2,2,2-Trifluoroethanol

for NMR spectroscopy,≥99.9%(GC)

Reagent Code: #241284
label
Alias 2,2,2-TFEA; Trifluoroethanol
fingerprint
CAS Number 75-89-8

science Other reagents with same CAS 75-89-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 100.04 g/mol
Formula C₂H₃F₃O
badge Registry Numbers
EC Number 200-913-6
MDL Number MFCD00004672
thermostat Physical Properties
Melting Point -44 °C(lit.)
Boiling Point 77-80 °C(lit.)
inventory_2 Storage & Handling
Density 1.391 g/mL at 20 °C
Storage Room temperature

description Product Description

Used as a solvent in organic synthesis, particularly in peptide coupling and polymer chemistry due to its ability to dissolve a wide range of organic and inorganic compounds. Enhances reaction rates in esterifications and acylations because of its strong hydrogen-bond donor properties. Employed in pharmaceutical manufacturing as a building block for fluorinated compounds, which often exhibit improved metabolic stability and bioavailability. Commonly used in NMR spectroscopy as a solvent for analyzing polar compounds. Also finds use in the formulation of liquid chromatography mobile phases for separating fluorinated molecules.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿340.00
inventory 5g
10-20 days ฿850.00
inventory 25g
10-20 days ฿1,990.00
inventory 100g
10-20 days ฿5,200.00
inventory 500g
10-20 days ฿17,400.00

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2,2,2-Trifluoroethanol
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Used as a solvent in organic synthesis, particularly in peptide coupling and polymer chemistry due to its ability to dissolve a wide range of organic and inorganic compounds. Enhances reaction rates in esterifications and acylations because of its strong hydrogen-bond donor properties. Employed in pharmaceutical manufacturing as a building block for fluorinated compounds, which often exhibit improved metabolic stability and bioavailability. Commonly used in NMR spectroscopy as a solvent for analyzing pol

Used as a solvent in organic synthesis, particularly in peptide coupling and polymer chemistry due to its ability to dissolve a wide range of organic and inorganic compounds. Enhances reaction rates in esterifications and acylations because of its strong hydrogen-bond donor properties. Employed in pharmaceutical manufacturing as a building block for fluorinated compounds, which often exhibit improved metabolic stability and bioavailability. Commonly used in NMR spectroscopy as a solvent for analyzing polar compounds. Also finds use in the formulation of liquid chromatography mobile phases for separating fluorinated molecules.

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