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BGC > Product Search > Triethylsilane | 617-86-7
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Suppliers for

Triethylsilane



Properties

CAS   617-86-7 
Formula   C6H16Si 
EINECS   210-535-3 

Structure

28 Registered suppliers


Molecular Formula: C6H16Si
Molecular Weight: 116.28
Hazard Symbols: F,Xi
UN Number: UN 1993 3/PG 2
WGKGermany: 1
PackingGroup: II
HS Code: 29310095

More details are to be found here
Molecular Formula: C6H16Si
Molecular Weight: 116.28
Hazard Symbols: F,Xi
UN Number: UN 1993 3/PG 2
WGKGermany: 1
PackingGroup: II
HS Code: 29310095

More details are to be found here
Molecular Formula: C6H16Si
Molecular Weight: 116.28
Hazard Symbols: F,Xi
UN Number: UN 1993 3/PG 2
WGKGermany: 1
PackingGroup: II
HS Code: 29310095

More details are to be found here
Molecular Formula: C6H16Si
Molecular Weight: 116.28
Hazard Symbols: F,Xi
UN Number: UN 1993 3/PG 2
WGKGermany: 1
PackingGroup: II
HS Code: 29310095

More details are to be found here
Molecular Formula: C6H16Si
Molecular Weight: 116.28
Hazard Symbols: F,Xi
UN Number: UN 1993 3/PG 2
WGKGermany: 1
PackingGroup: II
HS Code: 29310095

More details are to be found here
Molecular Formula: C6H16Si
Molecular Weight: 116.28
Hazard Symbols: F,Xi
UN Number: UN 1993 3/PG 2
WGKGermany: 1
PackingGroup: II
HS Code: 29310095

More details are to be found here
Molecular Formula: C6H16Si
Molecular Weight: 116.28
Hazard Symbols: F,Xi
UN Number: UN 1993 3/PG 2
WGKGermany: 1
PackingGroup: II
HS Code: 29310095

More details are to be found here
Molecular Formula: C6H16Si
Molecular Weight: 116.28
Hazard Symbols: F,Xi
UN Number: UN 1993 3/PG 2
WGKGermany: 1
PackingGroup: II
HS Code: 29310095

More details are to be found here
Molecular Formula: C6H16Si
Molecular Weight: 116.28
Hazard Symbols: F,Xi
UN Number: UN 1993 3/PG 2
WGKGermany: 1
PackingGroup: II
HS Code: 29310095

More details are to be found here
Molecular Formula: C6H16Si
Molecular Weight: 116.28
Hazard Symbols: F,Xi
UN Number: UN 1993 3/PG 2
WGKGermany: 1
PackingGroup: II
HS Code: 29310095

More details are to be found here
Molecular Formula: C6H16Si
Molecular Weight: 116.28
Hazard Symbols: F,Xi
UN Number: UN 1993 3/PG 2
WGKGermany: 1
PackingGroup: II
HS Code: 29310095

More details are to be found here
Molecular Formula: C6H16Si
Molecular Weight: 116.28
Hazard Symbols: F,Xi
UN Number: UN 1993 3/PG 2
WGKGermany: 1
PackingGroup: II
HS Code: 29310095

More details are to be found here
Molecular Formula: C6H16Si
Molecular Weight: 116.28
Hazard Symbols: F,Xi
UN Number: UN 1993 3/PG 2
WGKGermany: 1
PackingGroup: II
HS Code: 29310095

More details are to be found here
Product Name: Triethylsilane
Synonyms: SILANE E3H;SILICONTRIETHYL;TRIETHYLSILANE;Triethylsilyl hydride;(C2H5)3SiH;CT2523;triethyl-silan;Triethylsilicon hydride
CAS: 617-86-7
MF: C6H16Si
MW: 116.28
EINECS: 210-535-3
mp -157°C
bp 107-108 °C(lit.)
density 0.728 g/mL at 25 °C(lit.)
refractive index n20/D 1.412(lit.)
Fp 25 °F
storage temp. 2-8°C
Sensitive Moisture Sensitive
BRN 1098278
Stability: Stable, but moisture sensitive. Highly flammable. Generates highly flammable gas (hydrogen) in contact with water, acids and bases.

Chemical Properties:
Colorless transparent liquid

Usage:
For organic synthesis and pharmaceutical intermediates
Under the action of alkaline water, the Si-H bond breaks in the molecule, releasing hydrogen gas to form triethylsilanol. Is reacted with an alkyl lithium, and the hydrogen atom in the Si-H bond is substituted with an alkyl group. With lithium alkoxide reaction, generating triethylalkoxysilane. Aluminum chloride in the presence of, and hydrogen chloride reaction, generating triethyl chlorosilane. In the role of platinum catalyst, with the addition of olefin reaction. Triethyl chlorosilane can be used lithium hydride or lithium aluminum tetrahydride reduction to the system. Used to synthesize


Product Name: Triethylsilane
Synonyms: SILANE E3H;SILICONTRIETHYL;TRIETHYLSILANE;Triethylsilyl hydride;(C2H5)3SiH;CT2523;triethyl-silan;Triethylsilicon hydride
CAS: 617-86-7
MF: C6H16Si
MW: 116.28
EINECS: 210-535-3
mp -157°C
bp 107-108 °C(lit.)
density 0.728 g/mL at 25 °C(lit.)
refractive index n20/D 1.412(lit.)
Fp 25 °F
storage temp. 2-8°C
Sensitive Moisture Sensitive
BRN 1098278
Stability: Stable, but moisture sensitive. Highly flammable. Generates highly flammable gas (hydrogen) in contact with water, acids and bases.

Chemical Properties:
Colorless transparent liquid

Usage:
For organic synthesis and pharmaceutical intermediates
Under the action of alkaline water, the Si-H bond breaks in the molecule, releasing hydrogen gas to form triethylsilanol. Is reacted with an alkyl lithium, and the hydrogen atom in the Si-H bond is substituted with an alkyl group. With lithium alkoxide reaction, generating triethylalkoxysilane. Aluminum chloride in the presence of, and hydrogen chloride reaction, generating triethyl chlorosilane. In the role of platinum catalyst, with the addition of olefin reaction. Triethyl chlorosilane can be used lithium hydride or lithium aluminum tetrahydride reduction to the system. Used to synthesize


Product Name: Triethylsilane
Synonyms: SILANE E3H;SILICONTRIETHYL;TRIETHYLSILANE;Triethylsilyl hydride;(C2H5)3SiH;CT2523;triethyl-silan;Triethylsilicon hydride
CAS: 617-86-7
MF: C6H16Si
MW: 116.28
EINECS: 210-535-3
mp -157°C
bp 107-108 °C(lit.)
density 0.728 g/mL at 25 °C(lit.)
refractive index n20/D 1.412(lit.)
Fp 25 °F
storage temp. 2-8°C
Sensitive Moisture Sensitive
BRN 1098278
Stability: Stable, but moisture sensitive. Highly flammable. Generates highly flammable gas (hydrogen) in contact with water, acids and bases.

Chemical Properties:
Colorless transparent liquid

Usage:
For organic synthesis and pharmaceutical intermediates
Under the action of alkaline water, the Si-H bond breaks in the molecule, releasing hydrogen gas to form triethylsilanol. Is reacted with an alkyl lithium, and the hydrogen atom in the Si-H bond is substituted with an alkyl group. With lithium alkoxide reaction, generating triethylalkoxysilane. Aluminum chloride in the presence of, and hydrogen chloride reaction, generating triethyl chlorosilane. In the role of platinum catalyst, with the addition of olefin reaction. Triethyl chlorosilane can be used lithium hydride or lithium aluminum tetrahydride reduction to the system. Used to synthesize


Product Name: Triethylsilane
Synonyms: SILANE E3H;SILICONTRIETHYL;TRIETHYLSILANE;Triethylsilyl hydride;(C2H5)3SiH;CT2523;triethyl-silan;Triethylsilicon hydride
CAS: 617-86-7
MF: C6H16Si
MW: 116.28
EINECS: 210-535-3
mp -157°C
bp 107-108 °C(lit.)
density 0.728 g/mL at 25 °C(lit.)
refractive index n20/D 1.412(lit.)
Fp 25 °F
storage temp. 2-8°C
Sensitive Moisture Sensitive
BRN 1098278
Stability: Stable, but moisture sensitive. Highly flammable. Generates highly flammable gas (hydrogen) in contact with water, acids and bases.

Chemical Properties:
Colorless transparent liquid

Usage:
For organic synthesis and pharmaceutical intermediates
Under the action of alkaline water, the Si-H bond breaks in the molecule, releasing hydrogen gas to form triethylsilanol. Is reacted with an alkyl lithium, and the hydrogen atom in the Si-H bond is substituted with an alkyl group. With lithium alkoxide reaction, generating triethylalkoxysilane. Aluminum chloride in the presence of, and hydrogen chloride reaction, generating triethyl chlorosilane. In the role of platinum catalyst, with the addition of olefin reaction. Triethyl chlorosilane can be used lithium hydride or lithium aluminum tetrahydride reduction to the system. Used to synthesize


Product Name: Triethylsilane
Synonyms: SILANE E3H;SILICONTRIETHYL;TRIETHYLSILANE;Triethylsilyl hydride;(C2H5)3SiH;CT2523;triethyl-silan;Triethylsilicon hydride
CAS: 617-86-7
MF: C6H16Si
MW: 116.28
EINECS: 210-535-3
mp -157°C
bp 107-108 °C(lit.)
density 0.728 g/mL at 25 °C(lit.)
refractive index n20/D 1.412(lit.)
Fp 25 °F
storage temp. 2-8°C
Sensitive Moisture Sensitive
BRN 1098278
Stability: Stable, but moisture sensitive. Highly flammable. Generates highly flammable gas (hydrogen) in contact with water, acids and bases.

Chemical Properties:
Colorless transparent liquid

Usage:
For organic synthesis and pharmaceutical intermediates
Under the action of alkaline water, the Si-H bond breaks in the molecule, releasing hydrogen gas to form triethylsilanol. Is reacted with an alkyl lithium, and the hydrogen atom in the Si-H bond is substituted with an alkyl group. With lithium alkoxide reaction, generating triethylalkoxysilane. Aluminum chloride in the presence of, and hydrogen chloride reaction, generating triethyl chlorosilane. In the role of platinum catalyst, with the addition of olefin reaction. Triethyl chlorosilane can be used lithium hydride or lithium aluminum tetrahydride reduction to the system. Used to synthesize


Product Name: Triethylsilane
Synonyms: SILANE E3H;SILICONTRIETHYL;TRIETHYLSILANE;Triethylsilyl hydride;(C2H5)3SiH;CT2523;triethyl-silan;Triethylsilicon hydride
CAS: 617-86-7
MF: C6H16Si
MW: 116.28
EINECS: 210-535-3
mp -157°C
bp 107-108 °C(lit.)
density 0.728 g/mL at 25 °C(lit.)
refractive index n20/D 1.412(lit.)
Fp 25 °F
storage temp. 2-8°C
Sensitive Moisture Sensitive
BRN 1098278
Stability: Stable, but moisture sensitive. Highly flammable. Generates highly flammable gas (hydrogen) in contact with water, acids and bases.

Chemical Properties:
Colorless transparent liquid

Usage:
For organic synthesis and pharmaceutical intermediates
Under the action of alkaline water, the Si-H bond breaks in the molecule, releasing hydrogen gas to form triethylsilanol. Is reacted with an alkyl lithium, and the hydrogen atom in the Si-H bond is substituted with an alkyl group. With lithium alkoxide reaction, generating triethylalkoxysilane. Aluminum chloride in the presence of, and hydrogen chloride reaction, generating triethyl chlorosilane. In the role of platinum catalyst, with the addition of olefin reaction. Triethyl chlorosilane can be used lithium hydride or lithium aluminum tetrahydride reduction to the system. Used to synthesize



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