the time of analysis.
The disappearance of the parent compound after 5 days as well as after 28d is less than 10% at any pH (from 2 to 12) at 40°C. Therefore, it can be concluded that the substance is hydrolytically stable under the conditions of the test.
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