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Amination hydroxy

Water repellant To impart water-resistant properties, particularly in greases Aliphatic amines, hydroxy fatty acids and some organic silicone polymers... [Pg.450]

An adequate set of kinetic equations must describe the rate at which functional groups (epoxides, primary and secondary amines, hydroxy groups), rather than individual species (monomers, dimers, i-mers), evolve during reaction. This assumes that the rate at which a functional group reacts does not depend on the size (finite or infinite) of the molecule to which it is attached. The implication of this hypothesis may be understood if we write Eqs (5.6) and (5.7) in terms of the formation of an activated complex. [Pg.161]

The raw materials used to synthesize organic dyes are commonly referred to as dye intermediates. Largely, they are derivatives of aromatic compounds obtained from coal tar mixtures. The majority of these derivatives are benzene, naphthalene, and anthracene based compounds. This section provides an overview of the chemical reactions used to prepare the key intermediates employed in dye synthesis. In this regard, emphasis is placed on halogenated, aminated, hydroxy-lated, sulfonated, and alkylated derivatives of benzene, naphthalene, and anthraquinone. [Pg.538]

SA " r R1 aliphatic and aromatic amines, hydroxy, ester, protected [109] a- and p-amino acids amino, furyl, thienyl aromatic and heteroaromatic aldehydes 2-mercapto acids... [Pg.98]

The CR NR group can be introduced into ammonia, amines, hydroxy compounds, carboxamides, and sulfonamides to form amidines, imido-esters, etc., via imidosulfonates, obtained by the Beckmann rearrangement of oxime sulfonates.—B Benzophenone oxime benzene sulfonate and aniline warmed in benzene, and, after the exothermic reaction has ceased, further refluxed for 15-30 min. —>- N,N -diphenylbenzamidine. Y 92.5%. (F. e. s. P. Oxley and W. F. Short, Soc. 1948,1514.)... [Pg.355]

Redistribution during thermal processing is a common self-reaction in condensation polymers such as PA, PEST, and PC that often contain nucleophilic amine, hydroxy, or phenolic end-groups, along with electrophilic groups such as amide, ester, or carbonate linking the individual monomer units. [Pg.351]

With A5 acids (such as the C20 acids in meadowfoam oil), the 8 lactone is formed in high yield when the acid is refluxed for 3 h with perchloric acid in dichloromethane. The proportion of 8 to y lactone depends on the reaction solvent. In hexane, the ratio is 6 1 and in dichloromethane almost 40 1. The 8-lactone is much more reactive than its y isomer. It can be converted to hydroxy amides (amines), hydroxy acids (alkali), and alkoxy esters (alcohol and acid) wifli the reagents indicated in parentheses. [Pg.13]

Hydroxy Water Urea Amine Hydroxy Water Urea Amine... [Pg.108]

A wide range of fluorescent derivatization reagents and techniques have been developed to utilize the analytical advantages that fluorescence offers. These derivatization reagents are usually specific to functional groups (e.g., amine, hydroxy, thiol), and their specificity offers yet another opportunity for discriminating against interferents. For excellent reviews, the reader is referred to references [38] and [39]. [Pg.42]

Eric R. Taylor, Lethal Mists (Commack, New York Nova Science Publishers, Inc. 1999) p. 79. Phosgene reacts strongly with those groups found in amino acids, the amine, hydroxy, and sulfhydryl. [Pg.276]

Amines, Hydroxy and Ketoximes Methyl ethyl ketoxime... [Pg.147]


See other pages where Amination hydroxy is mentioned: [Pg.69]    [Pg.965]    [Pg.181]    [Pg.679]    [Pg.69]    [Pg.261]    [Pg.604]    [Pg.18]    [Pg.401]    [Pg.69]    [Pg.547]    [Pg.223]    [Pg.156]    [Pg.817]    [Pg.17]    [Pg.532]    [Pg.1092]    [Pg.178]    [Pg.1035]    [Pg.650]    [Pg.33]    [Pg.44]    [Pg.53]   


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3- Hydroxy-4-pentenyl amines

4-hydroxy-1-alkanone amine

Alkene Hydroxy amination

Amines hydroxy acids

Amines hydroxy, rearrangement

Amines quinolines, 4-hydroxy

Amines, 3-hydroxy asymmetric epoxidation

Amines, 3-hydroxy kinetic resolution

Amines, A-hydroxy

Amines, p-hydroxy

Carbonyl compounds, a-hydroxy via keto aminals

Hydroxy amines

Hydroxy amines

Hydroxy amines allyl alcohol

Hydroxy amines from /3-amino aldehydes

Hydroxy amines from aldehydes

Hydroxy amines from alkenes

Hydroxy amines from amides

Hydroxy amines from amino esters

Hydroxy amines from amino ketones

Hydroxy amines from ammonia

Hydroxy amines from carbamates

Hydroxy amines from epoxides

Hydroxy amines from halo alcohols

Hydroxy amines from imines

Hydroxy amines from ketones

Hydroxy amines from oxides

Hydroxy amines from phenols

Hydroxy amines imines

Hydroxy amines oxidation

Hydroxy amines oxidative cleavage

Hydroxy amines reaction with nitrous acid

Hydroxy amines reductive alkylation

Hydroxy diphenyl amine

Hydroxy halides, alkylation amination

Hydroxy propyl amine

Hydroxy-de-amination

Reaction with hydroxy amines

Silylation-amination of hydroxy N-heterocycles

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