Benzoyl-L-histidine Monohydrate TCI B0204

Chemical Identity

CAS No.: 5354-94-9
PubChem: CID 152263·SID 87563337
Formula: C13H13N3O3
Molecular weight: 259.26 g/mol
Purity: >98.0%(HPLC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

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

Rp 557.550,00

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Berat 100mg 1g

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Benzoyl-L-histidine Monohydrate is a chemical compound widely used in chemical and biochemical experiments. As a derivative of histidine, one of the 20 amino acids found in proteins, it plays a crucial role in peptide synthesis and molecular interaction studies. This compound is particularly valued for its stability and controlled reactivity, making it a reliable material for research in biochemical and pharmacological fields. Its molecular structure allows for precise manipulation in laboratory settings, supporting a wide range of experimental applications.

The compound’s properties, including its solubility in organic solvents such as ethyl acetate and acetone, make it a preferred choice for researchers. Its hydrophobic nature enables it to dissolve easily in specific mediums, offering flexibility in experimental design. These characteristics allow for precise control over reactivity and solubility, which are essential in high-precision chemical reactions. The compound’s stability further ensures consistent results, enhancing its reliability in laboratory environments.

In Indonesian laboratories, Benzoyl-L-histidine Monohydrate is commonly used in peptide research, biological compound synthesis, and chemical analysis. Its availability and consistent quality make it a go-to material for scientists working on diverse biochemical projects. The compound supports both fundamental and applied research, contributing to advancements in various scientific fields.

TCI brochures (PDF)

Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 16

Related TCI products

Peptide Synthesis: Ideal for constructing complex peptide structures due to its controlled reactivity and solubility properties.
Molecular Interaction Studies: Facilitates the investigation of protein-ligand interactions and other molecular binding processes.
Biochemical Research: Supports studies on enzyme activity and metabolic pathways in biological systems.
Organic Chemistry Reactions: Provides a stable and reactive component for synthesizing organic compounds with high precision.
Pharmaceutical Development: Used in the formulation of drug compounds and the study of pharmacological effects.

Brand	TCI
CAS number	5354-94-9
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	Available in various quantities as per standard laboratory requirements
Physical form	White crystalline solid
Storage	Store in a cool, dry place away from direct sunlight

Benzoyl-L-histidine Monohydrate should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep the compound in a sealed container to avoid moisture exposure, which can affect its physical properties. Suitable storage conditions include a controlled temperature range of 15–25°C with low humidity levels. When handling, laboratory personnel should use appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety. The compound is generally non-hazardous but should be handled with care to avoid contamination. Regular inspection of storage conditions is advised to maintain the integrity of the material for research purposes.

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