DE2012508A1 - QuaternSre Ammoniumsalze - Google Patents
QuaternSre AmmoniumsalzeInfo
- Publication number
- DE2012508A1 DE2012508A1 DE19702012508 DE2012508A DE2012508A1 DE 2012508 A1 DE2012508 A1 DE 2012508A1 DE 19702012508 DE19702012508 DE 19702012508 DE 2012508 A DE2012508 A DE 2012508A DE 2012508 A1 DE2012508 A1 DE 2012508A1
- Authority
- DE
- Germany
- Prior art keywords
- ammonium salts
- quaternary ammonium
- anion
- radical
- reaction
- 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.)
- Pending
Links
- 150000003863 ammonium salts Chemical class 0.000 title 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 6
- -1 alkylsulfonate anion Chemical class 0.000 claims description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 3
- 229940100198 alkylating agent Drugs 0.000 claims description 3
- 239000002168 alkylating agent Substances 0.000 claims description 3
- 150000001450 anions Chemical class 0.000 claims description 3
- 239000012442 inert solvent Substances 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 239000000575 pesticide Substances 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 150000003512 tertiary amines Chemical class 0.000 claims description 2
- 150000003254 radicals Chemical class 0.000 claims 5
- HNUALPPJLMYHDK-UHFFFAOYSA-N C[CH]C Chemical compound C[CH]C HNUALPPJLMYHDK-UHFFFAOYSA-N 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 125000004803 chlorobenzyl group Chemical group 0.000 claims 1
- 150000004820 halides Chemical class 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000005394 methallyl group Chemical group 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000004372 methylthioethyl group Chemical group [H]C([H])([H])SC([H])([H])C([H])([H])* 0.000 claims 1
- 239000000460 chlorine Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 230000029936 alkylation Effects 0.000 description 2
- 238000005804 alkylation reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 241001233037 catfish Species 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- CEOCDNVZRAIOQZ-UHFFFAOYSA-N pentachlorobenzene Chemical compound ClC1=CC(Cl)=C(Cl)C(Cl)=C1Cl CEOCDNVZRAIOQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/12—Quaternary ammonium compounds
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR6907630A FR2038503A5 (enrdf_load_stackoverflow) | 1969-03-18 | 1969-03-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE2012508A1 true DE2012508A1 (de) | 1970-09-24 |
Family
ID=9030779
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19702012508 Pending DE2012508A1 (de) | 1969-03-18 | 1970-03-17 | QuaternSre Ammoniumsalze |
Country Status (9)
Country | Link |
---|---|
AT (1) | AT299156B (enrdf_load_stackoverflow) |
BE (1) | BE746938A (enrdf_load_stackoverflow) |
BR (1) | BR7017554D0 (enrdf_load_stackoverflow) |
CA (1) | CA947770A (enrdf_load_stackoverflow) |
DE (1) | DE2012508A1 (enrdf_load_stackoverflow) |
FR (1) | FR2038503A5 (enrdf_load_stackoverflow) |
GB (1) | GB1290225A (enrdf_load_stackoverflow) |
LU (1) | LU60530A1 (enrdf_load_stackoverflow) |
NL (1) | NL7003532A (enrdf_load_stackoverflow) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3929886A (en) * | 1969-03-18 | 1975-12-30 | Ugine Kuhlmann | Quaternary ammonia salts of polyhalogenated aromatic compounds |
-
1969
- 1969-03-18 FR FR6907630A patent/FR2038503A5/fr not_active Expired
-
1970
- 1970-03-02 GB GB1290225D patent/GB1290225A/en not_active Expired
- 1970-03-06 BE BE746938D patent/BE746938A/xx unknown
- 1970-03-12 NL NL7003532A patent/NL7003532A/xx unknown
- 1970-03-16 LU LU60530D patent/LU60530A1/xx unknown
- 1970-03-16 AT AT241570A patent/AT299156B/de not_active IP Right Cessation
- 1970-03-17 DE DE19702012508 patent/DE2012508A1/de active Pending
- 1970-03-17 CA CA077,700*7A patent/CA947770A/en not_active Expired
- 1970-03-18 BR BR21755470A patent/BR7017554D0/pt unknown
Also Published As
Publication number | Publication date |
---|---|
NL7003532A (enrdf_load_stackoverflow) | 1970-09-22 |
FR2038503A5 (enrdf_load_stackoverflow) | 1971-01-08 |
LU60530A1 (enrdf_load_stackoverflow) | 1970-05-21 |
GB1290225A (enrdf_load_stackoverflow) | 1972-09-20 |
AT299156B (de) | 1972-06-12 |
BE746938A (fr) | 1970-08-17 |
BR7017554D0 (pt) | 1973-05-10 |
CA947770A (en) | 1974-05-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE2040270A1 (de) | Verfahren zur Herstellung Polyolefin-substituierter Amine | |
DE2213809A1 (de) | Dibenzoxazepin-N-carbonsäurehydrazide und deren Derivate | |
DE2012508A1 (de) | QuaternSre Ammoniumsalze | |
DE2045440C3 (de) | Verfahren zur Herstellung von trisubstituierten Chlorsulfenylharnstoffen | |
DE2447824A1 (de) | Herstellung von c tief 1 -c tief 7 aliphatischen hydrocarbylestern von n- eckige klammer auf 2,6-di(c tief 1 -c tief 7 -alkyl)phenyl eckige klammer zu alpha-aminocarbonsaeuren | |
DE627880C (de) | Verfahren zur Gewinnung quaternaerer Stickstoffverbindungen | |
DE1122053B (de) | Verfahren zur Herstellung von Chlorbenzylisothiuroniumchloriden | |
DE2725523A1 (de) | Stabilisiertes 1,1,1-trichloraethan, verfahren zu seiner herstellung und seine verwendung | |
DE1568622A1 (de) | Verfahren zur Herstellung neuartiger Phenolderivate | |
DE1670920A1 (de) | N-Disubstituierte 3-Amino-1,2-benzisothiazol-Derivate | |
DE2202204A1 (de) | Verfahren zur kontinuierlichen herstellung von 2-mercaptobenzimidazol | |
DE932964C (de) | Verfahren zur Herstellung von ª‡,ª‰-ungesaettigten Carbonsaeureamiden aus ª‰-Halogencarbonsaeureamiden | |
DE2056357A1 (de) | Verfahren zur Herstellung von Reaktionsprodukten aus Hydrazin und Carbonylverbindungen | |
DE929192C (de) | Verfahren zur Herstellung von am Stickstoffatom acylierten oder sulfonylierten aliphatischen Aminocarbonsaeureamiden | |
DE1793773A1 (de) | Verfahren zur herstellung von alkylenepisulfiden mit 2 bis 3 kohlenstoffatomen | |
DE1568203C (de) | Verfahren zur Herstellung von N-Phenyl-N-methyl-N-(2.3-dibrom-l-methylallyl)-harnstoffen | |
DE1518986A1 (de) | Verfahren zur Herstellung von mehrfuntionellen aliphatischen Isocyanaten | |
DE902849C (de) | Verfahren zur Herstellung aliphatischer Dicarbonsaeuren mit 4 oder mehr Kohlenstoffatomen | |
DE1593105C (de) | Verfahren zur Herstellung quater narer Ammoniumhalogenide | |
DE2759261B2 (de) | Mittel und Verfahren zur Kontrolle von Korrosion und Schaumbildung in Systemen zur Acrylnitrilerzeugung | |
DE1951587C (enrdf_load_stackoverflow) | ||
DE1618257A1 (de) | Verfahren zur Herstellung von halogenierten Phenoxysilanen | |
DE952084C (de) | Verfahren zur Herstellung von organischen Isothiocyanaten | |
DE726175C (de) | Verfahren zur Verringerung der Loeslichkeit bzw. Quellbarkeit von Eiweissstoffen | |
DE939748C (de) | Verfahren zur Herstellung von 2, 5-Dichlorterephthalsaeure |