SE175407C1 - - Google Patents
Info
- Publication number
- SE175407C1 SE175407C1 SE175407DA SE175407C1 SE 175407 C1 SE175407 C1 SE 175407C1 SE 175407D A SE175407D A SE 175407DA SE 175407 C1 SE175407 C1 SE 175407C1
- Authority
- SE
- Sweden
- Prior art keywords
- aminoquinaldinium
- dodecyl
- iodide
- acetate
- hours
- Prior art date
Links
- -1 quinaldinium compound Chemical class 0.000 claims description 19
- COCFIBRMFPWUDW-UHFFFAOYSA-N 2-methylquinolin-4-amine Chemical compound C1=CC=CC2=NC(C)=CC(N)=C21 COCFIBRMFPWUDW-UHFFFAOYSA-N 0.000 claims description 9
- 241000334216 Proteus sp. Species 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 150000004820 halides Chemical class 0.000 claims description 4
- 150000001450 anions Chemical class 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- 230000000845 anti-microbial effect Effects 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 150000001350 alkyl halides Chemical class 0.000 claims 1
- SMUQFGGVLNAIOZ-UHFFFAOYSA-N quinaldine Chemical class C1=CC=CC2=NC(C)=CC=C21 SMUQFGGVLNAIOZ-UHFFFAOYSA-N 0.000 claims 1
- 239000007858 starting material Substances 0.000 claims 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 36
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 33
- 239000007787 solid Substances 0.000 description 18
- 238000002360 preparation method Methods 0.000 description 16
- 239000000203 mixture Substances 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 14
- 239000000047 product Substances 0.000 description 13
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 230000000844 anti-bacterial effect Effects 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 244000005700 microbiome Species 0.000 description 5
- 238000010992 reflux Methods 0.000 description 5
- 241000588724 Escherichia coli Species 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 241000191938 Micrococcus luteus Species 0.000 description 3
- 150000001242 acetic acid derivatives Chemical class 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 3
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 3
- 229940011051 isopropyl acetate Drugs 0.000 description 3
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- UAIVMMIZGVQHRU-UHFFFAOYSA-N 1-decyl-2-methylquinolin-1-ium-4-amine;iodide Chemical compound [I-].C1=CC=C2[N+](CCCCCCCCCC)=C(C)C=C(N)C2=C1 UAIVMMIZGVQHRU-UHFFFAOYSA-N 0.000 description 2
- WFENCVFYUBXRSH-UHFFFAOYSA-N 1-dodecyl-2-methylquinolin-1-ium-4-amine;acetate Chemical compound CC([O-])=O.C1=CC=C2[N+](CCCCCCCCCCCC)=C(C)C=C(N)C2=C1 WFENCVFYUBXRSH-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 241000813862 Streptomyces saprophyticus Species 0.000 description 2
- 230000003385 bacteriostatic effect Effects 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 210000000245 forearm Anatomy 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 239000012488 sample solution Substances 0.000 description 2
- CQLFBEKRDQMJLZ-UHFFFAOYSA-M silver acetate Chemical compound [Ag+].CC([O-])=O CQLFBEKRDQMJLZ-UHFFFAOYSA-M 0.000 description 2
- 229940071536 silver acetate Drugs 0.000 description 2
- MJWHEEXHUDCWDA-UHFFFAOYSA-O 1-dodecyl-2-methylquinolin-1-ium-4-amine Chemical compound C1=CC=C2[N+](CCCCCCCCCCCC)=C(C)C=C(N)C2=C1 MJWHEEXHUDCWDA-UHFFFAOYSA-O 0.000 description 1
- ZOLWCVXOIXJAIJ-UHFFFAOYSA-N 1-hexadecyl-2-methylquinolin-1-ium-4-amine iodide Chemical compound [I-].C(CCCCCCCCCCCCCCC)[N+]1=C(C)C=C(C2=CC=CC=C12)N ZOLWCVXOIXJAIJ-UHFFFAOYSA-N 0.000 description 1
- SKIDNYUZJPMKFC-UHFFFAOYSA-N 1-iododecane Chemical compound CCCCCCCCCCI SKIDNYUZJPMKFC-UHFFFAOYSA-N 0.000 description 1
- GCDPERPXPREHJF-UHFFFAOYSA-N 1-iodododecane Chemical compound CCCCCCCCCCCCI GCDPERPXPREHJF-UHFFFAOYSA-N 0.000 description 1
- LMHCYRULPLGEEZ-UHFFFAOYSA-N 1-iodoheptane Chemical compound CCCCCCCI LMHCYRULPLGEEZ-UHFFFAOYSA-N 0.000 description 1
- KMWHQYDMBYABKL-UHFFFAOYSA-N 1-iodohexadecane Chemical compound CCCCCCCCCCCCCCCCI KMWHQYDMBYABKL-UHFFFAOYSA-N 0.000 description 1
- ZNJOCVLVYVOUGB-UHFFFAOYSA-N 1-iodooctadecane Chemical compound CCCCCCCCCCCCCCCCCCI ZNJOCVLVYVOUGB-UHFFFAOYSA-N 0.000 description 1
- FKUQOQPBCHJHAP-UHFFFAOYSA-N 1-iodoundecane Chemical compound CCCCCCCCCCCI FKUQOQPBCHJHAP-UHFFFAOYSA-N 0.000 description 1
- WVYWICLMDOOCFB-UHFFFAOYSA-N 4-methyl-2-pentanol Chemical compound CC(C)CC(C)O WVYWICLMDOOCFB-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- RKYLUMOHNQTGMB-UHFFFAOYSA-N C(C)(=O)[O-].C(CCCCCCCCCCCCC)[N+]1=C(C)C=C(C2=CC=CC=C12)N Chemical compound C(C)(=O)[O-].C(CCCCCCCCCCCCC)[N+]1=C(C)C=C(C2=CC=CC=C12)N RKYLUMOHNQTGMB-UHFFFAOYSA-N 0.000 description 1
- UWRLVAAGLWTEQH-UHFFFAOYSA-N CCCCCCCCCCCCCCCCCC[N+](C1=CC=CC=C11)=C(C)C=C1N.[I-] Chemical compound CCCCCCCCCCCCCCCCCC[N+](C1=CC=CC=C11)=C(C)C=C1N.[I-] UWRLVAAGLWTEQH-UHFFFAOYSA-N 0.000 description 1
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 1
- 241000187845 Dermatophilus congolensis Species 0.000 description 1
- IIUZTXTZRGLYTI-UHFFFAOYSA-N Dihydrogriseofulvin Natural products COC1CC(=O)CC(C)C11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 IIUZTXTZRGLYTI-UHFFFAOYSA-N 0.000 description 1
- 241000982822 Ficus obtusifolia Species 0.000 description 1
- UXWOXTQWVMFRSE-UHFFFAOYSA-N Griseoviridin Natural products O=C1OC(C)CC=C(C(NCC=CC=CC(O)CC(O)C2)=O)SCC1NC(=O)C1=COC2=N1 UXWOXTQWVMFRSE-UHFFFAOYSA-N 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- 241000251124 Mustelus canis Species 0.000 description 1
- DDUHZTYCFQRHIY-UHFFFAOYSA-N Negwer: 6874 Natural products COC1=CC(=O)CC(C)C11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 DDUHZTYCFQRHIY-UHFFFAOYSA-N 0.000 description 1
- 239000001888 Peptone Substances 0.000 description 1
- 108010080698 Peptones Proteins 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 241001312524 Streptococcus viridans Species 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- RZESOXIJGKVAAX-UHFFFAOYSA-L [Ag++].[O-]C(=O)CCC([O-])=O Chemical compound [Ag++].[O-]C(=O)CCC([O-])=O RZESOXIJGKVAAX-UHFFFAOYSA-L 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000001408 fungistatic effect Effects 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- DDUHZTYCFQRHIY-RBHXEPJQSA-N griseofulvin Chemical compound COC1=CC(=O)C[C@@H](C)[C@@]11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 DDUHZTYCFQRHIY-RBHXEPJQSA-N 0.000 description 1
- 229960002867 griseofulvin Drugs 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000037311 normal skin Effects 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- LMEWRZSPCQHBOB-UHFFFAOYSA-M silver;2-hydroxypropanoate Chemical compound [Ag+].CC(O)C([O-])=O LMEWRZSPCQHBOB-UHFFFAOYSA-M 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 238000001665 trituration Methods 0.000 description 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE175407T |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SE175407C1 true SE175407C1 (pl) | 1961-01-01 |
Family
ID=41964591
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE175407D SE175407C1 (pl) |
Country Status (1)
| Country | Link |
|---|---|
| SE (1) | SE175407C1 (pl) |
-
0
- SE SE175407D patent/SE175407C1/sv unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69518323T2 (de) | Oxaborole und deren salze, und deren verwendung als biozide | |
| JPH01131136A (ja) | 置換アクリル酸エステルおよび該化合物を含有する殺菌剤 | |
| EP2723743B1 (de) | 10h-benzo[g]pteridin-2,4-dion-derivate, verfahren zur herstellung und verwendung derselben | |
| US3235449A (en) | Disinfectant and fungicidal compositions | |
| JPS5913516B2 (ja) | 新規２−アミノ−１，３−チアジン類の製造方法 | |
| IL24814A (en) | N',n'-disubstituted-thiono carbamyl thiolo-imides and process for their preparation | |
| US4115588A (en) | Antibacterial novel soft n-chloroamino alcohol derivatives | |
| US3519624A (en) | Antimicrobial preparations containing n-acyl-3,4-dihydro-oxazines-(1,3) | |
| US4061764A (en) | Certain O-substituted thiophene oxime carbamates used as antibacterial and antifungal agents | |
| US2997476A (en) | 1-alkyl-4-aminoquinaldinium salts | |
| CN114097804A (zh) | 一种二氨基嘧啶类化合物在防治农业病原菌中的用途 | |
| EP0288493B1 (de) | 3-halogensuccinimide | |
| US3642807A (en) | Certain 1-/dilower-alkyl amino-loweralkyl/-2-phenyl indolizines and quaternary salts thereof | |
| CN115536543B (zh) | 一种含异丙醇胺结构的三氯生类化合物及其制备方法和应用 | |
| US3631175A (en) | Derivatives of pyrano(3 2-d)oxazole | |
| US2885320A (en) | Cycloheximide thiosemicarbazone | |
| AT211834B (de) | Verfahren zur Herstellung von neuen 1-Alkyl-4-aminochinaldiniumsalzen | |
| US3031373A (en) | 8-quinolyl carbonate derivatives | |
| US3876790A (en) | Dihalonitromethylpyridines as antimicrobials | |
| US4171452A (en) | Antibacterially active N-chloroamino ester derivatives of alkyl carboxylates | |
| CN110724097B (zh) | 一种治疗耐药性微生物菌的化合物及其制备方法 | |
| US4031248A (en) | Microbicidal agents containing as active ingredient monohydroxyphenyl carbinols | |
| Chhatriwala et al. | In vitro biological investigations of novel piperazine based heterocycles | |
| JPH04120004A (ja) | 防菌防かび剤 | |
| JPS63215668A (ja) | １−（２，３，３−トリヨ−ドアリル）ピリジニウムハライド系化合物、その製造法、それを含有する殺微生物剤およびそれによる殺微生物方法 |