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EC number: 259-160-7 | CAS number: 54423-67-5
- 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:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to O.E.C.D. Testing Guideline 412 with GLP compliance.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 000
- Report date:
- 2000
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 412 (Subacute Inhalation Toxicity: 28-Day Study)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Limit test:
- no
Test material
- Details on test material:
- As per IUCLID Sections 1.1. - 1.4.
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- Sprague-Dawley rats were acquired from Charles River (UK) Limited Maragate, Kent. The animals were approximately five weeks old and weighted 116 - 134 grams. Animals were acclimated nine days before being placed on study. The animals room coditions were 22 C +/- 3 C, 30 - 70% relative hmidity and 15 - 20 air exchanges per hour. The rats were housed individually in polycarbonate cages containing wood shaveings with stainless steel removal tops and bottoms. Rat and Mouse (Modified) No. 1 Diet SQC Expanded was acquired from Special Diet Services, Stepfield, Witham, Essex. Water was domestic mains quality water. Both feed and water were available ad libitum.
Administration / exposure
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure:
- nose only
- Vehicle:
- other: unchanged (no vehicle)
- Details on inhalation exposure:
- The test chamber atmospheres were generated by a vapourizing system. A test material reserviour was placed in water bath at approximately 60 C and through witch compressed air was passed at a fixed rate. The resulting test substance vapour was then ducted into the inhalation chambers. The various chamber dose levels were achieved by varying the air flow through the test substance reservior and diluting with air as needed. The inhalation chambers were cylindrical stainless steel flow-pass design with a volume of 4.0 liters. Chamber air flow rate was measured continuously and recorede every 30 minutes.
- Analytical verification of doses or concentrations:
- yes
- Details on analytical verification of doses or concentrations:
- The chamber sampling employeed two glass impingher tubes in series. The sampling devices was temporarily sealed in a port in the inhalation chambers st the animal breathing zone. Air samples were analyzed by a Gas Chromatography method supplied by the study sponsor.
- Duration of treatment / exposure:
- 28 d
- Frequency of treatment:
- 6 h/d
Doses / concentrationsopen allclose all
- Remarks:
- Doses / Concentrations:
0.06 mg/l
Basis:
analytical conc.
- Remarks:
- Doses / Concentrations:
0.25 mg/l
Basis:
analytical conc.
- Remarks:
- Doses / Concentrations:
1.43 mg/l
Basis:
analytical conc.
- No. of animals per sex per dose:
- 8
- Control animals:
- yes, sham-exposed
- Details on study design:
- The animals were exposed nose-only to vapours of vinyl neononanoate 6 hr/day for 28 consecutive days. Five animals/sex were subjected to a Functional Observational Battery (FOB) once pre-study once weekly during the 28-day exposure period. Clinical signs, body weights and feed consumptions were taken diring the in-life phase of the study. At study termination a variety of standard end-points were observed and/or measured. At study termination satellite groups of three rats/sex subjected to whole body perfusion with paraformaldehyde/glutaraldehyde to fix neural tisse.
- Positive control:
- No
Examinations
- Observations and examinations performed and frequency:
- FOB with grip strength and motor activity weekly, Clinical Signs daily, Body Weight and Feed consumption, weekly, blood samples for clinical chemistry measurments and hematology were collected at study termination.
- Sacrifice and pathology:
- At study termination the main study animals were sacrificed by carbon dioxide ashyxiation. The satellite animals were sacrificed by sublethal injection of sodium pentobarbitone followed by whole body perfusion with paraformaldehyde/gluaraldehyde. The necropsy was directed by a veterinary pathologist. A complete internal and extenal examination was conducted. The weights of protocol speciified organs were taken. Tissues taken from main study animals were fixed in 10% neutral bufferd formailn except eyes were fixed in Davidson's solution and the testis were fixed in Bouin's fluid. Following whole body perfusion peripheral nerve tissue was processed to metyacrylate resin blocks. Tissues from all control and high dose animals were histologically examined. Kidney sections from all low and mid-dose animals were also examined. Haematoxylin and eosin was generally for tissue staining.
- Statistics:
- Homogeneity of variance using the "F-max" test was generally for detemining statstical significance. Other stastical models were used as needed.
Results and discussion
Results of examinations
- Clinical signs:
- effects observed, treatment-related
- Mortality:
- mortality observed, treatment-related
- Body weight and weight changes:
- effects observed, treatment-related
- Food consumption and compound intake (if feeding study):
- effects observed, treatment-related
- Food efficiency:
- not specified
- Water consumption and compound intake (if drinking water study):
- no effects observed
- Ophthalmological findings:
- no effects observed
- Haematological findings:
- no effects observed
- Clinical biochemistry findings:
- effects observed, treatment-related
- Urinalysis findings:
- no effects observed
- Behaviour (functional findings):
- no effects observed
- Organ weight findings including organ / body weight ratios:
- effects observed, treatment-related
- Gross pathological findings:
- no effects observed
- Histopathological findings: non-neoplastic:
- effects observed, treatment-related
- Histopathological findings: neoplastic:
- no effects observed
- Details on results:
- High dose male animals had significantly reduced mean body weight (33%) at study termination. High dose male feed consumption was significantly reduced 13% at 28 days. Significantly lower plasma urea values were observed for both male and female high dose group animals. High dose female rat group mean liver weight was significantly elevated 16% relative to the control value. Histopathological evidence of adverse kidney effects were observed at all dose levels in male rats. These findings inclued: mild hyaline droplet formation, karyomegally and single cell necrosis.
Effect levels
- Dose descriptor:
- NOEL
- Effect level:
- 0.25 mg/L air (analytical)
- Sex:
- male/female
- Basis for effect level:
- other: Significantly reduced body weight (33%) males only, clinical signs suggestive of neurtoxicity, reduced plasma urea in both sexes and histological evidence of kidney damage, males only at the high concentration of 1.43 mg/L (190 ppm).
Target system / organ toxicity
- Critical effects observed:
- not specified
Applicant's summary and conclusion
- Conclusions:
- Daily exposure, via the nose only inhalation route to 1.43 mg/l VeoVa9 for 28 days produced treatment-related clinical signs, reduced bodyweight and food intake and reduced plasma urea. Histologically, treatment at this level produced hyaline droplets in the renal cortex and in some rats produced karyomegaly in both the renal cortex and outert stripe of the renal medulla assopciated with single cell necrosis. Since the only changes of note observed in the Low and Intermediate dose animals were related to hyaline droplet formulation and minor renal changes and since these effects are known to be sex and species selective and unlikely to be relevant to man, the no adverse effect level in this study is considered to be 0.25 mg/L (33.2 ppm).
- Executive summary:
Rats were exposed nose-only to vapours of vinyl neononaoate in a GLP, O.E.C.D. 412 Testing Guideline 28 -day repeated dose study with neurtoxicity screen. Primary findings of adverse effects occured in male rats at the high dose level of 1.43 mg/L (190 ppm). These cosisted of: a significant 33% reduction in group mean body weight, a significant 13% reduction in feed consumption, signficantly reduced plasma urea and histopathological evidence of adverse kidney effects. The histological evidence of male rat nephrotoxicity is believed to be due to the accumulation of alpha-2u-microglobin that is a mechcanism not relevant ot human health. Therefore, the NOAEL for this study is the mid-dose of 0.25 mg/l (33.2 ppm). This study's results can be used to assist in the development of Worker and General Population inhalation DNELs.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
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