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EC number: 278-031-6 | CAS number: 74931-55-8
- 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 corrosion: in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- May 2018
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 018
- Report date:
- 2018
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 431 (In Vitro Skin Corrosion: Reconstructed Human Epidermis (RHE) Test Method)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- 2-ethylhexanoic acid, compound with 2-aminoethanol (1:1)
- EC Number:
- 278-031-6
- EC Name:
- 2-ethylhexanoic acid, compound with 2-aminoethanol (1:1)
- Cas Number:
- 74931-55-8
- Molecular formula:
- C10H23NO3
- IUPAC Name:
- 2-ethylhexanoic acid, compound with 2-aminoethanol (1:1)
- Test material form:
- liquid
- Details on test material:
- - Density: 0.999 g/cm3
Constituent 1
In vitro test system
- Test system:
- human skin model
- Source species:
- human
- Cell type:
- non-transformed keratinocytes
- Vehicle:
- unchanged (no vehicle)
- Control samples:
- yes, concurrent negative control
- yes, concurrent positive control
- Amount/concentration applied:
- TEST MATERIAL
- Amount applied: Single topical application of 50µl of neat test item
NEGATIVE CONTROL
- Amount applied: 50µl
- Lot/batch no.: RNBG4913
POSITIVE CONTROL
- Amount applied: 50µl
- Lot/batch no.: SLBD3295V - Duration of treatment / exposure:
- 3 and 60 minutes
- Number of replicates:
- Triplicate
Results and discussion
In vitro
Resultsopen allclose all
- Irritation / corrosion parameter:
- % tissue viability
- Run / experiment:
- 3-minute
- Value:
- 97.6
- Vehicle controls validity:
- not applicable
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Irritation / corrosion parameter:
- % tissue viability
- Run / experiment:
- 60-minute
- Value:
- 8.6
- Vehicle controls validity:
- not applicable
- Negative controls validity:
- valid
- Positive controls validity:
- valid
Applicant's summary and conclusion
- Interpretation of results:
- Category 1B (corrosive) based on GHS criteria
- Conclusions:
- In the reported study, mean tissue viability (as a percentage of the negative control) was 8.6 % after a 60-minute exposure and 97.6 % after a 3-minute exposure. 2-Ethylhexanoic acid, compound with 2-aminoethanol (1:1) subsequently required classification as corrosive to skin (Skin Corr. 1B/1C) according to CLP Regulation (EC) No. 1272/2008.
- Executive summary:
An in vitro skin corrosion study was performed for 2-ethylhexanoic acid, compound with 2-aminoethanol (1:1) in line with OECD Guideline 431 (In Vitro Skin Corrosion: Reconstructed Human Epidermis (RHE) Test Method). The test was compliant with GLP. 2-Ethylhexanoic acid, compound with 2-aminoethanol (1:1) was applied neat at 50µl to reconstructed human epidermal model Epiderm™. A negative (sterile water) and positive control (potassium hydroxide) was prepared and run in parallel. Exposure was permitted for a 3- and 60-minute period at 37 °C, 5 % CO2, 95 % RH. Corrosion is directly related to cytotoxicity in the EpiDerm™ tissue. Cytotoxicity is determined by the reduction of MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl-tetrazolium bromide) to formazan by viable cells in the test item treated tissues relative to the corresponding negative control. The results are then used to make a prediction of the corrosivity potential of the test item.
All controls were valid and demonstrated the reliability of the test system. Mean tissue viability, calculated as a percentage of the negative control, was 8.6 % after a 60-minute exposure and 97.6 % after a 3-minute exposure. A classification for skin corrosion (Skin Corr. 1B/1C) is subsequently required for 2-ethylhexanoic acid, compound with 2-aminoethanol (1:1) according to CLP Regulation (EC) No. 1272/2008.
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