N-(tert-Butoxycarbonyl)-D-phenylalanine TCI B2989

Chemical Identity

Other names: Boc-D-Phe-OH
CAS No.: 18942-49-9
PubChem: CID 637610·SID 87559409
Formula: C14H19NO4
Molecular weight: 265.30 g/mol
Purity: >98.0%(T)
Reference databases: ChEBI·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoic acid
SMILES: CC(C)(C)OC(=O)N[C@H](CC1=CC=CC=C1)C(=O)O
InChIKey: ZYJPUMXJBDHSIF-LLVKDONJSA-N

Rp 637.350,00

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N-(tert-Butoxycarbonyl)-D-phenylalanine is a chemical compound widely used in peptide synthesis and biochemical research. This compound serves as a protected amino acid derivative, playing a crucial role in the development of bioactive molecules and pharmaceutical compounds. In the laboratory, it is a key reagent in the synthesis of peptides, particularly in the design and production of therapeutic agents and biomedicinal substances. Its chemical structure allows for controlled chemical reactions essential in the creation of complex molecular structures.

The compound is known for its chemical stability and resistance to degradation under appropriate storage conditions. These properties make it a preferred choice for researchers requiring reliable and consistent reagents in their experiments. Its ability to remain chemically inert until the desired reaction conditions are met ensures accuracy and reproducibility in laboratory settings. This stability also supports long-term storage, reducing the need for frequent replenishment of reagents.

In Indonesian laboratories, N-(tert-Butoxycarbonyl)-D-phenylalanine is commonly used by researchers in chemistry, molecular biology, and pharmacology. It supports ongoing research in biomedical sciences and drug development, which are key priorities in national scientific initiatives. Its application is essential in studies involving protein structure, enzyme function, and the development of bioactive compounds.

TCI brochures (PDF)

Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 13

Related TCI products

Peptide synthesis for studying protein structure and function benefits from this compound's controlled reactivity and stability.
Drug development with specific biological activity relies on its role as a protected amino acid in synthetic pathways.
Enzyme research utilizes its ability to participate in controlled chemical reactions under laboratory conditions.
Biomedical research applications benefit from its use in creating complex molecular structures for therapeutic purposes.
Molecular biology experiments require its stability and consistency for accurate and reproducible results.

Brand	TCI
CAS number	18942-49-9
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 light and moisture. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Due to its chemical stability, it does not require refrigeration but should be kept in a controlled laboratory setting. General laboratory precautions include handling with care to avoid contamination and ensuring proper ventilation when working with chemical reagents. Always follow standard safety protocols when handling chemical substances to maintain a safe and efficient laboratory environment.

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