2,2,2-Trifluoroethylamine hydrochloride, 98%, Thermo Scientific Chemicals
2,2,2-Trifluoroethylamine hydrochloride, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2,2,2-Trifluoroethylamine hydrochloride, 98%, Thermo Scientific Chemicals

Quantity:
100 g
10 g
50 g
Catalog number A14904.22
also known as A14904-22
Price (JPY)/ Each
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Quantity:
100 g
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Chemical Identifiers
CAS373-88-6
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to yellow
Assay (Titration ex Chloride)≥97.5 to ≤102.5%
Assay (Freebase GC)≥97.5%
Identification (FTIR)Conforms
Water Content (Karl Fischer Titration)≤1%
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2,2,2-Trifluoroethylamine hydrochloride, is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuff

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
2,2,2-Trifluoroethylamine hydrochloride, is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuff

Solubility
It is Soluble in 0.7 to water, but soluble in ethanol and chloroform, slightly soluble in benzene, hardly soluble in ether.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Hygroscopic. Keep away from strong oxidizing agents, acids, acid chlorides, acid anhydrides.
RUO – Research Use Only

General References:

  1. Quincy LaRon Ford .; Justina Marie Burns. Aqueous in situ derivatization of carboxylic acids by an ionic carbodiimide and 2,2,2-trifluoroethylamine for electron-capture detection. Journal of Chromatography A. 2007, 1145, (2), 241-245.·
  2. Sonyuan Lin .; Atmaram D. Khanolkar .; Pusheng Fan .; Andreas Goutopoulos .; Ce Qin .; Demetris Papahadjis .; and Alexandros Makriyannis. Novel Analogues of Arachidonylethanolamide (Anandamide): Affinities for the CB1 and CB2 Cannabinoid Receptors and Metabolic Stability. J. Med. Chem. 1998, 41, (27), 5353-5361.