GB745607A - Improvements relating to antiseptic, bactericidal, or the like agents for disinfection - Google Patents
Improvements relating to antiseptic, bactericidal, or the like agents for disinfectionInfo
- Publication number
- GB745607A GB745607A GB34095/53A GB3409553A GB745607A GB 745607 A GB745607 A GB 745607A GB 34095/53 A GB34095/53 A GB 34095/53A GB 3409553 A GB3409553 A GB 3409553A GB 745607 A GB745607 A GB 745607A
- Authority
- GB
- United Kingdom
- Prior art keywords
- radical
- meta
- bactericidal
- hydrocarbon radicals
- benzene rings
- 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
Links
- 230000000844 anti-bacterial effect Effects 0.000 title abstract 4
- 230000002421 anti-septic effect Effects 0.000 title 1
- 238000004659 sterilization and disinfection Methods 0.000 title 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- 239000004215 Carbon black (E152) Substances 0.000 abstract 4
- 125000005843 halogen group Chemical group 0.000 abstract 4
- 229930195733 hydrocarbon Natural products 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 abstract 2
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 239000003599 detergent Substances 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 2
- LEVJVKGPFAQPOI-UHFFFAOYSA-N phenylmethanone Chemical compound O=[C]C1=CC=CC=C1 LEVJVKGPFAQPOI-UHFFFAOYSA-N 0.000 abstract 2
- WKEDVNSFRWHDNR-UHFFFAOYSA-N salicylanilide Chemical compound OC1=CC=CC=C1C(=O)NC1=CC=CC=C1 WKEDVNSFRWHDNR-UHFFFAOYSA-N 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- LDMOEFOXLIZJOW-UHFFFAOYSA-N 1-dodecanesulfonic acid Chemical class CCCCCCCCCCCCS(O)(=O)=O LDMOEFOXLIZJOW-UHFFFAOYSA-N 0.000 abstract 1
- GKPNMUZVXNHWPX-UHFFFAOYSA-N 2,4-dipentylphenol Chemical compound CCCCCC1=CC=C(O)C(CCCCC)=C1 GKPNMUZVXNHWPX-UHFFFAOYSA-N 0.000 abstract 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 abstract 1
- -1 2-hydroxybenzoyl anilide Chemical class 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000007859 condensation product Substances 0.000 abstract 1
- 238000005108 dry cleaning Methods 0.000 abstract 1
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 abstract 1
- 239000003350 kerosene Substances 0.000 abstract 1
- MXMBAFVETQBLGP-ICYLSCGJSA-M potassium;(z,12r)-12-hydroxy-2-sulfooctadec-9-enoate Chemical compound [K+].CCCCCC[C@@H](O)C\C=C/CCCCCCC(C([O-])=O)S(O)(=O)=O MXMBAFVETQBLGP-ICYLSCGJSA-M 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000000344 soap Substances 0.000 abstract 1
- 159000000000 sodium salts Chemical class 0.000 abstract 1
- 229910052938 sodium sulfate Inorganic materials 0.000 abstract 1
- 235000011152 sodium sulphate Nutrition 0.000 abstract 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 1
- 239000004094 surface-active agent Substances 0.000 abstract 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
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)
- Detergent Compositions (AREA)
- Cosmetics (AREA)
Abstract
A cleansing composition comprises a bactericidal 2-hydroxy-benzanilide in which both benzene rings contain together at least two and preferably more halogen atoms, of which at least one, and preferably more, must be in the anilide radical and one must be in the meta- or para-position to the amino radical, a halogen substituent in the meta-position being replaceable by the trifluoromethyl group; both benzene rings, but preferably that of the benzoyl radical, can also be substituted by hydrocarbon radicals containing at most 10 carbon atoms. The hydrocarbon radicals specified are methyl, allyl, phenyl and tertiary amyl. The cleansing agents specified are soaps, the ethylene oxide condensation products of 2, 4-diamyl-phenol, lauryl sulphonates, the sodium salt of dodecylbenzene sulphonic acid and oleyl-N-methyl taurine. The compositions may also contain sodium sulphate, soda, alkali poly- or polymeta-phosphates, and a complex-forming agent such as iminodiacetic acid. The halogenated hydroxybenzanilides may also be included in dry-cleaning compositions comprising kerosene and a surface-active agent, e.g. potassium sulphoricinoleate or an alkanolamine salt of an anion-active sulphonic or carboxylic acid.ALSO:A bactericidal composition comprises a capillary active cleansing agent and a bactericidal 2-hydroxybenzoyl anilide in which both benzene rings contain together at least two and preferably more halogen atoms of which at least one and preferably more must be in the anilide radical and one must be in the meta- or paraposition to the amino radical, a halogen substituent in the meta-position being replaceable by the trifluoromethyl group, and in which both benzene rings but preferably that of the benzoyl radical can also be substituted by hydrocarbon radicals containing at most 10 carbon atoms. The hydrocarbon radicals specified are methyl, allyl, phenyl, and tertiary amyl.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH745607X | 1952-12-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB745607A true GB745607A (en) | 1956-02-29 |
Family
ID=4533462
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB34095/53A Expired GB745607A (en) | 1952-12-09 | 1953-12-08 | Improvements relating to antiseptic, bactericidal, or the like agents for disinfection |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE524930A (en) |
| CH (1) | CH311986A (en) |
| FR (1) | FR1094578A (en) |
| GB (1) | GB745607A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3041236A (en) * | 1959-09-18 | 1962-06-26 | Herbert C Stecker | Germicides containing trifluoromethyl halogenated salicylanilides |
| US3276955A (en) * | 1962-07-30 | 1966-10-04 | Armour & Co | Bacteriostatic compositions |
| US3445397A (en) * | 1962-04-20 | 1969-05-20 | Armour & Co | Synergistic combination of a halogenated bisphenol and a polyhalo-salicylanilide |
| US4170638A (en) * | 1976-11-05 | 1979-10-09 | S. S. Steiner, Inc. | Method for producing a deodorant |
| WO2006038980A2 (en) * | 2004-09-30 | 2006-04-13 | Kimberly-Clark Worldwide, Inc. | Non-absorbent and absorbent articles for inhibiting the production of exoproteins |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE604014A (en) * | 1960-05-20 | |||
| US4287191A (en) * | 1980-04-14 | 1981-09-01 | The Research Foundation Of State University Of New York | Novel salicylanilides and microbiocidal compositions and uses thereof |
| US4358443A (en) * | 1980-04-14 | 1982-11-09 | The Research Foundation Of State University Of New York | Method and composition for controlling the growth of microorganisms |
| US4725590A (en) * | 1983-08-24 | 1988-02-16 | Lever Brothers Company | Method of relieving pain and inflammatory conditions employing substituted salicylamides |
| US4742083A (en) * | 1983-08-24 | 1988-05-03 | Lever Brothers Company | Method of relieving pain and inflammatory conditions employing substituted salicylamides |
| US4560549A (en) * | 1983-08-24 | 1985-12-24 | Lever Brothers Company | Method of relieving pain and inflammatory conditions employing substituted salicylamides |
| US4939132A (en) * | 1985-04-15 | 1990-07-03 | The Research Foundation Of State University Of New York | Novel 5-alkylsulfonylsalicylanilides and microbiocidal compositions for controlling the growth of microorganisms |
-
0
- BE BE524930D patent/BE524930A/xx unknown
-
1952
- 1952-12-09 CH CH311986D patent/CH311986A/en unknown
-
1953
- 1953-12-08 GB GB34095/53A patent/GB745607A/en not_active Expired
- 1953-12-08 FR FR1094578D patent/FR1094578A/en not_active Expired
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3041236A (en) * | 1959-09-18 | 1962-06-26 | Herbert C Stecker | Germicides containing trifluoromethyl halogenated salicylanilides |
| US3445397A (en) * | 1962-04-20 | 1969-05-20 | Armour & Co | Synergistic combination of a halogenated bisphenol and a polyhalo-salicylanilide |
| US3276955A (en) * | 1962-07-30 | 1966-10-04 | Armour & Co | Bacteriostatic compositions |
| US4170638A (en) * | 1976-11-05 | 1979-10-09 | S. S. Steiner, Inc. | Method for producing a deodorant |
| WO2006038980A2 (en) * | 2004-09-30 | 2006-04-13 | Kimberly-Clark Worldwide, Inc. | Non-absorbent and absorbent articles for inhibiting the production of exoproteins |
| WO2006038980A3 (en) * | 2004-09-30 | 2006-06-29 | Kimberly Clark Co | Non-absorbent and absorbent articles for inhibiting the production of exoproteins |
Also Published As
| Publication number | Publication date |
|---|---|
| FR1094578A (en) | 1955-05-23 |
| BE524930A (en) | |
| CH311986A (en) | 1955-12-15 |
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