- Triethylamine is the
chemical compound with the formula N(CH2CH3)3, commonly abbreviated
Et3N.
- It is a
commonly encountered in organic synthesis probably because it is the
simplest symmetrically trisubstituted amine, i.e. a tertiary amine, that
is liquid at room temperature.
- Triethylamine is
commonly employed in organic synthesis as a base, most often in the
preparation of esters and amides from acyl chlorides.
- Such reactions lead
to the production of hydrogen chloride which combines with triethylamine
to form the salt triethylamine hydrochloride,
commonly called tri
ethyl ammonium chloride.
- Nitrogen compounds
such as triethylamine are odorants generally found in chemical plants
and foundries
in which cold-box cores are made.
- Either triethylamine
or di ethy lenetriamine can be conveniently used as a dynamic modifier
to suppress the adsorption of basic proteins in capillary
zone
electrophoresis.
-
Two methods are described for the
simultaneous determination of Atorvastatin calcium and Ezetimibe in
binary mixture.
-
The first method was based on
UV-spectrophotometric determination of two drugs, using simultaneous
equation method.
-
The second method was based on HPLC
separation of the two drugs in reverse phase mode using Luna C18
column.
-
The application of
triethylamine to guayule plants results in a 2-fold stimulation of
rubber synthesis and a 1.5- to 3-fold increase in mevalonic acid kinase,
isopentenyl pyrophosphate isomerase, and rubber
transferase.
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Introduction
Process
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Effects of Operational Conditions on
the Performance of Triethylamine Bio filtration.
-
Simplified HPLC/UV detection method
for measuring serum retinol
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Pd–H from Pd/C and triethylamine
Implications in palladium catalysed reactions involving amines
-
The Kinetics of the
Triethylamine-catalyzed Reaction of Diisocyanates with 1-Butanol in
Toluene
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Liquid source metalorganic chemical
vapor deposition of aluminum from triethylamine alane
-
Structural Analysis of Murine Zona
Pellucida Glycans
-
Synthesis of sulfate esters of
lithocholic acid, glycol it hocholic acid, and tau rol it hocholic acid
with suIfur trioxide-triethylamine
-
Hydraulics and Biofiltration of
Triethylamine
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Direct Synthesis of Weinreb Amides
from Carboxylic Acids Using Triphosgene
MSDS & Product
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Triethylamine acetate
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Triethylamine
-
Triethylamine
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Triethylamine Msds
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Safety data for triethylamine
-
Triethylamine
-
Triethylamine Product Details
-
Triethylamine
Consultants
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-
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-
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-
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Triethylamine Expert
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Application
-
Triethylamine or diethylenetriamine as
dynamic modifier for suppressing basic protein adsorption in capillary
electrophoresis
-
Effect of
2-(3,4-Dichlorophenoxy)-triethylamine on the Synthensis of
cis-Polyisoprene in Guayule Plants
-
Regio- and stereo-selective
cyclizations. Application to natural products synthesis
-
Synthesis and application in
asymmetric C–C bond formation of solution phase ligand libraries of
monodentate phosphoramidites
Application of UV-Spectrophotometry
and RP-HPLC for Simultaneous Determination of Atorvastatin Calcium and
Ezetimibe in Pharmaceutical Dosage Form
Technology
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Transfer and Extraction
Techniques
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Theoretical Study on the Isomerization
Mechanism of Enol Ester
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Hydrolysis and Partial Recycling of a
Chloroaluminate Ionic Liquid
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Study on Synthesis of 2-Imino-1,
2-dihydropyridine-1-acetic Acid
Patent
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Triethylamine Catalyzed Neopentyl
Glycol Production utilizing a gas sparged reactor
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Extraction of Triethylamine in
Polycarbonate by the use of static mixtures
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Hypergolic fuel Formulations
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Method for Producing
Ethyldimethylamine & Triethylamine
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Oxidation of Thiols employing Cobalt
Molybdate/Triethylamine catalyst
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Process For the Preparation of
Triethylamine
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