Benzenesulfonic acid sodium salt

Base Information

• Chemical Name: Benzenesulfonic acid sodium salt
• CAS No.: 515-42-4
• Molecular Formula: C6H5NaO3S
• Molecular Weight: 180.16
• Hs Code.: 29049090
• Mol file: 515-42-4.mol

Synonyms:Benzenesulfonicacid, sodium salt (7CI,8CI,9CI);Dispersant GN;Sodium benzene monosulfonate;Sodiumnonafluoro-1-butanesulfonate;Sodium phenylsulfonate;Supragil GN;Benzene sulfonic acid sodium salt;Benzenesulfonic acid,sodium salt (1:1);

Chemical Property of Benzenesulfonic acid sodium salt

Chemical Property:

• Appearance/Colour: off-white crystalline powder
• Melting Point: 450 °C
• PSA: 65.58000
• Density: 1.124 g/mL at 25 °C
• LogP: 1.67150
• Storage Temp.: Inert atmosphere,Room Temperature
• Sensitive.: Hygroscopic
• Solubility.: water: soluble
• Water Solubility.: soluble

Purity/Quality:

99.9% ^*data from raw suppliers

Sodium Benzenesulfonate >96.0%(T) ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn, Xi
• Hazard Codes: Xn,Xi
• Statements: 22-36/37/38
• Safety Statements: 26-24/25-22

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Uses: Sodium benzenesulfonate has been used in Raman spectroscopic determination of molecular structural features in sulfonated polystyrene resins. It was used as electrolyte in formation of polypyrrole coatings with varying surface morphology on stainless steel. It was used in the synthesis of 1-butyl-3-propanenitrile imidazolium benzenesulfonate.

Technology Process of Benzenesulfonic acid sodium salt

There total 29 articles about Benzenesulfonic acid sodium salt which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.6%

osanetant benzenesulfonate (258337-99-4) → sodium phenylsulfonate (515-42-4) + osanetant (172734-92-8,160492-56-8)

Guidance literature:

osanetant benzenesulfonate; With sodium hydroxide; In ethanol;

at 20 ℃; for 1h;

Reference yield: 62.0%

sodium benzenesulfonate (873-55-2) → sodium phenylsulfonate (515-42-4)

Guidance literature:

With oxygen; In various solvent(s); at 19 - 21 ℃; for 1h;

DOI:10.1246/bcsj.69.1391

Reference yield: 22.0%

sodium benzenesulfonate (873-55-2) → sodium phenylsulfonate (515-42-4) + diphenyldisulfane (882-33-7)

Guidance literature:

With potassium sulfite; 1,10-Phenanthroline; ethanol; copper(II) trifluoroacetate; In dimethyl sulfoxide; at 120 ℃; for 8h;

DOI:10.1021/acs.orglett.1c02299

upstream raw materials:

sodium acetate

benzenesulfonyl chloride

benzenesulfonic acid

Benzenesulfonic acid toluene-4-sulfonylmethyl ester

Downstream raw materials:

diphenylether

Phenetole

phenol

diphenyl sulfide

Refernces

• 1、 Lam, Long Yin,Ma, Cong. "Chan-Lam-Type C-S Coupling Reaction by Sodium Aryl Sulfinates and Organoboron Compounds". supporting information. p. 6164 - 6168. Retrieved 2021/08/16.
• 2、 Akhondi, Maryam,Jamalizadeh, Effat. "Fabrication of silver-modified halloysite nanotubes and their catalytic performance in rhodamine 6G and methyl orange reduction". . p. 136 - 144. Retrieved 2019/04/13.