Registration Dossier
Registration Dossier
Diss Factsheets
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EC number: 218-487-5 | CAS number: 2162-74-5
- 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

Toxicity to soil macroorganisms except arthropods
Administrative data
- Endpoint:
- toxicity to soil macroorganisms except arthropods: long-term
- Type of information:
- experimental study planned
- Study period:
- The study will be placed following ECHA`s acceptance of the Testing Proposal. Depending on the capacities of the test facilities, the results should be available at the latest 6 - 12 months thereafter.
- Justification for type of information:
- TESTING PROPOSAL for study according to Annex X of REACH
NON-CONFIDENTIAL NAME OF SUBSTANCE:
- Name of the substance on which testing is proposed to be carried out:
Bis(2,6-diisopropylphenyl)carbodiimide (CAS 2162-74-5)
CONSIDERATIONS THAT THE GENERAL ADAPTATION POSSIBILITIES OF ANNEX XI OF THE REACH REGULATION ARE NOT ADEQUATE TO GENERATE THE NECESSARY INFORMATION:
- Available GLP studies: No data from GLP studies with terrestrial organisms available.
- Available non-GLP studies: No data from non-GLP studies with terrestrial organisms available.
- Historical human/control data: No historical human/control data for the terrestrial compartment available.
- (Q)SAR: No QSAR data for terrestrial organisms available.
- In vitro methods: Not applicable
- Weight of evidence: Not applicable
- Grouping and read-across: Not applicable
CONSIDERATIONS THAT THE SPECIFIC ADAPTATION POSSIBILITIES OF ANNEXES VI TO X (AND COLUMN 2 THEREOF) OF THE REACH REGULATION ARE NOT ADEQUATE TO GENERATE THE NECESSARY INFORMATION:
As demonstrated in the environmental exposure and risk assessment of the CSR, releases to the terrestrial environment are low – even despite the worst-case approach applied in the assessment. Nonetheless, a robust justification of “unlikely exposure” based on Col. 2 of REACH Annex IX cannot be delivered because of the insufficient documentation on downstream uses available to the registrant. It is therefore deemed as reasonable to undertake an Annex XI.3.2. (a) route based on derived PNEC. Accordingly, a study on earthworms is planned to be conducted by the lead registrant/consortium, to verify absence of risk/hazard for the terrestrial compartment.
According to Table R.7.11-1 of ECHA Endpoint specific guidance, Chapter R.7c (V 3.0, June 2017), the exposure pathway for invertebrates is by diverse uptake routes (soil pore water, ingestion of soil material, soil air, secondary poisoning). The exposure pathway for plants and microorganisms is the soil pore water, which is expected to contain a negligible amount of substance due to its poor solubility (< 0.53 μg/L (Holzaht-Grimme, 2019)). Further, the same guidance states “The choice of test (invertebrate / plant / micro-organism) would be based on all the information available, but in the absence of a clear indication of selective toxicity, an invertebrate (earthworm or collembolan) test is preferred.” (R.7c, page 149, V 3.0, June 2017).
Under Annex IX of REACH, short-term studies are standardly required, but, taking into account the substance’s high adsorptivity and potential persistence, a long-term study is deemed adequate. For the same reason, it was decided against screening based on EPM.
Hence, an Earthworm Reproduction Test according to OECD 222 with Eisenia fetida/Eisenia Andrei as representative terrestrial invertebrate is envisaged to be conducted with test concentrations being at least 10-fold higher than the regional PEC determined for the soil compartment, which is 4.54E-6 mg/kg dw as presented in Table 161 of the regional assessment within the CSR for the registered substance.
The study result will then be used to calculate the PNECsoil of the substance and, subsequently, the PEC/PNEC ratio. Should it be <<1, “no significant exposure” will be deemed proven. Otherwise, further testing will be considered.
FURTHER INFORMATION ON TESTING PROPOSAL IN ADDITION TO INFORMATION PROVIDED IN THE MATERIALS AND METHODS SECTION:
- Details on study design / methodology proposed:
As outlined above an Earthworm Reproduction Test according to OECD 222 is envisaged to be conducted with the earthworm Eisenia fetida/Eisenia andrei as test organism. Following the recommendations of the Endpoint specific Guidance Version 3.0, Chapter R.7c of June 2017, the study will be conducted with test concentrations being at least 10-fold higher than the PEC soil determined for the regional assessment and based on the total releases to the soil compartment.
Due to the poor solubility of the registered substance, it will probably be necessary to apply the test material by the use of a suitable vehicle, which can be completely evaporated before the exposed soil can be used for the test performance. Therefore, respective pre-experiments will be conducted ahead to determine the most meaningful test design for the performance of the definitive test. If it is demonstrated to be sufficient by the results of the pre-experiments, the definite study will be performed as limit test only.
Data source
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 222 (Earthworm Reproduction Test (Eisenia fetida/Eisenia andrei))
Test material
- Reference substance name:
- Bis(2,6-diisopropylphenyl)carbodiimide
- EC Number:
- 218-487-5
- EC Name:
- Bis(2,6-diisopropylphenyl)carbodiimide
- Cas Number:
- 2162-74-5
- Molecular formula:
- C25H34N2
- IUPAC Name:
- N,N'-bis[2,6-bis(propan-2-yl)phenyl]methanediimine
- Test material form:
- solid
Constituent 1
Results and discussion
Applicant's summary and conclusion
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.

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