sodium 1,4-didodecyl sulphonatosuccinate

Base Information

• Chemical Name: sodium 1,4-didodecyl sulphonatosuccinate
• CAS No.: 4229-35-0
• Molecular Formula: C28H54 O7 S . Na
• Molecular Weight: 556.78
• Hs Code.: 2914509090
• Mol file: 4229-35-0.mol

Synonyms:Butanedioicacid, sulfo-, 1,4-didodecyl ester, sodium salt (9CI); Succinic acid, sulfo-,1,4-didodecyl ester, sodium salt (8CI); Succinic acid, sulfo-, didodecyl ester,S-sodium salt (7CI); Succinic acid, sulfo-, didodecyl ester, sodium salt (6CI);Didodecyl sodiosulfosuccinate; Didodecyl sodium sulfosuccinate; Didodecylsulfosuccinate sodium salt; Dilauryl sodiosulfosuccinate; Dilauryl sodiumsulfosuccinate; Dilauryl sulfosuccinate sodium salt; Sodium dilaurylsulfosuccinate; Sodium sulfosuccinate didodecyl ester; Sulfosuccinic acid1,4-didodecyl ester sodium salt

Chemical Property of sodium 1,4-didodecyl sulphonatosuccinate

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 118.18000
• Density: g/cm³
• LogP: 8.29930

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of sodium 1,4-didodecyl sulphonatosuccinate

There total 7 articles about sodium 1,4-didodecyl sulphonatosuccinate 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: 70.0%

di-n-dodecyl succinate (5980-15-4) → sodium 1,2-bis(dedecyloxycarbonyl)ethanesulfonate (4229-35-0)

Guidance literature:

With sodium hydrogensulfite;

Reference yield: 36.0%

di-dodecyl maleate (2915-52-8) → sodium 1,2-bis(dedecyloxycarbonyl)ethanesulfonate (4229-35-0)

Guidance literature:

With sodium hydrogensulfite; In water; Heating;

DOI:10.1016/j.tet.2005.04.037

Reference yield:

didodecyl fumarate (2402-58-6) → sodium 1,2-bis(dedecyloxycarbonyl)ethanesulfonate (4229-35-0)

Guidance literature:

With sodium hydrogensulfite; In ethanol; water; at 49.85 ℃; for 4h;

DOI:10.1039/a904815d

upstream raw materials:

di-n-dodecyl succinate

didodecyl fumarate

di-dodecyl maleate

1-dodecyl alcohol

Refernces

• 1、 Matsumoto, Jin,Ishizu, Masayuki,Kawano, Ryu-Ichiro,Hesaka, Daisuke,Shiragami, Tsutomu,Hayashi, Yoshimi,Yamashita, Toshiaki,Yasuda, Masahide. "Generation of quinone methide from aminomethyl(hydroxy)arenes precursors in aqueous solution". . p. 5735 - 5740. Retrieved 2007/10/03.
• 2、 Okahata, Yoshio,Niikura, Ken-ichi,Ijiro, Kuniharu. "Simple transphosphatidylation of phospholipids catalysed by a lipid-coated phospholipase D in organic solvents". . p. 919 - 926. Retrieved 2007/10/02.