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EC number: 402-950-5 | CAS number: 87826-41-3 CLEARLITE NU 005; DISORBENE M; GENISET MD; GLC NU 005; MILLAD 3940; NU 005
- 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:
- 21 March 1988 to 13 June 1988
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP Guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 988
- Report date:
- 1988
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Version / remarks:
- (adopted 24 February 1987)
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- 1-(2,6-bis(4-tolyl)-1,3-dioxano(5,4-d)-1,3-dioxan-4-yl)ethane-1,2-diol
- EC Number:
- 402-950-5
- EC Name:
- 1-(2,6-bis(4-tolyl)-1,3-dioxano(5,4-d)-1,3-dioxan-4-yl)ethane-1,2-diol
- Cas Number:
- 87826-41-3
- Molecular formula:
- C22 H26 O6
- IUPAC Name:
- (1R)-1-[(4R,4aR,8aS)-2,6-bis(4-methylphenyl)-hexahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-yl]ethane-1,2-diol
- Details on test material:
- - Name of test material (as cited in study report): Gel-All-MD
- Substance type: White powder
- Physical state: solid
- Analytical purity: Active ingredient concentration: 98.6% (specified 95%)
- Impurities (identity and concentrations): No data
- Composition of test material, percentage of components: No data
- Isomers composition: No data
- Purity test date: No data
- Lot/batch No.: 4140626
- Stability under test conditions: No data
- Storage condition of test material: When not in use the material was stored in the dark at room temperature
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: Healthy female rabbits were obtained from Goreside Rabbits, Northchurch, Berkhamsted, Hereford
- Age at study initiation: At receipt the animals were 8 weeks of age, but left to acclimatise for at least 9 days.
- Weight at study initiation: See table.
- Housing: The rabbits were individually housed in grid-bottomed metal cages.
- Diet (e.g. ad libitum): A commercially available antibiotic free rabbit diet (SQC standard rabbit pellets produced by Special Diet Services, Witham, Essex), ad libitum.
- Water (e.g. ad libitum): Mains drinking water via an automatic nozzle, ad libitum.
- Acclimation period: At least 9 days.
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 17 - 20°C
- Humidity (%): Relative humidity within the range 44 - 77%.
- Photoperiod (hrs dark / hrs light): Fluorescent lighting was controlled to give an artificial cycle of 12 hours light/12 hours dark per day.
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- yes, concurrent no treatment
- Amount / concentration applied:
- 0.1 mL of the supplied material (weighing approximately 30 mg)
- Duration of treatment / exposure:
- Single exposure with observation for 7 days
- Observation period (in vivo):
- One, 24, 48 and 72 hours and 7 days following instillation of the test material the animals eyes were examined macroscopically under a standard light source.
- Number of animals or in vitro replicates:
- 3
- Details on study design:
- One restrained rabbit was dosed initially to assess the severity of any irritant response. As no marked irritation was seen a further two restrained animals were dosed, bringing the group size to three.
The test material was instilled into the right eye of each restrained animal by gently pulling away the lower lid from the eyeball to form a cup into which the test material was placed. The lids were then held shut for a few seconds. The treated eyes of the rabbits were not rinsed after dosing. The left eye was untreated and served as a control.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- conjunctivae score
- Remarks:
- (redness)
- Basis:
- animal #1
- Remarks:
- (No 781)
- Time point:
- other: mean of scores at 24, 48 and 72 h
- Score:
- 0
- Max. score:
- 3
- Reversibility:
- fully reversible within: 24 hours
- Irritation parameter:
- conjunctivae score
- Remarks:
- (redness)
- Basis:
- animal #2
- Remarks:
- (No 777)
- Time point:
- other: mean of scores at 24, 48 and 72 h
- Score:
- 0.3
- Max. score:
- 3
- Reversibility:
- fully reversible within: 48 hours
- Irritation parameter:
- conjunctivae score
- Remarks:
- (redness)
- Basis:
- animal #3
- Remarks:
- (No 778)
- Time point:
- other: mean of scores at 24, 48 and 72 h
- Score:
- 0.3
- Max. score:
- 3
- Reversibility:
- fully reversible within: 48 hours
- Irritation parameter:
- chemosis score
- Basis:
- animal #1
- Remarks:
- (No 781)
- Time point:
- other: mean of scores at 24, 48 and 72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: No chemosis observed at any observation
- Irritation parameter:
- chemosis score
- Basis:
- animal #2
- Remarks:
- (No 777)
- Time point:
- other: mean of scores at 24, 48 and 72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: No chemosis observed at any observation
- Irritation parameter:
- chemosis score
- Basis:
- animal #3
- Remarks:
- (No 778)
- Time point:
- other: mean of scores at 24, 48 and 72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: No chemosis observed at any observation
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #1
- Remarks:
- (No 781)
- Time point:
- other: mean of scores at 24, 48 and 72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: No cornea effects observed at any observation
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #2
- Remarks:
- (No 777)
- Time point:
- other: mean of scores at 24, 48 and 72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: No cornea effects observed at any observation
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #3
- Remarks:
- (No 778)
- Time point:
- other: mean of scores at 24, 48 and 72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: No cornea effects observed at any observation
- Irritation parameter:
- iris score
- Basis:
- animal #1
- Remarks:
- (No 781)
- Time point:
- other: mean of scores at 24, 48 and 72 h
- Score:
- 0
- Max. score:
- 2
- Remarks on result:
- other: No iris effects observed at any observation
- Irritation parameter:
- iris score
- Basis:
- animal #2
- Remarks:
- (No 777)
- Time point:
- other: mean of scores at 24, 48 and 72 h
- Score:
- 0
- Max. score:
- 2
- Remarks on result:
- other: No iris effects observed at any observation
- Irritation parameter:
- iris score
- Basis:
- animal #3
- Remarks:
- (No 778)
- Time point:
- other: mean of scores at 24, 48 and 72 h
- Score:
- 0
- Max. score:
- 2
- Remarks on result:
- other: No iris effects observed at any observation
- Irritant / corrosive response data:
- One hour after instillation, well defined conjunctival redness was seen in two rabbits and slight redness in the third animal. Only slight conjunctival redness was seen after 24 hours in two animals. All eyes were normal within 48 hours.
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Slight to moderate conjunctival irritancy (redness) was observed up to 24 hours post-installation.
- Executive summary:
- The purpose of the study was to assess the eye irritation potential of Gel
All MD in rabbits.
The method used was designed to meet the requirements of OECD Guideline No. 405.
Gel All MD was instilled into the right eye of three rabbits. Assessments of eye irritation were made 1, 24, 48 and 72 hours and 7 days after installation.
One hour after instillation, well defined conjunctival redness was seen in two rabbits and slight redness in the third animal. Only slight conjunctival redness was seen after 24 hours in two animals. All eyes were normal within 48 hours. No chemosis, iridial irritation or cornea effects were observed.
The slight irritation (redness) was fully reversible and not sufficient for classification.
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