249998
Titanium(III) chloride solution
~10 wt. % in 20-30 wt. % hydrochloric acid
Synonym(s):
Titanium trichloride
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About This Item
Recommended Products
reaction suitability
reagent type: catalyst
core: titanium
concentration
~10 wt. % in 20-30 wt. % hydrochloric acid
density
1.192 g/mL at 25 °C
SMILES string
Cl[Ti](Cl)Cl
InChI
1S/3ClH.Ti/h3*1H;/q;;;+3/p-3
InChI key
YONPGGFAJWQGJC-UHFFFAOYSA-K
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Application
Catalyst for:
Hydrogen desorption properties
Nitrogen-nitrogen reductive bond cleavage
Reagent for:
Photocatalyst synthesis
Preparation of nanostructures titania/cetyltrimethyammonium bromide nanoskeleton
Hydrogen desorption properties
Nitrogen-nitrogen reductive bond cleavage
Reagent for:
Photocatalyst synthesis
Preparation of nanostructures titania/cetyltrimethyammonium bromide nanoskeleton
Other Notes
Exact concentration stated on label
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
8B - Non-combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Applied Physics Letters, 99 (2011)
Catalysis Today, 161, 169-174 (2011)
Nanoscale research letters, 5(11), 1829-1835 (2010-12-03)
Highly crystalline TiO(2) nanostructures were prepared through a facile inorganic acid-assisted hydrothermal treatment of hexagonal-structured assemblies of nanocrystalline titiania templated by cetyltrimethylammonium bromide (Hex-ncTiO(2)/CTAB Nanoskeleton) as starting materials. All samples were characterized by X-ray diffraction (XRD) and transmission electron microscopy
Analytical biochemistry, 133(1), 116-119 (1983-08-01)
Hydroxamic acid siderophores were observed to be inactivated by exposure to titanium(III) chloride. To study the reaction, a series of eight model hydroxamic acids were prepared and reacted with titanium(III) chloride. The products were shown by ir and NMR comparisons
Xenobiotica; the fate of foreign compounds in biological systems, 15(6), 503-511 (1985-06-01)
The metabolic fate of chlormethiazole in healthy male subjects has been investigated following the oral administration of a single dose of chlormethiazole edisylate. Five urinary C-oxidation metabolites were identified and shown to be identical with previously reported metabolites. A novel
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