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Diss Factsheets
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EC number: 201-186-8 | CAS number: 79-21-0
- 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: inhalation
Administrative data
- Endpoint:
- short-term repeated dose toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 3 (not reliable)
- Rationale for reliability incl. deficiencies:
- significant methodological deficiencies
- Remarks:
- Reporting deficiencies including the nature, concentration and the stability of the test substance. No analytical determination of atmospheric concentrations of peracetic acid was made. Furthermore, the study was not carried out in accordance with international GLP or study guidelines. The daily exposure (45 minutes) was short compared to standard guidelines and only one concentration was tested. No clinical chemistry was performed and extent of haematology investigations was limited.
Data source
Reference
- Reference Type:
- publication
- Title:
- Tolerability of Peracetic Acid Aerosols to Animals with Particular Reference to Impairment of Organic Defence (in German with English abstract)
- Author:
- Heinze, W. et al
- Year:
- 1 979
- Bibliographic source:
- Mh. Vet.-Med. 34, 212-217
Materials and methods
- Principles of method if other than guideline:
- The study aimed at testing any adverse impact on immunisation when mice exposed to peracetic acid aerosol were subsequently infected with a highly virulent tester germ strain.
- GLP compliance:
- no
- Limit test:
- no
Test material
- Reference substance name:
- Peracetic acid
- EC Number:
- 201-186-8
- EC Name:
- Peracetic acid
- Cas Number:
- 79-21-0
- Molecular formula:
- C2H4O3
- IUPAC Name:
- Peracetic acid generated by perhydrolysis of N-acetylcaprolactam by hydrogen peroxide in alkaline conditions
Constituent 1
Test animals
- Species:
- mouse
- Strain:
- not specified
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- Age and weight not indicated
Administration / exposure
- Route of administration:
- inhalation
- Type of inhalation exposure:
- whole body
- Vehicle:
- other: water
- Details on inhalation exposure:
- For the preparation of aerosol particles/droplets, and ultrasonic aerosol device TUR USI 4 was used.
- Analytical verification of doses or concentrations:
- no
- Duration of treatment / exposure:
- 45 min per day for a period of 14 days
- Frequency of treatment:
- daily
Doses / concentrations
- Dose / conc.:
- 1 500 mg/m³ air
- Remarks:
- 30 mg peracetic acid/20 L air = 1.5 g peracetic acid/m³ (1.2 mL 6.25 % Wofasteril/20 L) (nominal conc.)
- No. of animals per sex per dose:
- 50
- Control animals:
- yes, concurrent vehicle
- Details on study design:
- 2 groups of mice were immunised with the “Red Murrain Vaccine Dessau” by subcutaneous injection of 1 million germs into the sacral region. One of the immunised groups was exposed to peracetic acid, the other group remained untreated. Both immunised groups as well as a non-immunised control group (group 3) were treated with red murrain germs at the end of the study. Group 4 served as peractic acid treated control only.
Examinations
- Observations and examinations performed and frequency:
- - Clinical signs and mortality: not indicated
- Body weight: not indicated
- Haematology: not performed - Sacrifice and pathology:
- A pathological examination was performed; histopathology was conducted in particular on kidneys, liver and lungs.
- Statistics:
- Yes, method not mentioned.
Results and discussion
Results of examinations
- Clinical signs:
- no effects observed
- Mortality:
- no mortality observed
- Body weight and weight changes:
- no effects observed
- Food consumption and compound intake (if feeding study):
- not examined
- Food efficiency:
- not examined
- Water consumption and compound intake (if drinking water study):
- not examined
- Ophthalmological findings:
- not examined
- Haematological findings:
- not examined
- Clinical biochemistry findings:
- not examined
- Endocrine findings:
- not examined
- Urinalysis findings:
- not examined
- Behaviour (functional findings):
- not examined
- Immunological findings:
- not examined
- Organ weight findings including organ / body weight ratios:
- no effects observed
- Gross pathological findings:
- no effects observed
- Neuropathological findings:
- not examined
- Histopathological findings: non-neoplastic:
- no effects observed
- Histopathological findings: neoplastic:
- not examined
- Other effects:
- not examined
- Details on results:
- Mortality: No deaths were reported.
Gross and histopathology: no pathological/histopathological findings reported
Other examinations: In mice which have been subcutaneously treated and immunised with “Red Murrain Vaccine Dessau” and subsequently infected with the highly virulent tester germ strain “Frankfurt XI” it was demonstrated that exposure towards peracetic acid for a period of 14 days does not have an adverse impact on immunisation of mice. In contrast to immunised and peracetic acid exposed mice as well as immunised and not peracetic acid exposed mice, all mice which were not immunised but infected with the tester germs, died within 24 hours after infection. No effects were reported on mice which were not immunised and not infected but exposed to a peracetic acid aerosol for a period of 14 days only.
Effect levels
- Key result
- Dose descriptor:
- NOAEL
- Effect level:
- 1 500 mg/m³ air (nominal)
- Based on:
- test mat.
- Sex:
- not specified
- Basis for effect level:
- other: based on PAA (impairment of the immune defence)
Target system / organ toxicity
- Key result
- Critical effects observed:
- not specified
Applicant's summary and conclusion
- Conclusions:
- In mice which were immunised against red murrain germs followed by inhalation exposure towards peracetic acid for 14 days and subsequent infection with red murrain germs, no impairment of the immune defence could be observed when comparison to immunised and infected mice was made.
- Executive summary:
When groups of mice which have been subcutaneously treated and immunised with “Red Murrain Vaccine Dessau” were exposed to an aerosol of peracetic acid at a concentration of 1.5 g/m3 for a period of 14 days and subsequently infected with the highly virulent tester germ strain “Frankfurt XI”, no adverse impact on immunisation of mice was observable. In contrast to immunised and peracetic acid exposed mice, all mice which were not immunised but infected with the tester germs, died within 24 hours after infection. No treatment- or exposure-related effects were reported on mice which were not immunised and not infected but exposed to a peracetic acid aerosol for a period of 14 days only.
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