Acetic acid, 2-sulfo-,dodecyl ester, sodium salt (1:1)

Base Information

• Chemical Name: Acetic acid, 2-sulfo-,dodecyl ester, sodium salt (1:1)
• CAS No.: 1847-58-1
• Molecular Formula: C14H27NaO5S
• Molecular Weight: 330.421
• Hs Code.: 2914509090
• European Community (EC) Number: 217-431-7
• Mol file: 1847-58-1.mol

Synonyms:1847-58-1;Acetic acid, 2-sulfo-,dodecyl ester, sodium salt (1:1);C14H27O5S.Na;C14H28O5S.Na;Sodium 2- (dodecyloxy)- 2- oxoethane- 1- sulphonate;SCHEMBL121776;s3801;2-dodecoxy-2-oxoethanesulfonic acid;sodium;A812887;2-dodecoxy-2-oxidanylidene-ethanesulfonic acid

Chemical Property of Acetic acid, 2-sulfo-,dodecyl ester, sodium salt (1:1)

Chemical Property:

• PSA: 91.88000
• LogP: 4.07650
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility.: DMSO (Slightly), Methanol (Slightly, Heated)
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 14
• Exact Mass: 331.15551444
• Heavy Atom Count: 21
• Complexity: 332

Purity/Quality:

>98% ^*data from raw suppliers

SodiumLaurylSulfoacetate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Other Uses -> Emulsifiers/Surfactants
• Canonical SMILES: CCCCCCCCCCCCOC(=O)CS(=O)(=O)O.[Na]
• Description: Sodium lauryl sulfoacetate is an anionic surfactant. It increases proliferation of isolated chicken peripheral blood mononuclear cells (PBMCs) when used at concentrations ranging from 62.5 to 500 μg/ml. Sodium lauryl sulfoacetate (1, 2, and 4 mg/kg) increases the blood CD4+ to CD8+ T cell ratio induced by a Newcastle disease virus vaccine in chickens. Formulations containing sodium lauryl sulfoacetate have been used as surfactants in the manufacture of cosmetics. Sodium Lauryl Sulfoacetate is derived from coconut and palm oils; a safe, skin-friendly surfactant (foaming agent) for both skin and hair. This mild plant-derived surfactant creates a rich, luxurious lather that effectively removes surface oil, dirt, and bacteria without stripping or drying sensitive skin or hair.
• Uses: Sodium Lauryl Sulfoacetate,can be used in the preparation of new surfactants of sodium cocoyl threoninate and sodium cocoyl glutamate that offer outstanding mildness, moisturization properties, and good foaming ability.

Technology Process of Acetic acid, 2-sulfo-,dodecyl ester, sodium salt (1:1)

There total 4 articles about Acetic acid, 2-sulfo-,dodecyl ester, sodium salt (1:1) 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:

methanesulfonic acid (75-75-2,98527-29-8) + lauryl acetate (112-66-3) → sodium lauryl sulphoacetate (1847-58-1)

Guidance literature:

methanesulfonic acid; With sodium carbonate; at 55 ℃; for 0.666667h;

lauryl acetate; at 30 ℃; for 0.5h;

Reference yield:

dodecyl bromoacetate (3674-07-5) → sodium lauryl sulphoacetate (1847-58-1)

Guidance literature:

With sodium sulfite; In water; for 1h; Heating;

DOI:10.1007/BF00807558

Reference yield:

1-dodecyl alcohol (112-53-8) → sodium lauryl sulphoacetate (1847-58-1)

Guidance literature:

Multi-step reaction with 2 steps

1: conc. HCl / toluene / 4 h / Heating

2: Na₂SO₃ / H₂O / 1 h / Heating

With hydrogenchloride; sodium sulfite; In water; toluene;

DOI:10.1007/BF00807558

upstream raw materials:

dodecyl bromoacetate

1-dodecyl alcohol

methanesulfonic acid

lauryl acetate

Refernces

• 1、 -. "Dodecyl sodium sulfoacetate synthesis process". Paragraph 0034; 0037-0039. . Retrieved 2019/02/13.