Bapat
Abhijit S. Bapat, Delhi IN
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20140364440 | TOPICAL OIL COMPOSITION FOR THE TREATMENT OF FUNGAL INFECTIONS - The present invention is directed to anti-fungal compositions comprising an anti-fungal agent, an oil and excipients or additives. The compositions of the present invention are devoid of C-11 or greater fatty acids/esters. | 12-11-2014 |
20140364595 | CONJUGATE-BASED ANTIFUNGAL AND ANTIBACTERIAL PRODRUGS - The invention provides conjugate-based antifungal or antibacterial prodrugs formed by coupling at least one anti-fungal agent or antibacterial agent with at least one linker and/or carrier. The prodrugs are of formula: (i) (AFA) | 12-11-2014 |
Anil Bapat, Bangalore IN
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20140126532 | SEAMLESS MOBILITY FROM 3G NETWORK TO WIFI NETWORK - According to one aspect, a multi-function gateway device (MFG) receives a request for terminating a first data session identified by a first IP address, the request originating either directly from a user equipment (UE), or indirectly from the UE via a radio access controller (RNC), wherein the UE is communicatively coupled to a 3G radio access network (RAN), such that data traffic of the first data session is routed to a first serving GPRS support node (SGSN). According to one aspect of the invention, the MFG further determines whether the UE is connected to the MFG via a WiFi RAN, any 3G call teardown related messages are blocked in order to keep the 3G GTP-U tunnel up. Continue routing user's data originating via the WiFi RAN over the GTP-U tunnel with the SGSN. | 05-08-2014 |
Chintamani Prabhakar Bapat, Thane IN
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20110172425 | NOVEL WATER BASED PROCESS FOR THE PREPARATION OF SUBSTITUTED DIPHENYLMETHYL PIPERAZINES - The present invention relates to a novel water based process for the preparation of substituted diphenylmethyl piperazines of Formula I and pharmaceutically acceptable salts | 07-14-2011 |
Deepti Bapat, Bangalore IN
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20160053193 | Novel water based metal working fluid composition - This invention is a composition of an ester resulting from the reaction of an oligomer of ethylene oxide in presence or a catalyst, with fatty acids. The resulting water based metal working fluid additive is useful as it imparts property of stable micro-emulsion and helps improving the wear life, coefficient of friction and other tribological properties among other uses. | 02-25-2016 |
Kiran A. Bapat, Pune IN
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20110046416 | PROCESS FOR PREPARATION OF BENZPHETAMINE AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS - The present invention provides a simple method for preparation of benzphetamine and its acid addition salt comprising reaction of methamphetamine hydrochloride of formula (III) with benzyl chloride and treating the isolated benzphetamine of formula (II) with an acid dissolved in an organic solvent to provide benzphetamine acid addition salt, more specifically, benzphetamine hydrochloride of formula (I). | 02-24-2011 |
Mohini Anand Bapat, Mumbai IN
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20120094883 | PERSONAL CLEANSING COMPOSITION - This invention relates to a liquid or soft-solid personal cleansing composition that utilises the detergency properties of new materials which are more efficient, more inexpensive and are an environmentally friendly alternative to conventional soaps or synthetic surfactants. It more particularly relates to a cleansing composition in liquid, gel or cream formats. The present invention provides for a personal cleansing composition comprising (i) 1 to 50% of treated clay particles; and (ii) a cosmetically acceptable base; wherein said treated clay particles are asymmetric 1:1 or 2:1:1 clay particles having alternating tetrahedral and octahedral sheets terminating with a tetrahedral sheet at one external surface plane and an octahedral sheet at another external surface plane, with a fatty acid of carbon chain length 10 to 22 attached to coordinating cation on one of said exterior surface planes. | 04-19-2012 |
Pratap Sashikant Bapat, Bhavnagar IN
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20150107983 | HOUSEHOLD SOLAR STILL WITH EASY OPERATION AND MAINTENANCE AND ENHANCED OUTPUT - The invention discloses the design of an improved household solar still with enhanced output and high recovery. The output and recovery are enhanced by (i) aligning the top glass and basin so as to maximize the input solar radiation, (ii) using North-South reflectors in V trough configuration to further raise the incident radiation, (iii) employing metallic condensers on sides to maximize condensation efficiency, (iv) using suitably heated and cooled saline water by taking advantage of ambient temperature differential during a day and using such water as feed water and condenser water respectively. Use of detachable top glass assembly and teflon cork at the bottom allow for easy cleaning of the interior of the still and discharge of concentrate, respectively. The still is also demonstrated to be useful for other applications where, besides producing distilled water, the concentrate is a more value added product than the feed. | 04-23-2015 |
Pratap Shashikant Bapat, Bhavnagar IN
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20150196891 | PROCESS FOR CONDUCTING ORGANIC REACTIONS IN A STANDALONE AND AFFORDABLE LABORATORY SCALE SOLAR PHOTO THERMOCHEMICAL REACTOR - A process conducts organic reactions in a standalone laboratory scale solar photo thermo chemical reactor. For organic reactions require elevated temperature, light and mechanical agitation, all three energy forms can be simultaneously derived from solar radiation. Organic synthesis, such as bromination of toluene derivatives (benzylic bromination), bromination of cyclic acyclic hydrocarbon and oxidative cyclization of N-phenylethyl benzamide through bromination were successfully conducted in such reactors. | 07-16-2015 |
Rajaram Uday Bapat, Maharashtra IN
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20090264662 | PROCESS FOR THE PREPARATION OF 5,6 -DIHYDRO -4H-4(S)-ETHYLAMINO-6(S)-METHYLTHIENO[2,3-b] THIOPYRAN-2-SULFONAMIDE- 7,7 -DIOXIDE AND ITS SALT - The present invention relates to resolution of (cis, trans) 5,6-dihydro-4H-4-ethylamino-6-methylthieno[2,3-b] thiopyran-2-sulfonamide-7,7-dioxide using dibenzoyl-L-tartaric acid monohydrate or di-p-toluoyl-L-tarrtaric acid monohydrate as a chiral resolving agent in presence of methanol to obtain hemitartarate salt, purifying it to obtain hemitartarate salt of 5,6-dihydro-4 H-4 (S)-ethyl amino-6(S) methylthieno [2,3-b] thiopyran-2-sulfonamide-7,7-dioxide with de of >99% , Chemical purity >99.5% with cis isomer content of <0.1% and further converting into its pharmaceutically acceptable salts, preferably hydrochloride salt. | 10-22-2009 |
Sachin Bapat, Bangalore Krn IN
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20140177344 | METHOD AND APPARATUS FOR CLOCK POWER SAVING IN MULTIPORT LATCH ARRAYS - An integrated circuit element is disclosed having a memory device; a P-type semiconductor region including a first semiconductor device from a first memory port circuit coupled to the memory device and configured to enable access to the memory device when the first semiconductor device is activated; an N-type semiconductor region including a second semiconductor device from a second memory port circuit coupled to the memory device and configured to enable access to the memory device when the second semiconductor device is activated; and a plurality of signal lines distributed over the P-type and N-type semiconductor regions including a first memory port selection line coupled to allow the first semiconductor device to be activated; a second memory port selection line coupled to allow the second semiconductor device to be activated; and a clock signal line placed between the first memory port selection line and the second memory port selection line. | 06-26-2014 |
20140306735 | FLIP-FLOP WITH REDUCED RETENTION VOLTAGE - A circuit including a logic gate responsive to a clock signal and to a control signal. The circuit also includes a master stage of a flip-flop. The circuit further includes a slave stage of the flip-flop responsive to the master stage. The circuit further includes an inverter responsive to the logic gate and configured to output a delayed version of the clock signal. An output of the logic gate and the delayed version of the clock signal are provided to the master stage and to the slave stage of the flip-flop. The master stage is responsive to the control signal to control the slave stage. | 10-16-2014 |
Sarang Shashikant Bapat, Pune IN
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20120278277 | OBJECT-BASED MODELS IN DOCUMENT MANAGEMENT - Product Data Management systems, methods, and mediums. A method includes receiving a document component that includes business objects. The method includes receiving a document automation component. The method includes reading a document management part of the document component, and constructing a document model based on the document management part. | 11-01-2012 |
Shashidhara S. Bapat, Bangalore IN
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20130057338 | POWER CONTROLLER FOR SOC POWER GATING APPLICATIONS - A rush-in current controller includes a clock module connected to provide a delayed sleep control signal based on counting a preset number of clock cycles corresponding to an input sleep control signal. Additionally, the rush-in current controller includes a ring oscillator module connected to maintain the delayed sleep control signal based on counting a preset number of ring oscillator cycles corresponding to a virtual power supply line voltage. A method of controlling a rush-in current includes providing a delayed sleep control signal based on counting a preset number of clock cycles corresponding to an input sleep control signal and maintaining the delayed sleep control signal based on counting a preset number of ring oscillator cycles corresponding to a virtual power supply line voltage. | 03-07-2013 |
Uday Rajaram Bapat, Mumbai IN
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20090247553 | Highly Pure Paliperidone or a Pharmaceutically Acceptable Salt Thereof Substantially Free of Keto Impurity - Provided herein is a highly pure paliperidone or a pharmaceutically acceptable salt thereof substantially free of keto impurity, 3-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-2-methyl-7,8-dihydro-6H-pyrido[1,2-a]pyrimidin-4,9-dione, a process for the preparation thereof, and pharmaceutical compositions comprising highly pure paliperidone or a pharmaceutically acceptable salt thereof substantially free of keto impurity. | 10-01-2009 |
20100004447 | PROCESS FOR PREPARATION OF 9-HYDROXY-3-(2-CHLOROETHYL)-2-METHYL-4H-PYRIDO[1,2-A]PYRIMIDIN-4-ONE HYDROCHLORIDE - Described herein is an improved, commercially viable and industrially advantageous process for the preparation of paliperidone intermediate 9-hydroxy-3-(2-chloroethyl)-2-methyl-4h-pyrido[1,2-a]pyrimidin-4-one and its hydrochloride salt. The process provides the paliperidone intermediate in higher yield and reduced reaction time compared to the previously disclosed processes, thereby providing for production of paliperidone and its pharmaceutically acceptable acid addition salts in high purity and in high yield. | 01-07-2010 |
20100174073 | PROCESS FOR THE PREPARATION OF ALFUZOSIN AND SALTS THEREOF - The present invention relates to novel N-[3-[(4-acyl-/aroyl-substituted amino-6,7-dimethoxy-2-quinazolinyl)methylamino]propyl]tetrahydro-2-furancarboxamide derivatives, and a process for the preparation thereof. The novel compounds are useful for preparing alfuzosin or a pharmaceutically acceptable salt thereof in high yield and purity. | 07-08-2010 |
Uday Rajaram Bapat, Ahmedabed IN
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20130137852 | NOVEL COMPOUNDS AS DPP-IV INHIBITORS AND PROCESS FOR PREPARATION THEREOF - The present invention relates to process for preparation of novel compounds which are acting as inhibitors of dipeptidyl peptidase-IV enzyme and is depicted by the structural formula as given below: Formula VI. Which are useful in the treatment or prevention of diseases in which the dipeptidylpeptidase-IV enzyme is involved, such as diabetes and particularly type-2 diabetes. | 05-30-2013 |
Uday Rajaram Bapat, Kandivali IN
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20090061005 | Paliperidone Polymorphs - Described herein are novel polymorphic forms of paliperidone, processes for preparing the novel forms and use thereof. Also provided are processes for the preparation of novel polymorphic forms of paliperidone and the use thereof in the preparation of pharmaceutical compositions. | 03-05-2009 |
Uday Rajaram Bapat, Navi Mumbai IN
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20150112059 | PROCESS FOR THE PREPARATION OF A BENZAZEPINE DERIVATIVE - Provided is an industrially scalable process for the preparation of a benzazepine derivative, namely, 7-chloro-5-hydroxy-1-[2-methyl-4-(2-methyl benzoyl amino) benzoyl]-2,3,4,5-tetrahydro-1H-1-benzazepine (generically referred as Tolvaptan). | 04-23-2015 |