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Diss Factsheets
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EC number: 601-818-6 | CAS number: 122009-11-4
- 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:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Non-GLP, non-guideline study, available as unpublished report, limitations in design and/or reporting but otherwise adequate for assessment
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 976
- Report date:
- 1976
Materials and methods
- Principles of method if other than guideline:
- Six rats per sex per dose were exposed to the saturated vapour of the test substance. After an observation period of 7 days, animals were necropsied.
- GLP compliance:
- no
- Test type:
- other: Inhalation risk test
- Limit test:
- no
Test material
- Reference substance name:
- 4-(diethoxyphosphinyl)-2-methyl-2-butenoic acid ethyl ester
- EC Number:
- 601-818-6
- Cas Number:
- 122009-11-4
- Molecular formula:
- C11 H21 O5 P
- IUPAC Name:
- 4-(diethoxyphosphinyl)-2-methyl-2-butenoic acid ethyl ester
- Details on test material:
- - Name of test material (as cited in study report): C-5-Phosphonester
Constituent 1
Test animals
- Species:
- rat
- Strain:
- not specified
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Weight at study initiation: 206.3 g for males, 165.7 g for females
Administration / exposure
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure:
- whole body
- Vehicle:
- air
- Details on inhalation exposure:
- - An air stream was conducted through a 5-cm layer of the test substance at 20°C to achieve an atmosphere that was saturated with the vapour of the test substance.
- Rate of air: 200 L/h - Analytical verification of test atmosphere concentrations:
- not specified
- Duration of exposure:
- 8 h
- Concentrations:
- Saturated vapour: 0.09 mg/L
- No. of animals per sex per dose:
- 2 groups of 6 animals (3 males and 3 females each)
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 7 days
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight
Results and discussion
Effect levels
- Sex:
- male/female
- Dose descriptor:
- LC50
- Effect level:
- > 0.09 mg/L air
- Based on:
- test mat.
- Exp. duration:
- 8 h
- Mortality:
- No mortality was observed in all exposed rats.
- Clinical signs:
- other: No clinical signs of toxicity findings were observed.
- Body weight:
- see Table 1 in "any other information on results incl. tables"
- Gross pathology:
- No pathological effects were observed.
Any other information on results incl. tables
Table 1: Body weight
Days after | Males | Females | ||
treatment | First group | Second group | First group | Second group |
0 | 192.0 | 187.3 | 168.7 | 162.7 |
7 | 234.0 | 240.7 | 175.3 | 169.0 |
Applicant's summary and conclusion
- Conclusions:
- Exposure to the saturated vapour pressure for 8 hours to the test substance does not result in mortality.
- Executive summary:
Six rats per sex were exposed to the saturated vapour (0.09 mg/L air) of the test substance for 8 hours. After an observation period of 7 days, animals were necropsied. No clinical signs, pathological effects or mortality was observed in all exposed animals.
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