NO129951B - - Google Patents
Download PDFInfo
- Publication number
- NO129951B NO129951B NO00558/70A NO55870A NO129951B NO 129951 B NO129951 B NO 129951B NO 00558/70 A NO00558/70 A NO 00558/70A NO 55870 A NO55870 A NO 55870A NO 129951 B NO129951 B NO 129951B
- Authority
- NO
- Norway
- Prior art keywords
- compound
- bacteriological
- compounds
- effect
- alkyl
- Prior art date
Links
- -1 Diaminopyridine compound Chemical class 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 239000000645 desinfectant Substances 0.000 claims description 5
- 239000003755 preservative agent Substances 0.000 claims description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 230000002335 preservative effect Effects 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 description 37
- 230000000721 bacterilogical effect Effects 0.000 description 20
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 238000002360 preparation method Methods 0.000 description 15
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- 230000007794 irritation Effects 0.000 description 8
- VHNQIURBCCNWDN-UHFFFAOYSA-N pyridine-2,6-diamine Chemical compound NC1=CC=CC(N)=N1 VHNQIURBCCNWDN-UHFFFAOYSA-N 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000000344 soap Substances 0.000 description 6
- QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 description 5
- 102000002322 Egg Proteins Human genes 0.000 description 5
- 108010000912 Egg Proteins Proteins 0.000 description 5
- 239000012888 bovine serum Substances 0.000 description 5
- 235000014103 egg white Nutrition 0.000 description 5
- 210000000969 egg white Anatomy 0.000 description 5
- 239000013543 active substance Substances 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 239000012043 crude product Substances 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- 229940072033 potash Drugs 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 235000015320 potassium carbonate Nutrition 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- INYFHZSQWXOHAJ-UHFFFAOYSA-N 6-N-octylpyridine-2,6-diamine Chemical compound C(CCCCCCC)NC1=NC(=CC=C1)N INYFHZSQWXOHAJ-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 150000001348 alkyl chlorides Chemical class 0.000 description 3
- 150000001350 alkyl halides Chemical class 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 244000052616 bacterial pathogen Species 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 238000000921 elemental analysis Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- PBLNBZIONSLZBU-UHFFFAOYSA-N 1-bromododecane Chemical compound CCCCCCCCCCCCBr PBLNBZIONSLZBU-UHFFFAOYSA-N 0.000 description 2
- NCKMMSIFQUPKCK-UHFFFAOYSA-N 2-benzyl-4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1CC1=CC=CC=C1 NCKMMSIFQUPKCK-UHFFFAOYSA-N 0.000 description 2
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 241000589540 Pseudomonas fluorescens Species 0.000 description 2
- 150000001347 alkyl bromides Chemical class 0.000 description 2
- 239000003899 bactericide agent Substances 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- VMKOFRJSULQZRM-UHFFFAOYSA-N 1-bromooctane Chemical compound CCCCCCCCBr VMKOFRJSULQZRM-UHFFFAOYSA-N 0.000 description 1
- JQZAEUFPPSRDOP-UHFFFAOYSA-N 1-chloro-4-(chloromethyl)benzene Chemical compound ClCC1=CC=C(Cl)C=C1 JQZAEUFPPSRDOP-UHFFFAOYSA-N 0.000 description 1
- ZTEHOZMYMCEYRM-UHFFFAOYSA-N 1-chlorodecane Chemical compound CCCCCCCCCCCl ZTEHOZMYMCEYRM-UHFFFAOYSA-N 0.000 description 1
- YAYNEUUHHLGGAH-UHFFFAOYSA-N 1-chlorododecane Chemical compound CCCCCCCCCCCCCl YAYNEUUHHLGGAH-UHFFFAOYSA-N 0.000 description 1
- RKAMCQVGHFRILV-UHFFFAOYSA-N 1-chlorononane Chemical compound CCCCCCCCCCl RKAMCQVGHFRILV-UHFFFAOYSA-N 0.000 description 1
- VUQPJRPDRDVQMN-UHFFFAOYSA-N 1-chlorooctadecane Chemical compound CCCCCCCCCCCCCCCCCCCl VUQPJRPDRDVQMN-UHFFFAOYSA-N 0.000 description 1
- CNDHHGUSRIZDSL-UHFFFAOYSA-N 1-chlorooctane Chemical compound CCCCCCCCCl CNDHHGUSRIZDSL-UHFFFAOYSA-N 0.000 description 1
- RNHWYOLIEJIAMV-UHFFFAOYSA-N 1-chlorotetradecane Chemical compound CCCCCCCCCCCCCCCl RNHWYOLIEJIAMV-UHFFFAOYSA-N 0.000 description 1
- QLMJAWRMASJMBY-UHFFFAOYSA-N 2-N,6-N-dioctylpyridine-2,6-diamine Chemical compound C(CCCCCCC)NC1=NC(=CC=C1)NCCCCCCCC QLMJAWRMASJMBY-UHFFFAOYSA-N 0.000 description 1
- CQEASSXFQSFQIM-UHFFFAOYSA-N 6-N-dodecylpyridine-2,6-diamine Chemical compound C(CCCCCCCCCCC)NC1=NC(=CC=C1)N CQEASSXFQSFQIM-UHFFFAOYSA-N 0.000 description 1
- CAHQGWAXKLQREW-UHFFFAOYSA-N Benzal chloride Chemical compound ClC(Cl)C1=CC=CC=C1 CAHQGWAXKLQREW-UHFFFAOYSA-N 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 239000005708 Sodium hypochlorite Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 150000007514 bases Chemical class 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- BNMHIKTUFBWOAM-UHFFFAOYSA-N dioctadecyl sulfate Chemical compound CCCCCCCCCCCCCCCCCCOS(=O)(=O)OCCCCCCCCCCCCCCCCCC BNMHIKTUFBWOAM-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- ARBOVOVUTSQWSS-UHFFFAOYSA-N hexadecanoyl chloride Chemical compound CCCCCCCCCCCCCCCC(Cl)=O ARBOVOVUTSQWSS-UHFFFAOYSA-N 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 210000004400 mucous membrane Anatomy 0.000 description 1
- 231100000286 mucous membrane, eye irritation or corrosion testing Toxicity 0.000 description 1
- CBFCDTFDPHXCNY-UHFFFAOYSA-N octyldodecane Natural products CCCCCCCCCCCCCCCCCCCC CBFCDTFDPHXCNY-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyridine Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19691909065 DE1909065A1 (de) | 1969-02-18 | 1969-02-18 | N-substituierte Diaminopyridine und ihre Verwendung als Biocide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO129951B true NO129951B (en, 2012) | 1974-06-17 |
Family
ID=5726099
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO00558/70A NO129951B (en, 2012) | 1969-02-18 | 1970-02-17 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US3647808A (en, 2012) |
| AT (1) | AT296304B (en, 2012) |
| BE (1) | BE746090A (en, 2012) |
| CH (1) | CH534157A (en, 2012) |
| DE (1) | DE1909065A1 (en, 2012) |
| DK (1) | DK131464B (en, 2012) |
| ES (1) | ES376772A1 (en, 2012) |
| FR (1) | FR2031483B1 (en, 2012) |
| GB (1) | GB1256983A (en, 2012) |
| NL (1) | NL144273B (en, 2012) |
| NO (1) | NO129951B (en, 2012) |
| SE (1) | SE388609B (en, 2012) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2003299574A1 (en) * | 2002-12-02 | 2004-06-23 | Byocoat Llc | Composition ad method for treating plant fungal disease |
| MXPA05009507A (es) | 2003-03-05 | 2006-03-10 | Byocoat Entpr Inc | Solucion y proceso antimicrobianos. |
| WO2008033466A2 (en) * | 2006-09-14 | 2008-03-20 | Combinatorx (Singapore) Pre. Ltd. | Compositions and methods for treatment of viral diseases |
| US20100298386A1 (en) * | 2007-10-03 | 2010-11-25 | Burwell Steven R | Compositions and methods for treating mastitis |
-
1969
- 1969-02-18 DE DE19691909065 patent/DE1909065A1/de not_active Withdrawn
- 1969-07-17 FR FR6924302A patent/FR2031483B1/fr not_active Expired
-
1970
- 1970-02-09 NL NL707001778A patent/NL144273B/xx unknown
- 1970-02-10 US US10282A patent/US3647808A/en not_active Expired - Lifetime
- 1970-02-12 ES ES376772A patent/ES376772A1/es not_active Expired
- 1970-02-13 SE SE7001855A patent/SE388609B/xx unknown
- 1970-02-16 CH CH216870A patent/CH534157A/de not_active IP Right Cessation
- 1970-02-17 GB GB1256983D patent/GB1256983A/en not_active Expired
- 1970-02-17 DK DK75570AA patent/DK131464B/da unknown
- 1970-02-17 BE BE746090D patent/BE746090A/xx unknown
- 1970-02-17 NO NO00558/70A patent/NO129951B/no unknown
- 1970-02-18 AT AT146770A patent/AT296304B/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DK131464B (da) | 1975-07-21 |
| DK131464C (en, 2012) | 1975-12-08 |
| NL144273B (nl) | 1974-12-16 |
| BE746090A (fr) | 1970-07-31 |
| SE388609B (sv) | 1976-10-11 |
| DE1909065A1 (de) | 1970-08-20 |
| CH534157A (de) | 1973-02-28 |
| AT296304B (de) | 1972-02-10 |
| ES376772A1 (es) | 1972-05-01 |
| GB1256983A (en, 2012) | 1971-12-15 |
| FR2031483A1 (en, 2012) | 1970-11-20 |
| NL7001778A (en, 2012) | 1970-08-20 |
| US3647808A (en) | 1972-03-07 |
| FR2031483B1 (en, 2012) | 1975-08-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO129951B (en, 2012) | ||
| US2987505A (en) | Compositions of polymeric nu-vinyl-2-oxazolidone and halogens | |
| DE1542739A1 (de) | Schaedlingsbekaempfungsmittel | |
| NO140872B (no) | Plasmaovn. | |
| US3800048A (en) | Composition of halogenated hydroxy-diphenyl ethers | |
| US3904696A (en) | Halogenated hydroxy-diphenyl ethers | |
| US3100175A (en) | Antiseptic composition | |
| DE2113208C3 (de) | Octylaminderivate, deren Herstellung und Verwendung als Bioeide | |
| US4034046A (en) | Hydroxyaryldialkyl sulfonium halides | |
| RU2238268C2 (ru) | Дезинфицирующее средство | |
| US3459534A (en) | Methods of controlling bacteria,fungi,nematodes and weed pests with tetrahalohydroxybenzamides | |
| DE2218417A1 (de) | Verwendung substituierter oxazolidine als antimikrobielle wirkstoffe | |
| DE1645951A1 (de) | Verfahren zur Herstellung von Tetrahydro-1,3,5-thiadiazin-2-thionen und ihre Verwendung als Mikrobizide | |
| DE890958C (de) | Verfahren zur Herstellung von Sulfonamidverbindungen | |
| US4388302A (en) | Coacervated iodine | |
| AT208516B (de) | Verfahren zur Herstellung einer stark keimtötend wirkenden Substanz | |
| DE1909065C (de) | N-substituierte Diaminopyridine | |
| US4124637A (en) | Certain cyanodithioimidocarbonates | |
| US2860084A (en) | Germicidal composition comprising iodine and a n-acyl colamino formyl methyl quaternary ammonium salt | |
| DE2058661A1 (de) | Biocides Adamantylaminderivat | |
| DE676013C (de) | Verfahren zur Herstellung von Sulfonaethandicarbonsaeuren | |
| DE4005178A1 (de) | Pyridiniumsalze | |
| US3480639A (en) | Process for preparing crystalline pyridinium 2-nitro-1 butyl sulfate | |
| DE539806C (de) | Verfahren zur Darstellung von Isopropylallylbarbitursaeure | |
| DE1645950A1 (de) | Verfahren zur Herstellung von Tetrahydro-1,3,5-thiadiazin-2-thionen und ihre Verwendung als Mikrobizide |