CH633304A5 - Polymer-containing composition, process for the preparation thereof, and use thereof - Google Patents

Polymer-containing composition, process for the preparation thereof, and use thereof Download PDF

Info

Publication number: CH633304A5
Authority: CH; Switzerland
Prior art keywords: polymer; volatile; active ingredient; solution; hydrophilic
Prior art date: 1977-02-01

Application number

CH181477A

Other languages

German (de)

English (en)

Inventor

Robert David Kross

Original Assignee

Bush Boake Allen Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1977-02-01

Filing date

1977-02-14

Publication date

1982-11-30

1977-02-14 Application filed by Bush Boake Allen Ltd filed Critical Bush Boake Allen Ltd

1982-11-30 Publication of CH633304A5 publication Critical patent/CH633304A5/de

Links

229920000642 polymer Polymers 0.000 title claims description 70
239000000203 mixture Substances 0.000 title claims description 63
238000000034 method Methods 0.000 title claims description 15
230000008569 process Effects 0.000 title claims description 8
238000002360 preparation method Methods 0.000 title claims description 6
239000004480 active ingredient Substances 0.000 claims description 48
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 38
239000000178 monomer Substances 0.000 claims description 28
-1 polyoxyethylene Polymers 0.000 claims description 26
239000003795 chemical substances by application Substances 0.000 claims description 24
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 19
235000010323 ascorbic acid Nutrition 0.000 claims description 17
239000011668 ascorbic acid Substances 0.000 claims description 17
229960005070 ascorbic acid Drugs 0.000 claims description 17
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 16
CIWBSHSKHKDKBQ-DUZGATOHSA-N D-isoascorbic acid Chemical compound OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 claims description 12
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
239000003054 catalyst Substances 0.000 claims description 11
150000002148 esters Chemical class 0.000 claims description 10
HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 claims description 7
235000011187 glycerol Nutrition 0.000 claims description 6
239000000463 material Substances 0.000 claims description 6
239000003638 chemical reducing agent Substances 0.000 claims description 5
235000014113 dietary fatty acids Nutrition 0.000 claims description 5
239000000194 fatty acid Substances 0.000 claims description 5
229930195729 fatty acid Natural products 0.000 claims description 5
239000002917 insecticide Substances 0.000 claims description 5
238000000465 moulding Methods 0.000 claims description 5
239000002685 polymerization catalyst Substances 0.000 claims description 5
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 4
150000004665 fatty acids Chemical class 0.000 claims description 4
239000003752 hydrotrope Substances 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 4
239000000600 sorbitol Substances 0.000 claims description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 3
150000001735 carboxylic acids Chemical class 0.000 claims description 3
239000002861 polymer material Substances 0.000 claims description 3
239000004094 surface-active agent Substances 0.000 claims description 3
125000002091 cationic group Chemical group 0.000 claims description 2
235000010352 sodium erythorbate Nutrition 0.000 claims description 2
JUDXBRVLWDGRBC-UHFFFAOYSA-N [2-(hydroxymethyl)-3-(2-methylprop-2-enoyloxy)-2-(2-methylprop-2-enoyloxymethyl)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(CO)(COC(=O)C(C)=C)COC(=O)C(C)=C JUDXBRVLWDGRBC-UHFFFAOYSA-N 0.000 claims 2
229920001577 copolymer Polymers 0.000 claims 2
229920001519 homopolymer Polymers 0.000 claims 2
150000002978 peroxides Chemical class 0.000 claims 2
QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 claims 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 58
KMPQYAYAQWNLME-UHFFFAOYSA-N undecanal Chemical compound CCCCCCCCCCC=O KMPQYAYAQWNLME-UHFFFAOYSA-N 0.000 description 30
239000003921 oil Substances 0.000 description 22
235000019198 oils Nutrition 0.000 description 22
239000000243 solution Substances 0.000 description 12
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 11
239000010692 aromatic oil Substances 0.000 description 11
238000006116 polymerization reaction Methods 0.000 description 10
238000004132 cross linking Methods 0.000 description 9
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 8
239000013543 active substance Substances 0.000 description 8
239000012298 atmosphere Substances 0.000 description 8
239000011347 resin Substances 0.000 description 8
229920005989 resin Polymers 0.000 description 8
229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 7
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 7
ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 7
VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 7
229910001870 ammonium persulfate Inorganic materials 0.000 description 7
239000000470 constituent Substances 0.000 description 7
230000000694 effects Effects 0.000 description 7
FBWNMEQMRUMQSO-UHFFFAOYSA-N tergitol NP-9 Chemical compound CCCCCCCCCC1=CC=C(OCCOCCOCCOCCOCCOCCOCCOCCOCCO)C=C1 FBWNMEQMRUMQSO-UHFFFAOYSA-N 0.000 description 7
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
229920001328 Polyvinylidene chloride Polymers 0.000 description 6
239000002253 acid Substances 0.000 description 6
150000001875 compounds Chemical class 0.000 description 6
238000001704 evaporation Methods 0.000 description 6
239000000796 flavoring agent Substances 0.000 description 6
235000019634 flavors Nutrition 0.000 description 6
239000007800 oxidant agent Substances 0.000 description 6
239000005033 polyvinylidene chloride Substances 0.000 description 6
239000010666 rose oil Substances 0.000 description 6
235000019719 rose oil Nutrition 0.000 description 6
239000008137 solubility enhancer Substances 0.000 description 6
239000002904 solvent Substances 0.000 description 6
GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 5
DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 5
239000002202 Polyethylene glycol Substances 0.000 description 5
235000010350 erythorbic acid Nutrition 0.000 description 5
STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 5
230000008020 evaporation Effects 0.000 description 5
229920001223 polyethylene glycol Polymers 0.000 description 5
DWHJJLTXBKSHJG-HWKANZROSA-N (e)-5-hydroxy-2-methylpent-2-enoic acid Chemical compound OC(=O)C(/C)=C/CCO DWHJJLTXBKSHJG-HWKANZROSA-N 0.000 description 4
GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 4
239000000853 adhesive Substances 0.000 description 4
239000001569 carbon dioxide Substances 0.000 description 4
229910002092 carbon dioxide Inorganic materials 0.000 description 4
239000004318 erythorbic acid Substances 0.000 description 4
229940026239 isoascorbic acid Drugs 0.000 description 4
239000000344 soap Substances 0.000 description 4
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
KUXKWCPBFHIJJJ-UHFFFAOYSA-N 6-hydroxy-2-methylhex-2-enoic acid Chemical compound OC(=O)C(C)=CCCCO KUXKWCPBFHIJJJ-UHFFFAOYSA-N 0.000 description 3
241000205585 Aquilegia canadensis Species 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
235000016623 Fragaria vesca Nutrition 0.000 description 3
240000009088 Fragaria x ananassa Species 0.000 description 3
235000011363 Fragaria x ananassa Nutrition 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
241000220317 Rosa Species 0.000 description 3
150000001299 aldehydes Chemical class 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
239000012876 carrier material Substances 0.000 description 3
230000008859 change Effects 0.000 description 3
239000003205 fragrance Substances 0.000 description 3
125000000524 functional group Chemical group 0.000 description 3
239000000077 insect repellent Substances 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
239000002736 nonionic surfactant Substances 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
239000003973 paint Substances 0.000 description 3
229920003023 plastic Polymers 0.000 description 3
239000004033 plastic Substances 0.000 description 3
USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 3
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
241000272525 Anas platyrhynchos Species 0.000 description 2
241000167854 Bourreria succulenta Species 0.000 description 2
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
244000223760 Cinnamomum zeylanicum Species 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
235000019501 Lemon oil Nutrition 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
241000243142 Porifera Species 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
235000004338 Syringa vulgaris Nutrition 0.000 description 2
244000297179 Syringa vulgaris Species 0.000 description 2
235000016639 Syzygium aromaticum Nutrition 0.000 description 2
244000223014 Syzygium aromaticum Species 0.000 description 2
239000002386 air freshener Substances 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 2
SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 2
230000001588 bifunctional effect Effects 0.000 description 2
239000003093 cationic surfactant Substances 0.000 description 2
SVURIXNDRWRAFU-OGMFBOKVSA-N cedrol Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1[C@@](O)(C)CC2 SVURIXNDRWRAFU-OGMFBOKVSA-N 0.000 description 2
235000019693 cherries Nutrition 0.000 description 2
235000017803 cinnamon Nutrition 0.000 description 2
NEHNMFOYXAPHSD-UHFFFAOYSA-N citronellal Chemical compound O=CCC(C)CCC=C(C)C NEHNMFOYXAPHSD-UHFFFAOYSA-N 0.000 description 2
QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 2
229910017052 cobalt Inorganic materials 0.000 description 2
239000010941 cobalt Substances 0.000 description 2
238000000354 decomposition reaction Methods 0.000 description 2
HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 2
CBOQJANXLMLOSS-UHFFFAOYSA-N ethyl vanillin Chemical group CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 description 2
RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 2
239000004744 fabric Substances 0.000 description 2
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
229920001477 hydrophilic polymer Polymers 0.000 description 2
230000001965 increasing effect Effects 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
239000000171 lavandula angustifolia l. flower oil Substances 0.000 description 2
239000010501 lemon oil Substances 0.000 description 2
UWKAYLJWKGQEPM-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000002609 medium Substances 0.000 description 2
VLKZOEOYAKHREP-UHFFFAOYSA-N methyl pentane Natural products CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
239000011707 mineral Substances 0.000 description 2
125000005702 oxyalkylene group Chemical group 0.000 description 2
239000003016 pheromone Substances 0.000 description 2
239000010665 pine oil Substances 0.000 description 2
229920001451 polypropylene glycol Polymers 0.000 description 2
239000001044 red dye Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000000126 substance Substances 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
125000002348 vinylic group Chemical group 0.000 description 2
KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 description 1
QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 1
MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 1
229940058015 1,3-butylene glycol Drugs 0.000 description 1
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QUMXDOLUJCHOAY-UHFFFAOYSA-N 1-Phenylethyl acetate Chemical compound CC(=O)OC(C)C1=CC=CC=C1 QUMXDOLUJCHOAY-UHFFFAOYSA-N 0.000 description 1
YBUIAJZFOGJGLJ-SWRJLBSHSA-N 1-cedr-8-en-9-ylethanone Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1C(C)=C(C(C)=O)C2 YBUIAJZFOGJGLJ-SWRJLBSHSA-N 0.000 description 1
KJSATFDGRLXLPP-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical class OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OCC(CO)(CO)CO KJSATFDGRLXLPP-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
FACFHHMQICTXFZ-UHFFFAOYSA-N 2-(2-phenylimidazo[1,2-a]pyridin-3-yl)ethanamine Chemical compound N1=C2C=CC=CN2C(CCN)=C1C1=CC=CC=C1 FACFHHMQICTXFZ-UHFFFAOYSA-N 0.000 description 1
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
GTELLNMUWNJXMQ-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical class OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.CCC(CO)(CO)CO GTELLNMUWNJXMQ-UHFFFAOYSA-N 0.000 description 1
YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexanol Substances CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 1
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
RIWRBSMFKVOJMN-UHFFFAOYSA-N 2-methyl-1-phenylpropan-2-ol Chemical compound CC(C)(O)CC1=CC=CC=C1 RIWRBSMFKVOJMN-UHFFFAOYSA-N 0.000 description 1
HAUVRGZOEXGUJS-UHFFFAOYSA-N 2-methyl-4-(oxiran-2-yl)but-2-enoic acid Chemical compound OC(=O)C(C)=CCC1CO1 HAUVRGZOEXGUJS-UHFFFAOYSA-N 0.000 description 1
JJYWRQLLQAKNAD-UHFFFAOYSA-N 2-methylpent-2-enoic acid Chemical compound CCC=C(C)C(O)=O JJYWRQLLQAKNAD-UHFFFAOYSA-N 0.000 description 1
NFAVNWJJYQAGNB-UHFFFAOYSA-N 2-methylundecanal Chemical compound CCCCCCCCCC(C)C=O NFAVNWJJYQAGNB-UHFFFAOYSA-N 0.000 description 1
PSAURYCHUAGLFL-UHFFFAOYSA-N 2-prop-2-enylidenepropanedioic acid Chemical compound OC(=O)C(C(O)=O)=CC=C PSAURYCHUAGLFL-UHFFFAOYSA-N 0.000 description 1
CKPOABDCSSXDCY-UHFFFAOYSA-N 2-propan-2-yltetradecanoic acid Chemical compound CCCCCCCCCCCCC(C(C)C)C(O)=O CKPOABDCSSXDCY-UHFFFAOYSA-N 0.000 description 1
GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 description 1
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LVSQXDHWDCMMRJ-UHFFFAOYSA-N 4-hydroxybutan-2-one Chemical compound CC(=O)CCO LVSQXDHWDCMMRJ-UHFFFAOYSA-N 0.000 description 1
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XQIHFGYUMFFCFG-UHFFFAOYSA-N 4-methyl-2-methylidenepentanoic acid Chemical compound CC(C)CC(=C)C(O)=O XQIHFGYUMFFCFG-UHFFFAOYSA-N 0.000 description 1
MBZRJSQZCBXRGK-UHFFFAOYSA-N 4-tert-Butylcyclohexyl acetate Chemical compound CC(=O)OC1CCC(C(C)(C)C)CC1 MBZRJSQZCBXRGK-UHFFFAOYSA-N 0.000 description 1
LJSJTXAZFHYHMM-UHFFFAOYSA-N 7-methyloctyl acetate Chemical compound CC(C)CCCCCCOC(C)=O LJSJTXAZFHYHMM-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
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239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
235000003717 Boswellia sacra Nutrition 0.000 description 1
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244000183685 Citrus aurantium Species 0.000 description 1
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241000402754 Erythranthe moschata Species 0.000 description 1
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239000005770 Eugenol Substances 0.000 description 1
239000004863 Frankincense Substances 0.000 description 1
239000005792 Geraniol Substances 0.000 description 1
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WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
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AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
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DINKXUCRJBUQAZ-UHFFFAOYSA-N tert-butyl 5-bromopyridine-3-carboxylate Chemical compound CC(C)(C)OC(=O)C1=CN=CC(Br)=C1 DINKXUCRJBUQAZ-UHFFFAOYSA-N 0.000 description 1
BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 1
229910052723 transition metal Inorganic materials 0.000 description 1
150000003624 transition metals Chemical class 0.000 description 1
DXNCZXXFRKPEPY-UHFFFAOYSA-N tridecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCC(O)=O DXNCZXXFRKPEPY-UHFFFAOYSA-N 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
239000011718 vitamin C Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/08—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing solids as carriers or diluents
- A01N25/10—Macromolecular compounds
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/18—Vapour or smoke emitting compositions with delayed or sustained release
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0208—Tissues; Wipes; Patches
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/007—Pulmonary tract; Aromatherapy
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/2027—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/015—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone
- A61L9/04—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating
- A61L9/042—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating with the help of a macromolecular compound as a carrier or diluent
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/015—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone
- A61L9/04—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating
- A61L9/044—Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating with the help of an organic compound other than a macromolecular compound
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0058—Biocides

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Animal Behavior & Ethology (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Chemical & Material Sciences (AREA)
Epidemiology (AREA)
Medicinal Chemistry (AREA)
Engineering & Computer Science (AREA)
Pest Control & Pesticides (AREA)
Pharmacology & Pharmacy (AREA)
Birds (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Agronomy & Crop Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Plant Pathology (AREA)
Toxicology (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Biomedical Technology (AREA)
Pulmonology (AREA)
Biodiversity & Conservation Biology (AREA)
Dermatology (AREA)
Fats And Perfumes (AREA)
Compositions Of Macromolecular Compounds (AREA)
Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Processes Of Treating Macromolecular Substances (AREA)
Cosmetics (AREA)

CH181477A 1977-02-01 1977-02-14 Polymer-containing composition, process for the preparation thereof, and use thereof CH633304A5 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
SE7701076A SE421531B (sv)	1977-02-01	1977-02-01	Polymer komposition innehallande en for reglerad avgivning aktiv, flyktig bestandsdel, forfarande for framstellning av kompositionen samt anvendning derav

Publications (1)

Publication Number	Publication Date
CH633304A5 true CH633304A5 (en)	1982-11-30

Family

ID=20330329

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH181477A CH633304A5 (en)	1977-02-01	1977-02-14	Polymer-containing composition, process for the preparation thereof, and use thereof

Country Status (9)

Country	Link
JP (1)	JPS5946541B2 (fr)
AU (1)	AU513822B2 (fr)
BE (1)	BE881972Q (fr)
CA (1)	CA1099429A (fr)
CH (1)	CH633304A5 (fr)
DE (1)	DE2705218A1 (fr)
FR (1)	FR2380328A1 (fr)
NL (1)	NL7701526A (fr)
SE (1)	SE421531B (fr)

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0011924A1 (fr) *	1978-10-23	1980-06-11	BUSH BOAKE ALLEN Limited	Compositions polymères libérant un parfum et procédés pour leur préparation
US4320873A (en) *	1979-05-21	1982-03-23	S. C. Johnson & Son, Inc.	Controlled release air freshener using an absorbent generator
CA1150635A (fr) *	1979-10-23	1983-07-26	Philip L. Williams	Monomere lipophyle d'un polymere hydrophyle contenant un ingredient volatif captif
IT1129711B (it) *	1980-01-23	1986-06-11	Montedison Spa	Formulazioni solide contenenti ferormoni
USRE33429E (en) *	1981-03-23	1990-11-06	Dow Corning Corporation	Lattice-entrapped emollient-moisturizer composition
US4880617A (en) *	1981-03-23	1989-11-14	Dow Corning Corporation	Lattice-entrapped composition
US4724240A (en) *	1981-03-23	1988-02-09	Wickhen Products, Inc.	Lattice-entrapped emollient-moisturizer composition
CA1168157A (fr) *	1981-03-23	1984-05-29	Eric S. Abrutyn	Composition adoucissante-humidifiante, fixee dans un polymere
US4729190A (en) *	1983-10-27	1988-03-08	Ciba-Geigy Corporation	Membrane-forming polymeric systems
US4855127A (en) *	1986-07-07	1989-08-08	Dow Corning Corporation	Lattice-entrapped composition
CA2037282C (fr) *	1990-04-02	1997-01-28	Nuno M. Rei	Microbicides immobilises dans des resines polymeres thermoplastiques hydrosolubles et dispersions aqueuses de microbicides ainsi produites
DE4416672A1 (de) *	1994-05-11	1995-11-16	Grillmayer Juergen	Duftender Gegenstand
JP7846623B2 (ja) *	2021-06-21	2026-04-15	積水化学工業株式会社	（メタ）アクリル樹脂組成物、無機微粒子分散スラリー組成物及び無機微粒子分散成形物

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GB1205769A (en) *	1966-07-26	1970-09-16	Nat Patent Dev Corp	Polymer compositions containing flavouring or fragrance agents
GR34006B (el) *	1966-07-26	1968-03-06	National Patent Development Corporation	Υδροφιλα πολυμερη, ειδη και μεθοδοι παρασκευης αυτων.
FR2022100A6 (en) *	1967-07-05	1970-07-31	Nat Patent Developm	Acrylate polymer as binder in cosmetic composns
US3655129A (en) *	1968-07-17	1972-04-11	Ppg Industries Inc	Slow release films and methods of making same
US3567118A (en) *	1968-09-05	1971-03-02	Nat Patent Dev Corp	Entrapped essences in dry composite fiber base products giving a strong fragrance when wet in water
US3868447A (en) *	1972-02-02	1975-02-25	Nat Patent Dev Corp	Hema paste
AU1158276A (en) *	1975-03-03	1977-09-08	Airwick Ag	A solid air odor-improving agent-releasing diffuser system

1977
- 1977-02-01 SE SE7701076A patent/SE421531B/xx not_active IP Right Cessation
- 1977-02-04 CA CA271,072A patent/CA1099429A/fr not_active Expired
- 1977-02-07 AU AU22023/77A patent/AU513822B2/en not_active Expired
- 1977-02-08 DE DE19772705218 patent/DE2705218A1/de not_active Ceased
- 1977-02-10 JP JP52013112A patent/JPS5946541B2/ja not_active Expired
- 1977-02-14 NL NL7701526A patent/NL7701526A/xx not_active Application Discontinuation
- 1977-02-14 CH CH181477A patent/CH633304A5/de not_active IP Right Cessation
- 1977-02-14 FR FR7704127A patent/FR2380328A1/fr active Granted
1980
- 1980-02-28 BE BE0/199591A patent/BE881972Q/fr not_active IP Right Cessation

Also Published As

Publication number	Publication date
SE421531B (sv)	1982-01-04
AU513822B2 (en)	1981-01-08
DE2705218A1 (de)	1978-08-10
AU2202377A (en)	1978-08-17
SE7701076L (sv)	1978-08-02
CA1099429A (fr)	1981-04-14
BE881972Q (fr)	1980-08-28
JPS5946541B2 (ja)	1984-11-13
FR2380328A1 (fr)	1978-09-08
NL7701526A (nl)	1978-08-16
FR2380328B1 (fr)	1980-03-07
JPS5399252A (en)	1978-08-30

Legal Events

Date	Code	Title	Description
1986-07-31	PUE	Assignment	Owner name: HYDRO OPTICS INCORPORATED
1988-10-31	PL	Patent ceased
1989-06-15	PK	Correction
1989-10-31	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
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DE69917309T2 (de)	2005-05-12	Gelförmige dampfeinrichtung
EP0862590B1 (fr)	1999-08-18	Polymeres absorbant des liquides, procede de preparation et utilisation
CH633304A5 (en)	1982-11-30	Polymer-containing composition, process for the preparation thereof, and use thereof
DE19543368C2 (de)	1998-11-26	Wasserabsorbierende Polymere mit verbesserten Eigenschaften, Verfahren zu deren Herstellung und deren Verwendung
DE1935873C3 (de)	1973-12-20	Filme, die langsam einen verflüchtigbaren Wirkstoff abgeben
DE69615153T2 (de)	2002-06-13	Absorbierendes schaummaterial hergestellt in wasser in öl emulsion brauchbar zurgewinnung und abgabe von wässrigen flüssigkeiten
EP0028118B1 (fr)	1986-01-15	Articles conformés à base de polymère et d'ingrédients volatils occlus
DE69322913T2 (de)	1999-06-02	Harzformkörper mit langsamer Abgabe und Verfahren zu ihrer Herstellung
DE2059409A1 (de)	1972-06-22	Hydrophile Gelpolymere
CH656624A5 (de)	1986-07-15	Verfahren zur herstellung einer bis zu hohen temperaturen stabilen und homogenen polymerlegierung sowie verwendung derselben.
DE2608533A1 (de)	1976-09-30	Verfahren zur herstellung eines festen diffusionssystems zur abgabe eines den geruch der luft verbessernden mittels, sowie damit erhaltene systeme
DE2454969A1 (de)	1975-05-22	Mineralisches traegermaterial fuer fluechtige stoffe
DE3853604T2 (de)	1995-08-31	Polymerische Zusammensetzungen.
DE2703360A1 (de)	1977-08-04	Verfahren zur verbesserung der qualitaet des duftes eines parfuems
DE2654417A1 (de)	1978-06-08	Formkoerper, insbesondere verpackungsmaterial, auf basis von chemisch modifiziertem cellulosehydrat sowie verfahren zur herstellung der formkoerper
DE2256496C2 (de)	1983-01-20	Verfahren zur Herstellung von Formteilen mit Zellstruktur
EP1334735A1 (fr)	2003-08-13	Procédé pour la désodorisation des salles
WO1998000020A1 (fr)	1998-01-08	Nouvelles formulations insecticides
EP0171603A1 (fr)	1986-02-19	Polylactides microporeux en poudre
EP2844065B1 (fr)	2021-01-06	Composition attractive
DE1694055C3 (de)	1975-10-02	Herstellung eines geruchaussendenden Kunststoffes
DE2062995A1 (de)	1971-12-02	Hydrophiles Copolymerisat
DE69812129T2 (de)	2003-10-30	Gelmaterialien
DE1620814A1 (de)	1970-09-03	Verfahren zur Herstellung von mit Vinylpolymerisat impraegnierter Zellulose