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EC number: 216-374-5 | CAS number: 1569-02-4
- 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

Acute Toxicity: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1984
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Comparable to a guideline study.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 984
- Report date:
- 1984
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 403 (Acute Inhalation Toxicity)
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EU Method B.2 (Acute Toxicity (Inhalation))
- GLP compliance:
- no
- Test type:
- fixed concentration procedure
Test material
- Reference substance name:
- 1-ethoxypropan-2-ol
- EC Number:
- 216-374-5
- EC Name:
- 1-ethoxypropan-2-ol
- Cas Number:
- 1569-02-4
- Molecular formula:
- C5H12O2
- IUPAC Name:
- 1-ethoxypropan-2-ol
- Details on test material:
- - Name of test material (as cited in study report): Ethoxypropanol
- Physical state: Liquid
- Analytical purity: 91.1%
- Impurities (identity and concentrations):
8.0% 2-ethoxy-1-propanol
0.7% 1-methoxy-2-propanol
0.1% 2-methoxy-1-propanol
0.04% 1-(2-propenyloxy)-2-propanol
- Purity test date: 6 June 1983
- Lot/batch No.: Batch No. 96 from BP Chemie, Lavera
- Storage condition of test material: At room temperature
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.
- Weight at study initiation: 135 - 179 g when received
- Housing: Except during exposure, animals were housed in groups of three in polypropylene cages with stainless steel grid tops and floors.-
- Diet: Labsure PRD, C Hill Group Ltd.
- Water: Tap water replaced daily
- Acclimation period: 11 days
ENVIRONMENTAL CONDITIONS
- Temperature: 21 – 28 degrees C
- Humidity: 40 – 61 % relative humidity
- Photoperiod: 12 hour dark: 12 hour light cycle
IN-LIFE DATES: From: June 2, 1983 To: June 28, 1983
Administration / exposure
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure:
- nose only
- Vehicle:
- other: unchanged (no vehicle)
- Details on inhalation exposure:
- GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure apparatus: Using a peristaltic pump, ethoxypropanol was metered into a stainless steel tube so that the liquid dripped on a column of glass beads warmed to 125 degrees C and through which air flowed. The vapours emitted from the column were diluted in chilled, humidified air, thoroughly mixed and administered to the rats.
- Method of holding animals in test chamber: Individual glass exposure tubes.
- Temperature, humidity, pressure in air chamber: Mean temperature = 24 degrees C (test animals); 22 degrees C (control animals)
Mean relative humidity = 61 % (test animals); 57 % (control animals)
TEST ATMOSPHERE
- Brief description of analytical method used: Samples of the vapour atmosphere were taken from the exposure module using a 5 ml gas tight syringe and injected into the nitrogen input stream of a gas chromatograph with a Tenax packed column at 150 degrees C and a flame ionization detector. - Analytical verification of test atmosphere concentrations:
- yes
- Remarks:
- no further data
- Duration of exposure:
- 4 h
- Concentrations:
- The mean vapour concentration was 9.59 g/m3 (2213 ppm).
- No. of animals per sex per dose:
- 6 males and 6 females.
- Control animals:
- yes
- Details on study design:
- - Duration of observation period following administration: 14 days
- Frequency of observations and weighing: Clinical signs at the end of exposure. Body weights were recorded daily following exposure.
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight,organ weights, histopathology, other: Respiration rates and patterns were recorded using an optical technique every half hour during exposure.
Organ weights (lungs, liver, and testes).Tissues fixed in neutral buffered formalin (testes, grossly abnormal tissues). - Statistics:
- Differences in organ weights and respiration rates were analyzed using Student’s ‘t’ test.
Results and discussion
Effect levelsopen allclose all
- Sex:
- male/female
- Dose descriptor:
- LC0
- Effect level:
- > 9.59 mg/L air
- Exp. duration:
- 4 h
- Remarks on result:
- other: maximum achievable concentration
- Sex:
- male/female
- Dose descriptor:
- LC50
- Effect level:
- > 9.59 mg/L air
- Exp. duration:
- 4 h
- Remarks on result:
- other: maximum achievable concentration
- Mortality:
- There were no deaths during the study.
- Clinical signs:
- other: Animal movements were uncoordinated when removed from the exposure tubes. Three animals appeared sedated. All animals recovered within approximately 75 minutes after being returned to fresh air.
- Body weight:
- Exposure to ethoxypropanol vapour had no effect on body weight gain.
- Gross pathology:
- There were no findings attributable to exposure.
- Other findings:
- - Organ weights: Lung, liver and testes weights were not affected by treatment.
- Other observations: Mean respiration rates decreased to levels statistically significantly lower than control animals during the first 30 minutes of exposure.
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Based on these results, the LC0 (4-hour) for ethoxypropanol vapour is greater than 9.59 mg/l.
- Executive summary:
In a GLP acute nose-only inhalation toxicity study in rats, a single 4-hour exposure to ethoxypropanol at a concentration of 9.59 mg/l did not produce lethality. This was the maximum practically achievable vapour concentration under ambient dynamic conditions. A reduction in respiratory rate occurred during exposure, and some animals appeared sedated upon removal from exposure, but recovered within 75 minutes. No effect on body weight gain and no gross pathological changes were observed.
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