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CAS 99306-64-6

Nalpha-(tert-Butoxycarbonyl)-L-arginine 4-Nitroanilide Hydrochloride TCI B1497

Nalpha-(tert-Butoxycarbonyl)-L-arginine 4-Nitroanilide Hydrochloride TCI B1497

Chemical Identity

Other names
Boc-Arg-pNA·HCl
CAS No.
99306-64-6
PubChem
CID 13502326·SID 87564410
Formula
C17H27ClN6O5
Molecular weight
430.9 g/mol
Purity
>98.0%(HPLC)(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
tert-butyl N-[(2S)-5-(diaminomethylideneamino)-1-(4-nitroanilino)-1-oxopentan-2-yl]carbamate;hydrochloride
SMILES
CC(C)(C)OC(=O)N[C@@H](CCCN=C(N)N)C(=O)NC1=CC=C(C=C1)[N+](=O)[O-].Cl
InChIKey
OUVONNGVXPOXGB-ZOWNYOTGSA-N
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N-alpha-(tert-Butyloxycarbonyl)-L-arginine 4-nitroanilide hydrochloride is a specialized chemical compound used in laboratory settings for advanced chemical and biochemical experiments. This compound is particularly valuable in peptide chemistry due to its role as a protected amino acid derivative. It serves as a key intermediate in the synthesis of complex peptides and proteins, enabling researchers to manipulate and study molecular interactions with precision. Its unique structure allows for controlled chemical reactions, making it an essential tool in modern biochemical research.

The compound’s chemical properties, including its hydrochloride group and tert-butyloxycarbonyl (Boc) functionality, contribute to its stability and reactivity under specific laboratory conditions. These features make it a preferred choice for applications requiring precise control over reaction pathways. The presence of functional groups also enhances its utility in various synthetic processes, allowing for the selective modification of amino acid residues. Its reliability and consistency in performance are critical for reproducible results in research environments.

In Indonesian laboratories, this compound is widely used in chemical, biochemical, and pharmacological research. It supports the development of new synthetic methods and the investigation of molecular interactions. Many research institutions and universities in Indonesia rely on this compound to advance their studies in peptide chemistry and related fields. Its availability through AMI Scientific ensures that researchers have access to high-quality materials for their experiments.

TCI brochures (PDF)

  • Peptide Synthesis: This compound is ideal for synthesizing complex peptides due to its protected amino acid functionality, enabling controlled coupling reactions.
  • Molecular Interaction Studies: Its unique structure allows researchers to investigate specific molecular interactions and reactivity patterns in biochemical systems.
  • Drug Development Research: The compound is used in pharmacological studies to develop and test new therapeutic agents by mimicking peptide-based drug structures.
  • Chemical Modification Experiments: Its reactivity and functional groups make it suitable for experiments involving selective chemical modifications of amino acid residues.
  • Biochemical Reagent Testing: It serves as a standard reagent for testing reaction conditions and optimizing biochemical processes in laboratory settings.

Brand TCI
CAS number 99306-64-6
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 light

This compound should be stored in a cool, dry environment to maintain its chemical integrity and prevent degradation. It is recommended to use airtight containers to protect it from moisture and light exposure. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. It is important to keep it away from incompatible substances to avoid any potential chemical reactions. Proper labeling and storage conditions help maintain its stability and effectiveness for research applications. Always follow standard laboratory safety protocols when working with this compound to ensure safe and efficient use.

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