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EC number: 248-256-4 | CAS number: 27138-01-8
- 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
Short-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
Description of key information
48h EC50 for m/p DIOL to D. magna is > 100 mg/L, based on nominal concentrations of m/p DIOL. The 48h no observed effect concentration (NOEC) is concluded to be 100 mg/L.
Key value for chemical safety assessment
Additional information
The acute toxicity to Daphnia magna was evaluated for the meta-isomer as well as for the mixture of both isomers according to OECD Guideline 202.
One study was designed to estimate the median effect concentration (EC50) for immobilisation of Daphnia magna exposed to the reaction mass of a,a,a’,a’-tetramethyl-m-xylene-a,a’-diol and a,a,a’,a’-tetramethyl-p-xylene-a,a’-diol (m/p DIOL). This study was conducted of a 48h period, under semi-static conditions. Four replicate vessels were prepared for each treatment group, each containing five D. magna neonates. No immobile D. magna were recorded in the control or 100 mg/L nominal concentration throughout the test period. It is concluded that the 48h- EC50 for m/p DIOL to D. magna is > 100 mg/L, based on nominal concentrations of m/p DIOL. The 48h no observed effect concentration (NOEC) is concluded to be 100 mg/L.
A test performed according to “The guidelines for the testing of chemicals” (HJ/T 153 -2004) and with reference to Procedure 202 of the “Guidelines for Testing of Chemicals” of the OECD: “Daphnia sp., Acute Immobilisation Test” (2004) etc. was designed to determine the acute toxicity of meta-Diisopropanolbenzene.The study comprised at least one range-finding test followed by a limit test to determine the 48-hour median effective concentration (EC50) of the test substance. In addition, the NOEC (no observed effect concentration) was also determined.
Under valid test conditions the 48h EC50 is greater than 150 mg/L (nominal concentration). And 48h NOEC value (no observed effect concentration) is greater than 150 mg/L (nominal concentration).
To conclude, no immobilization was observed throughout both tests at their highest tested concentration. As a consequence, 48h-EC50 is considered to be > 100 mg/L.
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