Method and device for determining viscosity

Sample carrier

The sample carrier (1) has a number of cavities (2) i.e. at least one sample holder (3) for a sample fluid (4) and at least one sample chamber (6) linked to the holder through a distribution channel (5). A cover (7) shrouds the sample chamber and channel. The carrier has an additional store (8) for the sample fluid, under the cover, linked to the ambient environment through a channel (9). In the event of sample fluid evaporation, or other loss, fluid flows back from the store. Fluid in the outer channel link prevents the entry of air beyond the store into the carrier.

Substituted triplets

Test strips

Infrared spectrometric gas sensor

The spectrometric sensor has a single moulded block forming a microstructure body with a base plate, a mirror grid, an input slot for reception of a poly-frequency IR beam and an output slot for a mono-frequency IR beam. The sample gas is contained in the free space between the entry and exit slots and the mirror grid, enclosed by cover plates at either end with gas inlet and exit openings. Pref. the mirror grid is provided by a concave reflection grid, with the mirror grid and the entry and exit slots for the IR radiation positioned on a Rowland circle, or along a curve in the vicinity of the Rowland circle.

Microstructured platform and method for handling a liquid

Für die Untersuchung von Flüssigkeiten in der Biologie, Biochemie, Chemie, Medizin und Pharmazie werden Verfahren angewendet, die mit erheblichem Aufwand für das Handhaben der Flüssigkeiten und für Hilfsmittel verbunden sind und die eine Mindestmenge an Flüssigkeit benötigen. Die mikrostrukturierte Plattform enthält Hohlräume und Kapillaren, in denen die Flüssigkeit durch Kapillarkraft transportiert wird. Sie umfasst fluidische Schalter, Dosiereinrichtungen für die Flüssigkeit, Abtrennvorrichtungen für die Flüssigkeit aus einer Dispersion und Bereiche zum Zusammenhalten einer begrenzten Flüssigkeitsmenge. Das Kapillarsystem kann verzweigt sein. Die Plattform ist für eien Vielzahl von Untersuchungen mit Flüssigkeitsmengen im Mikroliterbereich geeignet. Es werden nur sehr geringe Mengen von Reagenzien und Hilfsmitteln benötigt, die in den Hohlräumen in eingetrockneter oder immobilisierter Form vorgelegt sein können. Auf einer Plattform sind unterschiedliche Untersuchungen, die gleichzeitig nebeneinander oder nacheinander ablaufen können, realisierbar. Die Plattform ist in großer Stückzahl wirtschaftlich herstellbar und an viele Forderungen zum Reaktionsablauf und zur Auswertung der Untersuchungsergebnisse anpassbar. For the study of liquids in biology, biochemistry, chemistry, medicine and pharmacy procedures are applied, which are associated with considerable effort for the handling of fluids and aids and require a minimum amount of liquid. The microstructured platform contains cavities and capillaries in which the liquid is transported by capillary force. It comprises fluidic switches, liquid metering devices, dispersion liquid separation devices, and limited fluid retention areas. The capillary system can be branched. The platform is suitable for a large number of investigations with liquid volumes in the microliter range. Only very small amounts of reagents and auxiliaries are required, which may be initially introduced in the cavities in dried or immobilized form ...

PROCESS FOR THE PRODUCTION OF MOLDED BODIES ON THE BASIS OF AETHYLENIMINE COMPOUNDS

Manually actuated atomiser

The manual sputterer for fluids, to apply a droplet spray to a surface, has energy stored by a spring (59) using a coil spring, a plate spring or a gas spring. together with a piston (81) and two channels. The spray action is triggered by manual release (58) of a locking mechanism (74). The spring is outside the fluid storage zone, and acts on the piston to force a small volume of the fluid out of the cylinder (53) at a pressure of 1-5 MPa (10-50 bar). The distribution of the droplet sizes can be adjusted, with a mean droplet size of ≤ 50 mu m. The mass flow through the jet (60) is ≤ 0.4 g/second.

Inhaler and storage for a dry drug formulation and methods and use thereof

Es werden ein Inhalator, ein Speicher und ein Verfahren zur Zerstäubung einer trockenen Arzneimittelformulierung vorgeschlagen. Die Arzneimittelformulierung wird zunächst von einem flüssigen Lösungsmittel gelöst und dann zusammen mit dem Lösungsmittel zerstäubt. Dies ermöglicht eine einfache Dosierung und gute Lagerung der Arzneimittelformulierung im trockenen Zustand. Besonders bevorzugt wird die trockene Arzneimittelformulierung durch das Eintrocknen einer zunächst flüssigen Arzneimittelformulierung bereitgestellt. Alternativ kann die eingetrocknete Arzneimittelformulierung auch in trockener Form durch einen Gasstrom ausgetragen und zerstäubt werden. An inhaler, a reservoir and a method for atomizing a dry drug formulation are proposed. The drug formulation is first dissolved by a liquid solvent and then atomized together with the solvent. This allows easy dosing and good storage of the drug formulation in the dry state. Most preferably, the dry drug formulation is provided by the drying of an initially liquid drug formulation. Alternatively, the dried drug formulation may also be discharged and atomized in dry form through a gas stream.

Alkoxymethyl-substituted pyridone biphenyls

4-PHENYL-PIRIDONES AND 4-PHENYL-2-ALCOXIPIRIDINAS SUBSTITUTED AS INHIBITORS OF HMG-COA-REDUCTASA.

3-FENILPIRIDONAS Y 4-FENILPIRIDINAS SUSTITUIDAS SE PRODUCEN, POR REDUCCION DE LOS CORRESPONDIENTES DERIVADOS 4-FENILO-PIRIDONAS POR EJEMPLO DERIVADOS 4-FENILOALCOXIPIRIDINAS. LAS 4-FENIL-PIRIDONAS Y 4-FENIL-2-ALCOXIPIRIDINAS SUSTITUIDAS PUEDEN EMPLEARSE COMO SUSTANCIAS ACTIVAS EN MEDICAMENTOS, PARTICULARMENTE PARA EL TRATAMIENTO DE HIPERLIPOPROTEINEMIA. 3-PHENYLPYRIDONES AND SUBSTITUTED 4-PHENYLPYRIDIDS ARE PRODUCED, BY REDUCTION OF THE CORRESPONDING DERIVATIVES 4-PHENYL-PYRIDONES BY EXAMPLE 4-PHENYLALALCOXIPYRIDINE DERIVATIVES. 4-PHENYL-PIRIDONES AND 4-PHENYL-2-ALCOXIPIRIDINAS CAN BE USED AS ACTIVE SUBSTANCES IN MEDICINES, PARTICULARLY FOR THE TREATMENT OF HYPERLIPOPROTEINEMIA.

IMIDAZOLYL SUBSTITUTED PHENYL ACIDANCE AMIDE

5-AMINO PYRAZOLES AND TRIAZOLES AS PESTICIDES

Derivados de 1,2-diazol y de 1,2,4-triazoles como plaguicidas; formulaciones que los comprenden y su uso para el control de plagas animales, en particular insectos, arácnidos o nematodos. Éstos compuestos también se emplean en la protección de semillas o plantas. Reivindicación 1: Compuesto de la fórmula (1) donde Ar representa fenilo o un anillo heteroaromático de 5 ó 6 miembros, en cada caso no sustituido o sustituido con 1 a 4 RAʳ; donde cada RAʳ considerado en forma independiente de los demás representa halógeno, ciano, nitro, SF₅, C(Q¹)Rᵃ, C(O)ORᵃ, C(Q¹)NRᵇRᶜ, NRᵈRᵉ, ORᵃ, S(O)ₙRᵃ o SO₂NRᵇRᶜ; o representa C₁₋₆-alquilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo o C₃₋₇-cicloalquilo, todos los cuales pueden en cada caso ser no sustituidos o de mono a tridecasustituidos con halógeno y/o opcionalmente con 1 a 3 Rᶠ; o representa fenilo, un anillo heteroaromático de 5 ó 6 miembros o un sistema anular heteroaromático de 7 a 11 miembros, cada uno de los cuales en cada caso no está sustituido o está sustituido con 1 a 3 Rᵍ; A representa N o CRA; donde RA representa H, halógeno, ciano, nitro, SF₅, C(Q¹)Rᵃ, C(O)ORᵃ, C(Q¹)NRᵇRᶜ, NRᵈRᵉ, ORᵃ, S(O)ₙRᵃ o SO₂NRᵇRᶜ; o representa C₁₋₆-alquilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo o C₃₋₇-cicloalquilo, todos los cuales pueden en cada caso ser no sustituidos o de mono a tridecasustituidos con halógeno y/o opcionalmente con 1 a 3 Rᶠ; o representa fenilo, un anillo heteroaromático de 5 ó 6 miembros o un sistema anular heterocíclico aromático de 7 a 11 miembros, cada uno de los cuales en cada caso no está sustituido o está sustituido con 1 a 3 Rᵍ; R¹ representa -NR¹¹R¹², -N(Rᵇ)NRᵈRᵉ, -N(Rᵇ)ORᵃ, -N(Rᵇ)-CN, -N(R¹¹)C(Q¹)Rᵇ, -N(R¹¹)C(Q¹)NRᵇRᶜ, -N(R¹¹)C(O)ORᵃ, -N(R¹¹)C(O)C(O)Rᵇ, -N(R¹¹)C(O)C(O)ORᵃ, -N(R¹¹)C(O)C(O)NRᵇRᶜ, -N(R¹¹)SO₂Rᵃ, -N=C(Rᵇ)N(Rᵇ)(Rᶜ), -N=C(Rᵇ)(Rᶜ), -N=S(O)RᵃRᵃ o -N=SSRᵃRᵃ; donde R¹¹ representa H; o representa C₁₋₆-alquilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo o C₃₋₇-cicloalquilo, todos los cuales pueden en cada caso ser no sustituidos o de mono a ...

Use of 4-(2- or 3-nitrophenyl) di:hydro:pyridin:amide derivs. - as natriuretic agents for treating hypertonia, coronary insufficiency, arrhythmia, pulmonary and cerebral oedema, diabetes, etc.

The use of 4-(2- or 3-nitrophenyl)-dihydropyridinamide derivs. (I) as natriuretic agents is claimed. In (I), R1 is 12- or 3-nitrophenyl; and R2 is 1-6C alkyl or 3-5C cycloalkyl. Cpds. (Ia), i.e. cpds. (I) where R1 is 2-nitrophenyl and R2 is methyl or ethyl or R1 is 3-nitrophenyl and R2 is methyl, ethyl, propyl or cyclopropyl, are also claimed. (I) may be prepd. by reaction of aldehyde (R1-CH), enamine of formula (III) and keto methyl ester of formula (IV). USE - Cpds. (I) are used for the treatment of hypertonia, coronary and kidney insufficiency, coronary arrhythmia, liver cirrhosis, ascites, pulmonary and cerebral oedema, pregnancy-associated oedema, glaucoma and diabetes. Admin. is orally, esp. perlingually or i.v., in conventional dosage forms. Dosages are pef. 0.01-0.5 mg/kg i.v. and 0.1-10 mg/kg p.o. In an example, 1,4-dihydro-2,6-dimethyl -3-carboxymethyl- 4-(2-nitrophneyl)-pyridine -5-carboxylic acid imidazolide (IX) (3g) was stirred in 40% methylamine soln. (40 ml) for 18 hrs. and the crystalline prod. obtd. was washed and dried to give 1,4-dihydro-2,6- dimethyl-3-methoxycarbonyl- 4-(2-nitrophenyl)-pyridine -5-carboxylic acid methylamide (I) (2.9 g; 79.2% yield); m.pt. 197-200 deg. C.

2-PIRIDONAS AND PIRIDO-2-TIONAS SUBSTITUTED, PROCEDURE FOR ITS MANUFACTURE AND ITS USE IN MEDICINES.

EL INVENTO TRATA DE UN PROCEDIMIENTO PARA PRODUCIR NUEVA PIRIDONA-2 Y PIRIDITIONA 2 SUSTITUIDA QUE CONSISTE EN REDUCIR LA PURIDONA Y PIRIDITIONA QUE ESTAN SUSTITUIDAS A TRAVES DE RESTOS CETONICOS , ESTERIFICAR LAS PURIDONAS, PURIDITIONAS, CIDIZAR O HIDROGENAR LAS PURIDONAS ESTERIFICADAS Y DESCRIBE LA APLICACION DEL COMPUESTO EN MEDICAMENTOS COMO MATERIA ACTIVA. THE INVENTION IS ABOUT A PROCEDURE TO PRODUCE NEW PIRIDONA-2 AND SUBSTITUTED PIRIDITIONA 2 WHICH CONSISTS OF REDUCING PURIDONA AND PIRIDITIONA WHICH ARE SUBSTITUTED THROUGH KETONIC PURIDES, THE PURIDIDAS, PURIDIAS, AND COMPOSED IN MEDICINES AS AN ACTIVE MATTER.

Method of joining two or more parts

Pentasubstituted phenyls

Substituted biphenyls can be prepared by reduction of appropriate ketones and, if appropriate, subsequent hydrolysis, cyclization, hydrogenation and separation of isomers. The substituted biphenyls can be used as active compounds in medicaments.

Method and device for determining the viscosity

Es werden ein Verfahren und eine Vorrichtung zur Bestimmung der Viskosität eines Fluids vorgeschlagen. Eine sehr einfache und genaue Bestimmung wird dadurch ermöglicht, daß magnetische Partikel im Fluid durch ein zeitlich variierendes Magnetfeld in Schwingung versetzt werden. Eine Messung der Amplitude und/oder Phase der Partikelschwingung wird zur Bestimmung der Viskosität oder einer damit zusammenhängenden Größe, wie die Gerinnung von Blut oder ein Glucosegehalt, verwendet. A method and apparatus for determining the viscosity of a fluid are proposed. A very simple and accurate determination is made possible by the fact that magnetic particles in the fluid are set in vibration by a time-varying magnetic field. A measurement of the amplitude and / or phase of the particle vibration is used to determine the viscosity or an associated quantity, such as the coagulation of blood or a glucose content.

Dishwashing and cleaning agents for mucous membranes

Device for draining a liquid from a capillary

AMINOALKYL AZOL COMPOUNDS SUBSTITUTED WITH HETEROARYL AS PESTICIDES

La presente se refiere a compuestos de aminoalquil azol sustituidos con heteroarilo de la fórmula general (1), donde los elementos estructurales Y, Q¹, Q², R¹, R², R³ y R⁴ tienen el significado dado en la descripción, a formulaciones y composiciones que comprenden tales compuestos y para su uso en el control de plagas animales que incluyen artrópodos e insectos en la protección de plantas y a su uso para el control de ectoparásitos en animales. The present refers to heteroaryl substituted aminoalkyl azole compounds of the general formula (1), where the structural elements Y, Q¹, Q², R¹, R², R³ and R⁴ have the meaning given in the description, to formulations and compositions which comprise such compounds and for their use in the control of animal pests including arthropods and insects in the protection of plants and their use for the control of ectoparasites in animals.

Process for the preparation of a new derivative of 6-amino-penicillanic acid

Method and apparatus for separating and eliminating gas bubbles from liquids

IMIDAZOLYL-propenoic acid derivatives

Heterocyclic substituted phenyl-cyclohexane-carboxylic acid derivatives

Device for fragmenting tissue

HIGH SELECTIVE METHOD FOR THE PREPARATION OF DERIVATIVES OF PHENYLATED, 3,4-DIHYDROPYRIDINE ACID, 3,4-DIHYDROPYRIDINE-3-DICARBOXYL ACID

Method and device for determining viscosity

Method for determining the viscosity, or an associated variable, for a fluid, or for microscopic particles (3) in a fluid (2). According to the method, at least a magnetic particle is moved in an inhomogeneous magnetic field (6) and set oscillating by temporally alternating the magnetic field. The amplitude and phase of the resultant particle oscillation is measured and from it the viscosity or an associated fluid variable is determined. An independent claim is made for a device for use in determining the viscosity, or an associated variable, for a fluid, or for microscopic particles in a fluid.

Substituted mono- and bihydridylmethylpyridones

Metal application process for torsional damper weight - uses magnetically shaped endless thin walled ring of polygonal form

Imidazolyl-substituted amides of phenylacetic acid

Imidazolyl-substituted phenylacetamides of the general formula <IMAGE> in which A represents straight-chain or branched alkyl or alkenyl, each of which has up to 8 carbon atoms, or represents cycloalkyl having 3 to 8 carbon atoms, B represents hydrogen, halogen or perfluoroalkyl having up to 5 carbon atoms, D represents a group of the formula -CH2OR<3>, -CO-R<4>, -CO-NR<5>R<6>, <IMAGE> or <IMAGE>, E represents hydrogen, halogen, nitro, hydroxyl, trifluoromethyl, trifluoromethoxy, straight-chain or branched alkyl, alkoxy or alkoxycarbonyl, each of which has up to 6 carbon atoms, cyano or carboxyl, L represents straight-chain or branched alkyl having up to 8 carbon atoms which is optionally substituted by cycloalkyl having 3 to 8 carbon atoms or phenyl, or represents cycloalkyl having 3 to 12 carbon atoms which is optionally substituted by straight-chain or branched alkyl having up to 6 carbon atoms, R<1> represents hydrogen or straight-chain or branched alkyl having up to 8 carbon atoms, R<2> represents a radical of the formula -C(CH3)2-CH2OH, <IMAGE> and salts thereof. The compounds are angiotensin-II antagonists and can be used as active substances in pharmaceuticals, in particular for the treatment of hypertension and atherosclerosis.

SUBSTITUTED IMIDAZOLYL-PROPENSAEUREDERIVATE

DERIVATIVES OF FENYL-CYCLLOHEXANE-CARBOXYLIC ACIDS HETEROTRICICLICAMENTE SUBSTITUTED.

DERIVADOS FENIL DO HETERO ONDE LOS COMPUESTOS HETEROCICLICOS SE TRANSFORMAN CON DERIVADOS CICLOEXANO ACIDO CARBOXILICO, QUE SON SUSTITUIDOS POR RESTO BENCIL HALOGENO. LOS COMPUESTOS PUEDEN SER UTILIZADOS COMO SUSTANCIA ACTIVA EN MEDICAMENTOS. DERIVATIVES FENIL DO HETERO ONDE THE HETEROCICLICOS COMPOUNDS ARE TRANSFORMED WITH CYCLOEXANE DERIVATIVES CARBOXILICO ACID, WHICH ARE REPLACED BY REST BENZL HALOGENO. THE COMPOUNDS MAY BE USED AS AN ACTIVE SUBSTANCE IN MEDICINES.

Alkoxymethyl-substituted pyridonebiphenyls

Alkoxymethyl-substituted pyridone biphenyls of the general formula <IMAGE> in which R<1> stands for a carboxyl group, or stands for a C1-C8-alkoxycarbonyl group, R<2> stands for C1-C10-alkyl (straight-chain or branched) which is optionally substituted by phenyl, R<3> stands for halogen, hydrogen, C1-C6-alkyl, hydroxyl, C1-C8-alkoxy, trifluoromethyl or trifluoromethoxy, R<4> stands for carboxyl or for tetrazolyl and X stands for oxygen or sulphur, and their salts. Alkoxymethyl-substituted pyridone biphenyls are prepared by reacting appropriate pyridones with biphenylmethyl halogen compounds. The alkoxy methyl-substituted pyridone biphenyls can be employed as active ingredients in medicaments, in particular for the treatment of high blood pressure and atherosclerosis.

sample carrier

Es wird ein Probenträger mit einer Probenaufnahme für Probenflüssigkeit und vorzugsweise mehreren daran angeschlossenen Probenkammern vorgeschlagen. Um ein Nachfüllen von Probenflüssigkeit bei Verdunstung oder sonstigem Verlust oder Verbrauch von Probenflüssigkeit zu vermeiden, ist zusätzlich ein Speicher für Probenflüssigkeit vorgesehen, der ebenso wie die Probenkammern abgedeckt ist und dessen Verbindungskanal zur Umgebung durch Probenflüssigkeit verschließbar ist. A sample carrier with a sample receptacle for sample liquid and preferably several sample chambers connected thereto is proposed. In order to avoid replenishment of sample liquid in the event of evaporation or other loss or consumption of sample liquid, an accumulator for sample liquid is additionally provided which, like the sample chambers, is covered and whose connection channel to the environment can be closed by sample liquid.

Use of (carboxy- or tetrazolyl-bi:phenyl)methyl)pyridone compounds

Substituted biphenyl derivatives of formula (I) are claimed for treating liver disease. R1 = carboxy or 1-8C alkoxycarbonyl; R2 = 1-8C alkyl; R3 = H, halo, OH, 1-6C alkoxy, 1-8C alkyl, CF3 or OCF3; and R4 = carboxy or tetrazolyl.

Sulfonylbenzyl-substituted imidazopyridines

Imidazopyridines of the formula (I) <IMAGE> in which R<1> represents alkyl or alkenyl, each of which is optionally substituted by cycloalkyl, or represents cycloalkyl, B and D together form a radical of the formula <IMAGE> A represents a 3- to 8-membered, saturated heterocycle bonded via the nitrogen atom and having up to two further heteroatoms from the group consisting of S, N and O and which is optionally substituted up to 2 times by identical or different perfluoroalkyl having up to 5 carbon atoms or by a radical of the formula <IMAGE> The sulphonylbenzyl-substituted imidazopyridines can be employed as active compounds in medicaments, in particular for the treatment of hypertension and atherosclerosis.

Method of manufacturing miniaturised hollow bodies

A coating of electrically conductive material is applied to a microstructured plastic layer. A metal layer is precipitated o the conductive areas of this plastic layer and on conductive areas of the carrier plate (1). To obtain the required miniaturized hol component, the microstructured plastic layer is removed, starting at least at one location (3, 13) where this layer is accessibl

Trisubstituted biphenyls

Trisubstituted biphenyls of the general formula <IMAGE> in which R<1> stands for a carboxyl radical, or for a C1-C8-alkoxycarbonyl radical, R<2> stands for straight-chain or branched C1-C8-alkyl, R<3> stands for halogen, hydroxyl, cyano, C1-C6-alkoxy, straight-chain or branched C1-C8-alkyl, trifluoromethyl, trifluoromethoxy, carboxamido, carboxyl, C1-C8-alkoxycarbonyl or nitro, and R<4> stands for a carboxyl radical, or for tetrazolyl, and their salts. The trisubstituted biphenyls can be employed as active ingredients in medicaments, for example as angiotensin II antagonists.

PROCESS OF PURE ENANTIOMERIC PREPARATION OF CYCALOALO-INDOL-AND AZAINDOL-AND PYRIMIDO {1,2a}

1 - substituierte 6-aryl-4h-striazolo eckige klammer auf 3,4c eckige klammer zu thieno-eckige klammer auf 2,3e eckige klammer zu 1,4-diazepine, verfahren zu ihrer herstellung und diese enthaltende arzneimittel

Hochselektives verfahren zur herstellung von enantiomerenreinen phenylsubstituierten 1,4- dihydropyridin-3,5-dicarbonsäurederivaten

Imidazolyl-substituierte phenylessigsäureprolinamide

Substituierte pyridyl-dihydroxy-heptensäure und deren salze

Hetero-tricyclisch-substituierte phenyl- cyclohexan-carbonsäurederivate

Method of new dihydropyridinamides production

Drehzahlstellbare anordnung mit einem einphasen-komutatormotor

Verfahren zur Polymerisation von Cyclopenten mittels aus Verbindungen von Ubergangsmetallen und Alkylalumlnlumhalogeniden hergestellter Mischkatalysatoren

Faserreaktive Anthrachinonfarbstoffe und deren Verwendung zum Färben und Bedrukken von Textilmaterial

Herstellung von Perfluorkohlenstoffsulfonylfluoriden

Substituierte pyridylmethylpyridone als angiotensin ii antagonisten

Verfahren zur elektrochemischen fluorierung von organischen verbindungen

Verfahren und Vorrichtung zur elektrochemischen Fluorierung

Verfahren zur elektrochemischen Fluorierung von organischen Verbindungen

Verfahren zur Veredelung von cellulosehaltigen Materialien

Vorrichtung zum Erwärmen von Stoffen mittels gebündelter Elektronenstrahlen im Vakuum

Substituierte biphenylpyridone als angiotensin ii antagonisten

Procedimiento para la preparaciòn de ( s , s ) - bencil - 2,8 - diazabiciclo 4.3.0. nonano.

LA INVENCIÒN SE REFIERE A UN PROCEDIMIENTO PARA LA PREPARACIÒN DE (S,S)8BENCIL2,8DIAZABICICLO[4.3.0]

Verfahren zur herstellung von enantiomeren reinen cycloalkano-indol- und azaindol- und pyrimido (1, 2a) -indol-carbonsäuren und deren aktivierte derivate

Verwendung von aminocarbonsaeuren als viskositaetserhoehende mittel

Verfahren zur Herstellung eines neuen Antibioticums

Schleudergu Bverf ahren

Substituierte pyridine als hmg-coa-reduktase- inhitoren

Sauger mit Ovalquerschnitt im Nippelteil

Diagnostisches Mittel zum Nachweis von Fett oder fettartigen Substanzen bzw. von Wasser

Gelatineschicht mit verringerter Quellung. %

Disposicion microfluidica para la dosificacion de fluidos.

Disposición microfluídica para dosificar una o varias primeras cantidades dosificadas de líquido (A) y para separar éstas de una segunda cantidad de líquido (B), que comprende las siguientes características: - la disposición presenta un primer canal (2) y varios segundos canales (16); - el canal (2) presenta una entrada (11) y una salida (12); - la disposición presenta en la zona de la salida (12) una fuerza capilar que es superior o igual a la fuerza capilar en la zona de la entrada; - los segundos canales (16) se ramifican en uno o varios puntos de derivación (4) del primer canal (2); - los segundos canales (16) tienen una mayor fuerza capilar que el primer canal (2) en los puntos de ramificación (4); - los segundos canales (16) tienen un volumen predeterminado; - los segundos canales (16) empiezan en los puntos de ramificación (4) y terminan en un cierre de capilaridad (9); - los segundos canales (16) están divididos en primeras secciones (6), segundas secciones (7) y terceras secciones (8), formando de esta manera un segundo sistema de canales; - la primera sección (6) está diseñada en forma de ranura y constituye un canal, la segunda sección (7) está diseñada en forma de rebaje y la tercera sección (8) está diseñada en forma de ranura y forma un canal; - la primera sección (6) está conectada al primer canal (2) en el punto de ramificación (4); - en la primera sección se une la segunda sección (7); - la tercer sección (8) se une a la segunda sección (7) y termina en el cierre capilar (9); - en el cierre capilar (9) se une de manera correspondiente un tercer canal (10); - cada uno de los terceros canales (10) presentan una segunda salida (13); - las segundas salidas (13) presentan de modo correspondiente un cierre capilar; - los canales (2, 16, 10) están dispuestos en forma de ranuras o cubetas en una superficie, estando recubiertos por una tapa.

Derivados heterociclos bicíclicos condensados como plaguicida

Reivindicación 1: Compuestos de la fórmula (1) caracterizada porque Aa significa nitrógeno o =C(R⁷)-, Ab significa nitrógeno o =C(R⁸)-, Ac significa nitrógeno o =C(R⁹)-, Ad significa nitrógeno o =C(R¹⁰)-, Ae significa nitrógeno o =C(R¹¹), a lo cual, Ab, Ac, Ad y Ae no pueden representar simultáneamente nitrógeno, R¹ significa C₁₋₆alquilo, C₁₋₆halógenoalquilo, C₁₋₆alquenilo, C₂₋₆halógenoalquenilo, C₂₋₆alquinilo, C₂₋₆halógenoalquinilo, C₃₋₈cicloalquilo, halógenoC₃₋₈cicloalquilo, C₃₋₆cicloalquilo-C₁₋₆alquilo, C₃₋₆cicloalquilo-C₁₋₆halógenoalquilo, C₁₋₆alquilo-C₃₋₈cicloalquilo, C₁₋₆halógenoalquilo-C₃₋₈cicloalquilo, C₃₋₈cicloalquilo-C₃₋₈cicloalquilo, espiro-C₃₋₈cicloalquilo-C₃₋₈cicloalquilo, C₄₋₁₂bicicloalquilo, C₁₋₆cianoalquilo, C₁₋₆hidroxialquilo, C₁₋₆alcoxi-C₁₋₆alquilo, C₂₋₆cianoalquenilo, C₃₋₆cicloalquilo-C₂₋₆alquenilo, C₂₋₆cianoalquinilo, C₃₋₆cicloalquilo-C₂₋₆alquinilo, C₁₋₆halógenoalcoxi-C₁₋₆alquilo, C₂₋₆alqueniloxi-C₁₋₆alquilo, C₂₋₆halógenoalqueniloxi-C₁₋₆alquilo, C₂₋₆alquiniloxi-C₁₋₄alquilo, C₂₋₆halógenoalquiniloxi-C₁₋₆alquilo, C₁₋₆alquiltio-C₁₋₆alquilo, C₁₋₆alquilosulfinilo-C₁₋₆alquilo, C₁₋₆alquilosulfonilo-C₁₋₆alquilo, C₁₋₆halógenoalquiltio-C₁₋₆alquilo, C₁₋₆halógenoalquilosulfinilo-C₁₋₆alquilo, C₁₋₆halógenoalquilosulfonilo-C₁₋₆alquilo, o tri-C₁₋₆alquilsililo, R⁷ significa hidrógeno, ciano, halógeno, acetilo, hidroxi, amino, C₃₋₈cicloalquilo, halógenoC₃₋₈cicloalquilo, C₁₋₆alquilo, C₁₋₆haloalquilo, C₁₋₆cianoalquilo, C₂₋₆alquenilo, C₂₋₆haloalquenilo, C₂₋₆alquinilo, C₂₋₆haloalquinilo, C₁₋₆alcoxi, C₁₋₆haloalcoxi, C₁₋₆alquiltio, C₁₋₆halógenoalquiltio, C₁₋₆alquilsulfinilo, C₁₋₆haloalquilsulfinilo, C₁₋₆alquilsulfonilo o C₁₋₆haloalquilsulfonilo, R⁸, R⁹, R¹⁰, R¹¹ independientemente uno del otro significan hidrógeno, halógeno, C₁₋₆alquilo, C₁₋₆haloalquilo, C₁₋₆alcoxi, C₁₋₆haloalcoxi, C₁₋₆haloalquiltio, C₁₋₆haloalquilsulfinilo, C₁₋₆haloalquilsulfonilo o C₁₋₆halógenoalquilo-C₃₋₈cicloalquilo, dado el caso, C₁₋₆cianoalquilo mono o polisustituido por halógeno, C₁₋₆cianoalquilo- ...

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