NO135852B - - Google Patents
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- Publication number
- NO135852B NO135852B NO3055/73A NO305573A NO135852B NO 135852 B NO135852 B NO 135852B NO 3055/73 A NO3055/73 A NO 3055/73A NO 305573 A NO305573 A NO 305573A NO 135852 B NO135852 B NO 135852B
- Authority
- NO
- Norway
- Prior art keywords
- gluconate
- lactate
- weight
- solution
- chlorhexidine
- Prior art date
Links
- 229940050410 gluconate Drugs 0.000 claims description 28
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 claims description 25
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 claims description 15
- WUJZVKDLOUTNMK-UHFFFAOYSA-N C(CCCCCCCCCCC)[N+](C(C1=CC=CC=C1)(C)C)(Cl)Cl Chemical compound C(CCCCCCCCCCC)[N+](C(C1=CC=CC=C1)(C)C)(Cl)Cl WUJZVKDLOUTNMK-UHFFFAOYSA-N 0.000 claims description 6
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 5
- CYDRXTMLKJDRQH-UHFFFAOYSA-N benzododecinium Chemical compound CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 CYDRXTMLKJDRQH-UHFFFAOYSA-N 0.000 claims description 4
- WNBGYVXHFTYOBY-UHFFFAOYSA-N benzyl-dimethyl-tetradecylazanium Chemical compound CCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 WNBGYVXHFTYOBY-UHFFFAOYSA-N 0.000 claims description 4
- 239000000645 desinfectant Substances 0.000 claims description 4
- 239000013543 active substance Substances 0.000 claims description 3
- ULBMBQLPJXAYAG-UHFFFAOYSA-N ethyl-dimethyl-(1-phenyltridecyl)azanium Chemical compound CCCCCCCCCCCCC([N+](C)(C)CC)C1=CC=CC=C1 ULBMBQLPJXAYAG-UHFFFAOYSA-N 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 2
- 239000007864 aqueous solution Substances 0.000 claims description 2
- WJLUBOLDZCQZEV-UHFFFAOYSA-M hexadecyl(trimethyl)azanium;hydroxide Chemical compound [OH-].CCCCCCCCCCCCCCCC[N+](C)(C)C WJLUBOLDZCQZEV-UHFFFAOYSA-M 0.000 claims 1
- 239000000243 solution Substances 0.000 description 25
- GHXZTYHSJHQHIJ-UHFFFAOYSA-N Chlorhexidine Chemical compound C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 GHXZTYHSJHQHIJ-UHFFFAOYSA-N 0.000 description 14
- 229960003260 chlorhexidine Drugs 0.000 description 14
- 229960003333 chlorhexidine gluconate Drugs 0.000 description 7
- YZIYKJHYYHPJIB-UUPCJSQJSA-N chlorhexidine gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O.C1=CC(Cl)=CC=C1NC(=N)NC(=N)NCCCCCCNC(=N)NC(=N)NC1=CC=C(Cl)C=C1 YZIYKJHYYHPJIB-UUPCJSQJSA-N 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000002585 base Substances 0.000 description 6
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- ZFKLWOJJZKGHQW-UHFFFAOYSA-M C(C(O)C)(=O)[O-].C(CCCCCCCCCCC)[N+](C(C1=CC=CC=C1)(C)C)(Cl)Cl Chemical compound C(C(O)C)(=O)[O-].C(CCCCCCCCCCC)[N+](C(C1=CC=CC=C1)(C)C)(Cl)Cl ZFKLWOJJZKGHQW-UHFFFAOYSA-M 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 5
- 244000052616 bacterial pathogen Species 0.000 description 5
- -1 dodecyldimethyldichlorobenzylammonium lactate dodecyldimethylbenzylammonium lactate tetradecyldimethylbenzylammonium lactate dodecyldimethylethylbenzylammonium lactate hexadecyltrimethylammonium Chemical compound 0.000 description 5
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 150000004820 halides Chemical class 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- RLGQACBPNDBWTB-UHFFFAOYSA-N cetyltrimethylammonium ion Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)C RLGQACBPNDBWTB-UHFFFAOYSA-N 0.000 description 3
- 235000014655 lactic acid Nutrition 0.000 description 3
- 239000004310 lactic acid Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 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 description 2
- 239000003513 alkali Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- RARSHUDCJQSEFJ-UHFFFAOYSA-N p-Hydroxypropiophenone Chemical compound CCC(=O)C1=CC=C(O)C=C1 RARSHUDCJQSEFJ-UHFFFAOYSA-N 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- WTXGYGWMPUGBAL-SQOUGZDYSA-N (3r,4s,5r,6r)-3,4,5,6-tetrahydroxyoxepan-2-one Chemical compound O[C@@H]1COC(=O)[C@H](O)[C@@H](O)[C@@H]1O WTXGYGWMPUGBAL-SQOUGZDYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- OCUCCJIRFHNWBP-IYEMJOQQSA-L Copper gluconate Chemical class [Cu+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O OCUCCJIRFHNWBP-IYEMJOQQSA-L 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 241000191940 Staphylococcus Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- DPXJRRNZAUKEHX-UHFFFAOYSA-M hexadecyl(trimethyl)azanium;2-hydroxypropanoate Chemical compound CC(O)C([O-])=O.CCCCCCCCCCCCCCCC[N+](C)(C)C DPXJRRNZAUKEHX-UHFFFAOYSA-M 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
- A01N47/42—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides containing —N=CX2 groups, e.g. isothiourea
- A01N47/44—Guanidine; Derivatives thereof
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)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Cosmetics (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT659572A AT318152B (de) | 1972-07-31 | 1972-07-31 | Desinfektionsmittel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO135852B true NO135852B (xx) | 1977-03-07 |
| NO135852C NO135852C (xx) | 1977-06-15 |
Family
ID=3587881
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO3055/73A NO135852C (xx) | 1972-07-31 | 1973-07-30 |
Country Status (13)
| Country | Link |
|---|---|
| AT (1) | AT318152B (xx) |
| AU (1) | AU468341B2 (xx) |
| BE (1) | BE802957A (xx) |
| CA (1) | CA1026232A (xx) |
| DD (1) | DD106780A5 (xx) |
| FI (1) | FI58424C (xx) |
| FR (1) | FR2194448B1 (xx) |
| GB (1) | GB1355636A (xx) |
| IL (1) | IL42716A (xx) |
| NL (1) | NL7306479A (xx) |
| NO (1) | NO135852C (xx) |
| SE (1) | SE397268B (xx) |
| ZA (1) | ZA735201B (xx) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE425043B (sv) * | 1977-05-10 | 1982-08-30 | Kenogard Ab | Fungicid komposition, foretredesvis for anvendning som treskyddsmedel, innehallande minst en kvarter ammoniumforening i blandning med en aminkomponent |
| AT381001B (de) * | 1983-11-28 | 1986-08-11 | Arcana Chem Pharm | Verfahren zur herstellung klarer waesseriger desinfektionsmittelloesungen |
| FR2691325B1 (fr) * | 1992-05-21 | 1997-06-06 | Hutchinson | Compositions a base d'antiseptiques et leurs applications. |
| IL100881A (en) * | 1992-02-06 | 1996-06-18 | Porat Michael | Causal drug prevents diseases, devices and methods of using it |
| US6303557B1 (en) | 1999-11-16 | 2001-10-16 | S. C. Johnson Commercial Markets, Inc. | Fast acting disinfectant and cleaner containing a polymeric biguanide |
| US20110117032A1 (en) * | 2008-07-22 | 2011-05-19 | Donna Gilding | Santising compositions and methods |
| GB2474017B (en) * | 2009-09-29 | 2015-07-15 | Europ First Aid Ltd | Biocidal solution |
-
1972
- 1972-07-31 AT AT659572A patent/AT318152B/de not_active IP Right Cessation
-
1973
- 1973-03-12 SE SE7303386A patent/SE397268B/xx unknown
- 1973-03-14 GB GB1230573A patent/GB1355636A/en not_active Expired
- 1973-05-08 FR FR7316482A patent/FR2194448B1/fr not_active Expired
- 1973-05-09 NL NL7306479A patent/NL7306479A/xx unknown
- 1973-07-11 IL IL42716A patent/IL42716A/en unknown
- 1973-07-27 DD DD172577A patent/DD106780A5/xx unknown
- 1973-07-30 AU AU58699/73A patent/AU468341B2/en not_active Expired
- 1973-07-30 CA CA177,588A patent/CA1026232A/en not_active Expired
- 1973-07-30 BE BE134004A patent/BE802957A/xx unknown
- 1973-07-30 NO NO3055/73A patent/NO135852C/no unknown
- 1973-07-30 FI FI2389/73A patent/FI58424C/fi active
- 1973-07-31 ZA ZA735201A patent/ZA735201B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE2310989A1 (de) | 1974-02-14 |
| NO135852C (xx) | 1977-06-15 |
| FI58424B (fi) | 1980-10-31 |
| DD106780A5 (xx) | 1974-07-05 |
| IL42716A0 (en) | 1973-10-25 |
| DE2310989B2 (de) | 1975-06-26 |
| FR2194448B1 (xx) | 1976-09-17 |
| ZA735201B (en) | 1974-09-25 |
| AU5869973A (en) | 1975-01-30 |
| BE802957A (fr) | 1973-11-16 |
| AU468341B2 (en) | 1976-01-08 |
| CA1026232A (en) | 1978-02-14 |
| NL7306479A (xx) | 1974-02-04 |
| SE397268B (sv) | 1977-10-31 |
| AT318152B (de) | 1974-09-25 |
| GB1355636A (en) | 1974-06-05 |
| IL42716A (en) | 1976-03-31 |
| FI58424C (fi) | 1981-02-10 |
| FR2194448A1 (xx) | 1974-03-01 |
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