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EC number: 213-138-3 | CAS number: 926-57-8
- 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
-Acute toxicity: oral: LD50=414 mg/kg bw (male rats); LD50=300 mg/kg bw (female rats) according to OECD TG 401
-Acute Toxicity: inhalation: LD50=546 ppm (male rats), no guideline followed
Key value for chemical safety assessment
Additional information
OECD SIDS, 2007:
Studies in Animals
Inhalation
The inhalation 4-hour LC50 of 1,3-DCB in the male rat ranged from 546 (Kwon and Waritz, 1968) to 756 ppm (2840 to 3930 mg/m³) (Barsegyan, 1969). At lethal levels, 1,3-DCB caused irregular breathing, lacrimation, salivation, and hyperemia of the ears. Histopathologic examination revealed hemorrhage of lungs, tracheitis, and cell degeneration in the liver, spleen, thymus, and lymph nodes; no changes were observed in the testes. Tubular degeneration of the kidneys was also noted (Kwon and Waritz, 1968). The 2-hour LC50 in the mouse was 846 ppm (4400 mg/m³) (Barsegyan, 1969).
Dermal
There are no rat or rabbit dermal LD50 studies available for 1,3-DCB.
Oral
The oral LD50 for 1,3-DCB was 300 and 414 mg/kg in fasted male and female rats, respectively (Bayer AG, 1991), and 1368 mg/kg in the non-fasted male rat (DuPont, 1982a). Clinical signs of toxicity included stained and wet fur, wet perineal area, diarrhea, weakness, hunched posture, alopecia, salivation, chromodacryorrhea, rough coat, sedation, and/or weight loss (Bayer AG, 1991; DuPont, 1982a). The pathology examinations of animals that died on study showed congested vessels of the stomach, reddened mucous membranes, reddened small intestine, and clear fluid in the stomach.
Studies in Humans
Inhalation
Exposure of workers to 1,3-DCB can cause dizziness and nausea (DuPont, 1993). Exposure details were not reported.
Conclusions
In rats, 1,3-DCB is acutely toxic via the inhalation and oral routes of exposure
Justification for classification or non-classification
On the basis of the test results the substance should be classified as Xn, R20/22 (Harmful; Harmful by inhalation and if swallowed) according to DSD, and Acute Tox 3 (Toxic if swallowed and if inhaled, H301, H331) according to CLP.
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