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Diss Factsheets
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EC number: 211-463-5 | CAS number: 646-06-0
- 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
Endpoint summary
Administrative data
Description of key information
One subacute oral (gavage) toxicity study with rats is available. For the inhalation route, two subacute toxicity studies with rat and one subchronic study with rats is available. No repeated dose toxicity data for the dermal route are available.
Key value for chemical safety assessment
Repeated dose toxicity: via oral route - systemic effects
Endpoint conclusion
- Dose descriptor:
- NOAEL
- 75 mg/kg bw/day
- Study duration:
- subacute
- Species:
- rat
Repeated dose toxicity: inhalation - systemic effects
Endpoint conclusion
- Dose descriptor:
- NOAEC
- 903 mg/m³
- Study duration:
- subchronic
- Species:
- rat
Additional information
In an oral gavage study, male and female rats were given 0, 75, 250, 750 or 2000 mg/kg bw of 1,3-Dioxolane during 14 days. For repeated dose oral toxicity, a NOAEL systemic of 75 mg/kg bw/day was observed in a subacute study with rats, based on observed reduced body weight gain in males and females, reduced leucocyte and lymphocyte counts in females and reduced platelet count in males observed at 250 mg/kg bw/day. No local effects were observed.
In a 13-week inhalation toxicity study, male and female rats were exposed to targeted concentrations of 0, 300, 1000 or 3000 ppm of 1,3-Dioxolane vapour. Satelite groups were allowed to recover for 8 weeks after the exposure period. For repeated dose inhalation toxicity, an overall NOAEC systemic of 298 ppm (0.90 mg/L or 903 mg/m³) was observed in the 90-day rat study, based on reduced WBC and lymphocyte count and increased platelet count in males and females, and reduced spleen weights in females at and above 1000 ppm (3.03 mg/L or 3030 mg/m³).
No local effects were observed.
Repeated dose toxicity: via oral route - systemic effects (target organ) cardiovascular / hematological: other
Repeated dose toxicity: inhalation - systemic effects (target organ) cardiovascular / hematological: other
Justification for classification or non-classification
Based on the oral NOAEL and NOAEC for systemic effects in the repeated dose toxicity studies, 1,3-dioxolane needs no classification for danger of serious health effects after prolonged exposure according to Regulation (EC) No 1272/2008.
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.
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