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EC number: 204-411-8 | CAS number: 120-61-6
- 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 22 June to 25 June 1989
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Proprietary GLP study, in accordance with US EPA guidelines (comparable to OECD 404)
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 989
- Report date:
- 1989
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- other: EPA FIFRA, Pesticide Assessment Guidelines Subdivision F; Hazard Evaluation Human and Domestic Animals Section 81-5 "Primary Dermal Irritation Study"
- Qualifier:
- according to guideline
- Guideline:
- other: EPA TSCA Health Effect Test Guidelines; Section HG "Primary Dermal Irritation"
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- use of 6 animals
- GLP compliance:
- yes
Test material
- Reference substance name:
- Dimethyl terephthalate
- EC Number:
- 204-411-8
- EC Name:
- Dimethyl terephthalate
- Cas Number:
- 120-61-6
- Molecular formula:
- C10H10O4
- IUPAC Name:
- dimethyl terephthalate
- Details on test material:
- Dimethyl terephthalate (DMT) was supplied by Hüls Troisdorf AG in a glass screw top jar. It was described as a white flaky solid, and was stored at room temperature. The identification and stability of the test material were not determined.
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- The animals were male New Zealand White rabbits supplied by David Percival Ltd. (UK). At the start of the study the animals werighed 2.27 -3.04 kg and were approximately 12-16 weeks old. They were acclimatised for a minimum of 5 days. Individuals were identified by black indelible marker pen numbers written on the inner surface of the ear.
The rabbits were individually housed in suspended metal cages. Free access to mains drinking water and food (Rabbit Diet, Preston Farmers Ltd., UK) was allowed throughout the study
The animal room was maintained at a temperature of 17-21°C and relative humidity of 55-57%. There were approximately 15 air changes per hour and the lighting was controlled to give 12 hours light and 12 hours dark.
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- water
- Controls:
- no
- Amount / concentration applied:
- 0.5 g test material moistened with 0.5 ml distilled water.
- Duration of treatment / exposure:
- Four hours
- Observation period:
- 72 hours after patch removal
- Number of animals:
- Six
- Details on study design:
- Approximately 24 hours prior to the start of the test, the rabbits were clipped free of fur from the dorsal/flank area using veterinary clippers. Only animals with a healthy intact epidermis by gross observation were selected for the study.
On the day of the test a suitable test site was selected on the back of each rabbit. 0.5 g of the moistened test material was introduced under a 2.5 cm² gauze patch and placed in position on the shorn skin. The patch was secured in position by a strip of adhesive tape (Blenderm). The trunk of each rabbit was then wrapped in an elasticated corset and the animals were returned to their cages.
Four hours after application the wrappings and patches were removed and any residual test material removed by gentle swabbing with cotton wool soaked in diethyl ether.
The test sites were examined for evidence of primary irritation 1 hour after patch removal, and 24, 48 and 72 hours later. The Draize (1959) scale was used (see below).
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: Mean 1, 24, 48 and 72 hours
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- other: not applicable
- Remarks on result:
- other: no reactions recorded
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: Mean 24, 48 and 72 hours
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- other: not relevant
- Remarks on result:
- other: no reactions recorded
- Irritant / corrosive response data:
- No signs of irritation were observed in any rabbit at any time point.
- Other effects:
- No other effects reported.
Any other information on results incl. tables
No further details.
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Dimethyl terephthalate was not irritating to the skin of rabbits under the conditions of this study.
- Executive summary:
The irritant potential of Dimethyl terephthalate (DMT) was determined according to ES EPA guidelines. A single 4 hour, semi-occluded application of DMT to the skin of six male New Zealand White rabbits produced no evidence of skin irritation. The test material produced a primary index of 0.0 and is not classified as irritating to rabbit skin.
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