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Catalog Number:
48116
TentaGel MB COOH (0.15 - 0.3 mmol/g, 280 - 320 µm)
Documents
$96.25 /1G
Pack Size Availability Price
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Product Information

TentaGel MB COOH is a high-performance resin designed for solid-phase peptide synthesis and other applications in organic chemistry. This versatile compound features a carboxylic acid functional group, which enhances its reactivity and makes it ideal for coupling reactions. With a loading capacity of 0.15 - 0.3 mmol/g and a particle size of 280 - 320 µm, TentaGel MB COOH is optimized for efficient synthesis and purification processes. Its unique structure allows for easy cleavage of the synthesized products, facilitating the rapid development of peptides and other complex molecules.

Researchers and industry professionals can leverage TentaGel MB COOH in various applications, including drug discovery, biomolecule synthesis, and the development of novel therapeutic agents. Its robust performance and compatibility with a wide range of reagents make it a preferred choice for laboratories focused on high-throughput screening and combinatorial chemistry. By choosing TentaGel MB COOH, customers benefit from enhanced yields and purity, streamlining their workflows and accelerating their research outcomes.

Appearance
Slightly yellow to beige powder
Substitution
0.15 - 0.3 mmol/g
Mesh Size
280 - 320 µm
Conditions
Store at 0 - 8 °C
General Information
Appearance
Slightly yellow to beige powder
Substitution
0.15 - 0.3 mmol/g
Mesh Size
280 - 320 µm
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 MB COOH (0.15 - 0.3 mmol/g, 280 - 320 µm) is widely utilized in research focused on:

  • Peptide Synthesis: This chemical is commonly used as a solid-phase support for synthesizing peptides, allowing for easy purification and isolation of the final product.
  • Drug Development: It serves as a crucial component in the development of new pharmaceuticals, particularly in creating libraries of compounds for high-throughput screening.
  • Bioconjugation: The carboxylic acid functional groups facilitate the attachment of biomolecules, making it ideal for creating bioconjugates for diagnostic and therapeutic applications.
  • Polymer Chemistry: It is employed in the synthesis of functionalized polymers, enhancing properties such as solubility and reactivity for various industrial applications.
  • Material Science: The compound is used in the development of advanced materials, including hydrogels and coatings, which benefit from its unique chemical properties.

Citations