Abstract: Compounds of the general formula (2) and isomeric and/or tautomeric forms thereof ##STR1## characterized in that R.sup.1 is selected from the group consisting of: hydrogen; alkyl; alkenyl; alkynyl; cycloalkyl; cycloalkenyl; substituted alkyl or substituted cycloalkyl wherein the alkyl or cycloalkyl group is substituted with a substituent selected from the group consisting of alkoxy, alkylthio, optionally substituted phenyl, optionally substituted heterocycle; optionally substituted phenyl; optionally substituted heterocycle, alkyl sulfonyl; optionally substituted benzene sulfonyl; an acyl group; and an inorganic or organic cation;R.sup.
Type:
Grant
Filed:
April 13, 1988
Date of Patent:
July 3, 1990
Assignee:
Dunlena Pty. Limited
Inventors:
Janet E. Anderson-McKay, Andris J. Liepa
Abstract: Recombinant plasmids containing the larvicidal delta-endotoxin gene were constructed by inserting HindIII fragments of the Bacillus thuringiensis var. israelensis 72-75 Md plasmid into the Escherichia coli vector pUC12. Two recombinants producing a 27-kdal toxin (pIP173 and pIP174) were indentified by screening clones in an E. coli in vitro transcription-translation system. Both recombinants comprised pUC12 and common 9.7 kb HindIII fragment of the B. thuringiensis plasmid. The 27,340 Da polypeptide synthesized in vito from pIP174 transformed into E. coli JM101 and from B. subtilis 168 and spoOJ87 containing the 1.2 kb TaqI fragment from pIP173 was lethal to mosquito larvae.
Abstract: A method for distinguishing between carcinomatous and/or precarcinomatous colo-rectal disease and histologically similar conditions due to diseases that are not carcinomatous or precarcinomatous comprising contacting colo-rectal tissue with an antibody that binds to blood group substance H and determining the presence of carcinomatous or precarcinomatous disease upon a finding of bound antibody, or the absence of such disease upon the finding of no bound antibody.
Abstract: An improved device for killing arthropods characterized by a sloped target area that contains a toxicant, the device being devoid of any containment vessel for dead arthropods.
Abstract: Methods are described for preparing aluminum nitride of controllable morphology for ceramic and heat conduction applications. The methods comprise forming spherical particles or flakes of an intermediate, RA1NH, followed by heating the spheres or flakes of RA1NH at elevated temperatures to produce high purity aluminum nitride of corresponding morphology. Spheres of RA1NH are formed by (i) freezing a suspension of RA1NH in a liquid medium and thawing, by (ii) aging the suspension, or by (iii) dissolving RA1NH in a liquid medium and precipitating it. Flakes are formed by freezing a suspension of RAINH in a liquid medium and removing frozen medium from the frozen suspension.
Type:
Grant
Filed:
April 7, 1989
Date of Patent:
March 13, 1990
Assignee:
E. I. Du Pont de Nemours and Company
Inventors:
John D. Bolt, Walter Mahler, Frederick N. Tebbe, Robert J. Young, Jr.
Abstract: Herbicidal sulfonamides having the general formula ##STR1## wherein J, W, R and A are more particularly described herein, such compounds and agricultural compositions containing them being useful as preemergent or postemergent herbicides or both, or as plant growth regulants, including the manner of their use.
Abstract: Compounds of the general formula ##STR1## in which each of A and B independently represents a halogen atom or an alkyl group; m is 0 or 1; Q represents a group of general formula ##STR2## in which R is as defined, or Q represents a group of general formula --CR.sup.2 R.sup.3 R.sup.4 in which R.sup.2, R.sup.3 and R.sup.4 are as defined; together with processes for the preparation of such compounds, pesticidal compositions containing them and their pesticidal use, and certain novel intermediates.
Abstract: Admixing an aluminum alkyl, and optionally a boron compound, with a hydride of nitrogen in the gas phase and maintaining a gas phase temperature, optionally in the presence of a carrier gas, and producing aluminum nitride alone or in admixture with a precursor thereof or boron nitride or both.
Type:
Grant
Filed:
January 27, 1988
Date of Patent:
September 12, 1989
Assignee:
E. I. Du Pont de Nemours and Company
Inventors:
Ulrich Klabunde, Edward J. Newitt, Frederick N. Tebbe
Abstract: A process for depositing metal in the form of an interlayer within a solid matrix. The process is characterized in the use of electroactive transfer agents to carry electrons from the cathode to the desired locus within the matrix where the metal cation (M.sup.n+) is reduced to its zero-valent state. Also disclosed are composites of metallic-interlayer-containing matrices.
Abstract: Deprotonation of polyamides employing alkoxide and/or alkali amide bases in solution in a liquid sulfoxide, the solutions being useful to make N-alkylated and N-acylated derivatives and to fabricate polyamide films, fibers, coatings, manufactured articles, and the like.
Abstract: Polyfluoro .gamma.-ketoester compounds are obtained by reaction of ethylenic monoolefins, a metal or quaternary ammonium cyanide, and a fluoroester. These compounds, which have a general formula R.sub.F C(O)CFYCF.sub.2 CO.sub.2 R.sup.1, can be copolymerized directly with fluorinated ethylenic monoolefins, or further reacted to form vinyl ether and allyl ether derivatives which may also be copolymerized with ethylenic comonomers, forming solid, moldable copolymers with useful properties determined by the nature of pendant functional groups R.sub.F.
Abstract: A monoclonal hybridoma antibody with specificity for an antigen that is present on tumors of epithelial origin; the cell line secreting said antibodies; a process for selecting the cell line; a diagnostic process for detecting the antigen and a therapeutic process for neutrailization of the angtigen.
Type:
Grant
Filed:
May 13, 1985
Date of Patent:
March 21, 1989
Assignee:
E.I. DuPont de Nemours and Company
Inventors:
Paul J. Durda, David J. Green, Marcia J. Stone, Dennis E. Vaccaro
Abstract: Ortho-Sulfonamide benzenesulfonylureas, such as N-cyclopropyl-N'-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-1,2-benzened isulfonamide, are useful as pre-emergent and post-emergent herbicides.
Abstract: Heteropentathiepins including pyrazolopentathiepins substituted in the 8-position; intermediate pyrazolo-1,2,3-thiadiazoles, pyrazolothiazathiolium chlorides, and 5-substituted aminopyrazoles; process for making the pentathiepins by reacting the corresponding 1,2,3-thiadiazoles with sulfur at elevated temperatures; process for making the thiazathiolium chlorides; and use of the pentathiepins as fungicides or as sulfur sensitizers in photographic emulsions.
Abstract: An aqueous solution of precursors for biologically active glass, support particles coated with the solution, support particles coated with the glass, spheroidal particles of biologically active glass, processes for making the solution, coating the support, and for making the coated support and the spheroidal glass particles. The materials that comprise the biologically active glass are useful in prosthetic devices and implants for the human body.
Abstract: Substituted benzopentathiepins, their preparation from 1,2,3-benzothiadiazoles and elemental sulfur, selected 1,2,3-benzothiadiazoles; the benzopentathiepins being useful as biologically active compounds or as intermediates to 1,2-benzenedithiols.