TWI329519B - Stabilized body care products, household products, textiles and fabrics - Google Patents
Stabilized body care products, household products, textiles and fabrics Download PDFInfo
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- TWI329519B TWI329519B TW092110122A TW92110122A TWI329519B TW I329519 B TWI329519 B TW I329519B TW 092110122 A TW092110122 A TW 092110122A TW 92110122 A TW92110122 A TW 92110122A TW I329519 B TWI329519 B TW I329519B
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- 239000004744 fabric Substances 0.000 title claims abstract description 32
- 239000004753 textile Substances 0.000 title claims abstract description 16
- 239000000047 product Substances 0.000 title abstract description 51
- -1 hydroxylamine salt compounds Chemical class 0.000 claims abstract description 70
- 239000003599 detergent Substances 0.000 claims abstract description 15
- 239000002979 fabric softener Substances 0.000 claims abstract description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 118
- 125000000217 alkyl group Chemical group 0.000 claims description 67
- 239000000203 mixture Substances 0.000 claims description 40
- 239000001257 hydrogen Substances 0.000 claims description 38
- 229910052739 hydrogen Inorganic materials 0.000 claims description 38
- 239000002253 acid Substances 0.000 claims description 23
- 239000003795 chemical substances by application Substances 0.000 claims description 23
- 150000001875 compounds Chemical class 0.000 claims description 22
- 238000002360 preparation method Methods 0.000 claims description 22
- 125000002947 alkylene group Chemical group 0.000 claims description 17
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
- 239000006096 absorbing agent Substances 0.000 claims description 12
- 210000004209 hair Anatomy 0.000 claims description 10
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 9
- 238000004140 cleaning Methods 0.000 claims description 9
- 239000007789 gas Substances 0.000 claims description 9
- 239000010985 leather Substances 0.000 claims description 9
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 8
- 150000001412 amines Chemical class 0.000 claims description 8
- 239000011521 glass Substances 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 8
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 claims description 7
- 238000011282 treatment Methods 0.000 claims description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 6
- 239000003963 antioxidant agent Substances 0.000 claims description 6
- 235000006708 antioxidants Nutrition 0.000 claims description 6
- 239000003205 fragrance Substances 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 230000000087 stabilizing effect Effects 0.000 claims description 6
- 229910019142 PO4 Inorganic materials 0.000 claims description 5
- 150000001450 anions Chemical class 0.000 claims description 5
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 5
- 239000010452 phosphate Substances 0.000 claims description 5
- 239000000843 powder Substances 0.000 claims description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 5
- 229920002554 vinyl polymer Polymers 0.000 claims description 5
- 229940072107 ascorbate Drugs 0.000 claims description 4
- 235000010323 ascorbic acid Nutrition 0.000 claims description 4
- 239000011668 ascorbic acid Substances 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 3
- FEWJPZIEWOKRBE-JCYAYHJZSA-L L-tartrate(2-) Chemical compound [O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O FEWJPZIEWOKRBE-JCYAYHJZSA-L 0.000 claims description 3
- 229910002651 NO3 Inorganic materials 0.000 claims description 3
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 3
- RXTCWPTWYYNTOA-UHFFFAOYSA-N O=P1OCCCCCO1 Chemical compound O=P1OCCCCCO1 RXTCWPTWYYNTOA-UHFFFAOYSA-N 0.000 claims description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 3
- 239000002386 air freshener Substances 0.000 claims description 3
- 150000001449 anionic compounds Chemical group 0.000 claims description 3
- LVHBHZANLOWSRM-UHFFFAOYSA-N itaconic acid Chemical compound OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 3
- 239000004611 light stabiliser Substances 0.000 claims description 3
- 238000012423 maintenance Methods 0.000 claims description 3
- 229940049920 malate Drugs 0.000 claims description 3
- BJEPYKJPYRNKOW-UHFFFAOYSA-L malate(2-) Chemical compound [O-]C(=O)C(O)CC([O-])=O BJEPYKJPYRNKOW-UHFFFAOYSA-L 0.000 claims description 3
- IWYDHOAUDWTVEP-UHFFFAOYSA-M mandelate Chemical compound [O-]C(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-M 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 150000002891 organic anions Chemical group 0.000 claims description 3
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims description 3
- 238000012545 processing Methods 0.000 claims description 3
- 239000000344 soap Substances 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- 239000007921 spray Substances 0.000 claims description 3
- 229940095064 tartrate Drugs 0.000 claims description 3
- 238000005406 washing Methods 0.000 claims description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 claims description 2
- WTBIAPVQQBCLFP-UHFFFAOYSA-N N.N.N.CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O Chemical compound N.N.N.CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O WTBIAPVQQBCLFP-UHFFFAOYSA-N 0.000 claims description 2
- 230000002378 acidificating effect Effects 0.000 claims description 2
- 150000008052 alkyl sulfonates Chemical class 0.000 claims description 2
- 125000005228 aryl sulfonate group Chemical group 0.000 claims description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 2
- 239000000919 ceramic Substances 0.000 claims description 2
- 239000003153 chemical reaction reagent Substances 0.000 claims description 2
- 238000011109 contamination Methods 0.000 claims description 2
- 238000004332 deodorization Methods 0.000 claims description 2
- 238000004851 dishwashing Methods 0.000 claims description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- 230000007935 neutral effect Effects 0.000 claims description 2
- 230000003287 optical effect Effects 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 2
- MPPPKRYCTPRNTB-UHFFFAOYSA-N 1-bromobutane Chemical compound CCCCBr MPPPKRYCTPRNTB-UHFFFAOYSA-N 0.000 claims 1
- BDDLHHRCDSJVKV-UHFFFAOYSA-N 7028-40-2 Chemical compound CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O BDDLHHRCDSJVKV-UHFFFAOYSA-N 0.000 claims 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims 1
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 claims 1
- 230000001166 anti-perspirative effect Effects 0.000 claims 1
- 239000003213 antiperspirant Substances 0.000 claims 1
- ZAKOWWREFLAJOT-UHFFFAOYSA-N d-alpha-Tocopheryl acetate Natural products CC(=O)OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-UHFFFAOYSA-N 0.000 claims 1
- FOYKKGHVWRFIBD-UHFFFAOYSA-N gamma-tocopherol acetate Natural products CC(=O)OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 FOYKKGHVWRFIBD-UHFFFAOYSA-N 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- YKYONYBAUNKHLG-UHFFFAOYSA-N propyl acetate Chemical compound CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 claims 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 1
- UIERETOOQGIECD-ONEGZZNKSA-N tiglic acid Chemical compound C\C=C(/C)C(O)=O UIERETOOQGIECD-ONEGZZNKSA-N 0.000 claims 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 abstract description 6
- 239000002537 cosmetic Substances 0.000 abstract description 3
- 230000015556 catabolic process Effects 0.000 abstract 1
- 238000006731 degradation reaction Methods 0.000 abstract 1
- 239000000551 dentifrice Substances 0.000 abstract 1
- ODUCDPQEXGNKDN-UHFFFAOYSA-N nitroxyl Chemical compound O=N ODUCDPQEXGNKDN-UHFFFAOYSA-N 0.000 abstract 1
- 239000003381 stabilizer Substances 0.000 description 35
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 21
- 125000004430 oxygen atom Chemical group O* 0.000 description 21
- 150000002431 hydrogen Chemical class 0.000 description 20
- 239000000975 dye Substances 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 16
- 239000002585 base Substances 0.000 description 16
- 238000009472 formulation Methods 0.000 description 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 14
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 13
- 125000003118 aryl group Chemical group 0.000 description 12
- 229910052799 carbon Inorganic materials 0.000 description 12
- 229910052757 nitrogen Inorganic materials 0.000 description 12
- 241000208340 Araliaceae Species 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
- 235000005035 Panax pseudoginseng ssp. pseudoginseng Nutrition 0.000 description 11
- 235000003140 Panax quinquefolius Nutrition 0.000 description 11
- 235000008434 ginseng Nutrition 0.000 description 11
- 239000004615 ingredient Substances 0.000 description 10
- 239000003921 oil Substances 0.000 description 10
- 239000012071 phase Substances 0.000 description 10
- 239000000654 additive Substances 0.000 description 9
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 9
- 239000003086 colorant Substances 0.000 description 9
- 239000003995 emulsifying agent Substances 0.000 description 9
- 150000002148 esters Chemical class 0.000 description 9
- 235000019198 oils Nutrition 0.000 description 9
- 125000003342 alkenyl group Chemical group 0.000 description 8
- 239000006071 cream Substances 0.000 description 8
- 239000000499 gel Substances 0.000 description 7
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 7
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 6
- 125000003710 aryl alkyl group Chemical group 0.000 description 6
- 150000001721 carbon Chemical group 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
- 239000013011 aqueous formulation Substances 0.000 description 5
- 239000012965 benzophenone Substances 0.000 description 5
- 239000003925 fat Substances 0.000 description 5
- 150000002191 fatty alcohols Chemical class 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- 235000011187 glycerol Nutrition 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 239000003755 preservative agent Substances 0.000 description 5
- 159000000000 sodium salts Chemical class 0.000 description 5
- 239000001993 wax Substances 0.000 description 5
- 229920002101 Chitin Polymers 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- NQRYJNQNLNOLGT-UHFFFAOYSA-O Piperidinium(1+) Chemical compound C1CC[NH2+]CC1 NQRYJNQNLNOLGT-UHFFFAOYSA-O 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 150000001335 aliphatic alkanes Chemical class 0.000 description 4
- 230000003078 antioxidant effect Effects 0.000 description 4
- 239000012459 cleaning agent Substances 0.000 description 4
- 125000000753 cycloalkyl group Chemical group 0.000 description 4
- 238000004043 dyeing Methods 0.000 description 4
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 4
- 239000002674 ointment Substances 0.000 description 4
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 4
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 4
- 230000002335 preservative effect Effects 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000003971 tillage Methods 0.000 description 4
- 239000002023 wood Substances 0.000 description 4
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 3
- RXFCIXRFAJRBSG-UHFFFAOYSA-N 3,2,3-tetramine Chemical compound NCCCNCCNCCCN RXFCIXRFAJRBSG-UHFFFAOYSA-N 0.000 description 3
- DFFGEOGRBCKSMA-UHFFFAOYSA-N 4-ethenoxy-1-hydroxy-2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CC(OC=C)CC(C)(C)N1O DFFGEOGRBCKSMA-UHFFFAOYSA-N 0.000 description 3
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
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- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- CEZCCHQBSQPRMU-UHFFFAOYSA-L chembl174821 Chemical compound [Na+].[Na+].COC1=CC(S([O-])(=O)=O)=C(C)C=C1N=NC1=C(O)C=CC2=CC(S([O-])(=O)=O)=CC=C12 CEZCCHQBSQPRMU-UHFFFAOYSA-L 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000008367 deionised water Substances 0.000 description 3
- 229910021641 deionized water Inorganic materials 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 3
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- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 3
- 229910021645 metal ion Inorganic materials 0.000 description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 3
- 125000001624 naphthyl group Chemical group 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
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- 238000003756 stirring Methods 0.000 description 3
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 3
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- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 2
- VKZRWSNIWNFCIQ-WDSKDSINSA-N (2s)-2-[2-[[(1s)-1,2-dicarboxyethyl]amino]ethylamino]butanedioic acid Chemical compound OC(=O)C[C@@H](C(O)=O)NCCN[C@H](C(O)=O)CC(O)=O VKZRWSNIWNFCIQ-WDSKDSINSA-N 0.000 description 2
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- CSGAUKGQUCHWDP-UHFFFAOYSA-N 1-hydroxy-2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)N1O CSGAUKGQUCHWDP-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 2
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
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Classifications
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- 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
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- D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
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| EP1507826A4 (en) * | 2002-05-17 | 2007-11-07 | Othera Pharmaceuticals Inc | IMPROVING THE EVOLUTION OF CATARACTS AND OTHER OPHTHALMIC DISEASES |
| JP5384791B2 (ja) * | 2003-11-03 | 2014-01-08 | チバ ホールディング インコーポレーテッド | 安定化されたボディケア製品、家庭用製品、生地及び繊維 |
| EP1614742B1 (en) * | 2004-07-08 | 2007-12-05 | The Procter & Gamble Company | Bleaching composition comprising a cyclic hindered amine |
| US7410936B2 (en) | 2004-08-23 | 2008-08-12 | Ciba Specialty Chemicals Corporation | Stabilized body care products, household products, textiles and fabrics |
| US7357920B2 (en) | 2004-10-19 | 2008-04-15 | L'oreal | Photostable photoprotective compositions comprising dibenzoylmethane and amide oil compounds and a compound that accepts the excited triplet level energy of said dibenzoylmethane(s) |
| US7357919B2 (en) | 2004-10-19 | 2008-04-15 | L'oreal | Photostable photoprotective compositions comprising dibenzoylmethane and arylalkyl benzoate compounds and a compound that accepts the excited triplet level energy of said dibenzoylmethane(s) |
| FR2876579B1 (fr) * | 2004-10-19 | 2007-04-13 | Oreal | Composition antisolaire a base d'un derive de dibenzoylmetha ne et d'un agent photostabilisant particulier;procede de pho tostabilisation |
| FR2876578B1 (fr) * | 2004-10-19 | 2007-03-02 | Oreal | Composition antisolaire a base d'un derive de dibenzoylmetha ne et d'un agent photostabilisant particulier;procede de pho tostabilisation |
| US7431917B2 (en) | 2004-10-19 | 2008-10-07 | L'oreal | Photostable photoprotective compositions comprising dibenzoylmethane and bis-resorcinyl triazine compounds and a compound that accepts the excited triplet level energy of said dibenzoylmethane(s) |
| FR2876580B1 (fr) * | 2004-10-19 | 2007-03-02 | Oreal | Composition antisolaire a base d'un derive de dibenzoylmetha ne et d'un agent photostabilisant particulier;procede de pho tostabilisation |
| EP1674133B1 (en) * | 2004-12-16 | 2010-07-07 | KPSS-Kao Professional Salon Services GmbH | Cleansing composition |
| MX2007014412A (es) * | 2005-05-18 | 2008-02-11 | Ciba Sc Holding Ag | Productos estabilizados para el cuidado del cuerpo, productos domesticos, textiles y telas que contienen compuestos de sales aminas, obstruidos estericamente. |
| ES2435525T3 (es) | 2005-06-30 | 2013-12-20 | Basf Se | Medios electrocrómicos estabilizados |
| MX301558B (es) | 2005-07-29 | 2012-07-20 | Ciba Sc Holding Ag | Estabilizacion de productos para el cuidado del cuerpo y el hogar contra la degradacion por radiacion uv usando derivados de merocianina. |
| KR100853088B1 (ko) * | 2006-03-14 | 2008-08-19 | 주식회사 엘지화학 | 광색성 염료의 나노 캡슐화 방법 |
| EP1994921A1 (fr) | 2007-05-21 | 2008-11-26 | L'Oreal | Composition parfumante comprenant l'association d'un filtre A hydroxyaminobenzophenone, d'un filtre B cinnamate et d'un composé C pipéridinol, benzotriazole ou dibenzoylméthane |
| KR101701548B1 (ko) | 2009-10-06 | 2017-02-01 | 바스프 에스이 | 벤조트로폴론을 함유하는 식물 추출물 및/또는 관련 벤조트로폴론 유도체의 사용에 의한 가정용 제품, 바디-관리 제품 및 식품의 안정화 |
| CN103502528B (zh) * | 2011-04-20 | 2017-10-20 | 亨斯迈先进材料(瑞士)有限公司 | 聚酯染色方法 |
| WO2012174091A2 (en) | 2011-06-13 | 2012-12-20 | The Procter & Gamble Company | PERSONAL CARE COMPOSITIONS COMPRISING A pH TUNEABLE GELLANT AND METHODS OF USING |
| JP2014524901A (ja) | 2011-06-13 | 2014-09-25 | ザ プロクター アンド ギャンブル カンパニー | ジアミドゲル化剤を含むパーソナルケア組成物及び使用方法 |
| WO2012177757A2 (en) | 2011-06-20 | 2012-12-27 | The Procter & Gamble Company | Personal care compositions comprising shaped abrasive particles |
| US20130011347A1 (en) | 2011-07-07 | 2013-01-10 | Paul Robert Tanner | Personal Care Compositions With Improved Solubility of a Solid Cosmetic Active |
| US9192552B2 (en) | 2011-07-07 | 2015-11-24 | The Procter & Gamble Company | Personal care compositions with improved solubility of a solid UV active |
| BR112014001418B1 (pt) | 2011-07-21 | 2021-05-11 | Basf Se | compostos, e, processo para a preparação dos compostos |
| EP2819643B1 (en) | 2012-03-01 | 2017-10-18 | The Procter and Gamble Company | Sunscreen composition comprising uv composite |
| US9549891B2 (en) | 2012-03-19 | 2017-01-24 | The Procter & Gamble Company | Superabsorbent polymers and sunscreen actives for use in skin care compositions |
| US20130243834A1 (en) | 2012-03-19 | 2013-09-19 | The Procter & Gamble Company | Cross linked silicone copolmyer networks in a thickened aqueous phase |
| JP2015510937A (ja) | 2012-03-19 | 2015-04-13 | ザ プロクター アンド ギャンブルカンパニー | ヘアケア組成物中で使用するための超吸収性ポリマー及びシリコーンエラストマー |
| US20140178314A1 (en) | 2012-12-19 | 2014-06-26 | The Procter & Gamble Company | Compositions and/or articles with improved solubility of a solid active |
| JP6604637B2 (ja) | 2015-06-29 | 2019-11-13 | ザ プロクター アンド ギャンブル カンパニー | スキンケア組成物において使用するための超吸収性ポリマー及びデンプン粉末 |
| US20180000715A1 (en) | 2016-06-30 | 2018-01-04 | The Procter & Gamble Company | Hair Care Compositions For Calcium Chelation |
| US11246816B2 (en) | 2016-06-30 | 2022-02-15 | The Procter And Gamble Company | Shampoo compositions comprising a chelant |
| US11786447B2 (en) | 2016-06-30 | 2023-10-17 | The Procter & Gamble Company | Conditioner composition comprising a chelant |
| US20180000706A1 (en) | 2016-06-30 | 2018-01-04 | The Procter & Gamble Company | Conditioner Composition Comprising a Chelant |
| US20180000705A1 (en) | 2016-06-30 | 2018-01-04 | The Procter & Gamble Company | Shampoo Compositions Comprising a Chelant |
| WO2018064284A1 (en) | 2016-09-30 | 2018-04-05 | Novaflux, Inc. | Compositions for cleaning and decontamination |
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| EP3775133B1 (en) | 2018-04-03 | 2024-10-09 | Novaflux, Inc. | Cleaning composition with superabsorbent polymer |
| EP3613835A1 (en) | 2018-08-24 | 2020-02-26 | The Procter & Gamble Company | Treatment compositions comprising a surfactant system and an oligoamine |
| EP3613834B1 (en) | 2018-08-24 | 2026-04-01 | The Procter & Gamble Company | Treatment compositions comprising low levels of an oligoamine |
| CN109405996B (zh) * | 2018-10-17 | 2021-01-08 | 京东方科技集团股份有限公司 | 一种温度计及其控制方法 |
| WO2021067872A1 (en) | 2019-10-03 | 2021-04-08 | Novaflux, Inc. | Oral cavity cleaning composition, method, and apparatus |
| US12064495B2 (en) | 2019-10-03 | 2024-08-20 | Protegera, Inc. | Oral cavity cleaning composition, method, and apparatus |
| EP4121503B1 (en) * | 2020-03-17 | 2024-08-21 | Basf Se | Process for making a granule |
| DE112023001807T5 (de) | 2022-03-31 | 2025-01-23 | Galderma Holding SA | Körperpflegezusammensetzungen für empfindliche Haut und Anwendungsmethoden |
| KR102759880B1 (ko) * | 2022-10-04 | 2025-02-03 | 애경산업(주) | 피부 또는 모발용 세정제 조성물 |
| DE102023203837A1 (de) * | 2023-04-26 | 2024-10-31 | Henkel Ag & Co. Kgaa | Verfahren zur Färbung von Keratinfasern, umfassend die Anwendung eines Färbemittels mit Chitosan und farbgebender Verbindung und die Anwendung eines Shampoos |
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| EP0157738B1 (de) * | 1984-03-22 | 1989-04-19 | Ciba-Geigy Ag | Verfahren zur Herstellung von Nitroxylen sterisch gehinderter Amine |
| US4786431A (en) | 1984-12-31 | 1988-11-22 | Colgate-Palmolive Company | Liquid laundry detergent-bleach composition and method of use |
| MX162823B (es) * | 1985-03-29 | 1991-06-28 | Colgate Palmolive Co | Mejoras a composicion de detergente blanqueadora liquida para lavar ropa |
| US4908040A (en) * | 1986-11-07 | 1990-03-13 | Ciba-Geigy Corporation | Anionic cyclodiylide compounds, their preparation and use in washing agents as shading dyes |
| EP0309401B2 (en) | 1987-09-21 | 2002-06-05 | Ciba Specialty Chemicals Holding Inc. | Stabilization of coatings with N-hydroxy hindered amines |
| US5574163A (en) * | 1994-08-31 | 1996-11-12 | Ciba-Geigy Corporation | Process for the preparation of N-oxyl hindered amine esters |
| ATE194596T1 (de) | 1994-11-15 | 2000-07-15 | Moreno Paolini | N-hydroxypiperidine als superoxid-radikalfänger |
| RU2223985C2 (ru) * | 1997-07-23 | 2004-02-20 | Циба Спешиалти Кемикалз Холдинг Инк. | Ингибирование пожелтения целлюлозы и бумаги с использованием нитроксидов и других совместно вводимых добавок |
| TWI224995B (en) * | 1998-03-19 | 2004-12-11 | Ciba Sc Holding Ag | Stabilization of wood substrates |
| GB9917450D0 (en) | 1999-07-23 | 1999-09-29 | Unilever Plc | Fabric treatment composition and a method of treating fabric |
| JP2001106903A (ja) * | 1999-08-04 | 2001-04-17 | Mitsubishi Engineering Plastics Corp | 耐候性の改良されたポリアミド樹脂組成物及びそれを用いた成形品 |
| JP3540759B2 (ja) * | 2000-04-06 | 2004-07-07 | 三菱レイヨン株式会社 | 難燃性ポリプロピレン繊維及びその製造方法 |
| PL205847B1 (pl) * | 2000-05-11 | 2010-06-30 | Ciba Sc Holding Ag | Sposób bejcowania drewna, wodna bejca drewna, zastosowanie stabilizatora barwnika oraz zastosowanie wodnej bejcy drewna |
| US6433073B1 (en) * | 2000-07-27 | 2002-08-13 | 3M Innovative Properties Company | Polyurethane dispersion in alcohol-water system |
| WO2002028854A1 (en) * | 2000-10-03 | 2002-04-11 | Ciba Specialty Chemicals Holding Inc. | Heteroaryl substituted hydroxyphenyltriazine uv-absorbers |
-
2003
- 2003-04-24 JP JP2004510742A patent/JP4594727B2/ja not_active Expired - Lifetime
- 2003-04-24 AU AU2003233054A patent/AU2003233054A1/en not_active Abandoned
- 2003-04-24 AT AT03727349T patent/ATE463228T1/de not_active IP Right Cessation
- 2003-04-24 EP EP03727349A patent/EP1499286B1/en not_active Expired - Lifetime
- 2003-04-24 KR KR1020047017595A patent/KR100975789B1/ko not_active Expired - Lifetime
- 2003-04-24 MX MXPA04010833A patent/MXPA04010833A/es active IP Right Grant
- 2003-04-24 US US10/512,528 patent/US9358195B2/en active Active
- 2003-04-24 CN CN038097516A patent/CN1649566B/zh not_active Expired - Lifetime
- 2003-04-24 WO PCT/EP2003/004262 patent/WO2003103622A1/en not_active Ceased
- 2003-04-24 ES ES03727349T patent/ES2342594T3/es not_active Expired - Lifetime
- 2003-04-24 DE DE60332012T patent/DE60332012D1/de not_active Expired - Lifetime
- 2003-04-24 BR BRPI0309692-0B1A patent/BR0309692B1/pt active IP Right Grant
- 2003-04-30 TW TW092110122A patent/TWI329519B/zh not_active IP Right Cessation
-
2010
- 2010-07-01 JP JP2010151413A patent/JP5323771B2/ja not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| US9358195B2 (en) | 2016-06-07 |
| CN1649566A (zh) | 2005-08-03 |
| JP4594727B2 (ja) | 2010-12-08 |
| JP5323771B2 (ja) | 2013-10-23 |
| ES2342594T3 (es) | 2010-07-09 |
| WO2003103622A1 (en) | 2003-12-18 |
| BR0309692B1 (pt) | 2014-07-29 |
| DE60332012D1 (de) | 2010-05-20 |
| MXPA04010833A (es) | 2005-02-14 |
| JP2005539100A (ja) | 2005-12-22 |
| KR100975789B1 (ko) | 2010-08-16 |
| CN1649566B (zh) | 2010-05-26 |
| AU2003233054A1 (en) | 2003-12-22 |
| TW200406226A (en) | 2004-05-01 |
| KR20040106444A (ko) | 2004-12-17 |
| JP2010254706A (ja) | 2010-11-11 |
| EP1499286B1 (en) | 2010-04-07 |
| ATE463228T1 (de) | 2010-04-15 |
| US20050220727A1 (en) | 2005-10-06 |
| BR0309692A (pt) | 2005-03-29 |
| EP1499286A1 (en) | 2005-01-26 |
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| MK4A | Expiration of patent term of an invention patent |