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Diss Factsheets
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EC number: 203-442-4 | CAS number: 106-92-3
- 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
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Basic data given, acceptable with restrictions (The study was performed before the establishment of GLP and OECD guidelines.)
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 978
Materials and methods
- Principles of method if other than guideline:
- Six male rats per dose group were exposed to the nominal concentrations of 100, 250, 300, 375 and 500 ppm allyl glycidyl ether vapor. All rats were observed for signs of toxicity and LC50 was calculated.
- GLP compliance:
- no
- Test type:
- acute toxic class method
- Limit test:
- no
Test material
- Reference substance name:
- Allyl 2,3-epoxypropyl ether
- EC Number:
- 203-442-4
- EC Name:
- Allyl 2,3-epoxypropyl ether
- Cas Number:
- 106-92-3
- Molecular formula:
- C6H10O2
- IUPAC Name:
- 2-[(prop-2-en-1-yloxy)methyl]oxirane
- Details on test material:
- - Name of test material (as cited in study report): allyl glycidyl ether
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Sparta Research Animals, Inc., Michigan
Administration / exposure
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure:
- not specified
- Vehicle:
- not specified
- Details on inhalation exposure:
- no data
- Analytical verification of test atmosphere concentrations:
- no
- Duration of exposure:
- 7 h
- Concentrations:
- 100, 250, 300, 375, 500, 700, 1175 and 2600 ppm (equivalent to 0.47, 1.18, 1.42, 1.78, 2.37, 3.32, 5.57 and 12.31 mg/l) Calculation of concentrations (mg/L) based on Derelanko MJ (2000). Toxicologist's Pocket Handbook, CRC Press, conversion table, p. 57.
- No. of animals per sex per dose:
- 6
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: no data
- Frequency of observations and weighing: no data
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs
Results and discussion
Effect levels
- Sex:
- male
- Dose descriptor:
- LC50
- Effect level:
- ca. 1.46 mg/L air
- 95% CL:
- 1.36 - 1.6
- Exp. duration:
- 7 h
- Mortality:
- 0/6, 0/6, 2/6, 6/6, 6/6, 6/6, 6/6 and 6/6 rats died in the dose levels of 100, 250, 300, 375, 500, 700, 1175 and 2600 ppm groups, respectively. In the 300 ppm group, 2 rats died within 24h of exposure. In the 375 ppm group, 2 rats died within 24 h, 2 died within 48 h and rest 2 died within 72h of exposure. In the 500 ppm group, all rats died within 24 h of exposure.
- Clinical signs:
- other: During exposure to the rats of top 3 exposed groups were gasping and had exudates around the nose and mouth. Slight nasal irritation and slight gasping were observed in rats of the 100 ppm group during exposure. These signs of toxicity occurred with incre
- Gross pathology:
- Rats of the 700 ppm group were found to have a distended stomach from gasping, and hyperemic nasal turbinates; rats of the 1175 ppm group had dark and congested lungs; rats of the 2600 ppm group exhibited the above signs of toxicity, in addition to congested livers, hydrothorax, and paleness of the cortex of the kidneys with an accentuated corticomedullary junction. No visible lesions were found upon gross pathological examination of rats of the 100 and 250 ppm groups. However, rats of the 300, 375, and 500 ppm groups had nasal exudate, nasal turbinates which were congested and edematous, a distended stomach from gasping, and corneal cloudiness. Congested livers and kidneys were also observed in rats of the 300 and 375 ppm groups, while rats of the 500 ppm group had lungs which were congested, hyperemic, and edematous.
Any other information on results incl. tables
The LC50 (7h exposure) was reported to be 308 ppm (287 -338 ppm) which is equivalent to approximately 1.46 mg/l (1.36 -1.6 mg/l).
The LC50 (4h exposure) = 1.46 x 1.75 = 2.56 mg/l
Applicant's summary and conclusion
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.