Sodium Vinyl Sulfonate Structure

Vinylsulfonic Acid Sodium Salt Solution 25 Wt In H2o Technical Grade Vinylsulfonic Acid Sodium Salt Sigma Aldrich

Vinylsulfonic Acid Sodium Salt Solution 25 Wt In H2o Technical Grade Vinylsulfonic Acid Sodium Salt Sigma Aldrich

Vinylsulfonic Acid Wikipedia

Vinylsulfonic Acid Wikipedia

Phenyl Vinylsulfonate 95 Sigma Aldrich

Phenyl Vinylsulfonate 95 Sigma Aldrich

Sodium Ethenesulfonate C2h3nao3s Pubchem

Sodium Ethenesulfonate C2h3nao3s Pubchem

Sodium Vinylsulfonate

Sodium Vinylsulfonate

Benzenesulfinic Acid Sodium Salt 98 Sodium Benzenesulfinate Sigma Aldrich

Benzenesulfinic Acid Sodium Salt 98 Sodium Benzenesulfinate Sigma Aldrich

Benzenesulfinic Acid Sodium Salt 98 Sodium Benzenesulfinate Sigma Aldrich

Sodium vinyl sulfonate is a polymerizable organic compound which has many industrial uses particularly as an antistatic agent and as an agent improving the tinctorial affinity of synthetic fibres such as polyacrylonitrile and polypropylene to cationic dyes as a dispersing agent in polymer emulsions.

Sodium vinyl sulfonate structure.

The free acids are widely used as catalysts in organic syntheses while the salts and other derivatives form the basis of the manufacture. The study group consisted of 53 workers 39 female aged 18 to 51 working in two factories in the peoples republic of china that manufactured sodium allyl sulfonate. Sodium vinyl sulfonate sodium vinyl sulfonate svs has both an olefinic bond and a reactive sulfonic acid group. Vinyl sulfonate sodium salt.

Many useful compounds and even some biochemicals feature sulfonates. Sulfonates are the conjugate base of sulfonic acids. Molecular weight 130 10. Linear formula c 2 h 3 nao 3 s n.

Pubchem substance id 24856814. A sulfonate is a salt or ester of a sulfonic acid. Vinylsulfonic acid sodium salt solution 25 wt. Sulfonates are generally stable in water non oxidizing and colorless.

It contains the functional group r so 3 where r is an organic group. Ethylenesulfonic acid sodium salt sodium vinylsulfonate solution vinylsulfonic acid sodium salt cas number 3039 83 6. Beilstein reaxys number 3711195. Do not use the medicine orally or rectally in a baby who has slow digestion caused by surgery or by using other medicines.

This bi functional structure suggest its applications ranging from its use as a monomer in polymerization of. Sulfonic acid sulfonic also spelled sulphonic any of a class of organic acids containing sulfur and having the general formula rso 3 h in which r is an organic combining group the sulfonic acids are among the most important of the organosulfur compounds. In h 2 o technical grade synonym. Sodium vinyl sulfonate polymer.

Linear formula ch 2 chso 3 na. An epidemiological survey of the effects of occupational exposure to allyl chloride was conducted. Ethenesulfonic acid homopolymer sodium salt. Sodium vinyl sulfonate 25 svs has both an olefinic bond and a reactive sulfonic acid group.

Do not give sodium polystyrene sulfonate orally by mouth to a newborn baby. This bifunctional structure suggests its applications ranging from its use as a monomer in the polymerisation of sulfonated vinyl type resins to its use as an organic intermediate in sulfoethylation reactions. Sodium polystyrene sulfonate can be given as a liquid by mouth through a stomach feeding tube or as a rectal enema. Sodium vinyl sulfonate 25 svs is used as polymerizable non migratory surfactant or copolymer in emulsion polymerization.

Sodium Vinylsulfonate 3039 83 6 Tokyo Chemical Industry Co Ltd Apac

Sodium Vinylsulfonate 3039 83 6 Tokyo Chemical Industry Co Ltd Apac

3711195 C2h3nao3s Chemspider

3711195 C2h3nao3s Chemspider

Industrial Chemical Tri Ethylene Glycol Teg Wholesaler From Mumbai

Industrial Chemical Tri Ethylene Glycol Teg Wholesaler From Mumbai

Controlled Synthesis Of Sulfonated Block Copolymers Having Thermoresponsive Property By Raft Polymerization Of Vinyl Sulfonate Esters Sciencedirect

Controlled Synthesis Of Sulfonated Block Copolymers Having Thermoresponsive Property By Raft Polymerization Of Vinyl Sulfonate Esters Sciencedirect

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