Registration Dossier
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EC number: 701-124-4 | 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

Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Meets generally accepted scientific standards; sufficiently documented and acceptable for assessment.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 977
- Report date:
- 1977
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- 0.1 ml of undiluted compound was placed in the conjunctival sac of the right eye of each of six albino male and female rabbits and observations made over a period of seven days for inflammation. The treated eyes were washed with sodium chloride solution USP after the 24-hour reading. The left eye served as control. The data were scored according to the method of Draize, Woodard and Calvery (Journal of Pharm. and Exp. Therapeutics, Vol. 82, Dec. 1944).
- GLP compliance:
- no
Test material
- Reference substance name:
- 52747-01-0
- Cas Number:
- 52747-01-0
- IUPAC Name:
- 52747-01-0
- Reference substance name:
- Mondur PF
- IUPAC Name:
- Mondur PF
- Details on test material:
- Name of test material (as cited in study report): Desmodur PF; no further data given
Constituent 1
Constituent 2
Test animals / tissue source
- Species:
- rabbit
- Strain:
- other: albino
- Details on test animals or tissues and environmental conditions:
- no data
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: the left eye served as control
- Amount / concentration applied:
- Amount(s) applied: 0.1 ml/animal
- Duration of treatment / exposure:
- 24 hours
- Observation period (in vivo):
- 1, 24, 48, 72 hours and 5, 7 days after instillation
- Number of animals or in vitro replicates:
- 3 males and 3 females
- Details on study design:
- see "Principles of method"
Results and discussion
In vivo
Results
- Irritation parameter:
- overall irritation score
- Basis:
- animal: #1, 2, 3, 4, 5, 6
- Time point:
- other: 24, 48, 72 hours
- Score:
- 8.4
- Max. score:
- 110
- Reversibility:
- fully reversible within: 7 days
- Irritant / corrosive response data:
- Observations following application:
Immediate: discomfort was slight
10 min and 1 hour: slight erythema, copius discharge
24 hours: areas of barely perceptible corneal dullness in four animals, slight to moderate erythema, copius discharge
48-120 hours: gradual improvement
168 hours: all scored zero - Other effects:
- none
Any other information on results incl. tables
.
Applicant's summary and conclusion
- Executive summary:
Mondur PF was not classed as an eye irritant in an eye irritation test on male and female rabbits. Slight to moderate erythema was observed 24 hours after instillation, which was fully reversible within 7 days.
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