US3375199A - Cleaner-disinfectant composition - Google Patents
Cleaner-disinfectant composition Download PDFInfo
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- US3375199A US3375199A US327081A US32708163A US3375199A US 3375199 A US3375199 A US 3375199A US 327081 A US327081 A US 327081A US 32708163 A US32708163 A US 32708163A US 3375199 A US3375199 A US 3375199A
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- 239000000203 mixture Substances 0.000 title claims description 47
- 239000000645 desinfectant Substances 0.000 title description 9
- 239000003599 detergent Substances 0.000 claims description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
- 150000003839 salts Chemical class 0.000 claims description 17
- 239000007787 solid Substances 0.000 claims description 10
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 9
- -1 INORGANIC ACID SALT Chemical class 0.000 claims description 8
- 230000000249 desinfective effect Effects 0.000 claims description 5
- 244000005700 microbiome Species 0.000 claims description 5
- 235000019832 sodium triphosphate Nutrition 0.000 claims description 5
- 238000004140 cleaning Methods 0.000 claims description 4
- 230000001747 exhibiting effect Effects 0.000 claims description 4
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- OJLOUXPPKZRTHK-UHFFFAOYSA-N dodecan-1-ol;sodium Chemical compound [Na].CCCCCCCCCCCCO OJLOUXPPKZRTHK-UHFFFAOYSA-N 0.000 claims description 3
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 2
- 229940090668 parachlorophenol Drugs 0.000 claims description 2
- 238000004659 sterilization and disinfection Methods 0.000 claims description 2
- 239000000243 solution Substances 0.000 description 25
- 230000002070 germicidal effect Effects 0.000 description 22
- 239000004615 ingredient Substances 0.000 description 19
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 14
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 13
- 150000002989 phenols Chemical class 0.000 description 11
- 238000012360 testing method Methods 0.000 description 10
- 229910000029 sodium carbonate Inorganic materials 0.000 description 7
- NCKMMSIFQUPKCK-UHFFFAOYSA-N 2-benzyl-4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1CC1=CC=CC=C1 NCKMMSIFQUPKCK-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 238000010790 dilution Methods 0.000 description 5
- 239000012895 dilution Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000006260 foam Substances 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000002304 perfume Substances 0.000 description 5
- 241000894006 Bacteria Species 0.000 description 4
- 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 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000001488 sodium phosphate Substances 0.000 description 4
- 241000607142 Salmonella Species 0.000 description 3
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 3
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 229920000388 Polyphosphate Polymers 0.000 description 2
- 239000004115 Sodium Silicate Substances 0.000 description 2
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 2
- 241000191940 Staphylococcus Species 0.000 description 2
- 241000191967 Staphylococcus aureus Species 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 239000001205 polyphosphate Substances 0.000 description 2
- 235000011176 polyphosphates Nutrition 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 2
- 235000019351 sodium silicates Nutrition 0.000 description 2
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 2
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 2
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 2
- 235000019801 trisodium phosphate Nutrition 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N 1-Tetradecanol Natural products CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 238000009631 Broth culture Methods 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 208000035473 Communicable disease Diseases 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 229910000318 alkali metal phosphate Inorganic materials 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229940096386 coconut alcohol Drugs 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000002458 infectious effect Effects 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- 230000017066 negative regulation of growth Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 238000012546 transfer Methods 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
-
- 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
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/06—Phosphates, including polyphosphates
-
- 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
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/10—Carbonates ; Bicarbonates
Definitions
- This invention relates to a cleaner-disinfectant composition particularly suitablefor hard surface cleansing comprising in particular combination a halogenated phenolic germicide and detersive ingredients which on dissolution in Water yields solutions having effective cleansing action combined with broadly effective disinfecting action, as hereinafter described.
- Solid, granular detergent compositions intended to be dissolved in water to form detergent solutions have been used in households and industry for cleaning floors, walls, etc. These powders may contain alkaline inorganic detergent salt such as phosphate or carbonate and a minor proportion of an organic anionic or nonionic detergent as the active constituents.
- alkaline inorganic detergent salt such as phosphate or carbonate
- an organic anionic or nonionic detergent as the active constituents.
- distribution and use of such compositions have been limited because these formulations are not particularly effective in destroying some of the common infectious bacteria. Therefore, the possible formulation of such a composition with both good disinfecting and detergent properties would be desira'ble, and such a product would be particularl valuable for use in hospitals, institutions, restaurants, hotels, the dairy and beverage industries, as Well as homes.
- cleanser-disinfectant compositions be effective in destroying vegetative cells, including pathogenic organisms such as staphylococcus, if possible. It is well known that phenols and especially chlorinated phenols are effective germicides. It is also recognized that the chlorinated phenols are less soluble in water than the non-chlorinated compounds.
- substituted chlorinated phenols having an alkyl or aralkyl group on the phenol molecule are known to have germicidal activity but such substituent reduces the solubility of the organic phenol still further, and the net result is that a difficult formulation problem exists because of their-limited solubility.
- compositions which are particularly suitable for hard surface cleansing such as on floors and Walls, comprise a major proportion, e.g. about 90 to 98.5% of water-soluble alkaline inorganic salts, and a minor proportion, e.g., about /2 to 5%, of a watersoluble aliphatic primary. sulfated.
- a solid, granular, free flowing detergent composition stable upon aging which comprises about 55 to of water-soluble alkaline inorganic normal builder salts, about 15 to 40% of Water-soluble alkaline inorganic acid salt, preferably with about /2 to 3% of a water-soluble aliphatic primary fatty alcohol sulfate and about 1 to 4% of ortho-benzylpara-halogenated phenol, the ratio of said'd'etergent to said halogenated phenol being from about 1:2 to 3:4 by weight, said amounts being by weight. of the above ingredients and proportioned to form 'a water solution having a pH of about 9.4 to 10.2 with said halogenated phenol essentially in solution and exhibiting effective disinfecting action.
- a preferred embodiment comprises about 35 to 55% by weight of sodium carbonate, about 15 to 25% by weight of sodium .polyphosphate, about 20 to 30% by weight of sodium bicarbonate, about 2% by weight of sodium lauryl alcohol sulfate and about 3 to 4% by weight of ortho-berizyl-para-chlorophenol having a pH of about 9.6 to 10:0.
- compositions of the present invention are the resultant or unitary effects produced by the particular combinations of ingredients and their proportions, alkalinity, etc. For the sake of simplicity, these factors will be discussed individually to some extent. In general, the exercise of careful choice in the components and in their proportions as described will result in satisfactory compositions exhibiting desired deter'sive and foaming properties, solubility in water under specific conditions at use concentrations and high phenol coefficients in the AOAC Phenol Coefiicienttest as herein described.
- the major ingredients are the water-soluble alkaline inorganic salts, usually from about 98.5% by weight. It is preferred for optimum effects to use .a mixture of alkaline inorganic normal builder salts and acid salts proportioned to yield desired detersive properties and pH in solution.
- a variety of water-soluble alkaline inorganic normal builder salts may be employed.
- suitable alkaline salts that may be mentioned are the alkali metal carbonates, phosphates and silicate salts such as sodium and potassium carbonate, sodium and potassium tripolyphosphates and pyrophosphates, trisodium orthophos-phate and sodium silicates having an Na O to SiOg ratio of about 1:1 to about 1:35 by weight.
- Such salts may be used alone or in any desired mixtures, the choice being influenced usually by economics or the par.- ticulate product features it is desired to emphasize. It is preferred to include an alkali metal polyphosphate such as sodium pyrophosphate or tripolyphosphate Which is particularly effective herein for water softening and as a detergent aid in combination with other low cost detergent builders such as sodium carbonate or the sodium silicates.
- alkaline normal builder salts will generally form a major proportion of the composition, usually. in an amount by weight of about 55 to 80% by Weight of said mixture of ingredients.
- the water soluble inorganic acid salts suitable for use are the alkali metal acid carbonates and various acid phosphates. Typical examples are sodium acid carbonate (bicarbonate). disodium phosphate and monosodium phosphate, with the acid carbonate as the preferred material for this composition.
- Such use of inorganic acid salts has multiple advantages also including added hard surface detergent action and buffering capacity for the composition.
- the proportion is generally a minor proportion of the total solids and is proportionedwith the other ingredients so that the water-solution containing /2 to 2% of the composition will have a pH from the range of 9.4 to about 10.2 as it has been found that germicidal efficiency in this pH range is at an optimum.
- said acid salts will be present in an amount by weight of about 15-40% of the said ingredients.
- the detergent should be a water-soluble aliphatic primary sulfated detergent compatible with said germicide and inorganic salts.
- Particularly suitable detergents are the water-soluble primary sulfuric esters of aliphatic alcohols having the necessary compatibility, especially those containing 10 to 14 carbon atoms in the aliphatic group. It is preferred to use the alkali metal lauryl, coconut and myristyl alcohol sulfates, though other suitable watersoluble salts such as the ammonium and alkylolamine, e.g., triethanolamine salts may be employed also in suitable amount.
- Such detersive salts enhance the detergent action of the inorganic salts, emulsify oily soils, provide a minor amount of unstable foam and assist in the solubilization of the ortho-benzyl-para-halogenated-phenol.
- suitable compositions should be characterized by low foam levels in dilute solutions to eliminate foam streaks on the hard surfaces and to minimize the need for rinsing which would necessarily dilute the germicidal effectiveness.
- the detergent should be in minor amounts required for effective hard surface cleansing and low foam and the proportion required should be sufficient to solubilize the germicidal phenol in diluted use concentrations of product.
- Concentrations of about /2 to preferably /2 to 3%, of such detergent have been found to be satisfactory when proportioned with 1 to 5%, preferably 14%, of ortho-benzyl-para-chlorophenol or the like.
- the ratio of detergent to said phenolic compound is from about 1:1 to 1:4 range, preferably 1:2 to 3:4 by weight in order to maintain the germicidal activity of the compositions at a high level without any substantial adverse effect by the detergent. Therefore, too high a proportion of said detergent tends to reduce germicidal effectiveness and too low a proportion also reduces germicidal effectiveness because of insolubilization of said germicide.
- water solutions containing 0.5 to 2% of said mixtures should be substantially clear because the germicidal compound tends to separate rapidly in cloudy water dispersions. Such separation during use results in non-homogeneous mixtures with respect to the germicide and, hence, the disinfectant action will vary widely. To achieve the desired clarity, both the type of detergent and its concentration should be carefully correlated with the type and amount of said germicide.
- the suitable phenolic germicidal compounds are the ortho-benzyl-para-halogenated-phenol derivatives wherein the halogen is selected from the group consisting of chlorine, bromine and iodine.
- Ortho-benzyl-para-chlorophenol is a particularly satisfactory compound in compositions of the invention.
- the instant compositions are outstanding because of their potency against a wide variety of bacteria and fungi in low concentrations in addition to the other desirable properties.
- alkaline detergent compositions containing phenolic germicides have generally been singularly effective against either Gram-negative (Salmonella typhosa) or Gram-positive (Staphylococcus aureus) organisms.
- the instant alkaline compositions are effective against both types of organisms as well as fungi.
- the metal loops are generally re-subcultured and incubated for another 48 hour period at 37 C. to demonstrate that a true kill is obtained as opposed to stasis or inhibition of growth.
- compositions may also beneficially include suitable amounts of adjuvant materials such as coloring agents, perfumes, and other additives.
- compositions are advantageously marketed in the form of dry, free flowing granules containing the ingredients in homogeneous admixture, such that a definite weight of product may be used to give a solution of definite proportions of the ingredients.
- the compositions are prepared by adding in a suitable manner either powdered ortho-benzyl-para-chlorophenol or a concentrated solution of ortho-benzyl-para-chlorophenol in isopropanol for example to a blend of the granular inorganic compounds and dry detergent using a suitable dry blender, e.g., ribbon mixer, sigma mixer, twin shell blender, twin cone blender, rotary drum, etc. Any suitable particle size may be employed as desired. Color solution and perfume may advantageously be combined with the concentrated germicidal solution in the manufacture of this product if desired.
- compositions containing various detergents such as sodium dodecyl benzene sulfonate, higher alkyl phenolethylene oxide condensates or sodium disu'lfonated dodecyl diphenyl oxide form cloudy solutions with decreased etfectiveness.
- compositions of this invention present several additional advantages.
- the compositions are relatively simple to prepare on present equipment without changes in design.
- the ingredients are readily available through commercial channels at economically attractive prices.
- the new compositions can be used on a Wide variety of surfaces without fear of damage.
- Other advantages will be readily apparent to those skilled in the art.
- a solid granular free flowing detergent composition particularly suit-able for hard surface cleaning and disinfection consisting essentially of about 35 to by weight of sodium carbonate and about 15 to 25% by weight of sodium tripolyphos-phate, as water soluble inorganic normal builder salts, about 20 to 30% by weight of sodium bicarbonate as water soluble inorganic acid salt, about 2% by weight of sodium lauryl alcohol sulfate and about 3 to 4% by Weight of ortho-benzyl-parach'lorophenol, said amounts being by weight of total solids proportioned to form a water solution containing from about /2 to 2% by weight of said solids having a pH of about 9.6 to 10 with said chlorophenol essentially in solution and exhibiting thereby effective disinfecting action against a broad spectrum of microorganisms.
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- 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)
Description
United States Patent 3,375,199 CLEANER-DISINFECTANT COMPOSITION Robert Henry Trimmer, East Brunswick, N.'J., assignor to Colgate-Palmolive Cmpauy,-New York, N .Y., a corporation of Delaware No'Drawing. Filed Nov. 29, 1963, Ser. No.'327,081 1 Claim. (Cl. 252106) This invention relates to a cleaner-disinfectant composition particularly suitablefor hard surface cleansing comprising in particular combination a halogenated phenolic germicide and detersive ingredients which on dissolution in Water yields solutions having effective cleansing action combined with broadly effective disinfecting action, as hereinafter described.
Solid, granular detergent compositions intended to be dissolved in water to form detergent solutions have been used in households and industry for cleaning floors, walls, etc. These powders may contain alkaline inorganic detergent salt such as phosphate or carbonate and a minor proportion of an organic anionic or nonionic detergent as the active constituents. However, distribution and use of such compositions have been limited because these formulations are not particularly effective in destroying some of the common infectious bacteria. Therefore, the possible formulation of such a composition with both good disinfecting and detergent properties would be desira'ble, and such a product would be particularl valuable for use in hospitals, institutions, restaurants, hotels, the dairy and beverage industries, as Well as homes.
The problem of microbial or bacterial contamination is an important one since man contacts infectious diseases through the spread of micro-organisms. Therefore, it is desirable that cleanser-disinfectant compositions be effective in destroying vegetative cells, including pathogenic organisms such as staphylococcus, if possible. It is well known that phenols and especially chlorinated phenols are effective germicides. It is also recognized that the chlorinated phenols are less soluble in water than the non-chlorinated compounds. Similarly, substituted chlorinated phenols having an alkyl or aralkyl group on the phenol molecule are known to have germicidal activity but such substituent reduces the solubility of the organic phenol still further, and the net result is that a difficult formulation problem exists because of their-limited solubility.
In addition to the problems of water solubility mentioned above, this formulation problem is further complicated by the fact that in general phenolic germicides are less active in alkaline solutions than acid solutions. In addition, other ingredients such as inorganic salts, organic detergents, organic solubilizers, e.g., alcohol, etc., are known to have adverse effects on germicidal activity. Such effects are readily apparent by the formation of a nonhomogeneous solution at use-dilution concentrations in water or by low phenol coefficients in the AOAC Phenol 1 Coefficient test.
It has now been found that highly effective alkaline cleaning-distinfectant compositions which are particularly suitable for hard surface cleansing such as on floors and Walls, comprise a major proportion, e.g. about 90 to 98.5% of water-soluble alkaline inorganic salts, and a minor proportion, e.g., about /2 to 5%, of a watersoluble aliphatic primary. sulfated. detergent and a minor proportion, e.g., 1 to 5%, of orthobenzyl-p araehalogenated phenol, said amounts being .by weight of the above ingredients and proportioned so that the ratio of said detergent to said halogenated phenol is from the range of about 1:1 to about 1:4 by weight and a water solution containing from about /2 to about 2% by weight of said composition has a pH of about 9:4 to 10.2, with 3,375,199 Patented Mar. '26, '1968 ice said halogenated phenol being presentin solution in a concentration thereby suitable for effective disinfectant action. In particular, there may be prepared a solid, granular, free flowing detergent composition stable upon aging which comprises about 55 to of water-soluble alkaline inorganic normal builder salts, about 15 to 40% of Water-soluble alkaline inorganic acid salt, preferably with about /2 to 3% of a water-soluble aliphatic primary fatty alcohol sulfate and about 1 to 4% of ortho-benzylpara-halogenated phenol, the ratio of said'd'etergent to said halogenated phenol being from about 1:2 to 3:4 by weight, said amounts being by weight. of the above ingredients and proportioned to form 'a water solution having a pH of about 9.4 to 10.2 with said halogenated phenol essentially in solution and exhibiting effective disinfecting action. A preferred embodiment comprises about 35 to 55% by weight of sodium carbonate, about 15 to 25% by weight of sodium .polyphosphate, about 20 to 30% by weight of sodium bicarbonate, about 2% by weight of sodium lauryl alcohol sulfate and about 3 to 4% by weight of ortho-berizyl-para-chlorophenol having a pH of about 9.6 to 10:0.
The desirable characteristics of the compositions of the present invention are the resultant or unitary effects produced by the particular combinations of ingredients and their proportions, alkalinity, etc. For the sake of simplicity, these factors will be discussed individually to some extent. In general, the exercise of careful choice in the components and in their proportions as described will result in satisfactory compositions exhibiting desired deter'sive and foaming properties, solubility in water under specific conditions at use concentrations and high phenol coefficients in the AOAC Phenol Coefiicienttest as herein described.
As indicated, the major ingredients are the water-soluble alkaline inorganic salts, usually from about 98.5% by weight. It is preferred for optimum effects to use .a mixture of alkaline inorganic normal builder salts and acid salts proportioned to yield desired detersive properties and pH in solution. A variety of water-soluble alkaline inorganic normal builder salts may be employed. Among the suitable alkaline salts that may be mentioned are the alkali metal carbonates, phosphates and silicate salts such as sodium and potassium carbonate, sodium and potassium tripolyphosphates and pyrophosphates, trisodium orthophos-phate and sodium silicates having an Na O to SiOg ratio of about 1:1 to about 1:35 by weight. Such salts may be used alone or in any desired mixtures, the choice being influenced usually by economics or the par.- ticulate product features it is desired to emphasize. It is preferred to include an alkali metal polyphosphate such as sodium pyrophosphate or tripolyphosphate Which is particularly effective herein for water softening and as a detergent aid in combination with other low cost detergent builders such as sodium carbonate or the sodium silicates. Such alkaline normal builder salts will generally form a major proportion of the composition, usually. in an amount by weight of about 55 to 80% by Weight of said mixture of ingredients.
The water soluble inorganic acid salts suitable for use are the alkali metal acid carbonates and various acid phosphates. Typical examples are sodium acid carbonate (bicarbonate). disodium phosphate and monosodium phosphate, with the acid carbonate as the preferred material for this composition. Such use of inorganic acid salts has multiple advantages also including added hard surface detergent action and buffering capacity for the composition. The proportion is generally a minor proportion of the total solids and is proportionedwith the other ingredients so that the water-solution containing /2 to 2% of the composition will have a pH from the range of 9.4 to about 10.2 as it has been found that germicidal efficiency in this pH range is at an optimum. Usually said acid salts will be present in an amount by weight of about 15-40% of the said ingredients.
The detergent should be a water-soluble aliphatic primary sulfated detergent compatible with said germicide and inorganic salts. Particularly suitable detergents are the water-soluble primary sulfuric esters of aliphatic alcohols having the necessary compatibility, especially those containing 10 to 14 carbon atoms in the aliphatic group. It is preferred to use the alkali metal lauryl, coconut and myristyl alcohol sulfates, though other suitable watersoluble salts such as the ammonium and alkylolamine, e.g., triethanolamine salts may be employed also in suitable amount. Such detersive salts enhance the detergent action of the inorganic salts, emulsify oily soils, provide a minor amount of unstable foam and assist in the solubilization of the ortho-benzyl-para-halogenated-phenol. In particular, suitable compositions should be characterized by low foam levels in dilute solutions to eliminate foam streaks on the hard surfaces and to minimize the need for rinsing which would necessarily dilute the germicidal effectiveness. Accordingly, the detergent should be in minor amounts required for effective hard surface cleansing and low foam and the proportion required should be sufficient to solubilize the germicidal phenol in diluted use concentrations of product. Concentrations of about /2 to preferably /2 to 3%, of such detergent have been found to be satisfactory when proportioned with 1 to 5%, preferably 14%, of ortho-benzyl-para-chlorophenol or the like. In general, the ratio of detergent to said phenolic compound is from about 1:1 to 1:4 range, preferably 1:2 to 3:4 by weight in order to maintain the germicidal activity of the compositions at a high level without any substantial adverse effect by the detergent. Therefore, too high a proportion of said detergent tends to reduce germicidal effectiveness and too low a proportion also reduces germicidal effectiveness because of insolubilization of said germicide.
It is significant that water solutions containing 0.5 to 2% of said mixtures should be substantially clear because the germicidal compound tends to separate rapidly in cloudy water dispersions. Such separation during use results in non-homogeneous mixtures with respect to the germicide and, hence, the disinfectant action will vary widely. To achieve the desired clarity, both the type of detergent and its concentration should be carefully correlated with the type and amount of said germicide.
The suitable phenolic germicidal compounds are the ortho-benzyl-para-halogenated-phenol derivatives wherein the halogen is selected from the group consisting of chlorine, bromine and iodine. Ortho-benzyl-para-chlorophenol is a particularly satisfactory compound in compositions of the invention. The instant compositions are outstanding because of their potency against a wide variety of bacteria and fungi in low concentrations in addition to the other desirable properties. Heretofore, alkaline detergent compositions containing phenolic germicides have generally been singularly effective against either Gram-negative (Salmonella typhosa) or Gram-positive (Staphylococcus aureus) organisms. The instant alkaline compositions are effective against both types of organisms as well as fungi.
The effectiveness of this composition against standard test micro-organisms can be demonstrated in the AOAC Phenol Coefficient test (8th Edition (1955), p. 87) and in the AOAC Use-dilution test (8th Edition (1955), p. 91). In the former, the diluted concentration sufficient to kill bacteria in broth culture during a ten minute exposure period is compared with the concentration of phenol required for a kill under identical conditions. In the latter test, the bacteria are dried on a metal loop which is then exposed to the germicidal solution before transfer to a subculture tube and incubation for 48 hours at 37 C. No growth should be evident in any of the subculture tubes if the diluted composition is effective. Further, as a check 4 against stasis because of carry-over of dried germicidal solution on the metal loop, the metal loops are generally re-subcultured and incubated for another 48 hour period at 37 C. to demonstrate that a true kill is obtained as opposed to stasis or inhibition of growth.
The new compositions may also beneficially include suitable amounts of adjuvant materials such as coloring agents, perfumes, and other additives.
The new compositions are advantageously marketed in the form of dry, free flowing granules containing the ingredients in homogeneous admixture, such that a definite weight of product may be used to give a solution of definite proportions of the ingredients. The compositions are prepared by adding in a suitable manner either powdered ortho-benzyl-para-chlorophenol or a concentrated solution of ortho-benzyl-para-chlorophenol in isopropanol for example to a blend of the granular inorganic compounds and dry detergent using a suitable dry blender, e.g., ribbon mixer, sigma mixer, twin shell blender, twin cone blender, rotary drum, etc. Any suitable particle size may be employed as desired. Color solution and perfume may advantageously be combined with the concentrated germicidal solution in the manufacture of this product if desired.
The invention is illustrated by the following examples, but it is not intended that the invention be limited solely to the variations and proportions set forth. All concentraions are expressed in percent by weight of the indicated ingredients unless otherwise specified.
EXAMPLE I A solid hard surface detergent composition with disinfectant properties was prepared from the following ingredients using the 'method of production described above:
Ingredient: Percent ('by wt.) Sodium carbonate 42.8 Sodium bicarbonate 26.0 Pentasodium tripolyphosphate 20.0 Trisodium phosphate 4.3 Sodium lauryl sulfate 2.0 Ortho-benzyl-para-chloropheno-l 3.0 Color, perfume, inert, etc. Remainder This composition was formed by dry-mixing the above ingredients resulting in a dry, free flowing, granular product whose color remained stable during accelerated aging tests at F. Hard surface cleansing performance of a 1.85 solution in water was characterized by excellent detergency, low unstable foam and a non-streaked appearance after cleaning. Further, the 1.85% solution in water was clear at pH 9.8 and exhibited good disinfectant properties against a broad spectrum of micro-organisms as measured by the AOAC P-henol Coefficient and use dilution tests. Test results follow:
(A) Phenol coefficient (10 min. kill at 20 C.) (1) Against Salmonella typhosa, 5.0' (2) Against Staph. aureus, 3.0 (B) Use dilution (1.85 concentration) (1) Against Staphylococcus aureus-no growth in the ten subculture or the ten resubculture tubes. (2) Against Salmonella ch0leraesuis-no growth in the 10 subculture or the 10 resubculture tubes. (3) Against T ri. interdigitaleno growth in the 10 subculture or the 10 resubculture tubes.
The foregoing test results are particularly significant since the germicidal activity is outstanding, particularly in said alkaline system.
As indicative of the importance of the pH range, a similar composition was prepared wherein the ingredients were proportioned so that a 1.5% Water solution had a pH of 10.8. This formulation contained 65.8% Sodium carbonate, 2% sodium bicarbonate, 25% tetrasodium pyrophosphate, 4% ortho-benzyl-para-chlorophenol, 1%
sodium lauryl sulfate, with perfume and color, as the remainder.
This composition exhibited markedly reduced disinfectant levels. The A.O.A.C. Use-dilution test results for the 1.5% concentration follow:
Staphylococcus aureus organism Subculture tubes Growth in 8 out of 10 tubes R-esubculture tubes Growth in 8 out of 10 tubes Percent (by wt.)
Ingredient II III IV V VI Sodium carbonate 53 37. 5 40 54 Sodium bicarbonate 20 26 26 20 Pentasodium tripolyphosphat 20 20 Tetrasodium pyrophosphateu 18 18 Trisodium phosphate 4 3 4 4 Ortho-benzyl-para-chlorophenol Sodium lauryl sulfate Color, perfume, inert, etc pH of 1.5% solution Remainder 10.1 9.8 9.7 10.0
As further indicative of the importance of said ingredients in the relationship set forth, it has been found that similar compositions containing various detergents such as sodium dodecyl benzene sulfonate, higher alkyl phenolethylene oxide condensates or sodium disu'lfonated dodecyl diphenyl oxide form cloudy solutions with decreased etfectiveness.
The new compositions of this invention present several additional advantages. For example, the compositions are relatively simple to prepare on present equipment without changes in design. Furthermore, the ingredients are readily available through commercial channels at economically attractive prices. In addition, the new compositions can be used on a Wide variety of surfaces without fear of damage. Other advantages will be readily apparent to those skilled in the art.
Numerous modifications and variations of the embodiments of this invention may be made without departing from the spirit and scope thereof. Accordingly, it is to be understood that the invention is not to be limited except as defined in the appended claim.
What is claimed is:
1. A solid granular free flowing detergent composition particularly suit-able for hard surface cleaning and disinfection consisting essentially of about 35 to by weight of sodium carbonate and about 15 to 25% by weight of sodium tripolyphos-phate, as water soluble inorganic normal builder salts, about 20 to 30% by weight of sodium bicarbonate as water soluble inorganic acid salt, about 2% by weight of sodium lauryl alcohol sulfate and about 3 to 4% by Weight of ortho-benzyl-parach'lorophenol, said amounts being by weight of total solids proportioned to form a water solution containing from about /2 to 2% by weight of said solids having a pH of about 9.6 to 10 with said chlorophenol essentially in solution and exhibiting thereby effective disinfecting action against a broad spectrum of microorganisms.
FOREIGN PATENTS 9/1960 Great Britain. 7/1956 Australia.
OTHER REFERENCES The Condensed Chemical Dictionary, Rose, Reinhold Publ. Co., New York (1962), pshr 143.
IJEON D. ROSDOL, Primary Examiner.
JULIUS GREENWALD, Examiner.
S. E. DARD-EN, Assistant Examiner.
Claims (1)
1. A SOLID GRANULAR FREE FLOWING DETERGENT COMPOSITION PARTICULARLY SUITABLE FOR HARD SURFACE CLEANING AND DISINFECTION CONSISTING ESENTIALLY OF ABOUT 35 TO 55% BY WEIGHT OF SOLIUM CARBONATE AND ABOUT 15 TO 25% BY WEIGHT OF SODIUM TRIPOLYPHOSPHATE, AS WATER SOLUBLE INORGANIC NORMAL BUILDER SALTS, ABOUT 20 TO 30% BY WEIGHT OF SODIUM BICARBONATE AS WATER SOLUBLE INORGANIC ACID SALT, ABOUT 2% BY WEIGHT OF SODIUM LAURYL ALCOHOL SULFATE AND ABOUT 3 TO 4% BY WEIGHT OF ORTHO-BENYL-PARACHLOROPHENOL, SAID AMOUNTS BEING BY WEIGHT OF TOTAL SOLIDS PROPORTIONED TO FORM A WATER SOLUTION CONTAINING FROM ABOUT 1/2 TO 2% BY WEIGHT OF SAID SOLIDS HAVING A PH OF ABOUT 9.6 TO 10 WITH SAID CHLOROPHENOL ESSENTIALLY IN SOLUTION AND EXHIBITING THEREBY EFFECTIVE DISINFECTING ACTION AGAINST A BROAD SPECTRUM OF MICROORGANISMS.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US327081A US3375199A (en) | 1963-11-29 | 1963-11-29 | Cleaner-disinfectant composition |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US327031A US3242311A (en) | 1963-11-29 | 1963-11-29 | Welding cable suspension device |
| US327081A US3375199A (en) | 1963-11-29 | 1963-11-29 | Cleaner-disinfectant composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3375199A true US3375199A (en) | 1968-03-26 |
Family
ID=26985691
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US327081A Expired - Lifetime US3375199A (en) | 1963-11-29 | 1963-11-29 | Cleaner-disinfectant composition |
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| Country | Link |
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| US (1) | US3375199A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3625904A (en) * | 1968-05-09 | 1971-12-07 | Henkel & Cie Gmbh | Washing agents, washing adjuvants and cleaning agents containing antimicrobial substances |
| WO2008132769A1 (en) * | 2007-04-24 | 2008-11-06 | Bicar Jet Srl | Detergentand disinfectant abrasive product |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB848306A (en) * | 1958-02-06 | 1960-09-14 | Colgate Palmolive Co | Antibacterial detergent compositions |
| US3063895A (en) * | 1959-01-29 | 1962-11-13 | William Pearson Ltd | Disinfectant compositions |
-
1963
- 1963-11-29 US US327081A patent/US3375199A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB848306A (en) * | 1958-02-06 | 1960-09-14 | Colgate Palmolive Co | Antibacterial detergent compositions |
| US3063895A (en) * | 1959-01-29 | 1962-11-13 | William Pearson Ltd | Disinfectant compositions |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3625904A (en) * | 1968-05-09 | 1971-12-07 | Henkel & Cie Gmbh | Washing agents, washing adjuvants and cleaning agents containing antimicrobial substances |
| WO2008132769A1 (en) * | 2007-04-24 | 2008-11-06 | Bicar Jet Srl | Detergentand disinfectant abrasive product |
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