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Diss Factsheets
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EC number: - | CAS number: -
- 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
Repeated dose toxicity: dermal
Administrative data
- Endpoint:
- repeated dose toxicity: dermal
- Adequacy of study:
- other information
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Test material insufficient characterised.
Data source
Reference
- Reference Type:
- publication
- Title:
- Zur perkutanen Intoxikation mit Diphenyl-Kresyl-Phosphat beim Meerschweinchen
- Author:
- Geffke I. et al.
- Year:
- 1 970
- Bibliographic source:
- Z. ges. Hyg. Grenzgeb. 16, 167-170 (1970)
Materials and methods
- Principles of method if other than guideline:
- Diphenyl cresyl phosphate (purity not known) in olive oil was applied to the shaved skin (3 cm2 exposed area, position not stated) of groups of four guinea pigs (strain and sex not given) daily for 73 days. Administered doses were equivalent to approximately 120, 240, 480, 720 or 960 mg/kg bw/day.
- GLP compliance:
- no
- Limit test:
- no
Test material
- Reference substance name:
- Not applicable
- Molecular formula:
- C19 H17 O4 P1
- IUPAC Name:
- Not applicable
Constituent 1
- Specific details on test material used for the study:
- According to the authors, the determination of the structures of the of the test substance was not possible, However the authors assumed, the test substance was a mixture of diphenyl cresy isomers.
Test animals
- Species:
- guinea pig
- Strain:
- not specified
- Sex:
- not specified
Administration / exposure
- Type of coverage:
- other: Animals were immobilised until the test material has dried.
- Vehicle:
- olive oil
- Details on exposure:
- Route of Administration: dermal
- Analytical verification of doses or concentrations:
- not specified
- Duration of treatment / exposure:
- 73 days
- Frequency of treatment:
- daily
Doses / concentrations
- Remarks:
- Doses / Concentrations:
0.1 to 0.8 ml/kg bw/d = ca. 120 to 960 mg/kg bw
Basis:
- Control animals:
- other: yes (olive oil)
- Details on study design:
- Post-exposure period: no
Examinations
- Observations and examinations performed and frequency:
- Mortality, clinical signs, body weight, liver weight.
- Sacrifice and pathology:
- Histopathological examination.
Results and discussion
Results of examinations
- Clinical signs:
- effects observed, non-treatment-related
- Description (incidence and severity):
- At 480 mg/kg bw/day, hind limb paralysis was observed in two animals. At doses greater than 480 mg/kg bw/day, paralysis of the hind limbs and lower portions of the back muscles were observed in all animals (the time of onset of signs of paralysis were not given).
- Dermal irritation:
- effects observed, treatment-related
- Description (incidence and severity):
- There was a dose-dependent increase in alopecia from 240 mg/kg bw/day, and body weight gains were reduced in the two highest doses.
- Mortality:
- mortality observed, treatment-related
- Body weight and weight changes:
- effects observed, treatment-related
- Description (incidence and severity):
- Body weight gains were reduced in the two highest doses.
- Food consumption and compound intake (if feeding study):
- not specified
- Food efficiency:
- not specified
- Water consumption and compound intake (if drinking water study):
- not specified
- Ophthalmological findings:
- not examined
- Haematological findings:
- not specified
- Clinical biochemistry findings:
- not specified
- Urinalysis findings:
- not specified
- Behaviour (functional findings):
- effects observed, treatment-related
- Description (incidence and severity):
- At 480 mg/kg bw/day, hind limb paralysis was observed in two animals. At doses greater than 480 mg/kg bw/day, paralysis of the hind limbs and lower portions of the back muscles were observed in all animals (the time of onset of signs of paralysis were not given).
- Immunological findings:
- not examined
- Organ weight findings including organ / body weight ratios:
- effects observed, treatment-related
- Description (incidence and severity):
- Liver weights were increased.
- Neuropathological findings:
- effects observed, treatment-related
- Description (incidence and severity):
- Histologic changes in the spinal cord were observed.
- Histopathological findings: non-neoplastic:
- effects observed, treatment-related
- Description (incidence and severity):
- Effects on the liver were apparent from 480 mg/kg bw/day. At 720 mg/kg bw/day, the severity of hepatic effects increased. The highest dose caused all of these effects plus necrosis of hepatocytes and complete glycogen depletion. At doses of 480 mg/kg bw/day or above, hyperplasia, formation of fatty cysts, lipid vacuoles in the cortex and hyperaemia in the cortex and medulla of the adrenal glands were noted.
- Histopathological findings: neoplastic:
- not examined
Effect levels
- Key result
- Dose descriptor:
- NOAEL
- Effect level:
- 120 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Sex:
- not specified
- Basis for effect level:
- other: Diphyl cresyl phosphate applied dermally caused injuries of the liver, the nervous system and of the adrenals in guinea pigs.
Target system / organ toxicity
- Key result
- Critical effects observed:
- yes
- Lowest effective dose / conc.:
- 120 mg/kg bw/day (nominal)
- System:
- other: Diphyl cresyl phosphate applied dermally caused injuries of the liver, the nervous system and of the adrenals in guinea pigs.
- Treatment related:
- yes
- Dose response relationship:
- yes
Any other information on results incl. tables
Alopezia, reduced body weight with 0.2 ml and higher doses dose dependant), increased liver weight, paralysis in the 0.4, 0.6 and 0.8 ml-groups, microscopical up to 0.2 ml no effects in the liver, with 0.4 and 0.6 ml hyperemia and fatty liver changes, with 0.8 ml liver cell necrosis; edema of the spinal cord in the high dose groups, hyperplasia and necrosis of the adrenal glands (purity not known).
Applicant's summary and conclusion
- Conclusions:
- Diphyl cresyl phosphate applied dermally caused injuries of the liver, the nervous system and of the adrenals in guinea pigs.
- Executive summary:
Diphenyl cresyl phosphate (purity not known) in olive oil was applied to the shaved skin (3 cm2 exposed area, position not stated) of groups of four guinea pigs (strain and sex not given) daily for 73 days. Administered doses were equivalent to approximately 120, 240, 480, 720 or 960 mg/kg bw/day.
All guinea pigs, including those in the control group, showed slight erythema with scale formation; this was attributed to the presence of the vehicle, olive oil. There was a dose-dependent increase in alopecia from 240 mg/kg bw/day, and body weight gains were reduced in the two highest doses. At 480 mg/kg bw/day, hind limb paralysis was observed in two animals. At doses greater than 480 mg/kg bw/day, paralysis of the hind limbs and lower portions of the back muscles were observed in all animals (the time of onset of signs of paralysis were not given). Effects on the liver were apparent from 480 mg/kg bw/day. At 720 mg/kg bw/day, the severity of hepatic effects increased. The highest dose caused all of these effects plus necrosis of hepatocytes and complete glycogen depletion. At doses of 480 mg/kg bw/day or above, hyperplasia, formation of fatty cysts, lipid vacuoles in the cortex and hyperaemia in the cortex and medulla of the adrenal glands were noted. The NOAEL for this study was considered to be the lowest dose tested; 120 mg/kg bw/day (Geffke et al. 1970, cited in BG Chemie 2000).
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