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Diss Factsheets
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EC number: 225-184-1 | CAS number: 4702-90-3
- 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
Link to relevant study record(s)
Description of key information
Key value for chemical safety assessment
Additional information
There were no studies available in which the toxicokinetic properties of the test substance were investigated. The test substance (molecular weight of 358 g/mol) is a yellow powder with a log Pow of 5.02 and a water solubility of 4.7 µg/L at 23°C. The vapor pressure was estimated at 1.3E-009 Pa at 25°C.
In an acute toxicity study in rats no mortality and no systemic findings were observed after oral administration of test substance at a dose level of 6400 mg/kg body weight. Therefore, no conclusion can be drawn regarding systemic distribution. Generally, the smaller the molecule, the more easily it may be taken up. Molecular weights below 500 g/mol are favorable for absorption; molecular weights above 1000 g/mol do not favor absorption (ECHA GD 7c, 2008). The test article is characterized by a molecular weight in a range supporting absorption in the gastrointestinal tract. The water solubility of the test article is low, thus not favoring the substance to be readily dissolved in gastrointestinal fluids. The findings reported in an OECD 422 study demonstrates that the substance is taken up and bioavailable. In this study, adverse findings were reported in the high dose level indicating that the substance has been absorbed. In addition, discoloration of adipose tissue was reported, obviously corresponding with duration of treatment and dose level since low-dose male animals did not show the discoloration (treated for 4 weeks), but females did (treated for about 8 weeks). These observations support the hypothesis of systemic bioavailability and lead to the conclusion that the test substance accumulates by time and dose. Therefore, absorption through the gastrointestinal tract has occurred. A sensitization study was negative, therefore not allowing for a conclusion regarding dermal absorption. The vapor pressure is very low therefore absorption by inhalation is considered less relevant. The excretion pathway is largely dependent on molecular size, polarity and water solubility. Potential metabolites are either excreted via feces or urine, depending on their molecular size and water solubility after phase II metabolism.
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.