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EC number: 220-666-8 | CAS number: 2855-13-2
- 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
Hydrolysis
Administrative data
Link to relevant study record(s)
- Endpoint:
- hydrolysis
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2002-08-02 to 2002-08-12
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.7 (Degradation: Abiotic Degradation: Hydrolysis as a Function of pH)
- Version / remarks:
- (1981)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 111 (Hydrolysis as a Function of pH)
- Version / remarks:
- (1992)
- Deviations:
- no
- GLP compliance:
- yes
- Radiolabelling:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- At test start (= 0 hours), 2.4 hours, 5 days
- Buffers:
- pH 4: citric acid - hydrochloric acid
pH 7: potassium dihydrogen phosphate - disodium hydrogen phosphate
pH 9: boric acid -potassium chloride - sodium hydroxide - Details on test conditions:
- Only preliminary test performed
- Duration:
- 5 d
- pH:
- 4
- Temp.:
- 50
- Initial conc. measured:
- 1 010 mg/L
- Duration:
- 5 d
- pH:
- 7
- Temp.:
- 50
- Initial conc. measured:
- 1 062 mg/L
- Duration:
- 5 d
- pH:
- 9
- Temp.:
- 50
- Initial conc. measured:
- 1 013 mg/L
- Number of replicates:
- 2
- Positive controls:
- not specified
- Negative controls:
- not specified
- Statistical methods:
- average of two determinations
- Preliminary study:
- Less than 10 % degradation was observed after 5 days at 50 degree C and pH 4, 7, and 9.
Observed degree of hydrolysis (determined twice):
pH 4: 2.58 %, 3.68 %
pH 7: 1.36 %, 2.59 %
pH 9: not detectable (-3.16 %, -1.18 %) - Test performance:
- Main test: not required
- Transformation products:
- not measured
- % Recovery:
- < 90
- Temp.:
- 50 °C
- Duration:
- 5 d
- pH:
- 4
- Temp.:
- 25 °C
- DT50:
- > 1 yr
- pH:
- 7
- Temp.:
- 25 °C
- DT50:
- > 1 yr
- pH:
- 9
- Temp.:
- 25 °C
- DT50:
- > 1 yr
- Details on results:
- at 50 °C: Degradation (in %): < 10 after 5day(s)
- Validity criteria fulfilled:
- not specified
- Conclusions:
- Isophorone diamine does not show a significant sensitivity towards hydrolysis. In the preliminary test, less than 10% of the test substance was observed to hydrolyse at 50 °C at pH 4,7 and 9 after 5 days. There was no need to perform a main test.
- Executive summary:
The hydrolysis as a function of pH of the test substance was determined by Infracor (2002) according to OECD TG 111 (1981) and EU method C.7 (1992). In the preliminary test, less than 10% of the test substance was observed to hydrolyse at 50 °C at pH 4,7 and 9 after 5 days. Thus additional testing (main test) is not required.
The study was assessed as "reliable without restrictions".
Reference
Description of key information
Isophorone diamine does not show a significant sensitivity towards hydrolysis. In the preliminary test, less than 10% of the test substance was observed to hydrolyse at 50 °C at pH 4,7 and 9 after 5 days. There was no need to perform a main test.
Key value for chemical safety assessment
Additional information
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