N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-valine TCI F1165

Chemical Identity

Other names: N-Fmoc-N-methyl-L-valine · Fmoc-N-Me-Val-OH
CAS No.: 84000-11-3
PubChem: CID 978328·SID 354335657
Formula: C21H23NO4
Molecular weight: 353.42 g/mol
Purity: >98.0%(HPLC)(T)
Storage: 0-10°C

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]-3-methylbutanoic acid
SMILES: CC(C)C(C(=O)O)N(C)C(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
InChIKey: YCXXXPZNQXXRIG-IBGZPJMESA-N
MDL: MDL00153395

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N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-valine is a chemical compound widely used in peptide synthesis. This material plays a crucial role in the construction of complex organic molecules, particularly in the field of chemical biology. It is an essential component in the development of synthetic peptides and proteins, where its unique structure enables precise molecular assembly. In laboratory settings, it is employed to facilitate the formation of peptide chains through amide bond formation, a fundamental process in biochemistry. Its importance extends to various research areas, including drug discovery and molecular design.

The compound is favored for its chemical stability and the presence of the Fmoc (Fluoren-9-ylmethoxy carbonyl) group, which is highly reactive in peptide synthesis. This functional group allows for efficient coupling with other amino acids, making it a versatile tool in solid-phase peptide synthesis. Its non-toxic nature and compatibility with controlled laboratory conditions further enhance its appeal. The compound's ability to maintain structural integrity under specific experimental conditions ensures reliable results in research applications.

In Indonesian laboratories, this compound is commonly used in chemical biology, pharmaceutical, and biotechnology research. It is a key reagent in the development of synthetic peptides and proteins, supporting advancements in drug discovery and molecular engineering. Researchers in academic and industrial settings rely on its consistent performance to achieve accurate and reproducible outcomes in their experiments. Its widespread use underscores its importance in modern biochemical research.

Related TCI products

Peptide Synthesis: This compound is ideal for solid-phase peptide synthesis due to its Fmoc group, which enables efficient coupling with amino acids.
Drug Discovery: It supports the development of synthetic peptides used in pharmaceutical research, aiding in the design of novel therapeutic agents.
Molecular Biology Research: Its role in constructing complex molecular structures makes it valuable for studying protein interactions and biochemical pathways.
Biochemical Analysis: The compound is used in experiments requiring precise molecular assembly, contributing to the understanding of biological processes.
Biotransformation Studies: It facilitates the study of molecular modifications, helping researchers analyze how compounds behave in biological systems.

Brand	TCI
CAS number	84000-11-3
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	Available in various quantities as per standard laboratory supply
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 non-toxic nature, general laboratory safety protocols should be followed, including proper ventilation and personal protective equipment when handling. The compound is stable under normal storage conditions and does not require refrigeration. It is important to ensure that the storage area is free from incompatible substances to avoid any potential chemical interactions. Proper labeling and secure storage are essential to prevent accidental exposure and ensure safe handling in laboratory settings.

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