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Titanium ethoxide

Titanium ethoxide structure

Titanium ethoxide 

structure
  • CAS No:

    3087-36-3

  • Formula:

    C2H6O.1/4Ti

  • Chemical Name:

    Titanium ethoxide

  • Synonyms:

    Ethanol,titanium(4+) salt (4:1);Ethyl alcohol,titanium(4+) salt;Ethyl titanate(IV);Ethanol,titanium(4+) salt;Titanium ethoxide (Ti(OEt)4);Titanium,tetraethoxy-;Tetraethyl titanate;Tetraethoxytitanium;Titanium tetraethoxide;Ethyl titanate;Titanium ethoxide;Titanic acid ethyl ester;Tetraethyl orthotitanate;Tetraethyl titanate (Ti(OC2H5)4);Titanium(4+) ethoxide;Titanium tetrakis(ethoxide);Titanium tetraethanolate;Titanium(IV) ethoxide;Titanium ethylate;TEOT;Tyzor ET;Tetrakis(ethanolato)titanium;97583-04-5;104814-62-2;260561-26-0;334497-44-8;426266-86-6;753456-54-1;1391846-91-5;2042146-99-4;2146162-29-8;2242883-31-2

  • Categories:

    Cosmetic Ingredient  >  Binding Agent

Description

colourless liquid

Titanium ethoxide Basic Attributes

228.11

228.086304

221-410-8

DTXSID60627994

29051900

Characteristics

92.2

1.94880

Pale yellow Liquid

1.107 g/cm3

38 °C

122 °C @ Press: 1 Torr

84 °F

n20/D 1.505(lit.)

Solubility in water: reaction.;soluble in organic solvents.

2-8°C

Safety Information

III

4.1

UN 1993 3/PG 3

3

10-36/37/38-67

26-37/39-16

Xi

Stability Incompatible with strong oxidizing agents, strong acids. May decompose upon exposure to air or moisture.

P210-P305 + P351 + P338-P370 + P378

H226-H319-H336

Titanium ethoxide Use and Manufacturing

Methods of Manufacturing

Derived from the reaction of titanium tetrachloride and ethanol. Add benzene to a glass-lined reactor, cool to 20°C, add titanium tetrachloride, and the temperature should not exceed 50°C. When the temperature drops below 15°C, start to pass ammonia, and control it to pass under 50°C for about 2.5 hours. When the temperature drops to about 20°C and the pH is 9-10, slowly pass ammonia, add water and absolute ethanol, and the temperature rises to 45-50°C for about half an hour. Continue to pass ammonia for 1h until the pH stabilizes at 9-10. After stirring for 2 hours, let it stand for 24 hours, filter out the crystals, and rinse once with a small amount of benzene. The filtrate and the washing liquid are combined, and the benzene is recovered and distilled under reduced pressure to obtain the finished product.

Uses

Used in organic synthesis, transesterification, to enhance the adhesion of rubber and plastic on metal surfaces

Computed Properties

Molecular Weight:93.94
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Exact Mass:93.9898055
Monoisotopic Mass:93.9898055
Topological Polar Surface Area:20.2
Heavy Atom Count:4
Complexity:2.8
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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