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EC number: 269-053-7 | CAS number: 68186-91-4 This substance is identified in the Colour Index by Colour Index Constitution Number, C.I. 77428.
- 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
Short description of key information on bioaccumulation potential result:
As dissolved Cr and Cu concentrations were below 74 µg/L and 366 µg/L respectively, even at the highest loading of 0.1g/L, referring to a solubility of 0.074 % and 0.37 %, the pigment is considered biologically inert.
Key value for chemical safety assessment
Additional information
The chemical and physiological properties of the pigment copper chromite black spinel are characterised by inertness because of the specific synthetic process (calcination at high temperatures, approximately1000°C), rendering the substance to be of a unique, stable crystalline structure in which all atoms are tightly bound and not prone to dissolution in environmental and physiological media. This manufacturing process leads to a very low bioaccessibility of the elements contained in the pigment. This has been investigated experimentally in vitro by simulating dissolution under physiological conditions considered to mimic the most relevant exposure routes (oral, dermal and inhalation), as follows:
1.) Gamble’s solution (GMB, pH7.4) which mimics the interstitial fluid within the deep lung under normal health conditions,
2.) phosphate-buffered saline (PBS, pH7.2), which is a standard physiological solution that mimics the ionic strength of human blood serum,
3.) artificial sweat (ASW, pH 6.5) which simulates the hypoosmolar fluid, linked to hyponatraemia (loss of Na+ from blood), which is excreted from the body upon sweating,
4.) artificial lysosomal fluid (ALF, pH4.5), which simulates intracellular conditions in lung cells occurring in conjunction with phagocytosis and represents relatively harsh conditions and
5.) artificial gastric fluid (GST, pH1.5), which mimics the very harsh digestion milieu of high acidity in the stomach.
The dissolution of Cr of the test item is between 16.5 µg/L /19.3 µg/L (GMB) and 43.3 µg/L/ 73.5 µg/L (GST) at a loading of 0.1g/L after 2 and 24 hours.
The dissolution of Cu of the test item is in a range of 8.44 µg/L/ 41,4 µg/L (PBS) and 290 µg/L/ 366 µg/L (GST) at a loading of 0.1g/L after 2 and 24 hours.
A pHdependent dissolution can be observed.In conclusion, since the dissolvedCr and Cu concentrations were below 74 µg/L and 370 µg/L, respectively even at the highest loading of 0.1g/L, referring to a solubility of < 0.08 and<0.4 %, this pigment may reasonably be considered biologically inert.
Discussion on bioaccumulation potential result:
The chemical and physiological properties of the pigment copper chromite black spinel are dominated by inertness due to the characteristics of the production process (calcination at high temperatures, approximately1000°C), rendering the substance to be of a unique, stable crystalline structure. This fundamental process leads to a very low bioaccessibility for the elements contained in the pigment. By simulating the typical physiological conditions of the presumed exposure routes (oral, dermal and inhalation) with
1.) Gamble’s solution (GMB, pH7.4) which mimics the interstitial fluid within the deep lung under normal health conditions,
2.) phosphate‐buffered saline (PBS, pH7.2), which is a standard physiological solution that mimics the ionic strength of human blood serum,
3.) artificial sweat (ASW, pH6.5) which simulates the hypoosmolar fluid, linked to hyponatraemia (loss of Na+ from blood), which is excreted from the body upon sweating,
4.) artificial lysosomal fluid (ALF, pH4.5), which simulates intracellular conditions in lung cells occurring in conjunction with phagocytosis and represents relatively harsh conditions and
5.) artificial gastric fluid (GST, pH1.5), which mimics the very harsh digestion milieu of high acidity in the stomach.
An oral, dermal or inhalative uptake of the substance for humans exposed to the pigment is negligible.
The dissolution of Cr of the test item is between 16.5 µg/L /19.3 µg/L (GMB) and 43.3 µg/L/ 73.5 µg/L (GST) at a loading of 0.1g/L after 2 and 24 hours.
The dissolution of Cu of the test item is in a range of 8.44 µg/L/ 41,4 µg/L (PBS) and 290 µg/L/ 366 µg/L (GST) at a loading of 0.1g/L after 2 and 24 hours.
A pH dependent dissolution can be observed.In conclusion, since the dissolved Cr and Cu concentrations were below 74 µg/L and 370 µg/L, respectively even at the highest loading of 0.1g/L, referring to a solubility of < 0.08 and<0.4 %, this pigment may reasonably be considered biologically inert.
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