4-Acetyl-L-phenylalanine Hydrochloride is a chemical compound widely used in laboratory experiments across chemical and biochemical fields. As a derivative of phenylalanine, an essential amino acid, it plays a crucial role in peptide chemistry and organic synthesis. This compound is particularly valuable for researchers aiming to develop complex molecules, as it offers a stable and reactive platform for various chemical reactions. Its presence in laboratory settings supports both academic and industrial research, making it a versatile tool for chemical innovation.
The compound is favored for its controlled reactivity and stable molecular structure, which simplifies handling and processing. Its solubility in organic solvents such as ethyl acetate and ethanol enhances its usability in both small and large-scale reactions. The hydrochloride salt form ensures consistent performance and predictable behavior, making it a reliable choice for chemical synthesis. Additionally, its physical properties allow for straightforward storage and handling, reducing the risk of degradation during experimentation.
In Indonesian laboratories, 4-Acetyl-L-phenylalanine Hydrochloride is commonly used in chemical and biochemical research, especially in the development of new compounds and molecular structure studies. Its reliability in chemical reactions makes it a preferred material for scientists working on advanced synthetic pathways and structural analysis. Its availability and consistent performance support ongoing research efforts in both academic and applied settings.
Advantages (TCI brochure)
- Contains a ketone moiety for oxime ligation
- Oxime ligation with alkoxyamines enables homogeneous ADCs with optimized properties
TCI brochures (PDF)
- Non-Canonical Amino Acids for Protein Site-specific Modification by Genetic Code Expansion 2024-04-16 · p. 2
- Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 6
Related TCI products
- TCI B5350 68856-96-2 N-(tert-Butoxycarbonyl)-4-methoxy-D-phenylalanine
- TCI B5011 85466-66-6 N-(tert-Butoxycarbonyl)-N-methyl-D-phenylalanine
- TCI B4369 114873-07-3 N-(tert-Butoxycarbonyl)-4-trifluoromethyl-L-phenylalanine
- TCI B4356 100564-78-1 N-(tert-Butoxycarbonyl)-L-homophenylalanine
- TCI B4289 147923-08-8 N-(tert-Butoxycarbonyl)-4-phenyl-L-phenylalanine
- TCI B3668 61280-75-9 N-(tert-Butoxycarbonyl)-4-nitro-D-phenylalanine
- Peptide Synthesis: Ideal for constructing complex peptide sequences due to its stable structure and reactivity.
- Organic Chemistry Reactions: Used in various synthetic pathways for its predictable behavior in organic solvents.
- Structural Analysis Studies: Provides a reliable compound for molecular modeling and spectroscopic investigations.
- Biochemical Research: Supports the development of new compounds in biotechnology and pharmaceutical applications.
- Teaching and Training: Serves as an essential material for demonstrating chemical synthesis techniques in educational settings.
From the TCI brochure
- Oxime ligation with alkoxyamines for ADC preparation
| Brand | TCI |
|---|---|
| CAS number | 20299-31-4 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Chemical Biology > Peptide Chemistry |
| Pack sizes | Available in standard laboratory quantities |
| Physical form | Solid powder |
| Storage | Store in a cool, dry place away from moisture and light |
This compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and light exposure. Due to its hydrochloride salt form, it is generally stable under normal laboratory conditions. Avoid prolonged exposure to high temperatures or direct sunlight. Always handle with appropriate personal protective equipment to ensure safety during use and storage. Proper labeling and storage conditions help maintain the compound’s integrity and usability over time.
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