6994-45-2

Basic information

• Product Name: 1-TETRADECANESULFONIC ACID SODIUM SALT
• Synonyms: 1-Tetradecanesulphonic acid sodium salt;1-TETRADECANESULFONIC ACID SODIUM SALT, FOR IPC;tetradecylsulfonic acid sodium salt;MYRISTOYLSULPHONATE;Sodium tetradecanesulfonate;Tetradecane-1-sulfonic acid sodium salt;1-TETRADECANESULFONIC A;1-Tetradecanesulfonic Acid Sodium Salt Tetradecylsulfonic Acid Sodium Salt
• CAS NO: 6994-45-2
• Molecular Formula: C14H29NaO3S
• Molecular Weight: 300.43
• EINECS: 248-288-9
• Product Categories: Anionic Surfactants;Functional Materials;Sulfonate (Surfactants);Surfactants
• Mol File: 6994-45-2.mol
• Article Data: 4

Chemical Properties

• Melting Point: 225-227 °C
• Appearance: /
• Water Solubility: almost transparency in hot Water
• BRN: 3920141
• CAS DataBase Reference: 1-TETRADECANESULFONIC ACID SODIUM SALT(CAS DataBase Reference)
• NIST Chemistry Reference: 1-TETRADECANESULFONIC ACID SODIUM SALT(6994-45-2)
• EPA Substance Registry System: 1-TETRADECANESULFONIC ACID SODIUM SALT(6994-45-2)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• F: 3
• Hazardous Substances Data: 6994-45-2(Hazardous Substances Data)

Usage

Uses

Sodium Myristylsulfonate is used as a surfactant for many other reactions.

InChI:InChI=1/C14H30O3S.Na/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-18(15,16)17;/h2-14H2,1H3,(H,15,16,17);/q;+1

Upstream product

• 112-71-0 1-Bromotetradecane 
• 2425-54-9 myristyl chloride 
• 629-59-4 tetradecane 
• 5981-19-1 5-undecyl-1,2-oxathiolane 2,2-dioxide 
• 563-43-9 ethylaluminum dichloride 

Downstream Products

• 1174585-91-1 C₂₃H₄₃N₂O₂S⁽¹⁺⁾*I^(1-) 
• 7314-37-6 tetradecane-1-sulfonic acid 

Relevant articles and documents

Preparation method for ion pair chromatographic reagent sodium 1-tetradecanesulphonate

The invention relates to a preparation method for ion pair chromatographic reagent sodium 1-tetradecanesulphonate. The method comprises the following steps: adding anhydrous sodium sulfite, water, 1-myristyl bromide and tetrapropylammonium bromide in sequence in a reaction container provided with a cooling reflux device and a mechanical stirring device, sulfonating for 16-24 hours, then evaporating water in a mixture after the sulfonation reaction through pressure reduction, drying and crushing remaining solid, putting in a Soxhlet extractor, extracting with absolute ethyl alcohol to generate a crude product, then recrystallizing the crude product with absolute ethyl alcohol, filtering and purifying twice to obtain a pure product, and finally drying for 2-4 hours to obtain a finished product. According to the preparation method, in the sulfonation reaction process of the sodium sulfite and the 1-myristyl bromide, the tetrapropylammonium bromide is taken as a crystal, and the activity of the 1-myristyl bromide is strengthened, so that the sulfonation reaction can be carried out successfully, the generation of byproducts is reduced, and the reaction time is obviously shortened.

Sulfonyl urea and carbamate ACAT inhibitors

A pharmaceutically useful compound which lowers blood cholesterol levels having the formula STR1 wherein X is oxygen or --NH--; Ar is phenyl, substituted phenyl, naphthyl or substituted naphthyl; R1 is hydrogen, lower alkyl or benzyl; and Rsub