Abstract: Compounds of formula (I): ##STR1## wherein: R.sup.1 represents an alkyl group having from 1 to 6 carbon atoms;R.sup.2 represents an alkyl group having from 8 to 24 carbon atoms;EO represents an ethyleneoxy group;PO represents a propyleneoxy group;k is 0 or an integer from 1 to 10; andm is an integer from 1 to 4;provided that the total of (k+m) is greater than 1 and not greater than 10;are useful as antioxidant stabilizers for polymeric materials.

Abstract: The present invention relates to weather resistant resin compositions consisting essentially of at least one polymeric substance and comprising discoloration effective amounts of:(i) a hindered amine stabilizer;(ii) a hindered-phenol-hindered amine stabilizer; and(iii) a UV absorber.

Abstract: The compounds of formula (I): ##STR1## [in which: R.sup.1 and R.sup.2 are the same or different and each represents hydrogen or C.sub.1 -C.sub.5 alkyl;R.sup.3 represents hydrogen, an acyl group, a (C.sub.1 -C.sub.6 alkoxy)carbonyl group or an aralkyloxycarbonyl group;R.sup.4 and R.sup.5 are the same or different and each represents hydrogen, C.sub.1 -C.sub.5 alkyl or C.sub.1 -C.sub.5 alkoxy, or R.sup.4 and R.sup.5 together represent a C.sub.1 14 C.sub.4 alkylenedioxy group;n is 1, 2 or 3;W represents the --CH.sub.2 --, >CO or >CH--OR.sup.6 group (in which R.sup.6 represents any one of the atoms or groups defined for R.sup.3 and may be the same as or different from R.sup.3); andY and Z are the same or different and each represents oxygen or imino]and pharmaceutically acceptable salts thereof have various valuable therapeutic effects on the blood system and may be prepared by a process which includes reacting a corresponding halopropionic acid derivative with thiourea.

Abstract: Bis(piperidylaminotriazylamino)-(piperidylaminotriazylaminomethyl)-octane derivatives are novel compounds which are valuable as stabilizers for synthetic polymers.

Abstract: Polymers containing polyalkylpiperidines, preparation and use thereof as stabilizers for synthetic polymer compositions are described. In said polymer, sterically hindered polyalkylpiperidines are laterally linked to the main chain. The polymers are distinguished by an improved stabilizing effect in various synthetic polymer compositions, such as polyolefins, against light- and/or heat-induced deterioration thereof. The polyalkylpiperidine-containing polymers of the invention are hardly volatile upon heat-processing or during storage of shaped articles containing said polymers, and are resistant to extraction with solvents.

Abstract: Piperidine derivatives in which two or three piperidine residues each substituted at the 2- and the 6-position by two methyl groups or by one methyl group and one ethyl group, the piperidine residues being attached by means of substituted alkylene groups, by means of polyoxyalkylene groups (whose oxyalkylene chain is optionally interrupted by one or more phenylene or cyclohexylene groups), by means of substituted isocyanurate groups or by means of glyceryl groups, and acid addition salts thereof are valuable as stabilizers for synthetic polymers.

Abstract: Novel triazine derivatives represented by the general formula (I) and use thereof as light stabilizers for synthetic polymers are described. ##STR1## The compounds are distinguished by an improved stabilizing effect in various synthetic polymer compositions, such as polyolefins, against light- and/or heat-induced deterioration thereof, low volatility upon heat-processing or during storage of shaped articles containing the compounds, and resistance to extraction with water and solvents.

Abstract: The invention entitled "Polymers containing polyalkylpiperidines and use thereof as stabilizers" provides a class of polymers in which groups containing sterically hindered polyalkylpiperidines are linked in the main chain of the polymers via bridging members containing 2-hydroxy-1,3-trimethylene groups.The polymers show superior stabilizing effects for various synthetic polymers such as polyolefins against degradation thereof induced by light and/or heat. The polymers have advantages, as compared with known stabilizer compounds, that they hardly volatile upon processing with heating or during storage of articles containing thereof, and that they are resistant to extraction with solvents from articles containing thereof.

Abstract: Piperidine derivatives having the formula ##STR1## wherein R' represents an alkyl, an acyl, an alkoxycarbonyl, an amino or nitroso group;X represents oxygen or sulfur;Y represents oxygen, sulfur or a group of the formula .dbd.N--R" in which R" is hydrogen or alkyl;Z represents oxygen or a group of the formula >N--R'" in which R'" is hydrogen or alkyl;n is an integer of 1 to 4; andR represents, when n is 1, alkyl, aryl, cycloalkyl, alkoxycarbonyl, substituted phosphino or substituted phosphinyl, when n is 2, alkylene, alkenylene, arylene, aralkylene; alkylenediphenylene, bis-(alkoxycarbonyl) alkylene, alkylene-bis-(oxycarbonylalkyl), dialkylene ether or diphenylene ether, when n is 3, alkanetriyl,tris-(alkoxycarbonyl)alkanetriyl, alkanetriyl-tris-(oxycarbonylalkyl) or a group of the formula ##STR2## in which p is an integer of 1 through 8 inclusive, and, when n is 4, alkanetetrayl,tetrakis-(alkoxycarbonyl) alkanetetrayl or alkanetetrayl-tetrakis-(oxycarbonylalkyl).

Abstract: 2,2,6,6-Tetramethylpiperidine derivatives having the formula ##STR1## wherein: X represents a group of formula ##STR2## R represents a hydrogen atom, methyl group, ethyl group, phenoxymethyl group or phenyl group;R' represents a methyl group or ethyl group; andm represents 0, 1 or 2,are excellent stabilizers for synthetic polymers.

Abstract: Novel piperidine-spiro-hydantoin derivatives represented by the general formula (I) and use thereof as light stabilizers for synthetic polymers are described: ##STR1## The compounds are distinguished by an improved stabilizing effect in various synthetic polymer compositions, such as polyolefins, against light- and/or heat-induced deterioration thereof, small volatility upon heat-processing or during storage of shaped articles containing the compounds, and resistance to extraction with water and solvents.

Abstract: A novel piperidine derivative having a stabilizing effect on a synthetic polymeric material and a composition comprising said piperidine derivative and a synthetic polymeric material.

Abstract: Derivatives of sterically hindered 4-aminopiperidines are effective as light-stabilizers for organic polymers, especially for polyolefins. The piperidine ring is substituted with at least five alkyl groups, preferably methyl and ethyl groups. The 4-amino group is substituted with mono- or divalent acyl groups. The nitrogen in 1-position may also be substituted with a monovalent organic substituent. The compounds can be synthesized starting from higher homologs of acetone in sequence of several reaction steps.

Abstract: New polyalkylated 4-aminopiperidine derivatives contain in their molecule two or three piperidine rings, each having two alkyl substituents at both the 2- and the 6- positions, optionally having substituents at the 1- and 3- positions and having an amino substituent at the 4- position. The piperidine rings are joined together by attachment of the 4-amino substituents through, where there are two piperidine rings, a polyalkylene, polyether or polyester chain, or through, where there are three piperidine rings, an isocyanurate or glycerol system. These compounds and their acid addition salts are useful as stabilizers for synthetic polymers.

Abstract: Hydantoin derivatives in which two or three piperidine spiro hydantoin residues are attached by means of substituted alkylene groups or polyoxyalkylene groups whose oxyalkylene chain is optionally interrupted by one or more phenylene or cyclohexylene groups or by means of substituted isocyanurate or glyceryl groups and, where they exist, acid addition salts thereof, are valuable as stabilizers for synthetic polymers.

Abstract: Polymers, both natural and synthetic, are stabilized against the deterioration resulting from heat and/or light by the incorporation of certain 2,2,6,6-tetra-substituted-4-piperidinol derivatives which additionally have an alkyl, alkenyl, alkynyl or aralkyl substituent at one or both of the 3- and 5- positions.

Abstract: Sterically hindered piperidines having at least 5 alkyl groups in ring positions 2,3,5 and 6 are usable as light-stabilizers for organic polymers. The nitrogen may be unsubstituted or may bear a mono- to tetravalent substituent. The compounds can be synthesized by a Wolf-Kishner reduction of polyalkyl 4-oxopiperidines optionally followed by a N-substitution reaction in a second step.The stabilizers are added to the polymers in an amount of from 0.01 to 5% by weight. Preferred is the stabilization of polyolefins, styrene polymers, polyamides and polyurethanes.

Abstract: A novel piperidine derivative having a stabilizing effect on a synthetic polymeric material and a composition comprising said piperidine derivative and a synthetic polymeric material.

Abstract: Novel derivatives of 4-amino-2,6-dimethylpiperidine have additional methyl or substituted-methyl substituents at positions 2 and 6, and a carboxylate ester substituent at position 4. Positions 1 and 3, and the amino group at position 4, can optionally also be substituted. These derivatives are useful for stabilizing synthetic polymers, especially polyolefins, polyamides and polyurethanes, against photo- and thermal-deterioration, generally in an amount of 0.01 - 5.0% by weight based on the polymer.

Abstract: Cyclic ketals of sterically hindered 4-oxopiperidines are effective light-stabilizers for organic polymers. These compounds have at least five alkyl groups in ring positions 2,3,5 and 6 and four alkyl groups in ring positions 2 and 6, preferably methyl and ethyl groups. The ring nitrogen may be unsubstituted or substituted with a monvalent substitutent. The new compounds can be synthesized by ketalization of the corresponding 4-oxopiperidines with diols, triols or tetrols. Using triols the obtained ketals possess hydroxyl groups which may be esterified or etherified in a subsequent reaction step. Ketalization with tetrols yields cyclic bis-ketals.