Triethylamine trihydrofluoride

99.9%

Reagent Code: #238115
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CAS Number 73602-61-6

science Other reagents with same CAS 73602-61-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.21 g/mol
Formula C₆H₁₅N·₃HF
badge Registry Numbers
EC Number 277-550-5
MDL Number MFCD00043294
thermostat Physical Properties
Melting Point -29-27 °C
Boiling Point 70 °C/15 mm Hg(lit.)
inventory_2 Storage & Handling
Density 0.989 g/mL at 25 °C(lit.)
Storage Room temperature, inert gas

description Product Description

Used as a selective fluorinating agent in organic synthesis, particularly for the conversion of alcohols, aldehydes, and ketones into their corresponding fluorinated compounds. It is effective in deprotecting silicon-based protecting groups in peptide and nucleotide synthesis due to its mild and controlled fluoride release. Commonly employed in pharmaceutical manufacturing for introducing fluorine atoms into drug molecules, enhancing metabolic stability and bioavailability. Also utilized in materials science for surface modification of polymers and semiconductors where precise fluorination is required. Its liquid form and thermal stability make it suitable for use in continuous flow reactors and industrial-scale processes.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,350.00
Triethylamine trihydrofluoride
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Used as a selective fluorinating agent in organic synthesis, particularly for the conversion of alcohols, aldehydes, and ketones into their corresponding fluorinated compounds. It is effective in deprotecting silicon-based protecting groups in peptide and nucleotide synthesis due to its mild and controlled fluoride release. Commonly employed in pharmaceutical manufacturing for introducing fluorine atoms into drug molecules, enhancing metabolic stability and bioavailability. Also utilized in materials sci

Used as a selective fluorinating agent in organic synthesis, particularly for the conversion of alcohols, aldehydes, and ketones into their corresponding fluorinated compounds. It is effective in deprotecting silicon-based protecting groups in peptide and nucleotide synthesis due to its mild and controlled fluoride release. Commonly employed in pharmaceutical manufacturing for introducing fluorine atoms into drug molecules, enhancing metabolic stability and bioavailability. Also utilized in materials science for surface modification of polymers and semiconductors where precise fluorination is required. Its liquid form and thermal stability make it suitable for use in continuous flow reactors and industrial-scale processes.

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