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:
WHEREIN R AND R'' ARE EITHER STRAIGHT CHAIN OR PREDOMINANTLY STRAIGHT CHAIN BUT DISSIMILAR SLKYS, EACH RANGING FROM 7 TO 15 CARBONS, AND AT LEAST ONE OF WHICH HAS AN ODD NUMBER OF CARBONS, THE SUM OF CARBON ATOMS IN R AND R'' BEING IN THE RANGE OF FROM 20 TO 22 CARBONS, AND WHEREIN X IS A BIOCIDALLY ACCEPTABLE ANION PREFERABLY DERIVED FROM A HALOGEN SUCH AS BROMINE OR CHLORINE, OR WHICH MAY BE METHOSULFATE. THESE COMPOUNDDS HAVE EFFECTIVE BIOCIDAL ACTIVITY EVEN IN HARD WATER, UNLIKE OTHER QUATERNARY AMONIUM COMPOUNDS WHICH ARE INHIBITED IN THEIR BIOCIDAL ACTIVITY BY HARD WATER. THEY ARE HIGHLY EFFECTIVE FOR THE SANITIZATION OF ALL TYPES OF SURFACES AS WELL AS EGGS, FRUITS, VEGETABLES AND SIMILAR PRODUCTS.
R-N(+)(-R'')(-CH3)2 X(-)
WATER-SOLUBLE UNSYMMETRRICAL DI-HIGHER ALKYL DIMETHYL AMMONIUM SALTS HAVING THE STRUCTURE:
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:
Slimicidal treatment of water in recirculated water systems such as in cooling towers, air-conditioners, humidifiers and the like. The treatment consists of the introduction into the water of an Alpha -halo, Alpha , Beta -unsaturated carbonyl compound, particularly of Alpha -halocinnamaldehyde.
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:
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