Fmoc-Cit-PAB-OH TCI F1249

Chemical Identity

Other names: (S)-(9H-Fluoren-9-yl)methyl [1-[[4-(Hydroxymethyl)phenyl]amino]-1-oxo-5-ureidopentan-2-yl]carbamate · Nalpha-Fmoc-L-citrulline (4-Hydroxymethyl)phenylamide
CAS No.: 870487-04-0
PubChem: CID 70879715·SID 468591879
Formula: C28H30N4O5
Molecular weight: 502.57 g/mol
Purity: >97.0%(HPLC)
Storage: 0-10°C

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 9H-fluoren-9-ylmethyl N-[(2S)-5-(carbamoylamino)-1-[4-(hydroxymethyl)anilino]-1-oxopentan-2-yl]carbamate
SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CCCNC(=O)N)C(=O)NC4=CC=C(C=C4)CO
InChIKey: KBTCNJJDJZRXCX-VWLOTQADSA-N

Rp 2.677.500,00

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TCI F1249 870487-04-0 Fmoc-Cit-PAB-OH is a chemical compound widely used in peptide synthesis within laboratory settings. As a protected amino acid, it plays a crucial role in the construction of complex peptide structures, particularly in the field of chemical biology. This compound is essential for researchers working on protein modification and conjugation processes, enabling the creation of bioactive molecules with specific functional properties. Its inclusion in the peptide chemistry category highlights its importance in both academic and industrial research environments.

The compound's unique properties make it a preferred choice for synthetic chemists and biochemists. The Fmoc (9-fluorenylmethyloxycarbonyl) group provides a stable protecting group that facilitates controlled deprotection during peptide synthesis, ensuring high specificity and yield. Additionally, its compatibility with a wide range of reagents and solvents enhances its utility in various synthetic protocols. The chemical stability under controlled conditions further supports its application in complex and sensitive reactions.

In Indonesian laboratories, Fmoc-Cit-PAB-OH is commonly utilized in biochemical and pharmacological research. It is particularly valuable in academic institutions and research centers focused on drug development, protein engineering, and biotechnology. Its role in synthesizing bioactive compounds aligns with the growing demand for advanced chemical tools in both teaching and research environments.

TCI brochures (PDF)

Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 22

Related TCI products

Peptide Synthesis: Fmoc-Cit-PAB-OH is ideal for solid-phase peptide synthesis due to its stable Fmoc group, enabling efficient coupling and deprotection steps.
Protein Conjugation: Its functional groups allow for the attachment of various biomolecules, making it suitable for antibody-drug conjugate development.
Bioactive Compound Development: The compound supports the creation of peptides with therapeutic potential in pharmaceutical research.
Chemical Biology Research: It is used in studies involving protein-protein interactions and molecular recognition mechanisms.
Biotransformation Studies: Its reactivity allows for the investigation of metabolic pathways and enzymatic modifications in biochemical processes.

Brand	TCI
CAS number	870487-04-0
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	Available in standard chemical laboratory quantities
Physical form	Solid powder
Storage	Store in a cool, dry place away from light and moisture

Fmoc-Cit-PAB-OH 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 humidity and air contaminants. Due to its chemical nature, it should be handled in a well-ventilated laboratory setting, ideally with appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances and ensure proper waste disposal procedures are followed. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in research applications.

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