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Catalog Number:
48141
TentaGel M NH2 (0.15 - 0.35 mmol/g, 10 µm), narrow particle size distribution
Documents
$170.00 /1G
Pack Size Availability Price
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Product Information

TentaGel M NH2 is a versatile and highly efficient amino-functionalized resin, designed for solid-phase peptide synthesis and other applications in organic and medicinal chemistry. With a loading capacity of 0.15 - 0.35 mmol/g and a narrow particle size distribution of 10 µm, this resin ensures consistent and reliable performance, making it an ideal choice for researchers and industry professionals. Its unique amino functionality allows for the easy attachment of various building blocks, facilitating the synthesis of complex peptides and other biomolecules.

This resin is particularly beneficial in high-throughput screening and combinatorial chemistry, where rapid and efficient synthesis is crucial. TentaGel M NH2 can also be employed in the development of drug candidates, enabling the exploration of diverse chemical libraries. Its robust nature and compatibility with various coupling reagents enhance its usability across different synthetic protocols, making it a valuable asset in both academic and industrial laboratories.

Appearance
White to slightly yellowish powder
Substitution
0.15 - 0.35 mmol/g
Mesh Size
10 µm, narrow particle size
Conditions
Store at 0 - 8 °C
General Information
Appearance
White to slightly yellowish powder
Substitution
0.15 - 0.35 mmol/g
Mesh Size
10 µm, narrow particle size
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

TentaGel M NH2 (0.15 - 0.35 mmol/g, 10 µm), narrow particle size distribution is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as an excellent support for solid-phase peptide synthesis, allowing for efficient coupling reactions and easy cleavage of the final product.
  • Drug Discovery: It is used in combinatorial chemistry to create diverse libraries of compounds, aiding researchers in the identification of potential drug candidates.
  • Bioconjugation: The amino groups allow for the attachment of biomolecules, making it ideal for creating bioconjugates for diagnostics and therapeutic applications.
  • Material Science: Its properties are leveraged in the development of functionalized materials, enhancing the performance of sensors and catalysts.
  • Environmental Applications: It can be employed in the removal of pollutants from water, showcasing its versatility in addressing environmental challenges.

Citations