SE201889C1 - - Google Patents
Info
- Publication number
- SE201889C1 SE201889C1 SE201889DA SE201889C1 SE 201889 C1 SE201889 C1 SE 201889C1 SE 201889D A SE201889D A SE 201889DA SE 201889 C1 SE201889 C1 SE 201889C1
- Authority
- SE
- Sweden
- Prior art keywords
- dialdehyde
- alkali metal
- cho
- spray drying
- glutaraldehyde
- Prior art date
Links
- ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical compound N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 claims description 13
- 239000007864 aqueous solution Substances 0.000 claims description 7
- 238000001694 spray drying Methods 0.000 claims description 7
- 229910052783 alkali metal Inorganic materials 0.000 claims description 5
- -1 alkali metal cation Chemical class 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- WBZKQQHYRPRKNJ-UHFFFAOYSA-L disulfite Chemical compound [O-]S(=O)S([O-])(=O)=O WBZKQQHYRPRKNJ-UHFFFAOYSA-L 0.000 claims description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 6
- 230000003330 sporicidal effect Effects 0.000 description 6
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- 230000003113 alkalizing effect Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 229940015043 glyoxal Drugs 0.000 description 2
- RWPGFSMJFRPDDP-UHFFFAOYSA-L potassium metabisulfite Chemical compound [K+].[K+].[O-]S(=O)S([O-])(=O)=O RWPGFSMJFRPDDP-UHFFFAOYSA-L 0.000 description 2
- 235000010263 potassium metabisulphite Nutrition 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- LUNMJPAJHJAGIS-UHFFFAOYSA-N 3-methylpentanedial Chemical compound O=CCC(C)CC=O LUNMJPAJHJAGIS-UHFFFAOYSA-N 0.000 description 1
- UMHJEEQLYBKSAN-UHFFFAOYSA-N Adipaldehyde Chemical compound O=CCCCCC=O UMHJEEQLYBKSAN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- WSMYVTOQOOLQHP-UHFFFAOYSA-N Malondialdehyde Chemical compound O=CCC=O WSMYVTOQOOLQHP-UHFFFAOYSA-N 0.000 description 1
- CNWMSQYZKMSPMJ-UHFFFAOYSA-M S([O-])(O)=O.C(=O)C=O.[K+] Chemical compound S([O-])(O)=O.C(=O)C=O.[K+] CNWMSQYZKMSPMJ-UHFFFAOYSA-M 0.000 description 1
- PCSMJKASWLYICJ-UHFFFAOYSA-N Succinic aldehyde Chemical compound O=CCCC=O PCSMJKASWLYICJ-UHFFFAOYSA-N 0.000 description 1
- YHFXJKYHUWPWSJ-UHFFFAOYSA-L [Na+].[Na+].OS([O-])=O.OS([O-])=O Chemical compound [Na+].[Na+].OS([O-])=O.OS([O-])=O YHFXJKYHUWPWSJ-UHFFFAOYSA-L 0.000 description 1
- 150000008043 acidic salts Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000012084 conversion product Substances 0.000 description 1
- CXEPVDIXZYCMFU-UHFFFAOYSA-L disodium;hydrogen sulfite;pentanedial Chemical compound [Na+].[Na+].OS([O-])=O.OS([O-])=O.O=CCCCC=O CXEPVDIXZYCMFU-UHFFFAOYSA-L 0.000 description 1
- 238000007323 disproportionation reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229940043349 potassium metabisulfite Drugs 0.000 description 1
- 239000004297 potassium metabisulphite Substances 0.000 description 1
- SCQHVYVXKOUGHQ-UHFFFAOYSA-M potassium;hydrogen sulfite;pentanedial Chemical compound [K+].OS([O-])=O.O=CCCCC=O SCQHVYVXKOUGHQ-UHFFFAOYSA-M 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- AMDXZOMRWVXZJX-UHFFFAOYSA-M sodium hydrogen sulfite 3-methylpentanedial Chemical compound S([O-])(O)=O.CC(CC=O)CC=O.[Na+] AMDXZOMRWVXZJX-UHFFFAOYSA-M 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE201889T |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SE201889C1 true SE201889C1 (de) | 1965-01-01 |
Family
ID=41986069
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE201889D SE201889C1 (de) |
Country Status (1)
| Country | Link |
|---|---|
| SE (1) | SE201889C1 (de) |
-
0
- SE SE201889D patent/SE201889C1/sv unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU1050565A3 (ru) | Способ получени натриевой соли @ -фосфонометилглицина | |
| EP0572957A2 (de) | Verfahren zur Herstellung von pulverförmigen, anionischen Tensiden | |
| JPS5692859A (en) | Preparation of hydroxyalkylaminosulfnonic acid | |
| Szarek et al. | Addition of pseudohalogens to unsaturated carbohydrates. III. Synthesis of 3-deoxy-3-C-nitromethyl-D-allose, a branched-chain nitro sugar | |
| US3829580A (en) | Fungicidal dithiomalonamides and their congeners | |
| SE201889C1 (de) | ||
| US3149152A (en) | Mono-alkali metal bisulfites of dialdehydes | |
| NO822165L (no) | Nytt ugressdrepende preparat, fremgangsmaate for dets fremstilling og bruk. | |
| US4372976A (en) | Novel aryl-aliphatic ketone and its use as an antiviral agent | |
| SU797572A3 (ru) | Способ выделени солей аспарагиновойКиСлОТы | |
| Herbst et al. | The nitration of 5-aminotetrazole | |
| KR870003967A (ko) | 살리실산의 분리 및 정제방법 | |
| KR910004434B1 (ko) | 치환된 티오펜설폰아미드 화합물의 제조방법 | |
| GB984481A (en) | Process for the preparation of polyfunctional diazonium phosphates | |
| US4258210A (en) | Process for manufacturing sodium pantothenate | |
| Chute et al. | SOME REACTIONS OF 5-CHLOROMERCURI-2-FURFURYL ALCOHOL1 | |
| Botta et al. | 6-Alkyl-2-hethoxy-4-(3h)-pyrimidinones in the transformation of pyrimidines: regiospecific preparation, antitumor and antimicrobial activity of 4-O-acylated pyrimidine derivatives. New agents for selective acylation of amines | |
| US5849933A (en) | Process for producing ascorbic acid-2-monophosphates | |
| JPS5524125A (en) | Preparation of substituted diphenyl ether | |
| Wolfe et al. | The Preparation of Nitrite Salts of Alkyl Amines1 | |
| NO822090L (no) | Nytt akaricid preparat, fremgangsmaate for dets fremstilling og bruk. | |
| US2580364A (en) | Preparation of crystalline penicillin salts | |
| RU2797970C1 (ru) | Способ очистки нуклеиновой кислоты | |
| Butz | The Dehydration of 1, 5-Hexadiene-3-ol to 1, 3, 5-Hexatriene and 1, 3-Cyclohexadiene1 | |
| DE1667463C3 (de) | Verfahren zur Herstellung von festem, kristallinem Natrium-Ammoniumperoxomonosulfat, im Gemisch mit Natrium- und Ammoniumsulfat und -bisulfat |