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EC number: 231-142-3 | CAS number: 7440-32-6
- 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
Titanium dioxide has been tested in three in vivo skin irritation and one eye irritation study. All tests show a negative response, thus titanium dioxide does not require classification either as skin or as eye irritant.
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)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Additional information
Titanium is a transition-metal and is subject at its surface to passivation by the formation of a passive and protective oxide (i. e. titanium dioxide) coating that effectively protects it from further reaction. In particular for titanium metal and granules, the oxide layer will form a quantitatively continuous layer to envelop the entire particle irrespective of product form. The reaction kinetics have been investigated and reported in various references (Uhlig, 1979; Schmets et al. 1953; Andreeva, 1964; Burleigh, 1989; El Din et al., 1988), indicating that the oxide layer is formed immediately after the interaction of the clean surface with the air atmosphere. Any melt processing of titanium metal has to be conducted under an inert atmosphere or vacuum to protect the metal from instant oxidation. Similarly the use of solid titanium at elevated temperatures is restricted due to its propensity for rapid oxidation.
Furthermore, transformation/dissolution testing according to “OECD 29 Environmental Health and Safety Publications, Series on testing and assessment, Guidance document on transformation/ dissolution of metals and metal compounds in Aqueous media” has shown that titanium metal compared to titanium dioxide has a similar release rate of titanium ions (please refer to the respective entry under the endpoint water solubility).
In view of this, it may be assumed that human exposure towards titanium metal is secondary to that of titanium dioxide.
Thus, unlimited read-across for skin and eye irritating properties is considered justified.Three in vivo key studies on the dermal irritation of titanium dioxide were identified which was conducted according or equivalent to OECD guideline 404. One study reported a mean erythema score of 0.7, 0.5 and 0.17 at time point 1, 24, 48h respectively after exposure. All further studies report no irritation whatsoever. Based on the outcome of these studies titanium dioxide is considered as not irritating to the skin. The supportive information undermine this interpretation since in none of the reliable studies, titanium dioxide was identified as irritating to the skin.
In a recent (2006) very well-conducted and reported acute eye irritation/corrosion test with highly pure titanium dioxide, performed according to OECD guideline 405 and in compliance with GLP regulations, the only observation was conjunctival redness (grade 1) observed in 2 animals at 1 hour after installation and grade 2 in 1 animal at 1 hour after instillation, respectively. This effect was fully reversible. There were no corneal lesions, the iris was not affected by instillation of the item, and there were no systemic intolerance reactions.
References
H.H. Uhlig (1979) Passivity in Metals and Alloys, Corrosion Science, Vol. 19, pp. 777-791
J. Schmets and M. Pourbaix (1953) Equilibrium Potential-pH Diagram for the System Ti-H2O, Corrosion of Titanium, Technical Report RT. 4, CEBELCOR, pp. 167-179
V.V. Andreeva (1964) Behavior and Nature of Thin Oxide Films on Some Metals in Gaseous Media and in Electrolyte Solutions, Corrosion, Vol. 20, No. 2, pp. 35-47
T.D. Burleigh (1989) Anodic Photocurrents and Corrosion Currents on Passive and Active-Passive Metals, Corrosion, Vol. 45, No. 6, pp.464-472
A.M. Shams El Din and A.A. Hammoud (1988) Oxide Film Formation and Thickening on Titanium in Water", Thin Solid Films, Vol. 167, No. 1, pp. 269-280
Justification for classification or non-classification
Skin irritation
References Finlay, C.(2006), Finlay, C.(2003), Filliben, T.A.(1994) are considered as the key studies for skin irritation and will be used for classification. The overall irritation results are as follows:
Finlay, C.(2006):
erythema, 0-72h after application: mean score=0.0
oedema, 0-72h after application: mean score=0.0
Finlay, C.(2003)
erythema, 0-48h after application: mean score=0.0
oedema, 0-48h after application: mean score=0.0
Filliben, T.A.(1994)
erythema, 1h after application: mean score=0.7 fully reversible
erythema, 24h after application: mean score=0.5 fully reversible
erythema, 48 and 72h after application: mean score=0.17 fully reversible
oedema, 0-72h after application: mean score=0.0
The classification criteria acc. to regulation (EC) 1272/2008 as irritating to skin are not met since the mean erythema score after 24h was 0.5, hence no classification required.
Eye irritation
Reference Finlay, C.(2006) is considered as the key study for eye irritation and will be used for classification. The overall irritation results are as follows:
conjunctival redness, 1h after application: mean score=1.3
conjunctival redness, 24h after application: mean score=0.3
conjunctival redness, 48 and 72h after application: mean score=0.0
The classification criteria acc. to regulation (EC) 1272/2008 as irritating to eyes are not met since the mean score after 24h was 0.3, hence no classification required.
Respiratory irritation
The classification as respiratory irritant is covered under the endpoint specific target organ toxicity- single exposure and repeated exposure. Please refer to the endpoint summaries on acute toxicity (endpoint 7.2) and repeated dose toxicity (endpoint 7.5) for further information.
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