US1696762A - Germicidal compound - Google Patents
Germicidal compound Download PDFInfo
- Publication number
- US1696762A US1696762A US235114A US23511427A US1696762A US 1696762 A US1696762 A US 1696762A US 235114 A US235114 A US 235114A US 23511427 A US23511427 A US 23511427A US 1696762 A US1696762 A US 1696762A
- Authority
- US
- United States
- Prior art keywords
- solution
- germicidal
- compound
- color
- tri
- Prior art date
- 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 - Lifetime
Links
- 230000002070 germicidal effect Effects 0.000 title description 27
- 150000001875 compounds Chemical class 0.000 title description 20
- 239000000243 solution Substances 0.000 description 26
- 239000000344 soap Substances 0.000 description 11
- 239000007864 aqueous solution Substances 0.000 description 10
- 235000013162 Cocos nucifera Nutrition 0.000 description 9
- 244000060011 Cocos nucifera Species 0.000 description 9
- 239000002253 acid Substances 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- 235000019198 oils Nutrition 0.000 description 9
- 239000001488 sodium phosphate Substances 0.000 description 9
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 9
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 9
- 235000019801 trisodium phosphate Nutrition 0.000 description 9
- 150000003839 salts Chemical class 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 239000010466 nut oil Substances 0.000 description 4
- 235000019488 nut oil Nutrition 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- AXDJCCTWPBKUKL-UHFFFAOYSA-N 4-[(4-aminophenyl)-(4-imino-3-methylcyclohexa-2,5-dien-1-ylidene)methyl]aniline;hydron;chloride Chemical compound Cl.C1=CC(=N)C(C)=CC1=C(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 AXDJCCTWPBKUKL-UHFFFAOYSA-N 0.000 description 3
- 230000003301 hydrolyzing effect Effects 0.000 description 3
- -1 hydroxyl ions Chemical class 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 2
- RZUBARUFLYGOGC-MTHOTQAESA-L acid fuchsin Chemical class [Na+].[Na+].[O-]S(=O)(=O)C1=C(N)C(C)=CC(C(=C\2C=C(C(=[NH2+])C=C/2)S([O-])(=O)=O)\C=2C=C(C(N)=CC=2)S([O-])(=O)=O)=C1 RZUBARUFLYGOGC-MTHOTQAESA-L 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 125000005456 glyceride group Chemical group 0.000 description 2
- 235000003441 saturated fatty acids Nutrition 0.000 description 2
- 150000004671 saturated fatty acids Chemical class 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- SOBHUZYZLFQYFK-UHFFFAOYSA-K trisodium;hydroxy-[[phosphonatomethyl(phosphonomethyl)amino]methyl]phosphinate Chemical compound [Na+].[Na+].[Na+].OP(O)(=O)CN(CP(O)([O-])=O)CP([O-])([O-])=O SOBHUZYZLFQYFK-UHFFFAOYSA-K 0.000 description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 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
- 159000000011 group IA salts Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000002147 killing effect Effects 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
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical class CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing 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
- C11D9/00—Compositions of detergents based essentially on soap
- C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
- C11D9/06—Inorganic compounds
- C11D9/08—Water-soluble compounds
- C11D9/10—Salts
- C11D9/14—Phosphates; Polyphosphates
Definitions
- This invention relates to compounds for making germicidal solutions having general application to medical, surgical, sanitary and household uses, and particularly to a.
- the invention has for its principal objects the provision of a germicidal compound in which the germicidal propertles of certain 0f the ingredients are accentuated, each by the presence of the other, and by the reaction incident to their going into solution; to provide a germicidal compound of ingredients, inherently germicidal, in which the germicidal strength is increased by the llberation of hydroxyl ions in the aqueous solu tion of the compound; to provide a germicidal solution of great potency which, on account of its ease of preparation, quickness of action, and non-poisonous nature, is admirably suited to medicinal, surgical, pharmaceutical, sanitary, and domestic uses; and in the provision of a compound of germicidal character, when in aqueous solution, having the power to quickly dissolve the fatty envelopes possessed by many bacteria, thus rendering them quickly susceptible to the action of the germicide.
- Another object of the invention is to furnish the compound with a color index in the form of an ingredient that will lend a fugitive color to the solution while incomplete, the color disappearing when the solution becomes complete and ready for use, thus serving as an indication of the preparedness of the solution, said color being capable of being restored for testing purposes by the use of a suitable reagent, by means of which not only the strength but also the genuineness of the solution may be ascertained.
- the invention is carried out by preparing a mixture of a soap of both saturated and unsaturated fatty acids common to cocoanut oil and palm nut oil, preferably in their saturated condition, with a sodium salt capable of hydrolyzing in water, tri-sodium Application filed November 22, 1927. Serial No. 235,114.
- a soap thus prepared consisting of the alkaline salts of the acids peculiar to cocoanut and palm nut oil, is mixed with an alkali salt capable of hydrolyzing in aqueous solution with the liberaton of free hydroxyl ions and produced by the hydrolyzat-ion attack and.
- a color index for the solution both for indicating its strength and the completion of the solution, as well as subsequently to permit of testing the solution for strength and genuineness.
- a minute quantity of some harmless coloring agent such as-acid fuchsin which reacts red to a I slightly acidulated solution, but becomes colorless in an alkaline solution.
- this acid fuchsin is added as an ingredient.
- a preparation of acid is added, which shows the genuineness of the solution by bringing back the original color,- the strength of the solution being indicated by the intensity of the color, which may be compared with a standard color chart.
- cocoanut oil soap containing salts of capric, caprillic, caprioic,..lauric, and myristic acids
- a germicidal compound for preparing germicidal aqueous solution comprising a mixture of soap including salts of the fatty acids common to cocoanut oil and palm nut oil, and tri-sodium phosphate.
- a germicidal compound for preparing germicidal aqueous solution comprising a mixture of a soap including salts of the fatty acids common to cocoanut oil and palm nut oil, and tri-sodium phosphate, and a trace of a substance se ving by its change of color when in solution to indicate acid and alkaline states of the solution of said compound.
- a germicidal compound for preparing germicidal aqueous solution comprising a mixture of cocoanut oil soap, and tri-sodium phosphate.
- a germicidal compound for preparing germicidal aqueous solution comprising a mixture of 40% of cocoanut oil soap and 60% of tri-sodium phosphate.
- a germicidal compound for preparing germicidal aqueous solution comprising a mixture of 40% of cocoanut oil soap, 60% of tri-sodium phosphate, and a trace of a substance serving by its change of color when in solution to indicate acid and alkaline states of the solution of said compound.
- a germicidal compound for preparing germicidal aqueous solution comprising a. mixture of 40% cocoanut oil soap, 60% trisodium phosphate, and a trace of acid fuch- SlIL JAMES JEFFRIES GooDwiN;
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)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
Patented Dec. 25, 1928.
UNITED STATES,
PATENT OFFICE.
JAMES JEFFRIES GOODWIN, OF LOUISVILLE, KENTUCKY, ASSIGNOR T GOODWIN LABORATORIES, INC., OF LOUISVILLE, KENTUCKY, A CORPORATION OF KENTUCKY.
GERMICIDAL COMPOUND.
No Drawing.
This invention relates to compounds for making germicidal solutions having general application to medical, surgical, sanitary and household uses, and particularly to a.
compound of the class described having special application to the preparation of antiseptic washing solution for the glassware used at public soda fountains and for other similar uses.
The invention has for its principal objects the provision of a germicidal compound in which the germicidal propertles of certain 0f the ingredients are accentuated, each by the presence of the other, and by the reaction incident to their going into solution; to provide a germicidal compound of ingredients, inherently germicidal, in which the germicidal strength is increased by the llberation of hydroxyl ions in the aqueous solu tion of the compound; to provide a germicidal solution of great potency which, on account of its ease of preparation, quickness of action, and non-poisonous nature, is admirably suited to medicinal, surgical, pharmaceutical, sanitary, and domestic uses; and in the provision of a compound of germicidal character, when in aqueous solution, having the power to quickly dissolve the fatty envelopes possessed by many bacteria, thus rendering them quickly susceptible to the action of the germicide.
Another object of the invention is to furnish the compound with a color index in the form of an ingredient that will lend a fugitive color to the solution while incomplete, the color disappearing when the solution becomes complete and ready for use, thus serving as an indication of the preparedness of the solution, said color being capable of being restored for testing purposes by the use of a suitable reagent, by means of which not only the strength but also the genuineness of the solution may be ascertained.
Other objects of the invention will appear as the following description of a preferred formula therefor proceeds. 1
The invention is carried out by preparing a mixture of a soap of both saturated and unsaturated fatty acids common to cocoanut oil and palm nut oil, preferably in their saturated condition, with a sodium salt capable of hydrolyzing in water, tri-sodium Application filed November 22, 1927. Serial No. 235,114.
phosphate and sodium per borate being tried examples of this class of salts.
Both the saturated and unsaturated fatty acids of the above oils have inherent germi= cidal properties of high value not possessed by the glycerides of the fatty acids used in making ordinary cleansing soaps. When a soap thus prepared, consisting of the alkaline salts of the acids peculiar to cocoanut and palm nut oil, is mixed with an alkali salt capable of hydrolyzing in aqueous solution with the liberaton of free hydroxyl ions and produced by the hydrolyzat-ion attack and.
dissolve the fatty envelopes of certain bacteria thus allowing more positive germicidal action of the germicidal agent, namely, the acids which are present in the form. of soap or sodium salts.
It has been found particularly advantageous to employ a color index for the solution, both for indicating its strength and the completion of the solution, as well as subsequently to permit of testing the solution for strength and genuineness. For this purpose, there is preferably added a minute quantity of some harmless coloring agent such as-acid fuchsin which reacts red to a I slightly acidulated solution, but becomes colorless in an alkaline solution. In the coinmercial preparation of the germicidal compound, this acid fuchsin is added as an ingredient. In subsequent testing of a solution, a preparation of acid is added, which shows the genuineness of the solution by bringing back the original color,- the strength of the solution being indicated by the intensity of the color, which may be compared with a standard color chart.
The following example illustrates what has been found to be a preferred embodimentof the invention A mixture of 40% cocoanut oil soap (containing salts of capric, caprillic, caprioic,..lauric, and myristic acids), and
60% of tri-sodium pho hate (Na PO to which is added a trace 0 acid fuchsin.
When this mixture is put into aqueous solution, preferably at about 75 C., the reaction is at first acid and the solution has a red tinge imparted by the fuchsin. In a minute or two the solution becomes clear, due to its progressive alkalization by the liberated hydroxyl ions. In the course of the hydrolysis of the tri-sodium phosphate, some of the sodium combines with the fuchsin, while the trisodium phosphate is reduced to the acid di-sodium phosphate (Na HPO which acts as a buffer, to prevent excess alkalinity of the solution.
Should extension of the solution from time to time be desired, in order to ascertain if the genuine solution is being ,used or one of the prescribed stren h, a measured quantity of acid is mixed with a sample of the solution which is to be tested, the color of the fuchsin being thus restored and the strength of the solution being determined by the intensity of the color.
It is to be understood that other glycerides of fatty acids than those herein enumerated may be found suitable for the purpose of making a germicidal compound according to the present invention, and that other salts, aside from the tri-sodium phosphate and sodium borate but which have a similar hydrolyzing action in water, may be substituted inplace of the salts above mentioned in the making of the compound. Therefore, the invention is not to be construed-as limited to the precise ingredients given or the precise properties indicated as being used, except where specifically limited bythe express terms of the appended claims.
I claim 1. A germicidal compound for preparing germicidal aqueous solution, comprising a mixture of soap including salts of the fatty acids common to cocoanut oil and palm nut oil, and tri-sodium phosphate.
'2. A germicidal compound for preparing germicidal aqueous solution, comprising a mixture of a soap including salts of the fatty acids common to cocoanut oil and palm nut oil, and tri-sodium phosphate, and a trace of a substance se ving by its change of color when in solution to indicate acid and alkaline states of the solution of said compound.
3. A germicidal compound for preparing germicidal aqueous solution, comprising a mixture of cocoanut oil soap, and tri-sodium phosphate.
4:- A germicidal compound for preparing germicidal aqueous solution, comprising a mixture of 40% of cocoanut oil soap and 60% of tri-sodium phosphate.
5. A germicidal compound for preparing germicidal aqueous solution comprising a mixture of 40% of cocoanut oil soap, 60% of tri-sodium phosphate, and a trace of a substance serving by its change of color when in solution to indicate acid and alkaline states of the solution of said compound.
6. A germicidal compound for preparing germicidal aqueous solution, comprising a. mixture of 40% cocoanut oil soap, 60% trisodium phosphate, and a trace of acid fuch- SlIL JAMES JEFFRIES GooDwiN;
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US235114A US1696762A (en) | 1927-11-22 | 1927-11-22 | Germicidal compound |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US235114A US1696762A (en) | 1927-11-22 | 1927-11-22 | Germicidal compound |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1696762A true US1696762A (en) | 1928-12-25 |
Family
ID=22884154
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US235114A Expired - Lifetime US1696762A (en) | 1927-11-22 | 1927-11-22 | Germicidal compound |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1696762A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4678658A (en) * | 1985-05-24 | 1987-07-07 | Larry Casey | Aerosol germicide and dye |
| US4793988A (en) * | 1985-05-24 | 1988-12-27 | Irene Casey | Germicide and dye composition |
| US4965063A (en) * | 1985-05-24 | 1990-10-23 | Irene Casey | Cleaner and disinfectant with dye |
-
1927
- 1927-11-22 US US235114A patent/US1696762A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4678658A (en) * | 1985-05-24 | 1987-07-07 | Larry Casey | Aerosol germicide and dye |
| US4793988A (en) * | 1985-05-24 | 1988-12-27 | Irene Casey | Germicide and dye composition |
| US4965063A (en) * | 1985-05-24 | 1990-10-23 | Irene Casey | Cleaner and disinfectant with dye |
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