DE234851C - - Google Patents
Info
- Publication number
- DE234851C DE234851C DENDAT234851D DE234851DA DE234851C DE 234851 C DE234851 C DE 234851C DE NDAT234851 D DENDAT234851 D DE NDAT234851D DE 234851D A DE234851D A DE 234851DA DE 234851 C DE234851 C DE 234851C
- Authority
- DE
- Germany
- Prior art keywords
- mercury
- halogen
- parts
- heated
- oxide
- 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
- 229910052736 halogen Inorganic materials 0.000 claims description 9
- 150000002731 mercury compounds Chemical class 0.000 claims description 6
- UKWHYYKOEPRTIC-UHFFFAOYSA-N mercury(ii) oxide Chemical compound [Hg]=O UKWHYYKOEPRTIC-UHFFFAOYSA-N 0.000 claims description 6
- -1 halogen nitrophenols Chemical class 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- 229910000474 mercury oxide Inorganic materials 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 150000002989 phenols Chemical class 0.000 claims description 4
- 150000002730 mercury Chemical class 0.000 claims description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 3
- 229910052753 mercury Inorganic materials 0.000 claims description 3
- 239000003085 diluting agent Substances 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 150000001875 compounds Chemical group 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000000243 solution Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
- 229940100892 mercury compound Drugs 0.000 description 5
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- IQUPABOKLQSFBK-UHFFFAOYSA-N 2-nitrophenol Chemical compound OC1=CC=CC=C1[N+]([O-])=O IQUPABOKLQSFBK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- NWSIFTLPLKCTSX-UHFFFAOYSA-N 4-chloro-2-nitrophenol Chemical compound OC1=CC=C(Cl)C=C1[N+]([O-])=O NWSIFTLPLKCTSX-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001447 alkali salts Chemical class 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- QQODMLTYWYCRQV-UHFFFAOYSA-M phenoxymercury Chemical class [Hg]OC1=CC=CC=C1 QQODMLTYWYCRQV-UHFFFAOYSA-M 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- DOBUSJIVSSJEDA-UHFFFAOYSA-L 1,3-dioxa-2$l^{6}-thia-4-mercuracyclobutane 2,2-dioxide Chemical compound [Hg+2].[O-]S([O-])(=O)=O DOBUSJIVSSJEDA-UHFFFAOYSA-L 0.000 description 1
- UMPSXRYVXUPCOS-UHFFFAOYSA-N 2,3-dichlorophenol Chemical class OC1=CC=CC(Cl)=C1Cl UMPSXRYVXUPCOS-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- RCTYPNKXASFOBE-UHFFFAOYSA-M chloromercury Chemical compound [Hg]Cl RCTYPNKXASFOBE-UHFFFAOYSA-M 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 230000000249 desinfective effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229940101209 mercuric oxide Drugs 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- RBXVOQPAMPBADW-UHFFFAOYSA-N nitrous acid;phenol Chemical class ON=O.OC1=CC=CC=C1 RBXVOQPAMPBADW-UHFFFAOYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F3/00—Compounds containing elements of Groups 2 or 12 of the Periodic Table
- C07F3/10—Mercury compounds
- C07F3/12—Aromatic substances containing mercury
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE234851C true DE234851C (enrdf_load_stackoverflow) |
Family
ID=494685
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT234851D Active DE234851C (enrdf_load_stackoverflow) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE234851C (enrdf_load_stackoverflow) |
-
0
- DE DENDAT234851D patent/DE234851C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1620024C3 (de) | 3'-Pyridylmethyl-2-(4-chlorphenoxy)-2-methylpropionat | |
| DE234851C (enrdf_load_stackoverflow) | ||
| DE1493776C3 (de) | Substituierte o-Phenoxyphenylester, Verfahren zu deren Herstellung und diese enthaltende Mittel | |
| DE1518289A1 (de) | Neue quaternaere Ammoniumsalze mit desinfizierender Wirkung und Verfahren zur Herstellung derselben | |
| DE568675C (de) | Verfahren zur Herstellung von O-Alkyl-, Oxyalkyl- oder Alkylaminoalkylaethern des Harmols oder Harmalols | |
| DE737193C (de) | Verfahren zur Herstellung von unsymmetrischen Heptamethincyaninfarbstoffen | |
| DE579224C (de) | Verfahren zur Darstellung von jodierten Abkoemmlingen des 4-Pyridons | |
| DE614196C (de) | Verfahren zur Herstellung von stickstoffhaltigen Kondensationsprodukten | |
| DE386743C (de) | Verfahren zur Darstellung von N-Alkylaminofettsaeuren und deren N-Acidylderivaten | |
| DE521458C (de) | Verfahren zur Darstellung von Kondensationsprodukten aus mehrwertigen Phenolen und aliphatischen Dicarbonsaeuren | |
| DE173729C (enrdf_load_stackoverflow) | ||
| DE673485C (de) | Verfahren zur Darstellung von 1-Ascorbinsaeure | |
| DE406148C (de) | Verfahren zur Darstellung am Stickstoff substituierter Anthranilsaeurederivate | |
| DE646703C (de) | Verfahren zur Herstellung von Metallkomplexverbindungen | |
| DE703227C (enrdf_load_stackoverflow) | ||
| AT205167B (de) | Verfahren zur Herstellung von 5a-6-Anhydrotetracyclinderivaten | |
| DE627251C (de) | Verfahren zur Reinigung von Milchsaeure | |
| DE386690C (de) | Verfahren zur Darstellung von Derivaten des Nortropinons | |
| AT149992B (de) | Verfahren zur Darstellung von 2-Keto-l-gulonsäure. | |
| DE69035C (de) | Verfahren zur Darstellung von p-Aethoxyacetylamidochinolin. (4 | |
| DE746578C (de) | Verfahren zur Herstellung von basischen 1, 3-Dialkoxypropanlen | |
| DE710225C (de) | Verfahren zur Darstellung von Verbindungen von Dioxydialkylstilbenen | |
| DE68240C (de) | Verfahren zur Darstellung von p-Aethoxyantipyrin | |
| DE448695C (de) | Verfahren zur Herstellung von Dipyridylen | |
| DE564786C (de) | Verfahren zur Darstellung von 3, 5-Dihalogenpyridin-2- oder -4-sulfonsaeuren |