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EC number: 208-235-2 | CAS number: 517-23-7
- 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

Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in vivo (LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 015
- Report date:
- 2015
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 429 (Skin Sensitisation: Local Lymph Node Assay)
- GLP compliance:
- yes
- Type of study:
- mouse local lymph node assay (LLNA)
Test material
- Reference substance name:
- α-acetyl-γ-butyrolactone
- EC Number:
- 208-235-2
- EC Name:
- α-acetyl-γ-butyrolactone
- Cas Number:
- 517-23-7
- Molecular formula:
- C6H8O3
- IUPAC Name:
- 3-acetyloxolan-2-one
- Test material form:
- other: liquid
Constituent 1
- Specific details on test material used for the study:
- No data
In vivo test system
Test animals
- Species:
- mouse
- Strain:
- CBA
- Sex:
- female
- Details on test animals and environmental conditions:
- Individual caging / mice were provided with glass tunnel-tubes.
Cage type: Type II pp/pc.
Bedding: Bedding was available to animals during study
Light: 12 hours daily, from 6 am to 6 pm
Temperature: 22*/- C
Relative humidity: 30-70%
Ventilation: 15-20 air exchanges/hour
-The temparature and relative humidity were recorded twice every day during the acclimatisation and experimental phases.
Study design: in vivo (LLNA)
- Vehicle:
- dimethylformamide
- Concentration:
- Preliminary irritation/toxicity test: 100% and 50% w/v in DMF
Main study Experiment 1 : 100% undiluted, 50% and 25% w/v
Main study Experiment 2 : 50% and 10% and 2% w/v - No. of animals per dose:
- 5 animals/group
3 groups/experiment - Details on study design:
- Preliminary irritation/toxicity test using two doses (undiluted 100%& and 50% w/v in DMF
Main study Experiment 1 : 5 animals/group; 100% undiluted, 50% and 25% w/v
Main study Experiment 2 : 5 animals/group; 50% and 10% and 2 w/v - Positive control substance(s):
- hexyl cinnamic aldehyde (CAS No 101-86-0)
Results and discussion
In vivo (LLNA)
Resultsopen allclose all
- Parameter:
- SI
- Value:
- 0.3
- Test group / Remarks:
- Based on 5 animals in 100% w/v group
- Parameter:
- SI
- Value:
- 0.5
- Test group / Remarks:
- Based on 5 animals in 50% w/v in DMF group
- Parameter:
- SI
- Value:
- 0.7
- Test group / Remarks:
- Based on 5 animals in 25% w/v in DMF group
- Cellular proliferation data / Observations:
- CELLULAR PROLIFERATION DATA
Mean DPM/node
100% undiluted = 74.7
50% w/v = 117.4
25% w/v = 167.3
Any other information on results incl. tables
The test item was a liquid, which was used undiluted or formulated in DMF. Since there were no confounding effects of irritation or systemic toxicity at the applied concentrations, the proliferation values obtained are considered to reflect the real potential of the test item to cause lymphoproliferation in the Local Lymph Node Assay. The resulted stimulation index values were under the threshold limit of 3 observed at the examined concentrations indicating that JAU 6476-ß-lacton (BCS-AA16476) is not a skin sensitizer.
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- In conclusion, under the conditions of the present assay JAU 6476-ß-lacton (BCS-AA16476) was shown to have no sensitization potential (non-sensitizer) in the Local Lymph Node Assay
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