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EC number: 234-426-5 | CAS number: 12003-38-2
- 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
Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- Aug 19 - Dec 16, 2011
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP study performed according to OECD TG 405.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 011
- Report date:
- 2011
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- Fluorphlogopite (Mg3K[AlF2O(SiO3)3])
- EC Number:
- 234-426-5
- EC Name:
- Fluorphlogopite (Mg3K[AlF2O(SiO3)3])
- Cas Number:
- 12003-38-2
- Molecular formula:
- AlF2O10Si33Mg
- IUPAC Name:
- Fluorphlogopite
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: Charles River Wiga GmbH, Kißlegg
- Age at study initiation: 17-18 weeks
- Mean weight at study initiation: 3.68 kg
- Housing: individual
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: 7 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C):19-24 °C
- Humidity (%): 48-84 %
- Air changes (per hr): no data
- Photoperiod (hrs dark / hrs light): 12/12 hours
IN-LIFE DATES: From: day 1 to day 8
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- 0.1 g
- Duration of treatment / exposure:
- 24 hours
- Observation period (in vivo):
- after 24, 48, and 72 hours, then daily up to day 8
- Number of animals or in vitro replicates:
- 3 females
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Washing (if done): --
- Time after start of exposure: --
SCORING SYSTEM: Draize
The right eye of each rabbit remained untreated and served as control
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- other: 24, 48, and 72 hours after treatment
- Score:
- 0
- Max. score:
- 0
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- other: 24, 48, and 72 hours after treatment
- Score:
- 0
- Max. score:
- 0
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Time point:
- other: 24, 48, and 72 hours after treatment
- Score:
- 0
- Max. score:
- 0
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- other: 24, 48, and 72 hours after treatment
- Score:
- 0
- Max. score:
- 0
- Irritant / corrosive response data:
- No signs of irritation were observed at the cornea or iris. All animals showed discharge (score 1) and redness of conjunctivae (score 1) one hour after instillation of the test material. In one animal chemosis (score 1) was seen one hour after instillation of the test material. No abnormalities were detected in the untreated eyes.
- Other effects:
- No signs of clinical toxicity were detected. All animals survived the observation period. The body weight development of the treated rabbits was inconspicuous.
Any other information on results incl. tables
For details see executive summary
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Fluorophlogopite did not show any eye irritating potential under the conditions of this test. According to EU Directive 67/548/EC amended and repealed by EU Regulation No. 1272/2008 and CLP, the test material should not be regarded as an irritant to the eyes.
- Executive summary:
Study design
For the test of primary eye irritation, 0.1 g of the solid test material was applied into the conjunctival sac in the left eye of rabbits. The right eye remained untreated and served as control. The first examination of the eyes followed 1 hour after instillation. The other examinations of the eyes were performed daily for a further 7 days.
The eyes were evaluated according to the DRAIZE scale (1959).Results
Ocular alterations
No signs of irritation were observed at the cornea or iris. All animals showed discharge (score l) and redness of conjunctivae (score 1) one hour after instillation of the test material. In one animal chemosis (score 1) was seen one hour after instillation of the test material. 24 hours after treatment, no signs of irritation were observed at the conjunctivae of all animals, No abnormalities were detected in the untreated eyes.
Signs of systemic toxicity, body weight, mortality
No signs of systemic toxicity were seen. The body weight development was not different from that of untreated rabbits of the same age. All animals survived the 8-day observation period.
Evaluation of all animals (24/48/72 hours mean score and max score)
Animal No Mean Score Max Score Cornea Iris Conjunctivae Cornea Iris Conjunctivae A A A B A A A B 1 0.00 0.00 0.00 0.00 0 0 0 0 1 0.00 0.00 0.00 0.00 0 0 0 0 3 0.00 0.00 0.00 0.00 0 0 0 0
Conclusions
Fluorphlogopite did not show any eye irritating potential under the conditions of this test. According to EU Directive 67/548/EC amended and repealed by EU Regulation No. 1272/2008 and CLP, the test material should not be regarded as an irritant to the eyes.
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