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EC number: 227-231-1 | CAS number: 5726-19-2
- 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
Acute Toxicity: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- January 8, 1997 - February 4, 1997
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 997
- Report date:
- 1997
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.2 (Acute Toxicity (Inhalation))
- Deviations:
- no
- GLP compliance:
- yes
- Test type:
- standard acute method
- Limit test:
- yes
Test material
- Reference substance name:
- 2-methylcyclohexyl acetate
- EC Number:
- 227-231-1
- EC Name:
- 2-methylcyclohexyl acetate
- Cas Number:
- 5726-19-2
- Molecular formula:
- C9H16O2
- IUPAC Name:
- 2-methylcyclohexyl acetate
- Details on test material:
- - Name of test material (as cited in study report): 2-Methyl cyclohexyl acetate
- Physical state: Liquid
- Analytical purity: >95%
- Lot/batch No.: 36586
- Expiration date of the lot/batch: June 1997
- Storage condition of test material: Room temperature in the dark.
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Charles River UK Ltd, Manston Road, Margate, Kent, England.
- Weight at study initiation: males: 248-281 g; females: 196-230 g.
- Housing: By sex in groups of 5. Stainless steel sheet and wire mesh cages, 35cm x 53cm x 25cm.
- Diet (e.g. ad libitum): Ad libitum (SDS RM1)
- Water (e.g. ad libitum): Ad libitum (tap water)
- Acclimation period: 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 16-22 ºC
- Humidity (%): 36-58%
- Photoperiod (hrs dark / hrs light): 12 hrs dark / 12 hrs light (artificial light, 8 am - 8 pm).
Administration / exposure
- Route of administration:
- other: inhalation: liquid droplet aerosol and vapour.
- Type of inhalation exposure:
- nose only
- Vehicle:
- air
- Details on inhalation exposure:
- GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure apparatus: Aerosol generator
- Exposure chamber volume: Snout-only exposure chamber (ADG Developments), cylindrical form (30 cm i.d., 45 cm height), made of aluminium alloy, with and enclosed volume of approx. 30 litres.
- Method of holding animals in test chamber: The rats were held in moulded polycarbonate restraining tubes which were attached at evenly spaced ports in the cylindrical section of the chamber. Each rat was restrained in a forward position by an adjustable foamed plastic stopper.
- Source and rate of air: A supply of clean dried air was connected to the aerosol generator giving a flow rate of 15 litres/minute at the atomising jet. The test item was introduced into the generator through a syringe pump, with an initial flow rate of 0.3 ml/minute. This flow rate was expected to give a concentration of 2-methylcyclohexyl acetate in air slightly in excess of 5 mg/L. Equilibration period: 5 minutes.
- Treatment of exhaust air: Each chamber was equipped with an extract fan exhausting to atmosphere through an absolute filter.
- Temperature, humidity, pressure in air chamber:
Temperature (mean): 20 ºC (both control and treatment chambers)
Relative humidity (mean): 42 % (control), 45 % (treatment)
TEST ATMOSPHERE
- Brief description of analytical method used:
Test item concentration in the chamber: Gas chromatography (Hewlett Packard 5890A fitted with a model 7673 autosampler). Five samples (every 30 minutes) were taken during the exposure.
Particle size distribution: Two additional samples (at 90 and 210 minutes following the equilibration period) were taken during the exposure.
The nominal concentration was calculated from the amount of 2-methylcyclohexyl acetate dispersed in the generator and the total air flow through the generator during exposure. - Analytical verification of test atmosphere concentrations:
- yes
- Remarks:
- (see above)
- Duration of exposure:
- 4 h
- Concentrations:
- 0 (control), 5.32 mg/L
- No. of animals per sex per dose:
- 5 animals per sex and per dose
- Control animals:
- yes
- Details on study design:
- - Duration of observation period following administration: 14 days
- Frequency of observations and weighing:
Mortality and clinical signs: at the end of chamber equilibration period, at 0.25, 0.5 and 1.0 hours and then at hourly intervals during the exposure. During the observation period, once in the morning and then as necessary following a later check.
Body weight: daily from the day of delivery until the end of the observation period.
Food and water consumption: daily from the day of arrival.
- Necropsy of survivors performed: yes, at the end of the 14-day observation period by intraperitoneal injection of pentobarbitone sodium and exsanguinated when clinically dead.
Gross pathology: all rats were subjected to a detailed macroscopic examination.
Organ weights: lungs
Histopathology: lungs, liver and kidneys (buffered 10% formalin)
Results and discussion
Effect levels
- Key result
- Sex:
- male/female
- Dose descriptor:
- LC50
- Effect level:
- > 5.32 mg/L air (analytical)
- Based on:
- test mat.
- Exp. duration:
- 4 h
- Mortality:
- There were no deaths.
- Clinical signs:
- other: There were no clinical signs during the exposure nor observation periods related to treatment.
- Body weight:
- The rate of bodyweight gain for rats following the exposure was similar to that of the control rats.
- Gross pathology:
- There were no macroscopic abnormalities in test or control rats.
- Other findings:
- - Food and water consumption: A slight reduction in the food consumption of male test rats was recorded for 1 day following exposure, but were otherwise similar to the control values.
- Organ weights: The mean lung weights for male and female test rats were similar to the respective control values.
- Histopathology: no data available.
Any other information on results incl. tables
Concentration of 2 -methylcyclohexyl acetate in the chamber air: 5.32 ± 0.230 mg/L
Nominal concentration: 20.3 mg/L
Particle size distribution: c.a. 85% of the test atmosphere was present as vapour or droplets of a respirable size (<6 mm).
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Remarks:
- Criteria used for interpretation of results: EU
- Conclusions:
- The acute 4h-LD50 for 2-methylcyclohexyl acetate was determined to be >5.32 mg/L of air in rats.
- Executive summary:
An acute inhalation toxicity test was performed on 2 -methylcyclohexyl acetate in accordance with EEC method B.2. Five rats per sex were exposed to the test item for 4 hours in a snout-only exposure system (liquid droplets aerosol and vapour). The concentration of 2 -methylcyclohexyl acetate was 5.32 mg/L. An additional group of control rats (five male and five females) was exposed to air only for 4 hours. The groups were observed for 14 days post-exposure and necropsy was performed at study termination. There were no deaths nor clinical signs during and following exposure. The rate of bodyweight gain for test rats was similar to that of the control rats. A slight reduction in food consumption was recorded for male rats on the day following exposure but were otherwise similar to that of the control rats. The lung weights were similar to control values and there were no macroscopic abnormalities. Based on these results, the acute 4h-LC50 for 2 -methylcyclohexyl acetate was determined to be >5.32 mg/L of air in rats.
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