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Merck

697079

Titanium tetrachloride

packaged for use in deposition systems

Sinónimos:

Titanium(IV) chloride, TTC, Titanium tetrachloride

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Fórmula lineal:
TiCl4
Número CAS:
Peso molecular:
189.68
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352103
EC Number:
231-444-5
MDL number:
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InChI key

XJDNKRIXUMDJCW-UHFFFAOYSA-J

InChI

1S/4ClH.Ti/h4*1H;/q;;;;+4/p-4

SMILES string

Cl[Ti](Cl)(Cl)Cl

vapor pressure

50 mmHg ( 55 °C), 9.6 mmHg ( 20 °C)

assay

≥99.995% (trace metals analysis)

Quality Level

reaction suitability

core: titanium, reagent type: catalyst

bp

135-136 °C (lit.)

mp

−25 °C (lit.)

density

1.73 g/mL at 20 °C (lit.)

General description

Atomic number of base material: 22 Titanium

Application

Titanium tetrachloride may be used in the vapor synthesis of titania powder by oxidaition. It may be used as a catalyst in cross and asymmetric aldol reactions. Other possible uses of titanium tetrachloride is in the synthesis of :
  • γ,δ-unsaturated alcohols from allylsilanes and carbonyl compounds,
  • N-Phosphinoylimines and N-sulphonylimines from aromatic aldehydes,
  • Homoallyl ethers from allylsilanes and acetals.6

pictograms

Skull and crossbonesCorrosion

signalword

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

supp_hazards

Clase de almacenamiento

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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    Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product. 

  5. Can the empty deposition cylinders be refilled?

    Yes, we are able to refill these cylinders through our SAFC Hitech group.  Please contact our Technical Service department by email at techserv@sial.com, and they will forward you to the appropriate SAFC Hitech representative for a quote.

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M T Crimmins et al.
The Journal of organic chemistry, 66(3), 894-902 (2001-06-30)
Asymmetric aldol additions using chlorotitanium enolates of N-acyloxazolidinone, oxazolidinethione, and thiazolidinethione propionates proceed with high diastereoselectivity for the Evans or non-Evans syn product depending on the nature and amount of the base used. With 1 equiv of titanium tetrachloride and
The titanium tetrachloride induced synthesis of N-phosphinoylimines and N-sulphonylimines directly from aromatic aldehydes
Jennings WB and Lovely CJ
Tetrahedron, 47(29), 5561-5568 (1991)
New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride
Mukaiyama T, et al.
Journal of the American Chemical Society, 96(24), 7503-7509 null
Syntheses of γ,δ-unsaturated alcohols from allylsilanes and carbonyl compounds in the presence of titanium tetrachloride
Hosomi A and Sakurai H
Tetrahedron Letters, 17(16), 1295-1298 (1976)
Ravit Madar et al.
Brain, behavior, and immunity, 48, 301-312 (2015-05-30)
Neuroinflammation in the central nervous system is detrimental for learning and memory, as evident form epidemiological studies linking developmental defects and maternal exposure to harmful pathogens. Postnatal infections can also induce neuroinflammatory responses with long-term consequences. These inflammatory responses can

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