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EC number: 202-936-7 | CAS number: 101-37-1
- 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
Endpoint summary
Administrative data
Description of key information
Key value for chemical safety assessment
Skin sensitisation
Link to relevant study records
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.6 (Skin Sensitisation)
- GLP compliance:
- yes
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- An in vivo test for skin sensitisation according to OECD Guidance 406 (guinea pig maximisation test) is already available. Thus, the informtion requirement is fulfilled, and for animal welfare reasons, another in vivo test is not conducted.
- Species:
- guinea pig
- Strain:
- other: Pirbright White (Bor: DAPW)
- Sex:
- male/female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Winkelmann /Borchen
- Age at study initiation: 9 weeks
- Weight at study initiation: males: 410-473 g; females 375-421 g
- Housing: individually, Macrolon cages Type III
- Diet (e.g. ad libitum): ssniff (G) ad libitum
- Water (e.g. ad libitum): tap water ad libitum (twice weekly + vitamin C)
- Acclimation period: 6 days
ENVIRONMENTAL CONDITIONS: according to guideline - Route:
- intradermal
- Vehicle:
- peanut oil
- Concentration / amount:
- 1st application: Induction with 0.1 mL of a 3 % (w/w) solution in peanut oil
- Adequacy of induction:
- other: maximum non-irritating concentration
- Route:
- epicutaneous, occlusive
- Vehicle:
- unchanged (no vehicle)
- Concentration / amount:
- 2nd application: Induction with 0.7 mL undiluted test substance (30-35°C)
- Day(s)/duration:
- 48 h
- Adequacy of induction:
- non-irritant substance, but skin pre-treated with 10% SDS
- Route:
- epicutaneous, occlusive
- Vehicle:
- unchanged (no vehicle)
- Concentration / amount:
- 3rd application: Challenge with 0.2 mL undiluted test substance (30-35°C)
- Day(s)/duration:
- 24 h
- No. of animals per dose:
- control group: 10 animals
treatment group: 10 animals - Details on study design:
- RANGE FINDING TESTS: In preliminary tests, the maximum non-irritating concentration for the intradermal or the slight to moderate irritating concentration for the epidermal application during the induction phase as well as a non-irritating concentration for the epidermal application during the challenge phase were determined
MAIN STUDY
A. INDUCTION EXPOSURE
- No. of exposures: 2
- Exposure period: day 1 intradermal and day 8 epicutaneous for 48 h
- Test groups: 1 with 10 animals
- Control group: 1 with 10 animals
- Site: intradermal - scapular region three pairs of intradermal injections in two parallel lines; epicutaneous - same region was covered with a patch
- Frequency of applications:
- Duration:
- Concentrations: treatment group: intradermal: pair one: FCA/ saline solution 1:1
pair two: test substance solution (3% (w/w) in peanut oil)
pair three: test substance solution / FCA 1:1
epicutaneous: undiluted (30-35°C)
control group: vehicle instead of tets substance
B. CHALLENGE EXPOSURE
- No. of exposures: 1
- Day(s) of challenge: day 22
- Exposure period: 24 h
- Test groups: occlusive patch with 0.2 mL undiluted test substance (30-35°C)
- Control group: identical to treatment group (right flank treated with vehicle alone in both groups)
- Site: right flank (vehicle), left flank (test substance)
- Concentrations: 0.2 mL undiluted test substance
- Evaluation (hr after challenge): 24 and 48 h after challenge - Positive control substance(s):
- yes
- Remarks:
- para-phenylenediamine
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 0.2 mL undiluted test substance (30-35°C)
- No. with + reactions:
- 1
- Total no. in group:
- 10
- Clinical observations:
- slight erythema
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 0.2 mL undiluted test substance (30-35°C)
- No. with + reactions:
- 1
- Total no. in group:
- 10
- Clinical observations:
- slight erythema
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 0.2 mL undiluted test substance (30-35°C)
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 0.2 mL undiluted test substance (30-35°C)
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Remarks on result:
- no indication of skin sensitisation
- Group:
- positive control
- Remarks on result:
- other: once per annum (latest examination: Sep./oct. 1989)
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- In this study under the given conditions the test item showed no skin sensitising effects. The test item is classified as “non-sensitiser“ based on CLP Regulation (EC) No.1272/2008.
Reference
1 of 10 animals exhibited a slight erythema at the treated site 24 and 48 hours after removal of the patch. None of the animals of the control group showed changes at the exposed skin areas. Systemic toxic effects could not be detected. The general condition and body weight development of the test animals were not affected.
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
Triallyl cyanurate was applied to the skin of 10 Pribright White guinea pigs to determine its skin sensitizing properties by the maximization test method according to OECD guideline 406 (90-0119-DGT). The test substance was injected intradermally as a solution in peanut oil (3% w/w) with or without the addition of FCA (three pairs of injections) and was applied undiluted epicutanously during the induction phase. Additionally a solution of sodium dodecylsulfate (10% w/w) in water was applied before the epidermal induction. Challenge was performed epicutanously using the pure test material. 1 out of 10 guinea pigs showed a slight erythema at the 24 and 48 h reading after removal of the patch. None of control animals exhibited changes at the exposed skin areas. Systemic effects could not be detected. The general condition and body weight development of the test animal were not affected.
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
- Additional information:
No evidence of respiratory sensitisation observed.
Justification for classification or non-classification
No classification according to EU and GHS classification criteria required according to DSD (67/548/EEC) and CLP (1272/2008/EC)
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