TCI B3167, with the CAS number 71989-18-9, is a specialized chemical compound known as 5-tert-Butyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-glutamate. This compound is widely used in chemical and biochemical research, particularly in the field of peptide chemistry. It serves as a key building block in the synthesis of complex peptides and proteins, offering a stable and reactive platform for chemical modifications. Its unique structure allows it to participate in various synthetic reactions, making it an essential component in modern laboratory workflows.
The compound's chemical properties, including its controlled reactivity and structural stability, make it a preferred choice for researchers. The fluorenyl group attached to the molecule enhances its resistance to degradation under varying reaction conditions, ensuring consistent performance in synthetic processes. Additionally, the tert-butyl group provides further stability, enabling efficient and controlled reactions. These characteristics make it particularly suitable for applications requiring high precision and reproducibility.
In Indonesian laboratories, this compound is commonly used in academic and industrial research settings. It plays a crucial role in the development of new therapeutic agents and biochemical tools. Its availability and reliability make it an ideal choice for scientists working on advanced peptide-based projects. The compound's versatility supports a wide range of experimental designs, contributing to the advancement of chemical and biological research in the region.
TCI brochures (PDF)
- Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 19
- Reagents for Biological Research 2025-03-11 · p. 58
Related TCI products
- TCI B4931 78081-87-5 Nalpha,Nepsilon-Bis[(9H-fluoren-9-ylmethoxy)carbonyl]-L-lysine
- TCI B4619 112883-39-3 4-tert-Butyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-aspartate
- TCI B4184 109425-55-0 Ndelta-(tert-Butoxycarbonyl)-Nalpha-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-ornithine
- TCI B3887 86060-84-6 4-Benzyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-aspartate
- TCI B3669 104091-08-9 5-tert-Butyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-glutamate
- TCI B3318 86061-04-3 5-tert-Butyl 1-Pentafluorophenyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-glutamate
- Peptide Synthesis: This compound is ideal for solid-phase peptide synthesis due to its stable fluorenyl group, which facilitates efficient coupling reactions and purification.
- Bioconjugation Studies: Its reactive carbonyl group enables specific conjugation with biomolecules, making it suitable for antibody-drug conjugate development.
- Organic Chemistry Research: The compound's controlled reactivity supports a variety of organic transformations, enhancing the efficiency of synthetic pathways.
- Protein Engineering: Its structure allows for the incorporation of functional groups, aiding in the design of modified proteins with enhanced properties.
- Analytical Chemistry: It serves as a standard in chromatographic and spectroscopic analyses, providing a reliable reference for method validation.
| Brand | TCI |
|---|---|
| CAS number | 71989-18-9 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Chemical Biology > Peptide Chemistry |
| Pack sizes | Available in various quantities as per supplier specifications |
| Physical form | Solid powder |
| Storage | Store in a cool, dry place away from light and moisture |
This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Due to its reactive nature, it should be handled in a well-ventilated area, with appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances, and ensure proper disposal procedures are followed to comply with laboratory safety standards. Regular monitoring of storage conditions is essential to ensure the compound remains suitable for use in research applications.
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