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EC number: 295-619-8 | CAS number: 92113-15-0
- 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

Endpoint summary
Administrative data
Description of key information
Key value for chemical safety assessment
Skin irritation / corrosion
Link to relevant study records
- Endpoint:
- skin corrosion: in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 431 (In Vitro Skin Corrosion: Reconstructed Human Epidermis (RHE) Test Method)
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- Batch no. EXP 7
- Test system:
- human skin model
- Source species:
- human
- Cell type:
- non-transformed keratinocytes
- Vehicle:
- unchanged (no vehicle)
- Irritation / corrosion parameter:
- % tissue viability
- Run / experiment:
- Viability measured after 3 minutes
- Value:
- ca. 40.3
- Positive controls validity:
- valid
- Irritation / corrosion parameter:
- % tissue viability
- Run / experiment:
- Tissue viability measured after 1 hour
- Value:
- ca. 28.1
- Positive controls validity:
- valid
- Interpretation of results:
- Category 1 (corrosive) based on GHS criteria
- Conclusions:
- Notes from study report: "After 3 min and 1h exposure on the surface of EpiDermTM reconstructed human epidermis, the viability of the tissues was assessed and compared to a negative control.
The percentage of viability obtained was 40.3% after 3 min and 28.1% after 1h and therefore:
Potassium Iso-Alpha Resin was classified as Corrosive, optional sub-category 1B/1C to human skin."
Since tetrahydroisoalpha acids are simply hydrogenated, with two side chain C=C double bonds converted to CH-CH, then it is appropriate to read across the classification from iso-alpha acids. - Endpoint:
- skin irritation: in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 1 (reliable without restriction)
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 439 (In Vitro Skin Irritation: Reconstructed Human Epidermis Test Method)
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- Batch no. EXP 7
- Test system:
- human skin model
- Source species:
- human
- Cell type:
- non-transformed keratinocytes
- Irritation / corrosion parameter:
- % tissue viability
- Value:
- ca. 7.323
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Remarks on result:
- positive indication of irritation
- Interpretation of results:
- Category 1 (corrosive) based on GHS criteria
- Conclusions:
- After 60 ± 1 minute exposure on the surface of the EpiDermTM reconstructed human epidermis, and a 42 ± 4 hours post-exposure incubation time, viability of the tissues was assessed and compared to the negative control.
The percentage of viability obtained was 7.323 % and therefore:
Potassium Iso-Alpha Resin was classified as an Irritant to the skin.
Since tetrahydroisoalpha acids are simply hydrogenated, with two side chain C=C double bonds converted to CH-CH, then it is appropriate to read across the classification from iso-alpha acids. The classification is based on endpoint 001 following a corrosion study.
Referenceopen allclose all
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (corrosive)
Eye irritation
Link to relevant study records
- Endpoint:
- eye irritation: in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Justification for type of information:
- An eye irritation study according to OECD test guideline 492 has been commissioned and an update will be made once results are available. The skin corrosion studies performed on this substance indicate that a preliminary classification of eye damage category 1 is appropriate, pending the results of the study planned.
- Qualifier:
- according to guideline
- Guideline:
- other: OECD 431: skin corrosion study used as supporting evidence for classification
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- Batch no. EXP 7
- Vehicle:
- unchanged (no vehicle)
- Irritation parameter:
- other: % tissue viability 3 minutes
- Value:
- ca. 40.3
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Irritation parameter:
- other: % tissue viability 1 hour
- Value:
- ca. 28.1
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Interpretation of results:
- Category 1 (irreversible effects on the eye) based on GHS criteria
- Conclusions:
- An eye irritation study according to OECD test guideline 492 has been commissioned and an update will be made once results are available. The skin corrosion studies performed on this substance indicate that a preliminary classification of eye damage category 1 is appropriate, pending the results of the study planned.
Notes from study report: "After 3 min and 1h exposure on the surface of EpiDermTM reconstructed human epidermis, the viability of the tissues was assessed and compared to a negative control.
The percentage of viability obtained was 40.3% after 3 min and 28.1% after 1h and therefore:
Potassium Iso-Alpha Resin was classified as Corrosive, optional sub-category 1B/1C to human skin."
Since tetrahydroisoalpha acids are simply hydrogenated, with two side chain C=C double bonds converted to CH-CH, then it is appropriate to read across the classification from iso-alpha acids.
Reference
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irreversible damage)
Additional information
Justification for classification or non-classification
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