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EC number: 287-836-1 | CAS number: 85586-34-1
- 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 10 August 1981 to 17 August 1981
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The experimental design is similar to that of OECD guideline 404 with enhanced exposure due to an extended exposure period - 24 hours - and inclusion of dermal abrasion prior to application of the test material.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 981
- Report date:
- 1981
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- other: Proposed Guidelines of the United States Environmental Agency (EPA) S 163.81-5 "Primary dermal irritation study" Federal Register, Vol. 43, No. 163, August 22, 1978
- Deviations:
- no
- GLP compliance:
- no
Test material
- Reference substance name:
- TK 11'278
- IUPAC Name:
- TK 11'278
- Reference substance name:
- ESBO
- IUPAC Name:
- ESBO
- Reference substance name:
- Epoxidised Soybean Oil
- IUPAC Name:
- Epoxidised Soybean Oil
- Reference substance name:
- Soybean oil, epoxidized
- EC Number:
- 232-391-0
- EC Name:
- Soybean oil, epoxidized
- IUPAC Name:
- 232-391-0
- Reference substance name:
- 8013-07-8
- Cas Number:
- 8013-07-8
- IUPAC Name:
- 8013-07-8
- Details on test material:
- - Name of test material (as cited in study report): TK 11'278
- Physical state: Yellow liquid
- Lot/batch No.: Prod. Oct. 80
- Storage condition of test material: not stated
- Other:
- Solubility in water: insoluble
Constituent 1
Constituent 2
Constituent 3
Constituent 4
Constituent 5
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- The test was performed on 3 male and 3 female adult New Zealand White rabbits bred and raised on the laboratory premises. They weighed 2 - 3 Kgs.
They were housed individually in metal cages numbered by ear tags.
They were kept at constant room temperature of 22 ± 2 °C, at a relative humidity of 55 ± 10 % and on a 12-hours light cycle day.
The animals received ad libitum standard rabbit food - NAFAG, No. 814, Gossau SG - and water.
Prior to treatment they were adapted to the laboratory for a minimum of 4 days.
Test system
- Type of coverage:
- occlusive
- Preparation of test site:
- other: skin was shaved. One site abraded one left unabraded
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- Gauze patches of 2.5 x 2.5 cm laden with 0.5 mL of the test material were applied to the prepared abraded and intact skin.
The patches were covered with an impermeable material and were fastened to the body of the rabbit with adhesive tape. - Duration of treatment / exposure:
- The dressings were removed after a 24 hour application.
- Observation period:
- Reactions were appraised using standard Draize assessment, on removal of dressing and during an observation period of 7 days.
- Number of animals:
- 3 male and 3 female adult New Zealand White rabbits
- Details on study design:
- Before treatment the entire back and the flank of the rabbits were shaved with an electric clipper and immediately before treatment the shaved skin on one side was lightly sacrified using a scalpel blade.
Gauze patches of 2.5 x 2.5 cm laden with 0.5 mL of the test material were applied to the prepared abraded and intact skin. The patches were covereed with an impermeable material and were fastened to the body of the rabbit with adhesive tape.
The skin reaction was appraised on ths basis of the following evaluation scheme:
Score for skin irritation in rabbits:
Erythema and eschar formation:
No erythema: .................................................................... 0
Very slight erythema (barely perceptible):.................... 1
Well defined erythema:..................................................... 2
Moderate to severe erythema:........................................ 3
Severe erythema (beet redness) to slight eschar
formation {injuries in depth) :......................................... 4
Total possible erythema score:...................................... 4
Oedema formation
No edema: .......................................................................0
Very sllght edema (barely perceptible): ..................... 1
Sllght edema (edges of area well defined by
definite raising):............................................................. 2
Moderate edema (raised approximately 1 mm): ...... 3
Severe edema {raised more than 1 mm and
extending beyond area of exposure): ........................4
Total possible oedema score: ........................................ 4
Results and discussion
In vivo
Results
- Irritation parameter:
- primary dermal irritation index (PDII)
- Basis:
- mean
- Time point:
- other: 24 and 72 h post application
- Score:
- 1.7
- Max. score:
- 8
- Reversibility:
- fully reversible within: 7 days
- Remarks on result:
- other: Only limited information is provided relating to 24 and 72 scores. Reversibility is presented graphically
- Irritant / corrosive response data:
- The results of the primary skin irritation test are reported in Table 1.
Tha calculated primary irritation index was 2.6 - this includes results from abraded and non-abraded skin.
TK 11'278 was found to cause a moderate irritation when applied to intact and abraded rabbit skin, according to the interpretation of PII results
After 24 hours the surface of the erythema was greater than the site of application on all sites except No. 415 (intact) and No. 416 (abraded). This observation was made after 48 hours on both sites of animal No. 417 and after 72 hours on the abraded side of the same animal.
Results were revaluated to determine a possble classification in accordance with EU/GHS criteria.
In the absence of individual animal scores, taking into account the extended exposure period and assuming a linear response for ameliorating dermal responses between 24 and 72 hours, the mean results for non-abraded skin were averaged for 24 and 72 hour responses as an approximation of the Draize result. On this basis, the mean erythema score for non-abraded skin over 24-72 h was 1.5 and for oedema the mean result was 0.75.
Neiher of these values exceeds the EU classification threshold. - Other effects:
- With the exception of the last day of the test, a slight sedation was observed.
Any other information on results incl. tables
Dermal reactions
Time after exposure (hours) |
Mean Reaction Score |
|||
Erythema |
Oedema |
|||
Intact Skin |
Abraded Skin |
Intact Skin |
Abraded Skin |
|
24 |
1.7 |
2.0 |
1.0 |
1.5 |
72 |
1.3 |
1.5 |
0.5 |
0.7 |
|
||||
Total |
3.0 |
3.5 |
1.5 |
2.2 |
Assessment of Irritation
0
0.1 - 1.0 = minimal
1.1 - 2.0 = slight
2.1 - 4.0 = moderate
4.1 - 6.0 = marked
6.1 - 8.0 = extreme
The scores read after 24 and 72 hours for erythema and edema for the intact as well as for the abraded skin were summed up and divided by 4. The primary irritation index was 2.6.
The abraded skin results are not appropriate for assessment under EU classification guidelines. The mean scores are 24 and 72 hours were used as approximations to the 24 -72h mean. Erythema and oedema mean scores were approximated to be 1.5 and 0.75 respectively. Neither results exceeds the EU classification threshold
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Under the condition of the present experiment TK 11'278 was found to cause a moderate irritation when applied to intact and abraded rabbit skin. The calculated primary irritation index was 2.6.
Individual values are not presented for each rabbit and so it is not possible to fully evaluate in accordance with EU criteria, however an approximation can be calculated that indicates the erythema score for intact skin was approximately 1 and slightly higher for the abraded sites, when averaged over the 24 and 72 hour assessments. On this basis the material would be considered to be only slightly or mildly irritating and would not warrant classification according to EU criteria. - Executive summary:
Under the condition of the present experiment TK 11'278 was found to cause a moderate irritation when applied to intact and abraded rabbit skin. The calculated primary irritation index was 2.6. The estimation of the mean score for irritation based on the 24 and 72 hour assessments was circa 1.0. According to Directive 67/548/EEC no classification is required for dermal irritation. According to Regulation (EC) No. 1272/2008, no classification is warranted.
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