GB1265919A - - Google Patents
Info
- Publication number
- GB1265919A GB1265919A GB1265919DA GB1265919A GB 1265919 A GB1265919 A GB 1265919A GB 1265919D A GB1265919D A GB 1265919DA GB 1265919 A GB1265919 A GB 1265919A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dimethyl
- weight
- ammonium chloride
- composition
- dichlorobenzyl ammonium
- 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
- 239000000203 mixture Substances 0.000 abstract 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 5
- -1 alkyl dimethyl dichlorobenzyl ammonium chloride Chemical compound 0.000 abstract 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 abstract 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 abstract 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 2
- 239000000645 desinfectant Substances 0.000 abstract 2
- 229910052740 iodine Inorganic materials 0.000 abstract 2
- 239000011630 iodine Substances 0.000 abstract 2
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Inorganic materials [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 abstract 2
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 abstract 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 1
- AKCDSOIBQNVSSJ-UHFFFAOYSA-M [Cl-].C(CCCCCCCCCCC)[N+](C(C1=CC=CC=C1)(C)C)(Cl)Cl Chemical compound [Cl-].C(CCCCCCCCCCC)[N+](C(C1=CC=CC=C1)(C)C)(Cl)Cl AKCDSOIBQNVSSJ-UHFFFAOYSA-M 0.000 abstract 1
- UEHVQSYTWKQNQB-UHFFFAOYSA-M [Cl-].C(CCCCCCCCCCCCC)[N+](C(C1=CC=CC=C1)(C)C)(Cl)Cl Chemical compound [Cl-].C(CCCCCCCCCCCCC)[N+](C(C1=CC=CC=C1)(C)C)(Cl)Cl UEHVQSYTWKQNQB-UHFFFAOYSA-M 0.000 abstract 1
- KIHQRAGIEGOUKX-UHFFFAOYSA-M [Cl-].C(CCCCCCCCCCCCCCC)[N+](C(C1=CC=CC=C1)(C)C)(Cl)Cl Chemical compound [Cl-].C(CCCCCCCCCCCCCCC)[N+](C(C1=CC=CC=C1)(C)C)(Cl)Cl KIHQRAGIEGOUKX-UHFFFAOYSA-M 0.000 abstract 1
- SQCUKHCINIPYGG-UHFFFAOYSA-M [Cl-].C(CCCCCCCCCCCCCCCCC)[N+](C(C1=CC=CC=C1)(C)C)(Cl)Cl Chemical compound [Cl-].C(CCCCCCCCCCCCCCCCC)[N+](C(C1=CC=CC=C1)(C)C)(Cl)Cl SQCUKHCINIPYGG-UHFFFAOYSA-M 0.000 abstract 1
- 229910001508 alkali metal halide Inorganic materials 0.000 abstract 1
- 150000008045 alkali metal halides Chemical class 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 abstract 1
- 229960004275 glycolic acid Drugs 0.000 abstract 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 abstract 1
- 229910000043 hydrogen iodide Inorganic materials 0.000 abstract 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 1
- 235000011007 phosphoric acid Nutrition 0.000 abstract 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 abstract 1
- 235000009518 sodium iodide Nutrition 0.000 abstract 1
- 239000004094 surface-active agent Substances 0.000 abstract 1
- 239000003021 water soluble solvent Substances 0.000 abstract 1
Classifications
-
- 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
- A01N31/08—Oxygen or sulfur directly attached to an aromatic ring system
- A01N31/12—Bis-chlorophenols
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
1,265,919. Disinfectant compositions. ECONOMICS LABORATORY Inc. 29 May, 1970 [29 May, 1969], No. 26093/70. Headings A5B and ASE. [Also in Division C2] A skin disinfectant composition comprises an aqueous solution of a complex of iodine with at least one alkyl dimethyl dichlorobenzyl ammonium chloride wherein the alkyl group contains 12 to 18 carbon atoms. The mixture of alkyl dimethyl dichlorobenzyl ammonium chlorides comprises 30 to 70% by weight dodecyl dimethyl dichlorobenzylammonium chloride, 25 to 45% by weight tetradecyl dimethyl dichlorobenzyl ammonium chloride, 8-27% by weight hexadecyl dimethyl dichlorobenzyl ammonium chloride and 0 to 8% by weight octadecyl dimethyl dichlorobenzyl ammonium chloride. The iodine is present in an amount of 2 to 10% by weight of the quaternary ammonium compounds. The pH of the composition is preferably not greater than 5. The composition may also contain orthophosphoric acid, hydroxyacetic acid, hydrogen iodide and one or more alkali metal halides e.g. sodium or potassium iodide. The composition may further contain a water-soluble solvent, e.g. an alcohol, 2-(2-butoxy ethoxy)-ethanol, propylene glycol or dimethyl sulphoxide and also a non-ionic surface active agent, e.g. an alkyl phenol polyethoxy ethanol, a butoxy-mixed poly (propoxy-ethoxy) polyethoxy ethanol or an ethylene oxide or propylene oxide condensate of a glycol.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US82913769A | 1969-05-29 | 1969-05-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1265919A true GB1265919A (en) | 1972-03-08 |
Family
ID=25253633
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1265919D Expired GB1265919A (en) | 1969-05-29 | 1970-05-29 |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1265919A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000057703A1 (en) * | 1999-03-26 | 2000-10-05 | Ecolab Inc. | Antimicrobial and antiviral compositions containing an oxidizing species |
| EP1108056A1 (en) * | 1998-08-28 | 2001-06-20 | Colgate-Palmolive Company | Method for testing anti-bacterial attachment compositions |
| US6534075B1 (en) | 1999-03-26 | 2003-03-18 | Ecolab Inc. | Antimicrobial and antiviral compositions and treatments for food surfaces |
| WO2003105583A3 (en) * | 2002-03-28 | 2004-04-15 | Ecolab Inc | ANTIMICROBIAL AND ANTIVIRAL COMPOSITIONS CONTAINING AN OXIDIZING SPECIES |
-
1970
- 1970-05-29 GB GB1265919D patent/GB1265919A/en not_active Expired
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1108056A1 (en) * | 1998-08-28 | 2001-06-20 | Colgate-Palmolive Company | Method for testing anti-bacterial attachment compositions |
| WO2000057703A1 (en) * | 1999-03-26 | 2000-10-05 | Ecolab Inc. | Antimicrobial and antiviral compositions containing an oxidizing species |
| US6436445B1 (en) | 1999-03-26 | 2002-08-20 | Ecolab Inc. | Antimicrobial and antiviral compositions containing an oxidizing species |
| US6534075B1 (en) | 1999-03-26 | 2003-03-18 | Ecolab Inc. | Antimicrobial and antiviral compositions and treatments for food surfaces |
| WO2003105583A3 (en) * | 2002-03-28 | 2004-04-15 | Ecolab Inc | ANTIMICROBIAL AND ANTIVIRAL COMPOSITIONS CONTAINING AN OXIDIZING SPECIES |
| US6855328B2 (en) | 2002-03-28 | 2005-02-15 | Ecolab Inc. | Antimicrobial and antiviral compositions containing an oxidizing species |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |