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EC number: 231-441-9 | CAS number: 7550-45-0
- 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

Genetic toxicity: in vitro
Administrative data
- Endpoint:
- in vitro DNA damage and/or repair study
- Remarks:
- Type of genotoxicity: DNA damage and/or repair
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Meets generally accepted scientific standards, well documented and acceptable for assessment
Data source
Reference
- Reference Type:
- publication
- Title:
- Mutagenicity evaluation of forty-one metal salts by the umu test
- Author:
- Yamamoto A,Kohyama Y, Hanawa T
- Year:
- 2 002
- Bibliographic source:
- J Biomed Mater Res. 59(1):176-83
Materials and methods
- Principles of method if other than guideline:
- Titanium terachloride was tested in the umu test, which can evaluate the genotoxicity of a substance by measuring the induction of the bacterial SOS response which is induced by single-strand DNA gaps or DNA fragments produced as the result of danage to DNA.
- GLP compliance:
- not specified
- Type of assay:
- SOS/umu assay
Test material
- Reference substance name:
- Titanium tetrachloride
- EC Number:
- 231-441-9
- EC Name:
- Titanium tetrachloride
- Cas Number:
- 7550-45-0
- Molecular formula:
- Cl4Ti
- IUPAC Name:
- titanium tetrachloride
- Details on test material:
- - Name of test material (as cited in study report): TiCl4
- Physical state: liquid
- Analytical purity: >99%
Constituent 1
Method
Species / strain
- Species / strain / cell type:
- S. typhimurium TA 1535 pSK1002
- Metabolic activation:
- with and without
- Metabolic activation system:
- S-9 mix
- Test concentrations with justification for top dose:
- 0.00042-0.021 mol/L
- Vehicle / solvent:
- - Vehicle(s)/solvent(s) used: [Phosphate-buffered saline without calcium and magnesium salts (PBS(-))]
Controlsopen allclose all
- Untreated negative controls:
- yes
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- not specified
- Positive controls:
- yes
- Positive control substance:
- other: 2-aminoanthracene
- Remarks:
- with S-9 mix
- Untreated negative controls:
- yes
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- not specified
- Positive controls:
- yes
- Positive control substance:
- furylfuramide
- Remarks:
- without S-9 mix
- Details on test system and experimental conditions:
- METHOD OF APPLICATION: in medium
DURATION
2 h at 37 °C, addition of X-Gal, 1 h at 37 °C
DETERMINATION OF CYTOTOXICITY
- Method: relative total growth - Evaluation criteria:
- To judge metal salt mutagenicity, the RAB curve of each metal salt is drawn based on more than six concentrations.
When the RABmax, is larger than 0.1, the metal salt is estimated to be "mutagenic". For mutagenic salts, the test was repeated until the RAB peak was
obtained. The starting range of the RAB curve (where RAB is equal to zero at relatively low concentrations) or the ending range of the
curve (where the RAB decreases below Zero at relatively high concentrations) is also confirmed. The metal salt mutagenicity was expressed
quantitatively by two Factors, Cmax and RABmax. For nonmutagenic metal salts, the test is repeated by changing the metal salt concentration range
until two points, described below are confirmed from its RAB curve: 1. the RAB is approximately zero over several ranges of the metal salt
concentration, and then 2. the RAB decreased to below zero at more than two concentrations of the metal salt by its toxicity. - Statistics:
- no data
Results and discussion
Test results
- Species / strain:
- S. typhimurium TA 1535 pSK1002
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not specified
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Remarks on result:
- other: all strains/cell types tested
- Remarks:
- Migrated from field 'Test system'.
Applicant's summary and conclusion
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.

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