NO810105L - Dikaliumpentapropionat og fremgangsmaate til fremstilling derav - Google Patents
Dikaliumpentapropionat og fremgangsmaate til fremstilling deravInfo
- Publication number
- NO810105L NO810105L NO810105A NO810105A NO810105L NO 810105 L NO810105 L NO 810105L NO 810105 A NO810105 A NO 810105A NO 810105 A NO810105 A NO 810105A NO 810105 L NO810105 L NO 810105L
- Authority
- NO
- Norway
- Prior art keywords
- potassium
- solution
- pentapropionate
- dipropionate
- solid
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 15
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 46
- JTXZVIXWVXOIFO-UHFFFAOYSA-L dipotassium propanoate propanoic acid Chemical compound [K+].[K+].CCC(O)=O.CCC(O)=O.CCC(O)=O.CCC([O-])=O.CCC([O-])=O JTXZVIXWVXOIFO-UHFFFAOYSA-L 0.000 claims description 36
- 239000000243 solution Substances 0.000 claims description 31
- IPDIUGJTVNBYTI-UHFFFAOYSA-L [K+].[K+].CCC([O-])=O.CCC([O-])=O Chemical compound [K+].[K+].CCC([O-])=O.CCC([O-])=O IPDIUGJTVNBYTI-UHFFFAOYSA-L 0.000 claims description 30
- 235000019260 propionic acid Nutrition 0.000 claims description 23
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims description 23
- 239000007787 solid Substances 0.000 claims description 22
- 238000001816 cooling Methods 0.000 claims description 18
- 230000007935 neutral effect Effects 0.000 claims description 17
- 239000013078 crystal Substances 0.000 claims description 10
- 239000007864 aqueous solution Substances 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 9
- BWILYWWHXDGKQA-UHFFFAOYSA-M potassium propanoate Chemical compound [K+].CCC([O-])=O BWILYWWHXDGKQA-UHFFFAOYSA-M 0.000 claims description 7
- 235000010332 potassium propionate Nutrition 0.000 claims description 7
- 239000004331 potassium propionate Substances 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 3
- 239000012452 mother liquor Substances 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims 2
- 239000000376 reactant Substances 0.000 claims 1
- 150000003839 salts Chemical class 0.000 description 17
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 16
- 239000002253 acid Substances 0.000 description 16
- 238000002425 crystallisation Methods 0.000 description 5
- 230000008025 crystallization Effects 0.000 description 5
- 238000001914 filtration Methods 0.000 description 5
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 241000228197 Aspergillus flavus Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 241000228150 Penicillium chrysogenum Species 0.000 description 1
- 150000008043 acidic salts Chemical class 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- KCIDZIIHRGYJAE-YGFYJFDDSA-L dipotassium;[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate Chemical compound [K+].[K+].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@H]1O KCIDZIIHRGYJAE-YGFYJFDDSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- -1 potassium pentapropionate Chemical compound 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/41—Preparation of salts of carboxylic acids
- C07C51/412—Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8001543 | 1980-01-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO810105L true NO810105L (no) | 1981-07-20 |
Family
ID=10510690
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO810105A NO810105L (no) | 1980-01-17 | 1981-01-14 | Dikaliumpentapropionat og fremgangsmaate til fremstilling derav |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP0032807B1 (da) |
| JP (1) | JPS56103133A (da) |
| AU (1) | AU540839B2 (da) |
| CA (1) | CA1155133A (da) |
| DE (1) | DE3160026D1 (da) |
| DK (1) | DK17681A (da) |
| FI (1) | FI69297C (da) |
| NO (1) | NO810105L (da) |
| NZ (1) | NZ196009A (da) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8308384D0 (en) * | 1983-03-26 | 1983-05-05 | Verdugt Bv | Producing solid potassium diproprionate |
| DE102005063109A1 (de) * | 2005-12-30 | 2007-07-05 | Basf Ag | Herstellung von sauren Propionaten |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE424017C (de) * | 1922-09-05 | 1926-01-14 | Egon Eloed Dr | Verfahren zur Herstellung saurer Natriumformiate |
| DE932607C (de) * | 1944-12-23 | 1955-09-05 | Benckiser Gmbh Joh A | Verfahren zur Herstellung von festem, haltbarem, saurem Natriumacetat |
| US3919307A (en) * | 1973-02-26 | 1975-11-11 | Eastman Kodak Co | Process for reacting solid particulate matter with a gas |
-
1981
- 1981-01-08 AU AU66072/81A patent/AU540839B2/en not_active Ceased
- 1981-01-14 DE DE8181300139T patent/DE3160026D1/de not_active Expired
- 1981-01-14 FI FI810086A patent/FI69297C/fi not_active IP Right Cessation
- 1981-01-14 NZ NZ196009A patent/NZ196009A/xx unknown
- 1981-01-14 EP EP81300139A patent/EP0032807B1/en not_active Expired
- 1981-01-14 NO NO810105A patent/NO810105L/no unknown
- 1981-01-15 DK DK17681A patent/DK17681A/da not_active Application Discontinuation
- 1981-01-16 JP JP490581A patent/JPS56103133A/ja active Pending
- 1981-01-19 CA CA000368753A patent/CA1155133A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DK17681A (da) | 1981-07-18 |
| FI69297B (fi) | 1985-09-30 |
| AU540839B2 (en) | 1984-12-06 |
| JPS56103133A (en) | 1981-08-18 |
| AU6607281A (en) | 1981-07-23 |
| FI810086L (fi) | 1981-07-18 |
| DE3160026D1 (en) | 1983-02-24 |
| CA1155133A (en) | 1983-10-11 |
| NZ196009A (en) | 1983-06-17 |
| EP0032807B1 (en) | 1983-01-19 |
| FI69297C (fi) | 1986-01-10 |
| EP0032807A1 (en) | 1981-07-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4966982A (en) | Process for the production of lactide | |
| KR20050042061A (ko) | 포름산 포르메이트의 제조 방법 | |
| NO118256B (da) | ||
| US4294766A (en) | Preparation of pure potassium ribonate and ribonolactone | |
| DK149473B (da) | Fremgangsmaade til fremstilling af aminomethan-phosphonsyrer | |
| US2620354A (en) | Production of guanidino fatty acids | |
| US4189591A (en) | Method of preparing 4-methyl-5-hydroxymethyl-imidazole | |
| EP0032807B1 (en) | Dipotassium pentapropionate and method of preparing the same | |
| US2564647A (en) | Hydantoin manufacture | |
| US3141035A (en) | Process for the preparation of choline salicylate | |
| US2870198A (en) | Production of choline salts | |
| US2504130A (en) | Process of making alkaline earth metal permanganates | |
| DE19835866B4 (de) | Verfahren zur Herstellung von 5-Perfluoralkyluracilderivaten | |
| US4014929A (en) | Ether carboxylate monohydrate | |
| US4062839A (en) | Resolution of α-amino-e-caprolactam optical isomers | |
| US2590067A (en) | Methanol complex of dehydro-l-ascorbic acid | |
| US2889347A (en) | Process for producing alkali metal methyl arsonates | |
| US2436739A (en) | Method of making 3,6-bis-(beta-hydroxy-ethyl)-2,5-diketopiperazine | |
| US2764612A (en) | Process for preparing salts of glutamic acid | |
| IL31743A (en) | Acids 1-) Phenyl-sulfonyl (- Cyclopropane carboxyls) | |
| US2798092A (en) | Glutamine synthesis | |
| US4837362A (en) | Preparation of pure hydroxylammonium salts of fatty acids of 1 to 4 carbon atoms | |
| US4534904A (en) | Process for producing N-phosphonomethylglycine | |
| US4263454A (en) | Lithium ribonate, lithium arabonate and the preparation and purification of these salts | |
| JPH02145565A (ja) | ２‐ピロリドン‐５‐カルボン酸の誘導体及びその製法 |