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EC number: 206-056-4 | CAS number: 298-07-7
- 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: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: scientifically acceptable and sufficient documented - but only 2 doses applied
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 982
- Report date:
- 1982
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 401 (Acute Oral Toxicity)
- Principles of method if other than guideline:
- Two groups of 5 male and 5 female rats were dosed once by oral gavage at dose levels of 500 or 5000 mg/kg bw. The animals were observed for mortality, body weight and clinical signs through day 14. After 14 days, the surviving animals were killed and discarded.
- GLP compliance:
- not specified
- Test type:
- standard acute method
Test material
- Reference substance name:
- Bis(2-ethylhexyl) hydrogen phosphate
- EC Number:
- 206-056-4
- EC Name:
- Bis(2-ethylhexyl) hydrogen phosphate
- Cas Number:
- 298-07-7
- Molecular formula:
- C16H35O4P
- IUPAC Name:
- bis(2-ethylhexyl) hydrogen phosphate
- Test material form:
- other: liquid
- Details on test material:
- no data
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- unchanged (no vehicle)
- Doses:
- 500 or 5000 mg/kg bw
- No. of animals per sex per dose:
- 5 male and 5 female rats/dose
- Control animals:
- not specified
Results and discussion
Effect levels
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- > 500 - < 5 000 mg/kg bw
- Based on:
- test mat.
Any other information on results incl. tables
All animals doses at 5000 mg/kg bw died within 24 hours after application of bis(2-ethylhexyl) hydrogen phosphate and were necropsied. Severly redness abdominal walls, enlarged blood vessels, reddened liningof the gastrointestinal tract were found at necrosy. The stomach lining had a dark red clour. Adrenals and pancreas were reddened. Lungs in most instances were found to be scarlet red, kidneys were pale and thymus darkened.
All animals dosed with 500 mg/kg bw survived 14 days and gained weight through the study. Clinically, the animals exhibited oral/nasal discharge and diarrhea on the day of dosing only.
Applicant's summary and conclusion
- Executive summary:
Two groups of 5 male and 5 female rats were dosed once by oral gavage of bis(2-ethylhexyl) hydrogen phosphate at dose levels of 500 or 5000 mg/kg bw. The animals were observed for mortality, body weight and clinical signs through day 14. After 14 days, the surviving animals were killed and discarded.
All animals doses at 5000 mg/kg bw died within 24 hours after application of bis(2-ethylhexyl) hydrogen phosphate and were necropsied. Severly redness abdominal walls, enlarged blood vessels, reddened liningof the gastrointestinal tract were found at necrosy. The stomach lining had a dark red clour. Adrenals and pancreas were reddened. Lungs in most instances were found to be scarlet red, kidneys were pale and thymus darkened.
All animals dosed with 500 mg/kg bw survived 14 days and gained weight through the study. Clinically, the animals exhibited oral/nasal discharge and diarrhea on the day of dosing only.
An oral LD50 > 500 and < 5000 mg/kg bw was determined.
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