N-Acetyl-DL-histidine Monohydrate is a chemical compound widely used in research applications across chemistry and biology. As a derivative of histidine, it plays a significant role in peptide synthesis and protein modification processes. This compound is commonly utilized in laboratories for the development of bioactive molecules and pharmaceutical research. Its chemical structure and functional groups make it a versatile reagent in various synthetic pathways. Due to its stability and solubility, it is a preferred choice for researchers working on complex chemical reactions.
This compound is known for its chemical stability and solubility in organic solvents such as ethylamine and acetone. Its ability to dissolve in both organic and aqueous environments makes it suitable for a wide range of experimental conditions. The monohydrate form enhances its compatibility with different reaction systems, allowing for more controlled and reproducible results. These properties make it an essential component in many biochemical and pharmaceutical applications.
In Indonesian laboratories, N-Acetyl-DL-histidine Monohydrate is frequently used in biochemistry, pharmacology, and organic chemistry research. It supports studies related to the synthesis of bioactive compounds and the development of new drugs. Its availability ensures that local research institutions can conduct experiments requiring this compound without relying on imports. This makes it a valuable resource for both academic and industrial research settings.
TCI brochures (PDF)
- Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 11
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- TCI F1145 135610-90-1 Nalpha-[(9H-Fluoren-9-ylmethoxy)carbonyl]-tele-(triphenylmethyl)-D-histidine
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- Biochemical research utilizes N-Acetyl-DL-histidine Monohydrate for synthesizing peptides and modifying proteins due to its structural compatibility with amino acid derivatives.
- Pharmaceutical development benefits from this compound as it is used in the creation of bioactive molecules with therapeutic potential.
- Organic chemistry experiments leverage its solubility and stability to perform complex reactions under controlled conditions.
- Protein modification studies rely on this compound to alter amino acid side chains, enhancing functional properties of biomolecules.
- Drug discovery processes incorporate it as a building block for designing new compounds with specific biological activities.
| Brand | TCI |
|---|---|
| CAS number | 213178-97-3 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Chemical Biology > Peptide Chemistry |
| Pack sizes | Available in various quantities as per standard laboratory requirements |
| Physical form | White crystalline powder |
| Storage | Store in a cool, dry place away from moisture and direct sunlight |
N-Acetyl-DL-histidine Monohydrate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in airtight containers to prevent exposure to moisture, which could affect its solubility properties. Due to its hygroscopic nature, it is important to ensure that the storage area is well-ventilated and free from sources of humidity. The compound should be handled with care using appropriate personal protective equipment to avoid direct contact. In laboratory settings, it should be stored away from incompatible substances to prevent any potential chemical interactions. Proper labeling of containers is essential for safe handling and easy identification.
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![Nalpha-[(9H-Fluoren-9-ylmethoxy)carbonyl]-tele-(triphenylmethyl)-D-histidine (CAS 135610-90-1) - TCI F1145 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510F1145.jpg?v=1769142458&width=533)

