Abstract: The present invention relates to an anhydrosugar alcohol composition having enhanced storage stability, and an anhydrosugar alcohol storage method, and more specifically, to an anhydrosugar alcohol composition having enhanced storage stability by comprising anhydrosugar alcohol and an amine-based additive; and to a method by which anhydrosugar alcohol having excellent quality may be provided by having the storing of the anhydrosugar alcohol performed under the existence of the amine-based additive, thereby remarkably enhancing the storage stability of the anhydrosugar alcohol.

Abstract: The present invention relates to a method for preparing an anhydrosugar alcohol using hydrol (namely, a crystalline mother liquor remaining after obtaining crystalline glucose from a crude glucose liquor). More particularly, the present invention relates to a method for preparing an anhydrosugar alcohol in a method for performing a dehydration reaction on the hydrogenated sugar so as to convert the hydrogenated sugar to an anhydrosugar alcohol, wherein the method for preparing an anhydrosugar alcohol is configured to use, as at least a portion of the hydrogenated sugar, the product obtained from the hydrogenation of the hydrol which is a by-product or waste generated during the production of glucose, thus relatively lowering the cost for a material as compared with a case of using a high purity raw material (for example, high purity sorbitol), to thus improve economical advantages, and further reduce the amount of waste and cost for disposal of the waste during the production of glucose.

Abstract: The photostabilizing electronic excited state energy—particularly singlet state energy from retinoid compounds—has been found to be readily transferred to (accepted by) ?-cyanodiphenylacrylate compounds having an alkoxy radical in the four (para) position (hereinafter “alkoxycrylenes”) on one of the phenyl rings having the formula (I): wherein one of R1 and R2 is a straight or branched chain C1-C30 alkoxy radical, preferably C1-C8, more preferably methoxy, and the non-alkoxy radical R1 or R2 is hydrogen; and R3 is a straight or branched chain C1-C30 alkyl radical, preferably C2-C20. The alkoxycrylene compounds of formula (I) significantly increase the photostability of retinoid compounds in a composition by at least 3-fold.

Abstract: The photostabilizing electronic excited state energy—particularly singlet state energy from resveratrol compounds—has been found to be readily transferred to (accepted by) ?-cyanodiphenylacrylate compounds having an alkoxy radical in the four (para) position (hereinafter “alkoxycrylenes”) on one of the phenyl rings having the formula (I): wherein one of R1 and R2 is a straight or branched chain C1-C30 alkoxy radical, preferably C1-C8, more preferably methoxy, and the non-alkoxy radical R1 or R2 is hydrogen; and R3 is a straight or branched chain C1-C30 alkyl radical, preferably C2-C20. The alkoxycrylene compounds of formula (I) significantly increase the photostability of resveratrol compounds in a composition by at least 3-fold and as much as 10-fold or greater. The ability of the alkoxycrylene compounds to stabilize the resveratrol compound is concentration dependent, with the amount of resveratrol photostabilization increasing with the concentration of the alkoxycrylene compound.

Abstract: An olefinically unsaturated monomer is stabilized by a retarder-containing composition which comprises a solvent and a quinone methide as a retarder.

Abstract: The photostabilizing electronic excited state energy—particularly singlet state energy from resveratrol compounds—has been found to be readily transferred to (accepted by) ?-cyanodiphenylacrylate compounds having an alkoxy radical in the four (para) position (hereinafter “alkoxycrylenes”) on one of the phenyl rings having the formula (I): wherein one of R1 and R2 is a straight or branched chain C1-C30 alkoxy radical, preferably C1-C8, more preferably methoxy, and the non-alkoxy radical R1 or R2 is hydrogen; and R3 is a straight or branched chain C1-C30 alkyl radical, preferably C2-C20. The alkoxycrylene compounds of formula (I) significantly increase the photostability of resveratrol compounds in a composition by at least 3-fold and as much as 10-fold or greater. The ability of the alkoxycrylene compounds to stabilize the resveratrol compound is concentration dependent, with the amount of resveratrol photostabilization increasing with the concentration of the alkoxycrylene compound.

Abstract: The present invention provides a process and its utilization in a process comprising the step of carrying out an addition reaction of an alkylene oxide to an addition-receiving substance in the presence of a resin catalyst, thereby producing the addition reaction product, when the resin catalyst as used for the reaction is persevered so as to recycle it after it is recovered, the unreacted alkylene oxide remaining in the resin catalyst can be prevented from polymerizing and solidifying during the preservation, and the resin catalyst accordingly can be preserved stably for a long time. The resin catalyst as recovered after it is used for the reaction may be preserved under any of the following conditions: 1) at a low temperature of not higher than 40° C.

Abstract: The subject of the present invention is a novel method for preparing a composition of internal dehydration product of a hydrogenated sugar, comprising:

Abstract: Fatty alcohol containing admixed therewith a small amount on the order of up to 1.0 wt. % of hypophosphorous acid, exhibits markedly reduced oxidation and oxidation-related deterioration such as discoloration and other side effects. This discovery is particularly useful when the fatty alcohol is subjected to reactions such as esterification under conditions which could cause or accelerate undesired oxidation.

Abstract: Described are compositions protected against thermal and oxidative degradation, comprisingA) a polyether polyol or mixtures of such polyols,B) at least one benzofuranone derivative of formula I ##STR1## wherein either two of R.sub.1, R.sub.7, R.sub.8, R.sub.9 and R.sub.10 are each independently of the other C.sub.1 -C.sub.4 alkyl or C.sub.1 -C.sub.4 alkoxy, the others being hydrogen,orR.sub.7 to R.sub.10 are hydrogen, or at most two of these radicals are each independently of the other methyl or methoxy, and R.sub.1 is --O--CHR.sub.3 --CHR.sub.5 --O--CO--R.sub.6,R.sub.2 and R.sub.4 are each independently of the other hydrogen or C.sub.1 -C.sub.6 alkyl,R.sub.3 is hydrogen or C.sub.1 -C.sub.4 alkyl,R.sub.5 is hydrogen, phenyl or C.sub.1 -C.sub.6 alkyl, andR.sub.6 is C.sub.1 -C.sub.4 alkyl,C) at least one compound from group of the phenolic antioxidants, and/orD) at least one compound from group of the amino antioxidants of the secondary amine type.

Abstract: A light colored basic alkali or alkaline earth metal organic salt is obtained by the reaction of a basic metal compound, an alkyl phenol and/or a carboxylic acid, carbon dioxide, and thereafter post-treating the reaction product with a C.sub.7 -C.sub.17 alkyl glycidyl ester such as glycidyl neodecanoate.

Abstract: Enzymatically cleavable chemiluminescent 1,2-dioxetane compounds capable of producing light energy when decomposed, substantially stable at room temperature before a bond by which an enzymatically cleavable labile substituent thereof is intentionally cleaved, are disclosed. These compounds can be represented by the formula: ##STR1## wherein: X and X.sup.1 each represent, individually, hydrogen, a hydroxyl group, a halo substituent, an unsubstituted lower alkyl group, a hydroxy (lower) alkyl group, a halo (lower) alkyl group, a phenyl group, a halophenyl group, an alkoxyphenyl group, a hydroxyalkoxy group, a cyano group or an amide group, with at least one of X and X.sup.1 being other than hydrogen; andR.sub.1 and R.sub.2, individually or together, represent an organic substituent that does not interfere with the production of light when the dioxetane compound is enzymatically cleaved and that satisfies the valence of the dioxetane compound's 4-carbon atom, with the provisos that if R.sup.1 and R.sub.

Abstract: A process in which carbon is used to catalyze production of alkylene glycols from alkylene oxides and water. Using this process, carbon may be employed to selectively catalyze the hydrolysis of alkylene oxides, such as ethylene oxide, to monoalkylene gylcols, such as monoethylene glycol. Typically, activated carbon is employed. Suitable forms of activated carbon or other carbon material include powders, granulates, extruded shapes, or mixtures thereof. The process may be carried out as a continuous or batch reaction process.

Abstract: A process comprising the addition of a degradation inhibiting effective amount of an amine having a boiling point above that of the phenol used in the process to a composition comprising the said phenol and a bisphenol, the addition occurring prior to a procedure which subjects the bisphenol to substantial heat, said bisphenol produced from an acidic ion exchange resin catalyzed reaction of the said phenol and a ketone or aldehyde.

Abstract: A process for improving the color of bisphenol-A and improving yields of bisphenol-A comprises the addition of hypophosphorus acid either prior to or concurrent with a distillation step.

Abstract: Phenyl acetylenic acetals and thioacetals and their use in the treatment of allergy, asthma, inflammation, arthritis, hyperproliferative skin disease, psoriasis or contact dermatitis are disclosed. Also disclosed are intermediates useful for producing said phenyl acetylenic acetals and thioacetals.

Abstract: A method for preventing the precipitation of ethylene-vinyl alcohol copolymers in a distillation vessel. The vessel contains water, methanol, and ethylene-vinyl alcohol copolymers. The method includes the step of adding to the distillation vessel from 1 to about 1,000 ppm of at least one surfactant selected from the group consisting of alkyl, aryl, alkylaryl and arylalkyl sulfonic acids having a carbon length of from 4 to about 30 carbons. Preferably, the surfactant is dodecylbenzenesulfonic acid.

Abstract: 6-chromanol derivatives are used as antioxidants in polyethers. These, particularly in conjunction with other antioxidants, provide excellent protection against oxidation at very low levels of use. They are particularly useful in polyethers for preparing polyurethane slabstock foam.

Abstract: Lactic, malic and glyceric acids have been found to be superior to the hydroxy acids here-to-fore employed for the stabilization of bisphenols. These hydroxy carboxylic acids or their ammonium or alkali metal salts can be added to the feed reactants used to make the bisphenols or to the reaction mixture after the reaction is complete or at any point in between. They are particularly useful when the bisphenol is exposed to high temperatures, e.g. during the separation of the bisphenol from the reaction mixture or in a melt.

Abstract: Certain substituted diaryl amines are used to inhibit the polymerization of ethylenically unsaturated monomers; for example, unsaturated carboxylic acids and derivatives thereof.

Abstract: A tablet for use in preserving samples of milk for analysis comprises bronopol (2-bromo-2-nitropropane-1,3-diol) and a water-soluble solid organic carboxylic acid, the amount of the organic acid being within the range 0.002-0.07 milli-equivalents per milligram of bronopol. The presence of the organic acid stabilizes the bronopol, thereby providing a tablet with an adequate shelf life. Suitable organic acids include citric acid, tartaric acid, malic acid, adipic acid, succinic acid and fumaric acid.

Abstract: Polyhydroxybutadiene compounds are storage stabilized against reactivity changes by incorporating therein an effective amount of a di or triphenyl phosphine compound of the formula ##STR1## wherein each x is hydrogen, a halogen or an alkyl or alkoxy group having from 1 to 10 carbon atoms and y is an alkyl group having from 1 to 10 carbon atoms or an aryl group which may be substituted with a halogen or an alkyl or alkoxy group having from 1 to 10 carbon atoms.

Abstract: A stabilizer system containing at least one compound of the formula I ##STR1## and one compound of the formula II ##STR2## the substituents R.sup.1, R.sup.2, R and R' having the meanings defined in the text, and x being 1 to 3. This stabilizer system is suitable for use as an additive to a polyalkylene glycol base liquid for preventing the formation of rust, especially on iron-containing surfaces, the use of these lubricant compositions being possible also in the high-temperature range.

Abstract: A process is disclosed for separating 5-isopropyl-m-cresol from other isopropylated m-cresols by treating a mixture of the isopropylated m-cresols with a metal halide salt. The metal halide salt preferentially forms a complex with 5-isopropyl-m-cresol over other related closely-boiling isopropylated m-cresols in the mixture. The preferentially-formed complex of 5-isopropyl-m-cresol may then be isolated from the mixture and the complex decomposed to provide a product substantially enriched in, or substantially entirely composed of, 5-isopropyl-m-cresol. The process is particularly suitable for isolating 5-isopropyl-m-cresol from closely-boiling isomers, and di-isopropylated m-cresols.

Abstract: A process is disclosed for separating closely-boiling chlorinated phenolic compounds from other chlorinated and unchlorinated phenolics by treating a mixture of the phenolics with a metal halide salt. The metal halide salt preferentially forms a complex with one of the phenolics over other related closely-boiling phenolics in the mixture. The preferentially-formed complex of one of the phenolics may then be isolated from the mixture and the complex decomposed to provide a product substantially enriched in, or substantially entirely composed of, one phenolic. The process is particularly suitable for resolving a mixture comprising phenol or cresol from their closely-boiling ortho-chlorinated derivatives, or a mixture of two isomeric chlorinated phenols or cresols or a mixture of closely-boiling mono- and dichlorinated phenols or cresols.

Abstract: A polyol composition comprising a solid polyol which is crystalline under normal conditions and, as an anti-caking agent therefor, a tertiary amine containing at least two identical organic substituents, each having two to twenty carbon atoms. A method of preventing caking of polyols is disclosed wherein to such polyols there is added at least one of such tertiary amines, preferably in a concentration of 0.05 to 0.25 percent by weight based on the weight of the polyol.

Abstract: Shelf stability of hydroxyl terminated liquid polymers is vastly improved by mixing a strong inorganic or organic acid, therewith in order to adjust acid number thereof up to about 12. Amount of the acid used is less than 1% by weight of the liquid polymer.

Abstract: Novel arylalkyl silicone sulfonate-silicate copolymers are disclosed which are useful in inhibiting the corrosion of metals below sodium in the electromotive series that come in contact with aqueous liquids, especially aqueous alcohol solutions used as heat transfer media. Antifreeze concentrates and a process for inhibiting corrosion are also disclosed.

Abstract: A bisphenol is stabilized against thermal decomposition in the molten state in a non-reactive environment by incorporation in the bisphenol of a small stabilizing amount of a quaternary ester of ortho titanic acid and an aliphatic alcohol.

Abstract: Salts of substituted nitrogen or sulfur containing siliconates are effective stabilizers for aqueous silicates in such applications as treating boiler water, geothermal water and other aqueous silicates. They are also useful in antifreeze and coolant solutions.

Abstract: Detrimental color change of phenolic antioxidants during production, storage and use in rubbers is inhibited by adding during the synthesis of the phenolic antioxidant a disubstituted hydroxylamine to the catalyst neutralization solution and a substituted oxime together with a disubstituted hydroxylamine to the reaction mixture prior to filtration.

Abstract: Disclosed is a tracer fluid for use in connection with surfactant waterflooding or other chemicalized enhanced oil, recovery processes, and an oil recovery process using the fluid. Fluids containing easily identifiable components such as water-soluble, inorganic salts, specifically water-soluble nitrate salts, as well as low molecular weight alcohols may be used as tracer fluids for determining numerous flow and formation conditions between injection wells and production wells. Many of the most desirable tracers are degraded by bacteria present in field water or surface contamination. Incorporation of from 10 to 2000 and preferably from 50 to 1500 parts per million of an aromatic treating compound, preferably benzene, toluene, or xylene, stabilizes the chemical tracer against microbial attack.

Abstract: Metals such as copper and the transition elements may give rise to serious problems in conventional rubber based solid propellant binders. These metals may accelerate the curing action to such a degree that the pot life of the freshly mixed propellant is reduced. Also the metals may promote oxidative degradation of cured and uncured binder systems. These undesirable effects can be prevented by adding to the uncured binder certain binder soluble agents which are capable of forming stable complexes with the undesirable metals in which the valence of the metal ion is fixed. A wide variety of chelating agents can be used and include, particularly, the condensation products of salicylaldehyde with aliphatic di- and polyamines and with o-aminophenols.

Abstract: Contaminant metal ions of the transition elements such as copper and iron for example may give rise to serious problems in the curing of polymeric binders for conventional rubber-based solid propellants. These metal ions may accelerate the curing action to such a degree that the potlife of the freshly mixed polymer is reduced. Also, the metal ions may promote oxidative degradation of cured and uncured polymeric systems. These undesirable effects can be prevented by adding to the uncured polymer certain polymer-soluble agents which are capable of forming stable complexes with the undesirable metal ions in which the valence of the metal ion is fixed. These agents are selected from a large group of compounds and compositions comprising certain hydroxy substituted aromatic compositions. The preferred embodiments are pyrogallol, propyl gallate, octyl gallate, decyl gallate, purpurogallin and alizarin.

Abstract: Salts of substituted nitrogen or sulfur containing siliconates are effective stabilizers for aqueous silicates in such applications as treating boiler water, geothermal water and other aqueous silicates. They are also useful in antifreeze and cooland solutions.