Examples of 'allyl chloride' in a sentence
Meaning of "allyl chloride"
Allyl chloride: A chemical compound used in various industrial processes, particularly in the production of plastics and pharmaceuticals. It is a colorless liquid with a pungent odor and is flammable and toxic if inhaled or ingested
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- The chlorinated derivative of propene 3-chloropropene that is used in the manufacture of pesticides and pharmaceuticals etc
How to use "allyl chloride" in a sentence
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allyl chloride
Allyl chloride is highly toxic and flammable.
The great majority of allyl chloride is converted to epichlorohydrin.
It is a byproduct in the chlorination of propene to make allyl chloride.
Propylene and allyl chloride are preferred.
One such process entails epoxidation of allyl chloride.
It is prepared by the reaction of allyl chloride with sodium hydroxide and methanethiol.
One example which may be mentioned is allyl chloride.
The above method of making allyl chloride commercially has several disadvantages.
Examples of allylic monomers include allyl alcohol and allyl chloride.
Infrared absorption spectrum elucidates that allyl chloride is adsorbed by the silanol groups.
Excess allyl chloride is stripped out on a kugelrohr apparatus to give the chloropropyl terminated oligomer.
The olefinic compound is preferably allyl chloride or propylene.
Crude allyl chloride often also contains residual propene from which the allyl chloride was made.
The photooxidation of allyl chloride.
Propylene and allyl chloride are preferred, and most particularly propylene.
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Substitution reactions are preferred in the production of allyl chloride from propylene and chlorine.
Allyl chloride is commercially prepared by the high-temperature chlorination of propene.
Selective distillation is a preferred method of removing hexadiene from commercially available allyl chloride feed.
Propylene, butylene and allyl chloride are suitable for use.
The olefin may be substituted, as for example in allyl chloride.
Distillation of the crude allyl chloride to remove light ends ;.
A process according to claim 7 where the azeotropic entrainer is allyl chloride.
It is prepared by the reaction of allyl chloride with tri-sodium cyanurate.
Reacting allyl chloride with hypochlorous acid to make a mixture of dichloropropanols ; and.
The monomer DADMAC is formed by reacting two equivalents of allyl chloride with dimethylamine.
Gaseous allyl chloride reacts too readily with the chlorine to trichloropropane, which is not useful.
The process according to claim 7 in which the azeotropic entrainer is allyl chloride.
Still another object is to manufacture allyl chloride in high yields from propane and / or propylene.
Epichlorohydrin, which is also industrially important, can be obtained from allyl chloride.
The process of claim 7, wherein the allyl chloride is methallyl chloride.
Second, less than half of the chlorine consumed is used to produce allyl chloride.
Then, 15 g of allyl chloride was added and the reaction was conducted for 36 hours.
The protocol of example 1 is carried out again with allyl chloride replacing bromoethane.
Subsequently, 15 g of allyl chloride was added to the reaction mixture, followed by reacting for 36 hours.
Preferably, an extraction solvent which also dissolves the starting allyl chloride well is used.
Similar free radical addition to allyl chloride and styrene gives 1-bromo-3-chloropropane and phenylethylbromide, respectively.
The procedure is as in Example 7, with replacement of the benzyl chloride with allyl chloride.
Belgian Patent 742,356 describes a process for synthesizing allyl chloride by gas phase substitutive chlorination of propylene.
The process of claim 1, wherein the allyl halide is allyl chloride.
Suitable alkenyl halides include, for example, allyl chloride or allyl bromide.
The process defined in claim 1, wherein the activator comprises allyl chloride.
Allyl isothiocyanate is produced commercially by the reaction of allyl chloride and potassium thiocyanate, [ 4 ].
The process of Claim 1 or 2 where the olefinic compound is allyl chloride.
The residue was triturated with 20 % ethyl acetate / toluene and the allyl chloride was collected by filtration.
For example, a carbamate ester of structure ( 13 ) is contacted with allyl bromide or allyl chloride.
Most preferred are hydrogen chloride, t-butyl chloride, allyl chloride and benzyl chloride.
There was obtained as an initial distillate 6.4 g of mixture of allyl chloride and allyl bromide.
Most preferred are hydrogen chloride, t - butyl chloride, allyl chloride and benzyl chloride.
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Examples of using Allyl
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Allyl alcohol can be obtained by many methods
A specific example of allyl bromide activation is as follows
Allyl chloride is highly toxic and flammable
Examples of using Chloride
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Do not use calcium chloride as a source of salt
Chloride pollution was one of the major concerns
The availability of chloride is not affected by soil pH
