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964 results about "Organophosphate" patented technology

Organophosphates (also known as phosphate esters, or OPEs) are a class of organophosphorus compounds with the general structure O=P(OR)₃. They can be considered as esters of phosphoric acid. Like most functional groups organophosphates occur in a diverse range of forms, with important examples including key biomolecules such as DNA, RNA and ATP, as well as many insecticides, herbicides, nerve agents and flame retardants.

Xylo-LNA analogues

Based on the above and on the remarkable properties of the 2′-O,4′-C-methylene bridged LNA monomers it was decided to synthesise oligonucleotides comprising one or more 2′-O,4′-C-methylene-β-D-xylofuranosyl nucleotide monomer(s) as the first stereoisomer of LNA modified oligonucleotides. Modelling clearly indicated the xylo-LNA monomers to be locked in an N-type furanose conformation. Whereas the parent 2′-deoxy-β-D-xylofuranosyl nucleosides were shown to adopt mainly an N-type furanose conformation, the furanose ring of the 2′-deoxy-β-D-xylofuranosyl monomers present in xylo-DNA were shown by conformational analysis and computer modelling to prefer an S-type conformation thereby minimising steric repulsion between the nucleobase and the 3′-O-phopshate group (Seela, F.; Wömer, Rosemeyer, H. Helv. Chem. Acta 1994, 77, 883). As no report on the hybridisation properties and binding mode of xylo-configurated oligonucleotides in an RNA context was believed to exist, it was the aim to synthesise 2′-O,4′-C-methylene-β-D-xylofuranosyl nucleotide monomer and to study the thermal stability of oligonucleotides comprising this monomer. The results showed that fully modified or almost fully modified Xylo-LNA is useful for high-affinity targeting of complementary nucleic acids. When taking into consideration the inverted stereochemistry at C-3′ this is a surprising fact. It is likely that Xylo-LNA monomers, in a sequence context of Xylo-DNA monomers, should have an affinity-increasing effect.
Owner:QIAGEN GMBH

Highly purified tocopheryl phosphate, process for producing the same, analytical method therefor and cosmetic

Disclosed herein are a highly purified tocopheryl phosphate and / or a salt thereof (tocopheryl phosphates) wherein a P,P'-bistocopheryl hypophosphate and / or a salt thereof (P,P'-bistocopheryl diphoshates) is contained in a proportion of not higher than 3% by weight; a process for producing a highly purified tocopheryl phosphate and / or a salt thereof, which comprises the steps of reacting a tocopherol with an oxyphosphorus trihalide followed by treating with an acid or basic aqueous solution to thereby form tocopheryl phosphates (i) in which P,P'-bistocopheryl diphoshates (ii) formed as by-products are contained, hydrolyzing the P,P'-bistocopheryl diphoshates (ii) under acid condition, and, optionally, rendering the hydrolyzate neutral or basic under basic condition; and a method of analyzing tocopheryl phosphates, comprising analyzing a sample containing components (i) and (ii) with the use of a high-performance liquid chromatograph column packed with a gel of a polymethacrylate having, bonded thereto, long-chain alkyl groups. None or only an extremely minute amount of P,P'-bistocopheryl diphoshates are contained in the highly purified tocopheryl phosphates, so that the highly purified tocopheryl phosphates exhibit antioxidant and blood circulation promoting effects, have excellent water solubility, are powdery so that the handling thereof is extremely easy, are free from cutaneous irritation and allergenecity and ensure dermal safety. Therefore, the highly purified tocopheryl phosphates are useful as cosmetic ingredients. The amounts of components (i) and (ii) can be simply measured with high accuracy by the above method.
Owner:SHOWA DENKO KK

Water-based epoxy modified phosphorus-containing styrene-acrylic antirust emulsion and synthesis method thereof

InactiveCN102127271ASmall sizeControl particle diameterAnti-corrosive paintsEpoxy resin coatingsWater basedEpoxy
The invention relates to a water-based epoxy modified phosphorus-containing styrene-acrylic antirust emulsion and a synthesis method thereof. The water-based epoxy modified phosphorus-containing styrene-acrylic antirust emulsion is prepared by a conventional emulsion polymerization method, and can be crosslinked with a crosslinking agent and cured at room temperature; and the particle size of thewater-based epoxy modified phosphorus-containing styrene-acrylic antirust emulsion is 80-140nm, the solid content is 40-50%, and the minimum filming temperature is not higher than 35 DEG C. The emulsion is prepared by introducing epoxy-group-containing epoxy resin and phosphate functional monomer with flash-etching-resistant function into the conventional emulsion polymerization process of acrylate. The polymerization technique is simple and practical, almost no gel is generated in the polymerization process, and the storage stability of the emulsion can reach more than 1 year. When the synthesized emulsion is crosslinked with the curing agent to form a film, a three-dimensional network structure is generated, and an efficiently-antirust paint film with high adhesive force can be formed after the emulsion is completely cured. When the water-based epoxy modified phosphorus-containing styrene-acrylic antirust emulsion is used as water-based antirust paint, the adhesive force can reach Level 1, and the water absorptivity is smaller than or equal to 10%; and the water-based epoxy modified phosphorus-containing styrene-acrylic antirust emulsion does not bubble after being soaked in a 3% NaCl solution for 450 hours, and has favorable corrosion resistance.
Owner:DALIAN POLYTECHNIC UNIVERSITY

Cyanine derivatives, fluorescent conjugates containing same and use thereof

A subject matter of the invention is cyanine derivatives of formula:
in which the dotted lines represent the atoms necessary for the formation of one or two fused aromatic rings, each ring comprising 5 or 6 carbon atoms;
  • R1, R2, R3 and R4 represent, independently of one another: H; substituted or unsubstituted C1-C15 alkyl; C1-C6 alkoxy; (C2-C12)dialkylamino; C1-C6 alkoxycarbonyl; di(C2-C12)alkylamido; a substituted or unsubstituted aryl, arylalkyl or aryloxy group; a halogen atom; a nitro; an L1-W, L2-M, L2-A or L2-G group;
  • R5 and R6 represent, independently of one another: substituted or unsubstituted C1-C15 alkyl; a substituted or unsubstituted aryl or arylalkyl group; an L1-W, L2-M, L2-A or L2-G group;
  • X is chosen from: O, S or CR7R8; Y is chosen from: O, S or CR9R10;
  • R7, R8, R9 and R10 independently represent: substituted or unsubstituted C1-C15 alkyl; substituted or unsubstituted aryl, arylalkyl or aryloxy; an L1-W, L2-M, L2-A or L2-G group;
  • R7 and R8 and/or R9 and R10 can also together form a ring comprising 5 or 6 atoms or a heterocycle comprising 4 to 5 carbon atoms and an oxygen atom;
  • B represents a polymethine bridge comprising 1 to 5 methine groups, said groups being in particular individually unsubstituted or substituted by a substituted or unsubstituted C1-C15 alkyl; a substituted or unsubstituted aryl, arylalkyl or aryloxy group; a nitro group; an L1-W, L2-M, L2-A or L2-G group;
  • L1 and L2 are connecting arms; G is a reactive group; A is a coupling agent; M is a conjugated molecule, W is a phosphate or phosphonate ester (preferably diester), with the proviso that the cyanine derivative comprises at least one L1-W group and at least one L2-A, L2-G or L2-M group.
Owner:CIS BIO INT

Preparation method of halogen-free flame retardant high-intensity polyvinyl alcohol fibers

The invention discloses a preparation method of halogen-free flame retardant high-intensity polyvinyl alcohol fibers, which is characterized by comprising the following steps of uniformly mixing 20-45 parts by weight of phosphate ester flame retardant powder with the average particle size no more than 1.0 microns, 1-10 parts by weight of dispersing agent, and 40-79 parts by weight of water to prepare flame retardant suspended slurry, continuously mixing the slurry and polyvinyl alcohol plus boron spinning solution with the polymerization degree of 1700-3000 and the alcoholysis degree more than 99 percent through a mode of spun injection, carrying out spinning with the mixed solution through a polyvinyl alcohol wet method plus a spinning process route, carrying out neutralization, wet-heat drawing, washing and drying on solidified fibers to obtain as-spun fibers, preheating the as-spun fibers to the temperature of 200-230 DEG C, drawing by 2-4 times, and then carrying out heat setting on the fibers at the temperature of 180-210 DEG C for 2-5min to obtain the halogen-free flame retardant high-intensity polyvinyl alcohol fibers. According to different uses, post-treatment steps such as formalization, oiling, curling, cutting and the like can be selectively carried out on the flame-retardant fibers. The flame-retardant fibers prepared through the method has the advantages of low toxicity and high intensity, realizes self-extinguishment after leaving fire, is free of halogen and the dripping phenomenon and is used for aspects of fabric flame retarding, enhancing flame retardant fabrics and the like, and the limited oxygen index can reach 28-30.
Owner:SICHUAN UNIV +2
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