O-(6-Chloro-1-hydrocibenzotriazol-1-yl)- -1,1,3,3-tetramethyluronium tetrafluoroborate

98%

Reagent Code: #56711
label
Alias 1-[bis(dimethylamino)methylene]-5-chlorobenzotriazolium 3-oxide tetrafluoroborate 6-chlorobenzotriazole-1,1,3,3-tetramethyl Urea Tetrafluoroborate TCTU
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CAS Number 330641-16-2

science Other reagents with same CAS 330641-16-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 355.53 g/mol
Formula C₁₁H₁₅BClF₄N₅O
badge Registry Numbers
MDL Number MFCD04973270
thermostat Physical Properties
Melting Point 201-205 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Widely used as a coupling reagent in peptide synthesis, it facilitates the formation of amide bonds between amino acids, enhancing efficiency and yield. It is particularly valued for its ability to minimize racemization, ensuring the stereochemical integrity of the synthesized peptides. Additionally, it is employed in the preparation of complex organic molecules, where it acts as a reliable activator for carboxylic acids, enabling smooth condensation reactions. Its stability and effectiveness in various solvents make it a preferred choice in both academic research and industrial applications.

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Test Parameter Specification
Elemental Analysis (Nitrogen) 19.3-19.9%
Melting point 198-204
Purity (GC) 98-100%
Appearance White to light yellow powder
Infrared Spectrometry Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿500.00
inventory 100g
10-20 days ฿6,180.00
inventory 25g
10-20 days ฿1,730.00

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O-(6-Chloro-1-hydrocibenzotriazol-1-yl)- -1,1,3,3-tetramethyluronium tetrafluoroborate
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Widely used as a coupling reagent in peptide synthesis, it facilitates the formation of amide bonds between amino acids, enhancing efficiency and yield. It is particularly valued for its ability to minimize racemization, ensuring the stereochemical integrity of the synthesized peptides. Additionally, it is employed in the preparation of complex organic molecules, where it acts as a reliable activator for carboxylic acids, enabling smooth condensation reactions. Its stability and effectiveness in various

Widely used as a coupling reagent in peptide synthesis, it facilitates the formation of amide bonds between amino acids, enhancing efficiency and yield. It is particularly valued for its ability to minimize racemization, ensuring the stereochemical integrity of the synthesized peptides. Additionally, it is employed in the preparation of complex organic molecules, where it acts as a reliable activator for carboxylic acids, enabling smooth condensation reactions. Its stability and effectiveness in various solvents make it a preferred choice in both academic research and industrial applications.

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