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EC number: 218-827-2 | CAS number: 2244-16-8
- 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
Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in vivo (LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- data from handbook or collection of data
- Justification for type of information:
- Data is from peer reviewed journal
Data source
Reference
- Reference Type:
- publication
- Title:
- Correlation between experimental human and murine skin sensitization induction thresholds
- Author:
- Anne Marie Api, David Basketter, and Jon Lalko
- Year:
- 2 015
- Bibliographic source:
- Cutaneous and ocular toxicology, 34, no. 4, (2015), 298-302.
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 429 (Skin Sensitisation: Local Lymph Node Assay)
- Principles of method if other than guideline:
- To evaluate the skin sensitization potential of D-Carvone by Mouse Local Lymph Node Assay.
- GLP compliance:
- not specified
- Type of study:
- mouse local lymph node assay (LLNA)
Test material
- Reference substance name:
- (5S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one
- Cas Number:
- 2244-16-8
- Molecular formula:
- C10H14O
- IUPAC Name:
- (5S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one
- Test material form:
- liquid
- Details on test material:
- - Name of test material: d-Carvone- IUPAC name: (5S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one- Molecular formula: C10H14O- Molecular Weight: 150.22 g/mole- Smiles Notation: C1[C@H](CC=C(C1=O)C)C(C)=C- Inchl: 1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3/t9-/m0/s1- Substance type: Organic- Physical state: Colorless to pale-yellow liquid
Constituent 1
- Specific details on test material used for the study:
- - Name of test material: d-Carvone- IUPAC name: (5S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one- Molecular formula: C10H14O- Molecular Weight: 150.22 g/mole- Smiles Notation: C1[C@H](CC=C(C1=O)C)C(C)=C- Inchl: 1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3/t9-/m0/s1- Substance type: Organic- Physical state: Colorless to pale-yellow liquid
In vivo test system
Test animals
- Species:
- mouse
- Strain:
- CBA/Ca
- Sex:
- female
- Details on test animals and environmental conditions:
- No data availlable
Study design: in vivo (LLNA)
- Vehicle:
- other: 1:3 ethanol :diethyl phthalate.
- Concentration:
- 25 µl (Each group received one of five test concentrations prepared as a w/v%.)
- No. of animals per dose:
- Total=5
- Details on study design:
- MAIN STUDYANIMAL ASSIGNMENT AND TREATMENT- Name of test method: LLNA- Criteria used to consider a positive response: EC 3 value TREATMENT PREPARATION AND ADMINISTRATION: Groups of female CBA/CA mice were dosed topically on the dorsum of each ear with 25 µl of test fragrance in 1:3 ethanol: diethyl phthalate.Each group received one of five test concentrations preparedas a w/v%.
- Positive control substance(s):
- other:
Results and discussion
In vivo (LLNA)
Results
- Key result
- Parameter:
- SI
- Value:
- 2 650
- Variability:
- not specified
- Test group / Remarks:
- 5 mice
- Remarks on result:
- other: Sensitizing to skin
- Cellular proliferation data / Observations:
- CELLULAR PROLIFERATION DATA: Suspensions of the lymph node cells were prepared by mechanical disaggregation through 200- mesh stainless steel gauze. The cell suspensions were washedthree times with phosphate buffered saline and precipitated overnight at 4°C with 5% w/v trichloroacetic acid (TCA). Thesamples were then pelleted by centrifugation. The cells wereresuspended in 1ml of TCA and transferred to scintillation vials containing 10 ml of scintillation fluid. The incorporationof 3HTdR was measured by b-scintillation counting and expressed as disintegrations per minute (dpm) per lymph node for each experimental group.DETAILS ON STIMULATION INDEX CALCULATION : The stimulation index (SI)values were calculated for each dose level. A SI of 3 or more was considered to give a positive response.EC3 CALCULATION : The EC3 valuewas taken as a measure of relative potency
Applicant's summary and conclusion
- Interpretation of results:
- Category 1 (skin sensitising) based on GHS criteria
- Conclusions:
- The EC3 value obtained from LLNA assay performed to assess the sensitizing potential of d-Carvone was 2650 microgram/sq cm. Based on this value, d-Carvone can be considered to be sensitizing to skin.
- Executive summary:
Skin sensitization potential of d-Carvone was evaluated by Local Lymph Node Assay (LLNA) The LLNAs were conducted according to the method described in OECD Guideline 429. Groups of female CBA/CA mice (n= 5) were dosed topically on the dorsum of each ear with 25 ml of test material in 1:3 ethanol :diethyl phthalate. Each group received one of five test concentrations prepared as a w/v%. A concurrent vehicle control group was similarly treated with 1:3 ethanol: diethyl phthalate.
Dosing occurred daily for three consecutive days. The animals received no treatment for two days and on the sixth day after the first application, all mice were injected intravenously via the tail vein with 250 ml of phosphate buffered saline containing 20 µCi of radiolabelled methyl thymidine (3HTdR). Five hours later, the mice were euthanized and the draining auricular lymph nodes were excised and pooled . Suspensions of the lymph node cells were prepared by mechanical disaggregation through 200-mesh stainless steel gauze. The cell suspensions were washed three times with phosphate buffered saline and precipitated overnight at 4 °C with 5% w/v trichloroacetic acid (TCA). The samples were then pelleted by centrifugation. The cells were resuspended in 1ml of TCA and transferred to scintillation vials containing 10 ml of scintillation fluid. The incorporation of 3HTdR was measured by β- scintillationcounting and expressed as disintegrations per minute (dpm) per lymph node.
The EC3 value obtained from LLNA assay performed to assess the sensitizing potential of d-Carvone was 2650 microgram/sq cm. Based on this value, d-Carvone can be considered to be sensitizing to skin.
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