GB593678A - Improvements in the manufacture and use of germicidal compounds - Google Patents
Improvements in the manufacture and use of germicidal compoundsInfo
- Publication number
- GB593678A GB593678A GB11907/43A GB1190743A GB593678A GB 593678 A GB593678 A GB 593678A GB 11907/43 A GB11907/43 A GB 11907/43A GB 1190743 A GB1190743 A GB 1190743A GB 593678 A GB593678 A GB 593678A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mercury
- phenyl
- germicidal
- general formula
- aqueous solution
- 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
- 230000002070 germicidal effect Effects 0.000 title abstract 3
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- 239000007864 aqueous solution Substances 0.000 abstract 2
- XEBWQGVWTUSTLN-UHFFFAOYSA-M phenylmercury acetate Chemical compound CC(=O)O[Hg]C1=CC=CC=C1 XEBWQGVWTUSTLN-UHFFFAOYSA-M 0.000 abstract 2
- RRFGSWMKSSCUSU-UHFFFAOYSA-M 2-hydroxypropanoate;phenylmercury(1+) Chemical compound CC(O)C(=O)O[Hg]C1=CC=CC=C1 RRFGSWMKSSCUSU-UHFFFAOYSA-M 0.000 abstract 1
- 229920000742 Cotton Polymers 0.000 abstract 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 abstract 1
- 150000001450 anions Chemical class 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 239000013078 crystal Substances 0.000 abstract 1
- 238000007598 dipping method Methods 0.000 abstract 1
- 239000004744 fabric Substances 0.000 abstract 1
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 239000010985 leather Substances 0.000 abstract 1
- 229940049920 malate Drugs 0.000 abstract 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 abstract 1
- 150000002730 mercury Chemical class 0.000 abstract 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 abstract 1
- 229910052753 mercury Inorganic materials 0.000 abstract 1
- 125000000962 organic group Chemical group 0.000 abstract 1
- 239000000123 paper Substances 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- -1 pyridyl mercury butyrate Chemical compound 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 239000005060 rubber Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 238000005507 spraying Methods 0.000 abstract 1
- 239000004753 textile Substances 0.000 abstract 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyridine Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Organo - mercury compounds, having germicidal and fungicidal properties, are obtained by reacting an alkylolamine with an organic mercury salt of the general formula R-Hg-X (where R indicates an aromatic or heterocyclic group having the mercury attached to a carbon atom thereof and X represents an anion), specified compounds of the above general formula being phenyl mercury acetate, phenyl mercury lactate, toluylmercury malate and pyridyl mercury butyrate. In an example, the reaction in aqueous solution of phenyl mercuryacetate with triethanolamine at room temperature is described, together with the treatment of a cotton fabric with the aqueous solution so obtained. If the reactants are mixed in the absence of a solvent, the reaction product is obtained as a mass of waxy crystals, which melt at 75 DEG C. In addition to the treatment of textiles, the product may also be used for imparting germicidal properties to paper, leather or rubber, by spraying padding, dipping or black-filling.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US593678XA | 1942-05-16 | 1942-05-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB593678A true GB593678A (en) | 1947-10-23 |
Family
ID=22022506
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB11907/43A Expired GB593678A (en) | 1942-05-16 | 1943-07-21 | Improvements in the manufacture and use of germicidal compounds |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB593678A (en) |
-
1943
- 1943-07-21 GB GB11907/43A patent/GB593678A/en not_active Expired
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB1016514A (en) | 2-aryl-amino-1,3-diazacyclopentenes | |
| US2423262A (en) | Compounds having the formula | |
| MX3240E (en) | PROCEDURE FOR PREPARING 1 - ARIL - 2 - (1 - IMIDAZOL IL) ETHERS - ALKYL AND TIO ETHERS | |
| GB593678A (en) | Improvements in the manufacture and use of germicidal compounds | |
| US3221021A (en) | Acylated oxazolidinones | |
| GB1029228A (en) | A method of preparing new quaternary ammonium salts with disinfectant activity | |
| FR2383175A1 (en) | PROCESS FOR PREPARING PHENYLPYRIDAZINONE DERIVATIVES | |
| GB1318298A (en) | 0,0-dialkyllthiophosphoric and 0,0-dialkyl-dithiophosphoric esters of oxadiazoles | |
| US2423121A (en) | Reaction product of phenyl mercury salts with hydroxy alkyl amino compounds and their preparation | |
| ES425533A1 (en) | Dichlorothiazolylureas processes for their preparation and their use as herbicides | |
| US2898262A (en) | Compositions and methods | |
| GB988253A (en) | Production of azoalkanes | |
| GB971219A (en) | Novel alkane sulphonanilides and herbicidal compositions containing them | |
| GB956027A (en) | 2,6-dihalobenzamidines and derivatives thereof | |
| GB728969A (en) | Manufacture of tribromo- and trichloro-methyl sulphone derivatives | |
| GB915751A (en) | Substituted alanines | |
| GB964699A (en) | Improvements in or relating to thiophosphonic acid esters | |
| GB877106A (en) | Substituted urea complex salts | |
| GB938727A (en) | Sulphonamides | |
| GB891862A (en) | New piperidine derivatives and processes for preparing the same | |
| GB1062877A (en) | Improvements in and relating to the preparation of substituted carbinols | |
| ES275615A1 (en) | Procedure for the preparation of a new derivative of piperacin (Machine-translation by Google Translate, not legally binding) | |
| GB890533A (en) | Improvements in or relating to heterocyclic quaternary ammonium salts | |
| GB667094A (en) | Manufacture of biguanide derivatives | |
| GB945892A (en) | Phenylalanines |