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Patent ID Patent name Patent application publication number Patent application publication date Patent application number Patent application date Patent authorization announcement number Patent grant date Patent priority date Patent inventor Patentee Classification number Brief description Number of patent claims Number of citations to other patents Number of patent citations Legal Status
EP0000002B1 Tetrahydrofurane derivatives, processes for their preparation and their use as herbicides EP0000002A1 1978/12/20 EP78100007A 1978/6/1 EP0000002B1 1981/8/26 1977/6/1 Thomas Dr. Schmidt,Wilfried Dr. Draber,Ludwig Dr. Eue,Robert Rudolf Dr. Schmidt Bayer AG C07D307/42;A01N43/08;A01N43/12;C07D307/12;C07D407/12;F01D1/00; 5 3 26 DE - Pending Expired Expired, DD - Pending Expired Expired, IL - Pending Expired Expired, PT - Pending Expired Expired, IT - Pending Expired Expired, ZA - Pending Expired Expired, JP - Pending Expired Expired, BR - Pending Expired Expired, DK - Pending Expired Expired, EP - Pending Expired Expired
EP0000004B1 Continuous filtration centrifuge for separation, washing or draining, and application to an automatic coffee machine EP0000004A1 1978/12/20 EP19780100037 1978/6/1 EP0000004B1 1980/9/3 1977/6/2 Serge Cailliot Cor Bertrand, Gastinne Arnaud, GENERALE POUR LE FINANCEMENT DE L'INNOVATION SOGINNOVE Ste, Agence National de Valorisation de la Recherche ANVAR, Normande de Services Ste B04B3/08;A47J31/22; 11 6 5 FR - Expired, IT - Expired Expired - Lifetime Expired, DE - Expired Expired - Lifetime Expired, US - Expired Expired - Lifetime Expired, EP - Expired Expired - Lifetime Expired
EP0000005A1 New cephalosporin derivatives, their preparations and their pharmaceutical compositions EP0000005A1 1978/12/20 EP78100078A 1978/6/1 EP0000005B1 1980/10/29 1977/6/3 Marc Dr. Montavon,Roland Dr. Reiner F Hoffmann La Roche AG C07D501/36;A61P31/04; 1. Cephalosporin derivatives of the general formula see diagramm : EP0000005,P15,F1 wherein R represents furyl, thienyl or phenyl optionally substituted by halogen, hydroxy, lower alkoxy or lower alkyl, R1 represents lower alkyl or aminocarbonylmethyl and X represents a group of the formulae see diagramm : EP0000005,P15,F2 see diagramm : EP0000005,P15,F3 see diagramm : EP0000005,P15,F4 in which one of the two symbols R2 and R3 or R4 and R5 represents hydrogen and the other represents lower alkyl, carboxymethyl or sulphomethyl, as well as salts of said compounds and hydrates of said salts. 18 6 6 GB - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , NL - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , NZ - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , MC - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , IE - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , AU - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , IL - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , HU - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , JP - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , SE - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , FR - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , GR - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , EP - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , DE - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , FI - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , IT - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , DK - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , NO - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , PT - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , ES - Expired, CA - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , PH - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , AT - IP Right Cessation, BR - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , AR - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation , CU - Expired Application Discontinuation Expired Pending Expired Expired Expired Application Discontinuation Withdrawn Application Discontinuation Expired Expired IP Right Cessation
EP0000006A1 Process for nitrification of waste water EP0000006A1 1978/12/20 EP78200030A 1978/6/1 EP0000006B1 1981/2/4 1977/6/6 Gerhard Bakker,Fokke Dijkstra,Johannes Petrus Zeeman Stamicarbon BV C02F3/34;C02F3/06;Y02W10/10; Process for the nitrification of waste water in a trickle phase reactor whereby the gas containing molecular oxygen contains more than 25% by weight of molecular oxygen, the off-gas in the column is vented and/or recycled, during the nitrification 0.5-10% by weight of CO2, with respect to the total quantity of molecular oxygen present, such a quantity of the liquid effluent of the reactor is recycled that the entire column contents are irrigated and the gas and the liquid contact each other counter-currently. This process can be used for the nitrification of industrial waste water, especially waste water of fertilizer plants. 8 3 1 NL - Application Discontinuation, EP - Expired Expired, DE - Expired Expired
EP0000009B1 Method for the oxidation of quinine to quininone and quinidinone. EP0000009A1 1978/12/20 EP78400019A 1978/6/14 EP0000009B1 1980/7/23 1977/6/15 Jacques Bourrelly Devinter Sa C07D453/04; 3 3 0 FR - Withdrawn, EP - Expired Expired , DE - Expired Expired , IE - Expired Expired
EP0000011A1 Rotary sheet printing machine. EP0000011A1 1978/12/20 EP78100018A 1978/6/1 EP0000011B1 1980/4/30 1977/6/2 Gerhard Pollich Heidelberger Druckmaschinen AG B41F21/106; Bei Bogenrotationsmaschinen für Schöndruck und Schön- und Widerdruck sind unter den Bogenübergabetrommeln (5, 7), die den Druckzylindern (4) aufeinanderfolgender Druckwerke vor- oder nachgeordnet sind, Bogenleitbleche (9, 10) vorgesehen. Die Ausbildung dieser Bogenleitbleche (9, 10) ist derart, daß sich zwischen der Unterseite eines von der jeweiligen Bogenübergabetrommel (5 bzw. 7) transportierten Bogens und dem zugeordneten Bogenleitblech (9 oder 10) bei jeder Maschinengeschwindigkeit zwangsläufig ein Luftkissen ausbildet.In sheet-fed rotary machines for straight printing and face and back printing, sheet guide plates (9, 10) are provided under the sheet transfer drums (5, 7) which are arranged upstream or downstream of the printing cylinders (4) of successive printing units. The design of these sheet guide plates (9, 10) is such that an air cushion inevitably forms between the underside of a sheet transported by the respective sheet transfer drum (5 or 7) and the associated sheet guide plate (9 or 10) at any machine speed. 3 12 12 DE - Expired, ZA - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , AU - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , CA - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , GB - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , JP - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , ES - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , AT - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , EP - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , BR - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , US - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , IT - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime
EP0000011B1 Rotary sheet printing machine. EP0000011A1 1978/12/20 EP78100018A 1978/6/1 EP0000011B1 1980/4/30 1977/6/2 Gerhard Pollich Heidelberger Druckmaschinen AG B41F21/106; 3 12 12 DE - Expired, ZA - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , AU - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , CA - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , GB - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , JP - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , ES - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , AT - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , EP - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , BR - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , US - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime , IT - Expired Expired Expired Expired Expired IP Right Cessation Expired Expired - Lifetime
EP0000015A1 Medicament for the treatment of depressions EP0000015A1 1978/12/20 EP78100027A 1978/6/1 EP0000015B1 1980/7/23 1977/6/1 Karl Dr. Schmitt,Irmgard Dr. Hoffmann,Werner Dr. Fülberth,Willi Dr. Stammberger Hoechst AG A61K31/55;A61P25/24;A61P25/26; Arzneimittel, die als Wirkstoff A eine Verbindung der Formel I in der R1, R3 und R4 gleich oder verschieden sein können und Wasserstoffatome oder niedere Alkyl- oder Aralkylgruppen und R2 und R2<'> gleich oder verschieden sein Können und Wasserstoff- oder Halogenatome, Hydroxy- oder Trifluormethylgruppen oder niedere Alkyl-, Alkoxy- oder Aralkoxygruppen bedeuten, wobei 2 benachbarte Reste auch zusammen ein Alkylendioxyrest sein können, und R5 ein Wasserstoff- oder Halogenatom, eine Hydroxy-, Trifluormethyl- oder Nitrogruppe oder einen niederen Alkyl-, Alkoxy- oder Aralkoxyrest bedeuten oder deren Salze mit Säuren und als Wirkstoff B 7-Chlor-1- methyl-5- phenyl-1 H-1,5-benzodiazepin-2,4 (3H, 5H)-dion enthalten und ihre Verwendung zur Behandlung von Depressionen.Medicaments which, as active ingredient A, can be a compound of the formula I in which R1, R3 and R4 can be the same or different and hydrogen atoms or lower alkyl or aralkyl groups and R2 and R2 <'> can be the same or different and hydrogen or Halogen atoms, hydroxyl or trifluoromethyl groups or lower alkyl, alkoxy or aralkoxy groups, where 2 adjacent radicals can also together be an alkylenedioxy radical, and R5 represents a hydrogen or halogen atom, a hydroxyl, trifluoromethyl or nitro group or a lower alkyl, Alkoxy or aralkoxy radical or their salts with acids and as active ingredient B contain 7-chloro-1-methyl-5-phenyl-1 H-1,5-benzodiazepine-2,4 (3H, 5H) -dione and their use for Treatment of depression. 2 1 4 DE - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, ZA - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, IT - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, US - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, IL - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, CA - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, AU - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, DK - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, AT - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, JP - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, EP - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired
EP0000015B1 Medicament for the treatment of depressions EP0000015A1 1978/12/20 EP78100027A 1978/6/1 EP0000015B1 1980/7/23 1977/6/1 Karl Dr. Schmitt,Irmgard Dr. Hoffmann,Werner Dr. Fülberth,Willi Dr. Stammberger Hoechst AG A61K31/55;A61P25/24;A61P25/26; 1 1 4 DE - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, ZA - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, IT - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, US - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, IL - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, CA - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, AU - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, DK - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, AT - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, JP - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired, EP - Expired - Lifetime Expired Expired Application Discontinuation IP Right Cessation Expired Pending Expired
EP0000020A1 Apparatus for measuring the water content of isotropic materials with the aid of microwave absorption EP0000020A1 1978/12/20 EP78100032A 1978/6/1 1977/6/2 Hans Georg Dr. Fitzky,Franz Schmitt,Norbert Bollongino,Helmut Rehrmann Bayer AG H01P7/06;G01N22/04; Der Wassergehalt von elektrisch nicht leitenden Pulvern, Granulaten, Pasten und Fasermaterialien kann auf der Basis der Mikrowellenabsorption gemessen werden. Ein frequenzmodulierter Mikrowellenoszillator speist in einer Transmissionsanordnung einen geschlossenen Multimode-Messresonator, der mit der Probe beschickt ist. Die in einen Behälter (3) abgefüllte Probe füllt den Multimode-Resonator (22) nahezu vollständig aus. Der Probenbehälter ist um seine Längsachse drehbar. Hierdurch wird eine weitgehende Homogenität der Feldverteilung in der Probe erzielt, so dass auch bei Schüttdichteschwankungen noch genaue Messungen möglich sind.The water content of electrically non-conductive powders, granules, pastes and fiber materials can be measured on the basis of microwave absorption. In a transmission arrangement, a frequency-modulated microwave oscillator feeds a closed multimode measuring resonator, which is loaded with the sample. The sample filled into a container (3) fills the multimode resonator (22) almost completely. The sample container can be rotated about its longitudinal axis. This results in a largely homogeneous field distribution in the sample, so that precise measurements are still possible even with fluctuations in bulk density. 8 9 22 DE - Withdrawn, US - Expired - Lifetime Withdrawn Pending, IT - Expired - Lifetime Withdrawn Pending, EP - Expired - Lifetime Withdrawn Pending, DK - Expired - Lifetime Withdrawn Pending, JP - Expired - Lifetime Withdrawn Pending
EP0000021A1 Process for the preparation of sulfonic acid groups and phosphonate groups bearing polyisocyanate mixtures EP0000021A1 1978/12/20 EP78100033A 1978/6/1 EP0000021B1 1980/7/23 1977/6/3 Hans-Joachim Dr. Scholl,Dieter Dr. Dieterich Bayer AG C07F9/4065;C08G18/776; Sulfonsäure- und Phosphonatgruppen aufweisende Polyisocyanate und Verfahren zu deren Herstellung. Bei Raumtemperatur flüssige Polyisocyanatgemische mit einem Gehalt an ggf. teilweise als Carbamidsäurechlorid vorliegenden Isocyanatgruppen von 10-42 Gewichtsprozent, an in Form von ggf. zumindest teilweise neutralisierten oder veresterten Sulfonsäuregruppen vorliegendem Schwefel von 0,5-5 Gewichtsprozent, an in Form von Phosphonsäurealkylester- oder Phosphonsäurearalkylestergruppen vorliegendem Phosphor von 0,5-5 Gewichtsprozent und eine Viskosität von 10-50000 cP bei 25°C werden durch Reaktion von Chlorsulfonsäure bei -10 bis +150°C mit aromatischen Polyisocyanaten bzw. Polyisocyanatgemischen in Gegenwart eines ggf. Halogensubstituierten Trialkylphosphits oder Tris-(aralkyl)- phosphits und inerten Lösungsmitteln hergestellt.Polyisocyanates containing sulfonic acid and phosphonate groups and process for their preparation. Polyisocyanate mixtures which are liquid at room temperature and contain 10-42% by weight of isocyanate groups, some of which are present as carbamic acid chloride, 0.5-5% by weight of sulfur, which may be at least partially neutralized or esterified sulfonic acid groups, or in the form of alkyl phosphates or Phosphonic acid aryl ester groups present phosphorus of 0.5-5 percent by weight and a viscosity of 10-50000 cP at 25 ° C by reacting chlorosulfonic acid at -10 to + 150 ° C with aromatic polyisocyanates or polyisocyanate mixtures in the presence of a possibly halogen-substituted trialkyl phosphite or Tris - (aralkyl) - phosphites and inert solvents. 4 3 2 DE - Expired - Lifetime Expired Expired , US - Expired - Lifetime Expired Expired , EP - Expired - Lifetime Expired Expired , IT - Expired - Lifetime Expired Expired
EP0000026A1 Process for the preparation of secondary amines EP0000026A1 1978/12/20 EP19780100041 1978/6/1 1977/6/6 Karl Dr. Merkel,Herbert Dr- Toussaint,Herbert Dr. Mueller,Herwig Dr. Hoffmann,Leopold Dr. Hupfer,Hans Jochen Dr. Mercker BASF SE C07C209/26; Secondary amines are prepared by N-alkylation of primary amines by means of aldehydes under hydrogenating conditions in the presence of a quaternary ammonium base. 5 1 2 DE - Expired, EP - Ceased
EP0000027A1 Process for the manufacture, according to the Levitherm process, of hard polyvinyl chloride films EP0000027A1 1978/12/20 EP78100042A 1978/6/1 EP0000027B1 1980/9/17 1977/6/14 Guenter Mueller,Martin Dr. Herner BASF SE B29C43/24; 1. A process for the production of rigid vinyl chloride polymer sheeting at elevated temperature and in the presence of a slip agent added during the production of the sheeting, in which vinyl chloride polymers are preplasticized by calendering at temperatures of from 150 to about 190 degrees C and luvithermizing the resulting brittle sheeting at from 200 to 280 degrees C, characterized in that a slip agent is continuously applied during calendering at least to the calendar roll which is the last in the direction of product flow in the form of a thin, uniform layer over the whole length of the calender roll. 2 3 0 DE - Expired Expired , EP - Expired Expired , IT - Expired Expired
EP0000031B1 Thermal and sound isolating glass unit EP0000031A1 1978/12/20 EP78100052A 1978/6/1 EP0000031B1 1981/1/7 1977/6/8 Edith Dr. Leicht,Friedrich Günther,Reinhard Strigl Linde GmbH E06B3/6715;E06B3/6707; 3 5 6 DE - Expired IP Right Cessation, AT - Expired IP Right Cessation, EP - Expired Application Discontinuation Expired, IT - Expired Application Discontinuation Expired, BR - Expired Application Discontinuation Expired, DK - Expired Application Discontinuation Expired, NO - Expired Application Discontinuation Expired, ZA - Expired Application Discontinuation Expired, AU - Expired Application Discontinuation Expired
EP0000032A1 Di EP0000032A1 1978/12/20 EP78100053A 1978/6/1 EP0000032B1 1982/5/19 1977/6/1 John James Baldwin,Gerald Salvatore Ponticello Merck and Co Inc C07D417/12;A61K31/425;A61K31/44;A61K31/505;A61K31/535;A61P25/02;C07D263/06;C07D277/34;C07D277/36;C07D277/56;C07D417/04; Di- and tri-substituted thiazoles, of the formula: their preparation and intermediates pharmaceutical compositions containing (I) useful as β-adrenolytica. 21 4 7 US - Expired - Lifetime Expired Expired, JP - Expired - Lifetime Expired Expired, EP - Expired - Lifetime Expired Expired
EP0000038B1 Method and apparatus for cancelling interference between area coverage and spot coverage antenna beams EP0000038A1 1978/12/20 EP19780100062 1978/6/1 EP0000038B1 1981/10/14 1977/6/3 Anthoney Acampora,Douglas Otto John Reudink,Yu Shuan Yeh Western Electric Co Inc H04B7/2041; 7 13 23 US - Expired - Lifetime, CA - Expired Expired Expired Pending, EP - Expired Expired Expired Pending, DE - Expired Expired Expired Pending, JP - Expired Expired Expired Pending
EP0000042B1 Process for the preparation of 2,4,5 EP0000042A1 1978/12/20 EP78100071A 1978/6/1 EP0000042B1 1980/8/20 1977/6/8 Gunther Dr. Beck,Helmut Dr. Heitzer Bayer AG C07D239/30; 3 4 1 DE - Expired Expired Expired - Lifetime Pending, EP - Expired Expired Expired - Lifetime Pending, US - Expired Expired Expired - Lifetime Pending, JP - Expired Expired Expired - Lifetime Pending
EP0000043B1 Bisphosphinic acid anhydrides and process for its preparation EP0000043A1 1978/12/20 EP78100072A 1978/6/1 EP0000043B1 1982/1/6 1977/6/11 Hans-Jerg Dr. Kleiner,Walter Dr. Dürsch,Fritz Dr. Linke Hoechst AG C07F9/3235;C07F9/305; 5 2 2 DE - Expired Expired Pending, EP - Expired Expired Pending, IT - Expired Expired Pending, JP - Expired Expired Pending
EP0000044B1 Carbamoyloxyalkyl phosphinic acid derivatives, process for their preparation and their use in the preparation of flame EP0000044A1 1978/12/20 EP78100073A 1978/6/1 EP0000044B1 1980/7/23 1977/6/10 Hans-Jerg Dr. Kleiner,Fritz Dr. Linke,Walter Dr. Dürsch Hoechst AG D06M13/453;C07F9/3211; 5 5 0 EP - Expired Expired Expired - Lifetime , DE - Expired Expired Expired - Lifetime , US - Expired Expired Expired - Lifetime , IT - Expired Expired Expired - Lifetime
EP0000050A1 Derivatives of 4 EP0000050A1 1978/12/20 EP78100090A 1978/6/5 1977/6/7 Heinz Dr. Förster,Ludwig Dr. Eue,Robert Rudolf Dr. Schmidt Bayer AG C07C205/38; 4-(2-chloro-4-nitrophenoxy)phenoxyalkanecarboxylic acid derivatives of the formula in which R represents hydrogen or alkyl, R<1> represents alkoxy which is mono- or polysubstituted by hydroxyl, halogen, alkoxy, alkoxyalkoxy, alkylthio, amino, monoalkylamino, dialkylamino or carbonyl-N-alkyl-N-aryl, or hydroxyalkenoxy, hydroxyalkynoxy, hydroxylamino, a nitrogen-containing heterocycle whose ring can be interrupted by further heteroatoms and/or can optionally be substituted by alkyl or halogen, arylamino or monoalkyl-monoarylamino, in which the aryl radical can in each case be substituted by alkyl, nitro, halogen or haloalkyl, R<2> represents hydrogen, halogen or alkyl and n represents an integer from 1 to 4; method for their preparation and their use as herbicides.i 6 2 0 IL - Pending Withdrawn Pending, IT - Pending Withdrawn Pending, JP - Pending Withdrawn Pending, EP - Pending Withdrawn Pending, BR - Pending Withdrawn Pending, DK - Pending Withdrawn Pending, AU - Pending Withdrawn Pending
EP0000054A1 Process for the preparation of olefinic unsaturated aliphatic or cycloaliphatic hydrocarbons EP0000054A1 1978/12/20 EP78100096A 1978/6/6 EP0000054B1 1980/10/29 1977/6/10 Peter Dr. Horn,Otto-Alfred Dr. Grosskinsky,Hugo Dr. Fuchs BASF SE C07C1/213;C07C1/2078;C07C2521/02;C07C2521/04;C07C2521/06;C07C2521/08;C07C2523/14;C07C2527/24;C07C2601/10;C07C2601/16;Y02P20/582; Herstellung von olefinisch ungesättigten aliphatischen oder cycloaliphatischen Kohlenwasserstoffen durch Erhitzen von Alkancarbonsäuren mit 3 bis 20 Kohlenstoffatomen, Alkandicarbonsäuren mit 4 bis 20 Kohlenstoffatomen oder 5- oder 6-gliedrigen Cycloalkancarbonsäuren oder deren Alkyl-, Cycloalkyl-, Aralkyl- oder Phenylester auf Temperaturen von 250 bis 800°C in der Gasphase in Gegenwart von Katalysatoren, wobei man Katalysatoren verwendet, deren katalytisch aktive Masse aus Bortrioxid, Borsäure und/oder Bornitrid sowie mindestens aus einem der Oxide von Aluminium, Silizium, Zinn, Blei, Titan oder Zirkonium besteht.Production of olefinically unsaturated aliphatic or cycloaliphatic hydrocarbons by heating alkane carboxylic acids with 3 to 20 carbon atoms, alkane dicarboxylic acids with 4 to 20 carbon atoms or 5- or 6-membered cycloalkane carboxylic acids or their alkyl, cycloalkyl, aralkyl or phenyl esters at temperatures of 250 to 800 ° C in the gas phase in the presence of catalysts, using catalysts whose catalytically active composition consists of boron trioxide, boric acid and / or boron nitride and at least one of the oxides of aluminum, silicon, tin, lead, titanium or zirconium. 9 5 12 DE - Expired - Lifetime Expired Expired Pending , US - Expired - Lifetime Expired Expired Pending , EP - Expired - Lifetime Expired Expired Pending , JP - Expired - Lifetime Expired Expired Pending , IT - Expired - Lifetime Expired Expired Pending
EP0000059A1 Process for the preparation of N EP0000059A1 1978/12/20 EP78100102A 1978/6/6 EP0000059B1 1980/9/17 1977/6/8 Dieter Dr. Arlt,Franz-Gerhard Behlau Bayer AG C07C231/00;C07C231/10; Verfahren zur Herstellung von N-alkylsubstituierten Carbonsäureamiden. Carbonium-lonen bildende Verbindungen werden mit einem Nitril in Gegenwart von Säuren zu N-alkylsubstituierten Carbonsäureamiden umgesetzt. Das Reaktionsgemisch wird durch Destillation aufgetrennt, wobei man die Umsetzung in Gegenwart einer Säure durchführt, die unter Destillationsbedingungen inert ist.Process for the preparation of N-alkyl substituted carboxamides. Compounds which form carbonium ions are reacted with a nitrile in the presence of acids to give N-alkyl-substituted carboxamides. The reaction mixture is separated by distillation, the reaction being carried out in the presence of an acid which is inert under distillation conditions. 4 15 6 DE - Expired - Lifetime Pending Expired Expired Expired , IN - Expired - Lifetime Pending Expired Expired Expired , US - Expired - Lifetime Pending Expired Expired Expired , JP - Expired - Lifetime Pending Expired Expired Expired , IT - Expired - Lifetime Pending Expired Expired Expired , EP - Expired - Lifetime Pending Expired Expired Expired , BR - Expired - Lifetime Pending Expired Expired Expired , ES - Expired - Lifetime Pending Expired Expired Expired , ZA - Expired - Lifetime Pending Expired Expired Expired
EP0000061A1 Derivatives of carboxylic acid that contain phosphorus, process for their preparation and their utilisation EP0000061A1 1978/12/20 EP78100104A 1978/6/6 EP0000061B1 1980/10/15 1977/6/14 Horst Dieter Dr. Thamm,Fritz Dr. Linke Hoechst AG C07F9/4046;C02F5/14;C07F9/305;C07F9/3235;C07F9/3869;C07F9/5312;C07F9/5329;C08K5/5393;D06M13/288; 1. Phosphorus-containing carboxylic acid derivates of the formula see diagramm : EP0000061,P18,F3 in which R, which may be the same or different, are radicals selected from the group consisting of H, (C1-20 )-alkyl, (C2-8 )-alkyenyl, both radicals being optionally substituted, preferably up to three times, especially once, by halogen, especially chloride or bromine, (C5-6 )-cycloalkyl, phenyl or phen(C1-4 )-alkyl, said radicals being optionally substituted in the ring, preferably up to three times, by halogen, preferably chlorine or bromine, or (C1-4 )-alkyl, an alkali metal or ammonium, preferably sodium or potassium, cation, but R cannot be H or a cation, if the pertinent m, n, p or q is 0, R1 is H, (C1-4 )-alkyl, R2 is CN, COOR4 , CONR5 R6 , CONH2-x (CH2 OH)x , with x being 1 or 2, R3 is H or the group see diagramm : EP0000061,P19,F1 with R'1 and R'2 having the same meaning as R1 and R2 R4 has the meaning given for R, and R5 , R6 is H, (C1-20 )-alkyl or phenyl, both radicals being optionally substituted by halogen, preferably chlorine or bromine, and/or (C1-4 )-alkyl, preferably up to three times, and m, n, p, q independent from each other are 0 or 1, with the restriction that, if R2 is CN or COOR4 , all members of the group m, n, p, q cannot be 1, and that for R = C6 H5 and m = n = p = q = 0, R3 not= H. 7 3 5 DE - Expired Expired Pending, EP - Expired Expired Pending, IT - Expired Expired Pending, JP - Expired Expired Pending
EP0000069A1 Image printing head EP0000069A1 1978/12/20 EP78100128A 1978/6/8 EP0000069B1 1981/2/18 1977/6/13 Marcel Yvard,Jean-Claude Decuyper,Michel Beduchaud Alcatel CIT SA G01D15/06;B41J2/395;H04N1/032; Barrette d'impression d'une image comportant un empilement de plaquettes (1) conductrices et isolées les unes des autres dont une extrémité de chacune forme un stylet d'impression (10) et n matrices diagonales (20) d'adressage des stylets dont les colonnes sont constituées par les plaquettes (1) et sont alimentées à travers des résistances (R) formées sur les plaquettes et dont les lignes communes aux n matrices sont constituées par des conducteurs électriques (24) reliés aux colonnes à travers des diodes (D), également formées sur les plaquettes. Application aux installations de transmission de fac-similés.Bar for printing an image comprising a stack of conductive plates (1) insulated from one another, one end of each of which forms a printing stylus (10) and n diagonal matrices (20) for addressing styli whose the columns are formed by the plates (1) and are supplied through resistors (R) formed on the plates and whose lines common to the n matrices are constituted by electrical conductors (24) connected to the columns through diodes (D ), also formed on the pads. Application to facsimile transmission facilities. 15 14 7 FR - Pending, EP - Expired Expired IP Right Cessation Expired Expired , DE - Expired Expired IP Right Cessation Expired Expired , IE - Expired Expired IP Right Cessation Expired Expired , IT - Expired Expired IP Right Cessation Expired Expired , DK - Expired Expired IP Right Cessation Expired Expired , CA - Expired Expired IP Right Cessation Expired Expired , JP - Expired Expired IP Right Cessation Expired Expired , BR - Expired Expired IP Right Cessation Expired Expired , US - Expired - Lifetime
EP0000069B1 Image printing head EP0000069A1 1978/12/20 EP19780100128 1978/6/8 EP0000069B1 1981/2/18 1977/6/13 Marcel Yvard,Jean-Claude Decuyper,Michel Beduchaud Alcatel CIT SA G01D15/06;B41J2/395;H04N1/032; 8 14 7 FR - Pending, DE - Expired Expired Expired IP Right Cessation Expired, EP - Expired Expired Expired IP Right Cessation Expired, IT - Expired Expired Expired IP Right Cessation Expired, CA - Expired Expired Expired IP Right Cessation Expired, IE - Expired Expired Expired IP Right Cessation Expired, DK - Expired Expired Expired IP Right Cessation Expired, BR - Expired Expired Expired IP Right Cessation Expired, JP - Expired Expired Expired IP Right Cessation Expired, US - Expired - Lifetime
EP0000070B1 Image printing head EP0000070A1 1978/12/20 EP19780100129 1978/6/8 EP0000070B1 1981/2/18 1977/6/13 Marcel Yvard,Jean-Claude Decuyper,Michel Beduchaud Alcatel CIT SA H04N1/032;B41J2/425;G01D15/06; 6 13 17 FR - Pending, DE - Expired Expired Expired - Lifetime Expired IP Right Cessation Expired , EP - Expired Expired Expired - Lifetime Expired IP Right Cessation Expired , US - Expired Expired Expired - Lifetime Expired IP Right Cessation Expired , IT - Expired Expired Expired - Lifetime Expired IP Right Cessation Expired , CA - Expired Expired Expired - Lifetime Expired IP Right Cessation Expired , IE - Expired Expired Expired - Lifetime Expired IP Right Cessation Expired , DK - Expired Expired Expired - Lifetime Expired IP Right Cessation Expired , JP - Expired Expired Expired - Lifetime Expired IP Right Cessation Expired , BR - Expired Expired Expired - Lifetime Expired IP Right Cessation Expired
EP0000071B1 Stabilised thymidine phosphorylase preparation and culture medium containing it EP0000071A1 1978/12/20 EP78100132A 1978/6/9 EP0000071B1 1981/8/5 1977/6/14 Thomas Anthony Krenitsky Wellcome Foundation Ltd C12N9/96;C12N9/1077; 12 1 3 DE - Expired Expired Application Discontinuation Expired - Lifetime IP Right Cessation Expired Expired Expired Expired, EP - Expired Expired Application Discontinuation Expired - Lifetime IP Right Cessation Expired Expired Expired Expired, DK - Expired Expired Application Discontinuation Expired - Lifetime IP Right Cessation Expired Expired Expired Expired, ZA - Expired Expired Application Discontinuation Expired - Lifetime IP Right Cessation Expired Expired Expired Expired, US - Expired Expired Application Discontinuation Expired - Lifetime IP Right Cessation Expired Expired Expired Expired, FI - Expired Expired Application Discontinuation Expired - Lifetime IP Right Cessation Expired Expired Expired Expired, CA - Expired Expired Application Discontinuation Expired - Lifetime IP Right Cessation Expired Expired Expired Expired, IL - Expired Expired Application Discontinuation Expired - Lifetime IP Right Cessation Expired Expired Expired Expired, HU - Expired Expired Application Discontinuation Expired - Lifetime IP Right Cessation Expired Expired Expired Expired, ES - Expired Expired Application Discontinuation Expired - Lifetime IP Right Cessation Expired Expired Expired Expired, IT - Expired Expired Application Discontinuation Expired - Lifetime IP Right Cessation Expired Expired Expired Expired, AU - Expired Expired Application Discontinuation Expired - Lifetime IP Right Cessation Expired Expired Expired Expired, JP - Expired Expired Application Discontinuation Expired - Lifetime IP Right Cessation Expired Expired Expired Expired
EP0000074A1 New bispidine derivatives, process for their preparation and medicinal preparations containing them EP0000074A1 1978/12/20 EP78100147A 1978/6/13 EP0000074B1 1980/8/6 1977/6/13 Fritz Dr. Binnig,Ludwig Dr. Friedrich,Hans Peter Dr. Hofmann,Horst Dr. Kreiskott,Claus Dr. Mueller,Manfred Dr. Raschack BASF SE C07D471/08;A61P9/06; Die vorliegende Erfindung betrifft Bispidinderivate der Formel worin R¹ H oder C6H5, R² H, C1 oder CF3, R³ H, F oder C1 und x 0 oder 1 bedeutet, sowie Arzneimittel, die diese Verbindungen enthalten. Die Verbindungen werden hergestellt durch Kondensation von N-Monobezylbispidin mit entsprechend substituierten Phenyläthylhalogeniden oder durch Mannich-Reaktion von N-Benxyl-piperidon-4 mit entsprechend substituierten Phenylalkylaminen und anschließender Reduktion. Die neuen Verbindungen besitzen vorwiegend antiarrhythmische Eigenschaften.The present invention relates to bispidine derivatives of the formula in which R 1 is H or C6H5, R 2 H, C1 or CF3, R 3 H, F or C1 and x is 0 or 1, and medicaments which contain these compounds. The compounds are prepared by condensation of N-monobezylbispidine with appropriately substituted phenylethyl halides or by Mannich reaction of N-benxyl-piperidone-4 with appropriately substituted phenylalkylamines and subsequent reduction. The new compounds have predominantly antiarrhythmic properties. 9 1 10 DE - Pending IP Right Cessation IP Right Cessation Expired Expired - Lifetime Expired Expired, JP - Pending IP Right Cessation IP Right Cessation Expired Expired - Lifetime Expired Expired, FI - Pending IP Right Cessation IP Right Cessation Expired Expired - Lifetime Expired Expired, AT - Pending IP Right Cessation IP Right Cessation Expired Expired - Lifetime Expired Expired, EP - Pending IP Right Cessation IP Right Cessation Expired Expired - Lifetime Expired Expired, US - Pending IP Right Cessation IP Right Cessation Expired Expired - Lifetime Expired Expired, CA - Pending IP Right Cessation IP Right Cessation Expired Expired - Lifetime Expired Expired
EP0000075A1 Dredging vessel EP0000075A1 1978/12/20 EP19780200009 1978/6/1 1977/6/8 Petrus Johannes Hermanus Nieuwendijk Ballast Nedam NV, Amsterdamse Ballast Bagger En Grond (Amsterdam Ballast Dredging) BV E02F3/885;E02F7/04;E02F7/065; When loading a loading space 2 of a dredging vessel 1 with sand the head water 5 is removed from the loading space 2 by means of more than one siphon 12 and is conducted away into the water stream 26 moving around the vessel 1. This head water can be polluted with much sludge or another pollutant. In order to reduce pollution of the environment with the aid of effluent means which are not very expensive and which can be easily adjusted, said effluent means comprises in accordance with the invention a tubular sheath 23, inside which is telescopically arranged a level-adjustable common outlet conduit 24 which can be withdrawn into said tubular sheath and be brought out thereof to a considerable distance below the vessel 1 respectively, and which is connected with coupled conducts 16 one siphon 12. 2 9 14 NL - IP Right Cessation, EP - Withdrawn Ceased Expired Expired - Lifetime Expired, DE - Withdrawn Ceased Expired Expired - Lifetime Expired, BE - Withdrawn Ceased Expired Expired - Lifetime Expired, GB - Withdrawn Ceased Expired Expired - Lifetime Expired, US - Withdrawn Ceased Expired Expired - Lifetime Expired, JP - Withdrawn Ceased Expired Expired - Lifetime Expired, FR - Expired
EP0000078A1 Preparation of salts of hydroxyphosphinylureidobenzylpenicillins. EP0000078A1 1978/12/20 EP78200017A 1978/6/1 EP0000078B1 1980/7/23 1977/6/1 Piet Johannes Akkerboom,Geertruida Johanna Löwer,Willem Jacob Timp Gist Brocades NV C07F9/65611;C07D499/00;Y02P20/55; Process for the preparation of compounds of the general formula:- wherein R is an optionally substituted phenyl group, Y is a group Me or a hydrocarbon group, Me is a metal cation and E is a hydrogen atom or a metal cation, which comprises wherein 0 is a hydrogen atom or a silyl protecting group, Rz is a group R, with the proviso that any hydroxy groups present on the phenyl group are replaced by a group -OQz, wherein Qz is a group Q, but excluding hydrogen, and Ez is a carboxyl-protecting group, with a compound of the general formula:- wherein Z is a halogen atom and X is a group OY or a group Z, at low temperatures under anhydrous conditions and carefully hydrolysing the product obtained either with just enough water to remove protecting groups and hydrolyse groups Z to hydroxy groups and, still under anhydrous conditions, reacting the compound obtained with an organic metal salt carrying a metal cation Me or, in which case the organic solvent is water-insoluble, with an excess of whter, followed by washing the mixture acidified with water, extracting the organic phase with neutral water and forming a salt with a hydroxide or a salt carrying a salt-forming cation Me. High yields may be dbtained by this salt-formation method. 9 2 2 US - Expired - Lifetime Application Discontinuation Pending Expired Expired, IT - Expired - Lifetime Application Discontinuation Pending Expired Expired, FI - Expired - Lifetime Application Discontinuation Pending Expired Expired, JP - Expired - Lifetime Application Discontinuation Pending Expired Expired, DK - , DE - Expired - Lifetime Application Discontinuation Pending Expired Expired, EP - Expired - Lifetime Application Discontinuation Pending Expired Expired
EP0000078B1 Preparation of salts of hydroxyphosphinylureidobenzylpenicillins. EP0000078A1 1978/12/20 EP78200017A 1978/6/1 EP0000078B1 1980/7/23 1977/6/1 Piet Johannes Akkerboom,Geertruida Johanna Löwer,Willem Jacob Timp Gist Brocades NV C07F9/65611;C07D499/00;Y02P20/55; 12 2 2 US - Expired - Lifetime Application Discontinuation Pending Expired Expired, IT - Expired - Lifetime Application Discontinuation Pending Expired Expired, FI - Expired - Lifetime Application Discontinuation Pending Expired Expired, JP - Expired - Lifetime Application Discontinuation Pending Expired Expired, DK - , DE - Expired - Lifetime Application Discontinuation Pending Expired Expired, EP - Expired - Lifetime Application Discontinuation Pending Expired Expired
EP0000082A1 Process for image EP0000082A1 1978/12/20 EP19780200022 1978/6/1 EP0000082B1 1982/7/21 1977/6/1 Hugo Vital Van Goetham,Marcel August Stroobants,Walter Frans De Winter Agfa Gevaert NV G03F7/0388; A radiation-sensitive material is described that comprises a hydrophilic colloid layer containing a dispersed phase of at least one radiation sensitive polymer the polymer chain of which comprises units with side substituents containing oxime ester groups. Upon imagewise exposure to actinic radiation of the polymer in the exposed areas reduces the permeability of the hydrophilic colloid layer for an etchant in the absence of any ethylenically unsaturated monomer. The layer having upon imagewise exposure to radiation image-wise differentiations in permeability for an etchant can be used as etch-resist, without needing a washing away step, to modify image-wise the surface of an element e.g. to produce printed circuits or printing forms. 12 11 26 FR - Expired, JP - Pending Expired - Lifetime Expired Expired, US - Pending Expired - Lifetime Expired Expired, EP - Pending Expired - Lifetime Expired Expired, DE - Pending Expired - Lifetime Expired Expired
EP0000085A1 Process for the production and separation of hydrogen iodide and sulphuric acid and their respective uses in the production of hydrogen and oxygen EP0000085A1 1978/12/20 EP78200029A 1978/6/1 EP0000085B1 1980/10/29 1977/12/16 Giancarlo De Beni,Giancarlo Pierini,Bruno Spelta European Atomic Energy Community Euratom C01B7/135;C01B13/02;C01B17/90;C01B3/068;Y02E60/36; A process for the separation of hydrogen iodide and sulphuric acid produced in the reaction between sulphus dioxide, water and iodine (the Bunsen Reaction) when using liquid sulphur dioxide as a solvent includes the addition of a trialkyl phosphate or dialkyl-alkyl phosphonate to the reaction mixture to inhibit migration of the hydrogen iodide into the sulphuric acid phase. The process may form part of processes respectively for the production of hydrogen and oxygen in which hydrogen iodide and sulphuric acid produced in the Bunsen Reaction are decomposed respectively to hydrogen and oxygen, thus providing a cycle of chemical reactions in which the net result is the production of hydrogen and oxygen from water. 6 4 1 DE - Expired Expired Application Discontinuation, EP - Expired Expired Application Discontinuation, IE - Expired Expired Application Discontinuation, IT - Expired Expired Application Discontinuation, DK - Expired Expired Application Discontinuation
EP0000093B1 A pump dispenser for a vacuum bottle EP0000093A1 1978/12/20 EP78300022A 1978/6/6 EP0000093B1 1982/4/7 1977/6/6 Albert A. Frazier,Howard W. Phillips Aladdin Industries LLC A47J41/0033;B05B11/06;B67D1/04;B67D1/0425;F04B45/02;F04F1/06;G01F11/028; 6 9 5 GB - Expired , BR - Expired , JP - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, CA - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, GR - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, IE - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, IT - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, NO - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, DK - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, FR - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, MX - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, FI - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, SE - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, EP - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, AU - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, LU - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, ES - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, DE - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, NL - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, CH - Pending Expired Application Discontinuation Expired Application Discontinuation Expired Expired Expired Withdrawn Application Discontinuation IP Right Cessation Expired, HK -
EP0000097A1 Polyarylene esters moulding compositions, process for their preparation and shaped articles therefrom EP0000097A1 1978/12/20 EP78300028A 1978/6/9 EP0000097B1 1981/2/11 1977/6/13 Oliver Desauze Deex,Virgil Wayne Weiss Monsanto Co C08G63/19;C08K3/013;C08K3/40; A molding resin comprising an intimate blend of a polyarylene ester and a reinforcing filler; the polyarylene ester consisting essentially of units derived from a C8 to C25 aromatic dicarboxylic acid and a diphenol comprising from 60 to 100 mol percent 1,2-bis- (4-hydroxyphenyl) ethane and from 40 to 0 mol percent of a C6 to C25 diphenol, said inherent viscosity of said polyarylene ester at 30°C. is at least 0.5 as determined at a concentration of 0.5 grams polyester per 100 ml solution in a solvent mixture of 60 parts by weight of phenol and 40 parts by weight of sym-tetrachloroethane. A process for preparing the said molding resin is also described. 12 4 3 EP - Expired Expired Expired Expired Pending , DE - Expired Expired Expired Expired Pending , CA - Expired Expired Expired Expired Pending , AU - Expired Expired Expired Expired Pending , AR - Expired Expired Expired Expired Pending , BR - Expired Expired Expired Expired Pending , JP - Expired Expired Expired Expired Pending , IT - Expired Expired Expired Expired Pending
EP0000103A1 Purification of glycoproteins and use of glycoproteins to form antiserum compositions EP0000103A1 1978/12/20 EP78300035A 1978/6/12 1977/6/14 John Krupey,Ewald Frank Welchner American Home Products Corp G01N33/76;A61K39/0006;C07K14/59;C07K16/26;A61K39/00; A method is disclosed for the purification of glycoproteins, particularly the beta subunit of human chorionic gonadotrophin, by polyacrylamide gel electrohoresis using the magnesium salt of8-anilino-1- naphthalene-sulfonic acid as a fluorescent probe. Also disclosed is an antiserum com- position produced by using spleen Immunization of glycoprotein antigens. 10 9 7 US - Expired - Lifetime, GB - Expired Expired Expired Withdrawn Pending , CA - Expired Expired Expired Withdrawn Pending , EP - Expired Expired Expired Withdrawn Pending , JP - Expired Expired Expired Withdrawn Pending , IT - Expired Expired Expired Withdrawn Pending
EP0000107A1 Metallic or metallised article coated with a polyphenylene oxide film carrying reactive groups, its electrochemical preparation and its use EP0000107A1 1978/12/20 EP78400001A 1978/6/1 EP0000107B1 1980/7/23 1977/6/10 Jacques Emile Dubois,Minh-Chau Pham,Pierre Camille Lacaze Agence National de Valorisation de la Recherche ANVAR C09D5/4476;C08G65/44;Y10T428/31504;Y10T428/31678; Films d'oxydes de polyphénylène comportant des groupes réactifs et leur préparation par voie électrochimique. Films obtenus à partir de monomères répondant à la formula: dans laquelle R représente un groupe acyle de 1 à 7 atomes de carbone, un groupe hydroxy, carboxy, alcoxy-carbonyle, amino, alkylamino ou phénylamino, et n est un nombre entier qui peut être nul dans le cas où R est un groupe acyle. Usage pour la fixation par voie chimique d'enzymes, résines, laques ou peintures, notamment sur des surfaces métalliques ou métallisées.Polyphenylene oxide films comprising reactive groups and their preparation by electrochemical means. Films obtained from monomers corresponding to the formula: in which R represents an acyl group of 1 to 7 carbon atoms, a hydroxy, carboxy, alkoxy-carbonyl, amino, alkylamino or phenylamino group, and n is a number integer which can be zero in the case where R is an acyl group. Use for the chemical fixing of enzymes, resins, lacquers or paints, in particular on metallic or metallized surfaces. 15 7 9 FR - Expired, EP - Expired Expired Expired - Lifetime , DE - Expired Expired Expired - Lifetime , US - Expired Expired Expired - Lifetime , IT - Expired Expired Expired - Lifetime
EP0000110B1 Process for obtaining acrylic acid from its solutions in tri EP0000110A1 1978/12/20 EP19780400011 1978/6/5 EP0000110B1 1984/8/29 1977/6/14 Georges Biola,Yves Komorn,Gérard Schneider Rhone Poulenc Chimie de Base SA C07C51/44; 6 7 17 FR - Expired, DE - Expired Expired Expired - Lifetime Expired Expired Expired , EP - Expired Expired Expired - Lifetime Expired Expired Expired , US - Expired Expired Expired - Lifetime Expired Expired Expired , CA - Expired Expired Expired - Lifetime Expired Expired Expired , BR - Expired Expired Expired - Lifetime Expired Expired Expired , IT - Expired Expired Expired - Lifetime Expired Expired Expired , JP - Expired Expired Expired - Lifetime Expired Expired Expired , ES - Expired Expired Expired - Lifetime Expired Expired Expired , SU - Expired Expired Expired - Lifetime Expired Expired Expired
EP0000113A1 Dihydropyridazones, their preparation and medicines containing them and dihydropyridazones for use in medical treatments EP0000113A1 1979/1/10 EP78100001A 1978/6/1 EP0000113B1 1981/9/16 1977/6/18 Rolf Dr. Lebkuecher,Marco Dr. Thyes,Horst Dr. Koenig,Hans Dieter Dr. Lehmann,Josef Dr. Gries,Dieter Dr. Lenke,Johannes Dr. Kunze BASF SE C07D237/04;A61P7/02;A61P9/12; Die Erfindung betrifft 6-(p-Acylaminophenyl)-4,5-dihydropyridazone -(3) der Formel I in eer für R¹ Wasserstoff oder ein Alkylrest mit 1 bis 3 C-Atomen steht und R², wenn für R¹ ein Wasserstoffatom steht, einen durch ein Halogenatom substituierten Alkylrest mit 3 bis 6 C-Atomen oder einen β-Halogenäthylrest oder, wenn für R¹ ein Alkylrest mit 1 bis 3 C-Atomen steht, einen durch ein Halogenatom substituierten Alkylrest mit 1 bis 6 C-Atomen bedeutet, ihre Herstellung und therapeutische Mittel, die eine Verbindung der Formel I als Wirkstoff, wobei R² auch einen Halogenmethyl- oder -Halogenäthylrest bedeutet für den Fall, daß R¹ Wasserstoff ist, enthalten. Diese Verbindungen sind als Anti-hypertensiva und zur Prophylaxe und Therapie thrombo-embolischer Erkrankungen geeignet.The invention relates to 6- (p-acylaminophenyl) -4,5-dihydropyridazone - (3) of the formula I in which R 1 is hydrogen or an alkyl radical having 1 to 3 C atoms and R 2 when R 1 is a hydrogen atom is an alkyl radical substituted by a halogen atom with 3 to 6 C atoms or a β-haloethyl radical or, when R 1 is an alkyl radical having 1 to 3 C atoms, means an alkyl radical substituted by a halogen atom with 1 to 6 C atoms , their preparation and therapeutic agents which contain a compound of formula I as an active ingredient, where R² also denotes a halogenomethyl or haloethyl radical in the case where R¹ is hydrogen. These compounds are suitable as anti-hypertensives and for the prophylaxis and therapy of thrombo-embolic diseases. 7 12 26 DE - Expired Expired IP Right Cessation Expired Expired, EP - Expired Expired IP Right Cessation Expired Expired, AT - IP Right Cessation, JP - Expired Expired IP Right Cessation Expired Expired, ZA - Expired Expired IP Right Cessation Expired Expired, CA - Expired Expired IP Right Cessation Expired Expired, US - Expired - Fee Related
EP0000114B1 Process for forming an integrated logic circuit comprising bipolar transistors, and integrated circuit formed by that process. EP0000114A1 1979/1/10 EP78100005A 1978/6/1 EP0000114B1 1980/4/30 1977/6/16 David L. Bergeron,Geoffrey B. Stephens International Business Machines Corp H01L21/02238;H01L21/02255;H01L21/31662;H01L21/8226;H01L27/0244;Y10S257/918;Y10S438/966; 2 18 14 US - Expired - Lifetime, JP - Pending Expired Expired, DE - Pending Expired Expired, EP - Pending Expired Expired

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