DE284234C - - Google Patents
Info
- Publication number
- DE284234C DE284234C DENDAT284234D DE284234DC DE284234C DE 284234 C DE284234 C DE 284234C DE NDAT284234 D DENDAT284234 D DE NDAT284234D DE 284234D C DE284234D C DE 284234DC DE 284234 C DE284234 C DE 284234C
- Authority
- DE
- Germany
- Prior art keywords
- gold
- hexamethylenetetramine
- alkyl
- composition
- solution
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000010931 gold Substances 0.000 claims description 26
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylene tetramine Natural products C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 claims description 20
- -1 hexamethylenetetramine alkyl hydroxides Chemical class 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 15
- 235000010299 hexamethylene tetramine Nutrition 0.000 claims description 13
- 239000004312 hexamethylene tetramine Substances 0.000 claims description 13
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- WOFVPNPAVMKHCX-UHFFFAOYSA-N N#C[Au](C#N)C#N Chemical class N#C[Au](C#N)C#N WOFVPNPAVMKHCX-UHFFFAOYSA-N 0.000 claims description 2
- KPQDSKZQRXHKHY-UHFFFAOYSA-N gold potassium Chemical compound [K].[Au] KPQDSKZQRXHKHY-UHFFFAOYSA-N 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- MUQNGPZZQDCDFT-JNQJZLCISA-N Halcinonide Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H]3OC(C)(C)O[C@@]3(C(=O)CCl)[C@@]1(C)C[C@@H]2O MUQNGPZZQDCDFT-JNQJZLCISA-N 0.000 claims 1
- 229940028332 halog Drugs 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 239000000243 solution Substances 0.000 description 13
- 239000000460 chlorine Substances 0.000 description 12
- 229960004011 methenamine Drugs 0.000 description 12
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 229910052740 iodine Inorganic materials 0.000 description 4
- 239000011630 iodine Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- IZLAVFWQHMDDGK-UHFFFAOYSA-N gold(1+);cyanide Chemical compound [Au+].N#[C-] IZLAVFWQHMDDGK-UHFFFAOYSA-N 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- DRVVOFZLVDYJRW-UHFFFAOYSA-M st51002549 Chemical compound [I-].C1N(C2)CN3CN2C[N+]1(C)C3 DRVVOFZLVDYJRW-UHFFFAOYSA-M 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- JGJLWPGRMCADHB-UHFFFAOYSA-N hypobromite Inorganic materials Br[O-] JGJLWPGRMCADHB-UHFFFAOYSA-N 0.000 description 2
- FJWLWIRHZOHPIY-UHFFFAOYSA-N potassium;hydroiodide Chemical compound [K].I FJWLWIRHZOHPIY-UHFFFAOYSA-N 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- ZYECOAILUNWEAL-NUDFZHEQSA-N (4z)-4-[[2-methoxy-5-(phenylcarbamoyl)phenyl]hydrazinylidene]-n-(3-nitrophenyl)-3-oxonaphthalene-2-carboxamide Chemical compound COC1=CC=C(C(=O)NC=2C=CC=CC=2)C=C1N\N=C(C1=CC=CC=C1C=1)/C(=O)C=1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 ZYECOAILUNWEAL-NUDFZHEQSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 208000035473 Communicable disease Diseases 0.000 description 1
- 239000004133 Sodium thiosulphate Substances 0.000 description 1
- ZHICPAJFTWEPCN-UHFFFAOYSA-N [I].N#CC#N Chemical compound [I].N#CC#N ZHICPAJFTWEPCN-UHFFFAOYSA-N 0.000 description 1
- ARHBWGMHXPPGCZ-UHFFFAOYSA-N [K].[Au](C#N)(C#N)C#N Chemical class [K].[Au](C#N)(C#N)C#N ARHBWGMHXPPGCZ-UHFFFAOYSA-N 0.000 description 1
- PPVNYSRNJQOELF-UHFFFAOYSA-N [K].[Au].N#CC#N Chemical class [K].[Au].N#CC#N PPVNYSRNJQOELF-UHFFFAOYSA-N 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 150000002344 gold compounds Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 150000004694 iodide salts Chemical class 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 229910001511 metal iodide Inorganic materials 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- XTFKWYDMKGAZKK-UHFFFAOYSA-N potassium;gold(1+);dicyanide Chemical compound [K+].[Au+].N#[C-].N#[C-] XTFKWYDMKGAZKK-UHFFFAOYSA-N 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 description 1
- SWGJCIMEBVHMTA-UHFFFAOYSA-K trisodium;6-oxido-4-sulfo-5-[(4-sulfonatonaphthalen-1-yl)diazenyl]naphthalene-2-sulfonate Chemical compound [Na+].[Na+].[Na+].C1=CC=C2C(N=NC3=C4C(=CC(=CC4=CC=C3O)S([O-])(=O)=O)S([O-])(=O)=O)=CC=C(S([O-])(=O)=O)C2=C1 SWGJCIMEBVHMTA-UHFFFAOYSA-K 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/18—Bridged systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
DE284234C true DE284234C (enrdf_load_stackoverflow) |
Family
ID=539735
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT284234D Active DE284234C (enrdf_load_stackoverflow) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE284234C (enrdf_load_stackoverflow) |
-
0
- DE DENDAT284234D patent/DE284234C/de active Active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE2746244C2 (de) | Derivate des Spiro [chroman-4,4'-imidazolidin] - 2',5'-dions | |
DE2351412C2 (de) | 2,2-Disubstituierte 1-Oxo-5-indanyloxy-carbonsäuren, Verfahren zu deren Herstellung und Spaltung racemischer Gemische, sowie diese enthaltende Arzneimittel | |
DE1795452A1 (de) | 2-Aryl-nitroimidazole und Verfahren zu deren Herstellung | |
DE3438440A1 (de) | Platin-diamin-komplex | |
DE2028950B2 (de) | Waessrige loesung zum stromlosen abschneiden von nickel, kobalt oder legierungen davon | |
DE284234C (enrdf_load_stackoverflow) | ||
DE2600668A1 (de) | Adamantanderivate und diese derivate enthaltender cerebral-vasodilatator | |
DE2061972A1 (de) | Lichtempfindliches photographisches Material | |
DE2129418A1 (de) | Sulfamoylsubstituierte 1,3,4-Thiadiazol-Harnstoff-Verbindungen | |
DE1770490C3 (de) | 2,4-Diamino-6-nitrosamino-chinazolinverbindungen und Verfahren zu ihrer Herstellung | |
DE1233405B (de) | Verfahren zur Herstellung von 7-(Oxoalkyl)-1, 3-dimethylxanthinen | |
DE284259C (de) | Verfahren zur Darstellung von Doppelverbindungen aus den Salzen der Hexamethylentetraminalkylhydroxyde und Salzen von Schwermetallen | |
CH626228A5 (enrdf_load_stackoverflow) | ||
DE1545652C (de) | 3-(alpha-Hydroxyäthyl)-6-chlor-7sulfamyl-1,2,4-benzothiadiazin-1,1 dioxyd | |
DE1294188B (de) | Stabilisiertes photographisches Aufzeichnungsmaterial und Stabilisatoren enthaltenderEntwickler | |
DE2062364A1 (de) | Verfahren zur Herstellung neuer Pyn dazone | |
DE139394C (enrdf_load_stackoverflow) | ||
DE1643410C3 (de) | 3-(4'-Cyanophenyl)-cumarinderivate und Verfahren zu deren Herstellung sowie diese Verbindungen enthaltende Textilbehandlungsmittel | |
DE852855C (de) | Verfahren zur Herstellung von neuen diquartaeren Salzen von Pyrimidylaminochinolinen | |
DE1670273A1 (de) | Verfahren zur Herstellung von Aminopenicillinen | |
AT202134B (de) | Verfahren zur Herstellung von gemischten, sekundären Aminen und deren Salzen | |
AT236414B (de) | Verfahren zur Herstellung von neuen Benzolsulfonylsemicarbaziden | |
DE2127177A1 (de) | Verfahren zur Herstellung von 1-Phenyl-2-aminoäthanolderivaten | |
DE2323021A1 (de) | 2-substituierte 4-alkylamino-6- eckige klammer auf (kleines alpha,kleines alphadimethyl)-(beta-acetyl)-aethylamino eckige klammer zu -1,3,5-triazine sowie ihre verwendung und verfahren zur herstellung derselben | |
DE2439104C3 (de) | Cyclohexanderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide |