Nalpha-(tert-Butoxycarbonyl)-Nepsilon-benzyloxycarbonyl-L-lysine TCI B1632

Chemical Identity

Other names: Boc-Lys(Z)-OH
CAS No.: 2389-45-9
PubChem: CID 2724765·SID 87564533
Formula: C19H28N2O6
Molecular weight: 380.4 g/mol
Purity: >98.0%(HPLC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-6-(phenylmethoxycarbonylamino)hexanoic acid
SMILES: CC(C)(C)OC(=O)N[C@@H](CCCCNC(=O)OCC1=CC=CC=C1)C(=O)O
InChIKey: BDHUTRNYBGWPBL-HNNXBMFYSA-N

Rp 822.150,00

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Nalpha-(tert-Butoxycarbonyl)-Nepsilon-benzyloxycarbonyl-L-lysine is a chemical compound widely used in peptide synthesis. This compound plays a crucial role in the laboratory by enabling the formation of peptide bonds through controlled chemical reactions. Its complex structure allows for precise modification of amino acid residues, making it essential in the development of bioactive molecules. In research settings, it is a key reagent for creating custom peptides with specific biological functions.

The compound's stability under certain conditions and its functional groups—tert-butoxycarbonyl and benzyloxycarbonyl—make it a preferred choice for synthetic chemists. These protecting groups prevent unwanted side reactions, ensuring the integrity of the final product. The compound’s chemical properties allow it to be used in a variety of synthetic pathways, offering versatility in laboratory applications. Its ability to withstand specific reaction conditions enhances its utility in complex peptide synthesis protocols.

In Indonesian laboratories, this compound is commonly used in research related to peptides and bioactive compounds. Scientists in universities and research institutions rely on it for developing new therapeutic agents and studying molecular interactions. Its availability in solid form simplifies storage and handling, making it a reliable material for consistent experimental results.

TCI brochures (PDF)

Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 12

Related TCI products

Peptide Synthesis: This compound is ideal for constructing custom peptides due to its protecting groups, which allow controlled deprotection during synthesis.
Bioactive Compound Development: Its role in forming stable peptide bonds makes it essential for creating molecules with pharmacological activity.
Molecular Interaction Studies: Researchers use it to study how specific amino acid modifications affect protein function and behavior.
Drug Discovery Research: Its application in synthesizing bioactive peptides supports the development of new therapeutic agents.
Chemical Biology Experiments: The compound is used to explore the structural and functional properties of peptides in various biological contexts.

Brand	TCI
CAS number	2389-45-9
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	Available in standard laboratory quantities
Physical form	Solid
Storage	Store in a cool, dry place away from light

This compound should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to keep it in a sealed container to prevent exposure to air and humidity. Due to its chemical stability, it does not require refrigeration but should be protected from extreme temperature fluctuations. In a laboratory setting, it is important to handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. The compound is non-hazardous under normal conditions but should be used in a well-ventilated area to minimize any potential risks associated with chemical exposure.

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