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Isocyanate esters (i.e., compounds containing the isocyanate group, -N=C=O, bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon)

Subclass of:

560 - Organic compounds -- part of the class 532-570 series

560000000 - ORGANIC COMPOUNDS (CLASS 532, SUBCLASS 1)

Patent class list (only not empty are listed)

Deeper subclasses:

Class / Patent application numberDescriptionNumber of patent applications / Date published
560336000 Processes 107
560335000 Biuret containing (i.e., -NH-C(=O)-NH-C(=O)-NH- containing, wherein substitution may be made for hydrogen only) 2
20120226071PROCESS FOR PREPARING POLYISOCYANATES COMPRISING BIURET GROUPS - The present invention relates to a process for preparing polyisocyanates comprising biuret groups from diisocyanates or polyisocyanates and diamines.09-06-2012
20080262261STABLE LIQUID BIURET MODIFIED AND BIURET ALLOPHANATE MODIFIED TOLUENE DIISOCYANATES, PREPOLYMERS THEREOF, AND PROCESSES FOR THEIR PREPARATION - This invention relates to stable liquid biuret modified toluene diisocyanates, prepolymers thereof, stable liquid biuret allophanate modified toluene diisocyanates, prepolymers thereof, and to processes for the preparation of these compositions. The stable liquid biuret modified toluene diisocyanates comprise a secondary amine based biuret modified TDI having an NCO group content of about 12 to about 46% by weight.10-23-2008
560334000 Carbodiimide containing (i.e., -N=C=N- containing) 1
20120065424LOW-CATALYST CARBODIIMIDE GROUPS AND/OR ISOCYANATE MIXTURES COMPRISING URETONIMINE GROUPS - A low-catalyst-content isocyanate mixture containing at least one of a carbodiimide group and a uretonimine groups, obtained by: reacting at least one monomeric diisocyanate (A) in the presence of phosphorus-containing catalyst (B), to obtain a reaction mixture comprising carbodiimide, where the reaction does not take place to complete conversion of the diisocyanate (A) and 1-80% by weight of the diisocyanate (A) employed remains in the reaction mixture as excess diisocyanate; and subsequently simultaneously removing, by distillation, a fraction of the excess of diisocyanate and the catalyst (B), to obtain the isocyanate mixture and a distillate, where the isocyanate mixture has a monomeric diisocyanate (A) content of 0.5%-20% by weight, based on the monomeric diisocyanate (A) employed, and a catalyst (B) content of 0% to 20% by weight, based on the catalyst (B) employed. In addition, a process for preparing a low-catalyst-content isocyanate mixture.03-15-2012
560358000 Benzene ring bonded directly to the isocyanate group 1
20110190535PROCESS FOR PREPARING POLYAROMATIC POLYISOCYANATE COMPOSITIONS - Process for the preparation of polyaromatic polyamines comprising the step of reacting formaldehyde with at least one monoaromatic monoamine and at least one monoaromatic compound containing at least two amino functions in the presence of an acidic catalyst where a) the total amount of di-aromatic compounds in the polyaromatic polyamine mixture is in the range from about 25 wt % to about 50 wt % and b) the amount of monoaromatic compound containing at least two amine functions is in the range 5 to 30 mole % relative to 100 mole % of the total amount of monoaromatic monoamines and c) the amount of acidic catalyst used in the preparation of the polyaromatic polyamine mixture is less than about 0.4 moles per mole of formaldehyde or formaldehyde equivalents.08-04-2011
Entries
DocumentTitleDate
20110178328Apparatus, Systems, and Methods for Purification of Isocyanate Mixtures - The present disclosure relates, according to some embodiments, to apparatus, systems, and/or methods for fractionating a feed mixture comprising, for example, one or more isocyanates, light components, solvents and/or heavier components. In some embodiments, fractionating an isocyanate feed mixture may comprise distilling the feed mixture in a non-adiabatic fractionating apparatus comprising a prefractionating section and/or column and a main section and/or column, which comprises a rectification section, a side section, and a stripping section. For example, isocyanates may be separated from light component(s), solvent(s) and/or heavier component(s). A fractionating apparatus may be configured and arranged, in some embodiments, as a dividing wall column. According to some embodiments of the disclosure, apparatus, systems, and/or methods may be energy efficient and/or may have a broad operating range.07-21-2011

Patent applications in all subclasses Isocyanate esters (i.e., compounds containing the isocyanate group, -N=C=O, bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon)