N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-proline TCI F0298

Chemical Identity

Other names: Fmoc-L-proline · Fmoc-Pro-OH
CAS No.: 71989-31-6
PubChem: CID 688135·SID 87570072
Formula: C20H19NO4
Molecular weight: 337.38 g/mol
Purity: >98.0%(HPLC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-1-(9H-fluoren-9-ylmethoxycarbonyl)pyrrolidine-2-carboxylic acid
SMILES: C1CC(N(C1)C(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)C(=O)O
InChIKey: ZPGDWQNBZYOZTI-SFHVURJKSA-N
MDL: MDL00037122

Rp 955.500,00

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N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-proline is a chemical compound widely used in peptide synthesis and organic chemical reactions. It functions as a protective group that shields the amino group from unwanted side reactions during the synthesis process. This compound plays a critical role in chemical biology, particularly in the development of complex molecules with biological activity. Its stability and controlled reactivity make it a reliable choice for high-precision research applications.

The compound's unique chemical structure enables specific reactions under controlled conditions, making it highly versatile in synthetic chemistry. It exhibits good solubility in organic solvents such as ethyl acetate and dimethyl sulfoxide, which facilitates its use in various chemical reactions and synthesis processes. Its resistance to degradation ensures long-term stability and reliability in experimental results.

In Indonesian laboratories, this compound is commonly used in scientific research across fields such as chemical biology, pharmaceuticals, and biotechnology. It is a key reagent in academic and industrial settings where precise chemical synthesis is required. Its availability through AMI Scientific ensures that researchers have access to high-quality materials for their experiments.

TCI brochures (PDF)

Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 20

Related TCI products

Peptide Synthesis: This compound is ideal for peptide synthesis due to its protective group functionality, allowing for selective chemical reactions and high yield.
Organic Chemistry Reactions: Its controlled reactivity and solubility make it suitable for a wide range of organic reactions, enhancing reaction efficiency and product purity.
Bioactive Compound Development: It is widely used in the creation of bioactive compounds, supporting the synthesis of molecules with therapeutic potential.
Research in Chemical Biology: Its role in protecting amino groups makes it essential for studies involving complex molecular structures and biological activity.
Pharmaceutical Research: It is a key reagent in drug development, enabling the synthesis of compounds with specific pharmacological properties.

Brand	TCI
CAS number	71989-31-6
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	Available in various quantities as per standard laboratory requirements
Physical form	Solid
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 stability and effectiveness. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid contact with incompatible substances to prevent unwanted reactions. Proper labeling of containers is essential for safe handling and storage. Regular monitoring of storage conditions ensures the compound remains in optimal condition for use in research applications.

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