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EC number: 213-944-5 | CAS number: 1068-27-5
- 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
No effects were pbserved in an in vivo test.
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
- Study period:
- from 2003-01-14 to 2003-04-04
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Version / remarks:
- (1992)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.6 (Skin Sensitisation)
- Version / remarks:
- (1996)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 870.2600 (Skin Sensitisation)
- Version / remarks:
- (August 1998)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: Japanese Ministry of Agriculture, Forestry and Fisheries (MAFF): Japanese Test Guidelines (draft). Test Reports accompanying an application for registration. Unauthorised English translation, July 2000.
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- One in vivo non-LLNA study is already available.
- Species:
- guinea pig
- Strain:
- Dunkin-Hartley
- Sex:
- female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Species: Dunkin Hartley strain, albino guinea pig (SPE-quality), females were nulliparous and non-pregnant.
- Source: Charles River Deutschland, Kisslegg, Germany
- Age at study initiation: Young adult animals (approx. 4 weeks old)
- Housing: Group housing of maximally 5 animals per labelled cage (74 cm x 54 cm x 25 cm geight) containing purified sawdust as bedding material (SAWI, Jelu Werk, Rosenberg, Germany).
- Identification: Ear tattoo
- Diet: Free access to standard guinea pig diet, including ascorbic acid (100 mg/kg); (Charles River Breeding and Maintenance Diet for Guinea Pigs, Altromin, Lage, Germany).
- Water: Free access to tap water. Vitamin C (Dopharma, Raamsdonkveer, Netherlands) 200 mg/L was added to the water of the animals of the main study to ensure sufficient availability.
- Acclimation period: At least 5 days before the start of treatment under laboratory conditions.
ENVIRONMENTAL CONDITIONS
- Temperature: 21 ± 3 °C
- Humidity: 30 - 70 %
- Air changes: 15 per hour
- Photoperiod: 12 hours artificial fluorescent light and 12 hours dark per day. - Route:
- intradermal and epicutaneous
- Vehicle:
- corn oil
- Concentration / amount:
- Induction:
- intradermal: 50%
- epidermal: 100%
Challange:
- epidermal. 50% - Route:
- epicutaneous, occlusive
- Vehicle:
- corn oil
- Concentration / amount:
- Induction:
- intradermal: 50%
- epidermal: 100%
Challange:
- epidermal. 50% - No. of animals per dose:
- Experimental group: 10 females
Control group: 5 females - Details on study design:
- RANGE FINDING TESTS: Practical feasibility of administration determined the highes starting-concentration for each route. The starting- and subsequent concentrations were taken from the series: 100 % (undiluted), 50 %, 20 %, 10 %, 5 %, 2 %, 1 % and if needed, further lower concentrations using the same steps.
The test system and procedures were identical to those used during the main study, unless otherwise specified. The four animals selected were between 4 and 9 weeks old. No body weights were determined.
A.1 INDUCTION EXPOSURE (intradermal, 0.1 mL/site; Day 1)
- No. of exposures: 1
- Exposure period: single treatment on day 1
- Test groups: A) A 1:1 w/w mixture of Freunds' Complete Adjuvant (Difco, Detroit, U.S.A.) with water for injection (Fresenius AG, Bad Homburg, Germany); B) The test substance at a 50% concentration; C) 1:1 w/w mixture of the undiluted test substance and Freunds' Complete Adjuvant.
- Control group: Treated with adjuvant and the vehicle
- Site: Scapular region
- Frequency of applications: Once
- Concentrations: 50 %
A.2 INDUCTION EXPOSURE (epidermal, 0.5 mL/site; Day 8)
- No. of exposures: 1
- Exposure period: 48 hours
- Test groups: The scapular region was treated with 0.5 mL of a 100 % test substance concentration.
- Control group: Treated with adjuvant and the vehicle
- Site: Scapular region (area between the injection sites)
- Concentrations: 100 %
B. CHALLENGE EXPOSURE (epidermal, 0.1 mL; Day 22)
- No. of exposures: 1
- Day(s) of challenge: 22 days after the epidermal exposure
- Exposure period: 24 hours
- Test groups: single treatment
- Control group: single treatment
- Site: Flank
- Concentrations: 50 %
- Evaluation: 24 and 48 hours - Positive control substance(s):
- no
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 50 %
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 50 %
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 50 %
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 50 %
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Group:
- positive control
- Remarks on result:
- not measured/tested
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Based on the results of this study, the test substance is not considered to be sensitising to the skin under the test conditions chosen.
- Executive summary:
2,5-Bis(tert-butylperoxy)-2,5-dimethyl-3-hexyne (85% in mineral oil) was tested in a Maximisation Test in albino guinea pig according to OECD guideline 406.
Test substance concentrations selected for the main study were based on the results of a preliminary study. In the main study, ten experimental animals were intradermally injected with a 50 % concentration and epidermally exposed to a 100 % concentration. Five control animals were similarly treated, but with vehicle alone (corn oil). Two weeks after the epidermal application all animals were epidermal challenged with a 50 % test substance concentration and the vehicle. No skin reactions were evident after the challenge exposure in the experimental and control animals. There was no evidence that the test item had caused skin hypersensitivity in the guinea pig, since no responses were observed in the experimental animals in the challenge phase.
Based on these results and according to the EC criteria for classification and labelling, the test substance does not have to be classified and has no obligatory labelling requirement for sensitisation by skin contact.
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
2,5-Bis(tert-butylperoxy)-2,5-dimethyl-3-hexyne (85 % in mineral oil) was tested in a Maximisation Test in albino guinea pig according to OECD guideline 406 (Akzo Nobel 2003, 366312). Test substance concentrations selected for the main study were based on the results of a preliminary study. In the main study, ten experimental animals were intradermally injected with a 50 % concentration and epidermally exposed to a 100 % concentration. Five control animals were similarly treated, but with vehicle alone (corn oil). Two weeks after the epidermal application all animals were epidermal challenged with a 50 % test substance concentration and the vehicle. No skin reactions were evident after the challenge exposure in the experimental and control animals. There was no evidence that the test item had caused skin hypersensitivity in the guinea pig, since no responses were observed in the experimental animals in the challenge phase.
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Justification for classification or non-classification
Classification, Labelling, and Packaging Regulation (EC) No 1272/2008:
The available experimental test data are reliable and suitable for classification purposes under Regulation (EC) No 1272/2008 (CLP). As a result the substance is not considered to be classified for skin sensitisation under Regulation (EC) No 1272/2008, as amended for the fifteenth time in Regulation (EU) 2020/1182.
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