4-(Aminomethyl)benzoic Acid TCI A0965

Chemical Identity

CAS No.: 56-91-7
PubChem: CID 65526·SID 87562468
Formula: C8H9NO2
Molecular weight: 151.16 g/mol
Purity: >97.0%(HPLC)(T)
Reference databases: ChEBI·ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4-(aminomethyl)benzoic acid
SMILES: C1=CC(=CC=C1CN)C(=O)O
InChIKey: QCTBMLYLENLHLA-UHFFFAOYSA-N

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4-(Aminomethyl)benzoic Acid is a chemical compound widely used in chemical and biochemical research. It serves as a key building block in the synthesis of complex molecules, particularly in peptide chemistry and organic synthesis. Its unique molecular structure, combining a benzoic acid group with an aminomethyl group, allows it to participate in various chemical reactions and interact with multiple functional groups. This versatility makes it an essential reagent for researchers aiming to develop new compounds or modify existing ones.

The compound is valued for its chemical stability and reactivity. It exhibits good solubility in organic solvents such as ethylamine and acetone, which simplifies handling and purification processes in the laboratory. Its ability to form stable intermediates and undergo various functional group transformations makes it a preferred choice for synthetic chemists. Additionally, its predictable behavior in different reaction conditions ensures reliable results in experimental setups.

In Indonesian laboratories, 4-(Aminomethyl)benzoic Acid is commonly used by researchers in academic and industrial settings. It plays a crucial role in the development of pharmaceuticals, bioactive compounds, and materials science. Its availability and compatibility with standard laboratory procedures make it a popular choice for both basic and advanced research applications.

Related TCI products

Peptide Synthesis: This compound is widely used in peptide chemistry due to its ability to form amide bonds, making it ideal for constructing amino acid sequences.
Organic Synthesis: Its reactive functional groups allow it to participate in a variety of chemical reactions, supporting the creation of complex organic molecules.
Functional Group Modification: The aminomethyl group enables the modification of other molecules, making it useful in the development of new chemical entities.
Biochemical Research: It is frequently used in studies involving protein interactions and molecular recognition due to its structural similarity to amino acid side chains.
Drug Development: Its role in synthesizing bioactive compounds makes it a valuable tool in pharmaceutical research and development.

Brand	TCI
CAS number	56-91-7
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 sunlight

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 reactivity, it should be handled in a well-ventilated area, preferably under a fume hood. Avoid contact with strong oxidizing agents or acids. Proper personal protective equipment, such as gloves and safety goggles, should be worn during handling. Regular monitoring of storage conditions ensures the compound remains suitable for use in laboratory applications.

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