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160342

Sigma-Aldrich

2-Fluoroethanol

95%

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About This Item

Linear Formula:
FCH2CH2OH
CAS Number:
371-62-0
Molecular Weight:
64.06
Beilstein/REAXYS Number:
1730857
EC Number:
206-740-2
MDL number:
MFCD00002828
UNSPSC Code:
12352100
PubChem Substance ID:
24849864
NACRES:
NA.22
form:
liquid
assay:
95%

vapor pressure

16 mmHg ( 20 °C)

assay

95%

form

liquid

refractive index

n20/D 1.365 (lit.)

bp

103 °C/757 mmHg (lit.)

mp

−26.5 °C (lit.)

density

1.091 g/mL at 25 °C (lit.)

SMILES string

OCCF

InChI

1S/C2H5FO/c3-1-2-4/h4H,1-2H2

InChI key

GGDYAKVUZMZKRV-UHFFFAOYSA-N

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General description

The microwave spectra of two isotopic species of 2-fluoroethanol have been investigated.[1] The Gg′ conformer of 2-fluoroethanol was isolated in low-temperature noble gas matrices.[2] Single-photon IR photolysis of 2-fluoroethanol in solid argon has been investigated.[3]

accessory

Product No.
Description
Pricing

pictograms

FlameSkull and crossbones
GHS02,GHS06

signalword

Danger

hcodes

H226,H300

Hazard Classifications

Acute Tox. 1 Oral - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

93.2 °F - closed cup

flash_point_c

34 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKBH2444V
S38310V
STBB9169V
S38310
14308TI

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Kiel D Neumann et al.
Journal of labelled compounds & radiopharmaceuticals, 60(7), 337-342 (2017-04-14)
O-(2-Fluoroethyl)-O-(p-nitrophenyl) methylphosphonate 1 is an organophosphate cholinesterase inhibitor that creates a phosphonyl-serine covalent adduct at the enzyme active site blocking cholinesterase activity in vivo. The corresponding radiolabeled O-(2-[
Microwave Spectrum and Intramolecular Hydrogen Bonding in 2-Fluoroethanol.
Buckton KS and Azrak RG.
J. Chem. Phys. , 52(11), 5652-5655 (1970)
Site-selective infrared photoisomerizations of 2-fluoroethanol in low-temperature matrices
Pourcin J, et al.
Journal of Molecular Spectroscopy, 109(1) (1985)
Infrared laser photoisomerization of 2-fluoroethanol in argon.
Hoffman III WF and Shirk JS.
Chemical Physics, 78(3), 331-338 (1983)
T J Tewson et al.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 21(6), 559-564 (1980-06-01)
No-carrier-added [18F] fluoroethanol has been prepared by two routes. The first involves fluoride-ion displacement on alpha-p-toluene sulfonyl ethyl glycolate followed by reduction of the alpha-fluoroethyl acetate. The second involves a ring-opening reaction on glycol sulfite to give an alpha-fluorosulfinic acid
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