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EC number: 603-837-5 | CAS number: 134605-64-4
- 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 sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1995
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: According to guideline; under GLP conditions
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 995
- Report date:
- 1995
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- EPA OPP 81-6 (Skin Sensitisation)
- Deviations:
- no
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Deviations:
- no
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EU Method B.6 (Skin Sensitisation)
- Deviations:
- no
- GLP compliance:
- yes
- Type of study:
- guinea pig maximisation test
Test material
- Reference substance name:
- 1-(allyloxy)-2-methyl-1-oxopropan-2-yl 2-chloro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]benzoate
- EC Number:
- 603-837-5
- Cas Number:
- 134605-64-4
- Molecular formula:
- C20H18ClF3N2O6
- IUPAC Name:
- 1-(allyloxy)-2-methyl-1-oxopropan-2-yl 2-chloro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]benzoate
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
- Details on test material:
- - Physical state: solid (tan powder)
- Stability under test conditions: Analysis of the test material/vehicle mixtures for concentration, homogeneity/solubility, and stability was not conducted.
- Storage condition of test material: Room temperature
Constituent 1
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- other: Crl :(HA)BR
- Sex:
- male
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Recognised animal supplier
- Age at study initiation: not reported
- Weight at study initiation: 351 - 421 g
- Housing: individually housed in screen-bottom stainless steel cages.
- Diet (e.g. ad libitum): certified guinea pig diet ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: at least 7 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 19 - 25
- Humidity (%): 50 +/- 20
- Air changes (per hr): not reported
- Photoperiod (hrs dark / hrs light): 12h light / 12h dark
IN-LIFE DATES: From: To: 1995-07-11 to 1995-08-21
Study design: in vivo (non-LLNA)
Inductionopen allclose all
- Route:
- intradermal and epicutaneous
- Vehicle:
- other: mineral oil and petrolatum
- Concentration / amount:
- Preliminary skin irritation study: 1, 10, 15 and 25 %w/w
Induction dose: 25% w/w
Challenge dose: 25% w/w
Challengeopen allclose all
- Route:
- epicutaneous, occlusive
- Vehicle:
- other: mineral oil and petrolatum
- Concentration / amount:
- Preliminary skin irritation study: 1, 10, 15 and 25 %w/w
Induction dose: 25% w/w
Challenge dose: 25% w/w
- No. of animals per dose:
- Group 1 - Preliminary skin irritation study: 4
Group 2 - Main test: 20
Group 3 - Irritation control: 10
Group 4 - Positive control (sulfathiazole): 10
Group 5 - Positive control-irritation control: 5 - Details on study design:
- RANGE FINDING TESTS:
The purpose of the irritation screening study was to find a moderately irritating dose level to use for the topical application and the highest non-irritating concentration to be used for the challenge application. Four animals were treated with the test material at concentrations of 1%, 10%, 15%, and 25% w/w in petrolatum. Each animal received two different concentrations of the test material. The test material concentrations were applied in a thick even layer to 2-cm x 2-cm Whatman No. 3 filter papers, applied to two sites (one on the right side and one on the left side) on the shaved back of each animal, covered with overlapping strips of Blenderm tape, and overwrapped with Elastoplast® tape. The patches remained in place for 24 hours after which they were removed. The application sites were observed for dermal reactions at approximately 24 and 48 hours after patch removal.
MAIN STUDY
A. INDUCTION EXPOSURE
Animals in Groups 2 and 4 received duplicate 0.1-ml intradermal injections on the shoulder area of a 1:1 dilution of Freund's Complete Adjuvant in sterile water, a 5% w/v suspension of the test material in mineral oil (Group 2) or a 5% w/v suspension of sulfathiazole in sterile water (Group 4), and a 5% w/v suspension of the test material in Freund's Complete Adjuvant in sterile water (Group 2) or a 5% w/v mixture of sulfathiazole in sterile water in Freund's Complete Adjuvant (Group 4). Animals in Groups 3 and 5 received duplicate 0.1-ml intradermal injections of a 1:1 dilution of Freund's Complete Adjuvant in sterile water, the respective vehicle (mineral oil for Group 3 or sterile water for Group 5) alone, and a 1:1 dilution of the respective vehicle in Freund's Complete Adjuvant in the same manner as for the animals in Groups 2 and 4. Six days later, the animals in Groups 2 through 5 were pretreated with sodium lauryl sulfate applied topically at the injection sites. On Day 8, a 25% w/w mixture of test material in petrolatum was applied over the injection sites of the animals in Group 2, a 25% w/w mixture of sulfathiazole in petrolatum was applied over the injection sites of the animals in Group 4, and petrolatum was applied over the injection sites of the animals in Groups 3 and 5. All induction sites were then occluded for 48 hours.
B. CHALLENGE EXPOSURE
Two weeks after the topical application, all animals received a challenge dose. A 25% w/w mixture of test material in petrolatum was applied to the
right side and the control material (petrolatum) was applied to the left side of each animal in Groups 2 and 3. A 10% w/w mixture of sulfathiazole in
petrolatum was applied to the right side and petrolatum alone was applied to the left side of each animal in Groups 4 and 5. All test and control sites
were occluded for 24 hours and then wiped clean. The challenge sites were examined for dermal reactions at 24 and 48 hours after patch removal. - Challenge controls:
- Petrolatum alone
- Positive control substance(s):
- yes
- Remarks:
- sulfathiazole
Results and discussion
- Positive control results:
- All animals in Group 4 {positive control) exhibited slight to moderate sensitization reactions on the test sites treated with sulfathiazole
In vivo (non-LLNA)
Resultsopen allclose all
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 25% w/w
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: test group. Dose level: 25% w/w. No with. + reactions: 0.0. Total no. in groups: 20.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 25% w/w
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: test group. Dose level: 25% w/w. No with. + reactions: 0.0. Total no. in groups: 20.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- Petrolatum (control)
- No. with + reactions:
- 0
- Total no. in group:
- 35
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: negative control. Dose level: Petrolatum (control). No with. + reactions: 0.0. Total no. in groups: 35.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- Petrolatum (control)
- No. with + reactions:
- 0
- Total no. in group:
- 35
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: negative control. Dose level: Petrolatum (control). No with. + reactions: 0.0. Total no. in groups: 35.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- 10% sulfathiazole
- No. with + reactions:
- 10
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: positive control. Dose level: 10% sulfathiazole. No with. + reactions: 10.0. Total no. in groups: 10.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- positive control
- Dose level:
- 10% sulfathiazole
- No. with + reactions:
- 10
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: positive control. Dose level: 10% sulfathiazole. No with. + reactions: 10.0. Total no. in groups: 10.0.
Applicant's summary and conclusion
- Interpretation of results:
- not sensitising
- Remarks:
- Migrated information Criteria used for interpretation of results: US EPA pesticides
- Conclusions:
- Under the conditions of this study, the test material is not considered to be a skin sensitiser.
- Executive summary:
The study was performed to assess the skin sensitisation potential of the test material in Crl :(HA)BR male guinea pigs following the guinea pig maximisation method. The study was performed to GLP and the method was designed to meet the requirements of EPA OPP 81-6 and equivalent methodology to OECD Guideline 406 and EU Method B.6. In a preliminary skin irritation screening test in 4 test animals were treated with the test material at concentrations of 1%, 10%, 15%, and 25% w/w in petrolatum and were applied to the shaved backs for a period of 24 hours. The test material caused no dermal reaction in any animal at any concentration and was therefore administered as a 25% w/w mixture in petrolatum for the topical induction application and for the challenge phase in the definitive study. In the main study, a group of 45 test animals (20 test animals treated with test material, 10 animals serving as an irritation control, 10 animals serving as a positive control and 5 animals serving as a positive control-irritation control) received induction doses by intradermal injection and topical application. The intradermal injections were made within the boundaries of a 2 -cm x 4 -cm area, one row of three injections on each side of the midline. Each animal received the following: anterior sites: 0.1 ml of a 1:1 dilution of Freund's Complete Adjuvant in sterile water; medial site: 0.1ml test material in Freund's Complete Adjuvant in sterile water / positive control in sterile water in Freund's Complete Adjuvant / vehicle in Freund's Complete Adjuvant. On Day 7 test animals backs were shaved and pretreated with a 10% w;w sodium lauryl sulfate (SLS) suspension in petrolatum before the topical induction application. A 25% w/w mixture of test material in petrolatum, a 25% w;w mixture of sulfathiazole (positive control substance) in petrolatum, or petrolatum was applied over the injection sites of the animals in the respective groups. The patches were covered with overlapping strips of BlendermN tape and secured by an overwrap of Elastoplast® tape wound around the trunk and remained in place for 48 hours. 2 weeks after the topical induction, a topical challenge dose was applied. A 25% w/w mixture of test material in petrolatum and petrolatum alone or a 10% w/w mixture of sulfathiazole in petrolatum and petrolatum alone were applied to the backs of the test animals. The filter paper containing the test or positive control material mixture was placed on the right side and the filter paper containing petrolatum alone was placed on the left side of each animal. The patches were sealed for 24 hours under occlussive dressing. Twenty-four hours after application, the wrappings were removed and the test sites wiped clean with wet disposable paper towels. The test sites were closely shaved approximately 3 hours before the 24-hour challenge observation.
None of the test animals exhibited a dermal reaction to the challenge application of the test or control materials. All animals of the positive control group exhibited slight to moderate sensitization reactions on the test sites treated with sulfathiazole and no dermal reactions on the test sites treated with petrolatum alone. None of the animals in the positive control-irritation control exhibited a dermal reaction to the challenge application of sulfathiazole or petrolatum. Based on these results, the test material is not considered to be a skin sensitizer in guinea pigs.
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