Sodium 2-Amino-4-chloro-5-methylbenzenesulfonate TCI A0896

Chemical Identity

CAS No.: 6627-59-4
PubChem: CID 23687607·SID 87562405
Formula: C7H7ClNNaO3S
Molecular weight: 243.64 g/mol
Purity: >98.0%(HPLC)(N)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: sodium 2-amino-4-chloro-5-methylbenzenesulfonate
SMILES: CC1=CC(=C(C=C1Cl)N)S(=O)(=O)[O-].[Na+]
InChIKey: KMIGBVSYNVXBEI-UHFFFAOYSA-M

Rp 452.550,00

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Sodium 2-Amino-4-chloro-5-methylbenzenesulfonate is a chemical compound widely used in organic synthesis reactions within laboratory settings. This compound serves as a key building block in the development of complex molecules, particularly those involving heterocyclic structures or carbon chains. Its versatility makes it a valuable resource for chemists working on a variety of synthetic pathways. Due to its chemical stability and controlled reactivity, it is frequently employed in research related to organic chemistry and pharmacology.

The compound's unique molecular structure, featuring both sulfonate and amino groups, contributes to its reactivity and functional versatility. These functional groups allow it to participate in various chemical reactions, including substitution, coupling, and reduction processes. Its solubility in organic solvents such as ethylamine and acetone further enhances its utility in laboratory applications. This combination of chemical properties and solubility makes it a preferred choice for researchers seeking reliable and effective reagents.

In Indonesian laboratories, Sodium 2-Amino-4-chloro-5-methylbenzenesulfonate is commonly used in both fundamental and applied chemical research. It plays a crucial role in the development of new compounds with potential applications in pharmaceuticals and materials science. Many research institutions and universities in Indonesia rely on this compound to advance their studies and innovations in the field of chemistry.

Related TCI products

Organic synthesis reactions benefit from its reactivity and structural versatility, enabling the creation of complex molecules.
It is ideal for substitution reactions due to its stable sulfonate group and reactive amino functionality.
Coupling reactions often utilize this compound as a key intermediate, facilitating the formation of new molecular frameworks.
Reduction processes can be effectively carried out using this compound, thanks to its controlled reactivity and chemical stability.
Pharmaceutical research leverages its structural features to develop new drug candidates with targeted biological activities.

Brand	TCI
CAS number	6627-59-4
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities to meet different research needs
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 and prevent degradation. It is recommended to use airtight containers to protect it from moisture and contaminants. Due to its potential reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid exposure to heat and direct sunlight to ensure long-term storage integrity. Regular checks of storage conditions are advised to maintain the compound's quality and usability in laboratory settings.

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