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Diss Factsheets
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EC number: 274-572-7 | CAS number: 70331-94-1
- 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
PBT assessment
Administrative data
PBT assessment: overall result
- Name:
- (1,2-dioxoethylene)bis(iminoethylene) bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate]
- Type of composition:
- legal entity composition of the substance
- State / form:
- solid: particulate/powder
- Reference substance:
- (1,2-dioxoethylene)bis(iminoethylene) bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate]
- PBT status:
- the substance is not PBT / vPvB
- Justification:
The following information is available for review:
Persistence
The substance is not readily biodegradable achieving 0-2% in 28 days. Due to high water insolubility (1.5 μg/l), it is not possible to assess the potential for hydrolysis by testing. The substance is, however, a stable organic molecule and is, therefore, considered to not potentially hydrolyse in the environment.
The substance potentially screens as persistent.
Bioaccumulation
The log Pow has been determined to be 8.1. The substance is highly insoluble in water (1.5 μg/l). The high log Pow is likely to be due in part to the hydrophobic nature of the molecule but is well outside the criteria by which that substance is considered to present a potential hazard.
The substance has a water solubility of 1.5 μg/l which clearly limits the bioavailability towards aquatic organisms. Furthermore, due to the high adsorption potential (log Koc > 5.63) it is expected that the substance will bind to sewage sludge and be removed from the water phase. In total, the concentrations in the environmental water phase are expected to be very low and not relevant for bioaccumulation.
The calculated BCF value is 713.4 L/kg wet-wt estimated by QSAR modelling. These values support the above-mentioned assessment that the substance is not expected to significantly accumulate in aquatic organisms.
No evidence of accumulation was noted in the repeated dose study conducted on the substance.
The substance does not screen as "B" based on the high log Kow value and calculated BCF.
Toxicity
The substance is highly insoluble in water. In consequence exposure to three aquatic species (algae, daphnia and fish) have been investigated at nominal concentrations. The toxicological examination of freshwater fish, daphnia and algae provided the following results:
· LC50 > 100 mg/l in fish
· EC50 > 100 mg/l in daphnia
· EC50 > 100 mg/l in algae
The substance is not classified on the basis of these results and no further toxicological examination is considered appropriate to determine that hazard of the substance.
The substance has been assessed for genetic toxicity utilising in vitro assays with and without metabolic activation. All endpoints demonstrated a lack of mutagenic response.
The reproduction/developmental screening test provided a result NOAEL 1000 mg/kg bw/day and showed no substance related effects on parents or offspring.
On the basis of the genetic and reproduction/developmental toxicity data available, in addition to the repeated dose toxicity data the substance is not classified for this endpoint.
The data from the 90-day mammalian toxicity oral repeated dose study achieved a NOAEL >2000 mg/kg/day. The substance is not classified on the basis of this data and no further toxicological examination is considered necessary for hazard assessment.
The substance demonstrates no toxicity in any of the test endpoints noted.
Conclusion.
The substance does not screen as PBT of vPvB on the basis of the available data.
Reference
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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