Registration Dossier
Registration Dossier
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EC number: 418-220-4 | CAS number: - RED JB 747
- 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
Oral rat LD50 > 2000 mg/kg bw
Inhalation: study scientifically unjustified
Dermal rat LD50 > 2000 mg/kg bw
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- LD50
- Value:
- 2 000 mg/kg bw
Acute toxicity: via inhalation route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Acute toxicity: via dermal route
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- LD50
- Value:
- 2 000 mg/kg bw
Additional information
In the assessment of both acute oral toxicity and acute dermal toxicity a limited test was performed on rats (males and females), with the application of a single dose of 2000 mg/kg bw. Both studies were conducted according to the OECD Guidelines (No. 401 and 402 for oral and dermal toxicity respectively. Since any relevant toxicity effect could not be observed, the test substance can be considered to be not acutely toxic, with a LD50 >2000 mg/kg bw by both dermal and oral routes.
The inhalation exposure route was not assessed because, according to column 2 (information requirement section 8.5), Annex VIII of REACH Regulation , the study does not need to be conducted since exposure by inhalation is very unlikely and acute toxicity studies are already available for both oral and dermal route.
Despite the MMD of the substance is 3.1 µm (i.e. respirable fraction), exposure by inhalation route is unlikely to happen because of the physical state of the substance when imported and adopted RMMs.
In fact, since the chemical is imported as a component of a liquid solution, dust inhalation will not be taken into account. Inhalation exposure can still occur if mists are produced, but this would only occur under certain conditions such as leaks from a pressurised system. Formation of vapours from the solution containing the chemical is also very unlikely, due to its negligible vapour pressure.
In addition, the substance is used in tanneries to dye hides and it was reported to be strongly chemically bound to the substrate one the hides are dried, limiting therefore the exposure to workers and general population.
Justification for classification or non-classification
The substance has a rat acute oral LD50 >2000 mg/kg bw. As a result, the substance does not meet the criteria for classification according to regulation EC 1272/2008 (CLP), Annex I section 3.
The substance has a rat acute dermal LD50 >2000 mg/kg bw. As a result, the substance does not meet the criteria for classification according to Regulation EC 1272/2008, Annex I section 3.
In addition, the inhalation route is very unlikely to be interested since the substance is a solid with negligible vapour pressure which decomposed before boiling.
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