Abstract: There is provided a polymer film including a polymer; and a high molecular weight plasticizer that has a number average molecular weight of 700 to 10,000 and has a repeating unit derived from a dicarboxylic acid and a diol, wherein the dicarboxylic acid for forming the high molecular weight plasticizer includes at least one aliphatic dicarboxylic acid having 2 to 20 carbon atoms and at least one aromatic dicarboxylic acid having 8 to 20 carbon atoms, and the diol includes at least one diol selected from the group consisting of an aliphatic diol having 2 to 12 carbon atoms, an alkyl ether diol having 4 to 20 carbon atoms and an aromatic ring-containing diol having 6 to 20 carbon atoms.

Abstract: Disclosed is a complex alcohol ester composition comprising a polyester in which at least two molecules of a polyol represented by a formula I: R(OH)n (wherein R represents an n-valent aliphatic, alicyclic or aromatic group, one or more carbon atoms not adjacent to each other in R may be individually substituted with an oxygen atom, and n indicates an integer of 2 or more) are linked through at least two ester bonds via at least one molecule of a polybasic acid, and at least a part of the non-linked side chain ends of the polyol have a group represented by a formula II: (AO)kR2 (wherein R2 represents a hydrocarbon group, A represents a divalent linking group, and k indicates an integer) via a polybasic acid. The complex alcohol ester composition can be used a lubricant agent.

Abstract: Addition-fragmentation agents of the formula are disclosed having the following functional groups: 1) a labile addition-fragmentation group that can cleave and reform to relieve strain, 2) a free-radically polymerizable group, and 3) a surface-modifying functional group that associates with the surface of a substrate.

Abstract: There is provided a method for production of a high-purity biodegradable polyoxyethylene derivative on an industrial scale using a polyoxyethylene compound containing polylactic acid at the terminal thereof. A biodegradable polyoxyethylene compound represented by formula (1) and a compound represented by formula (I) are caused to react with each other at 60° C. to 120° C. using toluene as a solvent in the presence of sodium acetate to obtain a biodegradable polyoxyethylene derivative represented by formula (2).

Abstract: Addition-fragmentation agents of the formula are disclosed having the following functional groups: 1) a labile addition-fragmentation group that can cleave and reform to relieve strain, 2) a free-radically polymerizable group, and 3) a surface-modifying functional group that associates with the surface of a substrate.

Abstract: Structural adhesives are prepared from an elastomeric toughener that contains urethane and/or urea groups, and have some terminal isocyanate groups that are capped with a phenol and other terminal isocyanate groups that are capped with a hydroxy-functional acrylate or a hydroxy-functional methacrylate. In certain embodiments, the presence of both types of capping on the toughener leads to higher impact peel strengths and a greater level of cohesive failure, than when the toughener is capped with a phenol an hydroxy-functional acrylate or hydroxy-functional methacrylate alone.

Abstract: Provided are compositions comprising one or more compounds having a structure comprising a node structure with from four to twelve carbon atoms, one or more (poly)glyceryl groups, and one or more hydrophobic moieties, wherein each of the one or more (poly)glyceryl groups is linked to the node structure by a first primary linking group, the one or more hydrophobic moieties are each independently linked either to the node structure by a primary linking group or to one of the (poly)glyceryl groups by a secondary linking group, and wherein the polyglyceryl thickener has an average degree of glyceryl polymerization of from greater than 3 to less than about 11 and an average number of hydrophobic groups per primary linking group of about 0.35 or greater. Also provided are polyglyceryl compounds, compositions comprising water, a surfactant, and a polyglyceryl thickener, as well as, methods of making polyglyceryl compounds and compositions of the present invention.

Abstract: Addition-fragmentation agents of the formula are disclosed: wherein R1, R2 and R3 are each independently Z-Q-, a (hetero)alkyl group or a (hetero)aryl group with the proviso that at least one of R1, R2 and R3 is Zm-Q-, Q is a linking group have a valence of m+1; Z is an ethylenically unsaturated polymerizable group, m is 1 to 6; each X1 is independently —O— or —NR4—, where R4 is H or C1-C4 alkyl, and n is 0 or 1.

Abstract: Provided are compositions comprising one or more compounds having a structure comprising a node structure with from four to twelve carbon atoms, one or more (poly)glyceryl groups, and one or more hydrophobic moieties, wherein each of the one or more (poly)glyceryl groups is linked to the node structure by a first primary linking group, the one or more hydrophobic moieties are each independently linked either to the node structure by a primary linking group or to one of the (poly)glyceryl groups by a secondary linking group, and wherein the polyglyceryl thickener has an average degree of glyceryl polymerization of from greater than 3 to less than about 11 and an average number of hydrophobic groups per primary linking group of about 0.35 or greater. Also provided are polyglyceryl compounds, compositions comprising water, a surfactant, and a polyglyceryl thickener, as well as, methods of making polyglyceryl compounds and compositions of the present invention.

Abstract: Structural adhesives are prepared from an elastomeric toughener that contains urethane and/or urea groups, and have some terminal isocyanate groups that are capped with a phenol and other terminal isocyanate groups that are capped with a hydroxy-functional acrylate or a hydroxy-functional methacrylate. In certain embodiments, the presence of both types of capping on the toughener leads to higher impact peel strengths and a greater level of cohesive failure, than when the toughener is capped with a phenol an hydroxy-functional acrylate or hydroxy-functional methacrylate alone.

Abstract: Disclosed is a method of denitrifying a solution including introducing into the solution an amount of a carbon source within a duration and at a frequency so that indigenous heterotrophic bacteria deplete dissolved oxygen in the solution and decompose oxygen from nitrate in the solution to obtain its combined oxygen. Related apparatuses and compounds also are disclosed.

Abstract: A process for preparing polymers containing polyortho ester groups and optionally NCO groups by reacting A) and B) where A) is a polyortho ester containing at least one isocyanate-reactive group prepared by reacting at least one or more acyclic ortho esters with low molecular weight polyols having a functionality of 4-8 and a number-average molecular weight of 80-500 g/mol and B) is least one polyisocyanate. The polymers obtained from the process can be used to produce coatings, adhesive bonds and/or seals. The coating compositions can include one or more of the above-described polymers, optionally polyisocyanates, catalysts, and optionally auxiliaries and additives and can be used to coat substrates.

Abstract: The invention provides acyloxymethyl esters of C6-14 alkane-dicarboxylic acids, or physiologically tolerable salts or esters thereof, for use in medicine as therapeutic or prophylactic agents.

Abstract: Novel mixed esters of dicarboxylic acids with monohydric fatty alcohols and propoxylated fatty alcohols show unexpected superior properties as pigment dispersants, especially for inorganic pigments used in foundations, make-ups, lipsticks and physical sunscreens. The compounds of the present invention show superior pigment wetting and dispersing properties, as demonstrated by their ability to form fluid, very high-solids dispersions, while exhibiting unusual emolliency and gloss formation.

Abstract: An ester compound represented by formula (1) R1OOC—(CH2)m—COOR2 ??(1) wherein R1 and R2 are different from each other and each represents a group of formula (2) —(R3O)nR4 ??(2) wherein R3 is a C1-6 alkylene group; R4 is a C1-10 straight- or branched-chain alkyl group, a C6-12 aryl group, C7-15 arylalkyl group or a C7-15 alkylaryl group; m is an integer from 0 to 8, and n is an integer from 0 to 6. This compound is suitable as a plasticizer for biodegradable aliphatic polyester resins.

Abstract: Novel mixed esters of dicarboxylic acids with monohydric fatty alcohols and propoxylated fatty alcohols show unexpected superior properties as pigment dispersants, especially for inorganic pigments used in foundations, make-ups, lipsticks and physical sunscreens. The compounds of the present invention show superior pigment wetting and dispersing properties, as demonstrated by their ability to form fluid, very high-solids dispersions, while exhibiting unusual emolliency and gloss formation.

Abstract: A process for the preparation of water-soluble polymers of esters of ethylenically unsaturated carboxylic acids and polyalkylene glycols by azeotropic esterification, in the presence of organic solvents which form an azeotrope with water, of ethylenically unsaturated carboxylic acids with polyalkylene oxides which are capped at one end by end groups, to a degree of at least 85 wt %, followed by free-radical polymerization of the resulting esters optionally together with other ethylenically unsaturated monomers, in aqueous medium, wherein the organic solvents are removed by azeotropic distillation from the reaction mixture during polymerization and the water that is removed by distillation is recycled or the quantity of water removed by distillation from the reaction mixture is replaced by a feed of fresh water.

Abstract: Water-soluble polymers of esters made from acrylic acid and alkylpolyalkylene glycols, obtainable by azeotropic esterification of a mixture of acrylic acid and alkylpolyalkylene glycol in a molar ratio of from 2 to 3:1 in the presence of at least 85% by weight, based on the alkylpolyalkylene glycol, of an organic solvent which forms an azeotrope with water, followed by free-radical polymerization, in an aqueous medium, of the mixture obtained during the esterification, where the organic solvent is distilled off azeotropically from the reaction mixture during the polymerization, and the water removed by distillation is returned to the mixture or replaced by a feed of fresh water, and preparation and use of these polymers as an additive to cementitious systems.

Abstract: This invention provides a process to produce a hydroxyl group-containing ester-forming addition reaction product having an acid value of 20 mgKOH/g or less, which process is characterized in that 2,2-dimethylolalkanoic acid having 6 to 8 carbon atoms is melted, and is then mixed with alkanoic acid monoglycidylester having 8 to 24 carbon atoms so that an ester-forming addition reaction may occur. Thus obtained reaction product contains almost no undesirable high-molecular components, is quite excellent in reactivity and compatibility with a curing agent, and is useful for the manufacture of high-solids paint etc.

Abstract: Monofunctional polyfluorooxetane oligomers and polymers are prepared by the cationic polymerization of fluorooxetane monomers with a monoalcohol. The fluorooxetane oligomers or polymers can be copolymerized with generally cyclic ethers. Alternatively, the polyfluorooxetane oligomer or polymer having a single hydroxyl end group can be functionalized with a variety of compounds so as to yield a functional end group such as an acrylate, a methacrylate, an allylic, an amine, etc., with the functionalized oligomer or polymer being suitable for use in radiation curable or thermal curable coating compositions. These functionalized polymers can be copolymerized and cured to provide improvements in wetting and surface properties that have previously been provided by migratory chemicals such as waxes and oils.

Abstract: Optionally fluorine-substituted alkyl or alkenyl poly(ethylene oxides) the compounds of the general formula in which R is an alkyl group with 10-20 carbon atoms, an alkenyl group with 10-20 carbon atoms or a fluoroalkyl or fluoroalkenyl group with f carbon atoms that each bear at least one fluorine atom and g carbon atoms that bear only hydrogen atoms, in which 1.5 f+g=10-20 and g may optionally be zero. R′ is an alkyl group with 1 to 4 carbon atoms, L is a linking group, a linking atom or a chemical bond, and p is at least 2, q is at least 2 and p+q=from 4 to 100, may be prepared by reacting maleic anhydride with a poly(ethylene glycol) alkyl. ether and reacting the resultant intermediate product with a compound of the formula RL′H in which L′ is a linking group or linking atom. Compounds of the formula (1) may also be prepared by reacting RL-substituted succinic anhydrides with a alkyl end-capped polyethylene glycol.

Abstract: Monofunctional polyfluorooxetane oligomers and polymers Zare prepared by the cationic polymerization of fluorooxetane monomers with a monoalcohol. The fluorooxetane oligomers or polymers can be copolymerized with generally cyclic ethers. Alternatively, the poly-fluorooxetane oligomer or polymer having a single hydroxyl end group can be functionalized with a variety of compounds so as to yield a functional end group such as an acrylate, a methacrylate, an allylic, an amine, etc., with the functionalized oligomer or polymer being suitable for use in radiation curable or thermal curable coating compositions. These functionalized polymers can be copolymerized and cured to provide improvements in wetting and surface properties that have previously been provided by migratory chemicals such as waxes and oils.

Abstract: An ester resulting from an esterification reaction between at least one polyfunctional alcohol and at least one polyfunctional carboxylic acid using a chain stopping agent to form ester bonds with the remaining hydroxyl or carboxyl groups is disclosed. The polyfunctional carboxylic acid comprises an aliphatic dicarboxylic acid containing from 9 to 18 carbon atoms, dimerised and/or trimerised fatty acids or mixtures thereof, with the proviso that dimerised and trimerised fatty acids do not constitute more than 80% by weight of the total amount of polyfunctional carboxylic acid used. The chain stopping agent may be a monocarboxylic acid or a monofuntional alcohol having at least 14 carbon atoms. The complex esters have a kinematic viscosity at 100 C of from 30 to 1000 cSt, preferably from 30 to 200 cSt.

Abstract: Monofunctional polyfluorooxetane oligomers and polymers are prepared by the cationic polymerization of fluorooxetane monomers with a monoalcohol. The fluorooxetane oligomers or polymers can be copolymerized with generally cyclic ethers. Alternatively, the polyfluorooxetane oligomer or polymer having a single hydroxyl end group can be functionalized with a variety of compounds so as to yield a functional end group such as an acrylate, a methacrylate, an allylic, an amine, etc., with the functionalized oligomer or polymer being suitable for use in radiation curable or thermal curable coating compositions. These functionalized polymers can be copolymerized and cured to provide improvements in wetting and surface properties that have previously been provided by migratory chemicals such as waxes and oils.

Abstract: Monofunctional polyfluorooxetane oligomers and polymers are prepared by the cationic polymerization of fluorooxetane monomers with a monoalcohol. The fluorooxetane oligomers or polymers can be copolymerized with generally cyclic ethers. Alternatively, the polyfluorooxetane oligomer or polymer having a single hydroxyl end group can be functionalized with a variety of compounds so as to yield a functional end group such as an acrylate, a methacrylate, an allylic, an amine, etc., with the functionalized oligomer or polymer being suitable for use in radiation curable or thermal curable coating compositions. These functionalized polymers can be copolymerized and cured to provide improvements in wetting and surface properties that have previously been provided by migratory chemicals such as waxes and oils.

Abstract: The invention concerns a process for manufacturing polyol complex esters. According to the method, a polyol, such as BEPD or NPG, is reacted with mono- and polyvalent acids in the presence of a catalyst to produce a reaction blend containing complex esters. According to the invention the acid components of the reaction blend are neutralized with a tertiary amine, and the complex esters are recovered from the thus treated reaction blend. The basic amines that are used form salt-like compounds with the carboxylic acids. The compounds enter the aqueous phase, from which they are easily separated, whereby the complex esters are recovered with high yield.

Abstract: The present invention discloses the synthesis of a novel crosslinker having the following structure: R1 is C(R8) (R9) wherein (R8) is H, or an alkyl group having 1-5 carbon atoms, and (R9) is H, or an alkyl group having 1-5 carbon atoms. R2 is H, or an alkyl group having 1-5 carbon atoms. R3 is H or an alkyl group having 1-5 carbon atoms. R4 is an alkyl group having 1-5 carbon atoms. R5 is H or an alkyl group having 1-5 carbon atoms. R6 is H or an alkyl group having 1-5 carbon atoms. R7 is C(R10) (R11) wherein (R10) is H, or an alkyl group having 1-5 carbon atoms, and (R11) is H, or an alkyl group having 1-5 carbon atoms. The crosslinker is stable in a basic environment, but decomposable in an acidic environment.

Abstract: A high solids coating composition comprising a branched hydroxy-functional polyester oligomer and a curing agent; and the oligomer itself containing at least 20% by weight of the binder of at least one of the following tertiary acid ester end groups: where R1, R2 and R3 are independently selected from CH3 and CH2OH; the composition being suitable as an automobile clearcoat or pigmented topcoat.

Abstract: The present invention provides a lubricating oil or a lubricating oil additive, particularly suitable for a R-134a (1,1,1,2-tetrafluoroethane) or R-134 (1,1,2,2-tetrafluoroethane) refrigerant, consisting of a compound (X) that can be prepared by esterification of a polyoxyethoxylated glycerol with at least one polycarboxylic acid compound having from 2 to 20 carbon atoms, preferably from 4 to 13 carbon atoms, and at least one monocarboxylic acid compound having from 2 to 20 carbon atoms, preferably from 6 to 13 carbon atoms.

Abstract: The present invention deals with the composition, and application of novel carboxylated polymers. The complexes are made by a series of reactions which include reaction of an anhydride with an allyl alcohol alkoxylate, polymerization of the carboxylated allyl alkoxylate, then formation of a complex of the poly carboxylate with quaternary compounds.

Abstract: The present invention deals with the composition, and application of novel carboxylated polymers, and complexes thereof. The complexes are made by a series of reactions which include reaction of an anhydride with an allyl alcohol alkoxylate, polymerization of the carboxylated allyl alkoxylate, then formation of a complex of the poly carboxylate with quaternary compounds.

Abstract: This invention relates to compositions for and methods of treating, preventing or ameliorating cancer and other proliferative diseases as well as methods of inducing wound healing, treating cutaneous ulcers, treating gastrointestinal disorders, treating blood disorders such as anemias, immunomodulation, enhancing recombinant gene expression, treating insulin-dependent patients, treating cystic fibrosis patients, inhibiting telomerase activity, treating virus-associated tumors, especially EBV-associated tumors, augmenting expression of a tumor suppressor gene and inducing tolerance to an antigen. The methods of the invention use tricarboxylic acid substituted oxyalkyl esters.

Abstract: A malonate group-containing acrylate monomer is produced by a transesterification reaction of dialkyl malonate with a hydroxyalkyl (meth)acrylate or a polyalkylene glycol mono(meth)acrylate. The malonate group-containing acrylate monomer finds use in the production of an acrylic polymer capable of crosslinking through a Michael reaction with an .alpha., .beta.-unsaturated carbonyl compound or resin.

Abstract: A high solids coating composition comprising a branched hydroxy-functional polyester oligomer and a curing agent; and the oligomer itself containing at least 20% by weight of the binder of at least one of the following tertiary acid ester end groups: ##STR1## where R.sub.1, R.sub.2 and R.sub.3 are independently selected from CH.sub.3 and CH.sub.2 OH; the composition being suitable as an automobile clearcoat or pigmented topcoat.

Abstract: Methods and devices for controlling the reaction rate of a hydrocarbon to an acid or other intermediate oxidation product by pressure drop rate adjustments. The pressure drop rate measurements arc conducted at predetermined time intervals, after stopping the feeding and exiting of gases. The pressure drop at a predetermined time interval is measured or the time it takes for the pressure to drop by a certain degree. Adjustments are then made in one or more temperature, feeding rates of hydrocarbon, solvent, catalyst, promoter, and the like until the pressure drop rate and the reaction rate fall within desirable predetermined limits.

Abstract: An oil-soluble polyester having a weight average molecular weight of 10,000 to 1 000,000, which is a polycondensate prepared by polycondensing the following ingredients (A), (B) and (C):(A) a divalent higher carboxylic acid ingredient,(B) a divalent alcohol ingredient comprising a glycol represented by the following formula:HO--CH.sub.2 --CR.sup.1 R.sup.2 --CH.sub.2 --OHwherein R.sup.1 and R.sup.2 represent a alkyl group, and the sum of carbon numbers in R.sup.1 and R.sup.2 is at least three, and(C) 0.1 to 15% by mole, based on the total of ingredients (A) and (B), of at least one multi-valent ingredient selected from a carboxylic acid with a valency of at least three and an alcohol with a valency of at least three. This oil-soluble polyester is useful as an additive for a lubricating oil.

Abstract: Esterification of an ultra-low unsaturation polyoxy(higher)alkylene polyol with a dicarboxylic acid or reactive derivative thereof to form a poly(half ester) followed by capping the poly(half ester) with a capping agent capable of forming an amide linkage or ester linkage while retaining primary hydroxyl functionality, generates high primary hydroxyl content polyols with substantially retained hydrophile/lipophile balance and low polydispersity. Low color products having primary hydroxyl contents in excess of 80 equivalent percent may be routinely achieved.

Abstract: A complex alcohol ester which comprises the reaction product of an add mixture of the following: a polyhydroxyl compound represented by the general formula:R(OH).sub.nwherein R is any aliphatic or cyclo-aliphatic hydrocarbyl group and n is at least 2, provided that the hydrocarbyl group contains from about 2 to 20 carbon atoms; a polybasic acid or an anhydride of a polybasic acid, provided that the ratio of equivalents of the polybasic acid to equivalents of alcohol from the polyhydroxyl compound is in the range between about 1.6:1 to 2:1; and a monohydric alcohol, provided that the ratio of equivalents of the monohydric alcohol to equivalents of the polybasic acid is in the range between about 0.84:1 to 1.2:1; wherein the complex alcohol ester exhibits a pour point of less than or equal to -20.degree. C., a viscosity in the range between about 100-700 cSt at 40.degree. C. and having a polybasic acid ester concentration of less than or equal to 70 wt. %, based on the complex alcohol ester.

Abstract: This invention relates to polymers, especially emulsion polymers, and their use for the thickening of a variety of aqueous systems, to methods of thickening utilizing the polymers, to enhancement of such thickening by the addition of surfactants, solvents or non-solvents, and to other aspects including coating compositions and other aqueous systems thickened with the polymers. This invention also relates to new complex hydrophobe-containing oligomers and their use in producing the polymers of this invention.

Abstract: A skin-moisture-regulating composition for cosmetic or dermatological preparations, the composition containing succinic acid derivatives corresponding to formula I:R.sup.1 O(C.sub.n H.sub.2n O).sub.x CO--CHR.sup.2 --CHR.sup.3 --CO(OC.sub.n H.sub.2n O).sub.y OR.sup.4 (I)wherein R.sup.1 is an alkyl, alkenyl, mono-or dihydroxyalkyl or hydroxyalkenyl group containing 6 to 22 carbon atoms, one of R.sup.2 and R.sup.3 is hydrogen and the other is an alkyl or alkenyl group containing 12 to 22 carbon atoms, n=2 or 3, x and y are average degrees of alkoxylation and have values of 0 to 20 and 1 to 20, respectively, and R.sup.4 is hydrogen or a group R.sup.1 O--(C.sub.n H.sub.2n O).sub.x --CO--CHR.sup.2 --CHR.sup.3 --CO--, or an alkyl, alkenyl, mono- or dihydroxyalkyl or hydroxyalkenyl group containing 6 to 22 carbon atoms.

Abstract: A compound of the formula (I) or its pharmaceutically acceptable salt or ester: ##STR1## and intermediates thereof.

Abstract: This invention pertains to perfluoropolyethers and perhalogenated chlorofluoropolyethers that can be prepared by fluorinating addition polymers made by polymerizing epoxides.

Abstract: The compound described in the present invention is represented by the following general formula: R.sub.1 (OCH.sub.2 CH.sub.2).sub.n O(COACOOXO).sub.m COACO(OCH.sub.2 CH.sub.2).sub.k OR.sub.2 wherein A is C.sub.2 -C.sub.4 alkylene group or a residual group of aromatic dicarboxylic acid, namely a group formed by removing two carboxylic groups from an aromatic dicarboxylic acid,X is straight or branched chain alkylene group, a residual group of glycols (namely a group formed by removing two hydroxyl groups from a glycol) selected from the group consisting of diethylene glycol, triethylene glycol, dipropylene glycol, and tripropylene glycol, or a residual group of thiodiethanol,n is 1 to 3,R.sub.1 is selected from the group consisting of C.sub.1 -C.sub.10 alkyl or benzyl,R.sub.2 is C.sub.1 -C.sub.8 alkyl or benzyl,m is 0 to 13 andk is 0 to 3.

Abstract: The invention provides a polyester based on dimeric fatty acid, a glycol without hydrogen atoms at an alpha carbon atom in which a C3-C12 monoalcohol chainstopper is present and which contains approximately equivalent quantities of acid and alcohol groups. Preferably the dimer acid contains 36 carbon atoms and the monoalcohol is a branched chain C6-C10 alkanol. The invention also provides lubricant compositions comprising 30-2% (w.w.) of the polyester and 70-98% (w.w.) of an synthetic lubricant base.

Abstract: The invention relates to new N-alkyl-N-(meth)acryloyloxyalkylcarboxamides of aromatic carboxylic acids and aromatic carboxylic acid anhydrides, their preparation and formulations of these compounds for use as adhesives for the treatment of dental hard substance.

Abstract: The present invention provides new allyl esters of the general formula:X--CH.sub.2 --CR.sup.1 .dbd.CR.sup.2 --CO--Y--R.sup.3 --A (I)wherein R.sup.1 and R.sup.2, which can be the same or different, are hydrn or halogen atoms or alkyl or aryl radicals, R.sup.3 is a linking grouping (spacer), X is an acyloxy radical in which acyl in the acyloxy radical is the residue of an aliphatic carboxylic acid or is the radical RCO-- in which R is an organic radical, Y is an oxygen or sulphur atom or especially an --NH-- group and A is a grouping which can react with a solid carrier material F, which contains appropriate functional groups B, either after selective deblocking or directly, whereby A and B are atom groupings which react with one another with condensation and/or addition and formation of a linkage between the solid carrier material and the radical X--CH.sub.2 --CR.sup.1 .dbd.CR.sup.2 --CO--Y--R.sup.3 --.The present invention also provides processes for the preparation of these new allyl esters.

Abstract: The present invention relates to compounds comprising ester groups having at least three ester functions, to processes for the production thereof, and to the use of the products.Compounds having at least three functional ester groups of the general formula: ##STR1## are described, wherein the abbreviations have the following meanings: X=--CH.sub.2 --CH.sub.2 -- or --CH.dbd.CH--,Y=bivalent, saturated aliphatic hydrocarbon residue optionally substituted,Z=optionally substituted acyl residue --CO--RR.sub.1 =the residue of an alcohol, or a group from an alkylene-oxide-adduct taking the alcohol function in the ester grouping.n=1 to 3 andm=1 to 3.

Abstract: Described is a composition imparting antistatic properties to polyamide materials and of the general formula: ##STR1## wherein R is a C.sub.1-9 alkyl group or hydrogen, Z is a difunctional chain modifier group, R' is a C.sub.1-4 alkyl group or hydrogen and x and y are between about 10 and about 50.

Abstract: The present invention deals with novel internal branched ether esters based upon novel ether alcohols. These materials are useful as viscosity index modifiers where outstanding liquidity, resistance to oxidation, and minimal variation in viscosity as a function of temperature is required.

Abstract: Synthetic polyol esters with lubricating oil properties based on substantially neutral esterification products of a polyhydric alcohol with selected monocarboxylic acids and, optionally, polybasic carboxylic acids, wherein the polyfunctional alcohol component is dipentaerythritol which is esterified withI--branched C.sub.8 -C.sub.16 fatty acids (class A acids) or withII--mixtures of linear C.sub.8 -C.sub.14 fatty acids (class B acids) with branched fatty acids of class Aand, optionally, limited quantities of polybasic carboxylic acids of the following classes C, D and/or E incorporated in the polyester molecular by condensation:class C acids: di- and/or tricarboxylic acids in the range from C.sub.6 to C.sub.54class D acids: difunctional fatty acids which have been obtained by addition of acrylic acid onto the double bonds of oleic acid, linoleic acid and/or linolenic acidclass E acids: aromatic and/or paraffinic, cyclic polycarboxylic acids containing from 2 to 6 acid functions.