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2-Sulfobenzaldehyde Sodium Salt (CAS NO : 17465-11-3)

We are one of the leading manufacturers, distributors, and suppliers of 2-Sulfobenzaldehyde Sodium Salt in USA. Its CAS Number is 17465-11-3, and the chemical formula is C7H5NaO4S.

2-Sulfobenzaldehyde Sodium Salt is a sulfonated aromatic aldehyde used as a versatile intermediate in the synthesis of fluorescent dyes, surfactants, & specialty chemicals. This Sodium Salt has dual functionality (aldehyde and sulfonate) allows for selective reactivity in organic synthesis, especially in coupling reactions and anion exchange processes. As it preferred in Functional Intermediate in Dye and Surfactant Chemistry, 2-Sulfobenzaldehyde Sodium Salt enables synthesis pathways requiring both electron-withdrawing sulfonate groups and reactive aldehyde moieties. Manufacturers known it as Sodium o-formylbenzenesulfonate as frequently used in azo dye coupling, optical brighteners, and functional polymers demanding ionic conductivity or hydrophilic aromatic backbones.

2-Sulfobenzaldehyde Sodium Salt
2-Sulfobenzaldehyde Sodium Salt

2-Sulfobenzaldehyde Sodium Salt is a sulfonated aromatic aldehyde used as a versatile intermediate in the synthesis of fluorescent dyes, surfactants, & specialty chemicals. This Sodium Salt has dual functionality (aldehyde and sulfonate) allows for selective reactivity in organic synthesis, especially in coupling reactions and anion exchange processes. As it preferred in Functional Intermediate in Dye and Surfactant Chemistry, 2-Sulfobenzaldehyde Sodium Salt enables synthesis pathways requiring both electron-withdrawing sulfonate groups and reactive aldehyde moieties. Manufacturers known it as Sodium o-formylbenzenesulfonate as frequently used in azo dye coupling, optical brighteners, and fu...

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Organic Intermediates

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Aromatic Sulfonates

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Chemical Properties & Specifications

Applications of 2-Sulfobenzaldehyde Sodium Salt

Dye Manufacturing

Intermediate in synthesis of fluorescent and azo dyes

Specialty Surfactants

Used in the creation of charged aromatic surfactants

Chemical Coupling Agent

Reacts via aldehyde group for Schiff base formation

Polymer Chemistry

Building block in sulfonated polymeric networks

Electronics

Research use in functionalized ionic conductors

Dual Functional Group

Facilitates both electrophilic and nucleophilic reactions

Water Soluble

Readily used in aqueous reaction systems

Anionic Character

Useful in ionic polymer systems and solubilizers

Non-volatile

High stability under ambient processing

Customizable Derivatives

Aldehyde group permits structural extension

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