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Triethoxysilane

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Triethoxysilane Basic information

Product Name:
Triethoxysilane
Synonyms:
  • CT2500
  • triethoxy-silan
  • Triethoxysilane ((C2H5O)3SiH)
  • Triethoxysilicane
  • TRIETHOXYSILANE
  • Triethoxysilane,96%
  • Triethoxysilaneelectronicgradeavailable
  • Silane, triethoxy-
CAS:
998-30-1
MF:
C6H16O3Si
MW:
164.27
EINECS:
213-650-7
Product Categories:
  • OthersSilsesquioxanes: POSS? Nanohybrids
  • RSi(OR)3Organometallic Reagents
  • Alkoxy Silanes
  • Organometallic Reagents
  • Organosilicon
  • POSS? Precursors and Intermediates
  • Si (Classes of Silicon Compounds)
  • Si-H Compounds
  • Si-O Compounds
  • Trialkoxysilanes
  • Hydrogensilanes Hydrogensiloxanes
  • Reducing Agents
Mol File:
998-30-1.mol
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Triethoxysilane Chemical Properties

Melting point:
-170°C
Boiling point:
134-135 °C(lit.)
Density 
0.89 g/mL at 25 °C(lit.)
vapor pressure 
9.21hPa at 20℃
refractive index 
n20/D 1.377(lit.)
Flash point:
80 °F
storage temp. 
Store at 0-5°C
solubility 
sol diethyl ether, THF, alkanes, aromatic and chlorinated solvents.
form 
A liquid
Specific Gravity
0.8753
Water Solubility 
Insoluble in water. Soluble in organic solvents.
Hydrolytic Sensitivity
7: reacts slowly with moisture/water
Sensitive 
Moisture Sensitive
BRN 
1738989
Stability:
Stable, but moisture sensitive. Flammable. Incompatible with strong oxidizing agents, strong acids, strong bases.
InChIKey
QQQSFSZALRVCSZ-UHFFFAOYSA-N
CAS DataBase Reference
998-30-1(CAS DataBase Reference)
NIST Chemistry Reference
Silane, triethoxy-(998-30-1)
EPA Substance Registry System
Triethoxysilane (998-30-1)
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Safety Information

Hazard Codes 
T+,C,T
Risk Statements 
10-26-34-23/24/25
Safety Statements 
26-28-36/37/39-45
RIDADR 
UN 3384 6.1/PG 1
WGK Germany 
3
RTECS 
VV6682000
10-21
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
II
HS Code 
29209090
Hazardous Substances Data
998-30-1(Hazardous Substances Data)

MSDS

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Triethoxysilane Usage And Synthesis

Description

Triethoxysilane is an organosilicon compound with the formula HSi(OC2H5)3. It is a colourless liquid used in precious metal-catalysed hydrosilylation reactions. The resulting triethoxysilyl groups are often valued for attachment to silica surfaces.Compared to most compounds with Si-H bonds, triethoxysilane exhibits relatively low reactivity. Like most silyl ethers, triethoxysilane is susceptible to hydrolysis. As reducing agent, triethoxysilane can for example be used in reduction of amides, reduction of carbonyl compounds in the presence of cobalt(II) chloride as catalyst, Cu-catalyzed reductive hydroxymethylation of styrenes, and Rh-catalyzed hydrodediazoniation.

Chemical Properties

Colorless, clear liquid

Physical properties

bp 134–135 °C; d 0.89 g cm?3.

Uses

Triethoxysilane is useful reagent for the hydrosilylation of carbon–carbon multiple bonds; reducing agent for carbonyl groups

Uses

Triethoxysilane is used in metal catalyzed hydrosilylation reactions.

Application

Reduces esters in the presence of zinc hydride catalyst. Reduces aldehydes and ketones to alcohols via the silyl ethers in presence of fluoride ion. Gives 1,2-reduction of enones to allyl alcohols.

General Description

Liquid. Used as a reducing agent.

Air & Water Reactions

May become pyrophoric, by generation of silane

Reactivity Profile

Triethoxysilane has been involved in cases where Triethoxysilane has disproportionated, generating silane (SiH4) which has a history of being pyrophoric.

Health Hazard

Toxicity is similar to silanes. Silanes are moderately irritating to skin, eyes, and mucous membranes. Silane compounds are toxic.

Fire Hazard

When heated to decomposition, Triethoxysilane emits acrid smoke and fumes.

Flammability and Explosibility

Highly flammable

Safety Profile

Poison by intravenous route.Moderately toxic by inhalation. Flammable liquid. Whenheated to decomposition it emits acrid smoke andirritating fumes.

Purification Methods

Fractionate it using a column packed with glass helices of ca 15 theoretical plates in an inert atmosphere. Store it in aliquots in sealed ampoules because it is sensitive to moisture. [Spauschus et al. J Am Chem Soc 72 1377 1950, MacKenzie et al. J Am Chem Soc 72 2032 1950, Havill et al. J Org Chem 13 280 1948, Beilstein 1 IV 1359.]

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