N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-isoleucine TCI F1129

Chemical Identity

Other names: N-Fmoc-N-methyl-L-isoleucine · Fmoc-N-Me-Ile-OH
CAS No.: 138775-22-1
Formula: C22H25NO4
Molecular weight: 367.45 g/mol
Purity: >98.0%(HPLC)(T)
Storage: 0-10°C

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S,3S)-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]-3-methylpentanoic acid
SMILES: CCC(C)C(C(=O)O)N(C)C(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
InChIKey: IQIOLCJHRZWOLS-XOBRGWDASA-N
MDL: MDL00153389
PubChem: CID 15433034

Rp 1.035.300,00

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N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-isoleucine is a chemical compound widely used in peptide synthesis. This compound plays a crucial role in the development of bioactive molecules, serving as a key building block in the creation of complex peptide structures. In laboratory settings, it is frequently employed as a starting material for the synthesis of various bioactive peptides, which are essential in pharmaceutical and biotechnological research. Its utility extends to the study of molecular interactions and the design of targeted therapeutic agents.

The compound is valued for its stable molecular structure and its ability to form ester bonds with other amino acids. These properties make it a preferred choice in peptide chemistry due to its reliability in chemical reactions and its compatibility with a range of synthetic methodologies. Its ester functionality allows for controlled cleavage during peptide synthesis, facilitating the isolation of desired peptide sequences. This makes it an essential reagent for researchers aiming to produce high-quality peptides with specific biological activities.

In Indonesian laboratories, this compound is commonly used in biochemical and pharmacological research. It is a key component in studies related to drug development, molecular structure analysis, and the exploration of new therapeutic agents. Its application is widespread in academic and industrial research settings, supporting advancements in biotechnology and medicinal chemistry. Researchers rely on its consistent performance and chemical stability to achieve accurate and reproducible results in their experiments.

Peptide synthesis for the development of new therapeutic agents due to its ability to form ester bonds with other amino acids.
Biochemical research to understand complex chemical reaction mechanisms and molecular interactions.
Pharmaceutical applications in the design and synthesis of targeted drug molecules with specific biological activities.
Structural studies to analyze molecular interactions and improve the design of bioactive compounds.
Drug discovery programs aimed at creating novel compounds with potential medical applications in pharmacology.

Brand	TCI
CAS number	138775-22-1
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide 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 environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and potential degradation. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Due to its chemical nature, it should be stored separately from incompatible substances to avoid any adverse reactions. Regular monitoring of storage conditions is advised to ensure the integrity of the compound remains intact throughout its shelf life. Proper labeling and documentation of storage conditions are essential for safe and effective laboratory practices.

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