Registration Dossier
Registration Dossier
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: 615-712-2 | CAS number: 720-94-5
- 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

Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation / corrosion
- Remarks:
- in vitro
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 6 June 2014 - 16 June 2014
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Test method according to OECD Guideline 430. GLP study.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 014
- Report date:
- 2014
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 430 (In Vitro Skin Corrosion: Transcutaneous Electrical Resistance Test Method (TER))
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.40 (In Vitro Skin Corrosion: Transcutaneous Electrical Resistance Test (TER))
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- 4,4,4-trifluoro-1-(4-methylphenyl)butane-1,3-dione
- EC Number:
- 615-712-2
- Cas Number:
- 720-94-5
- Molecular formula:
- C11H9F3O2
- IUPAC Name:
- 4,4,4-trifluoro-1-(4-methylphenyl)butane-1,3-dione
- Details on test material:
- - Name of test material: 4,4,4-Trifluoro-1-(4-methylphenyl)-1,3-butanedione
- Physical state: slightly coloured crystalline powder
- Analytical purity: 99.9%
- Lot/batch No.: M13696C
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Details on test animals or test system and environmental conditions:
- SOURCE OF THE BIOLOGICAL MATERIAL:
TEST ANIMALS:
- Source: Centre for Experimental Medicine at the Medical University in Katowice
- Age at study initiation: At the beginning of the experiment, the animals were 21 days old. The skin discs used in the experiment were obtained from two 29-day-old female rats.
- Housing: Plastic cage covered with a wire bar lid. Dimensions: 58 x 37 x 21 cm. Bedding: UV-sterilized wood shavings.
- Diet (e.g. ad libitum): ad libitum, "Murigran” standard granulated laboratory fodder
- Water (e.g. ad libitum): ad libitum, tap water
- Acclimation period: 3 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20ºC
- Humidity (%): 49-56%
- Air changes (per hr): about 16 times/hour
- Photoperiod (hrs dark / hrs light): 12 hours light/12 hours dark
Test system
- Type of coverage:
- other: Not applicable: in-vitro test
- Preparation of test site:
- other: Not applicable: in-vitro test
- Vehicle:
- water
- Controls:
- yes, concurrent vehicle
- Amount / concentration applied:
- VEHICLE
- Amount(s) applied (volume or weight with unit): 150 µl of distilled water - Duration of treatment / exposure:
- 24 hours
- Number of animals:
- 2
Results and discussion
In vivo
- Irritant / corrosive response data:
- On the grounds of the study, it may be stated that the test item belongs to a group of substances which do not lead to skin corrosion/severe irritation. The mean TER values for the test item were higher than 5 kΩ and there were not any visible changes on the skin discs.
Any other information on results incl. tables
Results of the control transcutaneous electrical resistance test (TER):
Animal number |
Skin disc number |
TER value (kΩ) |
1 |
1 |
16.21 |
2 |
15.78 |
|
2 |
1 |
12.60 |
2 |
11.53 |
The skin discs gave the resistance values greater than 10 kΩ; therefore, the remainder of the skin discs of the animals could have been used in the experiment.
Results of the transcutaneous electrical resistance test (TER):
Animal number |
Tested substance |
Skin disc number |
TER value (kΩ) |
Mean TER value ± SD (kΩ) |
1 |
Positive control – 36% HCl |
1 |
0.76 |
0.78 ± 0.02 |
2 |
0.79 |
|||
3 |
0.80 |
|||
Negative control – distilled water |
1 |
23.25 |
23.68 ± 0.40
|
|
2 |
24.03 |
|||
3 |
23.75 |
|||
Test item |
1 |
18.01 |
18.37 ± 0.38
|
|
2 |
18.33 |
|||
3 |
18.76 |
|||
2 |
Positive control – 36% HCl |
1 |
0.87 |
0.88 ± 0.01 |
2 |
0.88 |
|||
3 |
0.88 |
|||
Negative control – distilled water |
1 |
22.75 |
22.24 ± 0.45 |
|
2 |
21.90 |
|||
3 |
22.06 |
|||
Test item |
1 |
19.29 |
19.41 ± 0.30 |
|
2 |
19.75 |
|||
3 |
19.18 |
The concurrent mean values for the positive and negative controls were within the acceptable ranges for the method:
Positive control: 0.5-1.0 kΩ
Negative control: 10 -25 kΩ
The mean TER results for the skin discs treated with the test item were equal to 18.37 kΩ (animal no. 1) and 19.41 kΩ (animal no. 2).
Gross changes on the surface of the treated skin discs:
Animal number |
Tested substance |
Skin disc number |
Gross changes |
1 |
Positive control – 36% HCl |
1 |
perforation |
2 |
perforation |
||
3 |
perforation |
||
Negative control – distilled water |
1 |
no changes |
|
2 |
no changes |
||
3 |
no changes |
||
Test item |
1 |
no changes |
|
2 |
no changes |
||
3 |
no changes |
||
2 |
Positive control – 36% HCl |
1 |
perforation |
2 |
perforation |
||
3 |
perforation |
||
Negative control – distilled water |
1 |
no changes |
|
2 |
no changes |
||
3 |
no changes |
||
Test item |
1 |
no changes |
|
2 |
no changes |
||
3 |
no changes |
The gross examination showed that the positive control skin discs exhibited skin perforation, whereas the negative control skin discs and the ones treated with the test item did not reveal any changes.
Applicant's summary and conclusion
- Interpretation of results:
- other: non-corrosive
- Remarks:
- Criteria used for interpretation of results: EU
- Conclusions:
- The substance do not lead to skin corrosion/severe irritation. The mean TER values for the test item were higher than 5 kΩ and there were not any visible changes on the skin discs.
- Executive summary:
The in vitro skin corrosion: transcutaneous electrical resistance test (TER) was performed according to OECD Guideline 430 Guideline and EU Method B.40. (GLP study). Skin discs used in the experiment were obtained from two 29-day-old rats. The test item (ground to a powder) was uniformly applied to the epidermal surface of the skin disc placed inside a tube. Positive (36% hydrochloric acid) and negative (distilled water) controls were conducted concurrently. Three skin discs obtained from each animal were used for the test item and three for each control item. The test item and the control items were evenly applied to the discs for 24 hours and kept at 21-22°C. Then, they were removed by washing with a jet of tap water and the surface tension of the skin was reduced by adding 70% ethanol. After removing the ethanol the tissue was hydrated by the addition of 3 mL of a solution of MgSO4 (154 mM). A LCR 6401 low-voltage, alternating current databridge was used to measure the electrical resistance of the skin in kΩ by placing the databridge electrodes on either side of the skin disc. The skin discs were subjected to a gross examination. The mean TER results were equal to 18.37 kΩ (animal no. 1) and 19.41 kΩ (animal no. 2). The concurrent positive and negative control values fell within the acceptable ranges for the method. Gross examinations of the skin discs did not reveal any pathological changes. On the grounds of the study, it may be stated that the test item do not lead to skin corrosion/severe irritation. The mean TER values for the test item were higher than 5 kΩ and there were not any visible changes on the skin discs.
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.
