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EC number: 292-054-9 | CAS number: 90530-16-8
- 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
Key value for chemical safety assessment
Skin sensitisation
Link to relevant study records
- Endpoint:
- skin sensitisation
- Remarks:
- other: QSAR, read-across
- Type of information:
- (Q)SAR
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- results derived from a valid (Q)SAR model and falling into its applicability domain, with adequate and reliable documentation / justification
- Justification for type of information:
- QSAR prediction: migrated from IUCLID 5.6
- Principles of method if other than guideline:
- • TIMES modeling approach (Skin sensitization model);
• Available experimental data;
• Toolbox 3.3 read-across analysis. - Type of study:
- other: QSAR, read-across
- Value:
- 1
- Vehicle controls validity:
- not specified
- Negative controls validity:
- not specified
- Positive controls validity:
- not specified
- Remarks on result:
- positive indication of skin sensitisation
- Interpretation of results:
- sensitising
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Skin sensitiser category 1 H317
- Executive summary:
The assessment of 2-Propenenitrile, reaction products with 1,3-benzenedimethanamineis separated in two parts:
· Analysis of the individual constituents:Based on the TIMES Skin sensitization model and TB read-across analysis performed the constituents of analyzed UVCB 2-Propenenitrile, reaction products with 1,3-benzenedimethanamine(CAS 90530-16-8) are predicted as follows:
- ConstituentsMXDA, CandEare not expected to be skin-sensitizers;
- ConstituentsA, BandDare expected to cause Skin sensitization effect.
The predictions provided by TIMES SS model and Toolbox are consistent and supported by the experimental skin sensitization data of structural analogues. The only inconsistency is for MXDA: documented positive skin sensitizer but negative predictions by TIMES SS and Toolbox read-across. The analysis also showed that the structural analogues of the simulated skin metabolites of MXDA do not cause skin sensitization effect. Our assumption is that the corrosivity of MXDA may affect the outcome from skin sensitization tests and give false positive results [3].
· Analysis of the whole substance based on the predictions for the constituents and the concentration information provided by the client:
According to the classification criteria for mixtures discussed inCLP Annex I, 3.4.3.3.1. [30, 31]2-Propenenitrile, reaction products with 1,3-benzenedimethanamine(CAS 90530-16-8) is assessed as a skin sensitizer because three of its constituents (A,B and D) are predicted as Strong skin sensitizers by TIMES SS model and their concentrations in the analyzed UVCB are greater than the specified threshold of 1.0%.
Reference
The assessment of2-Propenenitrile, reaction products with 1,3-benzenedimethanamineis separated in two parts:
· Analysis of the individual constituents: Based on the TIMES Skin sensitization model and TB read-across analysis performed the constituents of analyzed UVCB 2-Propenenitrile, reaction products with 1,3-benzenedimethanamine (CAS 90530-16-8) are predicted as follows:
- ConstituentsMXDA, C and E are not expected to be skin-sensitizers;
- ConstituentsA, B and D are expected to cause Skin sensitization effect.
The predictions provided by TIMES SS model and Toolbox are consistent and supported by the experimental skin sensitization data of structural analogues. The only inconsistency is for MXDA: documented positive skin sensitizer but negative predictions by TIMES SS and Toolbox read-across. The analysis also showed that the structural analogues of the simulated skin metabolites of MXDA do not cause skin sensitization effect. Our assumption is that the corrosivity of MXDA may affect the outcome from skin sensitization tests and give false positive results [3].
· Analysis of the whole substance based on the predictions for the constituents and the concentration information provided by the client:
According to the classification criteria for mixtures discussed inCLP Annex I, 3.4.3.3.1. [30, 31]2-Propenenitrile, reaction products with 1,3-benzenedimethanamine(CAS 90530-16-8) is assessed as a skin sensitizer because three of its constituents (A,B and D) are predicted as Strong skin sensitizers by TIMES SS model and their concentrations in the analyzed UVCB are greater than the specified threshold of 1.0%.
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (sensitising)
- Additional information:
According to the classification criteria for mixtures discussed in CLP Annex I, 3.4.3.3.1. [30, 31] 2-Propenenitrile, reaction products with 1,3-benzenedimethanamine (CAS 90530-16-8) is assessed as a skin sensitizer because three of its constituents (A,B and D) are predicted as Strong skin sensitizers by TIMES SS model and their concentrations in the analyzed UVCB are greater than the specified threshold of 1.0%.
Migrated from Short description of key information:
H 317 skin sensitiser category 1
Justification for selection of skin sensitisation endpoint:
Read-across and QSAR prediction
Justification for classification or non-classification
According to the classification criteria for mixtures discussed inCLP Annex I, 3.4.3.3.1. [30, 31]2-Propenenitrile, reaction products with 1,3-benzenedimethanamine(CAS 90530-16-8) is assessed as a skin sensitizer because three of its constituents (A,BandD) are predicted as Strong skin sensitizers by TIMES SS model and theirconcentrations in the analyzed UVCB are greater than the specified threshold of 1.0%.
CLP classification: H317 skin sensibilsation category 1
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