BE458103A - - Google Patents
Info
- Publication number
- BE458103A BE458103A BE458103DA BE458103A BE 458103 A BE458103 A BE 458103A BE 458103D A BE458103D A BE 458103DA BE 458103 A BE458103 A BE 458103A
- Authority
- BE
- Belgium
- Prior art keywords
- mercury
- preparing
- organic
- inorganic
- compounds
- Prior art date
Links
- 230000002421 anti-septic effect Effects 0.000 claims description 13
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 10
- 239000000645 desinfectant Substances 0.000 claims description 9
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 9
- 229910052753 mercury Inorganic materials 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 8
- 150000002989 phenols Chemical group 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 6
- UKWHYYKOEPRTIC-UHFFFAOYSA-N mercury(ii) oxide Chemical compound [Hg]=O UKWHYYKOEPRTIC-UHFFFAOYSA-N 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 229940064004 antiseptic throat preparations Drugs 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 150000001555 benzenes Chemical class 0.000 claims description 3
- 150000002730 mercury Chemical class 0.000 claims description 3
- 229910000474 mercury oxide Inorganic materials 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 238000006467 substitution reaction Methods 0.000 claims description 3
- 230000001476 alcoholic effect Effects 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 239000000080 wetting agent Substances 0.000 claims description 2
- 239000012670 alkaline solution Substances 0.000 claims 1
- 150000002731 mercury compounds Chemical class 0.000 claims 1
- 150000002891 organic anions Chemical class 0.000 claims 1
- 230000000590 parasiticidal effect Effects 0.000 claims 1
- 239000003755 preservative agent Substances 0.000 claims 1
- 230000000717 retained effect Effects 0.000 claims 1
- 239000000243 solution Substances 0.000 description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 235000019441 ethanol Nutrition 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 230000000844 anti-bacterial effect Effects 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 229960000583 acetic acid Drugs 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- -1 alkyl radicals Chemical class 0.000 description 2
- 239000004599 antimicrobial Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 230000002070 germicidal effect Effects 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- WPWHSFAFEBZWBB-UHFFFAOYSA-N 1-butyl radical Chemical group [CH2]CCC WPWHSFAFEBZWBB-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- 241000271566 Aves Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 235000019687 Lamb Nutrition 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 241000191940 Staphylococcus Species 0.000 description 1
- 241000194017 Streptococcus Species 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 206010052428 Wound Diseases 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- WRYNUJYAXVDTCB-UHFFFAOYSA-M acetyloxymercury Chemical compound CC(=O)O[Hg] WRYNUJYAXVDTCB-UHFFFAOYSA-M 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 229960003093 antiseptics and disinfectants Drugs 0.000 description 1
- 230000003385 bacteriostatic effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 230000002920 convulsive effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- FWJGYFKCKCRGIV-UHFFFAOYSA-N dicyanomercury;oxomercury Chemical compound [Hg]=O.N#C[Hg]C#N FWJGYFKCKCRGIV-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000001077 hypotensive effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229940101209 mercuric oxide Drugs 0.000 description 1
- BRMYZIKAHFEUFJ-UHFFFAOYSA-L mercury diacetate Chemical compound CC(=O)O[Hg]OC(C)=O BRMYZIKAHFEUFJ-UHFFFAOYSA-L 0.000 description 1
- LWJROJCJINYWOX-UHFFFAOYSA-L mercury dichloride Chemical compound Cl[Hg]Cl LWJROJCJINYWOX-UHFFFAOYSA-L 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 210000004400 mucous membrane Anatomy 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 231100000344 non-irritating Toxicity 0.000 description 1
- 231100000926 not very toxic Toxicity 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 230000003285 pharmacodynamic effect Effects 0.000 description 1
- 239000000590 phytopharmaceutical Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F3/00—Compounds containing elements of Groups 2 or 12 of the Periodic Table
- C07F3/10—Mercury compounds
- C07F3/12—Aromatic substances containing mercury
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE458103A true BE458103A (enrdf_load_stackoverflow) |
Family
ID=111465
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE458103D BE458103A (enrdf_load_stackoverflow) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE458103A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2539418A1 (fr) * | 1983-01-13 | 1984-07-20 | Inst Textile De France | Nouveaux derives du mercurobutol et leur application a la protection de supports notamment textiles |
-
0
- BE BE458103D patent/BE458103A/fr unknown
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2539418A1 (fr) * | 1983-01-13 | 1984-07-20 | Inst Textile De France | Nouveaux derives du mercurobutol et leur application a la protection de supports notamment textiles |
| EP0116489A1 (fr) * | 1983-01-13 | 1984-08-22 | Centre Technique Industriel dit: INSTITUT TEXTILE DE FRANCE | Nouveaux dérivés du mercurobutol et leur application à la protection de supports notamment textiles |
| US4556721A (en) * | 1983-01-13 | 1985-12-03 | Centre Technique Industriel Styled: Institut Textile | Derivatives of mercurobutol, and their application to the protection of supports more particularly in textiles |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA1166578A (fr) | Composition cosmetique capillaire, contenant un extrait de salsepareille | |
| CA1116635A (fr) | Procede de preparation de nouveaux derives de la benzene propanamine et de leurs sels | |
| EP0078785A1 (fr) | Sels d'acide valproîque, leur préparation et leur utilisation | |
| EP0308328B1 (fr) | Dérivés de (benzyl pipéridino)-1 propanol-2, leur préparation, leur utilisation comme antimicrobiens et les produits les contenant | |
| EP0469983B1 (fr) | Clathrates de peroxyacides, leur préparation et leurs utilisations | |
| EP0288352A1 (fr) | Dérivés aromatiques, leur préparation et leur utilisation comme antimicrobiens | |
| EP0593506B1 (fr) | Lipoaminoacides, leur procede de preparation et leurs applications | |
| CA1242458A (fr) | Ethers-oxydes et ethers-oximes d'alcoylaminoalcools comme medicaments, produits nouveaux et procedes pour leur preparation | |
| BE458103A (enrdf_load_stackoverflow) | ||
| EP0135433B1 (fr) | Dérivés de l'acide benzoique pour utilisation comme médicament et utilisation de ces dérivés comme agents conservateurs ou désinfectants | |
| EP0136195A1 (fr) | Dérivés de la benzamidine à activité antimicrobienne, procédé d'obtention et application à titre de médicaments désinfectants ou conservateurs | |
| EP0520865B1 (fr) | Utilisation de dérivés d'acide pour la fabrication d'un médicament pédiculicide | |
| BE475167A (enrdf_load_stackoverflow) | ||
| BE475168A (enrdf_load_stackoverflow) | ||
| BE903568A (fr) | Nouveaux composes chimiques a activites antiphlogistiques, antiseptiques et detergentes | |
| CH623724A5 (enrdf_load_stackoverflow) | ||
| CH224646A (fr) | Procédé de préparation du 2,2'-dioxy-3,5,6,3',5',6'-hexachloro-diphénylméthane. | |
| CA1311683C (fr) | Procede de preparation d'une composition inhibitrice ou destructive d'aumoins un etre vivant unicellulaire renfermant un fluorure d'ammonium quaternaire et procede de preparation de ce sel | |
| FR2516919A1 (fr) | Nouveau derive de n, n''-bis (4-chlorophenyl)-3,12-diimino-2, 4, 11, 13-tetraaza-tetradecane-diimidoamide, son procede de preparation et son application en therapeutique | |
| BE489839A (enrdf_load_stackoverflow) | ||
| BE670235A (enrdf_load_stackoverflow) | ||
| BE492921A (enrdf_load_stackoverflow) | ||
| BE638810A (enrdf_load_stackoverflow) | ||
| BE572852A (enrdf_load_stackoverflow) | ||
| BE697820A (enrdf_load_stackoverflow) |