Skip to Content
MilliporeSigma
All Photos(2)

Documents

429058

Sigma-Aldrich

2-Fluoroethylamine hydrochloride

technical grade, 90%

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
FCH2CH2NH2 · HCl
CAS Number:
460-08-2
Molecular Weight:
99.54
EC Number:
207-302-3
MDL number:
MFCD00008161
UNSPSC Code:
12352100
PubChem Substance ID:
24866832
NACRES:
NA.22

grade

technical grade

Quality Level

100

Assay

90%

form

solid

mp

99-103 °C (lit.)

SMILES string

Cl.NCCF

InChI

1S/C2H6FN.ClH/c3-1-2-4;/h1-2,4H2;1H

InChI key

YRRZGBOZBIVMJT-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

2-Fluoroethylamine hydrochloride is a fluorinated alkylammonium salt. Studies suggest that adding a fluorine atom to it leads to double gauche effect in the resulting 2,2-difluoroethylamine chloride. Microwave spectral studies for 2-fluoroethylamine has been conducted.

Application

2-Fluoroethylamine hydrochloride may be used in the synthesis of the following:
  • 2-fluoroethylisocyanate
  • 1,3-bis-(2-fluoroethyl) urea (BFU)
  • N-2-fluoroethylmaleimide
  • [Cu4(O)(Ln)2(CH3COO)4] where HL= 4-methyl-2,6-bis(2-fluoroethyliminomethyl) phenol
  • 1-O-(4-(2-fluoroethyl-carbamoyloxymethyl)-2-nitrophenyl)-O-β-D-glucopyronuronate (FEAnGA)

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

4-Fluorobenzylamine 97%

Sigma-Aldrich

162493

4-Fluorobenzylamine

2-Bromoethylamine hydrobromide 99%

Sigma-Aldrich

B65705

2-Bromoethylamine hydrobromide

Development of a new thiol site-specific prosthetic group and its conjugation with [Cys40]-exendin-4 for in vivo targeting of insulinomas.
Yue X, et al.
Bioconjugate Chemistry, 24(7), 1191-1200 (2013)
Conformational analysis of 2, 2-difluoroethylamine hydrochloride: double gauche effect.
Silla JM, et al.
Beilstein Journal of Organic Chemistry, 10(1), 877-882 (2014)
Tetranuclear copper (II)-Schiff-base complexes as active catalysts for oxidation of cyclohexane and toluene.
Roy P and Manassero M.
Dalton Transactions, 39(6), 1539-1545 (2010)
Microwave-spectrum, conformational equilibrium, intramolecular hydrogen-bonding, dipole-moments, N-14 nuclear-quadrupole coupling-constants and centrifugal-distortion constants of 2-fluoroethylamine.
Marstokk KM and Mollendal H.
Acta Chemica Scandinavica, 34(1), 15-29 (1980)
Synthesis of 18F-labelled 2-fluoroethyl-nitrosoureas.
Farrokhzad S, et al.
Canadian Journal of Chemistry, 62(11), 2107-2112 (1984)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service