JP4005640B2 - 低極性液体中で透明ゲルを処方するのに有用な重合化脂肪酸のエステル末端ポリアミド - Google Patents
低極性液体中で透明ゲルを処方するのに有用な重合化脂肪酸のエステル末端ポリアミド Download PDFInfo
- Publication number
- JP4005640B2 JP4005640B2 JP51971798A JP51971798A JP4005640B2 JP 4005640 B2 JP4005640 B2 JP 4005640B2 JP 51971798 A JP51971798 A JP 51971798A JP 51971798 A JP51971798 A JP 51971798A JP 4005640 B2 JP4005640 B2 JP 4005640B2
- Authority
- JP
- Japan
- Prior art keywords
- ester
- groups
- etpa
- carbon atoms
- composition
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
- 235000014113 dietary fatty acids Nutrition 0.000 title claims description 51
- 229930195729 fatty acid Natural products 0.000 title claims description 51
- 239000000194 fatty acid Substances 0.000 title claims description 51
- 239000004952 Polyamide Substances 0.000 title claims description 39
- 229920002647 polyamide Polymers 0.000 title claims description 39
- 239000000499 gel Substances 0.000 title description 133
- 150000004665 fatty acids Chemical class 0.000 title description 47
- 239000007788 liquid Substances 0.000 title description 32
- 239000000203 mixture Substances 0.000 claims description 85
- 150000002430 hydrocarbons Chemical class 0.000 claims description 60
- 125000004432 carbon atom Chemical group C* 0.000 claims description 58
- 229930195733 hydrocarbon Natural products 0.000 claims description 51
- 150000002148 esters Chemical class 0.000 claims description 40
- 239000004215 Carbon black (E152) Substances 0.000 claims description 24
- 238000006243 chemical reaction Methods 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 23
- 125000000217 alkyl group Chemical group 0.000 claims description 22
- 239000001257 hydrogen Substances 0.000 claims description 22
- 229910052739 hydrogen Inorganic materials 0.000 claims description 22
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 20
- 239000011342 resin composition Substances 0.000 claims description 17
- 125000004185 ester group Chemical group 0.000 claims description 16
- 125000003368 amide group Chemical group 0.000 claims description 13
- 239000002537 cosmetic Substances 0.000 claims description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
- 150000005690 diesters Chemical class 0.000 claims description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 11
- 229910052760 oxygen Inorganic materials 0.000 claims description 11
- 239000001301 oxygen Substances 0.000 claims description 11
- 150000002431 hydrogen Chemical class 0.000 claims description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 229920000233 poly(alkylene oxides) Polymers 0.000 claims description 7
- 125000000962 organic group Chemical group 0.000 claims description 6
- 239000002674 ointment Substances 0.000 claims description 4
- 239000004909 Moisturizer Substances 0.000 claims description 2
- 210000001072 colon Anatomy 0.000 claims description 2
- 230000001333 moisturizer Effects 0.000 claims description 2
- 239000002304 perfume Substances 0.000 claims description 2
- 239000000829 suppository Substances 0.000 claims description 2
- 230000001225 therapeutic effect Effects 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 7
- 239000007934 lip balm Substances 0.000 claims 1
- 229920005989 resin Polymers 0.000 description 76
- 239000011347 resin Substances 0.000 description 76
- 239000000047 product Substances 0.000 description 50
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 47
- 239000002253 acid Substances 0.000 description 39
- 150000004985 diamines Chemical class 0.000 description 34
- BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 description 34
- 239000000376 reactant Substances 0.000 description 27
- 238000009472 formulation Methods 0.000 description 21
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 20
- 239000000463 material Substances 0.000 description 18
- 239000011541 reaction mixture Substances 0.000 description 17
- 239000000539 dimer Substances 0.000 description 16
- 239000003921 oil Substances 0.000 description 16
- 235000019198 oils Nutrition 0.000 description 16
- 239000002480 mineral oil Substances 0.000 description 15
- 150000001412 amines Chemical class 0.000 description 14
- 235000010446 mineral oil Nutrition 0.000 description 14
- 125000003118 aryl group Chemical group 0.000 description 13
- 229910052757 nitrogen Inorganic materials 0.000 description 13
- -1 --CH2CH2-) Chemical group 0.000 description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 12
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 12
- 239000003349 gelling agent Substances 0.000 description 12
- 239000007787 solid Substances 0.000 description 10
- 239000004480 active ingredient Substances 0.000 description 9
- 150000001298 alcohols Chemical class 0.000 description 9
- 150000001408 amides Chemical class 0.000 description 9
- 229910052799 carbon Inorganic materials 0.000 description 9
- 238000001816 cooling Methods 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 9
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 9
- 150000007513 acids Chemical class 0.000 description 8
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 8
- 239000002781 deodorant agent Substances 0.000 description 8
- 238000005755 formation reaction Methods 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 8
- 125000000623 heterocyclic group Chemical group 0.000 description 7
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
- 125000002947 alkylene group Chemical group 0.000 description 6
- 125000003277 amino group Chemical group 0.000 description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 6
- 239000000969 carrier Substances 0.000 description 6
- 239000003086 colorant Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 6
- 229920006122 polyamide resin Polymers 0.000 description 6
- 150000003141 primary amines Chemical class 0.000 description 6
- 150000003335 secondary amines Chemical class 0.000 description 6
- 125000003342 alkenyl group Chemical group 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000006227 byproduct Substances 0.000 description 5
- 125000002843 carboxylic acid group Chemical group 0.000 description 5
- 239000003153 chemical reaction reagent Substances 0.000 description 5
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 229920006395 saturated elastomer Polymers 0.000 description 5
- 239000005977 Ethylene Substances 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 230000001166 anti-perspirative effect Effects 0.000 description 4
- 239000003213 antiperspirant Substances 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
- BTFJIXJJCSYFAL-UHFFFAOYSA-N icosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 description 4
- 239000000944 linseed oil Substances 0.000 description 4
- 235000021388 linseed oil Nutrition 0.000 description 4
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 4
- 125000004430 oxygen atom Chemical group O* 0.000 description 4
- 239000002453 shampoo Substances 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- 239000003784 tall oil Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000001993 wax Substances 0.000 description 4
- CFQZKFWQLAHGSL-FNTYJUCDSA-N (3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e,17e)-18-[(3e,5e,7e,9e,11e,13e,15e)-octadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoyl]oxyoctadeca-3,5,7,9,11,13,15,17-octaenoic acid Chemical group OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\OC(=O)C\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C=C CFQZKFWQLAHGSL-FNTYJUCDSA-N 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000005642 Oleic acid Substances 0.000 description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 239000006071 cream Substances 0.000 description 3
- 238000005886 esterification reaction Methods 0.000 description 3
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- NEOZOXKVMDBOSG-UHFFFAOYSA-N propan-2-yl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OC(C)C NEOZOXKVMDBOSG-UHFFFAOYSA-N 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 238000000518 rheometry Methods 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 3
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 2
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 235000014698 Brassica juncea var multisecta Nutrition 0.000 description 2
- 235000006008 Brassica napus var napus Nutrition 0.000 description 2
- 240000000385 Brassica napus var. napus Species 0.000 description 2
- 235000006618 Brassica rapa subsp oleifera Nutrition 0.000 description 2
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical group CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 125000002015 acyclic group Chemical group 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 2
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 2
- 238000010640 amide synthesis reaction Methods 0.000 description 2
- 125000004429 atom Chemical group 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
- VHRGRCVQAFMJIZ-UHFFFAOYSA-N cadaverine Chemical compound NCCCCCN VHRGRCVQAFMJIZ-UHFFFAOYSA-N 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 229960000541 cetyl alcohol Drugs 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- 239000013065 commercial product Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 229960000735 docosanol Drugs 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 125000001033 ether group Chemical group 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 2
- 239000000976 ink Substances 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 229940093629 isopropyl isostearate Drugs 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 229960004488 linolenic acid Drugs 0.000 description 2
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 2
- 150000004668 long chain fatty acids Chemical class 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 2
- BAIZLGVGMIENLK-UHFFFAOYSA-N n-hexacosanyl palmitate Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC BAIZLGVGMIENLK-UHFFFAOYSA-N 0.000 description 2
- NTNWKDHZTDQSST-UHFFFAOYSA-N naphthalene-1,2-diamine Chemical compound C1=CC=CC2=C(N)C(N)=CC=C21 NTNWKDHZTDQSST-UHFFFAOYSA-N 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- RZJRJXONCZWCBN-UHFFFAOYSA-N octadecane Chemical compound CCCCCCCCCCCCCCCCCC RZJRJXONCZWCBN-UHFFFAOYSA-N 0.000 description 2
- 235000021313 oleic acid Nutrition 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 238000004537 pulping Methods 0.000 description 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- RXRMVTCLUMJEEX-UHFFFAOYSA-N tetratriacontyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC RXRMVTCLUMJEEX-UHFFFAOYSA-N 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- 239000012780 transparent material Substances 0.000 description 2
- 239000013638 trimer Substances 0.000 description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
- LWBHHRRTOZQPDM-UHFFFAOYSA-N undecanedioic acid Chemical compound OC(=O)CCCCCCCCCC(O)=O LWBHHRRTOZQPDM-UHFFFAOYSA-N 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
- XBTRYWRVOBZSGM-UHFFFAOYSA-N (4-methylphenyl)methanediamine Chemical compound CC1=CC=C(C(N)N)C=C1 XBTRYWRVOBZSGM-UHFFFAOYSA-N 0.000 description 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- OPCJOXGBLDJWRM-UHFFFAOYSA-N 1,2-diamino-2-methylpropane Chemical compound CC(C)(N)CN OPCJOXGBLDJWRM-UHFFFAOYSA-N 0.000 description 1
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- PWGJDPKCLMLPJW-UHFFFAOYSA-N 1,8-diaminooctane Chemical compound NCCCCCCCCN PWGJDPKCLMLPJW-UHFFFAOYSA-N 0.000 description 1
- WTFAGPBUAGFMQX-UHFFFAOYSA-N 1-[2-[2-(2-aminopropoxy)propoxy]propoxy]propan-2-amine Chemical compound CC(N)COCC(C)OCC(C)OCC(C)N WTFAGPBUAGFMQX-UHFFFAOYSA-N 0.000 description 1
- BDEHGQOUMOLWCN-UHFFFAOYSA-N 16-methylheptadecyl benzoate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)C1=CC=CC=C1 BDEHGQOUMOLWCN-UHFFFAOYSA-N 0.000 description 1
- FTVFPPFZRRKJIH-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CC1(C)CC(N)CC(C)(C)N1 FTVFPPFZRRKJIH-UHFFFAOYSA-N 0.000 description 1
- DDHUNHGZUHZNKB-UHFFFAOYSA-N 2,2-dimethylpropane-1,3-diamine Chemical compound NCC(C)(C)CN DDHUNHGZUHZNKB-UHFFFAOYSA-N 0.000 description 1
- WCZNKVPCIFMXEQ-UHFFFAOYSA-N 2,3,5,6-tetramethylbenzene-1,4-diamine Chemical compound CC1=C(C)C(N)=C(C)C(C)=C1N WCZNKVPCIFMXEQ-UHFFFAOYSA-N 0.000 description 1
- ZVDSMYGTJDFNHN-UHFFFAOYSA-N 2,4,6-trimethylbenzene-1,3-diamine Chemical compound CC1=CC(C)=C(N)C(C)=C1N ZVDSMYGTJDFNHN-UHFFFAOYSA-N 0.000 description 1
- JWTVQZQPKHXGFM-UHFFFAOYSA-N 2,5-dimethylhexane-2,5-diamine Chemical compound CC(C)(N)CCC(C)(C)N JWTVQZQPKHXGFM-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
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- ZJGLLMWPRVWKFA-UHFFFAOYSA-N 2-hexadecyloctadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCC(CO)CCCCCCCCCCCCCCCC ZJGLLMWPRVWKFA-UHFFFAOYSA-N 0.000 description 1
- BHIZVZJETFVJMJ-UHFFFAOYSA-N 2-hydroxypropyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(C)O BHIZVZJETFVJMJ-UHFFFAOYSA-N 0.000 description 1
- JZUHIOJYCPIVLQ-UHFFFAOYSA-N 2-methylpentane-1,5-diamine Chemical compound NCC(C)CCCN JZUHIOJYCPIVLQ-UHFFFAOYSA-N 0.000 description 1
- KOGSPLLRMRSADR-UHFFFAOYSA-N 4-(2-aminopropan-2-yl)-1-methylcyclohexan-1-amine Chemical compound CC(C)(N)C1CCC(C)(N)CC1 KOGSPLLRMRSADR-UHFFFAOYSA-N 0.000 description 1
- DZIHTWJGPDVSGE-UHFFFAOYSA-N 4-[(4-aminocyclohexyl)methyl]cyclohexan-1-amine Chemical compound C1CC(N)CCC1CC1CCC(N)CC1 DZIHTWJGPDVSGE-UHFFFAOYSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- SNCJAJRILVFXAE-UHFFFAOYSA-N 9h-fluorene-2,7-diamine Chemical compound NC1=CC=C2C3=CC=C(N)C=C3CC2=C1 SNCJAJRILVFXAE-UHFFFAOYSA-N 0.000 description 1
- 238000006596 Alder-ene reaction Methods 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical class CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
- 239000005700 Putrescine Substances 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- KJYGRYJZFWOECQ-UHFFFAOYSA-N [2-hydroxy-3-[2-hydroxy-3-[2-hydroxy-3-(16-methylheptadecanoyloxy)propoxy]propoxy]propyl] 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(O)COCC(O)COCC(O)COC(=O)CCCCCCCCCCCCCCC(C)C KJYGRYJZFWOECQ-UHFFFAOYSA-N 0.000 description 1
- QLBRROYTTDFLDX-UHFFFAOYSA-N [3-(aminomethyl)cyclohexyl]methanamine Chemical compound NCC1CCCC(CN)C1 QLBRROYTTDFLDX-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 125000005529 alkyleneoxy group Chemical group 0.000 description 1
- IYABWNGZIDDRAK-UHFFFAOYSA-N allene Chemical group C=C=C IYABWNGZIDDRAK-UHFFFAOYSA-N 0.000 description 1
- DNXNYEBMOSARMM-UHFFFAOYSA-N alumane;zirconium Chemical compound [AlH3].[Zr] DNXNYEBMOSARMM-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229940048506 aluminum zirconium tetrachlorohydrex gly Drugs 0.000 description 1
- WYANSMZYIOPJFV-UHFFFAOYSA-L aluminum;2-aminoacetic acid;zirconium(4+);chloride;hydroxide;hydrate Chemical compound O.[OH-].[Al+3].[Cl-].[Zr+4].NCC(O)=O WYANSMZYIOPJFV-UHFFFAOYSA-L 0.000 description 1
- IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 description 1
- 150000004984 aromatic diamines Chemical class 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 229960002903 benzyl benzoate Drugs 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- YQLZOAVZWJBZSY-UHFFFAOYSA-N decane-1,10-diamine Chemical compound NCCCCCCCCCCN YQLZOAVZWJBZSY-UHFFFAOYSA-N 0.000 description 1
- GJBRTCPWCKRSTQ-UHFFFAOYSA-N decanedioic acid Chemical compound OC(=O)CCCCCCCCC(O)=O.OC(=O)CCCCCCCCC(O)=O GJBRTCPWCKRSTQ-UHFFFAOYSA-N 0.000 description 1
- 238000007257 deesterification reaction Methods 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- LVYZJEPLMYTTGH-UHFFFAOYSA-H dialuminum chloride pentahydroxide dihydrate Chemical compound [Cl-].[Al+3].[OH-].[OH-].[Al+3].[OH-].[OH-].[OH-].O.O LVYZJEPLMYTTGH-UHFFFAOYSA-H 0.000 description 1
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- QFTYSVGGYOXFRQ-UHFFFAOYSA-N dodecane-1,12-diamine Chemical compound NCCCCCCCCCCCCN QFTYSVGGYOXFRQ-UHFFFAOYSA-N 0.000 description 1
- IINXALNHMRMYDC-UHFFFAOYSA-N dodecanedioic acid Chemical compound OC(=O)CCCCCCCCCCC(O)=O.OC(=O)CCCCCCCCCCC(O)=O IINXALNHMRMYDC-UHFFFAOYSA-N 0.000 description 1
- QQQMUBLXDAFBRH-UHFFFAOYSA-N dodecyl 2-hydroxypropanoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)O QQQMUBLXDAFBRH-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000013213 extrapolation Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229940097789 heavy mineral oil Drugs 0.000 description 1
- PWSKHLMYTZNYKO-UHFFFAOYSA-N heptane-1,7-diamine Chemical compound NCCCCCCCN PWSKHLMYTZNYKO-UHFFFAOYSA-N 0.000 description 1
- XEUHNWODXVYLFD-UHFFFAOYSA-N heptanedioic acid Chemical compound OC(=O)CCCCCC(O)=O.OC(=O)CCCCCC(O)=O XEUHNWODXVYLFD-UHFFFAOYSA-N 0.000 description 1
- YVSCCMNRWFOKDU-UHFFFAOYSA-N hexanedioic acid Chemical compound OC(=O)CCCCC(O)=O.OC(=O)CCCCC(O)=O YVSCCMNRWFOKDU-UHFFFAOYSA-N 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000003903 lactic acid esters Chemical class 0.000 description 1
- 229940059904 light mineral oil Drugs 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- 229960001047 methyl salicylate Drugs 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- SCZVXVGZMZRGRU-UHFFFAOYSA-N n'-ethylethane-1,2-diamine Chemical compound CCNCCN SCZVXVGZMZRGRU-UHFFFAOYSA-N 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical group 0.000 description 1
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 1
- WPBWJEYRHXACLR-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O.OC(=O)CCCCCCCC(O)=O WPBWJEYRHXACLR-UHFFFAOYSA-N 0.000 description 1
- DUUVLSQFLIAPFQ-UHFFFAOYSA-N octacosanyl hexadecanoate Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC DUUVLSQFLIAPFQ-UHFFFAOYSA-N 0.000 description 1
- 229940038384 octadecane Drugs 0.000 description 1
- TWHMVKPVFOOAMY-UHFFFAOYSA-N octanedioic acid Chemical compound OC(=O)CCCCCCC(O)=O.OC(=O)CCCCCCC(O)=O TWHMVKPVFOOAMY-UHFFFAOYSA-N 0.000 description 1
- WCJLCOAEJIHPCW-UHFFFAOYSA-N octyl 2-hydroxybenzoate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1O WCJLCOAEJIHPCW-UHFFFAOYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 238000010915 one-step procedure Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000006213 oxygenation reaction Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- WTSXICLFTPPDTL-UHFFFAOYSA-N pentane-1,3-diamine Chemical compound CCC(N)CCN WTSXICLFTPPDTL-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- ARFWEVQMYYLLPJ-UHFFFAOYSA-N phenanthrene-1,2-diamine Chemical compound C1=CC=C2C3=CC=C(N)C(N)=C3C=CC2=C1 ARFWEVQMYYLLPJ-UHFFFAOYSA-N 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000223 polyglycerol Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- BEKZXQKGTDVSKX-UHFFFAOYSA-N propyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCC BEKZXQKGTDVSKX-UHFFFAOYSA-N 0.000 description 1
- DPBVJRXPSXTHOL-UHFFFAOYSA-N propyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCCC DPBVJRXPSXTHOL-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 229940026235 propylene glycol monolaurate Drugs 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000029058 respiratory gaseous exchange Effects 0.000 description 1
- 150000003902 salicylic acid esters Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000007779 soft material Substances 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 230000009967 tasteless effect Effects 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- PGHWKVVGGRFTRY-UHFFFAOYSA-N tetradecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCC(O)=O.OC(=O)CCCCCCCCCCCCC(O)=O PGHWKVVGGRFTRY-UHFFFAOYSA-N 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 238000007056 transamidation reaction Methods 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 150000003626 triacylglycerols 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
- 238000005829 trimerization reaction Methods 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 238000001429 visible spectrum Methods 0.000 description 1
Images
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
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/042—Gels
-
- 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
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/88—Polyamides
-
- 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
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/02—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings containing insect repellants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/0052—Preparation of gels
- B01J13/0065—Preparation of gels containing an organic phase
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/26—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
- C08G69/34—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids using polymerised unsaturated fatty acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/44—Polyester-amides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/0206—Polyalkylene(poly)amines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/0273—Polyamines containing heterocyclic moieties in the main chain
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/0622—Polycondensates containing six-membered rings, not condensed with other rings, with nitrogen atoms as the only ring hetero atoms
- C08G73/0633—Polycondensates containing six-membered rings, not condensed with other rings, with nitrogen atoms as the only ring hetero atoms with only two nitrogen atoms in the ring
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C5/00—Candles
- C11C5/002—Ingredients
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C5/00—Candles
- C11C5/002—Ingredients
- C11C5/004—Ingredients dyes, pigments; products giving a coloured flame
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/26—Optical properties
- A61K2800/262—Transparent; Translucent
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Dermatology (AREA)
- Dispersion Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Polyamides (AREA)
- Cosmetics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/734,523 | 1996-10-18 | ||
| US08/734,523 US5783657A (en) | 1996-10-18 | 1996-10-18 | Ester-terminated polyamides of polymerized fatty acids useful in formulating transparent gels in low polarity liquids |
| PCT/US1997/019510 WO1998017705A1 (en) | 1996-10-18 | 1997-10-17 | Ester-terminated polyamides of polymerized fatty acids useful in formulating transparent gels in low polarity liquids |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007114875A Division JP4703599B2 (ja) | 1996-10-18 | 2007-04-24 | 低極性液体中で透明ゲルを処方するのに有用な重合化脂肪酸のエステル末端ポリアミド |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2001502742A JP2001502742A (ja) | 2001-02-27 |
| JP2001502742A5 JP2001502742A5 (enExample) | 2005-09-08 |
| JP4005640B2 true JP4005640B2 (ja) | 2007-11-07 |
Family
ID=24952036
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP51971798A Expired - Lifetime JP4005640B2 (ja) | 1996-10-18 | 1997-10-17 | 低極性液体中で透明ゲルを処方するのに有用な重合化脂肪酸のエステル末端ポリアミド |
| JP2007114875A Expired - Lifetime JP4703599B2 (ja) | 1996-10-18 | 2007-04-24 | 低極性液体中で透明ゲルを処方するのに有用な重合化脂肪酸のエステル末端ポリアミド |
| JP2009058711A Pending JP2009120856A (ja) | 1996-10-18 | 2009-03-11 | 低極性液体中で透明ゲルを処方するのに有用な重合化脂肪酸のエステル末端ポリアミド |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007114875A Expired - Lifetime JP4703599B2 (ja) | 1996-10-18 | 2007-04-24 | 低極性液体中で透明ゲルを処方するのに有用な重合化脂肪酸のエステル末端ポリアミド |
| JP2009058711A Pending JP2009120856A (ja) | 1996-10-18 | 2009-03-11 | 低極性液体中で透明ゲルを処方するのに有用な重合化脂肪酸のエステル末端ポリアミド |
Country Status (8)
| Country | Link |
|---|---|
| US (3) | US5783657A (enExample) |
| EP (2) | EP0939782B1 (enExample) |
| JP (3) | JP4005640B2 (enExample) |
| AU (1) | AU727433B2 (enExample) |
| CA (1) | CA2268452C (enExample) |
| DE (1) | DE69730144T2 (enExample) |
| TW (1) | TW385321B (enExample) |
| WO (1) | WO1998017705A1 (enExample) |
Families Citing this family (427)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6169160B1 (en) | 1996-09-26 | 2001-01-02 | Union Camp Corporation | Cable protectant compositions |
| US5783657A (en) * | 1996-10-18 | 1998-07-21 | Union Camp Corporation | Ester-terminated polyamides of polymerized fatty acids useful in formulating transparent gels in low polarity liquids |
| JP2002516619A (ja) | 1996-10-18 | 2002-06-04 | ユニオン キャンプ コーポレイション | エステル末端ポリアミドゲル |
| US6776792B1 (en) | 1997-04-24 | 2004-08-17 | Advanced Cardiovascular Systems Inc. | Coated endovascular stent |
| US6517343B2 (en) | 1997-09-26 | 2003-02-11 | Arizona Chemical Company | Coated candles and coating compositions |
| PL340595A1 (en) * | 1997-11-20 | 2001-02-12 | Schuemann Sasol Gmbh | Base material for making candles and method of obtaining such material |
| GB9821693D0 (en) * | 1998-10-06 | 1998-12-02 | Humphries Martyn | Improvements in or relating to insect repellents |
| WO2000026285A1 (en) * | 1998-10-29 | 2000-05-11 | Penreco | Gel compositions |
| US6503077B2 (en) | 1999-01-04 | 2003-01-07 | Arizona Chemical Company | Gelled articles containing tertiary amide-terminated polyamide |
| US6268466B1 (en) | 1999-01-04 | 2001-07-31 | Arizona Chemical Company | Tertiary amide terminated polyamides and uses thereof |
| US6132665A (en) | 1999-02-25 | 2000-10-17 | 3D Systems, Inc. | Compositions and methods for selective deposition modeling |
| GB9908218D0 (en) * | 1999-04-12 | 1999-06-02 | Unilever Plc | Antiperspirant compositions |
| US6544302B2 (en) * | 1999-06-01 | 2003-04-08 | Bush Boake Allen | Composite candle compositions |
| US6435694B1 (en) | 1999-06-10 | 2002-08-20 | Aromatic Technologies, Inc. | Candle with insert |
| FR2796270B1 (fr) * | 1999-07-15 | 2002-01-11 | Oreal | Composition a phase grasse liquide gelifiee par un polyamide a groupements ester terminaux |
| FR2796271B1 (fr) * | 1999-07-15 | 2002-01-11 | Oreal | Composition sans cire structuree sous forme rigide par un polymere |
| FR2796272B1 (fr) * | 1999-07-15 | 2003-09-19 | Oreal | Composition sans cire structuree sous forme rigide par un polymere |
| FR2796273B1 (fr) | 1999-07-15 | 2003-09-12 | Oreal | Composition a phase grasse liquide gelifiee par un polyamide a groupements ester terminaux |
| US6174937B1 (en) * | 1999-07-16 | 2001-01-16 | Xerox Corporation | Composition of matter, a phase change ink, and a method of reducing a coefficient of friction of a phase change ink formulation |
| US7807211B2 (en) | 1999-09-03 | 2010-10-05 | Advanced Cardiovascular Systems, Inc. | Thermal treatment of an implantable medical device |
| US20070032853A1 (en) | 2002-03-27 | 2007-02-08 | Hossainy Syed F | 40-O-(2-hydroxy)ethyl-rapamycin coated stent |
| ATE293425T1 (de) * | 1999-12-28 | 2005-05-15 | Oreal | Strukturierte langhaltige zubereitung enthaltend ein polymer und pastöse fettstoffe |
| FR2802806B1 (fr) * | 1999-12-28 | 2002-02-08 | Oreal | Composition longue tenue structuree par un polymere et un corps gras pateux |
| FR2804017B1 (fr) * | 2000-01-25 | 2002-07-26 | Oreal | Composition longue tenue structuree par un polymere et un corps gras pateux |
| FR2804018B1 (fr) | 2000-01-24 | 2008-07-11 | Oreal | Composition sans transfert structuree sous forme rigide par un polymere |
| US6439880B1 (en) | 2000-02-11 | 2002-08-27 | Robert Ray | Clear candle construction |
| US6214063B1 (en) * | 2000-03-01 | 2001-04-10 | Bath & Body Works, Inc. | Products with ETPA-based icons |
| US6645261B2 (en) | 2000-03-06 | 2003-11-11 | Cargill, Inc. | Triacylglycerol-based alternative to paraffin wax |
| US6706081B2 (en) * | 2000-04-28 | 2004-03-16 | The Dial Corporation | Decorative candle |
| DE10022247A1 (de) | 2000-05-08 | 2001-11-15 | Basf Ag | Polyurethan und dessen Verwendung zur Modifizierung rheologischer Eigenschaften |
| US20030124474A1 (en) * | 2000-06-07 | 2003-07-03 | David Elliott | Self extinguishing candles and method of making same |
| GB0014426D0 (en) * | 2000-06-13 | 2000-08-09 | Unilever Plc | Hair oils |
| US6423304B1 (en) * | 2000-06-15 | 2002-07-23 | Cognis Corporation | Dimerized fatty acid based polyamides useful for clear candle and gel applications |
| US6423324B1 (en) | 2000-06-20 | 2002-07-23 | Cosmolab, Inc. | Temperature-stable polyamide resin-based composition, and products |
| FR2810562B1 (fr) * | 2000-06-23 | 2003-04-18 | Oreal | Emulsion solide a phase grasse liquide structuree par un polymere |
| US6432391B1 (en) | 2000-07-07 | 2002-08-13 | L'ORéAL S.A. | Transparent scented solid cosmetic composition |
| FR2811225B1 (fr) * | 2000-07-07 | 2004-04-16 | Oreal | Composition solide parfumee transparente |
| US6309715B1 (en) | 2000-08-02 | 2001-10-30 | International Flavors & Fragrances Inc. | Decorative materials encased in a polymer with fragrance releasing characteristics |
| AR029272A1 (es) * | 2000-09-15 | 2003-06-18 | Perez Roldan Alberto Gonzalo | Compuesto transparente, elastico y autoportante para la fabricacion de velas y la vela autoportante obtenida con dicho compuesto |
| US6953560B1 (en) | 2000-09-28 | 2005-10-11 | Advanced Cardiovascular Systems, Inc. | Barriers for polymer-coated implantable medical devices and methods for making the same |
| US20020066974A1 (en) * | 2000-10-04 | 2002-06-06 | Jeffrey Bell | Item with decorative voids |
| US6783793B1 (en) | 2000-10-26 | 2004-08-31 | Advanced Cardiovascular Systems, Inc. | Selective coating of medical devices |
| US7807210B1 (en) | 2000-10-31 | 2010-10-05 | Advanced Cardiovascular Systems, Inc. | Hemocompatible polymers on hydrophobic porous polymers |
| FR2816630B1 (fr) * | 2000-10-31 | 2006-08-25 | Abt Sarl | Matiere combustible pour bougie, bougie et procede de fabrication associe |
| US6478830B2 (en) | 2000-11-15 | 2002-11-12 | Noville, Inc. | Transparent compositions and candles and methods for making the same |
| FR2816832B1 (fr) * | 2000-11-23 | 2003-09-26 | Oreal | Composition cosmetique comprenant des particules interferentielles et une matiere colorante |
| US8080257B2 (en) * | 2000-12-12 | 2011-12-20 | L'oreal S.A. | Cosmetic compositions containing at least one hetero polymer and at least one film-forming silicone resin and methods of using |
| US7276547B2 (en) * | 2000-12-12 | 2007-10-02 | L'oreal S.A. | Compositions comprising heteropolymers and at least one oil-soluble polymers chosen from alkyl celluloses and alkylated guar gums |
| WO2002047623A1 (en) * | 2000-12-12 | 2002-06-20 | L'oreal Sa | Composition comprising at least one heteropolymer and at least one inert filler and methods for use |
| FR2817743B1 (fr) * | 2000-12-12 | 2003-01-10 | Oreal | Utilisation d'un polymere pour obtenir un maquillage rapide des matieres keratiniques |
| AU2002256544A1 (en) | 2000-12-12 | 2002-06-24 | L'oreal Sa | Cosmetic compositions containing at least one heteropolymer and at least one gelling agent and methods of using the same |
| FR2817739B1 (fr) | 2000-12-12 | 2005-01-07 | Oreal | Composition cosmetique coloree transparente ou translucide |
| US20020111330A1 (en) * | 2000-12-12 | 2002-08-15 | Carlos Pinzon | Compositions containing heteropolymers and methods of using same |
| US6835399B2 (en) | 2000-12-12 | 2004-12-28 | L'ORéAL S.A. | Cosmetic composition comprising a polymer blend |
| ATE322310T1 (de) * | 2000-12-12 | 2006-04-15 | Oreal | Kosmetische zusammensetzung mit einem wachs und einem polymer |
| US6881400B2 (en) | 2000-12-12 | 2005-04-19 | L'oreal S.A. | Use of at least one polyamide polymer in a mascara composition for increasing the adhesion of and/or expressly loading make-up deposited on eyelashes |
| CN1230142C (zh) * | 2000-12-12 | 2005-12-07 | 莱雅公司 | 含聚合物和纤维的化妆品组合物 |
| AU2001220877A1 (en) | 2000-12-12 | 2002-06-24 | L'oreal S.A. | Cosmetic composition comprising heteropolymers and a solid substance and method of using same |
| US20020168335A1 (en) * | 2000-12-12 | 2002-11-14 | Nathalie Collin | Cosmetic composition comprising a wax and a polymer |
| US20080028669A1 (en) * | 2000-12-18 | 2008-02-07 | Hurwitz Marni M | Insect removal tape, debilitating spray formulation and method for using same |
| US20020076427A1 (en) * | 2000-12-18 | 2002-06-20 | Marni Hurwitz | Insect removal tape and method of using insect removal tape |
| AU2001220200A1 (en) * | 2000-12-21 | 2002-07-01 | L'oreal S.A. | Structured composition comprising a heteratome polymer and fibers |
| US7025953B2 (en) | 2001-01-17 | 2006-04-11 | L'oreal S.A. | Nail polish composition comprising a polymer |
| FR2819399B1 (fr) | 2001-01-17 | 2003-02-21 | Oreal | Composition cosmetique contenant un polymere et une huile fluoree |
| US6870011B2 (en) | 2001-01-24 | 2005-03-22 | Arizona Chemical Company | Hydrocarbon-terminated polyether-polyamide block copolymers and uses thereof |
| US20040094635A1 (en) * | 2001-02-21 | 2004-05-20 | Michael Harris | Air fresheners |
| US6592637B2 (en) | 2001-03-16 | 2003-07-15 | Mcgee Thomas | Decorative candle and process for making same |
| US6780424B2 (en) * | 2001-03-30 | 2004-08-24 | Charles David Claude | Controlled morphologies in polymer drug for release of drugs from polymer films |
| US6552160B2 (en) | 2001-05-14 | 2003-04-22 | Arizona Chemical Company | Ester-terminated poly(ester-amides) useful for formulating transparent gels in low polarity fluids |
| WO2002099022A1 (en) * | 2001-06-04 | 2002-12-12 | Novaflame Pty Ltd | Candles with coloured flames |
| FR2825628B1 (fr) * | 2001-06-07 | 2004-03-19 | Oreal | Composition cosmetique comportant un polymere comprenant des groupes de jonction capables d'etablir chacun au moins trois liaisons h |
| US6497861B1 (en) | 2001-06-21 | 2002-12-24 | Color Access, Inc. | Stable cosmetic emulsion with polyamide gelling agent |
| US20080233065A1 (en) * | 2001-06-21 | 2008-09-25 | Wang Tian X | Stable Cosmetic Emulsion With Polyamide Gelling Agent |
| US6695920B1 (en) | 2001-06-27 | 2004-02-24 | Advanced Cardiovascular Systems, Inc. | Mandrel for supporting a stent and a method of using the mandrel to coat a stent |
| US8741378B1 (en) | 2001-06-27 | 2014-06-03 | Advanced Cardiovascular Systems, Inc. | Methods of coating an implantable device |
| US6565659B1 (en) | 2001-06-28 | 2003-05-20 | Advanced Cardiovascular Systems, Inc. | Stent mounting assembly and a method of using the same to coat a stent |
| US7682669B1 (en) | 2001-07-30 | 2010-03-23 | Advanced Cardiovascular Systems, Inc. | Methods for covalently immobilizing anti-thrombogenic material into a coating on a medical device |
| US8303651B1 (en) | 2001-09-07 | 2012-11-06 | Advanced Cardiovascular Systems, Inc. | Polymeric coating for reducing the rate of release of a therapeutic substance from a stent |
| US6669468B2 (en) * | 2001-09-28 | 2003-12-30 | Bath & Body Works, Inc. | Candle with polyethersulfone barrier |
| US6716420B2 (en) | 2001-10-05 | 2004-04-06 | L′Oreal | Methods of use and of making a mascara comprising at least one coloring agent and at least one heteropolymer |
| US20030083209A1 (en) * | 2001-10-22 | 2003-05-01 | Moodycliffe Timothy I. | Viscosity modification of petroleum distillates |
| US20030126788A1 (en) * | 2001-11-07 | 2003-07-10 | Colloid Tech. Inc. | Storage stable translucent flammable article |
| EP1453885B1 (en) | 2001-12-13 | 2009-08-05 | Arizona Chemical Company | Aqueous suspensions containing polymerized fatty acid-based polyamides |
| US7160337B2 (en) * | 2001-12-17 | 2007-01-09 | International Flavors & Fragrances Inc. | Transparent, vegetable-based, substantially hydrocarbon-free candle article |
| US20030148239A1 (en) * | 2002-02-05 | 2003-08-07 | Margaret Szczerba | Polymerized wax candles |
| US20030199402A1 (en) * | 2002-04-22 | 2003-10-23 | Carl Triplett | Composition for reducing malodors and method for using the same |
| US20030235600A1 (en) * | 2002-05-31 | 2003-12-25 | L'oreal | Cosmetic compositions comprising at least one polyester and at least one polyheteroatom |
| US8449870B2 (en) * | 2002-06-11 | 2013-05-28 | Color Access, Inc. | Stable cosmetic emulsion with polyamide gelling agent |
| US8333956B2 (en) * | 2002-06-11 | 2012-12-18 | Color Access, Inc. | Stable cosmetic emulsion with polyamide gelling agent |
| US20040042980A1 (en) * | 2002-06-12 | 2004-03-04 | L'oreal | Cosmetic emulsions containing at least one hetero polymer and at least one sunscreen, and methods of using same |
| US20050008598A1 (en) | 2003-07-11 | 2005-01-13 | Shaoxiang Lu | Cosmetic compositions comprising a structuring agent, silicone powder and swelling agent |
| US7011842B1 (en) | 2002-06-21 | 2006-03-14 | Advanced Cardiovascular Systems, Inc. | Polycationic peptide coatings and methods of making the same |
| US7070798B1 (en) | 2002-06-21 | 2006-07-04 | Advanced Cardiovascular Systems, Inc. | Coatings for implantable medical devices incorporating chemically-bound polymers and oligomers of L-arginine |
| US7033602B1 (en) | 2002-06-21 | 2006-04-25 | Advanced Cardiovascular Systems, Inc. | Polycationic peptide coatings and methods of coating implantable medical devices |
| US8506617B1 (en) | 2002-06-21 | 2013-08-13 | Advanced Cardiovascular Systems, Inc. | Micronized peptide coated stent |
| US7217426B1 (en) | 2002-06-21 | 2007-05-15 | Advanced Cardiovascular Systems, Inc. | Coatings containing polycationic peptides for cardiovascular therapy |
| US7794743B2 (en) | 2002-06-21 | 2010-09-14 | Advanced Cardiovascular Systems, Inc. | Polycationic peptide coatings and methods of making the same |
| US7056523B1 (en) | 2002-06-21 | 2006-06-06 | Advanced Cardiovascular Systems, Inc. | Implantable medical devices incorporating chemically conjugated polymers and oligomers of L-arginine |
| US6994867B1 (en) | 2002-06-21 | 2006-02-07 | Advanced Cardiovascular Systems, Inc. | Biocompatible carrier containing L-arginine |
| US7008629B2 (en) | 2002-07-22 | 2006-03-07 | L'ORéAL S.A. | Compositions comprising at least one heteropolymer and fibers, and methods of using the same |
| US7220288B2 (en) | 2002-08-13 | 2007-05-22 | Belmay, Inc. | Protection of fragrance in a wax candle using an antioxidant |
| US20060128578A9 (en) * | 2002-09-20 | 2006-06-15 | Nathalie Jager Lezer | Cosmetic composition comprising rigid fibres and at least one compound chosen from film-forming polymers and waxes |
| MXPA03008714A (es) | 2002-09-26 | 2004-09-10 | Oreal | Polimeros secuenciados y composiciones cosmeticas que comprenden tales polimeros. |
| US7875265B2 (en) | 2002-09-26 | 2011-01-25 | L'oreal | Cosmetic composition comprising a sequenced polymer and a plasticizer |
| US6896965B1 (en) | 2002-11-12 | 2005-05-24 | Advanced Cardiovascular Systems, Inc. | Rate limiting barriers for implantable devices |
| US7758880B2 (en) | 2002-12-11 | 2010-07-20 | Advanced Cardiovascular Systems, Inc. | Biocompatible polyacrylate compositions for medical applications |
| US7776926B1 (en) | 2002-12-11 | 2010-08-17 | Advanced Cardiovascular Systems, Inc. | Biocompatible coating for implantable medical devices |
| US7074276B1 (en) | 2002-12-12 | 2006-07-11 | Advanced Cardiovascular Systems, Inc. | Clamp mandrel fixture and a method of using the same to minimize coating defects |
| US20060002968A1 (en) | 2004-06-30 | 2006-01-05 | Gordon Stewart | Anti-proliferative and anti-inflammatory agent combination for treatment of vascular disorders |
| US7758881B2 (en) | 2004-06-30 | 2010-07-20 | Advanced Cardiovascular Systems, Inc. | Anti-proliferative and anti-inflammatory agent combination for treatment of vascular disorders with an implantable medical device |
| US7094256B1 (en) | 2002-12-16 | 2006-08-22 | Advanced Cardiovascular Systems, Inc. | Coatings for implantable medical device containing polycationic peptides |
| US8435550B2 (en) | 2002-12-16 | 2013-05-07 | Abbot Cardiovascular Systems Inc. | Anti-proliferative and anti-inflammatory agent combination for treatment of vascular disorders with an implantable medical device |
| CN100404015C (zh) * | 2003-01-17 | 2008-07-23 | 莱雅公司 | 持久型化妆品组合物 |
| US20040156742A1 (en) * | 2003-02-11 | 2004-08-12 | Milan Jolanda Bianca | Synergistically-effective cyclohexylethan-1-yl ester mixtures as malodour counteractants as measured physiologically and psychometrically and methods for using same |
| US7063884B2 (en) | 2003-02-26 | 2006-06-20 | Advanced Cardiovascular Systems, Inc. | Stent coating |
| US7687037B2 (en) * | 2003-02-28 | 2010-03-30 | American Covers, Inc. | Air freshener and method |
| US7293719B2 (en) * | 2003-02-28 | 2007-11-13 | American Covers, Inc. | Air freshener and method |
| US8460609B1 (en) | 2003-02-28 | 2013-06-11 | American Covers, Inc. | Vent stick air freshener with grip head |
| US7687038B2 (en) * | 2003-02-28 | 2010-03-30 | American Covers, Inc. | Air freshener and method |
| US20050169793A1 (en) * | 2003-02-28 | 2005-08-04 | American Covers, Inc. | Air freshener and method |
| US7137570B2 (en) * | 2003-02-28 | 2006-11-21 | American Covers, Inc. | Air freshener and method |
| US6956099B2 (en) * | 2003-03-20 | 2005-10-18 | Arizona Chemical Company | Polyamide-polyether block copolymer |
| US7253249B2 (en) * | 2003-04-22 | 2007-08-07 | Arizona Chemical Company | Ester-terminated poly(ester-amide) in personal care products |
| US7279174B2 (en) | 2003-05-08 | 2007-10-09 | Advanced Cardiovascular Systems, Inc. | Stent coatings comprising hydrophilic additives |
| US20040224028A1 (en) * | 2003-05-09 | 2004-11-11 | Popplewell Lewis Michael | Polymer particles and methods for their preparation and use |
| US6995122B2 (en) | 2003-05-20 | 2006-02-07 | International Flavors & Fragrances Inc. | Method for imparting substantive fragrance and, optionally, anti-static properties to fabrics during washing and/or drying procedure and compositions useful for effecting such processes |
| US20050019286A1 (en) * | 2003-06-09 | 2005-01-27 | Wang Tian Xian | Stable cosmetic emulsion with polyamide |
| US20050118344A1 (en) | 2003-12-01 | 2005-06-02 | Pacetti Stephen D. | Temperature controlled crimping |
| US7785512B1 (en) | 2003-07-31 | 2010-08-31 | Advanced Cardiovascular Systems, Inc. | Method and system of controlled temperature mixing and molding of polymers with active agents for implantable medical devices |
| FR2860143B1 (fr) | 2003-09-26 | 2008-06-27 | Oreal | Composition cosmetique comprenant un polymere sequence et une huile siliconee non volatile |
| US7198675B2 (en) | 2003-09-30 | 2007-04-03 | Advanced Cardiovascular Systems | Stent mandrel fixture and method for selectively coating surfaces of a stent |
| US7201915B2 (en) * | 2003-10-10 | 2007-04-10 | International Flavors & Fragrances Inc. | Polyamide stick dispensing product and method of use |
| US20050106192A1 (en) * | 2003-11-13 | 2005-05-19 | Parekh Prabodh P. | Synergistically-effective composition of zinc ricinoleate and one or more substituted monocyclic organic compounds and use thereof for preventing and/or suppressing malodors |
| ES2287793T3 (es) * | 2003-11-14 | 2007-12-16 | Chemlink Specialities Ltd. | Composicion que incluye uno o mas componentes hidroliticamente inestables. |
| DE60314638T2 (de) * | 2003-11-14 | 2008-03-06 | The Procter & Gamble Company, Cincinnati | Polymere Zusammensetzungen für die anhaltende Freigabe flüchtiger Materialien |
| US9114198B2 (en) | 2003-11-19 | 2015-08-25 | Advanced Cardiovascular Systems, Inc. | Biologically beneficial coatings for implantable devices containing fluorinated polymers and methods for fabricating the same |
| US8192752B2 (en) | 2003-11-21 | 2012-06-05 | Advanced Cardiovascular Systems, Inc. | Coatings for implantable devices including biologically erodable polyesters and methods for fabricating the same |
| US7220816B2 (en) | 2003-12-16 | 2007-05-22 | Advanced Cardiovascular Systems, Inc. | Biologically absorbable coatings for implantable devices based on poly(ester amides) and methods for fabricating the same |
| US7435788B2 (en) | 2003-12-19 | 2008-10-14 | Advanced Cardiovascular Systems, Inc. | Biobeneficial polyamide/polyethylene glycol polymers for use with drug eluting stents |
| US20050158262A1 (en) * | 2003-12-19 | 2005-07-21 | Eric Parris | Cosmetic composition comprising a cationic agent, a polymer comprising a hetero atom and an oil, and cosmetic treatment process |
| US20050191327A1 (en) * | 2003-12-24 | 2005-09-01 | Wei Yu | Cosmetic composition comprising two different hetero polymers and method of using same |
| US7563324B1 (en) | 2003-12-29 | 2009-07-21 | Advanced Cardiovascular Systems Inc. | System and method for coating an implantable medical device |
| PL1553162T5 (pl) * | 2004-01-08 | 2011-07-29 | Unilever Nv | Toaletowe kostki |
| US7341736B2 (en) * | 2004-01-30 | 2008-03-11 | S.C. Johnson & Son, Inc. | Aerosol spray resistant to discoloration |
| US8685431B2 (en) | 2004-03-16 | 2014-04-01 | Advanced Cardiovascular Systems, Inc. | Biologically absorbable coatings for implantable devices based on copolymers having ester bonds and methods for fabricating the same |
| CN1781476B (zh) * | 2004-03-22 | 2013-10-16 | 莱雅公司 | 包含聚甘油化硅氧烷弹性体的化妆品组合物 |
| US8728451B2 (en) | 2004-03-25 | 2014-05-20 | L'oreal | Styling composition comprising, in a predominantly aqueous medium, a pseudo-block polymer, processes employing same and uses thereof |
| US8778014B1 (en) | 2004-03-31 | 2014-07-15 | Advanced Cardiovascular Systems, Inc. | Coatings for preventing balloon damage to polymer coated stents |
| US20060257336A1 (en) * | 2004-04-19 | 2006-11-16 | Veronique Ferrari | Cosmetic composition comprising silica particles, reflecting particles, and at least one polymer, preparative processes, and uses thereof |
| US7553377B1 (en) | 2004-04-27 | 2009-06-30 | Advanced Cardiovascular Systems, Inc. | Apparatus and method for electrostatic coating of an abluminal stent surface |
| US7820732B2 (en) | 2004-04-30 | 2010-10-26 | Advanced Cardiovascular Systems, Inc. | Methods for modulating thermal and mechanical properties of coatings on implantable devices |
| US8293890B2 (en) | 2004-04-30 | 2012-10-23 | Advanced Cardiovascular Systems, Inc. | Hyaluronic acid based copolymers |
| US9561309B2 (en) | 2004-05-27 | 2017-02-07 | Advanced Cardiovascular Systems, Inc. | Antifouling heparin coatings |
| US20110117156A1 (en) * | 2004-05-27 | 2011-05-19 | Arizona Chemical Company | Compositions and articles containing an active liquid in a polymeric matrix and methods of making and using the same |
| PL1604690T3 (pl) * | 2004-06-08 | 2014-07-31 | Procter & Gamble | Kompozycje polimerowe kleju termotopliwego do przedłużonego uwalniania substancji lotnych |
| US7563780B1 (en) | 2004-06-18 | 2009-07-21 | Advanced Cardiovascular Systems, Inc. | Heparin prodrugs and drug delivery stents formed therefrom |
| US20050287184A1 (en) | 2004-06-29 | 2005-12-29 | Hossainy Syed F A | Drug-delivery stent formulations for restenosis and vulnerable plaque |
| US6989052B1 (en) * | 2004-06-30 | 2006-01-24 | Xerox Corporation | Phase change ink printing process |
| US20060013790A1 (en) * | 2004-07-16 | 2006-01-19 | L'oreal | Cosmetic composition comprising a defined silicone polymer and a gelling agent |
| FR2873033A1 (fr) | 2004-07-16 | 2006-01-20 | Oreal | Composition cosmetique compenant un polymere de silicone defini et un agent gelifiant. |
| US7494665B1 (en) | 2004-07-30 | 2009-02-24 | Advanced Cardiovascular Systems, Inc. | Polymers containing siloxane monomers |
| US8357391B2 (en) | 2004-07-30 | 2013-01-22 | Advanced Cardiovascular Systems, Inc. | Coatings for implantable devices comprising poly (hydroxy-alkanoates) and diacid linkages |
| US7311980B1 (en) | 2004-08-02 | 2007-12-25 | Advanced Cardiovascular Systems, Inc. | Polyactive/polylactic acid coatings for an implantable device |
| US7648727B2 (en) | 2004-08-26 | 2010-01-19 | Advanced Cardiovascular Systems, Inc. | Methods for manufacturing a coated stent-balloon assembly |
| US7244443B2 (en) | 2004-08-31 | 2007-07-17 | Advanced Cardiovascular Systems, Inc. | Polymers of fluorinated monomers and hydrophilic monomers |
| US8110211B2 (en) | 2004-09-22 | 2012-02-07 | Advanced Cardiovascular Systems, Inc. | Medicated coatings for implantable medical devices including polyacrylates |
| US7166680B2 (en) | 2004-10-06 | 2007-01-23 | Advanced Cardiovascular Systems, Inc. | Blends of poly(ester amide) polymers |
| ATE540668T1 (de) | 2004-10-22 | 2012-01-15 | Oreal | Kosmetische zusammensetzung, die ein polyorganosiloxan enthält |
| US8603634B2 (en) | 2004-10-27 | 2013-12-10 | Abbott Cardiovascular Systems Inc. | End-capped poly(ester amide) copolymers |
| US7481835B1 (en) | 2004-10-29 | 2009-01-27 | Advanced Cardiovascular Systems, Inc. | Encapsulated covered stent |
| US7390497B2 (en) | 2004-10-29 | 2008-06-24 | Advanced Cardiovascular Systems, Inc. | Poly(ester amide) filler blends for modulation of coating properties |
| EP1655344A1 (en) * | 2004-11-05 | 2006-05-10 | The Procter & Gamble Company | Polymeric compositions for sustained release of volatile materials |
| US7214759B2 (en) | 2004-11-24 | 2007-05-08 | Advanced Cardiovascular Systems, Inc. | Biologically absorbable coatings for implantable devices based on polyesters and methods for fabricating the same |
| US8609123B2 (en) | 2004-11-29 | 2013-12-17 | Advanced Cardiovascular Systems, Inc. | Derivatized poly(ester amide) as a biobeneficial coating |
| US7892592B1 (en) | 2004-11-30 | 2011-02-22 | Advanced Cardiovascular Systems, Inc. | Coating abluminal surfaces of stents and other implantable medical devices |
| US7632307B2 (en) | 2004-12-16 | 2009-12-15 | Advanced Cardiovascular Systems, Inc. | Abluminal, multilayer coating constructs for drug-delivery stents |
| US7604818B2 (en) | 2004-12-22 | 2009-10-20 | Advanced Cardiovascular Systems, Inc. | Polymers of fluorinated monomers and hydrocarbon monomers |
| US7419504B2 (en) | 2004-12-27 | 2008-09-02 | Advanced Cardiovascular Systems, Inc. | Poly(ester amide) block copolymers |
| US8007775B2 (en) | 2004-12-30 | 2011-08-30 | Advanced Cardiovascular Systems, Inc. | Polymers containing poly(hydroxyalkanoates) and agents for use with medical articles and methods of fabricating the same |
| AU2006205023C1 (en) | 2005-01-10 | 2012-05-24 | Elevance Renewable Sciences, Inc. | Candle and candle wax containing metathesis and metathesis-like products |
| US7202325B2 (en) | 2005-01-14 | 2007-04-10 | Advanced Cardiovascular Systems, Inc. | Poly(hydroxyalkanoate-co-ester amides) and agents for use with medical articles |
| US9212332B2 (en) * | 2005-03-29 | 2015-12-15 | Arizona Chemical Company, Llc | Compositions containing fatty acids and/or derivatives thereof and a low temperature stabilizer |
| US7452855B2 (en) | 2005-04-14 | 2008-11-18 | Ecolab Inc. | Fragrance dispenser for a dryer and a method for dispensing fragrance onto fabric in a dryer |
| US7795467B1 (en) | 2005-04-26 | 2010-09-14 | Advanced Cardiovascular Systems, Inc. | Bioabsorbable, biobeneficial polyurethanes for use in medical devices |
| US20060240194A1 (en) * | 2005-04-26 | 2006-10-26 | Cargill, Incorporated | Polyglycerol fatty acid ester composition and coating |
| US8778375B2 (en) | 2005-04-29 | 2014-07-15 | Advanced Cardiovascular Systems, Inc. | Amorphous poly(D,L-lactide) coating |
| US7637941B1 (en) | 2005-05-11 | 2009-12-29 | Advanced Cardiovascular Systems, Inc. | Endothelial cell binding coatings for rapid encapsulation of bioerodable stents |
| US20060263438A1 (en) * | 2005-05-17 | 2006-11-23 | L'oreal | Gelled oil particles for targeting sebaceous glands and/or hair follicles |
| FR2885797B1 (fr) * | 2005-05-17 | 2007-07-27 | Oreal | Particules d'huile gelifiee comportant au moins un filtre solaire hydrophobe |
| US20060265233A1 (en) * | 2005-05-20 | 2006-11-23 | United Parcel Service Of America, Inc. | Systems and methods for facilitating stock product returns |
| US20060272199A1 (en) * | 2005-06-02 | 2006-12-07 | Bmc Manufacturing, Llc | Aqueous gel candle for use with a warming device |
| US7993662B2 (en) * | 2005-06-14 | 2011-08-09 | Kokyu Alcohol Kogyo Co., Ltd. | Transparent solid oil cosmetics |
| US7622070B2 (en) | 2005-06-20 | 2009-11-24 | Advanced Cardiovascular Systems, Inc. | Method of manufacturing an implantable polymeric medical device |
| US8025869B2 (en) * | 2005-06-28 | 2011-09-27 | L'oréal | Cosmetic compositions having enhanced wear properties |
| US7823533B2 (en) | 2005-06-30 | 2010-11-02 | Advanced Cardiovascular Systems, Inc. | Stent fixture and method for reducing coating defects |
| US8021676B2 (en) | 2005-07-08 | 2011-09-20 | Advanced Cardiovascular Systems, Inc. | Functionalized chemically inert polymers for coatings |
| US7563313B2 (en) * | 2005-07-13 | 2009-07-21 | Xerox Corporation | Ink carriers, phase change inks including same and methods for making same |
| WO2007008575A1 (en) * | 2005-07-13 | 2007-01-18 | L'oreal | Cosmetic compositions containing liposoluble polymers and tackifiers |
| US7785647B2 (en) | 2005-07-25 | 2010-08-31 | Advanced Cardiovascular Systems, Inc. | Methods of providing antioxidants to a drug containing product |
| US7735449B1 (en) | 2005-07-28 | 2010-06-15 | Advanced Cardiovascular Systems, Inc. | Stent fixture having rounded support structures and method for use thereof |
| US20070025941A1 (en) * | 2005-08-01 | 2007-02-01 | L'oréal | Liquid lip gloss compositions with enhanced shine |
| US20070025944A1 (en) * | 2005-08-01 | 2007-02-01 | L'oreal | Cosmetic compositions useful for lengthening lashes |
| US7871634B2 (en) * | 2005-08-11 | 2011-01-18 | L'oréal | Cosmetic compositions useful for lengthening lashes |
| WO2007022169A1 (en) * | 2005-08-15 | 2007-02-22 | Arizona Chemical Company | Low sulfur tall oil fatty acid |
| US7884158B2 (en) * | 2005-09-06 | 2011-02-08 | L'Oré´al | Cosmetic compositions containing block copolymers, tackifiers and phenylated silicones |
| US20070093619A1 (en) * | 2005-10-24 | 2007-04-26 | L'oreal | Compositions having enhanced cosmetic properties |
| US8685330B2 (en) | 2005-10-31 | 2014-04-01 | American Covers, Inc. | Air freshener flower with vent stick |
| US7563314B2 (en) * | 2005-11-30 | 2009-07-21 | Xerox Corporation | Ink carriers containing nanoparticles, phase change inks including same and methods for making same |
| US7572325B2 (en) * | 2005-11-30 | 2009-08-11 | Xerox Corporation | Ink carriers, phase change inks including same and methods for making same |
| US7665835B2 (en) * | 2005-11-30 | 2010-02-23 | Xerox Corporation | Phase change inks and methods for making same |
| US7578875B2 (en) * | 2005-11-30 | 2009-08-25 | Xerox Corporation | Black inks and method for making same |
| EP1795556B1 (en) * | 2005-12-07 | 2017-02-15 | The Procter and Gamble Company | Polymeric compositions for sustained release of volatile materials |
| US7655084B2 (en) * | 2005-12-12 | 2010-02-02 | Xerox Corporation | Carbon black inks and method for making same |
| US7591841B2 (en) | 2005-12-16 | 2009-09-22 | Advanced Cardiovascular Systems, Inc. | Implantable devices for accelerated healing |
| FR2894816B1 (fr) * | 2005-12-16 | 2008-02-01 | Oreal | Composition cosmetique ou pharmaceutique comprenant un copolymere comportant au moins un groupe ionisable, et procede de traitement cosmetique |
| US7976891B1 (en) | 2005-12-16 | 2011-07-12 | Advanced Cardiovascular Systems, Inc. | Abluminal stent coating apparatus and method of using focused acoustic energy |
| US7867547B2 (en) | 2005-12-19 | 2011-01-11 | Advanced Cardiovascular Systems, Inc. | Selectively coating luminal surfaces of stents |
| US7638156B1 (en) | 2005-12-19 | 2009-12-29 | Advanced Cardiovascular Systems, Inc. | Apparatus and method for selectively coating a medical article |
| US20070207096A1 (en) * | 2006-02-13 | 2007-09-06 | Virginie Puisset | Nail varnish having a gelled texture |
| US20070190011A1 (en) * | 2006-02-15 | 2007-08-16 | L'oreal | Cosmetic composition comprising a polyolefin and fumed silica particles |
| US20070190001A1 (en) * | 2006-02-15 | 2007-08-16 | L'oreal | Cosmetic composition comprising an ester of polyol(s) and of fatty diacid dimer and a polyamide |
| US20070196428A1 (en) | 2006-02-17 | 2007-08-23 | Thierry Glauser | Nitric oxide generating medical devices |
| US7601383B2 (en) | 2006-02-28 | 2009-10-13 | Advanced Cardiovascular Systems, Inc. | Coating construct containing poly (vinyl alcohol) |
| US7713637B2 (en) | 2006-03-03 | 2010-05-11 | Advanced Cardiovascular Systems, Inc. | Coating containing PEGylated hyaluronic acid and a PEGylated non-hyaluronic acid polymer |
| US8003156B2 (en) | 2006-05-04 | 2011-08-23 | Advanced Cardiovascular Systems, Inc. | Rotatable support elements for stents |
| US8304012B2 (en) | 2006-05-04 | 2012-11-06 | Advanced Cardiovascular Systems, Inc. | Method for drying a stent |
| US7985441B1 (en) | 2006-05-04 | 2011-07-26 | Yiwen Tang | Purification of polymers for coating applications |
| US7775178B2 (en) | 2006-05-26 | 2010-08-17 | Advanced Cardiovascular Systems, Inc. | Stent coating apparatus and method |
| US9561351B2 (en) | 2006-05-31 | 2017-02-07 | Advanced Cardiovascular Systems, Inc. | Drug delivery spiral coil construct |
| US8568764B2 (en) | 2006-05-31 | 2013-10-29 | Advanced Cardiovascular Systems, Inc. | Methods of forming coating layers for medical devices utilizing flash vaporization |
| US8703167B2 (en) | 2006-06-05 | 2014-04-22 | Advanced Cardiovascular Systems, Inc. | Coatings for implantable medical devices for controlled release of a hydrophilic drug and a hydrophobic drug |
| US8778376B2 (en) | 2006-06-09 | 2014-07-15 | Advanced Cardiovascular Systems, Inc. | Copolymer comprising elastin pentapeptide block and hydrophilic block, and medical device and method of treating |
| US7699922B2 (en) * | 2006-06-13 | 2010-04-20 | Xerox Corporation | Organic phase change carriers containing nanoparticles, phase change inks including same and methods for making same |
| US8114150B2 (en) | 2006-06-14 | 2012-02-14 | Advanced Cardiovascular Systems, Inc. | RGD peptide attached to bioabsorbable stents |
| US8603530B2 (en) | 2006-06-14 | 2013-12-10 | Abbott Cardiovascular Systems Inc. | Nanoshell therapy |
| US8048448B2 (en) | 2006-06-15 | 2011-11-01 | Abbott Cardiovascular Systems Inc. | Nanoshells for drug delivery |
| US8017237B2 (en) | 2006-06-23 | 2011-09-13 | Abbott Cardiovascular Systems, Inc. | Nanoshells on polymers |
| US9028859B2 (en) | 2006-07-07 | 2015-05-12 | Advanced Cardiovascular Systems, Inc. | Phase-separated block copolymer coatings for implantable medical devices |
| WO2008008420A1 (en) | 2006-07-12 | 2008-01-17 | Elevance Renewable Sciences, Inc. | Hot melt adhesive compositions comprising metathesized unsaturated polyol ester wax |
| FR2904320B1 (fr) | 2006-07-27 | 2008-09-05 | Oreal | Polymeres sequences, et leur procede de preparation |
| US8703169B1 (en) | 2006-08-15 | 2014-04-22 | Abbott Cardiovascular Systems Inc. | Implantable device having a coating comprising carrageenan and a biostable polymer |
| US8715634B2 (en) | 2006-10-24 | 2014-05-06 | L'oreal | Volumizing compositions |
| US7786209B2 (en) * | 2006-10-27 | 2010-08-31 | Xerox Corporation | Nanostructured particles, phase change inks including same and methods for making same |
| US8597673B2 (en) | 2006-12-13 | 2013-12-03 | Advanced Cardiovascular Systems, Inc. | Coating of fast absorption or dissolution |
| US7989002B2 (en) * | 2006-12-20 | 2011-08-02 | Avon Products, Inc | High gloss gel-based lipstick |
| US8580283B2 (en) * | 2006-12-20 | 2013-11-12 | Avon Products, Inc. | Gel-based lipstick having improved rheology |
| MX2007016506A (es) | 2006-12-29 | 2008-10-28 | Oreal | Composicion que contiene un polimero de poliorganosiloxano un agente espesante y al menos un alcohol volatil. |
| FR2915893B1 (fr) | 2007-05-10 | 2012-05-11 | Oreal | Composition cosmetique sous forme de mousse sans cire |
| FR2915892B1 (fr) | 2007-05-10 | 2009-07-03 | Oreal | Composition sous forme de mousse comprenant un structurant polymerique |
| US8147769B1 (en) | 2007-05-16 | 2012-04-03 | Abbott Cardiovascular Systems Inc. | Stent and delivery system with reduced chemical degradation |
| US9056155B1 (en) | 2007-05-29 | 2015-06-16 | Abbott Cardiovascular Systems Inc. | Coatings having an elastic primer layer |
| US8883128B2 (en) * | 2007-06-06 | 2014-11-11 | L'oréal | Cosmetic compositions containing a propylphenylsilsesquioxane resin and a cosmetically-acceptable aromatic solvent |
| US9089503B2 (en) * | 2007-06-06 | 2015-07-28 | L'oreal | Comfortable transfer-resistant colored cosmetic compositions containing a silsesquioxane wax |
| US8048441B2 (en) | 2007-06-25 | 2011-11-01 | Abbott Cardiovascular Systems, Inc. | Nanobead releasing medical devices |
| US8109904B1 (en) | 2007-06-25 | 2012-02-07 | Abbott Cardiovascular Systems Inc. | Drug delivery medical devices |
| EP2025320A1 (fr) | 2007-08-10 | 2009-02-18 | L'Oréal | Ensemble de conditionnement et d'application d'un vernis à ongles de viscosité élevée |
| US8012554B2 (en) * | 2007-09-12 | 2011-09-06 | Pactiv Corporation | Bags having odor management capabilities |
| CA2698316A1 (en) * | 2007-09-17 | 2009-03-26 | Arizona Chemical Company | Polyamide and emollient compositions, products made therefrom, and methods of making and using such compositions and products |
| FR2924608A1 (fr) * | 2007-12-06 | 2009-06-12 | Chanel Parfums Beaute Sas Unip | Composition cosmetique renfermant une resine de polyamide, un ester de glyceryle et une cire apolaire |
| FR2924940B1 (fr) * | 2007-12-13 | 2012-10-19 | Oreal | Composition cosmetique comprenant de l'huile de macadamia et une cire. |
| FR2924939B1 (fr) | 2007-12-13 | 2010-02-26 | Oreal | Procede de coloration des cheveux a partir d'une composition comprenant un polymere filmogene hydrophobe, un pigment et un solvant volatil |
| FR2931670B1 (fr) | 2008-06-02 | 2015-05-22 | Oreal | Compositions a base de polyester dans une phase grasse et leurs utilisations. |
| FR2932070B1 (fr) | 2008-06-10 | 2012-08-17 | Oreal | Ensemble de maquillage et/ou de soin des cils |
| FR2932980B1 (fr) * | 2008-06-27 | 2010-12-24 | Oreal | Composition cosmetique de maquillage et/ou de soin des levres |
| US7892524B2 (en) * | 2008-06-30 | 2011-02-22 | Conopco, Inc. | Sunscreen composite particles |
| US7776350B2 (en) * | 2008-06-30 | 2010-08-17 | Conopco, Inc. | Sunscreen composite particles in cosmetic compositions |
| US20090324661A1 (en) * | 2008-06-30 | 2009-12-31 | Conopco, Inc., D/B/A Unilever | Niacinamide containing cosmetic compositions with improved skinfeel properties |
| US7914772B2 (en) * | 2008-06-30 | 2011-03-29 | Conopco, Inc. | Sunscreen composite particles dispersed in water-in-oil cosmetic compositions |
| US8206730B2 (en) * | 2008-06-30 | 2012-06-26 | Conopco, Inc. | Sunscreen composite particles and porous particles in cosmetic compostions |
| US8119698B2 (en) * | 2008-06-30 | 2012-02-21 | Conopco, Inc. | Sunscreen formula vanishing cream |
| FR2934129B1 (fr) * | 2008-07-24 | 2014-05-02 | Oreal | Procede de traitement cosmetique. |
| EP2157209B1 (en) * | 2008-07-31 | 2014-10-22 | Rohm and Haas Electronic Materials LLC | Inhibiting Background Plating |
| US8058386B2 (en) * | 2008-09-16 | 2011-11-15 | Arizona Chemical Company, Llc | Polyalkylene glycol-based poly(ester-amide) polymers, methods of making and methods of using same, compositions and products comprising same |
| EP2186544B1 (fr) | 2008-11-17 | 2013-07-10 | L'Oréal | Utilisation de particules minérales amorphes expansées pour augmenter la rémanence d'un parfum ; composition parfumante, procédé de traitement des odeurs corporelles. |
| BRPI0916036B8 (pt) | 2008-11-17 | 2017-06-06 | Oreal | método cosmético para tratar a perspiração humana, composição e composição sólida anidra |
| FR2938759B1 (fr) | 2008-11-24 | 2012-10-12 | Oreal | Composition de coloration des fibres keratiniques comprenant un polymere supramoleculaire a base de polyalcene un pigment et un solvant volatil |
| FR2939033B1 (fr) | 2008-12-02 | 2012-08-31 | Oreal | Composition cosmetique de maquillage et/ou de soin des matieres keratiniques, et procede de maquillage |
| FR2940102B1 (fr) | 2008-12-19 | 2016-03-11 | Oreal | Composition de teinture d'oxydation des fibres keratiniques comprenant un corps gras, un epaississant et un precurseur de colorant d'oxydation |
| US8822610B2 (en) | 2008-12-22 | 2014-09-02 | ATRP Solutions, Inc. | Control over controlled radical polymerization processes |
| US8815971B2 (en) | 2008-12-22 | 2014-08-26 | ATRP Solutions, Inc. | Control over controlled radical polymerization processes |
| US9005484B2 (en) * | 2009-03-31 | 2015-04-14 | Xerox Corporation | Low polarity nano silver gels |
| FR2943541B1 (fr) | 2009-03-31 | 2011-04-22 | Oreal | Composition filtrante fluide anhydre oleoalcoolique comprenant un polycondensat polyamide lipophile |
| US8569421B2 (en) | 2009-04-23 | 2013-10-29 | ATRP Solutions, Inc. | Star macromolecules for personal and home care |
| US8173750B2 (en) | 2009-04-23 | 2012-05-08 | ATRP Solutions, Inc. | Star macromolecules for personal and home care |
| US9783628B2 (en) | 2009-04-23 | 2017-10-10 | ATRP Solutions, Inc. | Dual-mechanism thickening agents for hydraulic fracturing fluids |
| WO2010146147A2 (en) | 2009-06-18 | 2010-12-23 | L'oreal | Composition for treating keratin fibres comprising a block copolymer, a siloxane resin and a volatile solvent |
| FR2946873A1 (fr) | 2009-06-18 | 2010-12-24 | Oreal | Composition de traitement des fibres keratiniques comprenant un polymere supramoleculaire a base de polyalcene et un polymere sequence et un solvant volatil. |
| FR2948875B1 (fr) | 2009-08-10 | 2011-09-02 | Oreal | Composition cosmetique comprenant un copolymere silicone particulier, un solvant volatil et des particules metalliques |
| FR2949053B1 (fr) | 2009-08-13 | 2011-11-04 | Oreal | Composition cosmetique comprenant un copolymere silicone particulier et un ou plusieurs alcanes lineaires volatils liquides |
| FR2949955B1 (fr) | 2009-09-11 | 2011-12-09 | Oreal | Procede de maquillage et/ou de soin des matieres keratiniques |
| FR2951639B1 (fr) | 2009-10-22 | 2011-11-04 | Oreal | Utilisation de l'adenosine et/ou de l'un de ses derives comme agent de traitement de la transpiration humaine |
| FR2951717B1 (fr) | 2009-10-22 | 2012-04-20 | Oreal | Utilisation d'un dialkylphenyl-4-aminopiperidine comme agent de traitement de la transpiration humaine; nouveaux composes, compositions les contenant |
| FR2953715B1 (fr) | 2009-12-11 | 2012-02-17 | Oreal | Composition filtrante fluide anhydre comprenant une phase huileuse, un filtre triazine particulier et un agent rheologique epaississant ou gelifiant d'huile |
| FR2953716B1 (fr) | 2009-12-16 | 2015-03-27 | Oreal | Kit de formulation d'un produit cosmetique |
| FR2954140A1 (fr) | 2009-12-17 | 2011-06-24 | Oreal | Compositions cosmetiques ou dermatologiques a base de bacteriocines et de prebiotiques |
| FR2954138B1 (fr) | 2009-12-17 | 2012-03-02 | Oreal | Procede cosmetique de traitement des odeurs corporelles utilisant une composition a base de bacteriocines |
| FR2954130B1 (fr) | 2009-12-18 | 2012-02-24 | Oreal | Composition cosmetique comprenant un compose supramoleculaire capable d'etablir des liaisons hydrogene, et un ingredient additionnel particulier |
| CN102686643A (zh) * | 2009-12-22 | 2012-09-19 | 陶氏环球技术有限责任公司 | 聚双草酰胺 |
| FR2954113B1 (fr) | 2009-12-22 | 2013-03-08 | Oreal | Agent de coloration et/ou de decoloration des fibres keratiniques en deux parties ou plus, sous forme d'emulsion. |
| US8485454B1 (en) | 2009-12-30 | 2013-07-16 | American Covers, Inc. | Rotatable and adjustable air freshener |
| CN102906236B (zh) | 2010-03-10 | 2015-02-25 | 艾勒旺斯可再生科学公司 | 基本不含有脂肪花白的脂类基蜡组合物及其制备方法 |
| FR2958158B1 (fr) | 2010-03-30 | 2012-06-08 | Oreal | Composition cosmetique a base de polyester |
| US8685433B2 (en) | 2010-03-31 | 2014-04-01 | Abbott Cardiovascular Systems Inc. | Absorbable coating for implantable device |
| CN102210634B (zh) * | 2010-04-09 | 2013-07-31 | 上海轻工业研究所有限公司 | 防晒剂凝胶组合物及其制备方法和应用 |
| FR2958540B1 (fr) | 2010-04-12 | 2012-05-04 | Oreal | Procede de coloration mettant en oeuvre des silicones adhesives sensibles a la pression avec une etape de pre-traitement |
| FR2958539B1 (fr) | 2010-04-13 | 2012-07-06 | Oreal | Composition cosmetique comprenant des particules de pierre ponce |
| US8097661B2 (en) | 2010-04-22 | 2012-01-17 | Xerox Corporation | Ink compositions and methods |
| US8084637B2 (en) | 2010-04-22 | 2011-12-27 | Xerox Corporation | Amide gellant compounds with aromatic end groups |
| US8603612B2 (en) | 2010-04-22 | 2013-12-10 | Xerox Corporation | Curable compositions for three-dimensional printing |
| US8507584B2 (en) | 2010-04-22 | 2013-08-13 | Xerox Corporation | Phase change inks containing amide gellant compounds with aromatic end groups |
| WO2011143037A1 (en) | 2010-05-12 | 2011-11-17 | Elevance Renewable Sciences, Inc. | Natural oil based marking compositions and their methods of making |
| FR2961508A1 (fr) | 2010-06-17 | 2011-12-23 | Oreal | Derives d'acide amine ; compositions les contenant ; utilisation comme agent de traitement de la transpiration humaine |
| FR2961509B1 (fr) | 2010-06-17 | 2014-01-31 | Oreal | Derives d'acide amine ; compositions les contenant ; utilisation comme agent de traitement de la transpiration humaine |
| FR2961392A1 (fr) | 2010-06-17 | 2011-12-23 | Oreal | Utilisation de derives d'acide amine comme agent de traitement de la transpiration humaine ; nouveaux composes ; compositions les contenant |
| FR2961510A1 (fr) | 2010-06-17 | 2011-12-23 | Oreal | Utilisation comme agent de traitement de la transpiration humaine ; nouveaux derives d'acide amine ; compositions les contenant |
| US9249360B2 (en) | 2010-07-09 | 2016-02-02 | Elevance Renewable Sciences, Inc. | Compositions derived from metathesized natural oils and amines and methods of making |
| US8308286B2 (en) | 2010-09-14 | 2012-11-13 | Xerox Corporation | Curable phase change ink containing alkoxysilane monomer |
| EP2432035B1 (en) | 2010-09-21 | 2017-05-31 | Sun Chemical Corporation | Improved method of stripping hot melt etch resists from semiconductors |
| FR2965480B1 (fr) * | 2010-09-30 | 2013-03-08 | Oreal | Composition filtrante fluide anhydre sans alcanol en c1-c5 comprenant un polycondensat polyamide lipophile et un alcane volatil |
| WO2012041411A1 (en) * | 2010-09-30 | 2012-04-05 | Cognis Ip Management Gmbh | Air freshener gel with improved longevity |
| US8662480B1 (en) | 2010-10-29 | 2014-03-04 | American Covers, Inc. | Fan powered air freshener automobile power outlet |
| US8673223B1 (en) | 2010-10-29 | 2014-03-18 | American Covers, Inc. | Fan powered air freshener automobile visor clip |
| USD660950S1 (en) | 2010-10-29 | 2012-05-29 | American Covers, Inc. | Air freshener diffuser with air tunnel |
| USD640358S1 (en) | 2010-10-29 | 2011-06-21 | American Covers, Inc. | Screw top air freshener |
| USD640359S1 (en) | 2010-10-29 | 2011-06-21 | American Covers, Inc. | Vent stick air freshener with grip head |
| US8251299B1 (en) | 2010-10-29 | 2012-08-28 | American Covers, Inc. | Screw top air freshener |
| ES2727276T3 (es) | 2010-11-23 | 2019-10-15 | Cargill Inc | Composiciones de cera basada en lípidos sustancialmente libres de exudado de grasa y métodos de fabricación |
| EP3494956A3 (en) | 2010-11-25 | 2019-10-16 | L'Oréal | Procédé pour le décapage de fibres kératiniques utilisant une composition comprenant un dérive dacide sulfinique et une composition aqueuse acide |
| FR2967905B1 (fr) | 2010-11-25 | 2013-07-12 | Oreal | Procede de traitement de la transpiration utilisant un compose carbonyle susceptible de reagir selon la reaction de maillard |
| US9587064B2 (en) | 2010-12-08 | 2017-03-07 | ATRP Solutions, Inc. | Salt-tolerant star macromolecules |
| FR2968935B1 (fr) | 2010-12-21 | 2012-12-28 | Oreal | Utilisation de particules d'aerogel hydrophobes comme actif deodorant ; procede de traitement des odeurs corporelles humaines |
| US8450385B2 (en) | 2010-12-21 | 2013-05-28 | Xerox Corporation | Urea-urethane gellant compositions with controlled molecular weight and methods of preparation |
| US8490846B1 (en) | 2011-01-10 | 2013-07-23 | American Covers, Inc. | Frictional holding pad with inclined grip |
| FR2971936B1 (fr) | 2011-02-25 | 2013-02-15 | Oreal | Composition pour colorer les fibres keratiniques comprenant un colorant direct a fonction disulfure/thiol, un tensioactif non ionique, un tensioactif amphotere, un alcool gras ethoxyle, un agent alcalin, et un agent reducteur |
| FR2971939B1 (fr) | 2011-02-25 | 2013-02-15 | Oreal | Composition pour colorer les fibres keratiniques comprenant un colorant direct a fonction disulfure/thiol, un corps gras, un agent alcalin, et un agent reducteur |
| FR2971935B1 (fr) | 2011-02-25 | 2013-02-15 | Oreal | Composition pour colorer les fibres keratiniques comprenant un colorant direct a fonction disulfure/thiol, un polymere epaississant, un tensioactif non ionique, un agent alcalin, et un agent reducteur |
| FR2971938B1 (fr) | 2011-02-25 | 2013-08-02 | Oreal | Composition pour colorer les fibres keratiniques comprenant un colorant direct a fonction disulfure/thiol, un alcool gras faiblement ou non ethoxyle, un tensioactif cationique, un agent alcalin, et un agent reducteur |
| EP2677996B1 (en) | 2011-02-25 | 2017-11-29 | L'Oréal | Composition for dyeing keratinous fibres comprising a direct dye having a disulphide/thiol functional group, a thickening polymer, an ethoxylated fatty alcohol and/or a nonionic surfactant, an alkaline agent and a reducing agent |
| FR2971937B1 (fr) | 2011-02-25 | 2013-02-15 | Oreal | Composition pour colorer les fibres keratiniques comprenant un colorant direct a fonction disulfure/thiol, un polymere epaississant non cellulosique, un agent alcalin, et un agent reducteur |
| US8784788B2 (en) | 2011-03-29 | 2014-07-22 | Environmentally Sensitive Solutions, Inc. | Gel carrier for releasing active ingredients |
| DE102011100859A1 (de) | 2011-05-06 | 2012-11-08 | Buck-Chemie Gmbh | Stückförmiges Sanitärmittel |
| US8581000B2 (en) | 2011-06-06 | 2013-11-12 | Xerox Corporation | Process for preparing amide gellant compounds with aromatic end groups |
| BR112013032810B1 (pt) | 2011-06-20 | 2018-05-02 | L' Oreal | Uso de um polímero floculante e processo cosmético para tratar a transpiração |
| US9139801B2 (en) | 2011-07-10 | 2015-09-22 | Elevance Renewable Sciences, Inc. | Metallic soap compositions for various applications |
| CN103732211B (zh) | 2011-07-21 | 2017-03-01 | 禾大国际股份公开有限公司 | 支化的聚醚‑聚酰胺嵌段共聚物及其制造与使用方法 |
| FR2978036B1 (fr) | 2011-07-22 | 2013-07-19 | Oreal | Procede de traitement de la transpiration utilisant une composition anhydre comprenant deux reactifs produisant ensemble in situ sur la peau un effet transpirant |
| FR2978035B1 (fr) | 2011-07-22 | 2015-03-20 | Oreal | Utilisation comme antitranspirant d'un sel de cation multivalent sans antitranspirant halogene d'aluminium ni de compose susceptible de reagir avec ledit sel pour produire un effet antitranspirant |
| WO2013013902A2 (en) | 2011-07-22 | 2013-01-31 | L'oreal | Method for the treatment of human perspiration using a polyvalent cation salt and an anion salt |
| WO2013036878A1 (en) | 2011-09-09 | 2013-03-14 | Arizona Chemical Company, Llc | Polyamide compositions for personal care |
| US9155811B1 (en) | 2011-12-02 | 2015-10-13 | American Covers, Inc. | Packaged vent stick air freshener with custom head |
| US9144621B1 (en) | 2012-01-10 | 2015-09-29 | American Covers, Inc. | Air freshener canister with pull top |
| US8772416B2 (en) | 2012-04-09 | 2014-07-08 | Xerox Corporation | Ink compositions containing isosorbide-capped amide gellant |
| US9085546B2 (en) | 2012-04-09 | 2015-07-21 | Xerox Corporation | Amide gellant compositions containing isosorbide |
| US8702221B2 (en) | 2012-05-08 | 2014-04-22 | Xerox Corporation | Gellant compositions with aromatic end-caps and oligomeric molecular weight distributions |
| FR2990850B1 (fr) | 2012-05-25 | 2014-05-16 | Oreal | Composition cosmetique comprenant l'association d'un derive lipophile de l'acide salicylique, d'un sel ou complexe d'aluminium anti-transpirant et d'un sel d'acide amine n,n-diacide acetique |
| JP6294885B2 (ja) | 2012-08-30 | 2018-03-14 | エーティーアールピー ソリューションズ インコーポレイテッドATRP Solutions,Inc. | 星形高分子、星形高分子組成物および星形高分子の製造方法 |
| FR2996756B1 (fr) | 2012-10-15 | 2020-06-05 | L'oreal | Utilisation cosmetique d'un acide gras mono-insature ou l'un de ses sels et/ou de ses esters comme actif deodorant |
| US9399080B2 (en) | 2012-10-23 | 2016-07-26 | American Covers, Inc. | Heated air freshener with power port for 12v receptacle |
| US9138502B2 (en) | 2012-10-23 | 2015-09-22 | American Covers, Inc. | Air freshener with decorative insert |
| US9042712B2 (en) | 2012-10-23 | 2015-05-26 | American Covers, Inc. | Heated air freshener for 12V receptacle |
| USD684675S1 (en) | 2012-10-23 | 2013-06-18 | American Covers, Inc. | Dual axis vent rod air freshener |
| USD689181S1 (en) | 2012-10-23 | 2013-09-03 | American Covers, Inc. | Air freshener container |
| CN102925132B (zh) * | 2012-10-26 | 2015-04-22 | 东营华力石油技术有限公司 | 一种热力采油用耐高温的蒸汽化学辅助剂 |
| FR2998782B1 (fr) | 2012-11-30 | 2015-04-17 | Oreal | Emulsion cosmetique eau-dans-huile notamment conditionnee sous forme d'aerosol comprenant au moins un polymere vinylique, au moins un copolymere d'olefine et au moins un actif anti-transpirant |
| FR3001138B1 (fr) | 2013-01-21 | 2015-06-19 | Oreal | Composition anhydre cosmetique ou dermatologique comprenant une merocyanine et une phase huileuse |
| CA2899349C (en) | 2013-02-04 | 2021-09-21 | ATRP Solutions, Inc. | Salt-tolerant star macromolecules |
| USD711521S1 (en) | 2013-04-15 | 2014-08-19 | American Covers, Inc. | Skull on dog tag shaped air freshener |
| JP6313851B2 (ja) | 2013-06-18 | 2018-04-18 | アグファ・ナームローゼ・フェンノートシャップAgfa Nv | パターン化されたバック層を有する平版印刷版前駆体の製造方法 |
| JPWO2015016259A1 (ja) * | 2013-07-31 | 2017-03-02 | 富士フイルム株式会社 | 複合エステルポリアミド組成物、潤滑剤組成物、潤滑剤及び複合エステルポリアミド組成物の製造方法 |
| GB201405271D0 (en) * | 2014-03-25 | 2014-05-07 | Croda Int Plc | Agrochemical oil based concentrates |
| MX385886B (es) | 2014-07-03 | 2025-03-18 | Pilot Polymer Tech Inc | Macromoleculas estrellas compatibles con tensoactivos. |
| FR3023475B1 (fr) | 2014-07-09 | 2016-07-22 | Oreal | Composition cosmetique ou dermatologique solide anhydre a base de particules a liberation d'agent benefique |
| US9437754B2 (en) * | 2014-11-10 | 2016-09-06 | E I Du Pont De Nemours And Company | Method of manufacturing electrical device |
| CA2972613C (en) | 2015-01-06 | 2023-08-01 | Lawter, Inc. | Polyamide resins for coating of sand or ceramic proppants used in hydraulic fracturing |
| US20160310623A1 (en) * | 2015-04-21 | 2016-10-27 | Belle-Aire Fragrances, Inc. | Transparent Melt |
| US9688943B2 (en) * | 2015-05-29 | 2017-06-27 | beauty Avenues LLC | Candle containing non-ionic emulsifer |
| FR3041252B1 (fr) | 2015-09-18 | 2019-01-25 | Capsum | Dispersions stables de gouttes comprenant un agent gelifiant |
| US10342886B2 (en) | 2016-01-26 | 2019-07-09 | S.C. Johnson & Son, Inc. | Extruded wax melt and method of producing same |
| US10010638B2 (en) | 2016-06-14 | 2018-07-03 | S. C. Johnson & Son, Inc. | Wax melt with filler |
| FR3057768B1 (fr) | 2016-10-26 | 2018-12-07 | Capsum | Emulsions doubles comprenant une phase grasse gelifiee |
| FR3057767B1 (fr) | 2016-10-26 | 2018-12-07 | Capsum | Emulsions doubles avec double coacervat |
| WO2018094623A1 (en) * | 2016-11-23 | 2018-05-31 | L'oreal | Solid anhydrous composition comprising a hydrophobic polymer for removing makeup on the skin |
| FR3060605B1 (fr) * | 2016-12-15 | 2021-05-28 | Skf Ab | Compositions de graisse et leur procede de fabrication |
| FR3060604B1 (fr) | 2016-12-15 | 2021-05-28 | Skf Ab | Compositions de graisse et leur procede de fabrication |
| FR3060385B1 (fr) | 2016-12-21 | 2020-01-03 | L'oreal | Composition comprenant de l’eau, une resine siliconee, une huile siliconee non volatile et procede la mettant en oeuvre |
| FR3060384B1 (fr) | 2016-12-21 | 2018-12-07 | L'oreal | Composition sous forme d’une emulsion directe comprenant une resine siliconee, une huile siliconee non volatile et procede la mettant en oeuvre |
| FR3060386B1 (fr) | 2016-12-21 | 2020-10-02 | Oreal | Composition pour les levres sous forme d'une emulsion inverse liquide. |
| FR3061006B1 (fr) | 2016-12-22 | 2020-10-02 | Oreal | Composition cosmetique solide comprenant une polyamide silicone, une resine siliconee et une phase aqueuse dispersee |
| FR3061429B1 (fr) | 2016-12-29 | 2020-11-27 | Oreal | Composition anhydre comprenant un sel de magnesium |
| JP7118591B2 (ja) | 2017-02-28 | 2022-08-16 | ロレアル | レゾルシノール又はその誘導体を含む組成物 |
| JP7176836B2 (ja) | 2017-06-13 | 2022-11-22 | ロレアル | ポリイオンコンプレックス粒子と油とを含む組成物 |
| FR3067930B1 (fr) | 2017-06-27 | 2020-01-10 | Capsum | Dispersions comprenant au moins une huile volatile hydrocarbonee |
| FR3070858B1 (fr) | 2017-09-14 | 2020-02-21 | Capsum | Dispersion avec phase grasse dispersee a teneur elevee en pigments |
| FR3072029A1 (fr) | 2017-10-09 | 2019-04-12 | L'oreal | Procede de traitement de la transpiration humaine utilisant un cation et un anion en presence d'un modulateur |
| JP7063593B2 (ja) | 2017-12-12 | 2022-05-09 | ロレアル | 油と、少なくとも1つの脂肪鎖を有するセルロース系カチオン性ポリマーを含むポリイオンコンプレックスとを含む組成物 |
| US10696857B2 (en) | 2017-12-14 | 2020-06-30 | Xerox Corporation | Curable gellant ink |
| FR3075623B1 (fr) | 2017-12-22 | 2020-06-19 | L'oreal | Composition sous forme d’une emulsion directe comprenant une resine siliconee, un polymere filmogene en et procede la mettant en oeuvre |
| FR3075632B1 (fr) | 2017-12-22 | 2020-03-06 | L'oreal | Composition sous forme d’une emulsion comprenant une resine siliconee, une huile siliconee aminee et procede la mettant en oeuvre |
| EP3781376A4 (en) * | 2018-04-16 | 2022-02-23 | Lumetique, Inc. | WICKS FOR CANDLES AND OTHER LIGHTING DEVICES |
| FR3089813B1 (fr) | 2018-12-12 | 2021-03-05 | Oreal | Gelée de parfum |
| FR3103700B1 (fr) | 2019-12-03 | 2024-01-19 | Oreal | Mélange antimicrobien contenant du 4-(3-éthoxy-4-hydroxyphényl)butan-2-one et le 4-hydroxyacétophenone, et composition le contenant |
| JP7372330B2 (ja) | 2018-12-20 | 2023-10-31 | ロレアル | 4-(3-エトキシ-4-ヒドロキシフェニル)ブタン-2-オン及び4-ヒドロキシアセトフェノンを含有する抗微生物混合物並びにそれを含有する組成物 |
| US10574801B1 (en) | 2019-01-11 | 2020-02-25 | Handstands Promo, Llc | Grip pad |
| FR3102178B1 (fr) * | 2019-10-16 | 2021-11-05 | Polymerexpert Sa | Polyamides gélifiants biosourcés |
| FR3103678B1 (fr) | 2019-12-03 | 2022-07-01 | Oreal | Composition contenant du 4-(3-éthoxy-4-hydroxyphényl)butan-2-one, un conservateur et/ou antioxydant, un tensioactif, et un polymère, le procédé de traitement des matières kératiniques à partir de la composition |
| JP2021104934A (ja) | 2019-12-24 | 2021-07-26 | ロレアル | 活性成分を局所送達するための無水組成物 |
| CN115916934A (zh) * | 2020-04-24 | 2023-04-04 | 国际香料和香精公司 | 凝胶蜡烛 |
| FR3110405B1 (fr) | 2020-05-21 | 2022-05-13 | Capsum | Emulsion double stable sans écorce |
| FR3110406B1 (fr) | 2020-05-21 | 2022-12-23 | Capsum | Dispersion stable sans écorce |
| CN116437894A (zh) | 2020-08-31 | 2023-07-14 | 莱雅公司 | 用于护理角蛋白材料的组合物 |
| FR3117804B1 (fr) | 2020-12-22 | 2024-03-01 | Oreal | Procede de traitement de la transpiration humaine et des odeurs corporelles utilisant de l’oxyde de magnesium et un sel de phosphate |
| FR3119317B1 (fr) | 2021-02-04 | 2024-05-03 | Capsum | Composition sous forme d’émulsion macroscopique stable comprenant un pourcentage d’ingrédients d’origine naturelle supérieur ou égale à 95% selon la norme ISO 16128 |
| FR3119769B1 (fr) | 2021-02-12 | 2023-09-15 | Oreal | Méthode et système d’élimination de maquillage |
| US12378501B2 (en) | 2021-03-24 | 2025-08-05 | S. C. Johnson & Son, Inc. | Candle and method of making thereof |
| FR3126177B1 (fr) | 2021-08-19 | 2025-03-14 | Oreal | Applicateur pour formulation cosmétique |
| WO2023278622A1 (en) | 2021-06-30 | 2023-01-05 | L'oreal | Applicator for cosmetic formulation |
| US12478165B2 (en) | 2021-06-30 | 2025-11-25 | L'oreal | Packaging kit for cosmetic formulation |
| FR3129286A1 (fr) | 2021-11-24 | 2023-05-26 | Capsum | Dispersion macroscopique |
| FR3129590A1 (fr) | 2021-11-26 | 2023-06-02 | Capsum | Dispersion macroscopique solaire sans écorce |
| FR3140268A1 (fr) | 2022-09-29 | 2024-04-05 | L'oreal | Processus cosmétique utilisant une particule avec microprotubérance |
| WO2024048429A1 (en) | 2022-08-30 | 2024-03-07 | L'oreal | Cosmetic process using particle with microprotrusion |
| CN119306942A (zh) * | 2023-07-14 | 2025-01-14 | 宁德时代新能源科技股份有限公司 | 聚合物、制备方法、分散剂、正极浆料、正极极片、二次电池和用电装置 |
| CN116589676B (zh) * | 2023-07-14 | 2023-12-22 | 宁德时代新能源科技股份有限公司 | 聚合物、制备方法、分散剂、正极浆料、正极极片、二次电池和用电装置 |
| FR3158444A3 (fr) | 2024-01-19 | 2025-07-25 | L'oreal | Composition de protection contre les uv |
| FR3156653A1 (fr) | 2023-12-15 | 2025-06-20 | L'oreal | Composition cosmétique solide comprenant une résine hydrocarbonée indénique, une résine siliconée et une phase aqueuse dispersée |
| WO2025127157A1 (en) | 2023-12-15 | 2025-06-19 | L'oreal | Uv shielding composition |
| FR3158445A3 (fr) | 2024-01-19 | 2025-07-25 | L'oreal | Composition de protection contre les uv |
Family Cites Families (48)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2379413A (en) * | 1940-06-28 | 1945-07-03 | American Cyanamid Co | Amides of high molecular weight carboxylic acids |
| US2450940A (en) * | 1944-04-20 | 1948-10-12 | John C Cowan | Polyamides from polymeric fat acids |
| US2662068A (en) * | 1951-03-16 | 1953-12-08 | Gen Mills Inc | Organic solvent gels |
| NL254088A (enExample) * | 1959-07-29 | |||
| US3148125A (en) * | 1961-03-22 | 1964-09-08 | Yardley Of London Inc | Clear lipstick |
| US3156572A (en) * | 1961-10-18 | 1964-11-10 | Interchonical Corp | Printing inks |
| US3156272A (en) * | 1962-01-22 | 1964-11-10 | William G Indrunas | Bottle coupling device |
| US3341465A (en) * | 1965-01-14 | 1967-09-12 | Drew Chem Corp | Novel gel emulsions |
| US3615289A (en) * | 1969-03-26 | 1971-10-26 | Avon Prod Inc | Candle composition |
| US3645705A (en) * | 1970-03-03 | 1972-02-29 | Kolar Lab Inc | Transparent combustible material suitable for candle bodies |
| DE2210220C3 (de) * | 1971-03-26 | 1981-04-16 | Avon Products, Inc., New York, N.Y. | Durchsichtiges Kerzenmaterial |
| US3819342A (en) * | 1971-03-26 | 1974-06-25 | Avon Prod Inc | Transparent candle |
| US3741711A (en) * | 1972-03-27 | 1973-06-26 | G Bryant | Composite indefinitely reusable decorative candle |
| GB1390786A (en) * | 1972-05-17 | 1975-04-16 | Wolf Ltd Victor | Polyesteramides |
| DE2357567A1 (de) * | 1973-04-09 | 1974-10-24 | Minnetonka Lab Inc | Transparente masse und ihre verwendung als kerzenmaterial |
| US4128436A (en) * | 1974-05-29 | 1978-12-05 | Coats Brothers & Company Ltd. | Rheological agents |
| IT1031921B (it) * | 1975-02-21 | 1979-05-10 | Snia Viscosa | Poliesterammidi insature metodo per la loro produzione e resine induribili prodotte con le dette poliesterammidi |
| US4051159A (en) * | 1976-01-12 | 1977-09-27 | Avon Products, Inc. | Transparent fragrance releasing composition and method of making same |
| US4062819A (en) * | 1976-09-07 | 1977-12-13 | Emery Industries, Inc. | Polyamide blends having improved processing characteristics |
| LU76035A1 (enExample) * | 1976-10-20 | 1978-05-16 | ||
| NL185519C (nl) * | 1976-12-23 | 1990-05-01 | Schering Ag | Werkwijze voor het bereiden van smeltlijmen voor textiel en gevormde voortbrengselen. |
| US4369284A (en) * | 1977-03-17 | 1983-01-18 | Applied Elastomerics, Incorporated | Thermoplastic elastomer gelatinous compositions |
| DE2942680C2 (de) * | 1979-10-23 | 1986-02-27 | Schering AG, 1000 Berlin und 4709 Bergkamen | Schmelzkleber auf Basis von Polyesteramiden und deren Verwendung zum Verkleben von organischen und anorganischen Substraten |
| US4346024A (en) * | 1979-12-10 | 1982-08-24 | Rhone-Poulenc Industries | Heat-stable polyphase polyamide/polyesteramide compositions |
| US4376194A (en) * | 1979-12-21 | 1983-03-08 | Toray Industries, Inc. | Polyester amide and process for producing the same |
| US4337298A (en) * | 1980-11-19 | 1982-06-29 | Gulf Oil Corporation | Polymer compositions and laminates produced by bonding or coextrusion |
| US4449987A (en) * | 1981-10-29 | 1984-05-22 | Avon Products, Inc. | Fragrant insect repellent composition and combustible candle composition containing same |
| JPS58206628A (ja) * | 1982-05-27 | 1983-12-01 | Toray Ind Inc | ポリエ−テルエステルアミドの製造方法 |
| DE3243794A1 (de) * | 1982-11-26 | 1984-05-30 | Schering AG, 1000 Berlin und 4709 Bergkamen | Alkoholloesliche druckfarben |
| US4552693A (en) * | 1983-03-30 | 1985-11-12 | Avon Products, Inc. | Transparent fragrance emitting articles |
| US5102656A (en) * | 1983-07-29 | 1992-04-07 | The Mennen Company | Antiperspirant creams |
| DE3482475D1 (de) * | 1983-12-27 | 1990-07-19 | Daicel Chem | Polyesteramide. |
| US4769285A (en) * | 1985-07-23 | 1988-09-06 | Minnesota Mining And Manufacturing Company | Polyamide-acrylate blends |
| JPS6274931A (ja) * | 1985-09-28 | 1987-04-06 | Asahi Chem Ind Co Ltd | ポリアミドの新規な製造方法 |
| US4937069A (en) * | 1985-11-15 | 1990-06-26 | Bristol-Myers Squibb Company | Anhydrous semi-solid antiperspirant suspension |
| GB8617559D0 (en) * | 1986-07-18 | 1986-08-28 | Raychem Ltd | Gels |
| US5069897A (en) * | 1987-10-16 | 1991-12-03 | The Proctor & Gamble Company | Antiperspirant creams |
| US5221534A (en) * | 1989-04-26 | 1993-06-22 | Pennzoil Products Company | Health and beauty aid compositions |
| CA2033642A1 (en) * | 1990-01-11 | 1991-07-12 | Dilip R. Abayasekara | Graft polymers of epsilon-caprolactam |
| JPH045640A (ja) * | 1990-04-24 | 1992-01-09 | Ricoh Co Ltd | データ写し込み機能付カメラ |
| US5132355A (en) * | 1990-11-26 | 1992-07-21 | Boris Nahlovsky | Gels of polyethylene block copolymers and liquid hydrocarbons |
| DE4128748A1 (de) * | 1991-08-29 | 1993-03-04 | Beiersdorf Ag | Kosmetische stifte |
| US5372852A (en) * | 1992-11-25 | 1994-12-13 | Tektronix, Inc. | Indirect printing process for applying selective phase change ink compositions to substrates |
| US5500209A (en) * | 1994-03-17 | 1996-03-19 | The Mennen Company | Deodorant and antiperspirant compositions containing polyamide gelling agent |
| US5578089A (en) * | 1995-04-27 | 1996-11-26 | Lancaster Colony Corporation | Clear candle |
| JP3568963B2 (ja) * | 1995-08-29 | 2004-09-22 | ペンゾイル プロダクツ カンパニー | 透明ゲルろうそく |
| US5645632A (en) * | 1996-02-14 | 1997-07-08 | Union Camp Corporation | Diesters of polymerized fatty acids useful in formulating hot-melt inks |
| US5783657A (en) * | 1996-10-18 | 1998-07-21 | Union Camp Corporation | Ester-terminated polyamides of polymerized fatty acids useful in formulating transparent gels in low polarity liquids |
-
1996
- 1996-10-18 US US08/734,523 patent/US5783657A/en not_active Expired - Lifetime
-
1997
- 1997-09-26 US US08/939,034 patent/US6111055A/en not_active Expired - Lifetime
- 1997-10-17 CA CA002268452A patent/CA2268452C/en not_active Expired - Lifetime
- 1997-10-17 JP JP51971798A patent/JP4005640B2/ja not_active Expired - Lifetime
- 1997-10-17 AU AU50919/98A patent/AU727433B2/en not_active Expired
- 1997-10-17 WO PCT/US1997/019510 patent/WO1998017705A1/en not_active Ceased
- 1997-10-17 DE DE69730144T patent/DE69730144T2/de not_active Expired - Lifetime
- 1997-10-17 EP EP97913823A patent/EP0939782B1/en not_active Expired - Lifetime
- 1997-10-18 TW TW086115375A patent/TW385321B/zh not_active IP Right Cessation
- 1997-10-18 EP EP06004626A patent/EP1696022A1/en not_active Withdrawn
-
1998
- 1998-05-06 US US09/074,070 patent/US5998570A/en not_active Expired - Lifetime
-
2007
- 2007-04-24 JP JP2007114875A patent/JP4703599B2/ja not_active Expired - Lifetime
-
2009
- 2009-03-11 JP JP2009058711A patent/JP2009120856A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| EP0939782B1 (en) | 2004-08-04 |
| DE69730144T2 (de) | 2005-08-11 |
| WO1998017705A1 (en) | 1998-04-30 |
| EP0939782A4 (en) | 1999-12-15 |
| EP0939782A1 (en) | 1999-09-08 |
| CA2268452A1 (en) | 1998-04-30 |
| AU727433B2 (en) | 2000-12-14 |
| JP2009120856A (ja) | 2009-06-04 |
| US5998570A (en) | 1999-12-07 |
| TW385321B (en) | 2000-03-21 |
| US5783657A (en) | 1998-07-21 |
| EP1696022A1 (en) | 2006-08-30 |
| CA2268452C (en) | 2006-08-01 |
| AU5091998A (en) | 1998-05-15 |
| US6111055A (en) | 2000-08-29 |
| JP2001502742A (ja) | 2001-02-27 |
| DE69730144D1 (de) | 2004-09-09 |
| JP4703599B2 (ja) | 2011-06-15 |
| JP2007204762A (ja) | 2007-08-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP4005640B2 (ja) | 低極性液体中で透明ゲルを処方するのに有用な重合化脂肪酸のエステル末端ポリアミド | |
| EP1392759B1 (en) | Ester-terminated poly(ester-amides) useful for formulating transparent gels in low polarity fluids | |
| US6268466B1 (en) | Tertiary amide terminated polyamides and uses thereof | |
| KR100775189B1 (ko) | 탄화수소-말단 폴리에테르-폴리아미드 블록 공중합체 및그의 용도 | |
| US6592857B2 (en) | Tertiary amide terminated polyamides in cosmetics | |
| JP2006152269A (ja) | エステル末端ポリアミドゲル |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20041015 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20050207 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20061024 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20070119 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20070305 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20070426 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20070814 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20070824 |
|
| R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100831 Year of fee payment: 3 |
|
| S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313111 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100831 Year of fee payment: 3 |
|
| R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100831 Year of fee payment: 3 |
|
| S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313113 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100831 Year of fee payment: 3 |
|
| R360 | Written notification for declining of transfer of rights |
Free format text: JAPANESE INTERMEDIATE CODE: R360 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100831 Year of fee payment: 3 |
|
| R370 | Written measure of declining of transfer procedure |
Free format text: JAPANESE INTERMEDIATE CODE: R370 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100831 Year of fee payment: 3 |
|
| S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313113 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100831 Year of fee payment: 3 |
|
| R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110831 Year of fee payment: 4 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110831 Year of fee payment: 4 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120831 Year of fee payment: 5 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120831 Year of fee payment: 5 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20130831 Year of fee payment: 6 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313113 |
|
| S531 | Written request for registration of change of domicile |
Free format text: JAPANESE INTERMEDIATE CODE: R313531 |
|
| R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| EXPY | Cancellation because of completion of term |