43211-62-7

Basic information

• Product Name: ALLYL PALMITATE
• Synonyms: PALMITIC ACID ALLYL ESTER;ALLYL HEXADECANOATE;ALLYL PALMITATE;Allylpalmitate=Allylhexadecanoate
• CAS NO: 43211-62-7
• Molecular Formula: C₁₉H₃₆O₂
• Molecular Weight: 296.49
• Product Categories: monomer
• Mol File: 43211-62-7.mol
• Article Data: 7

Chemical Properties

• Melting Point: 25-26°C
• Boiling Point: 371.415°C at 760 mmHg
• Flash Point: 164.706°C
• Appearance: /
• Density: 0.87g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.45
• CAS DataBase Reference: ALLYL PALMITATE(CAS DataBase Reference)
• NIST Chemistry Reference: ALLYL PALMITATE(43211-62-7)
• EPA Substance Registry System: ALLYL PALMITATE(43211-62-7)

Safety Data

• Hazardous Substances Data: 43211-62-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C19H36O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-19(20)21-18-4-2/h4H,2-3,5-18H2,1H3

Upstream product

• 72165-62-9 2-chloro-1-(ichloromethyl)ethyl palmitate 
• 36653-82-4 1-Hexadecanol 
• 78-93-3 butanone 
• 51479-73-3 allyl trichloroacetimidate 
• 57-10-3 1-hexadecylcarboxylic acid 
• 107-18-6 allyl alcohol 
• 112-67-4 n-hexadecanoyl chloride 

Downstream Products

• 57-10-3 1-hexadecylcarboxylic acid 
• 542-44-9 (S)-2,3-dihydroxypropyl hexadecanoic acid ester 

Relevant articles and documents

Synthesis and characterization of allyl fatty acid derivatives as reactive coalescing agents for latexes

This work evaluated the use of allyl fatty acid esters derived from vegetable oil (palmitic acid, soybean and sunflower oils) as reactive coalescing agents in a waterborne latex system. Allyl fatty acid derivatives (AFAD) from vegetable oils were synthesized by two different processes. The synthesis was monitored by IR-spectroscopy and the final product characterized by FT-IR, GC-MS, 1H and 13C NMR. The presence of conjugated double bonds in the aliphatic chain was confirmed, which is a determinant for the proposed autoxidative latexes drying mechanism. Each of the AFAD were subsequently added to a standard acrylic emulsion, in order to study its potential as reactive coalescing agent. The minimum film-forming temperature (MFT), glass transition temperature (Tg), drying time and rubbing resistance to solvents were evaluated. The results showed that, when added to water-borne acrylic resins, an AFAD acts as a non-volatile plasticizer capable of autoxidative crosslinking with itself. AOCS 2012.

A tandem Finkelstein-rearrangement-elimination reaction: a straightforward synthetic route to allyl esters

Allyl esters can be obtained by a Finkelstein-rearrangement-elimination reaction of 2-chloro-1-(chloromethyl)ethyl esters induced by NaI. Sodium iodide can be used below equivalence using a reductive agent as sodium thiosulfate. High yields are obtained with most of the diverse esters studied. The method described avoids the use of allyl alcohol as a reagent. 2-Chloro-1-(chloromethyl)ethyl esters are prepared from glycerol, the main by-product of biodiesel industry. The effectiveness of iodine as reagent to hydrolyze allyl esters is also confirmed.

Esters, retroesters, and a retroamide of palmitic acid: Pool for the first selective inhibitors of N-palmitoylethanolamine-selective acid amidase

Cyclohexyl hexadecanoate, hexadecyl propionate, and N-(3-hydroxypropionyl)pentadecanamide, respectively ester, retroester, and retroamide derivatives of N-palmitoylethanolamine, represent the first selective inhibitors of "N-palmitoylethanolamine hydrolase" described so far. These compounds are devoid of affinity for CB1 and CB 2 receptors and characterized by high percentages of inhibition of N-palmitoylethanolamine-selective acid amidase (84.0, 70.5, and 76.7% inhibition at 100 μM, respectively) with much lower inhibitory effect on either fatty acid amide hydrolase or the uptake of anandamide.