514381
Titanium(III) chloride
≥99.995% trace metals basis
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Synonym(s):
Titanium trichloride
Linear Formula:
TiCl3
CAS Number:
Molecular Weight:
154.23
EC Number:
MDL number:
UNSPSC Code:
26111700
PubChem Substance ID:
Recommended Products
Assay
≥99.995% trace metals basis
form
crystalline
reaction suitability
reagent type: catalyst
core: titanium
mp
440 °C (dec.) (lit.)
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
Used for the vapor-phase formation of intermetallic compounds with ultrafine particle size.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Pyr. Sol. 1 - Skin Corr. 1B
Supplementary Hazards
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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C Noubactep et al.
Journal of hazardous materials, 132(2-3), 202-212 (2005-11-08)
The effectiveness of elemental iron (Fe(0)) to remove uranium (U) from the aqueous phase has been demonstrated. While the mitigation effect is sure, discrepancies in the removal mechanism have been reported. The objective of this study was to investigate the
Catalytic oxidation of hydrazo derivatives promoted by a TiCl3/HBr system.
Eyal Drug et al.
Journal of the American Chemical Society, 129(45), 13784-13785 (2007-10-26)
C P Offen et al.
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
Investigation into the effectiveness of surface treatment on poly(methyl methacrylate) when exposed in the mouth.
M D Murray
The Journal of prosthetic dentistry, 59(3), 368-373 (1988-03-01)
Yan Zhang et al.
Organic & biomolecular chemistry, 9(13), 4977-4982 (2011-05-21)
N-N bond cleavage in hydrazines is widely used in the preparation of amines and thus occupies a significant place in organic synthesis. In this paper, we report a new method for the reductive cleavage of N-N bonds in hydrazines by
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