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687502

Sigma-Aldrich

Titanium(IV) isopropoxide

packaged for use in deposition systems

Synonyme(s) :

TTIP, Tetraisopropyl orthotitanate

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About This Item

Formule linéaire :
Ti[OCH(CH3)2]4
Numéro CAS:
546-68-9
Poids moléculaire :
284.22
Numéro Beilstein :
3679474
Numéro CE :
208-909-6
Numéro MDL:
MFCD00008871
Code UNSPSC :
12352107
ID de substance PubChem :
329761133
Nomenclature NACRES :
NA.23

Niveau de qualité

100

Pureté

99.999%

Forme

liquid

Pertinence de la réaction

core: titanium
reagent type: catalyst

Indice de réfraction

n20/D 1.464 (lit.)

Point d'ébullition

232 °C (lit.)

Pf

14-17 °C (lit.)

Densité

0.96 g/mL at 20 °C (lit.)

Chaîne SMILES 

CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C

InChI

1S/4C3H7O.Ti/c4*1-3(2)4;/h4*3H,1-2H3;/q4*-1;+4

Clé InChI

VXUYXOFXAQZZMF-UHFFFAOYSA-N

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Description générale

Atomic number of base material: 22 Titanium

Application

Precursors Packaged for Depositions Systems
Novel metal oxide/phosphonate hybrids were formed from titanium(IV) isopropoxide in a two-step sol-gel process. Starting material for barium-strontium-titanate thin films. Used to make porous titanosilicates, potential ion-exchange materials for cleanup of radioactive wastes. Applied in the formation of a heterosupermolecule consisting of a TiO2 nanocrystallite-viologen electron acceptor complex whose light-induced electron transfer has been demonstrated.

Pictogrammes

FlameExclamation mark
GHS02,GHS07

Mention d'avertissement

Warning

Mentions de danger

H226,H319,H336

Classification des risques

Eye Irrit. 2 - Flam. Liq. 3 - STOT SE 3

Organes cibles

Central nervous system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

105.8 °F - Pensky-Martens closed cup

Point d'éclair (°C)

41 °C - Pensky-Martens closed cup

Équipement de protection individuelle

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

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
SHBC6447V
MKBD2717V
00804DJ
11906HH

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Consulter la Bibliothèque de documents

Catalytic asymmetric aryl transfer reactions to aldehydes with Grignard reagents as the aryl source.
Yusuke Muramatsu et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 14(34), 10560-10563 (2008-10-31)
Manas K Panda et al.
Dalton transactions (Cambridge, England : 2003), 39(9), 2428-2440 (2010-02-18)
Controlled oxidation of organic sulfides to sulfoxides under ambient conditions has been achieved by a series of titanium isopropoxide complexes that use environmentally benign H(2)O(2) as a primary oxidant. Specifically, the [N,N'-bis(2-oxo-3-R(1)-5-R(2)-phenylmethyl)-N,N'-bis(methylene-R(3))-ethylenediamine]Ti(O(i)Pr)(2) [R(1) = t-Bu, R(2) = Me, R(3) =
Laszlo Sipos et al.
Biomacromolecules, 6(5), 2570-2582 (2005-09-13)
A poly(styrene-b-isobutylene-b-styrene) (SIBS) triblock polymer is employed as the polymer drug carrier for the TAXUS Express2 Paclitaxel-Eluting Coronary Stent system (Boston Scientific Corp.). It has been shown that the release of paclitaxel (PTx) from SIBS can be modulated by modification
Alfred J Wooten et al.
Organic letters, 9(3), 381-384 (2007-01-26)
[reaction: see text] We report the catalytic asymmetric allylation of ketones under highly concentrated reaction conditions with a catalyst generated from titanium tetraisopropoxide and BINOL (1:2 ratio) in the presence of isopropanol. This catalyst promotes the addition of tetraallylstannane to
Henrique Antonio Mendonça Faria et al.
Materials science & engineering. C, Materials for biological applications, 56, 260-268 (2015-08-08)
The structural and electronic properties of titanium oxide nanotubes (TiO2) have attracted considerable attention for the development of therapeutic devices and imaging probes for nanomedicine. However, the fluorescence response of TiO2 has typically been within ultraviolet spectrum. In this study
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