Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 247-956-7 | CAS number: 26748-47-0
- 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
![](https://poisoncentres.echa.europa.eu/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/print_toxicological-information.png)
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1992-11-24 to 1993-03-16
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 993
- Report date:
- 1993
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Version / remarks:
- 1981
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- 1-methyl-1-phenylethyl peroxyneodecanoate
- EC Number:
- 247-956-7
- EC Name:
- 1-methyl-1-phenylethyl peroxyneodecanoate
- Cas Number:
- 26748-47-0
- Molecular formula:
- C19H30O3
- IUPAC Name:
- 1-methyl-1-phenylethyl 2-ethyl-2,5-dimethylhexaneperoxoate
Constituent 1
- Specific details on test material used for the study:
- - Name: Cumylperoxyneodecanoate
- Brand name: Trigonox 99-C75
- Batch No.: 0509207222002
- Purity: 75% in aromatic free mineral spirit (CAS No.: 31807-55-3 and 26748-47-0)
- Storage: freezer
TREATMENT OF TEST MATERIAL PRIOR TO TESTING
- Treatment of test material prior to testing:
An appropriate quantity of the test material, as supplied by the Sponsor, was dispensed on the day of dosing.
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Froxfield S.P.F. Rabbits, Broadway Farm, Froxfield, Hampshire, England
- Age at study initiation: Animals were approximately 4 months old
- Weight at study initiation: 3.35 - 3.60 kg
- Housing: The animals were individually housed in suspended stainless steel cages mounted in mobile batteries. The cages were fitted with perforated counter-sunk floor panels. A tray beneath the floor was lined with absorbent paper which was changed regularly.
- Diet (e.g. ad libitum): ad libitum; commercially available standard pelleted rabbit diet (S.Q.C. Rabbit Diet, Special Diets Services Limited, Witham, Essex, England).
- Water (e.g. ad libitum): ad libitum; tap water taken from the public supply; in England the supply and quality of this water is governed by Department of the Environment regulations.
- Acclimation period: no data
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 16 - 20 °C
- Humidity (%): 52 - 60%
- Air changes (per hr): 15 complete air changes per hour without re-circulation
- Photoperiod (hrs dark / hrs light): electric time-switches operated a lighting cycle of 12 hours of artificial light per day
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- clipped
- Vehicle:
- unchanged (no vehicle)
- Controls:
- yes, concurrent no treatment
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): a single dose (0.5 mL) was applied directly to the skin - Duration of treatment / exposure:
- 4 hours exposure period
- Observation period:
- 1, 24, 48, 72 hours after removal of the bandages. Additional observation of persistent effects of treatment were made 6, 9, 12 and 15 days after treatment.
- Number of animals:
- 3.
A single animal was initially treated. In the absence of a severe irritation response in this sentinel animal, the remaining two animals were committed to the study. - Details on study design:
- TEST SITE
- Area of exposure: 6 x 6 cm
- Type of wrap if used: Test material was covered by an unmedicated gauze patch which was held in place on the place on the left test site by strips of Blenderm (Community Care Products, 3M Health Care, Loughborough, England). Pads of cotton whool and elasticated bandage were used to protect the patches and ensure good contact between the skin and the test material.
REMOVAL OF TEST SUBSTANCE
- Washing (if done): the treatment sites were gently washed with warm water and dried with paper towels to remove excess test material adhering to the skin.
OBSERVATION TIME POINTS
Assessment of skin irritation responses at the control and treated test sites were made 1, 24, 48 and 72 hours after removal of the bandages. Additional observations of persistent effects of treatment were made 6, 9, 12 and 15 days after treatment.
SCORING SYSTEM:
- Method of calculation:
Reactions of the test sites were assessed according to the criteria of Draize (1959) (for details see Table 1 in box 'Any other information on material and methods').
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 3
- Max. score:
- 4
- Reversibility:
- fully reversible within: 15 days
- Remarks on result:
- positive indication of irritation
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- fully reversible within: 15 days
- Remarks on result:
- positive indication of irritation
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- fully reversible within: 15 days
- Remarks on result:
- positive indication of irritation
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 1.3
- Max. score:
- 4
- Reversibility:
- fully reversible within: 15 days
- Remarks on result:
- positive indication of irritation
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- fully reversible within: 15 days
- Remarks on result:
- positive indication of irritation
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- no indication of irritation
- Irritant / corrosive response data:
- Well-defined or moderate erythema and very slight to moderate eedema were observed in two rabbits during the first 72 hours following bandage removal. Loss of elasticity was observed in both of these rabbits during the first week of observation. The area affected by these changes extended 2-3 cm beyond the test site of one of these rabbits. On the sixth day, very slight erythema and edema were observed, with the addition of exfoliation. On the ninth and twelfth days, exfoliation was still present in both animals. The test sites of these two animals were overtly normal on the 15th day.
The remaining rabbit showed very slight erythema during the first 72 hours following bandage removal. Very slight edema was also observed at the one-hour examination. Loss of elasticity was observed at 24-hour examination, and persisted until the 12th day. Exfoliation was evident during the latter part of the first week of observation. The test site of this animal was overtly normal on the fifteenth day after treatment.
The test sites of all three animals were sticky to touch at the one and 24-hour examinations. The effect was considered to have been caused by residual dose material and adhering to the skin after the washing procedure. This occurrence did not affect the assessment of the skin responses.
The control site of each animal did not show any response to the control procedure.
The mean values for erythema in two animals and edema in one animal, recorded 24, 48 and 72 hours after treatment, equaled or exceeded the EEC limit values considered to indicate a significant inflammatory response to treatment.
Mean Values for erythema and oedema are summed up in table 2 in box 'Any other information on results incl. tables'.
Any other information on results incl. tables
Table 2: Mean values for erythema and oedema 24, 48, 72 hours after treatment
Animal number and sex | Erythema* | Oedema* | ||
Test | Control | Test | Control | |
23TJ 811F | 3.0 | 0.0 | 2.0 | 0.0 |
23TJ 816F | 2.0 | 0.0 | 1.3 | 0.0 |
23TJ 823F | 1.0 | 0.0 | 0.0 | 0.0 |
* Values based on criteria documented in Table 1 in box 'Any other information on material and methods'.
Table 3: Scoring of irritance responses*
Test site: 0.5 mL Trigonox 99 -C75
Control site: No treatment
both: semioccluded for 4 hours
Score after removal of dressings | |||||||||
Animal number and sex | Type of Response | 1 hour | 24hour | 48 hour | 72 hours | ||||
Test site | Control site | Test site | Control site | Test site | Control site | Test site | Control site | ||
23TJ 811F | Erythema | 3 | 0 | 3 | 0 | 3 | 0 | 3 | 0 |
STW | STW | TW | TW | ||||||
Oedema | 3 | 0 | 2 | 0 | 2 | 0 | 2 | 0 | |
23TJ 816F | Erythema | 2 | 0 | 2 | 0 | 2 | 0 | 2 | 0 |
ST | ST | T | T | ||||||
Oedema | 2 | 0 | 2 | 0 | 1 | 0 | 1 | 0 | |
23TJ 823F# | Erythema | 1 | 0 | 1 | 0 | 1 | 0 | 1 | 0 |
S | ST | TX | TX | ||||||
Oedema | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
* Criteria documented in Table 1 in box 'Any other information on material and methods'.
# Sentinel animal
S Sticky to touch
T Loss of elasticity
W Area affected extends to 2 -3 cm beyond test site/application site
X Exfoliation
Table 4 : Scoring of irritance response*
Test site: 0.5 mL Trigonox 99 -C75
Control site: No treatment
both: semioccluded for 4 hours
Score after removal of dressings | |||||||||
Animal number and sex | Type of Response | 6 days | 9 days | 12 days | 15 days | ||||
Test site | Control site | Test site | Control site | Test site | Control site | Test site | Control site | ||
23TJ 811F | Erythema | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
TWX | WX | X | |||||||
Oedema | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |
23TJ 816F | Erythema | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
TX | X | X | |||||||
Oedema | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |
23TJ 823F# | Erythema | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
TX | T | T | |||||||
Oedema | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
* Criteria documented in Table 1 (in box "Any other information on material and methods").
# Sentinel animal
S Sticky to touch
T Loss of elasticity
W Area affected extends to 2 -3 cm beyond test site/application site
X Exfoliation
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Based on the results and in accordance to the CLP regulation no classification for skin irritation is warranted.
- Executive summary:
In a primary dermal irritation study according to guideline OECD 404, 3 female New Zealand White rabbits (4 months old, 3.35 - 3.60 kg) were dermally exposed to 0.5 mL of Trigonox 99 -C75 to the closely-clipped dorsal (6 x 6 cm) of the left site. Test sites were covered with a semi-occlusive dressing for 4 hours. Animals were then observed for 15 days.
Well-defined or moderate erythema and very slight to moderate edema were observed in two rabbits during the first 72 hours following bandage removal. Loss of elasticity was observed in both of these rabbits during this time. On the sixth day very slight erythema and edema and loss of elasticity were observed, with the addition of exfoliation. On the ninth and twelfth days, exfoliation was still present in both animals. The remaining rabbit showed very slight erythema during the first 72 hours following bandage removal. Very slight edema was also observed at the one-hour examination. Loss of elasticity was observed at the 24-hour examination and persisted until the 12th day. Exfoliation was evident during the latter part of the first week of observation. The test sites of all animals were overtly normal on the 15th day after treatment.
In this study, Trigonox 99 -C75 is not a dermal irritant based on CLP criteria.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
![ECHA](/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/echa_logo.png)