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EC number: 202-627-7 | CAS number: 98-01-1
- 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
Specific investigations: other studies
Administrative data
- Endpoint:
- specific investigations: other studies
- 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 animal experimental research study, published in peer reviewed literature. Restrictions in design and reporting but otherwise adequate for reporting.
Data source
Reference
- Reference Type:
- publication
- Title:
- Experimental research on toxicity of furfural
- Author:
- Castellino N, Elmino O, Rozera G
- Year:
- 1 963
- Bibliographic source:
- Archives of Environmental Health 1963; 7: 574 582
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Inhalation exposure 4 hours/day/5 days per week until death (<80 days)
- GLP compliance:
- not specified
- Type of method:
- in vivo
- Endpoint addressed:
- respiratory irritation
Test material
- Reference substance name:
- 2-furaldehyde
- EC Number:
- 202-627-7
- EC Name:
- 2-furaldehyde
- Cas Number:
- 98-01-1
- Molecular formula:
- C5H4O2
- IUPAC Name:
- 2-furaldehyde
- Reference substance name:
- furfural
- IUPAC Name:
- furfural
- Details on test material:
- - Name of test material (as cited in study report): Furfural
- Physical state: Amber coloured oily liquid
- No further details reported
Constituent 1
Constituent 2
Test animals
- Species:
- rabbit
- Strain:
- not specified
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- No details reported
Administration / exposure
- Route of administration:
- inhalation
- Vehicle:
- not specified
- Details on exposure:
- Exposure: 200, 500 add 1000 mg/m3/h for 4 hours/day, 5 days per week until death.
1g furfural was evaporated in 1000 L air, with flow of 1000 L of air per hour.
GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure apparatus: Metallic cylindrical cage, volume 0.288 m3
- Source and rate of air: 1000L air/hour produced by a compressor, measured and heated.
- System of generating particulates/aerosols: The air flow bubbled through a furfural water solution, heated by water bath. The furfural solution was renewed hourly. Even distribution was achieved by use of an agitator in the cage. - Analytical verification of doses or concentrations:
- not specified
- Details on analytical verification of doses or concentrations:
- No data
- Duration of treatment / exposure:
- Until death (<80 days)
- Frequency of treatment:
- 4 hours/day, 5 days/week,
Doses / concentrations
- Remarks:
- Doses / Concentrations:
200, 500 and 1000 mg/m3/hour by inhalation
Basis:
nominal conc.
- No. of animals per sex per dose:
- No data
- Control animals:
- no
Examinations
- Examinations:
- Limited toxicological parameters assessed, including kidney and liver function and histopathologiacl assessment.
- Positive control:
- none
Results and discussion
- Details on results:
- At 1000 mg/m3/h the rabbits the rabbits died after 8-10 days of exposure. There were signs of irritation of the conjunctiva and the mucosa of the upper respiratory tract at the end of each exposure. At autopsy, the lungs appeared congested and oedematous. There were no further detailed assessments of the animals or histopathology at this exposure level.
Rabbits died after 17-20 days exposure to 500 mg/m3/h. There was a significant reduction in the glomerular filtration and maximal tubular excretion capacity values indicative of renal impairment, which was confirmed by histopathological findings of minor glomerular and tubular lesions. There was no effect on hepatic function. There was a normochromic anaemia with slight signs of hyperplasia of the erytroblastic medullar parenchyma but number of platelets, fibrinogen and coagulation tests were normal.
Animals exposed to 200 mg/m3 showed no signs of intoxication (biochemical or histopathological) after 60-80 days exposure.
Any other information on results incl. tables
At 1000 mg/m3/h the rabbits the rabbits died after 8-10 days of exposure. There were signs of irritation of the conjunctiva and the mucosa of the upper respiratory tract at the end of each exposure. At autopsy, the lungs appeared congested and oedematous. There were no further detailed assessments of the animals or histopathology at this exposure level. Rabbits died after 17-20 days exposure to 500 mg/m3/h. There was a significant reduction in the glomerular filtration and maximal tubular excretion capacity values indicative of renal impairment, which was confirmed by histopathological findings of minor glomerular and tubular lesions. There was no effect on hepatic function. There was a normochromic anaemia with slight signs of hyperplasia of the erytroblastic medullar parenchyma but number of platelets, fibrinogen and coagulation tests were normal. Animals exposed to 200 mg/m3 showed no signs of intoxication (biochemical or histopathological) after 60-80 days exposure.
Biochemical measurements of rabbits exposed to 500 mg/m3/hour (death after 17 -20 exposures) indicated some renal impairment as evidenced by a reduction in glomerular filtration and maximal tubular excretion capacity values. This was confirmed by histopathological findings of minor glomerular and tubular lesions. Hepatic function however was normal
Applicant's summary and conclusion
- Conclusions:
- Rabbits showed signs of irritation of the conjunctivae and the mucosa of the upper respiratory tract after exposure to 1000 mg/m3 for 4 hours, 5 days per week until death (8-10 days).
- Executive summary:
Groups of rabbits were exposed, whole body, 4 hours/day for 5 days/week until death, to furfural at concentrations of 200, 500 or 1000 mg/m3/hour.
At 1000 mg/m3/h the rabbits the rabbits died after 8-10 days of exposure. There were signs of irritation of the conjunctiva and the mucosa of the upper respiratory tract at the end of each exposure. At autopsy, the lungs appeared congested and oedematous. There were no further detailed assessments of the animals or histopathology at this exposure level.
Rabbits died after 17-20 days exposure to 500 mg/m3/h. There was a significant reduction in the glomerular filtration and maximal tubular excretion capacity values indicative of renal impairment, which was confirmed by histopathological findings of minor glomerular and tubular lesions. There was no effect on hepatic function. There was a normochromic anaemia with slight signs of hyperplasia of the erytroblastic medullar parenchyma but number of platelets, fibrinogen and coagulation tests were normal. The anaemia is considered to be due to myeloininhibitory effect.
Animals exposed to 200 mg/m3 showed no signs of intoxication (biochemical or histopathological) after 60-80 days exposure.
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