CID 16211742

Base Information

• Chemical Name: CID 16211742
• CAS No.: 143-19-1
• Molecular Formula: C18H33NaO2
• Molecular Weight: 304.449
• Hs Code.: 29161500
• Mol file: 143-19-1.mol

Synonyms:SCHEMBL3583

Chemical Property of CID 16211742

Chemical Property:

• Appearance/Colour: white powder
• Vapor Pressure: 3.7E-06mmHg at 25°C
• Melting Point: 232-235 °C(lit.)
• Boiling Point: 359.999 °C at 760 mmHg
• Flash Point: 270.099 °C
• PSA: 40.13000
• Density: 0.9 g/cm³
• LogP: 4.77380
• Storage Temp.: −20°C
• Solubility.: Methanol (Slightly)
• Water Solubility.: soluble H2O, partially decomposes; soluble alcohol [HAW93]
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 15
• Exact Mass: 305.24564961
• Heavy Atom Count: 21
• Complexity: 234

Purity/Quality:

99% ^*data from raw suppliers

Sodium Oleate ^*data from reagent suppliers

Safty Information:

• Safety Statements: 22-24/25-25-24

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCCCCCCC=CCCCCCCCC(=O)O.[Na]
• Isomeric SMILES: CCCCCCCC/C=C\CCCCCCCC(=O)O.[Na]
• Uses: Sodium Oleate is the sodium salt of oleic acid. it functions as a binder, emulsifier, and anticaking agent. preparation of Turkey red oil, soft soap and other oleates; in polishing Compounds; waterproofing textiles, oiling wool; manufacture of driers; thickening lubricating oils. Pharmaceutic aid (solvent). The barium salt in rodent extermination. sodium oleate is a mild cleansing and foaming agent generally used in soaps. It is derived from natural fats and oils.

Technology Process of CID 16211742

There total 5 articles about CID 16211742 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:

Sodium laurate (629-25-4) + water (7732-18-5) + 1-dodecylthiol (112-55-0) → styrene (100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6) + 2,5-dimethyl-1,5-hexadiene (627-58-7) + sodium Oleate (143-19-1) + isoprene (78-79-5,9003-31-0)

Guidance literature:

at 50 ℃; Kinetics; entstehenden Dodecan-1-thiyl-Radikals;

DOI:10.1021/ja01137a055

Reference yield:

→ sodium Oleate (143-19-1) + potassium oleate (143-18-0)

Guidance literature:

Reference yield:

cis-Octadecenoic acid (112-80-1,2027-47-6) → sodium Oleate (143-19-1)

Guidance literature:

With sodium hydroxide; In water;

upstream raw materials:

Sodium laurate

water

1-dodecylthiol

cis-Octadecenoic acid

Downstream raw materials:

1,3-diolein

octadec-9-enoic acid propane-1,2,3-triyl ester

Elaidic acid

erythro-9,10-dihydroxystearic acid

Refernces

Preparation of sorbitol fatty acid polyesters, potential fat substitutes: optimization of reaction conditions by response surface methodology

10.1007/BF02518120

The research aimed to optimize the reaction conditions for the synthesis of sorbitol fatty acid polyesters (SFPE), potential fat substitutes, using response surface methodology. The study focused on four parameters: reaction temperature, reaction time, mole ratio of fatty acid methyl esters (FAME) to sorbitol, and mole ratio of fatty acid sodium soaps (FASS) to sorbitol. The chemicals used included sorbitol, methyl oleate, sodium oleate, and potassium carbonate. The research concluded that the optimum conditions for high yield of SFPE were a reaction temperature of 144°C, a reaction time of 6.65 hours, a mole ratio of FAME to sorbitol of 10.7:1, and a mole ratio of FASS to sorbitol of 0.77:1, resulting in an experimental yield close to the predicted value of 94%.