Nalpha-Carbobenzoxy-L-histidine TCI B0265

Chemical Identity

Other names: Z-His-OH
CAS No.: 14997-58-1
PubChem: CID 736313·SID 87563375
Formula: C14H15N3O4
Molecular weight: 289.29 g/mol
Purity: >99.0%(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-3-(1H-imidazol-5-yl)-2-(phenylmethoxycarbonylamino)propanoic acid
SMILES: C1=CC=C(C=C1)COC(=O)N[C@@H](CC2=CN=CN2)C(=O)O
InChIKey: WCOJOHPAKJFUDF-LBPRGKRZSA-N

Rp 955.500,00

~~Rp 683.550,00~~ Rp 955.500,00

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N-alpha-Carbobenzoxy-L-histidine is a chemical compound widely used in chemical biology and peptide chemistry. It serves as a key reagent in laboratory settings, particularly in the synthesis of peptides and biological compounds. This compound is derived from L-histidine and features a complex structure that enables it to participate in specific chemical activation processes. Its role in molecular research makes it essential for scientists working on drug development and molecular studies.

The compound is valued for its chemical stability and reactivity, which allow it to engage in molecular screening and coupling reactions. These properties make it a preferred choice for controlled reactivity in research applications. Its ability to bind with various chemical reagents enhances its utility in organic synthesis and modification processes. This versatility supports its application in a wide range of experimental setups.

In Indonesian laboratories, N-alpha-Carbobenzoxy-L-histidine is commonly used by researchers in educational and research institutions. It plays a crucial role in studies related to biological mechanisms and pharmacological compound development. Its availability in the local market ensures that scientists have access to this essential reagent for their experiments.

TCI brochures (PDF)

Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 17

Related TCI products

Peptide Synthesis: This compound is ideal for peptide synthesis due to its ability to participate in chemical activation and coupling reactions.
Molecular Screening: Its chemical stability and reactivity make it suitable for molecular screening applications in drug discovery.
Organic Modification: The compound is used in organic modification processes because of its capacity to bind with various reagents.
Drug Development Research: It supports research into pharmacological compounds by enabling controlled reactivity in synthesis processes.
Biological Mechanism Studies: Its role in chemical activation makes it valuable for studying biological mechanisms in molecular research.

Brand	TCI
CAS number	14997-58-1
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 moisture and direct light

This compound should be stored in a cool, dry environment, away from moisture and direct sunlight. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its chemical reactivity, it should be handled in a well-ventilated laboratory setting. Always wear appropriate personal protective equipment, such as gloves and safety goggles, when working with this material. Proper labeling of containers is essential to ensure safe handling and prevent accidental exposure. Regular monitoring of storage conditions is advised to maintain the compound’s integrity and effectiveness in research applications.

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