| Class / Patent application number | Description | Number of patent applications / Date published |
|---|
| 204157810 | Nitrogen product produced | 17 |
| 20110083956 | Continuous Method For Producing Fatty Acid Alkanol Amides - The invention relates to a continuous method for producing fatty acid alkanol amides, wherein at least one fatty acid of the formula (I) | 04-14-2011 |
| 20110089020 | Continuous Method for Producing Amides of Ethylenically Unsaturated Carboxylic Acids - The invention relates to a continuous method for producing amides, according to which at least one carboxylic acid of formula (I) R | 04-21-2011 |
| 20110089021 | Method For Producing Amides In The Presence Of Superheated Water - The invention relates to a method for producing carboxylic acid amides, according to which at least one carboxylic acid of formula (I) | 04-21-2011 |
| 20120055781 | MICROWAVE-ASSISTED PEPTIDE SYNTHESIS - An instrument and method for accelerating the solid phase synthesis of peptides are disclosed. The method includes the steps of deprotecting a protected first amino acid linked to a solid phase resin by admixing the protected linked acid with a deprotecting solution in a microwave transparent vessel while irradiating the admixed acid and solution with microwaves, activating a second amino acid, coupling the second amino acid to the first acid while irradiating the composition in the same vessel with microwaves, and cleaving the linked peptide from the solid phase resin by admixing the linked peptide with a cleaving composition in the same vessel while irradiating the composition with microwaves. | 03-08-2012 |
| 204157820 | Oxygen containing | 12 |
| 20100032284 | Method For Producing Alkaline (Meth)Acrylamides - The invention relates to a method for producing alkaline amides or imides of ethylenically unsaturated C | 02-11-2010 |
| 20100116642 | Method For Producing Alkaline Fatty Acid Amides - The invention relates to a method for producing alkaline fatty acid amides by reacting at least one amine that contains at least one primary or secondary amino group and at least one tertiary amino group with at least one fatty acid to form an ammonium salt, said ammonium salt being subsequently converted into the alkaline amide by means of microwave radiation. | 05-13-2010 |
| 20110083957 | Continuous Method For Producing Amides Of Aliphatic Hydroxycarboxylic Acids - The invention relates to a continuous method for producing hydroxycarboxylic acid amides, according to which at least one hydroxycarboxylic acid of formula (I) | 04-14-2011 |
| 20110226610 | SYNTHESIS OF NITRODIBENZYLFURAN CHROMOPHORE FOR PHOTODEPROTECTION OF ORGANIC MOLECULES - Inventors have developed a chromophore (nitrodibenzylfuranyl, or NBDF) for ultra efficient uncaging of a caged substrate (e.g., an organic molecule such as, for example, an amino acid, a biological molecules, such as, for example, second messengers inside cells). Photolysis of a NBDF derivative of EGTA (i.e. caged calcium) is about 50 times more efficient than others calcium cages (the quantum yield of photolysis is 0.6 and the extinction coefficient is 18,400. NDBF-EGTA has a 2-photon cross section of about 0.3-0.6 GM). | 09-22-2011 |
| 20110233048 | PHOTOBASE GENERATOR - There is intended to provide the novel compounds which generate a base easily when irradiated with long wavelength light (active energy rays), a photobase generator containing the compounds and a photobase generation method, and the present invention relates to the compounds represented by the general formula [1], a photobase generator containing the compounds and a photobase generation method: | 09-29-2011 |
| 20120234669 | PRECAST GEL FOR ELECTROPHORESIS, METHOD FOR PRODUCING THE SAME, AND USE OF THE SAME - This invention relates to a precast gel for electrophoresis comprising a support filled with an aqueous gel prepared by polymerizing an aqueous solution comprising a radically polymerizable monomer, a crosslinkable monomer, a buffer, a redox initiator comprising an oxidizer/reducer, and a photo sensitizer and having a pH level of 6.0 to 7.5 via light application. The slab gel for electrophoresis of the present invention can produce a precast gel for electrophoresis within a shorter period of time and in an easier manner than is possible with conventional techniques. Accordingly, the present invention enables production of a high-quality precast gel for electrophoresis in terms of productivity, cost, and quality, and the industrial applicability thereof is remarkable. | 09-20-2012 |
| 20130228449 | MICROWAVE-ASSISTED PEPTIDE SYNTHESIS - An instrument and method for accelerating the solid phase synthesis of peptides are disclosed. The method includes the steps of deprotecting a protected first amino acid linked to a solid phase resin by admixing the protected linked acid with a deprotecting solution in a microwave transparent vessel while irradiating the admixed acid and solution with microwaves, activating a second amino acid, coupling the second amino acid to the first acid while irradiating the composition in the same vessel with microwaves, and cleaving the linked peptide from the solid phase resin by admixing the linked peptide with a cleaving composition in the same vessel while irradiating the composition with microwaves. | 09-05-2013 |
| 20130327633 | Microchannel Gel Electrophoretic Separation Systems and Methods for Preparing and Using - A micro-analytical platform for performing electrophoresis-based immunoassays was developed by integrating photopolymerized cross-linked polyacrylamide gels within a microfluidic device. The microfluidic immunoassays are performed by gel electrophoretic separation and quantifying analyte concentration based upon conventional polyacrylamide gel electrophoresis (PAGE). To retain biological activity of proteins and maintain intact immune complexes, native PAGE conditions were employed. Both direct (non-competitive) and competitive immunoassay formats are demonstrated in microchips for detecting toxins and biomarkers (cytokines, c-reactive protein) in bodily fluids (serum, saliva, oral fluids). Further, a description of gradient gels fabrication is included, in an effort to describe methods we have developed for further optimization of on-chip PAGE immunoassays. The described chip-based PAGE immunoassay method enables immunoassays that are fast (minutes) and require very small amounts of sample (less than a few microliters). Use of microfabricated chips as a platform enables integration, parallel assays, automation and development of portable devices. | 12-12-2013 |
| 20140374238 | CONTROL APPARATUS FOR DISPENSING SMALL PRECISE AMOUNTS OF LIQUID REAGENTS - A precision volumetric liquid dispensing instrument is disclosed that includes two pressure sensors and a fluid passageway with a defined volume portion in communication with the two sensors for receiving and distributing liquid in relatively small volumes. One of the pressure sensors is positioned to measure pressure at one portion of the defined volume portion of the fluid passageway and the other of the gas pressure sensors is positioned to measure gas pressure at a different portion of the defined volume portion of the passageway. At least one valve is in communication with the passageway for moving fluids into or out of the defined volume portion of the fluid passageway, and a processor carries out a step selected from the group consisting of (i) calculating the volume of the liquid based upon the measured pressure and (ii) metering a liquid into the defined volume portion of the fluid passageway until the measured pressure indicates that a desired volume of fluid is in the fluid passageway. | 12-25-2014 |
| 20150343413 | METHOD FOR DIRECT PHOTOPATTERNING OF MOLECULES ON SURFACES - The disclosure relates to methods of photopatterning molecules directly on a surface by photochemical means. | 12-03-2015 |
| 20160067670 | MICROWAVE-ASSISTED PEPTIDE SYNTHESIS - An instrument and method for accelerating the solid phase synthesis of peptides are disclosed. The method includes the steps of deprotecting a protected first amino acid linked to a solid phase resin by admixing the protected linked acid with a deprotecting solution in a microwave transparent vessel while irradiating the admixed acid and solution with microwaves, activating a second amino acid, coupling the second amino acid to the first acid while irradiating the composition in the same vessel with microwaves, and cleaving the linked peptide from the solid phase resin by admixing the linked peptide with a cleaving composition in the same vessel while irradiating the composition with microwaves. | 03-10-2016 |
| 204157830 | Nitroso or oxime containing | 1 |
| 20140158522 | METHOD OF PRODUCING CYCLOALKANONE OXIME - A method produces a cycloalkanone oxime by photonitrosation using light emitting diodes as the light source for the next generation that replaces an electric discharge lamp with, for example, mercury or sodium sealed therein. The method produces the cycloalkanone oxime by a photochemical reaction of a cycloalkane with a photo nitrosating agent in a liquid by light irradiation. The method uses a light source satisfying conditions that, in an emission energy distribution with respect to wavelength of the light source, a wavelength at which emission energy has a maximum value is in a range of 550 nm to 700 nm and a wavelength range outputting energy of or over 5% strength of the peak strength is equal to or less than 150 nm. An irradiation distance in the liquid is equal to or greater than 200 mm, and concentration of the photo nitrosating agent in the liquid is 0.1 mol % to 0.5 mol %. | 06-12-2014 |
| 204157860 | Halogen containing | 1 |
| 20090260971 | METHOD OF PREPARING FLUOROALKYL COMPOUNDS USING RADIATION - Disclosed herein is a method of preparing a fluoroalkyl compound using radiation, including: mixing an alkyl compound having a leaving group with tetrabutylammonium fluoride (TBAF) in the presence of a reaction solvent at room temperature to form a mixed solution (step 1); and applying radiation to the mixed solution while stirring it to prepare a fluoroalkyl compound (step 2). The method of preparing a fluoroalkyl compound using radiation is advantageous in that fluoroalkyl compounds can be easily prepared in a short reaction time at room temperature, in that the method is safe because it is not required to use fluorine gas, which is harmful to the human body, in that the method can be usefully used to prepare fluoroalkyl compounds because the yield of fluoroalkyl compounds obtained using the method is higher than when using conventional SN2 reaction methods, and in that fluorine | 10-22-2009 |
