2,4,6-tri(pyrrolidin-1-yl)-1,3,5-triazine

95%

Reagent Code: #242699
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CAS Number 5794-91-2

science Other reagents with same CAS 5794-91-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.39 g/mol
Formula C₁₅H₂₄N₆
badge Registry Numbers
MDL Number MFCD00738806
thermostat Physical Properties
Melting Point 186.6-189.8 °C
Boiling Point 486.3±28.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.239±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a coupling agent in peptide synthesis, facilitating the formation of amide bonds between amino acids. It activates carboxylic acid groups, making them more reactive toward nucleophilic attack by amine groups. This reagent is particularly valued in solid-phase peptide synthesis due to its efficiency and minimal racemization. Also employed in the preparation of bioconjugates and pharmaceutical intermediates where selective and mild coupling conditions are required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,130.00
inventory 1g
10-20 days ฿13,680.00
inventory 5g
10-20 days ฿26,130.00

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2,4,6-tri(pyrrolidin-1-yl)-1,3,5-triazine
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Used as a coupling agent in peptide synthesis, facilitating the formation of amide bonds between amino acids. It activates carboxylic acid groups, making them more reactive toward nucleophilic attack by amine groups. This reagent is particularly valued in solid-phase peptide synthesis due to its efficiency and minimal racemization. Also employed in the preparation of bioconjugates and pharmaceutical intermediates where selective and mild coupling conditions are required.

Used as a coupling agent in peptide synthesis, facilitating the formation of amide bonds between amino acids. It activates carboxylic acid groups, making them more reactive toward nucleophilic attack by amine groups. This reagent is particularly valued in solid-phase peptide synthesis due to its efficiency and minimal racemization. Also employed in the preparation of bioconjugates and pharmaceutical intermediates where selective and mild coupling conditions are required.

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