Abstract: A multi-component curable composition which is reactive upon admixing of the components and which comprises: (i) an acrylic polymer having acetoacetoxy functionality; and (ii) an acetoacetoxy functional derivative of a low molecular weight polyol; and (iii) a crosslinking component comprising at least one imine functional compound having an average of at least two imine groups per molecule which are reactive with acetoacetoxy functionality.

Abstract: This invention involves a process for minimizing corrosion of metals in contact with aqueous acid solutions wherein said process comprises adding to the aqueous acid solution a corrosion inhibiting amount of a dialkylaminomethyl aromatic triazole having the structure: ##STR1## wherein R.sub.1 is from 1 to 4 substituents and is hydrogen, aliphatic of 1 to about 12 carbons, alkoxy of 2 to about 10 carbons, aroxy of 2 to about 10 carbons, or --COOR.sub.4 wherein R.sub.4 is aliphatic of 1 to about 12 carbons; and R.sub.2 and R.sub.3 are the same or different and are alkyl of 1 to about 4 carbons.

Abstract: Antimicrobial compounds of the formula: ##STR1## where R is a heterocyclic radical selected from the group consisting of thienyl; furanyl; pyrrolyl; isoxazolyl; oxazolyl; isothiazolyl, thiazolyl; pyrazolyl; imidazolyl; pyridazinyl; pyrimidinyl; pyrazinyl; pyridinyl; and N-oxides thereof; andn is 0 to 4.

Abstract: Antimicrobial compounds of the formula: ##STR1## where R is C.sub.3-12 alkyl, straight or branched chain C.sub.3 -C.sub.8 cycloalkyl; C.sub.3-8 cycloalkylC.sub.1-3 alkyl; or saturated heterocyclic radical selected from the group consisting of pyrrolidinyl, tetrahydrofuranyl, tetrahydrothienyl, isoxazolidinyl, oxazolidinyl, isothiazolidinyl, pyrazolidinyl, imidazolidinyl, piperazinyl, and piperidinyl.

Abstract: Antimicrobial compounds of the formula: ##STR1## wherein Hal is bromine or chlorine; R is C.sub.1-4 alkyl, straight or branched chain; and one of R.sup.1 and R.sup.2 is hydrogen and the other is selected from the group consisting of C.sub.3-8 cycloalkyl; C.sub.3-8 cycloalkyl C.sub.1-3 alkyl; phenyl; phenyl C.sub.1-3 alkyl; mono- or disubstituted phenyl or phenyl C.sub.1-3 alkyl wherein the substituents are halo, C.sub.1-4 alkyl, C.sub.1-4 alkoxy, hydroxy, nitro, cyano, or trifluoromethyl; a heterocyclic radical selected from the group consisting of thienyl, furanyl, pyrrolyl, isoxazolyl, oxazolyl, isothiazolyl, thiazolyl, pyrazolyl, imidazolyl, pyridazinyl, pyrimidinyl, pyrazinyl, and pyridinyl, and N-oxides thereof; and a saturated heterocyclic radical selected from the group consisting of pyrrolidinyl, tetrahydrofuranyl, tetrahydrothienyl, isoxazolidinyl, oxazolidinyl, isothiazolidinyl, thiazolidinyl, pyrazolidinyl, imidazolidinyl, piperazinyl, and piperidinyl.

Abstract: Antimicrobial compounds of the formulas: ##STR1## where R.sup.1 and R.sup.2 are hydrogen; halo; C.sub.1-4 alkyl; C.sub.1-4 alkoxy; hydroxy; nitro; cyano; or trifluoromethyl;m is 0 or 1; andn is 1 or 2.