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Diss Factsheets
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EC number: - | CAS number: -
- 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
- Study period:
- 19 August 2010 – 12 October 2010
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Study was conducted according to EC and OECD test guidelines, and in compliance with GLP.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 010
- Report date:
- 2011
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 429 (Skin Sensitisation: Local Lymph Node Assay)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.42 (Skin Sensitisation: Local Lymph Node Assay)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- The study report included a current certificate of GLP compliance for the test facility, issued by the MHRA.
- Type of study:
- mouse local lymph node assay (LLNA)
Test material
- Details on test material:
- - Physical state: Off-white powder
- Storage condition of test material: aprox. -20 degrees in the dark.
Constituent 1
In vivo test system
Test animals
- Species:
- mouse
- Strain:
- other: CBA/Ca
- Sex:
- female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Harlan UK Ltd
- Age at study initiation: Approximately 8 to 12 weeks of age prior to dosing on Day 1.
- Weight at study initiation: 17.4 to 20.6 g.
- Housing:The animals were housed in pairs in polycarbonate cages with woodflake bedding. The mice were also given Nestlets and a plastic shelter for environmental enrichment.
- Diet (e.g. ad libitum): The animals were allowed free access to a standard pelleted rodent diet (Rat & Mouse No. 1 Maintenance diet).
- Water (e.g. ad libitum): Potable water taken from the public supply was freely available via polycarbonate bottles fitted with sipper tubes.
- Acclimation period: 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 19 to 23°C
- Humidity (%): 40 to 70%
- Air changes (per hr): Not reported
- Photoperiod (hrs dark / hrs light): 12 hours dark / 12 hours light
IN-LIFE DATES: From: 19 August 2010 (date of animal allocation to groups) To: 11 October 2010
Study design: in vivo (LLNA)
- Vehicle:
- dimethylformamide
- Concentration:
- 0 (Dimethylformamide control), 1, 2.5, 5 and 10% w/v
- No. of animals per dose:
- 4
- Details on study design:
- RANGE FINDING TESTS:
- Compound solubility: Very thick suspensions were formed at 25% and 50% (w/v) in acetone:olive oil (4:1 (v/v), which were too thick for administration using a micropipette. In dimethylformamide, the test substance formed a pale brown solution at 50% (w/v) which was satisfactory for dose administration.
MAIN STUDY
ANIMAL ASSIGNMENT AND TREATMENT
- Criteria used to consider a positive response: The test substance is regarded as a sensitizer if at least one concentration of the test substance
results in a three-fold greater increase in 3HTdR incorporation compared to control values. (3HTdR = 3H-methyl Thymidine). - Positive control substance(s):
- hexyl cinnamic aldehyde (CAS No 101-86-0)
- Statistics:
- The results for this study included one concentration which had an SI greater than 3 and one concentration which had an SD of less than 3, therefore the EC3 value was calculated according to the following formula:
EC3 = c+[(3-d)/(b-d)](a-c)
a=concentration giving SI greater than 3, b=SI at concentration a, c=concentration giving SI less than 3, d=SI at concentration c.
Results and discussion
- Positive control results:
- The stimulation index for the positive control substance (HCA) was 7.5, which demonstrates the validity of this study
In vivo (LLNA)
Resultsopen allclose all
- Parameter:
- SI
- Remarks on result:
- other: The test/control ratios obtained for 1, 2.5, 5 and 10% w/v test substance were 1.3, 2.3, 5.0 and 9.4 respectively.
- Parameter:
- other: disintegrations per minute (DPM)
- Remarks on result:
- other: see Remark
- Remarks:
- Control (DMF): 807.9 (=100.99 dpm/node, 8 nodes) 1% (w/v): 1017.2 (=127.15 dpm/node, 8 nodes) 2.5% (w/v): 1851.1 (=231.39 dpm/node, 8 nodes) 5% (w/v): 4074.3 (=509.29 dpm/node, 8 nodes) 10% (w/v): 7605 (=950.63 dpm/node, 8 nodes) HCA (positive control): 6021.3 (=752.66 dpm/node, 8 nodes)
Applicant's summary and conclusion
- Interpretation of results:
- sensitising
- Remarks:
- Migrated information
- Conclusions:
- The test substance is regarded as a potential skin sensitizer.
- Executive summary:
A localised lymph node assay (LLNA) study was conducted by Huntingdon Life Sciences, UK, to determine the potential for skin sensitization of the test substance. The study was conducted according to OECD 429 and EEC B.42 Test Guidelines, and was performed in compliance with GLP. The test substance is regarded as a sensitizer if at least one concentration of the test substance results in a three-fold greater increase in 3HTdR incorporation compared to control values.
The test substance was found to generate a test/control ratio greater than 3 at two of the concentration tested (5 and 10% (w/v)), and so the test substance was considered to have the potential to cause skin sensitization (delayed contact hypersensitivity).
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.
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