Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 230-565-0 | CAS number: 7195-44-0
- 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:
- 1976
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Non-GLP study that meets accepted scientific standard, well document and acceptable for assessment.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 976
- Report date:
- 1976
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- The test was performed according to the method given in the "Hazardous Substances Regulations" under the U.S. Federal Hazardous Labelling Act Sect. 191.12 (February 1965).
- GLP compliance:
- no
Test material
- Reference substance name:
- Bis(2,3-epoxypropyl) terephthalate
- EC Number:
- 230-565-0
- EC Name:
- Bis(2,3-epoxypropyl) terephthalate
- Cas Number:
- 7195-44-0
- Molecular formula:
- C14H14O6
- IUPAC Name:
- 1,4-bis[(oxiran-2-yl)methyl] benzene-1,4-dicarboxylate
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- Healthy New Zealand White rabbits aged 12 - 16 weeks with average body weights of 2.93 kgs for the males and 2.80 kgs for the females, bred on the premises and maintained under semi-barrier system. The animals were acclimatized in the test area for one week prior to the start of the trial.
Experimental room was maintained at a temperature of 20C and a relative humidity of 50-70%. Light cycle of 10 Hours / 14 hours per day. A commercial irradiated diet was fed ad lib. and filtered sterile water was available at all times.
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: The right eye serve as control
- Amount / concentration applied:
- 100 mg of the test compound
- Duration of treatment / exposure:
- The eye lids were held closed for 1 second.
In three out of the six rabbits, after 30 seconds the compound was, as far as possible, flushed out of the eyes with approx. 200 mL of warm water. - Observation period (in vivo):
- The rabbits were examined 1, 24, 48 and 72 hours after application as well as 6 and 10 days.
- Number of animals or in vitro replicates:
- 6 animals
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Washing: in three animals the compound was flushed out with approx. 200 mL warm water
- Time after start of exposure: 30 seconds
SCORING SYSTEM:
CORNEA
Opacity: degree of density (area most dense taken for reading)
No ulceration or opacity.................................................................................................................... 0
Scattered or diffuse areas of opacity ,details of iris clearly visible..............................................1
Easily discernible translucent area, details of iris slightly obscured...........................................2
Oaplescent area, no details of iris visible, size of pupil barely discernible.................................3
Opaque cornea, iris invisible...............................................................................................................4
IRIS
Normal.....................................................................................................................................................0
Folds above normal, congestion, swelling, moderate circumcorneal injection,
any of these or combination of any thereof, iris still reacting to light
(sluggish reaction is positive) .............................................................................................................1
No reaction to light, hemorrhage, gross destruction (any or all of these)...................................2
CONHJUNCTIVAE
Redness (refers to palpebral and bulbar conjunctivae excluding cornea and iris)
vessels normal........................................................................................................................................0
vessels definitely injected above normal.............................................................................................1
More diffuse, deeper crimson red, individual vessels not easily discernible................................2
Diffuse beefy red.....................................................................................................................................3
Chemosis:
No swelling...............................................................................................................................................0
Any swelling above normal (including nictitating membranes).......................................................1
Obvious swelling with partial eversion of lids ....................................................................................2
Swelling with lids about half-closed.....................................................................................................3
Swelling with lids more than half-closed.............................................................................................4
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- other: 24 h
- Score:
- 25
- Max. score:
- 80
- Reversibility:
- other: Animals sacrificed after 6 days
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- other: 48 h
- Score:
- 22
- Max. score:
- 80
- Reversibility:
- other: Animlas sacrificed after 6 days
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- other: 72 h
- Score:
- 28
- Max. score:
- 80
- Reversibility:
- other: Animals sacrificed after 6 days
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Time point:
- other: 24
- Score:
- 2
- Max. score:
- 3
- Reversibility:
- other: Animals sacrificed after 6 days
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- other: 24 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- other: Animals sacrificed after 6 days
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Time point:
- other: 48 h
- Score:
- 2.66
- Max. score:
- 3
- Reversibility:
- other: Animals sacrificed after 6 days
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- other: 48 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- other: Animals sacrificed after 6 days
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Time point:
- other: 72 h
- Score:
- 3
- Max. score:
- 3
- Reversibility:
- other: Animals sacrificed after 6 days
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- other: 72 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- other: Animals sacrificed after 6 days
- Irritant / corrosive response data:
- Conjunctiva. A uery slight to mild reaction was seen in all treated eyes one hour after the application of the compound. By 24 hours this had
increased in severity in the unwashed eyes but had remained the same in the washed ones. By 72 hours all unwashed eyes were showing necrotic
areas, whereas one washed eye was normal at this time and the other 2 returned to normal by 6 days. There was no change in the unwashed eyes
by 6 days when the animals were killed. If sufficient time had been allowed to elapse it is considered there might have been some residual
scarring of the conjunctivae.
Cornea. Slight opacity with damage to the surface epithelium was seen in all treated eyes at one hour. This was still present at 24 hours inthe
3 unwashed eyes and 2/3 washed eyes. ' These 2 washed eyes had returned to normal by 48 hours and 10 days whereas 2/3 of the unwashed eyes
showed ulceration from 72 hours onwards. By 6 days there was slight pannus formation in the 3 unwashed eyes. It is considered that if sufficiënt
time had been allowed to elapse there might have been some residual . scarring of the cornea in the unwashed eyes.
Iris. Increased folding was seen in one unwashed eye at one hour and in 3 unwashed eyes and 2 washed eyes at 24 hours. The washed eyes
had returned to normal by 48 hours, but the unwashed eyes were still showing a reaction when the rabbits were killed at 6 days.
Washing the eyes reduced the severity of the reactions to a very great extent in that only slight reaction was present at 24 hours and all eyes
had returned to normal by 10 days.
Because of the severity of the reactions the 3 rabbits with unwashed eyes were killed after 6 days.
Applicant's summary and conclusion
- Interpretation of results:
- corrosive
- Remarks:
- Migrated information Criteria used for interpretation of results: expert judgment
- Conclusions:
- Based on the above mentioned data and as the animals were sacrificed for animal welfare reasons the substance is considered to be corrosive.
- Executive summary:
100 mg of the substance was instilled into the conjunctval sac of the left eye of six healthy new zealand white rabbits. The right eye served as control. After 30 seconds the substance was flushed out of the eyes of three rabbits with approx 200 mL water.
The rabbits were examined after 1, 24, 48, 72 hours as well as 6 and 10 days after treatment.
Washing the eyes reduced the severity of the reactions to a very great extent in that only slight reaction was present at 24 hours and all eyes had returned to normal by 10 days.
Because of the severity of the reactions the 3 rabbits with unwashed eyes were killed after 6 days.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.