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TETRAETHYLAMMONIUM BICARBONATE

TETRAETHYLAMMONIUM BICARBONATE Structure
  • ₹18878.8
  • Product name: TETRAETHYLAMMONIUM BICARBONATE
  • CAS: 17351-61-0
  • MF: C9H21NO3
  • MW: 191.27
  • EINECS:
  • MDL Number:MFCD08277046
  • Synonyms:Tetraethylammonium bicarbonate purum, >=95.0% (T);Tetraethylammonium bicarbonate >=95.0% (T);Ethanaminium, N,N,N-triethyl-, carbonate (1:1)
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Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 25G
  • ManufacturerSigma-Aldrich(India)
  • Product number11268
  • Product descriptionTetraethylammonium bicarbonate ≥95.0% (T)
  • Packaging25G
  • Price₹18878.8
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) 11268 Tetraethylammonium bicarbonate ≥95.0% (T) 25G ₹18878.8 2022-06-14 Buy

Properties

storage temp. :Inert atmosphere,Room Temperature

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H315 Causes skin irritation Skin corrosion/irritation Category 2 Warning GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 Causes serious eye irritation Serious eye damage/eye irritation Category 2A Warning GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 May cause respiratory irritation Specific target organ toxicity, single exposure;Respiratory tract irritation Category 3 Warning GHS hazard pictograms
Precautionary statements:
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P264 Wash hands thoroughly after handling.
P264 Wash skin thouroughly after handling.
P271 Use only outdoors or in a well-ventilated area.
P280 Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352 IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Description

Tetraethylammonium bicarbonate is used:
  • In the synthesis of carbamate esters from amines.
  • As a precipitant for synthesizing Cu/ZnO catalysts via coprecipitation method.
  • As an alternative to the traditional phase-transfer system in [18F]radiofluorinations for preventing microreactor blockages.
  • To promote carboxylation of secondary carboxamides bearing a leaving group at the α-position in the synthesis of oxazolidine-2,4-diones.


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