Abstract: This invention provides certain N-phenyl-N'-substitutedphenylsulfonylureas compounds, formulations, and a method for treating susceptible neoplasms in mammals using the sulfonylurea compounds.

Abstract: This invention relates to inhibiting leaching of crop treating chemicals into the ground water, aqua-system and surrounding soil of the treatment site by contacting the plant or plant site with an effective leach inhibiting, plant tolerating amount of a lactam containing polymer selected from the group of a crosslinked or non-crosslinked N-alkenyl lactam homopolymer or copolymer with a C.sub.2 to C.sub.30 comonomer selected from the group of an alkenoic acid; an alkenyl- anhydride, ester, ether, amino ester or amino amide and an alpha mono- or di- olefin, in which the lactam unit of the polymer is represented by the formula ##STR1## wherein R is C.sub.3 to C.sub.6 alkylene optionally substituted with C.sub.1 to C.sub.20 alkyl; R.sub.1 and R.sub.2 are each independently C.sub.2 to C.sub.20 alkyl or hydrogen and n has a value of from 0 or 2.

Abstract: A method for treating ALS (Amyotrophic Lateral Sclerosis) is disclosed. The inventive method comprises the administration of controlled dosages of dextromethorphan in therapeutically effective amounts in a pharmaceutically acceptable vehicle Dextromethorphan (DMP) is a dimethylaminomethyl-substituted phenol, a sigma receptor antagonist known also as d-3-methoxy-N methylmorphinan, a d-isomer of the codeine analog, levorphanol. The inventive method has proven useful in controlling the progression of ALS in afflicted patients.

Abstract: This invention relates to inhibiting leaching of crop treating chemicals into the ground water, aqua-system and surrounding soil of the treatment site by contacting the plant or plant site with an effective leach inhibiting, plant tolerating amount of a nitrogen-containing copolymer having pendant nitrogeneous groups which contains between about 40 and about 98 wt. % of monomer unit A defined by the formula ##STR1## and 2 to 40 wt. % of comonomer unit B ##STR2## wherein X is hydrogen, a C.sub.1 to C.sub.22 radical of the group alkyl, alkoxy, aryl, alkaryl, aryloxy and alkaryloxy;R.sub.2 is hydrogen or --(CO).sub.y' OR';R, R.sub.1, R.sub.3 and R' are each selected from the group of hydrogen and lower alkyl;R.sub.6 is hydrogen or ##STR3## x, y, y' and z each have a value of 0 or 1; a has a value of from 2 to 4;Z is --O-- or --NH--Y is an optionally quaternized group of ##STR4## and R.sub.4 and R.sub.5 are hydrogen or lower alkyl except that at least one of R.sub.4 and R.sub.5 is lower alkyl.

Abstract: This invention relates to inhibiting leaching of crop treating chemicals into the ground water, aqua-system and surrounding soil of the treatment site by contacting the plant or plant site with an effective leach inhibiting, plant tolerating amount of a copolymer of a maleic acid, the corresponding C.sub.1 to C.sub.6 alkyl ester of said acid or a mixture thereof and a comonomer of an alkyl alpha alkenyl ether; which copolymers have a molecular weight (Mw) of from about 8,000 to about 3,000,000 and can be directly incorporated into a standard agrichemical formulation.

Abstract: Compounds of the formula IV for use as local anesthesia and analgesia, as well as a method for their preparation, their pharmaceutical preparations and their use.

Abstract: Methods and compositions for the protection of plant tissue from damage upon exposure to certain environmental and handling stresses, and to assist plant tissue in recovering from environmental and handling stress injuries, include the application of an effective amount of stress-protectant compositions selected from the group consisting of tetrahydrofurfuryl alcohol, tetrahydrofurfuryl amine and mixtures thereof. The compositions are applied as aqueous solutions containing between about 0.005 and about 25 wt % of the stress-protectant components. Surfactants may be included to improve application of the compositions to the plant tissues.

Abstract: Methods and compositions for the protection of plant tissue from damage upon exposure to chemical stresses, and to assist plant tissue in recovering from chemical stress injuries, include the application of an effective amount of chemical stress-protectant compositions selected from the group consisting of tetrahydrofurfuryl alcohol, tetrahydrofurfuryl amine and mixtures thereof. The compositions are applied as aqueous solutions containing between about 0.005 and about 25 wt % of the stress-protectant components. Surfactants may be included to improve application of the compositions to the plant tissues.

Abstract: Microcapsule formulations are combined with emulsions or particle dispersions in a single-package formulation which is storage-stable and provides substantially the full efficacy of each of the two forms as if applied individually. The single-package formulation is suspension having two dispersed phases--the first being an active species encapsulated in a shell of inert polymeric diffusion-limiting material (i.e., a microcapsule), and the second being an active species in water-insoluble form with no diffusion-limiting barrier at its surface. An appropriate suspension system is included to prevent the dispersed phases from agglomerating within themselves and with each other. The invention is useful in combining two different active ingredients as well as in combining immediate-delivery and delayed-delivery forms of the same active ingredient.

Abstract: Disclosed is a 1,3,2-dioxathiolan-S-oxide derivative as represented by the general formula (I): ##STR1## (where R.sub.1 and R.sub.2 are identical to or different from each other and each is a hydrogen atom or a lower alkyl group;X is a halogen atom, a cyano group, a lower alkyl group, a haloalkyl group or a phenyl group;m is 0 or an integer from 1 to 5; and when small m is greater than 1 each x can be the same or different andn is 1 or 2).A 1,3,2-dioxathiolan-2-oxide derivative of the compound as represented by the general formula (I-I) is prepared by reacting a hydroxymethylcyclopentanol derivative with thionyl chloride; and a 1,3,2-dioxathiolan-2,2-dioxide derivative (I-II) thereof is prepared by oxidizing the compound (I-I). The compounds (I) can be employed as fungicides and intermediate compounds for the preparation of azolylmethylcyclopentanol derivatives.

Abstract: A process for preparing suture-grade .beta.-glycolide by purifying crude glycolide which comprises contacting the crude glycolide with a primary solvent which will dissolve the crude glycolide and residual impurities without dissolving primary impurities; removing the primary impurities; recovering the glycolide and residual impurities by evaporating the primary solvent at a temperature below 42.degree. C.; removing residual impurities by washing the glycolide with a washing solvent in which the residual impurities are soluble; and isolating the .beta.-glycolide crystals which remain.

Abstract: A dry, water-soluble, substituted phenoxy and/or benzoic acid herbicide is prepared by dry blending the herbicide in acid form with a dry solid solubilization medium selected from the group consisting of diammonium phosphate, dipotassium phosphate, and disodium phosphate. At least about 1.15 moles of the medium are provided for each mole of active herbicidal agent in the initially dry blended mixture.

Abstract: The invention relates to synergistic herbicidally active compositions. The quantity required for a given herbicidal effect is substantially lower than that required for the herbicide itself. The compositions of the invention comprise in combination a herbicide which brings about active oxygen species formation in plants and a substance which binds copper or zinc, or a substance which reacts with a thiol moiety of a thiol containing enzyme. The herbicide and metal binding or thiol binding component can be applied together or separately.

Abstract: Disclosed are novel compounds of the formula ##STR1## wherein: R is ##STR2## where Ph is phenyl, or ##STR3## X is --NR.sub.5 R.sub.6 or --OR.sub.7 ; R.sub.1 and R.sub.2 are independently hydrogen, methyl, ethyl, cyclohexyl, ##STR4## butyl, or heptyl; R.sub.4 is o-phenylene or p-phenylene and R.sub.4 can be alkyl- halo- or alkoxy- substituted;R.sub.3 is hydrogen;R.sub.5, R.sub.6, and R.sub.7 are independently hydrogen, methyl, ethyl, tert-butyl, isobutyl, butyl, alkoxy, acyl, acylamino, aryl, amino, cyclohexyl, aminoalkyl and substituted or unsubstituted phenylamino;Y is sulfur and oxygen atom; and n is zero or 1; provided n=1 when Y is sulfur.

Abstract: Magnetic resonance imaging contrast media used to affect the relaxation times of atoms in body tissues undergoing NMR diagnosis are disclosed. Such media comprise (1) a paramagnetic, physiologically compatible complex of (a) a chelant consisting of a N-carboxy methylated tetraazacyclododecane, and (b) a paramagnetic ion of a lanthanide element of atomic numbers 59-70, or of a transition metal of atomic numbers 21-29, 42 or 44, or a physiologically compatible salt of such a complex, and (2) a toxicity-reducing amount of labile calcium ions. The labile calcium ions can be derived from a source other than a salt of said chelant, e.g. an inorganic or organic calcium salt. NMR image-enhancing compositions comprising NMR image-enhancing effective amounts of said contrast media and pharmaceutically acceptable diluents are also disclosed.

Abstract: A method for the treatment of a harvested plant part with L(+) adenosine or 1-triacontanol to improve the quality of the parts, such as fruit, vegetables (including root vegetables) and leaves. The method includes applying the L(+) adenosine or 1-triacontanol to the part of the plant after harvest of the fruit or vegetable. The acidity or sugar content of the plant part and thus the sugar to acid ratio is particularly affected by the treatment.

Abstract: This invention relates to compounds which are derivatives of cyclopentane which are useful as antihypertensive agents, to pharmaceutical compositions including such compounds, and to their use in treating hypertension.

Abstract: The present invention provides pharmaceutically useful compounds which are aminosulfonyl urea compounds which are ACAT inhibitors rendering them useful in controlling blood cholesterol levels, pharmaceutical compositions and methods of using the ACAT inhibitors and closely related compounds which are also aminosulfonyl urea compounds.

Abstract: Phenolic compounds, particularly phenol, are aminated by reaction with ammonia in the presence of a catalyst made by calcining bayerite.

Abstract: Rare earth pillared clays, and especially cerium and lanthanum aluminum chlorohydrite pillared clays, are quite effective catalysts in the alkylation of diaryl amines at temperatures in the range of 100.degree.-225.degree. C. The catalysts effect alkylation using olefins as the alkylating agent with high conversion and with minimal cracking of either the olefin or the alkylated product. Catalysts may be regenerated by heating in air at temperatures of at least about 550.degree.-600.degree. C. Water in small amounts also modifies the reaction to further reduce cracking although it also reduces the activity of the catalyst.