3-(2-Oxo-1,2-dihydro-4-quinolinyl)-DL-alanine Hydrochloride TCI O0468

Chemical Identity

CAS No.: 4876-14-6
PubChem: CID 11514549·SID 468592523
Formula: C12H13ClN2O3
Molecular weight: 268.69 g/mol
Purity: >98.0%(HPLC)(N)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-amino-3-(2-oxo-1H-quinolin-4-yl)propanoic acid;hydrochloride
SMILES: C1=CC=C2C(=C1)C(=CC(=O)N2)CC(C(=O)O)N.Cl
InChIKey: MPTXVJCCTVAVNL-UHFFFAOYSA-N

Rp 1.060.500,00

~~Rp 757.050,00~~ Rp 1.060.500,00

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Berat 5g 25g

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3-(2-Oxo-1,2-dihydro-4-quinolinyl)-DL-alanine Hydrochloride is a specialized chemical compound widely used in laboratory settings for its unique structural properties and reactivity. This compound plays a crucial role in chemical and biochemical experiments, particularly in the field of peptide chemistry. Its application extends to the synthesis of complex molecules and the development of bioactive compounds. Due to its stability and reactivity, it is a valuable tool for researchers aiming to explore molecular interactions and functional group modifications.

The compound is preferred for its solubility in organic solvents and its chemical stability under controlled conditions. As a hydrochloride salt, it dissolves well in solvents such as ethylamine and acetone, making it suitable for a variety of chemical reactions. Its molecular structure allows for versatility in synthetic pathways, enabling researchers to design and test new compounds efficiently. These properties make it a reliable choice for both academic and industrial research.

In Indonesian laboratories, this compound is commonly used in scientific research related to the synthesis of bioactive compounds, drug development, and molecular interaction studies. Its availability and performance in controlled environments make it a preferred material for researchers working in chemical biology and peptide chemistry. Its role in advancing scientific understanding in these fields is significant.

TCI brochures (PDF)

Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 10

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Drug development research benefits from this compound’s ability to participate in complex synthetic pathways, enabling the creation of bioactive molecules with targeted biological functions.
Peptide chemistry studies utilize its structural features to explore modifications and interactions in protein-based systems, aiding in the design of novel therapeutic agents.
Molecular interaction studies leverage its chemical stability and reactivity to investigate binding affinities and functional group behavior in biochemical environments.
Bioactive compound synthesis relies on its solubility and reactivity to facilitate the formation of complex structures in controlled laboratory settings.
Organic synthesis experiments take advantage of its compatibility with organic solvents, allowing for efficient reaction conditions and product isolation.

Brand	TCI
CAS number	4876-14-6
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	—
Physical form	—
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 stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and exposure to air, which can affect its solubility and reactivity. Due to its hydrochloride nature, it is sensitive to humidity and should be kept in a controlled atmosphere. Laboratory personnel should handle it with care, using appropriate personal protective equipment when necessary. Proper storage conditions ensure the compound remains effective for its intended applications in research settings.

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