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Catalog Number:
04313
Cysteamine 2-chlorotrityl resin (200-400 mesh, 0.4-1.6 meq/g)
Synonym(s):
H-Aminoethylthio-2-chlorotrityl resin
Documents
$80.00 /1G
Pack Size Availability Price
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Product Information

Cysteamine 2-chlorotrityl resin is a versatile and highly functional resin widely utilized in peptide synthesis and drug development. This compound serves as a solid-phase support for the efficient synthesis of peptides and other bioactive molecules, enabling researchers to streamline their processes and enhance yields. Its unique chlorotrityl functionality allows for easy attachment and subsequent cleavage of peptides, making it an invaluable tool in the pharmaceutical and biotechnology industries.

In addition to its application in peptide synthesis, Cysteamine 2-chlorotrityl resin is also employed in the development of targeted drug delivery systems and in the production of various therapeutic agents. Its stability and reactivity make it suitable for a range of chemical reactions, providing researchers with a reliable platform for exploring new compounds. By choosing this resin, professionals can benefit from improved efficiency and precision in their synthesis processes, ultimately leading to faster development times and enhanced product quality.

Synonyms
H-Aminoethylthio-2-chlorotrityl resin
Molecular Weight
0
MDL Number
MFCD00283006
Appearance
Pale yellow
Substitution
0.4 - 1.5 meq/g
Mesh Size
200 - 400 mesh
Conditions
Store at 0 - 8 °C
%DVB
1% DVB
General Information
Synonyms
H-Aminoethylthio-2-chlorotrityl resin
Molecular Weight
0
MDL Number
MFCD00283006
Appearance
Pale yellow
Substitution
0.4 - 1.5 meq/g
Mesh Size
200 - 400 mesh
Conditions
Store at 0 - 8 °C
%DVB
1% DVB
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Cysteamine 2-chlorotrityl resin is widely utilized in research focused on:

  • Peptide Synthesis: This resin serves as a solid support for the synthesis of peptides, allowing for efficient coupling and deprotection steps in solid-phase peptide synthesis (SPPS).
  • Drug Development: It is employed in the development of pharmaceuticals, particularly in creating drug candidates that require specific amino acid sequences for therapeutic efficacy.
  • Bioconjugation: The resin is used to attach biomolecules, such as antibodies or enzymes, to surfaces or other molecules, enhancing the functionality of bioconjugates in diagnostics and therapeutics.
  • Research in Neuroscience: Cysteamine derivatives can be studied for their neuroprotective properties, making this resin valuable in the exploration of treatments for neurodegenerative diseases.
  • Custom Resin Development: Researchers can modify the resin to create tailored supports for specific applications, allowing for greater flexibility and innovation in chemical synthesis.

Citations