GB1063995A - Process for the manufacture of organic mercury compounds and products obtained thereby - Google Patents
Process for the manufacture of organic mercury compounds and products obtained therebyInfo
- Publication number
- GB1063995A GB1063995A GB35950/63A GB3595063A GB1063995A GB 1063995 A GB1063995 A GB 1063995A GB 35950/63 A GB35950/63 A GB 35950/63A GB 3595063 A GB3595063 A GB 3595063A GB 1063995 A GB1063995 A GB 1063995A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- compounds
- slimicides
- polybasic
- dimercuric
- 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
- 238000000034 method Methods 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- 150000002731 mercury compounds Chemical class 0.000 title 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 11
- 150000001875 compounds Chemical class 0.000 abstract 11
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 abstract 8
- 239000002253 acid Substances 0.000 abstract 7
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 abstract 6
- 239000005695 Ammonium acetate Substances 0.000 abstract 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 6
- 235000019257 ammonium acetate Nutrition 0.000 abstract 6
- 229940043376 ammonium acetate Drugs 0.000 abstract 6
- XJMWHXZUIGHOBA-UHFFFAOYSA-N azane;propanoic acid Chemical compound N.CCC(O)=O XJMWHXZUIGHOBA-UHFFFAOYSA-N 0.000 abstract 6
- 235000010290 biphenyl Nutrition 0.000 abstract 6
- 239000004305 biphenyl Substances 0.000 abstract 6
- 125000006267 biphenyl group Chemical group 0.000 abstract 6
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 6
- 239000000417 fungicide Substances 0.000 abstract 5
- -1 heterocyclic carboxylic Chemical class 0.000 abstract 5
- 230000002378 acidificating effect Effects 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 4
- 125000002252 acyl group Chemical group 0.000 abstract 3
- 125000004423 acyloxy group Chemical group 0.000 abstract 3
- 125000001931 aliphatic group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 239000004744 fabric Substances 0.000 abstract 3
- 150000002484 inorganic compounds Chemical class 0.000 abstract 3
- 150000007522 mineralic acids Chemical class 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 125000001624 naphthyl group Chemical group 0.000 abstract 3
- 150000002894 organic compounds Chemical class 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 150000007519 polyprotic acids Polymers 0.000 abstract 3
- 229920006395 saturated elastomer Polymers 0.000 abstract 3
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 2
- 150000001298 alcohols Chemical class 0.000 abstract 2
- 229910021529 ammonia Inorganic materials 0.000 abstract 2
- HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical compound O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 abstract 2
- 239000004927 clay Substances 0.000 abstract 2
- 150000002085 enols Chemical class 0.000 abstract 2
- 150000002334 glycols Chemical class 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 2
- 150000003141 primary amines Chemical class 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 150000004760 silicates Chemical class 0.000 abstract 2
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 2
- 239000000454 talc Substances 0.000 abstract 2
- 229910052623 talc Inorganic materials 0.000 abstract 2
- 150000003512 tertiary amines Chemical class 0.000 abstract 2
- 150000003573 thiols Chemical class 0.000 abstract 2
- 239000007789 gas Substances 0.000 abstract 1
- 239000004009 herbicide Substances 0.000 abstract 1
- 229910000069 nitrogen hydride Inorganic materials 0.000 abstract 1
- 239000002904 solvent 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)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises compounds of the formula R2Hg2NH2X and their preparation, where R is unsubstituted or substituted benzene or naphthyl, X represents the residue of an inorganic or organic compound having an active acidic hydrogen atom, X being, e.g. the acid or acyl group of a monobasic or polybasic inorganic acid, or an acyloxy group of a saturated or unsaturated monobasic or polybasic aliphatic acid, or of an aromatic, cycloaliphatic or heterocyclic carboxylic or sulphonic acid, possibly substituted compounds having reactive methylene groups, e.g. barbituric acid, thiols and enols. X may also be a polybasic acid radical partially neutralized by, e.g. NH4 or Na. The compounds of the invention are prepared using anhydrous conditions by one or more of the following methods (1) by reacting RHgOH with dry NH3 gas in a solvent which will dissolve the formed R2Hg2NH2OH, and then reacting this with an acid or salt, to form R2Hg2NH2X, (2) by reacting RHgX in an organic liquid with dry ammonia gas at about 10-100 DEG C., (3) by reacting a mixture of a compound having an acidic hydrogen atom or its salt and RHgOH in an organic liquid with dry ammonia gas.ALSO:Slimicides comprise compounds with the formula R2 Hg2 NH2X where R is unsubstituted or substituted phenyl or naphthyl, X represents the residue of an inorganic or organic compound having an active acidic hydrogen atom, X being e.g. the acid or acyl group of a monobasic or polybasic inorganic acid, or an acyloxy group of a saturated or unsaturated monobasic or polybasic aliphatic acid, or of an aromatic, cycloaliphatic or heterocyclic carboxylic or sulphonic acid, possibly substituted compounds having reactive methylene groups e.g. barbituric acid, thiols and enols. X may also be a polybasic acid radical partially neutralized by e.g. NH4 or Na. For use as slimicides and fungicides, the compounds may be diluted with talc, clay or synthetic silicates. For use as slimicides, fungicides and mildew proofing for fabrics, solutions may be used containing the compounds together with ammonium acetate, propionate, sulphate, free ammonia, primary or tertiary amines, alkanolamines, alcohols and glycols. Special compositions for use as slimicides in the paper industry are:- Example B: Diphenyl dimercuric ammonium propionate and "HY - FLO" (Trade Mark). Example K: Methanol, ammonium acetate, diphenyl dimercuric ammonium propionate, water, morpholine Example L: Ethylene glycol, ammonium acetate, diphenyl dimercuric ammonium propionate, morpholine and water.ALSO:Herbicides, fungicides, fungistats, slimicides, mildew proofer for fabrics comprise the compound R2 Hg2NH2X where R is unsubstituted or substituted benzene or naphthyl, X represents the residue of an inorganic or organic compound having an active acidic hydrogen atom, X being e.g. the acid or acyl group of a monobasic or polybasic inorganic acid, or an acyloxy group of a saturated or unsaturated monobasic or polybasic aliphatic acid, or of an aromatic, cycloaliphatic or heterocyclic carboxylic or sulphonic acid, possibly substituted. X may also be a polybasic acid radical partially neutralized by e.g. NH4 or Na. For use as slimicides and fungicides, the compounds may be diluted with talc, clay or synthetic silicates. For use as slimicides, fungicides and mildew proofing for fabrics, solutions may be used containing the compounds together with ammonium acetate, propionate, sulphate, free ammonia, primary or tertiary amines, alkanolamines, alcohols and glycols. Special compositions for use as slimicides in the paper industry are: Example B: Diphenyl dimercuric ammonium propionate and "HY-FLO" (Trade Mark). Example K: Methanol, ammonium acetate, diphenyl dimercuric ammonium propionate, water, morpholine Example L: Ethylene glycol, ammonium acetate, diphenyl dimercuric ammonium propionate, morpholine and water.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR947377A FR1537656A (en) | 1963-09-12 | 1963-09-12 | Production and applications of new organic mercury compounds |
GB35950/63A GB1063995A (en) | 1963-09-12 | 1963-09-12 | Process for the manufacture of organic mercury compounds and products obtained thereby |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB35950/63A GB1063995A (en) | 1963-09-12 | 1963-09-12 | Process for the manufacture of organic mercury compounds and products obtained thereby |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1063995A true GB1063995A (en) | 1967-04-05 |
Family
ID=10383296
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB35950/63A Expired GB1063995A (en) | 1963-09-12 | 1963-09-12 | Process for the manufacture of organic mercury compounds and products obtained thereby |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1063995A (en) |
-
1963
- 1963-09-12 GB GB35950/63A patent/GB1063995A/en not_active Expired
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