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Diss Factsheets
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EC number: - | CAS number: -
- 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:
- LE composition_Reaction mass of N-butylphthalimide and N-sec-butylphthalimide and N-propylphthalimide
- Type of composition:
- legal entity composition of the substance
- State / form:
- liquid
- Reference substance:
- LE composition_Reaction mass of N-butylphthalimide and N-sec-butylphthalimide and N-propylphthalimide
- Reference substance:
- LE composition_Reaction mass of N-butylphthalimide and N-sec-butylphthalimide and N-propylphthalimide
- Reference substance:
- LE composition_Reaction mass of N-butylphthalimide and N-sec-butylphthalimide and N-propylphthalimide
- PBT status:
- the substance is not PBT / vPvB
- Justification:
Evaluating the PBT/vPvB potential of multi-constituent substances is known to be difficult as persistence and bioaccumulation testing methods are not applicable (or at least difficult to apply) for these substances. Therefore, an evaluation based on experimental results of the multi-constituent substance and constituents as well as QSARs of the constituents and the most probable abiotic degradation products was performed.
Reaction mass of N-butylphthalimide and N-propylphthalimide and N-sec-butylphthalimide was ready biodegradable failing the 10 days window according to testing. It can therefore be concluded that reaction mass of N-butylphthalimide and N-propylphthalimide and N-sec-butylphthalimide do not fulfil the criteria for P and vP in the environment. In addition, the main abiotic degradations products of the consitutents N-butylphthalimide, N-propylphthalimide and N-sec-butylphthalimide are not expected to meet the P and vP criteria based on estimation performed with the Biowin 3, 5 and 6 models.
The evaluation of the bioaccumulation potential of reaction mass of N-butylphthalimide and N-propylphthalimide and N-sec-butylphthalimide was based on the measured Log Kow values of all three constituents as well as of the corresponding most probable abiotic degradation products. All Log Kow values reported were below 4.5. Even if the log Koa of all constituents were estimated to be above 5, the vapour pressures of reaction mass of N-butylphthalimide and N-propylphthalimide and N-sec-butylphthalimide and the corresponding abiotic degradation products were measured/estimated to be rather low (< 0.04 hPa) indicating that these substances are not very volatile. Therefore, reaction mass of N-butylphthalimide and N-propylphthalimide and N-sec-butylphthalimide and its abiotic degradtation products are expected to have a limited potential to be taken up via the air by air breathing organisms. Based on the available data, the constituents of reaction mass of N-butylphthalimide and N-propylphthalimide and N-sec-butylphthalimide as well as the corresponding most probable abiotic products are considered not to meet the criteria for a classification as B or vB.
Finally, reaction mass of N-butylphthalimide and N-propylphthalimide and N-sec-butylphthalimide does not fulfil the T screening criteria based on acute aquatic toxicity data and currently available human toxicity data. Concerning the abiotic degradation products, no further assessment was performed since the most probable abiotic degradation products of all constituents did not fulfill the criteria for B or vB.
In conclusion, reaction mass of N-butylphthalimide and N-propylphthalimide and N-sec-butylphthalimide and the abiotic degradation products of its constituents do not fulfill the criteria for PBT or vPvB.
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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