10044-00-5

Basic information

• Product Name: sodium 1,4-dihexadecyl sulphonatosuccinate
• Synonyms: sodium 1,4-dihexadecyl sulphonatosuccinate;Butanedioic acid,sulfo-, 1,4-dihexadecyl ester,sodium salt;Butanedioic acid,sulfo-,1,4-dihexadecyl ester,sodium salt;Dihexadecyl 2-sodiosulfobutanedioate;Sodium 1,4-dihexadecyl sulfonatosuccinate
• CAS NO: 10044-00-5
• Molecular Formula: C₃₆H₆₉O₇S*Na
• Molecular Weight: 668.98363
• EINECS: 233-147-6
• Mol File: 10044-00-5.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: sodium 1,4-dihexadecyl sulphonatosuccinate(CAS DataBase Reference)
• NIST Chemistry Reference: sodium 1,4-dihexadecyl sulphonatosuccinate(10044-00-5)
• EPA Substance Registry System: sodium 1,4-dihexadecyl sulphonatosuccinate(10044-00-5)

Safety Data

• Hazardous Substances Data: 10044-00-5(Hazardous Substances Data)

Usage

General Description

Sodium 1,4-dihexadecyl sulphonatosuccinate is a chemical compound that belongs to the class of sulphonatosuccinate surfactants. It is commonly used as a surfactant in various industrial and household products such as detergents, shampoos, and soaps due to its ability to reduce the surface tension of liquids, allowing them to spread more easily. sodium 1,4-dihexadecyl sulphonatosuccinate is made up of sodium, carbon, hydrogen, oxygen, and sulphur atoms in its structure. It is known for its excellent cleaning properties and its ability to stabilize the mixture of water and oil, making it an important ingredient in many cleaning and personal care products. Additionally, it is considered to be biodegradable and has low toxicity, making it relatively safe for use in consumer products.

InChI:InChI=1/C36H70O7S.Na/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-42-35(37)33-34(44(39,40)41)36(38)43-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2;/h34H,3-33H2,1-2H3,(H,39,40,41);/q;+1/p-1

Upstream product

• 36653-82-4 1-Hexadecanol 
• 220624-94-2 C₃₆H₆₈O₄ 
• 7003-73-8 maleic acid dihexadecyl ester 

Relevant articles and documents

Preparation and characterization of phase-segregated vesicles of photopolymerizable diacetylene mixed with nonpolymerizable amphiphiles

A mixture of sodium 1,2-di(hexadecyloxycarbonyl)ethanesulfonate (2C16S) with photopolymerizable 1,2-di(10,12- tricosadiynoyl)-sn-glycerol 3-phosphocholine (DTPC) in a 2:100 ratio was treated by modified thin-film hydration to give an aggregate which became polymerized giant vesicles (GVs) under irradiation at 254 nm. The autofluorescence of the GVs was analyzed with a confocal laser scanning microscope at the cross section, revealing a 3.8-μm diameter ring shape and the presence of a dark part of ca. 1 μm in the ring. When octadecylrhodamine B (RhB) as an amphiphilic fluorescence probe was added to the GV, the fluorescence of RhB was emitted from the whole ring. Therefore, phase segregation of 2C16S from DTPC was confirmed. Similarly, mixed vesicles of N,N-di(2-hexadecanoyloxyethyl)dimethylammonium iodide with DTPC were found to be 3.7-μm diameter phase-segregated vesicles with a dark portion of ca. 1 μm on the ring in the cross sectional image. On the other hand, DTPC vesicles mixed with 1,2-di(dodecyloxycarbonyl)ethanesulfonate, N,N-di(2- dodecanoyloxyethyl)dimethylammonium iodide, and N,N-di(2-tetradecanoyloxyethyl) dimethylammonium iodide formed sphere structures filling the inside of the vesicles. The segregation mechanism was explained by the difference in the main phase transition temperature of each amphiphile.