CA1214607A - Compositions au peroxygene - Google Patents

Compositions au peroxygene

Info

Publication number: CA1214607A
Authority: CA; Canada
Prior art keywords: composition according; hydrogen peroxide; peroxyacid; generator; weight
Prior art date: 1983-04-14
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

Application number

CA000452050A

Other languages

English (en)

Inventor

William R. Sanderson

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Solvay Interox Ltd

Original Assignee

Interox Chemicals Ltd

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

1983-04-14

Filing date

1984-04-16

Publication date

1986-12-02

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26285818&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CA1214607(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1983-04-14 Priority claimed from GB838310081A external-priority patent/GB8310081D0/en

1983-10-26 Priority claimed from GB838328655A external-priority patent/GB8328655D0/en

1984-04-16 Application filed by Interox Chemicals Ltd filed Critical Interox Chemicals Ltd

1986-12-02 Application granted granted Critical

1986-12-02 Publication of CA1214607A publication Critical patent/CA1214607A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 187
150000001875 compounds Chemical class 0.000 title claims abstract description 46
MHAJPDPJQMAIIY-UHFFFAOYSA-N hydrogen peroxide Substances OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims abstract description 165
150000004965 peroxy acids Chemical class 0.000 claims abstract description 67
238000005406 washing Methods 0.000 claims abstract description 59
-1 Compounds Hydrogen peroxide Chemical class 0.000 claims abstract description 56
238000000034 method Methods 0.000 claims abstract description 28
239000001257 hydrogen Substances 0.000 claims abstract description 21
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 21
230000008569 process Effects 0.000 claims abstract description 19
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 12
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 11
230000000249 desinfective effect Effects 0.000 claims abstract description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 5
DGZNTAVAPWEJPK-UHFFFAOYSA-N 1,5,5-triacetyloxypentyl acetate Chemical compound CC(=O)OC(OC(C)=O)CCCC(OC(C)=O)OC(C)=O DGZNTAVAPWEJPK-UHFFFAOYSA-N 0.000 claims abstract description 4
XXXVHMNOHZWOKW-UHFFFAOYSA-N 5,5-diacetyloxypent-1-enyl acetate Chemical compound CC(=O)OC=CCCC(OC(C)=O)OC(C)=O XXXVHMNOHZWOKW-UHFFFAOYSA-N 0.000 claims abstract description 3
150000002431 hydrogen Chemical class 0.000 claims abstract 2
239000012190 activator Substances 0.000 claims description 98
239000003995 emulsifying agent Substances 0.000 claims description 71
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical class CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 59
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 38
239000000839 emulsion Substances 0.000 claims description 33
239000004094 surface-active agent Substances 0.000 claims description 33
125000000217 alkyl group Chemical group 0.000 claims description 29
239000002904 solvent Substances 0.000 claims description 28
239000007788 liquid Substances 0.000 claims description 27
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 26
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 23
150000002148 esters Chemical class 0.000 claims description 23
125000004432 carbon atom Chemical group C* 0.000 claims description 22
239000003599 detergent Substances 0.000 claims description 20
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 16
239000002736 nonionic surfactant Substances 0.000 claims description 16
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 15
239000008346 aqueous phase Substances 0.000 claims description 15
GOKCJCODOLGYQD-UHFFFAOYSA-N 4,6-dichloro-2-imidazol-1-ylpyrimidine Chemical group ClC1=CC(Cl)=NC(N2C=NC=C2)=N1 GOKCJCODOLGYQD-UHFFFAOYSA-N 0.000 claims description 14
125000000129 anionic group Chemical group 0.000 claims description 14
239000003945 anionic surfactant Substances 0.000 claims description 14
239000007787 solid Substances 0.000 claims description 14
230000002378 acidificating effect Effects 0.000 claims description 12
125000001931 aliphatic group Chemical group 0.000 claims description 12
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 11
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 10
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 9
150000004996 alkyl benzenes Chemical class 0.000 claims description 8
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
150000001298 alcohols Chemical class 0.000 claims description 7
150000003077 polyols Chemical class 0.000 claims description 7
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims description 6
125000003118 aryl group Chemical group 0.000 claims description 6
150000002334 glycols Chemical class 0.000 claims description 6
229920001223 polyethylene glycol Polymers 0.000 claims description 6
229920005862 polyol Polymers 0.000 claims description 6
XSVSPKKXQGNHMD-UHFFFAOYSA-N 5-bromo-3-methyl-1,2-thiazole Chemical group CC=1C=C(Br)SN=1 XSVSPKKXQGNHMD-UHFFFAOYSA-N 0.000 claims description 5
239000002202 Polyethylene glycol Substances 0.000 claims description 5
125000002947 alkylene group Chemical group 0.000 claims description 5
150000001412 amines Chemical class 0.000 claims description 5
POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims description 4
230000001804 emulsifying effect Effects 0.000 claims description 4
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
NABSNBPOXKZXAJ-UHFFFAOYSA-N 1-benzoyloxyethyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OC(C)OC(=O)C1=CC=CC=C1 NABSNBPOXKZXAJ-UHFFFAOYSA-N 0.000 claims description 3
YEYKMVJDLWJFOA-UHFFFAOYSA-N 2-propoxyethanol Chemical group CCCOCCO YEYKMVJDLWJFOA-UHFFFAOYSA-N 0.000 claims description 3
125000002877 alkyl aryl group Chemical group 0.000 claims description 3
150000002170 ethers Chemical class 0.000 claims description 3
125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 claims description 3
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims description 3
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims description 2
GJQSALGXUFKDQA-UHFFFAOYSA-N C(C)(=O)O.C(C)(=O)O.C1(CCCCC(=O)OC(C)O1)=O Chemical group C(C)(=O)O.C(C)(=O)O.C1(CCCCC(=O)OC(C)O1)=O GJQSALGXUFKDQA-UHFFFAOYSA-N 0.000 claims description 2
125000003710 aryl alkyl group Chemical group 0.000 claims description 2
125000004429 atom Chemical group 0.000 claims description 2
229940067597 azelate Drugs 0.000 claims description 2
239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 2
BPBOWYWUOUJKLO-UHFFFAOYSA-N ethylidenecyclohexane Chemical group CC=C1CCCCC1 BPBOWYWUOUJKLO-UHFFFAOYSA-N 0.000 claims description 2
229920000151 polyglycol Polymers 0.000 claims description 2
239000010695 polyglycol Substances 0.000 claims description 2
229920002554 vinyl polymer Polymers 0.000 claims description 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 3
SVYKMRMTEYKNQE-UHFFFAOYSA-N 1,4,4-triacetyloxybutyl acetate Chemical compound CC(=O)OC(OC(C)=O)CCC(OC(C)=O)OC(C)=O SVYKMRMTEYKNQE-UHFFFAOYSA-N 0.000 claims 1
VFHKRVAEPRQMIC-UHFFFAOYSA-N 4,4-diacetyloxybut-1-enyl acetate Chemical group CC(=O)OC=CCC(OC(C)=O)OC(C)=O VFHKRVAEPRQMIC-UHFFFAOYSA-N 0.000 claims 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
125000005907 alkyl ester group Chemical group 0.000 claims 1
150000001414 amino alcohols Chemical class 0.000 claims 1
125000000753 cycloalkyl group Chemical group 0.000 claims 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
238000004659 sterilization and disinfection Methods 0.000 abstract description 4
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 abstract 1
GXCZOZXAPFPAFV-UHFFFAOYSA-N CC=CC(O)=O.CC=CC(O)=O.OC(=O)CCCCC(O)=O Chemical compound CC=CC(O)=O.CC=CC(O)=O.OC(=O)CCCCC(O)=O GXCZOZXAPFPAFV-UHFFFAOYSA-N 0.000 abstract 1
IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 abstract 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical class CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 abstract 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 38
239000000243 solution Substances 0.000 description 28
239000000047 product Substances 0.000 description 17
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 16
239000002253 acid Substances 0.000 description 14
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 12
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 12
150000005690 diesters Chemical class 0.000 description 12
238000003860 storage Methods 0.000 description 11
238000006243 chemical reaction Methods 0.000 description 10
239000012074 organic phase Substances 0.000 description 10
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
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 9
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
239000011541 reaction mixture Substances 0.000 description 9
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 8
238000004061 bleaching Methods 0.000 description 8
238000010992 reflux Methods 0.000 description 8
239000011734 sodium Substances 0.000 description 8
229910052708 sodium Inorganic materials 0.000 description 8
238000012360 testing method Methods 0.000 description 8
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 7
230000003115 biocidal effect Effects 0.000 description 7
239000003139 biocide Substances 0.000 description 7
239000007844 bleaching agent Substances 0.000 description 7
238000009472 formulation Methods 0.000 description 7
239000003112 inhibitor Substances 0.000 description 7
239000012071 phase Substances 0.000 description 7
229920001983 poloxamer Polymers 0.000 description 7
235000002639 sodium chloride Nutrition 0.000 description 7
238000003756 stirring Methods 0.000 description 7
229910021653 sulphate ion Inorganic materials 0.000 description 7
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 6
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 6
238000009835 boiling Methods 0.000 description 6
239000000975 dye Substances 0.000 description 6
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 6
239000004530 micro-emulsion Substances 0.000 description 6
238000002156 mixing Methods 0.000 description 6
229920000847 nonoxynol Polymers 0.000 description 6
150000003839 salts Chemical class 0.000 description 6
239000001632 sodium acetate Substances 0.000 description 6
235000017281 sodium acetate Nutrition 0.000 description 6
239000004907 Macro-emulsion Substances 0.000 description 5
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 5
239000000654 additive Substances 0.000 description 5
239000012736 aqueous medium Substances 0.000 description 5
239000007864 aqueous solution Substances 0.000 description 5
239000002585 base Substances 0.000 description 5
230000008901 benefit Effects 0.000 description 5
125000004185 ester group Chemical group 0.000 description 5
150000004665 fatty acids Chemical class 0.000 description 5
235000011187 glycerol Nutrition 0.000 description 5
244000005700 microbiome Species 0.000 description 5
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 5
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 5
150000002978 peroxides Chemical class 0.000 description 5
235000013772 propylene glycol Nutrition 0.000 description 5
239000000126 substance Substances 0.000 description 5
IEORSVTYLWZQJQ-UHFFFAOYSA-N 2-(2-nonylphenoxy)ethanol Chemical compound CCCCCCCCCC1=CC=CC=C1OCCO IEORSVTYLWZQJQ-UHFFFAOYSA-N 0.000 description 4
239000005711 Benzoic acid Substances 0.000 description 4
ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical compound N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 description 4
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
239000004166 Lanolin Substances 0.000 description 4
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 4
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
235000021355 Stearic acid Nutrition 0.000 description 4
239000002250 absorbent Substances 0.000 description 4
230000002745 absorbent Effects 0.000 description 4
150000001299 aldehydes Chemical class 0.000 description 4
239000012752 auxiliary agent Substances 0.000 description 4
235000010233 benzoic acid Nutrition 0.000 description 4
150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
239000003054 catalyst Substances 0.000 description 4
125000002091 cationic group Chemical group 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
235000014113 dietary fatty acids Nutrition 0.000 description 4
239000003085 diluting agent Substances 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
229930195729 fatty acid Natural products 0.000 description 4
230000002209 hydrophobic effect Effects 0.000 description 4
125000001165 hydrophobic group Chemical group 0.000 description 4
229940039717 lanolin Drugs 0.000 description 4
235000019388 lanolin Nutrition 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 4
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 4
VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 4
239000012418 sodium perborate tetrahydrate Substances 0.000 description 4
229910052938 sodium sulfate Inorganic materials 0.000 description 4
235000011152 sodium sulphate Nutrition 0.000 description 4
IBDSNZLUHYKHQP-UHFFFAOYSA-N sodium;3-oxidodioxaborirane;tetrahydrate Chemical compound O.O.O.O.[Na+].[O-]B1OO1 IBDSNZLUHYKHQP-UHFFFAOYSA-N 0.000 description 4
241000894007 species Species 0.000 description 4
239000008117 stearic acid Substances 0.000 description 4
239000010457 zeolite Substances 0.000 description 4
QFMDFTQOJHFVNR-UHFFFAOYSA-N 1-[2,2-dichloro-1-(4-ethylphenyl)ethyl]-4-ethylbenzene Chemical compound C1=CC(CC)=CC=C1C(C(Cl)Cl)C1=CC=C(CC)C=C1 QFMDFTQOJHFVNR-UHFFFAOYSA-N 0.000 description 3
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 3
FKOKUHFZNIUSLW-UHFFFAOYSA-N 2-Hydroxypropyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(C)O FKOKUHFZNIUSLW-UHFFFAOYSA-N 0.000 description 3
229920000742 Cotton Polymers 0.000 description 3
239000005977 Ethylene Substances 0.000 description 3
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 3
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
244000078534 Vaccinium myrtillus Species 0.000 description 3
235000017537 Vaccinium myrtillus Nutrition 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
229910052783 alkali metal Inorganic materials 0.000 description 3
239000012874 anionic emulsifier Substances 0.000 description 3
238000013459 approach Methods 0.000 description 3
239000011575 calcium Substances 0.000 description 3
229960000541 cetyl alcohol Drugs 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
VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 3
238000004821 distillation Methods 0.000 description 3
239000004744 fabric Substances 0.000 description 3
238000007429 general method Methods 0.000 description 3
230000003993 interaction Effects 0.000 description 3
239000012669 liquid formulation Substances 0.000 description 3
238000005259 measurement Methods 0.000 description 3
239000002184 metal Substances 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 3
239000012875 nonionic emulsifier Substances 0.000 description 3
230000003287 optical effect Effects 0.000 description 3
239000012044 organic layer Substances 0.000 description 3
239000002304 perfume Substances 0.000 description 3
229910052698 phosphorus Inorganic materials 0.000 description 3
239000011574 phosphorus Substances 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
238000012545 processing Methods 0.000 description 3
229940093625 propylene glycol monostearate Drugs 0.000 description 3
239000000377 silicon dioxide Substances 0.000 description 3
229940045872 sodium percarbonate Drugs 0.000 description 3
239000002689 soil Substances 0.000 description 3
239000003381 stabilizer Substances 0.000 description 3
239000007858 starting material Substances 0.000 description 3
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 3
239000002562 thickening agent Substances 0.000 description 3
238000012546 transfer Methods 0.000 description 3
ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 2
OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 2
LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 2
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 2
HXDLWJWIAHWIKI-UHFFFAOYSA-N 2-hydroxyethyl acetate Chemical class CC(=O)OCCO HXDLWJWIAHWIKI-UHFFFAOYSA-N 0.000 description 2
CTXGTHVAWRBISV-UHFFFAOYSA-N 2-hydroxyethyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCO CTXGTHVAWRBISV-UHFFFAOYSA-N 0.000 description 2
RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 2
KDSNLYIMUZNERS-UHFFFAOYSA-N 2-methylpropanamine Chemical compound CC(C)CN KDSNLYIMUZNERS-UHFFFAOYSA-N 0.000 description 2
HMFKFHLTUCJZJO-UHFFFAOYSA-N 2-{2-[3,4-bis(2-hydroxyethoxy)oxolan-2-yl]-2-(2-hydroxyethoxy)ethoxy}ethyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCOCC(OCCO)C1OCC(OCCO)C1OCCO HMFKFHLTUCJZJO-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 2
229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
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230000008859 change Effects 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
235000012000 cholesterol Nutrition 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000007957 coemulsifier Substances 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000011109 contamination Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000013256 coordination polymer Substances 0.000 description 1
239000004064 cosurfactant Substances 0.000 description 1
150000001923 cyclic compounds Chemical class 0.000 description 1
VZFUCHSFHOYXIS-UHFFFAOYSA-N cycloheptane carboxylic acid Natural products OC(=O)C1CCCCCC1 VZFUCHSFHOYXIS-UHFFFAOYSA-N 0.000 description 1
NZNMSOFKMUBTKW-UHFFFAOYSA-M cyclohexanecarboxylate Chemical group [O-]C(=O)C1CCCCC1 NZNMSOFKMUBTKW-UHFFFAOYSA-M 0.000 description 1
230000001066 destructive effect Effects 0.000 description 1
238000011161 development Methods 0.000 description 1
229940099371 diacetylated monoglycerides Drugs 0.000 description 1
125000005265 dialkylamine group Chemical group 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
238000007865 diluting Methods 0.000 description 1
238000010790 dilution Methods 0.000 description 1
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150000002009 diols Chemical class 0.000 description 1
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 description 1
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239000003651 drinking water Substances 0.000 description 1
229960001484 edetic acid Drugs 0.000 description 1
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238000004508 fractional distillation Methods 0.000 description 1
IREPGQRTQFRMQR-UHFFFAOYSA-N furantetracarboxylic acid Chemical compound OC(=O)C=1OC(C(O)=O)=C(C(O)=O)C=1C(O)=O IREPGQRTQFRMQR-UHFFFAOYSA-N 0.000 description 1
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238000004817 gas chromatography Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000000174 gluconic acid Substances 0.000 description 1
235000012208 gluconic acid Nutrition 0.000 description 1
JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
125000005456 glyceride group Chemical group 0.000 description 1
RZRNAYUHWVFMIP-HXUWFJFHSA-N glycerol monolinoleate Natural products CCCCCCCCC=CCCCCCCCC(=O)OC[C@H](O)CO RZRNAYUHWVFMIP-HXUWFJFHSA-N 0.000 description 1
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 1
231100001261 hazardous Toxicity 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000008235 industrial water Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
238000011835 investigation Methods 0.000 description 1
239000002563 ionic surfactant Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
230000007794 irritation Effects 0.000 description 1
229940099367 lanolin alcohols Drugs 0.000 description 1
239000010410 layer Substances 0.000 description 1
239000012263 liquid product Substances 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
239000000155 melt Substances 0.000 description 1
BQPIGGFYSBELGY-UHFFFAOYSA-N mercury(2+) Chemical compound [Hg+2] BQPIGGFYSBELGY-UHFFFAOYSA-N 0.000 description 1
229910021645 metal ion Inorganic materials 0.000 description 1
XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
150000004682 monohydrates Chemical class 0.000 description 1
239000000178 monomer Substances 0.000 description 1
BTSRIWFABHLYDQ-UHFFFAOYSA-N n,n-dimethyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)N(C)C BTSRIWFABHLYDQ-UHFFFAOYSA-N 0.000 description 1
AMQJEAYHLZJPGS-UHFFFAOYSA-N n-butyl carbinol Natural products CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000011356 non-aqueous organic solvent Substances 0.000 description 1
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 1
WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 1
WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
229940055577 oleyl alcohol Drugs 0.000 description 1
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
UFOIOXZLTXNHQH-UHFFFAOYSA-N oxolane-2,3,4,5-tetracarboxylic acid Chemical compound OC(=O)C1OC(C(O)=O)C(C(O)=O)C1C(O)=O UFOIOXZLTXNHQH-UHFFFAOYSA-N 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000003973 paint Substances 0.000 description 1
229910052763 palladium Inorganic materials 0.000 description 1
239000002245 particle Substances 0.000 description 1
244000052769 pathogen Species 0.000 description 1
230000001717 pathogenic effect Effects 0.000 description 1
125000005342 perphosphate group Chemical group 0.000 description 1
150000003009 phosphonic acids Chemical class 0.000 description 1
150000004714 phosphonium salts Chemical class 0.000 description 1
PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical class NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920000570 polyether Chemical group 0.000 description 1
229920002523 polyethylene Glycol 1000 Polymers 0.000 description 1
239000001205 polyphosphate Substances 0.000 description 1
235000011176 polyphosphates Nutrition 0.000 description 1
150000003109 potassium Chemical class 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
159000000001 potassium salts Chemical class 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
NJEVMKZODGWUQT-UHFFFAOYSA-N propane-1,1,3,3-tetracarboxylic acid Chemical compound OC(=O)C(C(O)=O)CC(C(O)=O)C(O)=O NJEVMKZODGWUQT-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
229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 1
229940005657 pyrophosphoric acid Drugs 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
238000009877 rendering Methods 0.000 description 1
238000011160 research Methods 0.000 description 1
239000011369 resultant mixture Substances 0.000 description 1
238000002390 rotary evaporation Methods 0.000 description 1
OARRHUQTFTUEOS-UHFFFAOYSA-N safranin Chemical compound [Cl-].C=12C=C(N)C(C)=CC2=NC2=CC(C)=C(N)C=C2[N+]=1C1=CC=CC=C1 OARRHUQTFTUEOS-UHFFFAOYSA-N 0.000 description 1
238000005070 sampling Methods 0.000 description 1
238000005204 segregation Methods 0.000 description 1
239000003352 sequestering agent Substances 0.000 description 1
239000010865 sewage Substances 0.000 description 1
238000010008 shearing Methods 0.000 description 1
230000035939 shock Effects 0.000 description 1
239000002002 slurry Substances 0.000 description 1
238000002791 soaking Methods 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000001509 sodium citrate Substances 0.000 description 1
NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
229960001922 sodium perborate Drugs 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
229910052911 sodium silicate Inorganic materials 0.000 description 1
235000019832 sodium triphosphate Nutrition 0.000 description 1
RBWSWDPRDBEWCR-RKJRWTFHSA-N sodium;(2r)-2-[(2r)-3,4-dihydroxy-5-oxo-2h-furan-2-yl]-2-hydroxyethanolate Chemical compound [Na+].[O-]C[C@@H](O)[C@H]1OC(=O)C(O)=C1O RBWSWDPRDBEWCR-RKJRWTFHSA-N 0.000 description 1
RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
BTJYKXPSPBJJDQ-UHFFFAOYSA-M sodium;1,4-bis(4-methylpentan-2-yloxy)-1,4-dioxobutane-2-sulfonate Chemical compound [Na+].CC(C)CC(C)OC(=O)CC(S([O-])(=O)=O)C(=O)OC(C)CC(C)C BTJYKXPSPBJJDQ-UHFFFAOYSA-M 0.000 description 1
FNXKBSAUKFCXIK-UHFFFAOYSA-M sodium;hydrogen carbonate;8-hydroxy-7-iodoquinoline-5-sulfonic acid Chemical class [Na+].OC([O-])=O.C1=CN=C2C(O)=C(I)C=C(S(O)(=O)=O)C2=C1 FNXKBSAUKFCXIK-UHFFFAOYSA-M 0.000 description 1
MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
239000012265 solid product Substances 0.000 description 1
229940035044 sorbitan monolaurate Drugs 0.000 description 1
239000001587 sorbitan monostearate Substances 0.000 description 1
235000011076 sorbitan monostearate Nutrition 0.000 description 1
229940035048 sorbitan monostearate Drugs 0.000 description 1
229960005078 sorbitan sesquioleate Drugs 0.000 description 1
239000001589 sorbitan tristearate Substances 0.000 description 1
235000011078 sorbitan tristearate Nutrition 0.000 description 1
229960004129 sorbitan tristearate Drugs 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000010186 staining Methods 0.000 description 1
TYFQFVWCELRYAO-UHFFFAOYSA-L suberate(2-) Chemical compound [O-]C(=O)CCCCCCC([O-])=O TYFQFVWCELRYAO-UHFFFAOYSA-L 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
229940032085 sucrose monolaurate Drugs 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical class S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 description 1
239000001117 sulphuric acid Substances 0.000 description 1
235000011149 sulphuric acid Nutrition 0.000 description 1
239000000271 synthetic detergent Substances 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
239000003784 tall oil Substances 0.000 description 1
150000003899 tartaric acid esters Chemical class 0.000 description 1
150000004685 tetrahydrates Chemical class 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
125000005270 trialkylamine group Chemical group 0.000 description 1
229940087291 tridecyl alcohol Drugs 0.000 description 1
150000004684 trihydrates Chemical class 0.000 description 1
210000001635 urinary tract Anatomy 0.000 description 1
244000000072 vaginal pathogen Species 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
229940082509 xanthan gum Drugs 0.000 description 1
235000010493 xanthan gum Nutrition 0.000 description 1
229910052724 xenon Inorganic materials 0.000 description 1
FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
239000002888 zwitterionic surfactant Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0004—Non aqueous liquid compositions comprising insoluble particles
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/0017—Multi-phase liquid compositions
- C11D17/0021—Aqueous microemulsions
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
- C11D3/3907—Organic compounds
- C11D3/391—Oxygen-containing compounds
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3945—Organic per-compounds
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3947—Liquid compositions

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Inorganic Chemistry (AREA)
Detergent Compositions (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CA000452050A 1983-04-14 1984-04-16 Compositions au peroxygene Expired CA1214607A (fr)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
GB8310081		1983-04-14
GB838310081A GB8310081D0 (en)	1983-04-14	1983-04-14	Peroxygen compounds
GB8328655		1983-10-26
GB838328655A GB8328655D0 (en)	1983-10-26	1983-10-26	Peroxygen compound compositions

Publications (1)

Publication Number	Publication Date
CA1214607A true CA1214607A (fr)	1986-12-02

Family

ID=26285818

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000452050A Expired CA1214607A (fr)	1983-04-14	1984-04-16	Compositions au peroxygene

Country Status (6)

Country	Link
EP (1)	EP0125781B1 (fr)
BR (1)	BR8401735A (fr)
CA (1)	CA1214607A (fr)
DE (1)	DE3465334D1 (fr)
ES (2)	ES8605571A1 (fr)
YU (1)	YU68184A (fr)

Families Citing this family (45)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4772413A (en) *	1986-08-28	1988-09-20	Colgate-Palmolive Company	Nonaqueous liquid nonbuilt laundry detergent bleach booster composition containing diacetyl methyl amine and method of use
NZ221555A (en) *	1986-09-09	1989-08-29	Colgate Palmolive Co	Detergent composition containing inorganic bleach and a liquid activator
DE3918525A1 (de) *	1989-06-07	1990-12-13	Hoechst Ag	Polymerisate, verfahren zu deren herstellung und deren verwendung als bleichaktivatoren mit buildereigenschaften
GB9025624D0 (en) *	1990-11-26	1991-01-09	S B Chemicals Limited	Liquid built detergent concentrates
GB9025691D0 (en) *	1990-11-26	1991-01-09	S B Chemicals Limited	Liquid built detergent concentrates
GB9109929D0 (en) *	1991-05-08	1991-07-03	Interox Chemicals Ltd	Thickened compositions
DE4123333A1 (de) *	1991-07-15	1993-01-21	Henkel Kgaa	Mehrkomponenten-waschmittelsystem
DE69226072T2 (de) *	1992-04-03	1999-02-25	The Procter & Gamble Co., Cincinnati, Ohio	Durch Säure aktivierte Bleichzusammensetzung
GB9302442D0 (en) *	1993-02-08	1993-03-24	Warwick Int Group	Oxidising agents
GB9302441D0 (en) *	1993-02-08	1993-03-24	Warwick Int Group	Oxidising agents
GB9323634D0 (en) *	1993-11-16	1994-01-05	Warwick Int Ltd	Bleach activator compositions
US5902354A (en) *	1994-04-12	1999-05-11	The Procter & Gamble Company	Bleaching compositions
EP0677575A1 (fr) *	1994-04-12	1995-10-18	The Procter & Gamble Company	Compositions de blanchiment
FR2728171B1 (fr) *	1994-12-14	1997-01-24	Chemoxal Sa	Production de formulations desinfectantes biocides, a base d'ions peracetiques
EP0751214A1 (fr) *	1995-06-30	1997-01-02	The Procter & Gamble Company	Compositions de blanchiment stables contenant des agents de blanchiment péroxydés
ES2173151T3 (es) *	1995-03-27	2002-10-16	Procter & Gamble	Composiciones blanqueantes liquidas activadas.
US5792385A (en) *	1995-05-25	1998-08-11	The Clorox Company	Liquid peracid precursor colloidal dispersions: liquid crystals
US5681805A (en) *	1995-05-25	1997-10-28	The Clorox Company	Liquid peracid precursor colloidal dispersions: microemulsions
US5954998A (en) *	1995-05-25	1999-09-21	The Clorox Company	Liquid peracid precursor colloidal dispersions: oil-core vesicles
US5776877A (en) *	1995-05-25	1998-07-07	The Clorox Company	Liquid peracid precursor colloidal dispersions: macroemulsions
EP0751210A1 (fr) *	1995-06-27	1997-01-02	The Procter & Gamble Company	Compositions de blanchiment
CA2238620C (fr) *	1995-11-27	2002-01-22	The Procter & Gamble Company	Composition pour traiter des taches sur des textiles a laver et procede de traitement
GB9600159D0 (en) *	1996-01-05	1996-03-06	Warwick Int Group	Process for bleaching or disinfecting a substrate
DE19712095A1 (de) *	1997-03-22	1998-09-24	Henkel Kgaa	Bisacylacetale als Bleichaktivatoren für Wasch- und Reinigungsmittel
ITVR980033A1 (it) *	1998-04-30	1999-10-30	Farmec Di Tabasso Renato & C S	Procedimento per l'ottenimento estemporaneo di un disinfettante a base di acido peracetico.
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US7150884B1 (en)	2000-07-12	2006-12-19	Ecolab Inc.	Composition for inhibition of microbial growth
US7316824B2 (en)	2000-12-15	2008-01-08	Ecolab Inc.	Method and composition for washing poultry during processing
US6514556B2 (en)	2000-12-15	2003-02-04	Ecolab Inc.	Method and composition for washing poultry during processing
GB0128052D0 (en)	2001-11-22	2002-01-16	Drug Discovery Lab As	Compounds
US6740193B2 (en) *	2001-12-21	2004-05-25	Henkel Corporation	Gem-diesters and epoxidized derivatives thereof
US7504123B2 (en)	2004-01-09	2009-03-17	Ecolab Inc.	Methods for washing poultry during processing with medium chain peroxycarboxylic acid compositions
US7887641B2 (en)	2004-01-09	2011-02-15	Ecolab Usa Inc.	Neutral or alkaline medium chain peroxycarboxylic acid compositions and methods employing them
US8999175B2 (en)	2004-01-09	2015-04-07	Ecolab Usa Inc.	Methods for washing and processing fruits, vegetables, and other produce with medium chain peroxycarboxylic acid compositions
US7771737B2 (en)	2004-01-09	2010-08-10	Ecolab Inc.	Medium chain peroxycarboxylic acid compositions
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EP1703791B1 (fr)	2004-01-09	2014-07-23	Ecolab Inc.	Compositions d'acide peroxycarboxylique a chaine moyenne
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JP6802166B2 (ja)	2014-12-18	2020-12-16	エコラボユーエスエーインコーポレイティド	多価アルコールホルマートによるペルオキシギ酸の生成
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US4496473A (en)	1982-04-27	1985-01-29	Interox Chemicals Limited	Hydrogen peroxide compositions
GB8310080D0 (en)	1983-04-14	1983-05-18	Interox Chemicals Ltd	Bleach composition

1984
- 1984-04-09 EP EP19840302410 patent/EP0125781B1/fr not_active Expired
- 1984-04-09 DE DE8484302410T patent/DE3465334D1/de not_active Expired
- 1984-04-13 ES ES531633A patent/ES8605571A1/es not_active Expired
- 1984-04-13 BR BR8401735A patent/BR8401735A/pt not_active IP Right Cessation
- 1984-04-13 YU YU68184A patent/YU68184A/xx unknown
- 1984-04-16 CA CA000452050A patent/CA1214607A/fr not_active Expired
1985
- 1985-07-01 ES ES544775A patent/ES8604638A1/es not_active Expired

Also Published As

Publication number	Publication date
ES8605571A1 (es)	1986-03-16
DE3465334D1 (en)	1987-09-17
ES544775A0 (es)	1986-02-01
EP0125781A1 (fr)	1984-11-21
EP0125781B1 (fr)	1987-08-12
ES531633A0 (es)	1986-03-16
ES8604638A1 (es)	1986-02-01
BR8401735A (pt)	1984-11-20
YU68184A (en)	1988-04-30

Legal Events

Date	Code	Title	Description
2004-04-16	MKEX	Expiry
2023-08-23	MKEX	Expiry	Effective date: 20040416

Publication	Publication Date	Title
CA1214607A (fr)	1986-12-02	Compositions au peroxygene
US4541944A (en)	1985-09-17	Compositions and processes employing activators for the generation of peroxyacids
AU662501B2 (en)	1995-09-07	Liquid detergent compositions containing a suspended peroxygen bleach
EP0086511B1 (fr)	1986-07-02	Compositions détergentes liquides contenant un agent de blanchiment oxydant
US5597790A (en)	1997-01-28	Liquid detergent compositions containing a suspended peroxygen bleach
US4347149A (en)	1982-08-31	Aqueous bleach compositions
EP0293040B1 (fr)	1991-12-11	Composition détergente liquide contenant un agent de blanchiment peroxydant
AU2007317613B2 (en)	2012-12-06	Liquid detergent formulation with hydrogen peroxide
EP0241137B1 (fr)	1990-07-18	Composition de blanchiment au peroxyde d'hydrogène liquide contenant un activeur peracide
CA1299054C (fr)	1992-04-21	Agent de renfort de blanchiment, liquide, non aqueux et sans adjuvant
US4783278A (en)	1988-11-08	Concentrated liquid compositions containing a peroxygen compound
US4704404A (en)	1987-11-03	Peroxygen-compounds
US4497725A (en)	1985-02-05	Aqueous bleach compositions
EP0273472A1 (fr)	1988-07-06	Compositions détergentes aqueuses contenant du diéthylenglycol monohexyl éther comme solvant
JPH073293A (ja)	1995-01-06	半透明で等方性の水性液状漂白剤組成物
JPH03200899A (ja)	1991-09-02	安定化された漂白剤含有液体洗剤組成物
US5250212A (en)	1993-10-05	Liquid detergent containing solid peroxygen bleach and solvent system comprising water and lower aliphatic monoalcohol
IE900096L (en)	1990-07-10	Liquid detergent composition containing enzyme and enzyme¹stabilization system
EP0037184A2 (fr)	1981-10-07	Compositions détergentes liquides, leur préparation et leur utilisation dans des procédés de lavage
JPH03210399A (ja)	1991-09-13	塩素を含まない液体自動皿洗い組成物
US4536313A (en)	1985-08-20	Peroxygen compound
GB2072643A (en)	1981-10-07	Aqueous H2O2 bleach compositions
IE860858L (en)	1986-09-29	Liquid laundry detergent-bleach composition
JPH0625700A (ja)	1994-02-01	過酸素漂白剤組成物
EP0105690A1 (fr)	1984-04-18	Compositions de blanchiment