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Diss Factsheets
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EC number: 249-828-6 | CAS number: 29761-21-5
- 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
Endpoint summary
Administrative data
Description of key information
- Acute Dermal Irritation/Corrosion:
In vivo skin irritation test (similar to OECD 404): not irritating.
- Acute Eye Irritation:
In vivo eye irritation test (similar to OECD 405): not irritating.
Key value for chemical safety assessment
Skin irritation / corrosion
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Eye irritation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Additional information
Acute Dermal Irritation/Corrosion:
In the key skin irritation and corrosion study, IDDPP was found not to be irritating or corrosive to the skin when treated on the intact and abraded skin of albino rabbits. The average mean scores calculated from the numerical values given to the skin irritation observed at the 4, 24, and 48 hour examinations were 0.84 for erythema and 0.22 for edema.
In the additional 3 supporting skin irritation/corrosion studies the test substance was also not irritating to the rabbit and human skin.
Based on these results and according to the EU criteria outlined in 67/548/EEC and 1272/2008/EC (CLP/EU-GHS), the test substance was considered not irritating and does not have to be classified and has no obligatory labelling requirement for skin irritation.
Acute Eye Irritation:
In the key eye irritation test the guidelines described by Draize (1965) were used to assign numerical scores for corneal, iridic and conjunctival irritation (redness/chemosis/discharge) to the observed effects and to develop a weighted total score for each rabbit for each day of observations. The mean scoring results was < 1.00 for all 9 rabbits. IDDPP was considered a non-irritant in the eyes of albino rabbits.
In the supporting eye irritation study the average maximum score was 21.3, 17.6, and 8.0 out of a possible 110 in 24, 48, and 72 hours, resp. Effects were completely reversible within 7 days. Interpretation of these results and classification of the test substance was not possible, since the scoring system used is not according to OECD guideline 405 or EU classification criteria. In the report it is concluded that IDDPP is mildly irritating to the eye.
Based on the results of the key study and according to the EU criteria outlined in 67/548/EEC and 1272/2008/EC (CLP/EU-GHS), the test substance does not have to be classified and has no obligatory labelling requirement for eye irritation.
The respiratory irritation was not studied for IDDPP.
Justification for classification or non-classification
The 2 key in vivo studies indicate that IDDPP does not induce any significant irritation to the skin and eye. Therefore, it can be concluded that the substance is not irritating and therefore does not need to be classified as such according to the criteria outlined in Annex I of 1272/2008/EC (CLP/EU-GHS) and Annex VI of 67/548/EEC.
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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