BRPI0614442B1 - Uso de derivados de merocianina, produto de tratamento para o corpo e agente de tratamento e limpeza doméstica - Google Patents

Info

Publication number

BRPI0614442B1

BRPI0614442B1 BRPI0614442-0A BRPI0614442A BRPI0614442B1 BR PI0614442 B1 BRPI0614442 B1 BR PI0614442B1 BR PI0614442 A BRPI0614442 A BR PI0614442A BR PI0614442 B1 BRPI0614442 B1 BR PI0614442B1

Authority

BR

Brazil

Prior art keywords

formula

radical

c22alkyl

preparations

acid

Prior art date

2005-07-29

Links

• Espacenet
• Global Dossier
• Discuss

• DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical class [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 title abstract description 5
• 239000012459 cleaning agent Substances 0.000 title description 8
• 150000001875 compounds Chemical class 0.000 claims abstract description 58
• 238000004140 cleaning Methods 0.000 claims abstract description 9
• 238000010525 oxidative degradation reaction Methods 0.000 claims abstract description 6
• -1 polysiloxane moiety Polymers 0.000 claims description 102
• 229910052739 hydrogen Inorganic materials 0.000 claims description 24
• 239000001257 hydrogen Substances 0.000 claims description 23
• 239000003795 chemical substances by application Substances 0.000 claims description 22
• 239000003381 stabilizer Substances 0.000 claims description 17
• 125000003118 aryl group Chemical group 0.000 claims description 14
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
• 125000006735 (C1-C20) heteroalkyl group Chemical group 0.000 claims description 12
• 125000000217 alkyl group Chemical group 0.000 claims description 10
• 229910052736 halogen Inorganic materials 0.000 claims description 10
• 150000002367 halogens Chemical class 0.000 claims description 9
• 125000000623 heterocyclic group Chemical group 0.000 claims description 9
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
• 239000004611 light stabiliser Substances 0.000 claims description 8
• RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 7
• 125000006736 (C6-C20) aryl group Chemical group 0.000 claims description 6
• YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 6
• GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 6
• NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 6
• 125000002837 carbocyclic group Chemical group 0.000 claims description 6
• 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims description 5
• 125000003342 alkenyl group Chemical group 0.000 claims description 5
• 125000005647 linker group Chemical group 0.000 claims description 5
• 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
• 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 4
• 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims description 3
• 125000006833 (C1-C5) alkylene group Chemical group 0.000 claims description 3
• 101100134929 Gallus gallus COR9 gene Proteins 0.000 claims description 3
• 229910006069 SO3H Inorganic materials 0.000 claims description 3
• 125000000304 alkynyl group Chemical group 0.000 claims description 3
• 125000000732 arylene group Chemical group 0.000 claims description 3
• 125000002993 cycloalkylene group Chemical group 0.000 claims description 3
• 125000001072 heteroaryl group Chemical group 0.000 claims description 3
• 125000005549 heteroarylene group Chemical group 0.000 claims description 3
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
• 125000004430 oxygen atom Chemical group O* 0.000 claims description 3
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
• 125000005843 halogen group Chemical group 0.000 claims 1
• 238000002360 preparation method Methods 0.000 description 77
• 239000000203 mixture Substances 0.000 description 47
• 239000000047 product Substances 0.000 description 45
• 150000003254 radicals Chemical class 0.000 description 37
• 239000003921 oil Substances 0.000 description 34
• 235000019198 oils Nutrition 0.000 description 34
• 238000009472 formulation Methods 0.000 description 28
• 239000006071 cream Substances 0.000 description 27
• 235000014113 dietary fatty acids Nutrition 0.000 description 24
• 239000000194 fatty acid Substances 0.000 description 24
• 229930195729 fatty acid Natural products 0.000 description 24
• 239000002453 shampoo Substances 0.000 description 21
• GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 20
• 239000000126 substance Substances 0.000 description 20
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 18
• 229920001577 copolymer Polymers 0.000 description 18
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• 239000003963 antioxidant agent Substances 0.000 description 16
• 235000006708 antioxidants Nutrition 0.000 description 16
• 125000004432 carbon atom Chemical group C* 0.000 description 16
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• 229940081733 cetearyl alcohol Drugs 0.000 description 14
• 239000002537 cosmetic Substances 0.000 description 14
• 239000003995 emulsifying agent Substances 0.000 description 14
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• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
• 150000004665 fatty acids Chemical class 0.000 description 13
• DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 12
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• 239000006210 lotion Substances 0.000 description 12
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 12
• 239000001993 wax Substances 0.000 description 12
• PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 11
• 239000002253 acid Substances 0.000 description 11
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• 239000002304 perfume Substances 0.000 description 11
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• LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 10
• VBICKXHEKHSIBG-UHFFFAOYSA-N beta-monoglyceryl stearate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 9
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• 150000002191 fatty alcohols Chemical class 0.000 description 9
• 239000007788 liquid Substances 0.000 description 9
• KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
• 239000006096 absorbing agent Substances 0.000 description 8
• 150000001298 alcohols Chemical class 0.000 description 8
• 125000002091 cationic group Chemical group 0.000 description 8
• 239000002781 deodorant agent Substances 0.000 description 8
• 239000003205 fragrance Substances 0.000 description 8
• 229920005862 polyol Polymers 0.000 description 8
• 150000001412 amines Chemical class 0.000 description 7
• 239000003925 fat Substances 0.000 description 7
• 235000019197 fats Nutrition 0.000 description 7
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
• 238000007254 oxidation reaction Methods 0.000 description 7
• 229920000642 polymer Polymers 0.000 description 7
• 239000000344 soap Substances 0.000 description 7
• 239000011734 sodium Substances 0.000 description 7
• 229910052708 sodium Inorganic materials 0.000 description 7
• DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
• UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 6
• ZFOZVQLOBQUTQQ-UHFFFAOYSA-N Tributyl citrate Chemical compound CCCCOC(=O)CC(O)(C(=O)OCCCC)CC(=O)OCCCC ZFOZVQLOBQUTQQ-UHFFFAOYSA-N 0.000 description 6
• 238000010521 absorption reaction Methods 0.000 description 6
• 150000001299 aldehydes Chemical class 0.000 description 6
• MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
• RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 description 6
• 239000011521 glass Substances 0.000 description 6
• RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
• QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 6
• 230000003647 oxidation Effects 0.000 description 6
• 229910052760 oxygen Inorganic materials 0.000 description 6
• 150000003077 polyols Chemical class 0.000 description 6
• 150000003839 salts Chemical class 0.000 description 6
• 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 6
• 229920002554 vinyl polymer Polymers 0.000 description 6
• 229920001661 Chitosan Polymers 0.000 description 5
• MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 5
• OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 5
• 229910019142 PO4 Inorganic materials 0.000 description 5
• XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 description 5
• 150000007513 acids Chemical class 0.000 description 5
• 230000001166 anti-perspirative effect Effects 0.000 description 5
• 239000003213 antiperspirant Substances 0.000 description 5
• 238000004061 bleaching Methods 0.000 description 5
• 239000003599 detergent Substances 0.000 description 5
• 235000013870 dimethyl polysiloxane Nutrition 0.000 description 5
• 229940075529 glyceryl stearate Drugs 0.000 description 5
• 150000002430 hydrocarbons Chemical group 0.000 description 5
• 239000004615 ingredient Substances 0.000 description 5
• 150000002576 ketones Chemical class 0.000 description 5
• 238000000034 method Methods 0.000 description 5
• 235000013336 milk Nutrition 0.000 description 5
• 210000004080 milk Anatomy 0.000 description 5
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• 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 5
• 239000000243 solution Substances 0.000 description 5
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• 239000000606 toothpaste Substances 0.000 description 5
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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 4
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• NLMKTBGFQGKQEV-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-hexadecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO NLMKTBGFQGKQEV-UHFFFAOYSA-N 0.000 description 4
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