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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
Some information in this page has been claimed confidential.
Administrative data
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 22/05/2018 - 30/06/2018
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- test procedure in accordance with national standard methods
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 018
- Report date:
- 2018
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: Human Repeated Insult Patch Test (HRIPT)
- Version / remarks:
- The methodology used by the laboratory is an adaptation from that described by Marzulli and Maibach Human 'Repeated Insult Patch Test for delayed contact hypersensitivity: Marzulli F.N., Maibach H.I., Contact allergy : predictive testing in man, Contact Dermatitis, '1976, 2, pp. 1 -17.
- GLP compliance:
- yes
- Type of study:
- patch test
- Justification for non-LLNA method:
- No laboratory animal studies are available, but human experience indicates upsalite is not a skin sensitiser.
Test material
Reference
- Name:
- Unnamed
- Test material form:
- solid: particulate/powder
- Details on test material:
- They have different version of synthesis based on scale (small, medium, large) There is differences between different scales are related to materials physical properties.
- Specific details on test material used for the study:
- Lot:Q0002-1701
In vivo test system
Test animals
- Species:
- other: human
- Sex:
- male/female
- Details on test animals and environmental conditions:
- The equipment used for the occluded patch is composed of a small plastic cavity of 0.64 cm 2 with a filter tissue at the bottom which is made to receive the product to test. All this is fixed to a hypoallergenic non woven adhesive tape.
Study design: in vivo (non-LLNA)
Induction
- Route:
- epicutaneous, occlusive
- Vehicle:
- not specified
- Concentration / amount:
- The amount of test material applied to each patch 0.02ml
- Day(s)/duration:
- 9 times on the same site over a period of 3 consecutive weeks
Challenge
- No.:
- #1
- Route:
- epicutaneous, occlusive
- Vehicle:
- not specified
- Concentration / amount:
- 0,02ml
- Day(s)/duration:
- a single application
- No. of animals per dose:
- 50 volunteers
- Details on study design:
- A skin examination of the application site is performed by the dermatologist before the 1st product application of the
induction phase, after each patch removal, the application of the challenge and its removal.The area on which the patch is applied is previously cleaned up with demineralised water and dried with cellulose cotton wool tissue.
The patches are put on the back of the volunteer.
Treatment sites are assessed before the first application of test material (baseline) and after treatment at 30 minutes
after patch removal during the induction period.
After a rest period of 2 weeks a patch was applied on a previously unpatched and patched skin site. This site was evaluated
on 30 minutes, 24, 48, 72 and 96 hours after removal.
Skin reactions are scored throughout the test by the same experienced assessor who made the baseline assessment and
under the same lighting source, following a pre-defined irritation and sensitization scoring scales. - Challenge controls:
- A "negative" control is a patch without any product, applied in the same conditions as the product to be tested:
if the product is tested pure: empty patch.
if the product is tested diluted: patch with 0.02ml of the solvent used (demineralised water or mineral oil).
Results and discussion
In vivo (non-LLNA)
Resultsopen allclose all
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 0.5
- Group:
- test chemical
- Dose level:
- 0,02
- No. with + reactions:
- 0
- Total no. in group:
- 50
- Clinical observations:
- On 0 volunteers (0%) noticed slight erythema & dryness. In this clinical study there was no evidence of oedema.
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 0,02
- No. with + reactions:
- 0
- Total no. in group:
- 50
- Clinical observations:
- On 0 volunteers (0%) noticed slight erythema & dryness. In this clinical study there was no evidence of oedema.
- Key result
- Reading:
- other: 3rd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 0,02
- No. with + reactions:
- 0
- Total no. in group:
- 50
- Clinical observations:
- On 0 volunteers (0%) noticed slight erythema & dryness. In this clinical study there was no evidence of oedema.
- Key result
- Reading:
- other: 4th reading
- Hours after challenge:
- 72
- Group:
- test chemical
- Dose level:
- 0,02
- No. with + reactions:
- 0
- Total no. in group:
- 50
- Clinical observations:
- On 0 volunteers (0%) noticed slight erythema & dryness. In this clinical study there was no evidence of oedema.
- Key result
- Reading:
- other: 5th reading
- Hours after challenge:
- 96
- Group:
- test chemical
- Dose level:
- 0,02
- No. with + reactions:
- 0
- Total no. in group:
- 50
- Clinical observations:
- On 0 volunteers (0%) noticed slight erythema & dryness. In this clinical study there was no evidence of oedema.
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 0.5
- Group:
- negative control
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 50
- Clinical observations:
- On 0 volunteers (0%) noticed slight erythema & dryness. In this clinical study there was no evidence of oedema.
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 50
- Clinical observations:
- On 0 volunteers (0%) noticed slight erythema & dryness. In this clinical study there was no evidence of oedema.
- Key result
- Reading:
- other: 3rd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 50
- Clinical observations:
- On 0 volunteers (0%) noticed slight erythema & dryness. In this clinical study there was no evidence of oedema.
- Key result
- Reading:
- other: 4th reading
- Hours after challenge:
- 72
- Group:
- negative control
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 50
- Clinical observations:
- On 0 volunteers (0%) noticed slight erythema & dryness. In this clinical study there was no evidence of oedema.
- Key result
- Reading:
- other: 5th reading
- Hours after challenge:
- 96
- Group:
- negative control
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 50
- Clinical observations:
- On 0 volunteers (0%) noticed slight erythema & dryness. In this clinical study there was no evidence of oedema.
Any other information on results incl. tables
Skin reactions are scored throughout the test by the same experienced assessor who made the baseline assessment and under the same lighting source, following a pre-defined irritation and sensitization scoring scales.
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Throughout the study, the product induced no reaction or irritation. The number of volunteers that presented an allergic reaction was 0 percent (0%).According to the experimental conditions of the study, the test product, can be considered as “Non Sensitizing”.
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