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Class 564/201 - Hydroxy, bonded directly to carbon, or ether in substituent Q (H of -OH may be replaced by a substituted or unsubstituted ammonium ion or a Group IA or IIA light metal)


Subclass of Class 564 - Organic compounds -- part of the class 532-570 series
Definition: Compounds wherein the carboxylic acid residue contains a
No. of applications: 15
Last issue date: 01/05/2012


Application No.Application TitleIssue Date
20120004183Unnatural reactive amino acid genetic code additions
This invention provides compositions and methods for producing translational components that expand the number of genetically encoded amino acids in eukaryotic cells. The components include orthogonal tRNAs, orthogonal aminoacyl-tRNA synthetases, pairs of tRNAs/syntheta...
01/05/2012
20110313147CHROMATOGRAPHIC MATERIAL FOR THE ABSORPTION OF PROTEINS AT PHYSIOLOGICAL IONIC STRENGTH
Ion exchange and hydrophobic interaction chromatographic materials are constructed by tethering a terminal binding functionality to a solid support via a hydrophobic linker. The backbone of the linker typically comprises sulfur-containing moieties. Suitable terminal bin...
12/22/2011
20110292141NONAQUEOUS INK COMPOSITION FOR INK JET RECORDING AND INK JET RECORDING METHOD
A nonaqueous ink composition for ink jet recording includes a solvent represented by general formula (1) and having a hydrophile-lipophile balance value of 10.5 to 20.0:

where R1 denotes an alkyl g...

12/01/2011
20110263898ETHER-AMIDE COMPOUNDS AND PREPARATION AND USES THEREOF
Novel ether-amide compounds having the formula RaRbC(OR1)—CHRc—CONR2R3 and processes for the preparation and use thereof, especially as solvents, for example in phytosanitary formulations....
10/27/2011
20110237765Amide-linked Perfluoropolyether Thiol Compounds and Processes for their Preparation and Use
A perfluoropolyether thiol compound comprises a perfluoropolyether segment, at least one mercapto group (—SH), and at least one intervening divalent carbonylimino moiety (—C(═O)—NR—, wherein R is hydrogen or alkyl). The compound can be produced, for example, b...
09/29/2011
2011013690212-MEMBERED-RING MACROLACTAM DERIVATIVES
There provided a 12-membered-ring macrolactam derivative having antitumor activity: A compound represented by Formula (1) or a salt thereof. In this Formula, R1 is a hydrogen atom, a C1-6 alkyl group, a C1-6 alkylcarbonyl group or a C
06/09/2011
20100256412FLUORINATED POLYETHERS AND POLYETHER OILS AND METHODS OF PREPARATION
Provided are fluorinated polyethers and polyether oils and methods of preparation. The preparation involves a catalytic oxidation process of fluorinated vinyl ethers employing free oxygen....
10/07/2010
20100063135POLYETHYLENE GLYCOL LIPID CONJUGATES AND USES THEREOF
Polyethylene glycol (PEG)-lipid conjugates, polyethylene glycol (PEG)-lipid conjugate based drug delivery systems, ways to make them and methods of treating diseases using them are disclosed....
03/11/2010
20090325246PROCESS FOR PRODUCTION OF BETAINE
According to the present invention, by using 4-halogeno-3-hydroxybutanamide as a substrate in quaternary amination reaction with trialkylamine which is an important step in betaine (such as carnitine) preparation processes, it becomes possible to reduce the production o...
12/31/2009
20090227453FORUMLATIONS
This invention relates to the use of lactamide compounds of formula (I): CH3CH(OH)C(═O)NR1R2, where R1 and R2 are each independently hydrogen; or C1-6 alkyl, C2-6 alkenyl or C3-6 c...
09/10/2009
20090221853PROCESS FOR THE PREPARATION OF 2-CHLOROETHOXY-ACETIC ACID-N,N-DIMETHYLAMIDE
According to the present invention, 2-chloroethoxy-acetic acid-N,N-dimethylamide of the Formula (I) is prepared by reacting 2-hydroxyethoxy-acetic acid-N,N-dimethylamide of the Formula (II) in a solvent optionally in the presence of a catalyst with thionyl chloride and ...
09/03/2009
20080087861Wrinkle-Removing Composition
The present invention provides a wrinkle-removing composition capable of removing wrinkles in fiber products without deteriorating the texture, even if heat treatment such as ironing and steam pressing is not carried out. The present relates to a wrinkle-removing compos...
04/17/2008
20070232806Hydride reduction process for preparing quinolone intermediates
Hydride process for making acyclic diol intermediates from cyclic intermediates, useful in antibacterial quinolone synthesis....
10/04/2007
20070037978Preparation of 2-amino-thiazole-5-carboxylic-acid derivatives
A method for preparing a compound of the structure I, ...
02/15/2007
20050123481Radio-opaque polymeric biomaterials
A radio-opaque dihydroxy compound substituted with at least one bromine or iodine atom. Radio-opaque medical implants and drug delivery devices and methods for therapeutic site-specific or systemic drug delivery comprising implanting in the body of a patient are also di...
06/09/2005
 
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