Examples of 'chloroacetic acid' in a sentence
Meaning of "chloroacetic acid"
chloroacetic acid: Chloroacetic acid is a chemical compound that is often used in various industrial processes, such as the production of pharmaceuticals, herbicides, and dyes. It is a type of organic acid with the chemical formula ClCH2COOH
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- The chlorinated derivative of acetic acid CHâ‚‚Cl-COOH that is used in organic synthesis
How to use "chloroacetic acid" in a sentence
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chloroacetic acid
Preparation of malonic acid from chloroacetic acid.
Chloroacetic acid is prepared industrially via two routes.
The source of carboxylic acid was chloroacetic acid.
Chloroacetic acid is used widely in various activities in mining.
Sodium chloroacetate is the sodium salt of chloroacetic acid.
The chloroacetic acid concentration is determined from calibration standards.
The first permeation standard contains chloroacetic acid.
Chloroacetic acid is especially preferred.
The react is continued until chloroacetic acid is consumed completely.
Chloroacetic acid also works.
The system was reacted until chloroacetic acid was completely consumed.
Chloroacetic acid solution.
Thioindigo is generated by the alkylation of the sulfur in thiosalicylic acid with chloroacetic acid.
Mono chloroacetic acid was further used as soon as the solution was still fluid.
This method is used for the production of thioglycolic acid from chloroacetic acid.
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The present synthetic route uses chloroacetic acid and benzyl alcohol as the starting materials.
Another class of amphoteric surfactants is formed by the reaction of imidazoline with chloroacetic acid.
Such a conversion can be accomplished through reaction with chloroacetic acid followed by reaction with carbodiimide.
Chloroacetic acid easily penetrates skin and mucous membranes and interferes with cellular energy production.
The obtained reaction mixture was washed with water to remove excess chloroacetic acid.
Chloroacetic acid is converted to chloroacetyl chloride, a precursor to adrenaline epinephrine.
The sorption standard for evaluating the nonwoven test mats contains chloroacetic acid.
Chloroacetic acid in an alcoholic solvent selected from the group comprising of,.
Particularly preferred is the use of bromoacetic acid and chloroacetic acid in the carboxymethylation step a.
Like other chloroacetic acids and related halocarbons, chloroacetic acid is a hazardous alkylating agent.
This conversion can be accomplished through reaction with chloroacetic acid followed by reaction with carbodiimide.
Iodoacetic acid is more toxic than bromoacetic acid and much more toxic than chloroacetic acid.
It may be prepared from chloroacetic acid and thionyl chloride, phosphorus pentachloride, or phosgene.
Subsequently, the thiouronium is converted to an acid with chloroacetic acid.
Chloroacetic acid ( Fluka ) was coupled by freshly prepared symmetrical anhydride.
In an embodiment, the halogenated acid is chloroacetic acid or a salt thereof.
Preferred acids are acetic acid, propionic acid, trifluoroacetic acid, methanesulfonic acid and chloroacetic acid.
Composition according to claim 8, wherein the chloroacetic acid is dichloroacetic acid.
CMC, for instance, is synthesized by the alkali-catalyzed reaction of cellulose with chloroacetic acid.
The physical and chemical parameters of chloroacetic acid are provided in Table 4.
It is synthesized by the alkali-catalyzed reaction of cellulose with chloroacetic acid.
The amino acids and chloroacetic acid were pre-activated using HBTU before coupling.
In the laboratory, it may be synthesized from chloroacetic acid and methylamine.
Chloroacetic acid ( and its salts ).
Exposure can be fatal if greater than 6 % body surface area is exposed to chloroacetic acid.
XII is then treated with carbon disulfide, chloroacetic acid and triethylamine to yield intermediate XIII.
Para-Nitrophenol is alkylated by means of an ester of chloroacetic acid.
Subsequently, 83 g of chloroacetic acid methyl ester was added dropwise.
The method of claim 1 wherein the halogenated acid is chloroacetic acid or a salt thereof.
Additional chloroacetic acid ( 2.0 g ) was added as necessary to drive the reaction to completion.
The desired thioamide was produced by activating 2 with chloroacetic acid and treating with amine 3.
The chloroacetic acid ( 64 equivalents ) is linked twice with one activation with diisopropylcarbodiimide ( 32 equivalents ).
The most hazardous chemicals to the environment were phenol, chloroacetic acid and acrylamide solution.
Chloroacetic acid ( monochloroacetic acid, MCA ), dichloroacetic acid ( considered a by-product ), and trichloroacetic acid.
This was deprotected with chloroacetic acid to give 55.
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