BG107311A - Фенолатни състави с ниска точка на замръзване - Google Patents
Фенолатни състави с ниска точка на замръзване Download PDFInfo
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- BG107311A BG107311A BG107311A BG10731102A BG107311A BG 107311 A BG107311 A BG 107311A BG 107311 A BG107311 A BG 107311A BG 10731102 A BG10731102 A BG 10731102A BG 107311 A BG107311 A BG 107311A
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- 239000000203 mixture Substances 0.000 title claims abstract description 102
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 title claims abstract description 29
- 229940031826 phenolate Drugs 0.000 title claims abstract description 29
- 230000008014 freezing Effects 0.000 title claims abstract description 15
- 238000007710 freezing Methods 0.000 title claims abstract description 15
- 238000009472 formulation Methods 0.000 title abstract 3
- 238000002425 crystallisation Methods 0.000 claims abstract description 116
- 230000008025 crystallization Effects 0.000 claims abstract description 116
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 95
- 239000003112 inhibitor Substances 0.000 claims abstract description 44
- 239000004615 ingredient Substances 0.000 claims abstract description 11
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical class OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 claims description 187
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 146
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 89
- 239000000725 suspension Substances 0.000 claims description 41
- 150000004707 phenolate Chemical class 0.000 claims description 36
- 229910052700 potassium Inorganic materials 0.000 claims description 34
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 28
- 150000003839 salts Chemical class 0.000 claims description 20
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 19
- 239000011591 potassium Substances 0.000 claims description 19
- 239000000049 pigment Substances 0.000 claims description 18
- -1 aliphatic glycol compound Chemical class 0.000 claims description 16
- 239000007900 aqueous suspension Substances 0.000 claims description 16
- 239000006185 dispersion Substances 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 16
- 150000001896 cresols Chemical class 0.000 claims description 15
- 150000002989 phenols Chemical class 0.000 claims description 14
- 239000003755 preservative agent Substances 0.000 claims description 13
- 230000003115 biocidal effect Effects 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 11
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 11
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 10
- 239000011707 mineral Substances 0.000 claims description 10
- 238000006386 neutralization reaction Methods 0.000 claims description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 9
- 239000000945 filler Substances 0.000 claims description 9
- 229910001854 alkali hydroxide Inorganic materials 0.000 claims description 8
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 230000001737 promoting effect Effects 0.000 claims description 8
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical class OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 8
- VAJVDSVGBWFCLW-UHFFFAOYSA-N 3-Phenyl-1-propanol Chemical compound OCCCC1=CC=CC=C1 VAJVDSVGBWFCLW-UHFFFAOYSA-N 0.000 claims description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 6
- 239000011230 binding agent Substances 0.000 claims description 6
- 239000002738 chelating agent Substances 0.000 claims description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- 239000002855 microbicide agent Substances 0.000 claims description 6
- 230000002335 preservative effect Effects 0.000 claims description 6
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 239000002585 base Substances 0.000 claims description 5
- 230000003472 neutralizing effect Effects 0.000 claims description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- 239000005068 cooling lubricant Substances 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 239000003381 stabilizer Substances 0.000 claims description 4
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 claims description 3
- SZHQPBJEOCHCKM-UHFFFAOYSA-N 2-phosphonobutane-1,2,4-tricarboxylic acid Chemical compound OC(=O)CCC(P(O)(O)=O)(C(O)=O)CC(O)=O SZHQPBJEOCHCKM-UHFFFAOYSA-N 0.000 claims description 3
- WFJIVOKAWHGMBH-UHFFFAOYSA-N 4-hexylbenzene-1,3-diol Chemical class CCCCCCC1=CC=C(O)C=C1O WFJIVOKAWHGMBH-UHFFFAOYSA-N 0.000 claims description 3
- 238000004090 dissolution Methods 0.000 claims description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 3
- 230000001502 supplementing effect Effects 0.000 claims description 3
- 150000005207 1,3-dihydroxybenzenes Chemical class 0.000 claims description 2
- WYTRYIUQUDTGSX-UHFFFAOYSA-N 1-phenylpropan-2-ol Chemical compound CC(O)CC1=CC=CC=C1 WYTRYIUQUDTGSX-UHFFFAOYSA-N 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 229910003002 lithium salt Inorganic materials 0.000 claims description 2
- 159000000002 lithium salts Chemical class 0.000 claims description 2
- 230000001590 oxidative effect Effects 0.000 claims description 2
- 239000003973 paint Substances 0.000 claims description 2
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 claims description 2
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims description 2
- 230000037452 priming Effects 0.000 claims description 2
- 159000000000 sodium salts Chemical class 0.000 claims description 2
- JUEAPPHORMOWPK-UHFFFAOYSA-M tributylstannyl benzoate Chemical compound CCCC[Sn](CCCC)(CCCC)OC(=O)C1=CC=CC=C1 JUEAPPHORMOWPK-UHFFFAOYSA-M 0.000 claims description 2
- 239000002966 varnish Substances 0.000 claims description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims 2
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 claims 2
- 239000003963 antioxidant agent Substances 0.000 claims 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 2
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 claims 2
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 claims 2
- NGFPWHGISWUQOI-UHFFFAOYSA-N 2-sec-butylphenol Chemical class CCC(C)C1=CC=CC=C1O NGFPWHGISWUQOI-UHFFFAOYSA-N 0.000 claims 1
- 230000003078 antioxidant effect Effects 0.000 claims 1
- HHTWOMMSBMNRKP-UHFFFAOYSA-N carvacrol Natural products CC(=C)C1=CC=C(C)C(O)=C1 HHTWOMMSBMNRKP-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 150000002902 organometallic compounds Chemical class 0.000 claims 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims 1
- 239000012530 fluid Substances 0.000 abstract 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 294
- 235000010292 orthophenyl phenol Nutrition 0.000 description 90
- 239000000243 solution Substances 0.000 description 72
- 239000012085 test solution Substances 0.000 description 48
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 45
- HSDKCIYHTPCVAU-UHFFFAOYSA-M potassium;2-phenylphenolate Chemical compound [K+].[O-]C1=CC=CC=C1C1=CC=CC=C1 HSDKCIYHTPCVAU-UHFFFAOYSA-M 0.000 description 43
- 238000003756 stirring Methods 0.000 description 28
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 27
- 210000002257 embryonic structure Anatomy 0.000 description 25
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 20
- 238000003760 magnetic stirring Methods 0.000 description 20
- 239000000523 sample Substances 0.000 description 18
- 239000012153 distilled water Substances 0.000 description 17
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 16
- 235000019445 benzyl alcohol Nutrition 0.000 description 15
- 239000000047 product Substances 0.000 description 14
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- 235000010216 calcium carbonate Nutrition 0.000 description 10
- KSQXVLVXUFHGJQ-UHFFFAOYSA-M Sodium ortho-phenylphenate Chemical compound [Na+].[O-]C1=CC=CC=C1C1=CC=CC=C1 KSQXVLVXUFHGJQ-UHFFFAOYSA-M 0.000 description 9
- 230000002411 adverse Effects 0.000 description 8
- 235000010755 mineral Nutrition 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 239000005995 Aluminium silicate Substances 0.000 description 7
- 235000012211 aluminium silicate Nutrition 0.000 description 7
- 230000000845 anti-microbial effect Effects 0.000 description 7
- 229910000019 calcium carbonate Inorganic materials 0.000 description 7
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 6
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 6
- 230000002269 spontaneous effect Effects 0.000 description 6
- 238000003860 storage Methods 0.000 description 6
- HSQFVBWFPBKHEB-UHFFFAOYSA-N 2,3,4-trichlorophenol Chemical compound OC1=CC=C(Cl)C(Cl)=C1Cl HSQFVBWFPBKHEB-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000012496 blank sample Substances 0.000 description 5
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- 238000007711 solidification Methods 0.000 description 5
- 230000008023 solidification Effects 0.000 description 5
- 244000052616 bacterial pathogen Species 0.000 description 4
- 230000035876 healing Effects 0.000 description 4
- 230000003641 microbiacidal effect Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 150000001447 alkali salts Chemical group 0.000 description 3
- 239000004599 antimicrobial Substances 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
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- 230000003647 oxidation Effects 0.000 description 3
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- 230000001681 protective effect Effects 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000001888 Peptone Substances 0.000 description 2
- 108010080698 Peptones Proteins 0.000 description 2
- 239000006004 Quartz sand Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
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- 239000000839 emulsion Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N formic acid Substances OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
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- 150000002334 glycols Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 235000019319 peptone Nutrition 0.000 description 2
- NJVOHKFLBKQLIZ-UHFFFAOYSA-N (2-ethenylphenyl) prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1C=C NJVOHKFLBKQLIZ-UHFFFAOYSA-N 0.000 description 1
- OHCWFJHNCNKOLE-UHFFFAOYSA-N 2-methylphenol;potassium Chemical compound [K].CC1=CC=CC=C1O OHCWFJHNCNKOLE-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- 241000192125 Firmicutes Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 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 1
- 235000019738 Limestone Nutrition 0.000 description 1
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- 241000589516 Pseudomonas Species 0.000 description 1
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- 229920002472 Starch Polymers 0.000 description 1
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- 150000007513 acids Chemical class 0.000 description 1
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- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
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- FFWMQDHRQQNYGT-UHFFFAOYSA-N didodecyl(2-phenylethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[NH+](CCCCCCCCCCCC)CCC1=CC=CC=C1 FFWMQDHRQQNYGT-UHFFFAOYSA-N 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
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- UWHRNIXHZAWBMF-UHFFFAOYSA-N n-dodecyl-n-methyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)CCCCCCCCCCCC UWHRNIXHZAWBMF-UHFFFAOYSA-N 0.000 description 1
- MJCJUDJQDGGKOX-UHFFFAOYSA-N n-dodecyldodecan-1-amine Chemical compound CCCCCCCCCCCCNCCCCCCCCCCCC MJCJUDJQDGGKOX-UHFFFAOYSA-N 0.000 description 1
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- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
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- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
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- 159000000001 potassium salts Chemical class 0.000 description 1
- GLRAIAFGAKIYID-UHFFFAOYSA-M potassium;2,3,4-trichlorophenolate Chemical compound [K+].[O-]C1=CC=C(Cl)C(Cl)=C1Cl GLRAIAFGAKIYID-UHFFFAOYSA-M 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
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- 125000001424 substituent group Chemical group 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical class CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
- C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
- C09K15/06—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing oxygen
- C09K15/08—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing oxygen containing a phenol or quinone moiety
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/08—Oxygen or sulfur directly attached to an aromatic ring system
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/08—Oxygen or sulfur directly attached to an aromatic ring system
- A01N31/16—Oxygen or sulfur directly attached to an aromatic ring system with two or more oxygen or sulfur atoms directly attached to the same aromatic ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/68—Purification; separation; Use of additives, e.g. for stabilisation
- C07C37/88—Use of additives, e.g. for stabilisation
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Environmental Sciences (AREA)
- Materials Engineering (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10023458 | 2000-05-12 | ||
| DE10027588A DE10027588B4 (de) | 2000-05-12 | 2000-06-02 | Phenolate enthaltende Formulierung mit tiefem Gefrierpunkt |
| PCT/EP2001/004729 WO2001085659A1 (de) | 2000-05-12 | 2001-04-26 | Phenolate enthaltende formulierung mit tiefem gefrierpunkt |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BG107311A true BG107311A (bg) | 2003-06-30 |
Family
ID=26005666
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BG107311A BG107311A (bg) | 2000-05-12 | 2002-11-25 | Фенолатни състави с ниска точка на замръзване |
Country Status (16)
| Country | Link |
|---|---|
| US (3) | US6994798B2 (cs) |
| EP (1) | EP1283822B1 (cs) |
| KR (1) | KR100832378B1 (cs) |
| AR (1) | AR028441A1 (cs) |
| AU (2) | AU6590701A (cs) |
| BG (1) | BG107311A (cs) |
| BR (1) | BR0110780B1 (cs) |
| CA (1) | CA2408643C (cs) |
| CZ (1) | CZ304058B6 (cs) |
| HU (1) | HUP0301864A3 (cs) |
| MX (1) | MXPA02011032A (cs) |
| NO (1) | NO330782B1 (cs) |
| NZ (1) | NZ522720A (cs) |
| RU (1) | RU2298543C2 (cs) |
| SK (1) | SK287821B6 (cs) |
| WO (1) | WO2001085659A1 (cs) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6994798B2 (en) * | 2000-05-12 | 2006-02-07 | Omya Ag | Phenolate-containing formulation with low freezing point |
| FR2812173B1 (fr) * | 2000-07-28 | 2003-01-03 | Aventis Cropscience Sa | Association fongicide a base d'huile d'origine vegetale |
| DE10040165A1 (de) * | 2000-08-17 | 2002-02-28 | Bayer Ag | ortho-Phenylphenolat-Konzentrate |
| FR2881064A1 (fr) * | 2005-01-26 | 2006-07-28 | Omya Development Ag | Procede de controle de la contamination microbienne, suspensions minerales obtenues et leurs utilisations |
| WO2010010700A1 (ja) * | 2008-07-23 | 2010-01-28 | 花王株式会社 | 抗菌剤含有液の製造方法 |
| EP2158813A1 (en) | 2008-08-28 | 2010-03-03 | Omya Development AG | Stabilisation of aqueous mineral preparations by reuterin |
| PL2482652T3 (pl) * | 2009-09-28 | 2016-03-31 | Dow Global Technologies Llc | Kompozycje dibromomalonamidu oraz ich zastosowanie jako biocydów |
| RS52656B (en) | 2010-04-09 | 2013-06-28 | Omya Development Ag | PROCEDURE FOR MAINTENANCE OF AQUATIC MINERAL MATERIALS, PROTECTED AQUATIC MINERAL MATERIALS, AND USE OF PROTECTIVE UNITS IN AQUATIC MINERAL MATERIALS |
| EP2982247A1 (en) | 2014-08-07 | 2016-02-10 | Omya International AG | Antiseptic product, process for preparing same and its use |
| CN109232192B (zh) * | 2018-10-29 | 2021-09-17 | 国家能源投资集团有限责任公司 | 一种对甲酚的分离方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU34050A1 (cs) * | 1955-02-26 | |||
| GB804257A (en) * | 1955-08-12 | 1958-11-12 | Monsanto Chem Australia Ltd | Liquid concentrates of sodium pentachlorophenate |
| NL7018669A (cs) * | 1969-12-23 | 1971-06-25 | ||
| DE2732441A1 (de) * | 1977-07-18 | 1979-02-01 | Boehme Fritz | Verfahren zur herstellung eines desinfektionsmittels |
| DE4202051A1 (de) * | 1992-01-25 | 1993-07-29 | Bayer Ag | Fliessfaehige mikrobizide mittel |
| GB2277749B (en) * | 1993-05-08 | 1996-12-04 | Ciba Geigy Ag | Fluorescent whitening of paper |
| US6019941A (en) * | 1996-01-30 | 2000-02-01 | Porcello; Joseph A. | Method for disinfecting dermal surfaces and inanimate surfaces, and particularly air ducts |
| EP0937130A1 (en) * | 1996-10-22 | 1999-08-25 | Kimberly-Clark Worldwide, Inc. | Method of increasing the antimicrobial activity of an aqueous, antimicrobial liquid cleaning formulation |
| US5837274A (en) * | 1996-10-22 | 1998-11-17 | Kimberly Clark Corporation | Aqueous, antimicrobial liquid cleaning formulation |
| DE19859136A1 (de) * | 1998-12-21 | 2000-06-29 | Pluss Stauffer Ag | Phenol und/oder Phenolderivate enthaltende Formulierung mit tiefem Gefrierpunkt |
| US6362152B1 (en) * | 2000-04-07 | 2002-03-26 | The Dow Chemical Company | Low color and low haze formulations of sodium o-phenylphenate |
| US6994798B2 (en) * | 2000-05-12 | 2006-02-07 | Omya Ag | Phenolate-containing formulation with low freezing point |
-
2001
- 2001-04-26 US US10/275,861 patent/US6994798B2/en not_active Expired - Fee Related
- 2001-04-26 AU AU6590701A patent/AU6590701A/xx active Pending
- 2001-04-26 KR KR1020027015159A patent/KR100832378B1/ko not_active Expired - Fee Related
- 2001-04-26 BR BRPI0110780-1A patent/BR0110780B1/pt not_active IP Right Cessation
- 2001-04-26 SK SK1742-2002A patent/SK287821B6/sk not_active IP Right Cessation
- 2001-04-26 NZ NZ522720A patent/NZ522720A/en not_active IP Right Cessation
- 2001-04-26 CZ CZ20024072A patent/CZ304058B6/cs unknown
- 2001-04-26 AU AU2001265907A patent/AU2001265907B2/en not_active Ceased
- 2001-04-26 HU HU0301864A patent/HUP0301864A3/hu unknown
- 2001-04-26 CA CA2408643A patent/CA2408643C/en not_active Expired - Lifetime
- 2001-04-26 WO PCT/EP2001/004729 patent/WO2001085659A1/de active IP Right Grant
- 2001-04-26 EP EP01943291.3A patent/EP1283822B1/de not_active Expired - Lifetime
- 2001-04-26 RU RU2002133454/04A patent/RU2298543C2/ru not_active IP Right Cessation
- 2001-04-26 MX MXPA02011032A patent/MXPA02011032A/es active IP Right Grant
- 2001-05-11 AR ARP010102227A patent/AR028441A1/es active IP Right Grant
-
2002
- 2002-11-11 NO NO20025400A patent/NO330782B1/no not_active IP Right Cessation
- 2002-11-25 BG BG107311A patent/BG107311A/bg unknown
-
2005
- 2005-11-18 US US11/281,622 patent/US7309452B2/en not_active Expired - Fee Related
-
2007
- 2007-04-20 US US11/737,971 patent/US20070191494A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| MXPA02011032A (es) | 2003-09-10 |
| HUP0301864A3 (en) | 2007-10-29 |
| CZ20024072A3 (cs) | 2003-05-14 |
| EP1283822A1 (de) | 2003-02-19 |
| AR028441A1 (es) | 2003-05-07 |
| SK17422002A3 (sk) | 2003-04-01 |
| US20060065875A1 (en) | 2006-03-30 |
| KR20030001481A (ko) | 2003-01-06 |
| US20070191494A1 (en) | 2007-08-16 |
| CZ304058B6 (cs) | 2013-09-11 |
| SK287821B6 (sk) | 2011-11-04 |
| CA2408643A1 (en) | 2002-11-08 |
| EP1283822B1 (de) | 2014-01-15 |
| RU2298543C2 (ru) | 2007-05-10 |
| AU6590701A (en) | 2001-11-20 |
| NO330782B1 (no) | 2011-07-18 |
| BR0110780B1 (pt) | 2013-04-30 |
| NO20025400D0 (no) | 2002-11-11 |
| NZ522720A (en) | 2005-09-30 |
| NO20025400L (no) | 2002-12-02 |
| US20040023939A1 (en) | 2004-02-05 |
| BR0110780A (pt) | 2003-05-06 |
| WO2001085659A1 (de) | 2001-11-15 |
| KR100832378B1 (ko) | 2008-05-26 |
| US6994798B2 (en) | 2006-02-07 |
| CA2408643C (en) | 2011-01-11 |
| HUP0301864A2 (hu) | 2003-09-29 |
| US7309452B2 (en) | 2007-12-18 |
| AU2001265907B2 (en) | 2006-08-17 |
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