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EC number: 232-504-3 | CAS number: 8060-28-4
- 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
Key value for chemical safety assessment
Effects on fertility
Link to relevant study records
- Endpoint:
- reproductive toxicity, other
- Remarks:
- See experimental details and the weight of evidence data in the background material.
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- 90 days
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study without detailed documentation
- Qualifier:
- no guideline available
- Version / remarks:
- The experiment has been cited, discussed and referred to as evidence for low toxicity in Chappel et al. (1998) Food Chem. Toxicol. volume 36, pp. 915-922 and in Gerhauser C (2005) Eur. J. Cancer vol. 41, pp. 1941-1954.
- Principles of method if other than guideline:
- 90-day subactue toxicity feeding study set up using 1, 0.1 and 0.01% of hop iso-alpha acids in corn oil, plus a negative control, fed to 21-day-old Sprague-Dawley rats. Histopathological examinations of tissues including reproductive tissues.
- GLP compliance:
- not specified
- Specific details on test material used for the study:
- Isomerized hop extract present as a 50% suspension in corn oil. This will be an extract enriched in hop iso-alpha acids.
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Route of administration:
- oral: unspecified
- Vehicle:
- corn oil
- Details on exposure:
- Rats provided with test ration and water ad libitum
- Duration of treatment / exposure:
- 90 days
- Dose / conc.:
- 0 ppm
- Remarks:
- Iso-alpha acids present at 0, 0.01, 0.1 and 1% in the study design
- Dose / conc.:
- 100 ppm
- Remarks:
- Iso-alpha acids present at 0, 0.01, 0.1 and 1% in the study design
- Dose / conc.:
- 1 000 ppm
- Remarks:
- Iso-alpha acids present at 0, 0.01, 0.1 and 1% in the study design
- Dose / conc.:
- 10 000 ppm
- Remarks:
- Iso-alpha acids present at 0, 0.01, 0.1 and 1% in the study design
- No. of animals per sex per dose:
- 10
- Parental animals: Observations and examinations:
- Animals weighed and their food consumption measured weekly. Periodic check for abnormal blood elements and urine elements made on high level groups and control.
- Postmortem examinations (parental animals):
- Certain organs weighed (body, liver, heart, spleen, kidneys, gonads); certain organs examined microscopically (heart, lung, spleen, liver, pancreas, stomach and intestine, mesenteric lymph nodes, salivary glands, thyroid, kidney, urinary bladder, ovary or testis, uterus or prostate, bone and bone marrow)
- Clinical signs:
- effects observed, treatment-related
- Description (incidence and severity):
- Reduced weight gain at the highest level (1%), but no changes in weights of liver, heart, spleen, kidneys or gonads, and no histopathological changes. The reduced weight gain is likely to be due to the unpalatibility of teh bitter iso-alpha acids.
- Key result
- Dose descriptor:
- dose level: NOAEL can be estimated from effects at highest dose level
- Effect level:
- ca. 10 000 ppm
- Based on:
- act. ingr.
- Sex:
- male/female
- Basis for effect level:
- body weight and weight gain
- Key result
- Dose descriptor:
- other: F1 offspring not tested in this experiment
- Remarks:
- Histopathological examination of reproductive tissues in parents only
- Generation:
- other: F1 offspring not tested in this experiment
- Effect level:
- 0 other: Histopathological examination of reproductive tissues in parents only
- Based on:
- act. ingr.
- Sex:
- male/female
- Basis for effect level:
- other: F1 offspring not tested in this experiment
- Remarks on result:
- other: See the attached background material that gives an analysis of existing data. Further animal studies are not warranted.
- Key result
- Reproductive effects observed:
- not specified
- Lowest effective dose / conc.:
- 10 000 ppm
- Treatment related:
- yes
- Conclusions:
- See the attached background material that gives an analysis of existing data. Further animal studies are not warranted.
Reference
Effect on fertility: via oral route
- Endpoint conclusion:
- no adverse effect observed
Justification for classification or non-classification
Additional information
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