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Diss Factsheets
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EC number: 204-809-1 | CAS number: 126-86-3
- 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
Endpoint summary
Administrative data
Description of key information
Key value for chemical safety assessment
Skin sensitisation
Link to relevant study records
- Endpoint:
- skin sensitisation: in vivo (LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2012
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: according to EC Directive 92/69/EEC and Regulation EC/440/2008 guideline methods under GLP conditions
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 429 (Skin Sensitisation: Local Lymph Node Assay)
- Deviations:
- no
- GLP compliance:
- yes
- Type of study:
- mouse local lymph node assay (LLNA)
- Species:
- mouse
- Strain:
- CBA
- Sex:
- female
- Details on test animals and environmental conditions:
- The animals were individually housed in suspended solid-floor polypropylene cages
furnished with softwood woodflakes. Free access to mains tap water and food (2014C
Teklad Global Rodent diet supplied by Harlan Laboratories UK Ltd., Oxon, UK) was
allowed throughout the study.
The temperature and relative humidity were controlled to remain within target ranges of
19 to 25°C and 30 to 70%, respectively. Any occasional deviations from these targets
were considered not to have affected the purpose or integrity of the study. The rate of
air exchange was approximately fifteen changes per hour and the lighting was controlledby a time switch to give twelve hours continuous light (06.00 to 18.00) and twelve hours darkness.
The animals were provided with environmental enrichment items which were considered
not to contain any contaminant of a level that might have affected the purpose or integrity
of the study. - Vehicle:
- acetone/olive oil (4:1 v/v)
- Concentration:
- 50%
25%
10% - No. of animals per dose:
- 5 mice
- Details on study design:
- The mice were treated by daily application of 25 μl of the
appropriate concentration of the test item to the dorsal surface of each ear for three
consecutive days (Days 1, 2, 3). The test item formulation was administered using an
automatic micropipette and spread over the dorsal surface of the ear using the tip of the
pipette. - Positive control substance(s):
- hexyl cinnamic aldehyde (CAS No 101-86-0)
- Positive control results:
- alpha-Hexylcinnamaldehyde, 85% was considered to be a sensitiser under the conditions of the test.
- Parameter:
- other: disintegrations per minute (DPM)
- Remarks on result:
- other: Vehicle: 1817.54 (+/- 657.13) dpm/Animal 10%: 3037.60 (+/-1145.05) dpm/Animal 25%: 5009.25 (+/-639.45) dpm/Animal 50%: 6698.23 (+/-2082.90) dpm/Animal
- Key result
- Parameter:
- SI
- Value:
- 1.67
- Test group / Remarks:
- 10 %
- Key result
- Parameter:
- SI
- Value:
- 2.76
- Test group / Remarks:
- 25 %
- Key result
- Parameter:
- SI
- Value:
- 3.69
- Test group / Remarks:
- 50 %
- Interpretation of results:
- sensitising
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- The test item was considered to be a sensitiser under the conditions of the test.
- Executive summary:
The test item was considered to be a sensitiser under the conditions of the test.
Reference
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (sensitising)
- Additional information:
The Stimulation Index expressed as the mean radioactive incorporation for
each treatment group divided by the mean radioactive incorporation of the vehicle control
group has been 3.69 at 50 % concentration.
Migrated from Short description of key information:
Sensitizer according to OECD TG 429
Justification for selection of skin sensitisation endpoint:
Only one study on this substance available. Most recent study on substance according to OECD TG 429, which meets the criteria set forth in Regulation EC No. 440/2008 for filling REACH endpoints. The data is generated in a reliable laboratory using established protocols.
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Justification for classification or non-classification
According to the UN Globally Harmonized System of Classification and Labelling of Chemicals (GHS) Part 3 Chapter 3.4 this substance is causing concern to be sensitizing.
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.