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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 242-361-9 | CAS number: 18479-57-7
- 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
Biodegradation in water: screening tests
Administrative data
Link to relevant study record(s)
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 10 October - 7 November 2000
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study
- Remarks:
- No CoA, no clarity on meeting time window of 14 days for a CBT, only SOP numbers are given but no summary provided
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 D (Ready Biodegradability: Closed Bottle Test)
- Deviations:
- no
- GLP compliance:
- yes
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic, non-adapted
- Details on inoculum:
- Secondary effluent of a domestic sewage treatment plant, collected 6 Oct 2000, (Kläranlage Odenthal). The effluent was preconditioned by seperation of coarse particles by filtration and aeration of mineral medium plus inoculum (filtrate) for 4 days.
The effluent concentration in the reaction mixture was 5 ml/L - Duration of test (contact time):
- 28 d
- Initial conc.:
- 2.3 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- O2 consumption
- Details on study design:
- Reference is made to SOPs, no summary description available.
Incubation temperature was 20 +/- 1 C - Reference substance:
- benzoic acid, sodium salt
- Remarks:
- at 2.9 mg/L
- Test performance:
- Test was considered acceptable as all validity criteria were met.
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 72
- Sampling time:
- 28 d
- Parameter:
- % degradation (O2 consumption)
- Value:
- 66
- Sampling time:
- 21 d
- Parameter:
- % degradation (O2 consumption)
- Value:
- 56
- Sampling time:
- 14 d
- Parameter:
- % degradation (O2 consumption)
- Value:
- 35
- Sampling time:
- 7 d
- Results with reference substance:
- The reference substance showed 80% degradation after 14 days.
- Validity criteria fulfilled:
- yes
- Remarks:
- The reference substance, toxicity of the test substance, the difference of the replicates at 28d, O2 depletion (inoculum blank) and residual O2 conc in the test bottles met the validity criteria.
- Interpretation of results:
- readily biodegradable
- Conclusions:
- The substance showed 72% biodegradation in an OECD TG 301D test meeting the 14-day time window and is considered to be readily biodegradable.
- Executive summary:
The ready biodegradability of Tetrahydromyrcenol was investigated in a study conducted in accordance with OECD TG 301D (closed bottle test) and GLP. The concentration tested was 2.3 mg/l test substance, with a secondary effluent concentration of 5 mg/l. There was 80% biodegradation of the reference substance sodium benzoate at 14 d. A toxicity control was included not showing toxicity of the test substance. The test substance biodegrades for 72% meeting the 14-day time window.
Reference
Name |
Substance |
% degradation 7 d |
% degradation 14 d |
% degradation 21 d |
% degradation 28 d |
Test substance |
Tetrahydro-myrcenol (THM) |
35 |
56 |
66 |
72 |
Reference substance |
Sodium benzoate (SB) |
67 |
80 |
82 |
84 |
Toxicity control |
THM & SB |
42 |
59 |
68 |
66 |
The following criteria were met: The reference substance was degradaed >60% (80%) in 14 days; No toxicity of the test substance was observed in the toxicity control; The difference of the extremes of the replicates at the end of the test is less than 20%; Oxygen depletion in the inoculum blank did not exceed 1.5 mg/L dissoved oxygen after 28 days and residual oxygen concentrations in the test bottles were > 0.5 mg/L at all times.
Description of key information
The ready biodegradability of Tetrahydromyrcenol was investigated in a study conducted in accordance with OECD TG 301D (closed bottle test) and GLP. The concentration tested was 2.3 mg/l test substance, with a secondary effluent concentration of 5 mg/l. There was 80% biodegradation of the reference substance sodium benzoate at 14 d. A toxicity control was included not showing toxicity of the test substance. The test substance biodegrades for 72% meeting the 14-day time window.
Key value for chemical safety assessment
- Biodegradation in water:
- readily biodegradable
Additional information
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.