PL44410B1 - - Google Patents

Info

Publication number

PL44410B1

PL44410B1 PL44410A PL4441060A PL44410B1 PL 44410 B1 PL44410 B1 PL 44410B1 PL 44410 A PL44410 A PL 44410A PL 4441060 A PL4441060 A PL 4441060A PL 44410 B1 PL44410 B1 PL 44410B1

Authority

PL

Poland

Prior art keywords

weight

parts

polyfamazine

sodium

anhydrous

Prior art date

1960-02-16

Links

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• 238000000034 method Methods 0.000 claims description 8
• 159000000000 sodium salts Chemical class 0.000 claims description 6
• 229910052708 sodium Inorganic materials 0.000 claims description 5
• 239000011734 sodium Substances 0.000 claims description 5
• -1 aliphatic alcohols Chemical class 0.000 claims description 4
• 238000002360 preparation method Methods 0.000 claims description 4
• 239000003960 organic solvent Substances 0.000 claims description 2
• ASWVTGNCAZCNNR-UHFFFAOYSA-N sulfamethazine Chemical compound CC1=CC(C)=NC(NS(=O)(=O)C=2C=CC(N)=CC=2)=N1 ASWVTGNCAZCNNR-UHFFFAOYSA-N 0.000 claims 1
• 239000000725 suspension Substances 0.000 claims 1
• KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 5
• DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
• 238000000354 decomposition reaction Methods 0.000 description 3
• CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
• 238000006243 chemical reaction Methods 0.000 description 2
• 239000011541 reaction mixture Substances 0.000 description 2
• 150000003839 salts Chemical class 0.000 description 2
• 235000011121 sodium hydroxide Nutrition 0.000 description 2
• 239000002904 solvent Substances 0.000 description 2
• MNWVJNSMYXMEIX-UHFFFAOYSA-N 4-amino-n-(4,6-dimethylpyrimidin-2-yl)benzenesulfonamide;sodium Chemical compound [Na].CC1=CC(C)=NC(NS(=O)(=O)C=2C=CC(N)=CC=2)=N1 MNWVJNSMYXMEIX-UHFFFAOYSA-N 0.000 description 1
• 241000019229 Dinia Species 0.000 description 1
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
• KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
• 230000015572 biosynthetic process Effects 0.000 description 1
• 238000009835 boiling Methods 0.000 description 1
• 239000001569 carbon dioxide Substances 0.000 description 1
• 229910002092 carbon dioxide Inorganic materials 0.000 description 1
• 238000001816 cooling Methods 0.000 description 1
• 238000002425 crystallisation Methods 0.000 description 1
• 230000008025 crystallization Effects 0.000 description 1
• 238000010438 heat treatment Methods 0.000 description 1
• 238000004519 manufacturing process Methods 0.000 description 1
• 239000002244 precipitate Substances 0.000 description 1
• 239000000047 product Substances 0.000 description 1
• 238000003756 stirring Methods 0.000 description 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1