Triethylamine - Wikipedia
WEBTriethylamine is mainly used in the production of quaternary ammonium compounds for textile auxiliaries and quaternary ammonium salts of dyes. It is also a catalyst and acid neutralizer for condensation reactions and is useful as an intermediate for manufacturing medicines, pesticides and other chemicals.
Triethylamine | (C2H5)3N | CID 8471 - PubChem
WEBTriethylamine | (C2H5)3N or C6H15N | CID 8471 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
Triethylamine = 99.5 121-44-8 - MilliporeSigma
WEBTriethylamine (TEA, Et 3 N) is an aliphatic amine. Its addition to matrix-assisted laser desorption/ionization (MALDI) matrices affords transparent liquid matrices with enhanced ability for spatial resolution during MALDI mass spectrometric (MS) imaging.
Triethylamine = 99 121-44-8 - MilliporeSigma
WEBSigma-Aldrich offers Sigma-Aldrich-T0886, Triethylamine for your research needs. Find product specific information including uses,density, molecular weight, CAS, MSDS, protocols and references.
TRIETHYLAMINE | CAMEO Chemicals | NOAA
WEBTRIETHYLAMINE reacts violently with oxidizing agents. Reacts with Al and Zn. Neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols …
Triethylamine - NIST Chemistry WebBook
WEBFormula: C 6 H 15 N. Molecular weight: 101.1900. IUPAC Standard InChI: InChI=1S/C6H15N/c1-4-7 (5-2)6-3/h4-6H2,1-3H3. Copy Sheet of paper on top of another sheet. IUPAC Standard InChIKey: ZMANZCXQSJIPKH-UHFFFAOYSA-N. Copy Sheet of paper on top of another sheet.
Triethylamine - NIST Chemistry WebBook
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Triethylamine: Properties, Production and Uses - chemcess.com
WEBTriethylamine: Properties, Production and Uses. Triethylamine (TEA) is tertiary amine, represented by the chemical formula N (CH2CH3)3. It is a colorless easily flammable liquid with an ammonia-like odor. It is one of the most widely used organic amine base in synthetic organic chemistry.
Triethylamine - NIST Chemistry WebBook
WEBQuantity Value Units Method Reference Comment; Δ f H° gas-134.1: kJ/mol: N/A: Baroody and Carpenter, 1972: Value computed using Δ f H liquid ° value of -169 kj/mol from Baroody and Carpenter, 1972 and Δ vap H° value of 34.94±0.06 kj/mol from missing citation.: Δ f H° gas-92.9 ± 0.5: kJ/mol: N/A: Lebedeva, 1966
Triethylamine - an overview | ScienceDirect Topics
WEB9.2.2.4 Binary Biphasic Systems Containing Triethylamine. Triethylamine is a weak cohesive and dipolar/polarizable solvent, moderately hydrogen-bond basic and non-hydrogen-bond acidic. The triethylamine-dimethyl sulfoxide biphasic system has similar selectivity to the isopentyl ether-propylene carbonate biphasic system, the triethylamine ...
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