Nalpha-(tert-Butoxycarbonyl)-L-histidine TCI B1634

Chemical Identity

Other names: Boc-His-OH
CAS No.: 17791-52-5
PubChem: CID 87308·SID 87564535
Formula: C11H17N3O4
Molecular weight: 255.27 g/mol
Purity: >98.0%(HPLC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-3-(1H-imidazol-5-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
SMILES: CC(C)(C)OC(=O)N[C@@H](CC1=CN=CN1)C(=O)O
InChIKey: AYMLQYFMYHISQO-QMMMGPOBSA-N

Rp 1.008.000,00

~~Rp 720.300,00~~ Rp 1.008.000,00

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Berat 5g 25g

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Nalpha-(tert-Butoxycarbonyl)-L-histidine is a chemical compound widely used in peptide chemistry and the synthesis of complex molecules in laboratory settings. This compound plays a crucial role in the construction of peptides, particularly in coupling and amino acid chain modification reactions. Its chemical structure allows for controlled and precise reactions, making it an essential component in various biochemical and pharmaceutical applications. In both chemical and biochemical laboratories, it is frequently utilized to develop more complex peptide structures, such as peptide analogs, enzyme inhibitors, and biological therapeutic molecules.

The compound's chemical stability and reactivity make it a preferred choice for researchers. It can participate in a variety of chemical reactions, including hydrolysis, coupling, and deprotonation. Its specific molecular structure enables controlled chemical transformations, ensuring accuracy and reproducibility in experimental outcomes. These properties are particularly valuable in applications requiring high precision and consistency, such as drug development and molecular modeling. Its solid form also facilitates easy handling and accurate weighing, which is essential for laboratory-scale experiments.

In Indonesian laboratories, this compound is commonly used in biochemical, pharmacological, and food science research. Local researchers leverage it to develop pharmaceutical products, study biological mechanisms, or test the biological activity of specific compounds. Its versatility and reliability make it a key reagent in both academic and industrial research settings across Indonesia.

TCI brochures (PDF)

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

Related TCI products

Peptide Synthesis: This compound is ideal for peptide synthesis due to its role in amino acid chain modification and coupling reactions.
Enzyme Inhibition Studies: It is used to develop enzyme inhibitors by providing a stable and reactive building block for peptide analogs.
Biological Therapeutic Development: Its chemical structure supports the creation of biological therapeutic molecules, making it useful in pharmaceutical research.
Biochemical Research: It is frequently employed in biochemical experiments to study molecular interactions and reaction mechanisms.
Food Science Applications: It contributes to the analysis of amino acid profiles and the development of food-related compounds in food science laboratories.

Brand	TCI
CAS number	17791-52-5
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid
Storage	Store in a cool, dry place away from moisture and direct light

This compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its chemical reactivity, it should be handled with appropriate laboratory safety measures, such as using gloves and a fume hood when necessary. It is important to avoid direct contact with skin or inhalation of vapors. Proper labeling and storage conditions ensure the compound remains effective for its intended applications. Always follow standard laboratory safety protocols when working with this material.

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