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EC number: 274-581-6 | CAS number: 70356-09-1
- 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:
- comparable to guideline study with acceptable restrictions
- Remarks:
- Comparable to guideline study under GLP with acceptable restrictions in documentation
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 978
- Report date:
- 1978
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- The test item was dissolved in diethylphtalate, concentration: 5 - 20 %.
- GLP compliance:
- yes
Test material
- Reference substance name:
- 1-[4-(1,1-dimethylethyl)phenyl]-3-(4-methoxyphenyl)propane-1,3-dione
- EC Number:
- 274-581-6
- EC Name:
- 1-[4-(1,1-dimethylethyl)phenyl]-3-(4-methoxyphenyl)propane-1,3-dione
- Cas Number:
- 70356-09-1
- Molecular formula:
- C20H22O3
- IUPAC Name:
- 1-(4-tert-butylphenyl)-3-(4-methoxyphenyl)propane-1,3-dione
- Test material form:
- liquid
- Details on test material:
- - Name of test material : tert.Butyl-4-methoxy-4' dibenzoylmethane
- Physical state: liquid
- Stability under test conditions: no changes noted during storage
- Storage condition of test material: room temperature
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
Test system
- Vehicle:
- other: diethylphtalate
- Controls:
- not required
- Amount / concentration applied:
- 0.1 mL of a solution containing 5 %, 10 % and 20 % BMDBM.
- Duration of treatment / exposure:
- Single application of a 5 %, 10 % and 20 % solution each
- Observation period (in vivo):
- After 1, 24, 48, and 72 h. Post-observation after 7 and 14 days.
- Number of animals or in vitro replicates:
- Three animals per dose group.
- Details on study design:
- SCORING SYSTEM: Draize system
Corneal opacity: 0 - 4
Iris: 0 - 2
Conjunctival redness: 0 - 3
Conjunctival swelling (chemosis): 0 - 4
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Remarks:
- of 3 animals
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- fully reversible
- Remarks on result:
- other: 5 % solution
- Irritation parameter:
- iris score
- Basis:
- mean
- Remarks:
- of 3 animals
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Reversibility:
- fully reversible
- Remarks on result:
- other: 5 % solution
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Remarks:
- of 3 animals
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 3
- Reversibility:
- fully reversible
- Remarks on result:
- other: 5 % solution
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Remarks:
- of 3 animals
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- fully reversible
- Remarks on result:
- other: 5 % solution
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Remarks:
- of 3 animals
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- fully reversible
- Remarks on result:
- other: 10 % solution
- Irritation parameter:
- iris score
- Basis:
- mean
- Remarks:
- of 3 animals
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Reversibility:
- fully reversible
- Remarks on result:
- other: 10 % solution
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Remarks:
- of 3 animals
- Time point:
- 24/48/72 h
- Score:
- 0.44
- Max. score:
- 3
- Reversibility:
- fully reversible within: 2 - 3 d
- Remarks on result:
- other: 10 % solution
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Remarks:
- of 3 animals
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- fully reversible
- Remarks on result:
- other: 10 % solution
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Remarks:
- of 3 animals
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- fully reversible
- Remarks on result:
- other: 20 % solution
- Irritation parameter:
- iris score
- Basis:
- mean
- Remarks:
- of 3 animals
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Reversibility:
- fully reversible
- Remarks on result:
- other: 20 % solution
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Remarks:
- of 3 animals
- Time point:
- 24/48/72 h
- Score:
- 0.67
- Max. score:
- 3
- Reversibility:
- fully reversible within: 3 d
- Remarks on result:
- other: 20 % solution
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Remarks:
- of 3 animals
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- fully reversible
- Remarks on result:
- other: 20 % solution
- Irritant / corrosive response data:
- As given above, single application of a 5 - 20 % solution of BMDBM in diethylphtalate caused weak shortlasting conjuncticval irritation of the rabbit eye. No alteration of the cornea was observed macroscopically.
- Other effects:
- No further effects were reported.
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- The 20 % solution of butyl methoxydibenzoylmethane (BMDBM) dissolved in diethylphtalate caused weak shortlasting conjunctival irritation of the rabbit eye. No alterations of the cornea was observed macroscopically. Therefore, BMDBM can be considered as non-irritant to the eye and no classification according to EU CLP is needed.
- Executive summary:
The determination of eye irritating effects of butyl methoxydibenzoylmethane (BMDBM) was performed in a study similar to OECD Guideline 405 on three rabbits: BMDBM as 5 %, 10 %, and 20 % solution in diethylphtalate was placed in the conjunctival sac of one rabbit eye and the effects are recorded after 1 h, 24 h, 48 h, 72 h, 7 days and 14 days. Observations comprised opacity of the cornea, iris reaction, conjunctival redness and swelling (chemosis).
The instillation of a solution of BMDBM caused concentration-dependent weak conjunctival irritation of the rabbit eye which was fully reversible within up to 3 days. The mean irritation scores for the 20 % solution (3 animals, 24 - 72 h after administration) were 0 (Cornea opacity), 0 (Iris), 0.67 (Conjunctivae redness), 0 (Chemosis). Therefore, BMDBM can be considered as non-irritant to the eye and no classification according to EU CLP is needed.
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