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Sku CI04817_1_G
Chem Impex
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Product Information

Product Name
Fmoc-L-histidine(2-chlorotrityl resin)amide
Brand Name
Chem Impex
Product Number
04817
CAS
109425-51-6
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
11422193
IUPAC Name
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(1-tritylimidazol-4-yl)propanoic acid
InChI Key
XXMYDXUIZKNHDT-QNGWXLTQSA-N
SMILES
C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)N4C=C(N=C4)CC@@H(C(=O)O)NC(=O)OCC5C6=CC=CC=C6C7=CC=CC=C57

Description

Fmoc-L-histidine(2-chlorotrityl resin)amide is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a key building block in solid-phase peptide synthesis, allowing researchers to create complex peptides efficiently. Its protective Fmoc group facilitates easy deprotection, making it ideal for sequential synthesis.

Drug Development: In pharmaceutical research, it is used to develop peptide-based drugs. Its unique structure can enhance the stability and bioavailability of therapeutic peptides, which is crucial for effective treatment.

Bioconjugation: The resin can be used in bioconjugation processes, where it helps attach peptides to other molecules, such as antibodies or drugs, improving targeted delivery systems in cancer therapy.

Protein Engineering: Researchers utilize this compound to modify histidine residues in proteins, enabling the study of protein interactions and functions, which is essential in understanding biological processes.

Analytical Chemistry: It plays a role in the development of analytical methods for detecting and quantifying peptides, aiding in quality control and research applications in various industries.

References Data Source From Pubchem

A bioinformatics approach to design minimal biomimetic metal-binding peptides

Publication Name: Communications Chemistry
Publication Date: 2025-10-06
DOI: 10.1038/s42004-025-01702-z

Genetic variance in the murine defensin locus modulates glucose homeostasis

Publication Name: The EMBO Journal
Publication Date: 2025-09-09
DOI: 10.1038/s44318-025-00555-5

Design and Evaluation of ATN-161 Analogues as Fusion Inhibitors Targeting Integrins in SARS-CoV-2

Publication Name: International Journal of Peptide Research and Therapeutics
Publication Date: 2025-05-30
DOI: 10.1007/s10989-025-10734-x

Stabilization of a miniprotein fold by an unpuckered proline surrogate

Publication Name: Communications Chemistry
Publication Date: 2025-03-12
DOI: 10.1038/s42004-025-01474-6

Rapid peptide synthesis using a methylimidazolium sulfinyl fluoride salt

Publication Name: Communications Chemistry
Publication Date: 2025-02-22
DOI: 10.1038/s42004-025-01456-8