CA1295550C - Stabilized hypochlorite disinfectant composition - Google Patents
Stabilized hypochlorite disinfectant compositionInfo
- Publication number
- CA1295550C CA1295550C CA000521327A CA521327A CA1295550C CA 1295550 C CA1295550 C CA 1295550C CA 000521327 A CA000521327 A CA 000521327A CA 521327 A CA521327 A CA 521327A CA 1295550 C CA1295550 C CA 1295550C
- Authority
- CA
- Canada
- Prior art keywords
- hypochlorite
- weight
- solution
- butanol
- sodium
- 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
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
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/02—Acyclic compounds
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic 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
- C11D3/395—Bleaching agents
- C11D3/3956—Liquid compositions
Abstract
ABSTRACT
This invention provides a novel disinfectant composi-tion which is an aqueous solution containing hypochlorite ions, such as sodium hypochlorite, containing a tertiary al-iphatic alcohol, such as tertiary-butanol. The alcohol acts as an odour masking agent and as a stabilizer for hypochlor-ite ions while itself possessing disinfecting properties.
The composition is useful as a disinfectant.
This invention provides a novel disinfectant composi-tion which is an aqueous solution containing hypochlorite ions, such as sodium hypochlorite, containing a tertiary al-iphatic alcohol, such as tertiary-butanol. The alcohol acts as an odour masking agent and as a stabilizer for hypochlor-ite ions while itself possessing disinfecting properties.
The composition is useful as a disinfectant.
Description
~ ~.55~0 This invention relates to a novel disinfectant compo-sition and more particularly it relates to a novel disinfec-tant composition containing hypochlorite ions.
It is known that chlorine-based disinfectants such as those containing hypochlorite ions, for example sodium hypo-chlorite, are useful in destroying pathogens such as bacter-ia. These disinfectants suffer from the disadvantage that they have an offensive odour of chlorine and potential users of such disinfectants object to the smell of chlorine and thus such disinfectants tend not to be the disinfectant of choice.
We have now found, and herein lies our invention, that the offensive odour of an aqueous solution containing hypo-chlorite ions can be reduced by the addition of a particular odour masking ingredient.
According to the invention, as claimed herein, there is provided a novel aqueous solution containing hypochlorite ions wherein there is present a tertiary aliphatic alcohol.
As an example of an aqueous solution containing hypo-chlorite ions there may be mentioned an aqueous solution con-taining an alkali metal or an alkaline earth metal hypochlor-ite such as lithium, sodium, potassium, calcium or barium hypochlorite. The hypochlorite compound may be present to an extent of up to about 2% w/w of the solution. A preferred hypochlorite is sodium hypochlorite which may be present in a concentration of 0.5% w/w.
The tertiary aliphatic alcohol present in the novel aqueous hypochlorite solution may be a tertiary alcohol con-taining from 4 to 8 carbon atoms such as tertiary-butanol, 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pentanediol.
Of these tertiary aliphatic alcohols, a preferred alcohol is tertiary-butanol. The presence of a tertiary aliphatic alco-3~
- 2 _ 1Z~55,'~
hol is advantageous in that it not only acts as an odour mask-ing agent but it also has biocidal activity in possessing mild disinfectant properties and it additionally functions as a sta-bilizer for hypochlorite ions.
As a further preferred feature of the invention there is provided an aqueous solution containing a compound provid-ing hypochlorite ions, such as sodium, potassium, lithium or calcium hypochlorite, in the presence of a tertiary aliphatic alcohol, such as tertiary-butanol, 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pentanediol, wherein for each 1 part by weight of said compound there is present from about 2 parts by weight to about 30 parts by weight of tertiary aliphatic alcohol, preferably from about 5 parts to about 15 parts by weight of tertiary aliphatic alcohol.
For example, an aqueous solution containing 1 part by weight of sodium hypochlorite may have present therein from about 2 parts by weight to about 30 parts by weight, prefer-ably from about 5 parts to about 15 parts by weight, of ter-tiary-butanol, 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pentanediol. A particularly useful aqueous solution is one containing about 1 part by weight of sodium hypochlorite and about 10 parts by weight of tertiary-butanol, 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pentanediol.
The aqueous solution containing hypochlorite ions may optionally have present therein one or more additional in-gredients. Thus, for example, the aqueous solution may also contain a synthetic organic detergent, such as sodium dodecyl sulphate. Thus, for example, for each part by weight of com-pound providing hypochlorite ions, such as sodium hypochlor-ite, there may be present from about 0.005 to about 0.1 part by weight, preferably about 0.02 part by weight, of synthetic organic detergent, such as sodium dodecyl sulphate.
The aqueous solution containing hypochlorite ions may also optionally have present therein one or more chlorine 55~;0 stable fragrances, such as a lemon fragrance or a pine frag-rance. Such fragrances may be present in an amount such that for each part by weight of hypochlorite compound there is present from about 0.005 to about 0.2 part by weight of frag-rance, preferably about 0.02 part by weight of fragrance, preferably a lemon fragrance.
The amount of fragrance may vary according to the strength and volume of the fragrance used. A weaker frag-rance may be present to an extent of 0.2% w/w whereas a stronger fragrance may be present to an extent of 0.02~ w/w.
The synthetic organic detergent, such as sodium dodecyl sul-phate, not only provides a cleaning power to the disinfec-tant but it also helps to dissolve or maintain the fragrance in solution. Since suitable fragrances mentioned above are usually oil-based fragrances, the synthetic organic deter-gent may be used to dissolve the fragrance prior to addition to the aqueous solution and thereafter it maintains the frag-rance in solution. When a fragrance is present to an extent of from about 0.005 to about 0.2~ w/w, the range of detergent may generally be from about 0.005 to about 0.01~ w/w. Quan-tities of detergent in excess of this amount may be present to provide additional detergency to the solution.
Other optional ingredients may be present in the novel aqueous solution of the invention such as a chlorine stable colouring agent.
The novel aqueous solutions of this invention are use-ful in destroying pathogens including viruses, bacteria and fungi.
The invention is illustrated by, but not limited by, the following Examples in which the ingredients are given as percentages of parts by weight.
129~5SO
An aqueous solution is prepared containing 0.5~ w/w of sodium hypochlorite and 5% w/w of tertiary-butanol. There is thus obtained a disinfectant solution having an acceptable masked chlorine odour compared with a corresponding 0.5% w/w sodium hypochlorite solution containing no tertiary-butanol.
The 0.5% w/w of sodium hypochlorite may be replaced by 0.5% w/w of potassium, lithium or calcium hypochlorite and there is likewise obtained a satisfactory and acceptable dis-infectant solution.
The 5~ w/w of tertiary-butanol may be replaced by 5%
w/w of 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pen-tanediol and there is likewise obtained a satisfactory and acceptable disinfectant solution.
An aqueous solution is prepared containing 0.5% w/w of sodium hypochlorite, 5% w/w of tertiary-butanol and 0.01%
w/w of sodium dodecyl sulphate. There is thus obtained a disinfectant solution having an acceptable masked chlorine odour.
The 0.5~ w/w of sodium hypochlorite may be replaced by 0.5% w/w of potassium, lithium or calcium hypochlorite and there is likewise obtained a satisfactory and acceptable disinfectant solution.
The 5~ w/w of tertiary-butanol may be replaced by 5%
w/w of 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pen-tanediol and there is likewise obtained a satisfactory and acceptable disinfectant solution.
An aqueous solution is prepared containing 0.5~ w/w 12~5' 0 of sodium hypochlorite and 2.5~ w/w of tertiary-butanol, 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pentanediol. There is thus obtained a disinfectant solution having an acceptable masked chlorine odour compared with a corresponding sodium hy-pochlorite solution containing no tertiary-butanol.
An aqueous solution is prepared containing 0.5% w/w of sodium hypochlorite and 7.5% w/w of tertiary-butanol, 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pentanediol. There is thus obtained a disinfectant solution having an acceptable masked chlorine odour compared with a corresponding sodium hy-pochlorite solution containing no tertiary-butanol.
An aqueous solution is prepared containing the follow-ing ingredients:
O.S % w/w of sodium hypochlorite, 5.0 ~ w/w of tertiary-butanol;
0.01% w/w of sodium dodecyl sulphate; and 0.01% w/w of lemon fragrance.
There is thus prepared an aqueous disinfectant solution which has an acceptable masked chlorine odour when used for its in-tended purpose of destroying pathogens.
The 0.5% w/w of sodium hypochlorite may be replaced by 0.5% w/w of potassium, lithium or calcium hypochlorite and there is likewise obtained a satisfactory and acceptable dis-infectant solution.
The 5% w/w of tertiary-butanol may be replaced by 5%
w/w of 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pen-tanediol and there is likewise obtained a satisfactory and acceptable disinfectant solution.
It is known that chlorine-based disinfectants such as those containing hypochlorite ions, for example sodium hypo-chlorite, are useful in destroying pathogens such as bacter-ia. These disinfectants suffer from the disadvantage that they have an offensive odour of chlorine and potential users of such disinfectants object to the smell of chlorine and thus such disinfectants tend not to be the disinfectant of choice.
We have now found, and herein lies our invention, that the offensive odour of an aqueous solution containing hypo-chlorite ions can be reduced by the addition of a particular odour masking ingredient.
According to the invention, as claimed herein, there is provided a novel aqueous solution containing hypochlorite ions wherein there is present a tertiary aliphatic alcohol.
As an example of an aqueous solution containing hypo-chlorite ions there may be mentioned an aqueous solution con-taining an alkali metal or an alkaline earth metal hypochlor-ite such as lithium, sodium, potassium, calcium or barium hypochlorite. The hypochlorite compound may be present to an extent of up to about 2% w/w of the solution. A preferred hypochlorite is sodium hypochlorite which may be present in a concentration of 0.5% w/w.
The tertiary aliphatic alcohol present in the novel aqueous hypochlorite solution may be a tertiary alcohol con-taining from 4 to 8 carbon atoms such as tertiary-butanol, 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pentanediol.
Of these tertiary aliphatic alcohols, a preferred alcohol is tertiary-butanol. The presence of a tertiary aliphatic alco-3~
- 2 _ 1Z~55,'~
hol is advantageous in that it not only acts as an odour mask-ing agent but it also has biocidal activity in possessing mild disinfectant properties and it additionally functions as a sta-bilizer for hypochlorite ions.
As a further preferred feature of the invention there is provided an aqueous solution containing a compound provid-ing hypochlorite ions, such as sodium, potassium, lithium or calcium hypochlorite, in the presence of a tertiary aliphatic alcohol, such as tertiary-butanol, 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pentanediol, wherein for each 1 part by weight of said compound there is present from about 2 parts by weight to about 30 parts by weight of tertiary aliphatic alcohol, preferably from about 5 parts to about 15 parts by weight of tertiary aliphatic alcohol.
For example, an aqueous solution containing 1 part by weight of sodium hypochlorite may have present therein from about 2 parts by weight to about 30 parts by weight, prefer-ably from about 5 parts to about 15 parts by weight, of ter-tiary-butanol, 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pentanediol. A particularly useful aqueous solution is one containing about 1 part by weight of sodium hypochlorite and about 10 parts by weight of tertiary-butanol, 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pentanediol.
The aqueous solution containing hypochlorite ions may optionally have present therein one or more additional in-gredients. Thus, for example, the aqueous solution may also contain a synthetic organic detergent, such as sodium dodecyl sulphate. Thus, for example, for each part by weight of com-pound providing hypochlorite ions, such as sodium hypochlor-ite, there may be present from about 0.005 to about 0.1 part by weight, preferably about 0.02 part by weight, of synthetic organic detergent, such as sodium dodecyl sulphate.
The aqueous solution containing hypochlorite ions may also optionally have present therein one or more chlorine 55~;0 stable fragrances, such as a lemon fragrance or a pine frag-rance. Such fragrances may be present in an amount such that for each part by weight of hypochlorite compound there is present from about 0.005 to about 0.2 part by weight of frag-rance, preferably about 0.02 part by weight of fragrance, preferably a lemon fragrance.
The amount of fragrance may vary according to the strength and volume of the fragrance used. A weaker frag-rance may be present to an extent of 0.2% w/w whereas a stronger fragrance may be present to an extent of 0.02~ w/w.
The synthetic organic detergent, such as sodium dodecyl sul-phate, not only provides a cleaning power to the disinfec-tant but it also helps to dissolve or maintain the fragrance in solution. Since suitable fragrances mentioned above are usually oil-based fragrances, the synthetic organic deter-gent may be used to dissolve the fragrance prior to addition to the aqueous solution and thereafter it maintains the frag-rance in solution. When a fragrance is present to an extent of from about 0.005 to about 0.2~ w/w, the range of detergent may generally be from about 0.005 to about 0.01~ w/w. Quan-tities of detergent in excess of this amount may be present to provide additional detergency to the solution.
Other optional ingredients may be present in the novel aqueous solution of the invention such as a chlorine stable colouring agent.
The novel aqueous solutions of this invention are use-ful in destroying pathogens including viruses, bacteria and fungi.
The invention is illustrated by, but not limited by, the following Examples in which the ingredients are given as percentages of parts by weight.
129~5SO
An aqueous solution is prepared containing 0.5~ w/w of sodium hypochlorite and 5% w/w of tertiary-butanol. There is thus obtained a disinfectant solution having an acceptable masked chlorine odour compared with a corresponding 0.5% w/w sodium hypochlorite solution containing no tertiary-butanol.
The 0.5% w/w of sodium hypochlorite may be replaced by 0.5% w/w of potassium, lithium or calcium hypochlorite and there is likewise obtained a satisfactory and acceptable dis-infectant solution.
The 5~ w/w of tertiary-butanol may be replaced by 5%
w/w of 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pen-tanediol and there is likewise obtained a satisfactory and acceptable disinfectant solution.
An aqueous solution is prepared containing 0.5% w/w of sodium hypochlorite, 5% w/w of tertiary-butanol and 0.01%
w/w of sodium dodecyl sulphate. There is thus obtained a disinfectant solution having an acceptable masked chlorine odour.
The 0.5~ w/w of sodium hypochlorite may be replaced by 0.5% w/w of potassium, lithium or calcium hypochlorite and there is likewise obtained a satisfactory and acceptable disinfectant solution.
The 5~ w/w of tertiary-butanol may be replaced by 5%
w/w of 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pen-tanediol and there is likewise obtained a satisfactory and acceptable disinfectant solution.
An aqueous solution is prepared containing 0.5~ w/w 12~5' 0 of sodium hypochlorite and 2.5~ w/w of tertiary-butanol, 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pentanediol. There is thus obtained a disinfectant solution having an acceptable masked chlorine odour compared with a corresponding sodium hy-pochlorite solution containing no tertiary-butanol.
An aqueous solution is prepared containing 0.5% w/w of sodium hypochlorite and 7.5% w/w of tertiary-butanol, 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pentanediol. There is thus obtained a disinfectant solution having an acceptable masked chlorine odour compared with a corresponding sodium hy-pochlorite solution containing no tertiary-butanol.
An aqueous solution is prepared containing the follow-ing ingredients:
O.S % w/w of sodium hypochlorite, 5.0 ~ w/w of tertiary-butanol;
0.01% w/w of sodium dodecyl sulphate; and 0.01% w/w of lemon fragrance.
There is thus prepared an aqueous disinfectant solution which has an acceptable masked chlorine odour when used for its in-tended purpose of destroying pathogens.
The 0.5% w/w of sodium hypochlorite may be replaced by 0.5% w/w of potassium, lithium or calcium hypochlorite and there is likewise obtained a satisfactory and acceptable dis-infectant solution.
The 5% w/w of tertiary-butanol may be replaced by 5%
w/w of 2,3-dimethyl-2,3-butanediol or 2,4-dimethyl-2,4-pen-tanediol and there is likewise obtained a satisfactory and acceptable disinfectant solution.
Claims (46)
1. A stabilised aqueous disinfectant solution containing an alkali metal or an alkaline earth metal hypochlorite wherein there is present a tertiary aliphatic alcohol containing from 4 to 8 carbon atoms.
2. A solution, as claimed in claim 1, wherein the hypochlorite is selected from the group consisting of lithium, sodium, potassium, calcium and barium hypochlorite.
3. A solution, as claimed in claim 1, wherein the hypochlorite is sodium hypochlorite.
4. A solution, as claimed in claim 1, wherein the tertiary alcohol is selected from the group consisting of tertiary-butanol, 2,3-dimethyl-2,3-butanediol and 2,4-dimethyl-2,4-pentanediol.
5. A solution, as claimed in claim 1, wherein for each 1 part by weight of said hypochlorite there is present from about 2 parts by weight to about 30 parts by weight of tertiary aliphatic alcohol.
6. A solution, as claimed in claim 1, wherein for each 1 part by weight of said hypochlorite there is present from about 5 parts by weight to about 15 parts by weight of tertiary aliphatic alcohol.
7. A solution, as claimed in claim 1, wherein said solution contains 1 part by weight of sodium hypochlorite and from about 2 parts by weight to about 30 parts by weight of alcohol selected from the group consisting of tertiary-butanol, 2,3-dimethyl-2,3-butanediol and 2,4-dimethyl-2,4-pentanediol.
8. A solution, as claimed in claim 1 wherein said solution contains 1 part by weight of sodium hypochlorite and from about 5 parts by weight to about 15 parts by weight of alcohol selected from the group consisting of tertiary-butanol, 2,3-dimethyl-2,3-butanediol and 2,4-dimethyl-2,4-pentanediol.
9. A solution, as claimed in claim 1, wherein said solution contains about 1 part by weight of sodium hypochlorite and about 10 parts by weight of alcohol selected from the group consisting of tertiary-butanol, 2,3-dimethyl-2,3-butanediol and 2,4-dimethyl-2,4-pentanediol.
10. A solution, as claimed in claim 1, 2, 3, 4, 5, 6, 7, 8 or 9, wherein there is additionally present a synthetic organic detergent.
11. A solution, as claimed in claim 10, wherein the detergent is sodium dodecyl sulphate.
12. A solution, as claimed in claim 10, wherein for each part by weight of hypochlorite there is present from about 0.005 to about 0.1 part by weight of said synthetic organic detergent.
13. A solution, as claimed in claim 12, wherein there is present 0.02 part by weight of said detergent.
14. A solution, as claimed in claim 10, wherein for each part by weight of sodium hypochlorite there is present 0.02 part by weight of sodium dodecyl sulphate.
15. A solution, as claimed in claim 1, 2, 3, 4, 5, 6, 7, 8 or 9, wherein there is present a fragrance.
16. A solution, as claimed in claim 15, wherein the fragrance is a lemon fragrance or a pine fragrance.
17. A solution, as claimed in claim 15, wherein for each part by weight of hypochlorite there is present from about 0.005 to about 0.2 part by weight of said fragrance.
18. A solution, as claimed in claim 17, wherein there is present about 0.02 part by weight of said fragrance.
19. An aqueous solution, as claimed in claim 1, wherein there is present:
0.5% w/w of hypochlorite selected from sodium hypochlorite, lithium hypochlorite, potassium hypochlorite and calcium hypochlorite;
5.0% w/w of tertiary alcohol selected from tertiary-butanol, 2,3-dimethyl-2,3-butanediol and 2,4-dimethyl-2,4-pentanediol;
0.01% w/w sodium dodecyl sulphate; and 0.01% w/w lemon fragrance.
0.5% w/w of hypochlorite selected from sodium hypochlorite, lithium hypochlorite, potassium hypochlorite and calcium hypochlorite;
5.0% w/w of tertiary alcohol selected from tertiary-butanol, 2,3-dimethyl-2,3-butanediol and 2,4-dimethyl-2,4-pentanediol;
0.01% w/w sodium dodecyl sulphate; and 0.01% w/w lemon fragrance.
20. An aqueous solution, as claimed in claim 1, wherein there is present:
0.5% w/w sodium hypochlorite;
5.0% w/w tertiary-butanol;
0.01% w/w sodium dodecyl sulphate; and 0.01% w/w lemon fragrance.
0.5% w/w sodium hypochlorite;
5.0% w/w tertiary-butanol;
0.01% w/w sodium dodecyl sulphate; and 0.01% w/w lemon fragrance.
21. A stabilized disinfectant composition, consisting essentially of, in aqueous solution:
about 0.5% w/w of hypochlorite selected from the group consisting of sodium hypochlorite, lithium hypochlorite, potassium hypochlorite and calcium hypochlorite;
about 5.0% w/w of t-butanol;
about 0.01% w/w sodium dodecyl sulphate; and about 0.01% w/w lemon fragrance.
about 0.5% w/w of hypochlorite selected from the group consisting of sodium hypochlorite, lithium hypochlorite, potassium hypochlorite and calcium hypochlorite;
about 5.0% w/w of t-butanol;
about 0.01% w/w sodium dodecyl sulphate; and about 0.01% w/w lemon fragrance.
22. The disinfectant composition of claim 21, comprising:
about 0.5% w/w sodium hypochlorite;
about 5.0% w/w tertiary-butanol;
about 0.01% w/w sodium dodecyl sulphate; and about 0.01% w/w lemon fragrance.
about 0.5% w/w sodium hypochlorite;
about 5.0% w/w tertiary-butanol;
about 0.01% w/w sodium dodecyl sulphate; and about 0.01% w/w lemon fragrance.
23. A stabilized aqueous disinfectant solution containing an alkali metal or an alkaline earth metal hypochlorite and t-butanol, wherein for each 1 part by weight of hypochlorite there is present from about 2 parts by weight to about 30 parts by weight t-butanol.
24. The solution of claim 23, wherein the hypochlorite is selected from the group consisting of lithium, sodium, potassium, calcium and barium hypochlorite.
25. The solution of claim 23, wherein the hypochlorite is sodium hypochlorite.
26. The solution of claim 23, wherein for each 1 part by weight of said hypochlorite compound there is present from about 5 parts by eight to about 15 parts by weight of t-butanol.
27. The solution of claim 23, wherein said solution contains 1 part by weight of sodium hypochlorite and from about 2 parts by weight to about 30 parts by weight of t-butanol.
28. The solution of claim 23, wherein said solution contains 1 part by weight of sodium hypochlorite and from about 5 parts by weight to about 15 parts by weight of t-butanol.
29. The solution of claim 23, wherein said solution contains 1 part by weight of sodium hypochlorite and about 10 parts by weight of t-butanol.
30. The solution of claim 23, 24, 25, 26, 27, 28 or 29, wherein there is additionally present a synthetic organic detergent.
31. The solution of claim 30, wherein the detergent is sodium dodecyl sulphate.
32. The solution of claim 30, wherein for each part by weight of hypochlorite, there is present from about 0.005 to about 0.1 part by weight of said synthetic organic detergent.
33. The solution of claim 32, wherein there is present 0.02 part by weight of said detergent.
34. The solution of claim 30, wherein said hypochlorite is sodium hypochlorite, and wherein for each part by weight of sodium hypochlorite there is present 0.02 part by weight of sodium dodecyl sulphate.
35. The solution of claim 23, 24, 25, 26, 27, 28 or 29, wherein there is present a fragrance.
36. The solution of claim 35, wherein the fragrance is a lemon fragrance or a pine fragrance.
37. The solution of claim 35, wherein for each part by weight of hypochlorite there is present from about 0.005 to about 0.2 part by weight of said fragrance.
38. The solution of claim 37, wherein there is present about 0.02 part by weight of said fragrance.
39. A method of masking the odor of an aqueous hypochlorite solution containing an alkali metal or an alkaline earth metal hypochlorite comprising adding to such a solution an amount of t-butanol effective as an odor-masking agent, wherein the weight ratio of t-butanol to hypochlorite is from about 2:1 to about 30:1.
40. The method of claim 39, wherein the weight ratio of t-butanol to hypochlorite is from about 5:1 to about 15:1.
41. The method of claim 39, wherein the weight ratio of t-butanol to hypochlorite is about 10:1.
42. The method of claim 39, 40 or 41, wherein said hypochlorite is selected from the group consisting of sodium hypochlorite, lithium hypochlorite, potassium hypochlorite and calcium hypochlorite.
43. A method of stabilizing an aqueous hypochlorite solution containing an alkali metal or an alkaline earth metal hypochlorite comprising adding to such a solution an amount of t-butanol effective as a hypochlorite stabilizing agent under conditions which substantially prevent degradation or reaction of said hypochlorite wherein the weight ratio of t-butanol to hypochlorite is from about 2:1 to about 30:1.
44. The method of claim 43, wherein the weight ratio of t-butanol to hypochlorite is from about 5:1 to about 15:1.
45. The method of claim 43, wherein the weight ratio of t-butanol to hypochlorite is about 10:1.
46. The method of claim 43, 44 or 45, wherein said hypochlorite is selected from the group consisting of sodium hypochlorite, lithium hypochlorite, potassium hypochlorite and calcium hypochlorite.
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA000521327A CA1295550C (en) | 1986-10-24 | 1986-10-24 | Stabilized hypochlorite disinfectant composition |
US07/112,205 US4839079A (en) | 1986-10-24 | 1987-10-22 | Hypochlorite: tertiary alcohol disinfectants with reduced offensive odor |
EP87309358A EP0267707A1 (en) | 1986-10-24 | 1987-10-22 | A novel disinfectant composition |
JP62269135A JPS63198606A (en) | 1986-10-24 | 1987-10-23 | Novel disinfectant composition |
US07/362,356 US5075025A (en) | 1986-10-24 | 1989-06-06 | Disinfectant composition |
US07/547,772 USRE34065E (en) | 1986-10-24 | 1990-07-03 | Hypochlorite: tertiary alcohol disinfectants with reduced offensive odor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA000521327A CA1295550C (en) | 1986-10-24 | 1986-10-24 | Stabilized hypochlorite disinfectant composition |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1295550C true CA1295550C (en) | 1992-02-11 |
Family
ID=4134212
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000521327A Expired - Lifetime CA1295550C (en) | 1986-10-24 | 1986-10-24 | Stabilized hypochlorite disinfectant composition |
Country Status (4)
Country | Link |
---|---|
US (2) | US4839079A (en) |
EP (1) | EP0267707A1 (en) |
JP (1) | JPS63198606A (en) |
CA (1) | CA1295550C (en) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5075025A (en) * | 1986-10-24 | 1991-12-24 | Kam Scientific Inc. | Disinfectant composition |
CA2045687A1 (en) * | 1989-01-27 | 1990-07-28 | Francois Jooste | Stabilized sterilizing or disinfecting halogen containing composition, method and apparatus |
US5290470A (en) * | 1992-11-25 | 1994-03-01 | Agri-Products Special Markets, Inc. | Aqueous cleaning composition containing a chlorinated bleach, an alcohol and a surfactant |
ZA935882B (en) * | 1992-10-19 | 1994-03-11 | Clorox Co | Composition and method for developing extensional viscosity in cleaning compositions. |
EP0916719A3 (en) | 1992-11-03 | 1999-07-14 | The Procter & Gamble Company | Cleaning with short-chain surfactants |
CA2107938C (en) * | 1993-01-11 | 2005-01-11 | Clement K. Choy | Thickened hypochlorite solutions with reduced bleach odor and methods of manufacture and use |
EP0651051A3 (en) * | 1993-10-29 | 1996-02-28 | Clorox Co | Gelled hypochlorite-based cleaner. |
US5753217A (en) * | 1996-08-14 | 1998-05-19 | William C. Christopfel | Method of reducing oral malodor |
JP3783071B2 (en) * | 2002-07-11 | 2006-06-07 | 味の素株式会社 | Cosmetic composition |
US7153438B2 (en) * | 2003-02-21 | 2006-12-26 | Pur Water Purification Products, Inc. | Water treatment compositions with masking agent |
US20050282722A1 (en) * | 2004-06-16 | 2005-12-22 | Mcreynolds Kent B | Two part cleaning composition |
US20080311227A1 (en) * | 2007-06-18 | 2008-12-18 | Wd-40 Company | Long-lasting mildew stain remover and method for making same |
US9637708B2 (en) | 2014-02-14 | 2017-05-02 | Ecolab Usa Inc. | Reduced misting and clinging chlorine-based hard surface cleaner |
US20170273305A1 (en) * | 2014-11-18 | 2017-09-28 | 3M Innovative Properties Company | Compositions comprising biguanide compound and diol surfactant |
JP6741489B2 (en) * | 2016-06-27 | 2020-08-19 | ライオン株式会社 | Method for producing smoke agent composition |
KR102257568B1 (en) * | 2020-09-21 | 2021-05-27 | 김주한 | Composition for inhibiting scattering dust and sterilization using natural materials, and method for using the same |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2694722A (en) * | 1954-11-16 | Preparation of alkyl hypocplomtes | ||
US2694772A (en) * | 1949-12-14 | 1954-11-16 | Gelardin Albert | Flashlight with hermetically sealed casing |
US4113645A (en) * | 1977-07-26 | 1978-09-12 | Polak's Frutal Works, Inc. | Bleach compositions containing perfume oils |
US4196140A (en) * | 1978-09-28 | 1980-04-01 | Olin Corporation | Recovery of waste streams containing recoverable chlorine |
US4287080A (en) * | 1979-09-17 | 1981-09-01 | The Procter & Gamble Company | Detergent compositions which contain certain tertiary alcohols |
-
1986
- 1986-10-24 CA CA000521327A patent/CA1295550C/en not_active Expired - Lifetime
-
1987
- 1987-10-22 US US07/112,205 patent/US4839079A/en not_active Ceased
- 1987-10-22 EP EP87309358A patent/EP0267707A1/en not_active Ceased
- 1987-10-23 JP JP62269135A patent/JPS63198606A/en active Pending
-
1990
- 1990-07-03 US US07/547,772 patent/USRE34065E/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
EP0267707A1 (en) | 1988-05-18 |
USRE34065E (en) | 1992-09-15 |
US4839079A (en) | 1989-06-13 |
JPS63198606A (en) | 1988-08-17 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MKLA | Lapsed | ||
MKLA | Lapsed |
Effective date: 19950812 |