Benzenesulfonyl Hydrazide TCI B0038

Chemical Identity

CAS No.: 80-17-1
PubChem: CID 65723·SID 87563250
Formula: C6H8N2O2S
Molecular weight: 172.21 g/mol
Purity: >98.0%(HPLC)(T)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: benzenesulfonohydrazide
SMILES: C1=CC=C(C=C1)S(=O)(=O)NN
InChIKey: VJRITMATACIYAF-UHFFFAOYSA-N

Rp 1.563.450,00

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Benzenesulfonyl Hydrazide (BCS) is a chemical compound widely used in organic chemistry reactions, particularly in the synthesis of heterocyclic compounds and complex molecular structures. As a key building block in chemical synthesis, it plays a crucial role in laboratories where researchers are engaged in the development of new compounds with specific biological activities. Its ability to react with various functional groups makes it an essential reagent in a range of chemical transformations, including hydrazone formation and condensation reactions.

The chemical properties of BCS make it a preferred choice for synthetic chemists. It exhibits stability under certain conditions but remains highly reactive towards electrophilic reagents such as aldehydes, ketones, and other reactive species. This reactivity enables it to participate effectively in a variety of reaction mechanisms, making it a versatile tool in organic synthesis. Additionally, its solubility in organic solvents like ethyl acetate and acetone facilitates efficient processing and purification in laboratory settings.

In Indonesian laboratories, BCS is commonly used by chemists and researchers working in academic institutions, research centers, and pharmaceutical industries. Its application spans across organic chemistry, pharmacology, and analytical chemistry, supporting the development of compounds with targeted biological properties. Its reliability and effectiveness in chemical reactions make it a standard component in many experimental protocols.

Related TCI products

Organic synthesis of heterocyclic compounds due to its reactivity with electrophilic species and functional groups.
Production of hydrazone derivatives through condensation reactions with aldehydes and ketones.
Development of bioactive compounds in pharmaceutical research for drug discovery and formulation.
Analytical chemistry applications for the detection and quantification of specific chemical species.
Support in complex molecular structure synthesis where precise chemical reactivity is required.

Brand	TCI
CAS number	80-17-1
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid
Storage	Store in a cool, dry place away from moisture and direct sunlight

Benzenesulfonyl Hydrazide should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air, which can affect its reactivity. Due to its potential to react with electrophilic reagents, it should be handled in a well-ventilated area with appropriate personal protective equipment. Avoid contact with incompatible substances such as strong oxidizers. In laboratory settings, it is important to follow standard safety protocols to ensure safe handling and storage. Regular monitoring of storage conditions is advised to maintain the integrity of the compound.

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