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CAS 831-59-4

Disodium 1,3-Benzenedisulfonate TCI B0023

Disodium 1,3-Benzenedisulfonate TCI B0023

Chemical Identity

CAS No.
831-59-4
PubChem
CID 71577·SID 87563237
Formula
C6H4Na2O6S2
Molecular weight
282.2 g/mol
Purity
>55.0%(HPLC)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
disodium;benzene-1,3-disulfonate
SMILES
C1=CC(=CC(=C1)S(=O)(=O)[O-])S(=O)(=O)[O-].[Na+].[Na+]
InChIKey
XWPWZOJBTOJEGW-UHFFFAOYSA-L
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Disodium 1,3-Benzenedisulfonate is a chemical compound widely used in laboratory settings as a foundational building block in various chemical reactions. It serves as a key reagent in the synthesis of organic compounds, particularly in the development of complex molecular structures. This compound is valued for its stability and controlled reactivity, making it a reliable choice for chemists working on diverse synthetic pathways. Its molecular structure features two sulfonate groups attached to a benzene ring, which allows it to participate in multiple reaction types, including substitution and condensation reactions.

The compound's chemical properties make it a preferred choice in laboratory environments. It is water-soluble and can interact with a variety of reagents, enabling its use in a wide range of experimental setups. Its stability under standard laboratory conditions ensures ease of handling and storage, reducing the risk of degradation during experiments. Additionally, it does not contain harmful or toxic components, enhancing its safety profile for routine use. These characteristics contribute to its popularity among researchers and chemists in both academic and industrial settings.

In Indonesian laboratories, Disodium 1,3-Benzenedisulfonate is commonly used in chemical research and development. It plays a significant role in pharmaceutical synthesis experiments, where it helps in the creation of various drug compounds. Its versatility and reliability make it an essential component in both basic and applied chemical studies, supporting advancements in scientific research across multiple disciplines.

  • Pharmaceutical synthesis where it acts as a key intermediate in the creation of complex drug molecules.
  • Organic chemistry experiments requiring sulfonate-based building blocks for structural modifications.
  • Analytical chemistry applications for standardization and calibration of chemical reagents.
  • Polymer science research for the development of functionalized materials and coatings.
  • Environmental chemistry studies to assess the behavior of sulfonate compounds in aqueous systems.

Brand TCI
CAS number 831-59-4
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid powder
Storage Store in a cool, dry place away from direct sunlight

Disodium 1,3-Benzenedisulfonate should be stored in a cool, dry place, away from direct sunlight and moisture. It is recommended to keep the compound in a sealed container to prevent exposure to air and humidity, which could affect its stability. While it is not classified as hazardous, standard laboratory safety practices should be followed, such as wearing protective gloves and goggles when handling. The compound is water-soluble, so it should be stored in a location that minimizes the risk of spills or contamination. Proper labeling of containers is essential to ensure safe handling and prevent accidental use. These precautions help maintain the integrity of the compound and ensure safe laboratory operations.

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