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Key Documents

514381

Sigma-Aldrich

Titanium(III) chloride

≥99.995% trace metals basis

Sinonimo/i:

Titanium trichloride

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About This Item

Formula condensata:
TiCl3
Numero CAS:
Peso molecolare:
154.23
Numero CE:
Numero MDL:
Codice UNSPSC:
26111700
ID PubChem:

Saggio

≥99.995% trace metals basis

Forma fisica

crystalline

Impiego in reazioni chimiche

reagent type: catalyst
core: titanium

Punto di fusione

440 °C (dec.) (lit.)

Stringa SMILE

Cl[Ti](Cl)Cl

InChI

1S/3ClH.Ti/h3*1H;/q;;;+3/p-3
YONPGGFAJWQGJC-UHFFFAOYSA-K

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Applicazioni

Used for the vapor-phase formation of intermetallic compounds with ultrafine particle size.

Pittogrammi

FlameCorrosion

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Pyr. Sol. 1 - Skin Corr. 1B

Rischi supp

Codice della classe di stoccaggio

4.2 - Pyrophoric and self-heating hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Gnana S Siluvai et al.
Biochemistry, 48(51), 12133-12144 (2009-11-20)
Sco-like proteins contain copper bound by two cysteines and a histidine residue. Although their function is still incompletely understood, there is a clear involvement with the assembly of cytochrome oxidases that contain the Cu(A) center in subunit 2, possibly mediating
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)
D J Kushner et al.
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
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
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

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