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About This Item
Linear Formula:
Ti(OC2H5)4
CAS Number:
Molecular Weight:
228.11
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12161600
MDL number:
Beilstein/REAXYS Number:
3678992
Product Name
Titanium(IV) ethoxide,
form
liquid
reaction suitability
core: titanium, reagent type: catalyst
impurities
≤3% tetraisopropyl orthotitanate (NMR)
refractive index
n20/D 1.505 (lit.), n20/D 1.509
bp
150-152 °C/10 mmHg (lit.)
density
1.088 g/mL at 25 °C (lit.)
SMILES string
CCO[Ti](OCC)(OCC)OCC
InChI
1S/4C2H5O.Ti/c4*1-2-3;/h4*2H2,1H3;/q4*-1;+4
InChI key
JMXKSZRRTHPKDL-UHFFFAOYSA-N
Application
Titanium(IV) ethoxide can be used:
- As an activator and dehydrating agent for by condensation of (S)-(+)-p-toluenesulfinamide with aldehydes and ketones to form sulfinimines.
- As a Ti4+ ion source to form complexes of titanium (IV) acrylate with methacrylic acid.
- As a catalyst to synthesize esters of sterically hindered alcohols via transesterification reactions.
Disclaimer
During storage a gelatinous residue may form, which dissolves after heating up to 40 °C
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
107.6 °F - closed cup
flash_point_c
42 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Two-photon polymerization of metal ions doped acrylate monomers and oligomers for three-dimensional structure fabrication
Duan, Xuan-Ming and Sun, Hong-Bo and Kaneko, Koshiro and Kawata, Satoshi
Thin Solid Films, 453(4), 518-521 (2004)
Synthesis of sterically hindered esters via titanium catalyzed transesterification
Krasik, Pavel
Tetrahedron Letters, 39(24), 4223-4226 (1998)
Improved synthesis of enantiopure sulfinimines (thiooxime s-oxides) from p-toluenesulfinamide and aldehydes and ketones
Davis FA, et al.
The Journal of Organic Chemistry, 64(4), 1403-1406 (1999)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 86710-50ML | 04061833041697 |