Abstract:
A METHOD OF PRESERVING METAL-WORKING FLUIDS AGAINST MICROORGANISMS BY ADDING THE COMPOUND 1-AMINOETHYL2-NAPHTHENYL IMIDAZOLINE, HAVING THE STRUCTURE:
1-(H2N-CH2-CH2-),2-R-2-IMIDAZOLINE
WHEREIN R IS THE RESIDUE OF NAPHTHENE-CARBOXYLIC ACID AS A MICROBIOCIDAL PRESERVATIVE AGENT.
Abstract:
Antimicrobial 1, 2, 4, 5-tetrasubstituted benzenes having the structure:
WHEREIN R and R'' and may be methyl, or a halogen when R'''''' is CH2-; or R and R'', taken together, may be methylene dioxy; R'''' may be methyl or nitro; R'''''' may be absent or may be -CH2 - or CH ; and X is the residue of a substituted amino or a polyamino radical.
Abstract:
MICROBIOCIDAL BIS-AMINO SUBSTITUTED HALOGENATED BIPHENYLS, AS WELL AS THE NITROGEN DERIVATIVES THEREOF SUCH AS QUATERNARY AMMONIUM COMPOUNDS, AMINE OXIDES, IMIDAZOLINES, AMIDES, ENAMINES, AMPHOLYTES, AND THE LIKE.
Abstract:
MICROBIOCIDAL AMMONIA AND AMINO SUBSTITUTED HALOGENATED BIPHENYLS, AS WELL AS THE NITROGEN DERIVATIVES THEREOF SUCH AS QUATERNARY AMMONIUM COMPOUNDS, AMINE OXIDES, IMIDAZOLINES, AMIDES, ENAMINES, AMPHOLYTED, AND THE LIKE. THE AMMONIA AND AMINO HALOBIPHENYLS ARE PREPARED BY REACTING THE AMMONIA OR THE AMINE AND THE HALOBIPHENYL REACTANTS IN SUCH A MANNER THAT THE RATIO OF AMINE TO HALOBIPHENYL IS PREFERABLY LIMITED TO BETWEEN TWO AND FIVE MOLS OF AMINE TO EACH MOL OF HALOBIPHENYL.
Abstract:
Microbiocidal ammonia and amino substituted halogenated biphenyls, as well as the nitrogen derivatives thereof such as quaternary ammonium compounds, amine oxides, imidazolines, amides, enamines, ampholytes, and the like. The ammonia and amino halobiphenyls are prepared by reacting the ammonia or the amine and the halobiphenyl reactants in such a manner that the ratio of amine to halobiphenyl is preferably limited to between two and five mols of amine to each mol of halobiphenyl.
Abstract:
MICROBIOCIDAL AMMONIA AND AMINO SUBSTITUTED HALOGENATED BIPHENYLS, AS WELL AS THE NITROGEN DERIVATIVES THEREOF SUCH AS QUATERNARY AMMONIUM COMPOUNDS, AMINE OXIDES, IMIDAZOLINES, AMIDES, ENAMINES, AMPHOLYTES, AND THE LIKE. THE AMMONIA AND AMINO HALOBIPHENYLS ARE PREPARED BY REACTING THE AMMONIA OR THE AMINE AND THE ALOBIPHENYL REACTANS IN SUCH A MANNER THAT THE RATIO OF AMINE TO HALOBIPHENYL IS PREFERABLY LIMITED TO BETWEEN TWO AND FIVE MOLS OF AMINE TO EACH MOL OF HALOBIPHENYL.
Abstract:
ANTIMICROBIAL 1, 2, 4, 5-TETRASUBSTITUTED BENZENES HAVING THE STRUCTURE:
1-R,2-R'',4-R",5-(X-R"''-)-BENZENE
WHEREIN R AND R'' MAY BE MEHYL, OR A HALOGEN WHEN R"'' IS-CH2-; OR R'', TAKEN TOGETHER, MAY BE METHYLENE DIOXY; R" MAY BEMETHYL OR NITRO; R" MAY BE ABSENT OR MAY BE -CH2 OR--CH=;AND X IS THE RESIDUE OF A SUBSTITUTED AMINO OR A POLYAMINO RADICALS.
Abstract:
A METHOD OF INHIBITING MICROORGANISMS WHICH COMPRISES APPLYING TO THE ENVIROMENT IN WHICH SUCH MICROORGANISMS ARE FOUND AMMONIA AND AMINOSUBSTITUTED HALOGENATED BIPHENYLS, AS WELL AS THE NITROGEN DERIVATIVES THEREOF SUCH AS QUENTERNARY AMMONIUM COMPOUNDS AMINE OXIDES, IMIDAZOLINES, AMIDES, ENAMINES, AMPHOLYTES, AND THE LIKE. THE AMMONIA AND AMINO HALOBIPHENYLS ARE PREPARED BY REACTING THE AMMONIA OR THE AMINE AND THE HALOBIPHENYL REACTANTS IN SUCH A MANNER THAT THE RATIO OF AMINE TO HALOBIPHENYL IS PREFERABLY LIMITED TO BETWEEN TWO AND FIVE MOLS OF AMINE TO EACH MOL OF HALOBIPHENYLo