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Catalog Number:
05541
CAS Number:
248921-84-8
Boc-His-Met-OH
Purity:
≥ 99 % (CCM)
Documents
$58.39 /100 mg
Taille
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Product Information

Boc-His-Met-OH is a valuable compound widely utilized in peptide synthesis and biochemistry research. This protected derivative of histidine and methionine offers researchers a versatile building block for the development of peptides and proteins. Its unique structure, featuring a tert-butoxycarbonyl (Boc) protecting group, enhances stability and solubility, making it an ideal choice for various applications in drug discovery and development.

In the pharmaceutical industry, Boc-His-Met-OH is particularly beneficial for the synthesis of bioactive peptides, which can serve as therapeutic agents or research tools in understanding biological processes. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups makes it a preferred choice among chemists. Furthermore, the compound's compatibility with automated peptide synthesizers streamlines the production process, allowing for efficient and reproducible results. Researchers can leverage Boc-His-Met-OH to explore new therapeutic avenues, making it an essential addition to any laboratory focused on peptide chemistry.

CAS Number
248921-84-8
Purity
≥ 99 % (CCM)
Molecular Formula
C16H26N4O5S
Molecular Weight
386.47
MDL Number
MFCD00237557
PubChem ID
78480744
Melting Point
191-195? C
Appearance
Poudre blanche
Conditions
Conserver à 0-8°C
General Information
CAS Number
248921-84-8
Purity
≥ 99 % (CCM)
Molecular Formula
C16H26N4O5S
Molecular Weight
386.47
MDL Number
MFCD00237557
PubChem ID
78480744
Melting Point
191-195? C
Appearance
Poudre blanche
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-His-Met-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those that require histidine and methionine residues. Its protective Boc group allows for selective reactions, making it easier to construct complex peptide sequences.
  • Drug Development: In pharmaceutical research, Boc-His-Met-OH is used to create peptide-based drugs. Its unique structure can enhance the bioactivity and stability of therapeutic peptides, which is crucial for effective drug formulation.
  • Bioconjugation: This chemical is employed in bioconjugation processes, where it can be linked to various biomolecules. This application is particularly beneficial in creating targeted drug delivery systems or diagnostic agents in the medical field.
  • Protein Engineering: Researchers utilize Boc-His-Met-OH in the design of modified proteins. By incorporating this compound, scientists can improve the properties of proteins, such as their solubility and stability, which are essential for various industrial applications.
  • Research in Cancer Therapy: The compound is also explored in cancer research, where it can be part of peptide-based therapies. Its ability to enhance the targeting of cancer cells makes it a valuable tool in developing more effective treatment options.

Citations