4-Amino-4'-dimethylaminoazobenzene TCI A1672

Chemical Identity

CAS No.: 539-17-3
PubChem: CID 10872·SID 87563089
Formula: C14H16N4
Molecular weight: 240.30 g/mol
Purity: >97.0%(HPLC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4-[[4-(dimethylamino)phenyl]diazenyl]aniline
SMILES: CN(C)C1=CC=C(C=C1)N=NC2=CC=C(C=C2)N
InChIKey: BVRIUXYMUSKBHG-UHFFFAOYSA-N

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4-Amino-4'-dimethylaminoazobenzene is a chemical compound widely used in laboratory settings for the synthesis of complex organic molecules. As a building block in organic chemistry, it plays a crucial role in the development of new compounds and materials. Its unique molecular structure, which includes two amino groups and an azo group, allows for high reactivity and versatility in chemical reactions. This compound is particularly valuable for researchers seeking to explore various synthetic pathways and functional group transformations.

The compound's azo group and amino functionalities make it a preferred choice for a range of chemical reactions, including coupling, nitroso, and reduction reactions. These properties enable it to participate in multiple synthetic strategies, making it a flexible tool for organic chemists. Its ability to undergo substitution and aromatic reactions further enhances its utility in laboratory applications. The compound's reactivity and structural characteristics make it a reliable and effective reagent for advanced chemical synthesis.

In Indonesian laboratories, 4-Amino-4'-dimethylaminoazobenzene is commonly used in organic chemistry research, especially in the synthesis of complex compounds and the development of new materials. It is a staple in research institutions and universities, where it supports ongoing studies in chemical synthesis and molecular design. Its availability and chemical properties make it an essential component in the toolkit of chemists working on innovative projects.

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Organic synthesis applications benefit from this compound's reactivity and structural versatility, enabling the creation of complex molecules through various chemical transformations.
It is ideal for coupling reactions due to its azo group, which facilitates the formation of new bonds between different molecular entities.
In the development of new materials, this compound serves as a building block for functional group modifications and molecular design.
Its use in nitroso reactions allows for the synthesis of nitrogen-containing compounds with specific functional properties.
Reduction reactions involving this compound are valuable in the preparation of aromatic and heterocyclic compounds for further chemical processing.

Brand	TCI
CAS number	539-17-3
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid
Storage	Store in a cool, dry place away from light and incompatible materials

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its chemical stability. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment such as gloves and safety goggles should be worn. Avoid contact with incompatible substances, including strong oxidizers and acids. Proper labeling and storage conditions are essential to maintain the integrity and safety of the compound in a laboratory setting.

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