Nalpha-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-tryptophan TCI F0307

Chemical Identity

Other names: Nalpha-Fmoc-L-tryptophan · Fmoc-Trp-OH
CAS No.: 35737-15-6
PubChem: CID 978343·SID 87570081
Formula: C26H22N2O4
Molecular weight: 426.47 g/mol
Purity: >98.0%(HPLC)(T)
Reference databases: ChemSpider

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(1H-indol-3-yl)propanoic acid
SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CNC5=CC=CC=C54)C(=O)O
InChIKey: MGHMWKZOLAAOTD-DEOSSOPVSA-N
MDL: MDL00037126

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N-alpha-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-tryptophan is a chemical compound widely used in laboratory settings for its role in peptide chemistry and chemical biology. This compound serves as a key building block in the synthesis of complex molecules with biological activity, making it essential for researchers working in the field of organic chemistry and biochemistry. Its unique molecular structure enables it to participate in various chemical reactions under controlled laboratory conditions, supporting the development of new pharmaceuticals and bioactive compounds.

The compound's chemical stability and solubility in organic solvents such as ethyl acetate and acetone make it a preferred choice for synthetic applications. These properties allow for efficient handling and processing in laboratory environments, ensuring reliable results in chemical reactions and analytical procedures. Its ability to maintain structural integrity during synthesis and analysis further enhances its utility in research settings.

In Indonesian laboratories, N-alpha-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-tryptophan is commonly used in studies related to peptides, proteins, and bioactive organic compounds. Its versatility and reactivity make it an ideal material for both academic and industrial research, supporting the development of new drugs and biochemical applications. The compound’s clear structure also facilitates accurate analysis using techniques like spectroscopy and chromatography, making it a valuable tool in modern chemical research.

TCI brochures (PDF)

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

Related TCI products

Peptide Synthesis: This compound is ideal for synthesizing peptides due to its reactive N-alpha-carbonyl group, which facilitates coupling reactions in solid-phase peptide synthesis.
Bioactive Compound Development: Its structural features make it suitable for creating bioactive molecules with pharmaceutical potential, supporting drug discovery efforts.
Analytical Chemistry: The compound’s distinct molecular structure allows for accurate identification and analysis using advanced spectroscopic and chromatographic techniques.
Organic Reaction Studies: Its solubility in organic solvents enables its use in a wide range of organic reactions, supporting research in chemical reactivity and functional group transformations.
Protein Modification Research: The compound is used in studies involving protein modification, where its functional groups can be chemically manipulated to alter protein properties.

Brand	TCI
CAS number	35737-15-6
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 sunlight and sources of moisture to maintain its chemical stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled with care in a well-ventilated laboratory setting, using appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to incompatible substances, and ensure that storage areas are free from potential sources of heat or ignition. Proper labeling and storage conditions are essential to ensure the compound remains effective for its intended applications.

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