Trifluoroacetic acid (TFA)

Reagent grade, 99.0%

Reagent Code: #239654
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Alias Trifluoroacetic acid (TFA); trifluoroacetic acid
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CAS Number 76-05-1

science Other reagents with same CAS 76-05-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 114.02 g/mol
Formula C₂HO₂F₃
badge Registry Numbers
EC Number 200-929-3
MDL Number MFCD00004169
thermostat Physical Properties
Melting Point -15 °C
Boiling Point 72.4 °C(lit.)
inventory_2 Storage & Handling
Density 1.489 g/mL at 20 °C(lit.)
Storage Room temperature

description Product Description

Widely used in peptide synthesis as a reagent for deprotection and cleavage from solid supports due to its strong acidity and ability to volatilize easily, allowing for simple removal. Commonly employed in high-performance liquid chromatography (HPLC) as an ion-pairing agent to improve separation of polar and basic compounds. Serves as a catalyst and solvent in organic reactions, including esterifications and Friedel-Crafts acylations, where its non-nucleophilic nature is advantageous. Also utilized in the production of pharmaceuticals, agrochemicals, and specialty fluorinated compounds thanks to its stability and reactivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿500.00
inventory 100ml
10-20 days ฿1,050.00
inventory 500g
10-20 days ฿3,200.00
inventory 2.5L
10-20 days ฿15,980.00
inventory 12X500ml
10-20 days ฿43,710.00
inventory 25ml
10-20 days ฿520.00
inventory 500ml
10-20 days ฿3,680.00
inventory 100g
10-20 days ฿720.00

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Trifluoroacetic acid (TFA)
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Widely used in peptide synthesis as a reagent for deprotection and cleavage from solid supports due to its strong acidity and ability to volatilize easily, allowing for simple removal. Commonly employed in high-performance liquid chromatography (HPLC) as an ion-pairing agent to improve separation of polar and basic compounds. Serves as a catalyst and solvent in organic reactions, including esterifications and Friedel-Crafts acylations, where its non-nucleophilic nature is advantageous. Also utilized in t

Widely used in peptide synthesis as a reagent for deprotection and cleavage from solid supports due to its strong acidity and ability to volatilize easily, allowing for simple removal. Commonly employed in high-performance liquid chromatography (HPLC) as an ion-pairing agent to improve separation of polar and basic compounds. Serves as a catalyst and solvent in organic reactions, including esterifications and Friedel-Crafts acylations, where its non-nucleophilic nature is advantageous. Also utilized in the production of pharmaceuticals, agrochemicals, and specialty fluorinated compounds thanks to its stability and reactivity.

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