TCI P3021 610794-20-2 H-L-Tyr(Propargyl)-OH is a chemical compound widely used in research applications within the field of chemical biology. This compound belongs to the category of conjugation chemistry and click chemistry, which are essential techniques for the development of bioactive molecules, including peptides and proteins. It serves as a key building block in the synthesis of complex molecules requiring precise and specific chemical reactions. Its role in laboratory settings is critical for creating stable and functional molecular structures that can be further modified or analyzed for biological activity.
One of the main reasons this compound is preferred is its ability to participate in click chemistry reactions, particularly the Copper-Catalyzed Azide-Alkyne Cycloaddition (CuAAC) reaction. This reaction is known for its high efficiency, specificity, and reliability, making it a popular choice in synthetic chemistry. The compound’s stable and reactive structure allows for the formation of strong and specific covalent bonds, which are essential in applications such as bioconjugation and molecular labeling. These properties make it a versatile and reliable tool for researchers working in various biochemical and pharmaceutical fields.
In Indonesian laboratories, TCI P3021 610794-20-2 H-L-Tyr(Propargyl)-OH is commonly used in biomedical, pharmacological, and organic chemistry research. Researchers in academic institutions and research centers rely on this compound for drug development, diagnostic testing, and molecular modification projects. Its availability and performance make it a valuable resource for advancing scientific studies in these areas.
TCI brochures (PDF)
- Bio-Orthogonal Non-Canonical Amino Acid Tagging (BONCAT) Related Reagents 2025-12-23 · p. 1
- Non-Canonical Amino Acids for Protein Site-specific Modification by Genetic Code Expansion 2024-04-16 · p. 1
- Click Chemistry 2026-09-08 · p. 13
- Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 10
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- Biomedical Research: This compound is ideal for creating bioconjugates used in diagnostic and therapeutic applications due to its reactivity and stability in click chemistry reactions.
- Peptide and Protein Modification: Its ability to form specific covalent bonds makes it useful for modifying peptides and proteins for structural and functional studies.
- Drug Development: It is frequently used in the synthesis of drug molecules that require precise chemical modifications and high specificity in reaction conditions.
- Molecular Labeling: The compound's reactivity allows for the efficient labeling of biomolecules, aiding in tracking and analysis in biochemical assays.
- Organic Synthesis: It serves as a key reagent in the synthesis of complex organic molecules requiring high precision and controlled reaction conditions.
| Brand | TCI |
|---|---|
| CAS number | 610794-20-2 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Chemical Biology > Conjugation Chemistry/Click Chemistry |
| Pack sizes | — |
| Physical form | — |
| Storage | Store in a cool, dry place away from light and moisture |
This compound should be stored in a cool, dry place, away from direct light and moisture to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its chemical integrity. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. Due to its chemical nature, it should be stored separately from incompatible substances to avoid any potential reactions. Proper labeling and storage conditions are essential to ensure its effectiveness and safety in research applications.
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Product Categories
- Chemical BiologyConjugation Chemistry/Click ChemistryAmino Acid Azides/Alkynes [Conjugation Chemistry/Click Chemistry]
- Chemical BiologyConjugation Chemistry/Click ChemistryTerminal Alkynes [Conjugation Chemistry/Click Chemistry]
- Chemical BiologyPeptide ChemistryUnnatural Amino Acid Derivatives
- Pharmaceutical Development and Drug Discovery Research ReagentsPeptide ChemistryUnnatural Amino Acid Derivatives
- Biochemicals and ReagentsAmino Acidsnon-Proteinogenic Amino Acids
- Molecular BiologyProteomicsCo-Translational Modification
- Pharmaceutical Development and Drug Discovery ResearchPeptide ChemistryUnnatural Amino Acid Derivatives
- Pharmaceutical Development and Drug Discovery ResearchConjugation Chemistry/Click ChemistryAmino Acid Azides/Alkynes [Conjugation Chemistry/Click Chemistry]
- Pharmaceutical Development and Drug Discovery ResearchConjugation Chemistry/Click ChemistryTerminal Alkynes [Conjugation Chemistry/Click Chemistry]

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