Vinyl laurate

Base Information

• Chemical Name: Vinyl laurate
• CAS No.: 2146-71-6
• Molecular Formula: C14H26 O2
• Molecular Weight: 226.359
• Hs Code.: 29159000
• European Community (EC) Number: 218-414-7
• NSC Number: 32650
• UNII: CP59R9UN62
• DSSTox Substance ID: DTXSID7074953
• Nikkaji Number: J42.302E
• Wikidata: Q82003058
• Mol file: 2146-71-6.mol

Synonyms:ethenyl dodecanoate;vinyl laurate

Chemical Property of Vinyl laurate

Chemical Property:

• Vapor Pressure: 0.00237mmHg at 25°C
• Melting Point: 7℃
• Refractive Index: n20/D 1.441
• Boiling Point: 288.2°Cat760mmHg
• Flash Point: 100.8°C
• PSA: 26.30000
• Density: 0.876g/cm³
• LogP: 4.59400
• Solubility.: H2O: slightly soluble1g/L at 20°C
• XLogP3: 5.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 12
• Exact Mass: 226.193280068
• Heavy Atom Count: 16
• Complexity: 176

Purity/Quality:

99% ^*data from raw suppliers

Vinyl laurate ^*data from reagent suppliers

Safty Information:

• Safety Statements: 23-24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCCCCCCCCCC(=O)OC=C
• Uses: Vinyl laurate was used in the synthesis of laurate and stearate esters of corn starch. It was used as the acyl donor during synthesis of sucrose laurate esters catalyzed by Bacillus pseudofirmus AL-89 . Vinyl laurate was also used in the preparation of chirally deuterated benzyl chlorides. Vinyl laurate can be used to synthesize the following:sucrose laurate esters from sucrose in organic solventspoly(vinyl laurate) (PVL)latexesporous conducting ‘‘soft′′ polymer foams which can be used as gas sensors

Technology Process of Vinyl laurate

There total 6 articles about Vinyl laurate 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: 75.0%

lauric acid (143-07-7) + vinyl acetate (108-05-4,9003-20-7) → vinyl laurate (2146-71-6)

Guidance literature:

With [Ru₃O(OAc)₆(H₂O)₃]OAc; acetic acid; at 140 ℃; under 5250.53 Torr; Flow reactor;

Reference yield: 68.0%

→ vinyl laurate (2146-71-6)

Guidance literature:

With 1,10-Phenanthroline; palladium diacetate; at 140 ℃; for 1.25h; under 15001.5 Torr;

Reference yield: 16.0%

lauric acid (143-07-7) + ethene (74-85-1) → vinyl laurate (2146-71-6)

Guidance literature:

With trihexyl(tetradecyl)phosphonium chloride; tetrabutyl-ammonium chloride; copper diacetate; palladium diacetate; tetrahexylammonium chloride; copper dichloride; Catalytic behavior; High pressure;

upstream raw materials:

lauric acid

vinyl acetate

n-dodecanoyl chloride

acetaldehyde

Downstream raw materials:

1,3-dilauroylglycerol

lauric acid

prostaglandin A₂

(S)-1-phenylethanol

Refernces

• 1、 -. "PROCESS FOR THE PRODUCTION OF HIGHER CARBOXYLIC ACID VINYL ESTERS". Page/Page column 40-41. . Retrieved 2017/01/31.
• 2、 -. "Transvinylation as a First Stage of Coupling Production of Vinyl Esters and Acetic Acid or Propionic Acid Reaction Products". Paragraph 0058-0059. . Retrieved 2014/12/09.