Abstract: A method for removing residual cresidine from impure p-cresidine sulfonic acid which impure p-cresidine sulfonic acid contains from above two parts per billion to about 1500 parts per million of cresidine. The method comprises contacting an aqueous solution of the p-cresidine sulfonic acid with a sufficient quantity of particles of a crosslinked lipophilic porous resin for a sufficient time to reduce the concentration of p-cresidine in the cresidine sulfonic acid to less than 2 parts per billion.

Abstract: New compounds and a method for inhibiting the growth of fungus is disclosed which comprises contacting said fungus with a fungicidal amount of a phenyl glycine compound of the formula: ##STR1## wherein R.sub.1 and R.sub.2 are independently hydrogen, lower alkyl, substituted lower alkyl, cycloalkyl, substituted cycloalkyl, alkenyl, phenyl, substituted phenyl, halogen, amino or hydroxy groups; R.sub.3 is a hydrogen, lower alkyl, substituted lower alkyl, cycloalkyl, benzoyl, halo or nitro substituted benzoyl, substituted cycloalkyl, methylcarbamoyl, cyclohexylcarbamoyl, phenylcarbamoyl, halophenylcarbamoyl, methylphenylcarbamoyl, methylthiocarbamoyl, phenyl, substituted phenyl, napthyl group or --SO.sub.2 R.sub.7 where R.sub.7 is a hydrogen, alkyl, substituted alkyl, phenyl, substituted phenyl or amino group; R.sub.4 and R.sub.5 are independently hydrogen, lower alkyl or substituted lower alkyl groups and R.sub.6 is a hydrogen, lower alkyl or substituted lower alkyl, alkenyl or substituted alkenyl group.

Abstract: The invention describes a method for inhibiting the growth of pests comprising applying thereto a pesticidal amount of a compound of the formula ##STR1## wherein R.sub.1, and R.sub.2 are independently hydrogen, substituted or unsubstituted lower alkyl, cycloalkyl, phenyl, or alkenyl, and halogen, amino or hydroxy groups, R.sub.3 and R.sub.4 are independently hydrogen or substituted or unsubstituted lower alkyl, R.sub.5 is hydrogen, substituted or unsubstituted lower alkyl, cycloalkyl or phenyl, and naphthyl groups; pesticidal compositions containing at least one of said compounds; and novel thiohydantoin compounds having pesticidal activity.

Abstract: N-phenyl carbamoyl glycinate compounds of the formula ##STR1## wherein R is lower alkyl, are disclosed as having anti-convulsant activity; and, methods are disclosed for producing anti-convulsant activity by administering pharmaceutical compositions containing at least one of said compounds.

Abstract: A process for the preparation of meta sulfobenzoic acid wherein after solution sulfonation of benzoic acid, meta sulfobenzoic alkali metal salt is precipitated by treating the solution with an alkali metal salt at a temperature below about 120.degree. C. The precipitate is then filtered from the solution and rinsed at least once with a cold rinse solution containing from 3 to 10 percent of an alkali metal salt The resulting product has a lower concentration of alkali metal salt, usually sodium chloride, than was obtained using prior art methods. The product is especially suitable for use in a process to manufacture m-hydroxy benzoic acid.

Abstract: A method for recovering purified m-hydroxybenzoic acid from crude m-hydroxybenzoic acid alkali metal salt. The method comprises dissolving the crude m-hydroxy benzoic acid alkali metal salt in water at a ratio of between about 13 and 20 milliliters of water per gram of pure m-hydroxybenzoic acid alkali metal salt contained in the crude salt; acidifying the resulting solution to a pH of below 2 with a mineral acid to neutralize all alkali metal hydroxide present and to convert the m-hydroxybenzoic acid alkali metal salt to free m-hydroxybenzoic acid; and cooling the solution to from about 0.degree. C. to about 15.degree. C. for a sufficient time to crystallize purified m-hydroxybenzoic acid from the solution.The method is particularly effective for removing impurities of parahydroxybenzoic acid, alkali metal hydroxide and water soluble inorganic salts.

Abstract: A process for purifying 4,4'-dihydroxydiphenyl comprising contacting a solution of 4,4'-dihydroxydiphenyl alkali metal salt with activated carbon followed by removing the activated carbon from the solution and acidifying the solution with sufficient acid to convert essentially all of the 4,4'-dihydroxydiphenyl alkali metal salt to water insoluble 4,4'-dihydroxydiphenyl and 4,4'-dihydroxydiphenyl product containing less than 0.45 weight percent of 4-monohydroxydiphenyl impurity.

Abstract: A composition comprising polyethylene having from about 0.002 to about 1 weight percent of indigo dye uniformly melt dispersed therein. The average particle size of the dispersed indigo being less than about 1 micron. And the process for coloring polyethylene which comprises blending indigo into melted polyethylene at a concentration of from about 0.002 to about 1 percent by weight of polyethylene until a uniform dispersion is obtained.

Abstract: An anhydride blend of from 7 to 25 weight percent methyl endomethylenetetrahydrophathalic anhydride and from 75 to 93 weight percent hexahydrophthalic anhydride which is liquid at room temperature and imparts excellent properties to epoxy resins cured with the blend including unexpectedly high impact strength.

Abstract: A process for the preparation of 4,4' dihydroxydiphenyl by acidifying an alkali metal salt of 4,4' dihydroxydiphenyl. The alkali metal salt of 4,4' dihydroxydiphenyl is prepared by fusion of an alkali metal hydroxide with alkali metal diphenyl 4,4' disulfonic acid. Because the reaction may be carried out in granular form, or in a reaction which is made highly fluid by using potassium hydroxide with potassium diphenyl 4,4' disulfonic acid, or by reacting the alkali metal 4,4' disulfonic acid in increments with the hydroxide, low molar ratios of hydroxide to alkali metal diphenyl 4'4, disulfonic acid may be used. When potassium diphenyl 4,4' disulfonic acid is used in accordance with the invention, it is prepared by reacting 4,4' diphenyl disulfonic acid with an inorganic neutral potassium salt.

Abstract: Sulfonation of anthraquinone by a sulfur trioxide component including SO.sub.3 or oleum in a liquid sulfur dioxide solvent. When a mercury catalyst is used to give alpha anthraquinone sulfonate products, most of the mercury is left in the reactor or recovered with unreacted anthraquinone by precipitation with water after vaporization of the sulfur dioxide. High sulfuric acid and mercury pollution are thus avoided.