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N,O-Bis(trimethylsilyl)acetamide, 95%, Thermo Scientific Chemicals

$77.34 - $191.92

Chemical Identifiers

CAS 10416-59-8
Molecular Formula C8H21NOSi2
Molecular Weight (g/mol) 203.43
MDL Number MFCD00008270
InChI Key SIOVKLKJSOKLIF-UHFFFAOYSA-N
Synonym n,o-bis trimethylsilyl acetamide, trimethylsilyl 1z-n-trimethylsilylethanimidate
PubChem CID 6913588
SMILES CC(O[Si](C)(C)C)=N[Si](C)(C)C
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Products 2
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAL0018314
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Thermo Scientific Chemicals
L0018314
25 g
Each for $77.34
 
AAL0018322
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Thermo Scientific Chemicals
L0018322
100 g
Each for $191.92
 
Description

Description

N,O-Bis(trimethylsilyl)acetamide is used as a regioselective desulfation reagent as well as a preparatory agent for carbohydrate and alcohol trimethylsilyl ethers. It is also used for the derivatization of polar functional groups such as carboxylic acids, phenols, steroids, amines, alcohols, alkaloids and amides. It is employed in the formation of stable trimethylsilyl derivatives. Further, it is used in analytical chemistry for the derivatization of compounds in analysis to increase their volatility and to introduce the trimethylsilyl protecting group in organic synthesis. In addition to this, it is used in the protection of hydroxyl groups in natural products, functional groups in organic intermediates and derivatization reagent for gas chromatography-Mass spectral analysis of phenolic acids in fruits.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
N,O-Bis(trimethylsilyl)acetamide is used as a regioselective desulfation reagent as well as a preparatory agent for carbohydrate and alcohol trimethylsilyl ethers. It is also used for the derivatization of polar functional groups such as carboxylic acids, phenols, steroids, amines, alcohols, alkaloids and amides. It is employed in the formation of stable trimethylsilyl derivatives. Further, it is used in analytical chemistry for the derivatization of compounds in analysis to increase their volatility and to introduce the trimethylsilyl protecting group in organic synthesis. In addition to this, it is used in the protection of hydroxyl groups in natural products, functional groups in organic intermediates and derivatization reagent for gas chromatography-Mass spectral analysis of phenolic acids in fruits.

Solubility
Miscible with many nonpolar and polar aprotic solvents.

Notes
Air and moisture sensitive. Incompatible with strong oxidizing agents, water and acids.
Specifications

Chemical Identifiers

10416-59-8
203.43
SIOVKLKJSOKLIF-UHFFFAOYSA-N
6913588
C8H21NOSi2
MFCD00008270
n,o-bis trimethylsilyl acetamide, trimethylsilyl 1z-n-trimethylsilylethanimidate
CC(O[Si](C)(C)C)=N[Si](C)(C)C

Specifications

71°C to 73°C (35mmHg)
10416-59-8
C8H21NOSi2
UN2920
42°C (107°F)
Miscible with many nonpolar and polar aprotic solvents.
CC(O[Si](C)(C)C)=N[Si](C)(C)C
203.43
203.43
1.417
0.829
-24°C
25 g
MFCD00008270
1306669
n,o-bis trimethylsilyl acetamide, trimethylsilyl 1z-n-trimethylsilylethanimidate
SIOVKLKJSOKLIF-UHFFFAOYSA-N
trimethylsilyl N-(trimethylsilyl)ethanimidate
6913588
95%
Moisture sensitive
N,O-Bis(trimethylsilyl)acetamide
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Safety and Handling

Safety and Handling

GHS H Statement
H301-H314-H318-H226
Toxic if swallowed.
Causes severe skin burns and eye damage.
Causes serious eye damage.
Flammable liquid and vapor.

P210-P233-P235-P240-P241-P242-P243-P260-P264b-P270-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P370+P378q-P501c

H226-H302-H314-H335

DOTInformation : Transport Hazard Class: 8; Packing Group: II; Proper Shipping Name: CORROSIVE LIQUIDS, FLAMMABLE, N.O.S.

EINECSNumber : 233-892-7

RTECSNumber : AK3000000

TSCA : Yes

Recommended Storage : Keep cold

SDS
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RUO – Research Use Only