BE560641A - - Google Patents
Info
- Publication number
- BE560641A BE560641A BE560641DA BE560641A BE 560641 A BE560641 A BE 560641A BE 560641D A BE560641D A BE 560641DA BE 560641 A BE560641 A BE 560641A
- Authority
- BE
- Belgium
- Prior art keywords
- radical
- hydrocarbon radical
- polyquaternary
- polyquaternary compounds
- solution
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 19
- 239000004215 Carbon black (E152) Substances 0.000 claims description 11
- 229930195733 hydrocarbon Natural products 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 238000011282 treatment Methods 0.000 claims description 6
- 125000005842 heteroatom Chemical group 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 150000003512 tertiary amines Chemical class 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000000982 direct dye Substances 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 239000000243 solution Substances 0.000 description 14
- 239000000975 dye Substances 0.000 description 10
- 238000003756 stirring Methods 0.000 description 8
- 239000007788 liquid Substances 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 5
- -1 chlorine or bromine Chemical class 0.000 description 5
- 230000007935 neutral effect Effects 0.000 description 5
- YMDNODNLFSHHCV-UHFFFAOYSA-N 2-chloro-n,n-diethylethanamine Chemical compound CCN(CC)CCCl YMDNODNLFSHHCV-UHFFFAOYSA-N 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- LBUJPTNKIBCYBY-UHFFFAOYSA-N 1,2,3,4-tetrahydroquinoline Chemical compound C1=CC=C2CCCNC2=C1 LBUJPTNKIBCYBY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- WNRWEBKEQARBKV-UHFFFAOYSA-N 1-(2-chloroethyl)piperidine Chemical compound ClCCN1CCCCC1 WNRWEBKEQARBKV-UHFFFAOYSA-N 0.000 description 1
- RMGFLMXDCGQKPS-UHFFFAOYSA-N 1-(2-chloroethyl)pyrrolidine Chemical group ClCCN1CCCC1 RMGFLMXDCGQKPS-UHFFFAOYSA-N 0.000 description 1
- ZAPMTSHEXFEPSD-UHFFFAOYSA-N 4-(2-chloroethyl)morpholine Chemical compound ClCCN1CCOCC1 ZAPMTSHEXFEPSD-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 101100136062 Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) PE10 gene Proteins 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 1
- 125000005605 benzo group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000004699 copper complex Chemical class 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- PTVDYARBVCBHSL-UHFFFAOYSA-N copper;hydrate Chemical compound O.[Cu] PTVDYARBVCBHSL-UHFFFAOYSA-N 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- RXSFYJAXRSVQRN-UHFFFAOYSA-N n-(2-chloroethyl)-2-methyl-n-(2-methylpropyl)propan-1-amine Chemical compound CC(C)CN(CCCl)CC(C)C RXSFYJAXRSVQRN-UHFFFAOYSA-N 0.000 description 1
- BXRWQPSRWVPOOX-UHFFFAOYSA-N n-(2-chloroethyl)-n-ethylcyclohexanamine Chemical compound ClCCN(CC)C1CCCCC1 BXRWQPSRWVPOOX-UHFFFAOYSA-N 0.000 description 1
- QKWHKHPUGFKVCP-UHFFFAOYSA-N n-(2-chloroethyl)-n-propylpropan-1-amine Chemical compound CCCN(CCC)CCCl QKWHKHPUGFKVCP-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229940066771 systemic antihistamines piperazine derivative Drugs 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/06—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by halogen atoms or nitro radicals
- C07D295/067—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by halogen atoms or nitro radicals with the ring nitrogen atoms and the substituents attached to the same carbon chain, which is not interrupted by carbocyclic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE560641A true BE560641A (ca) |
Family
ID=182864
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE560641D BE560641A (ca) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE560641A (ca) |
-
0
- BE BE560641D patent/BE560641A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0017568B1 (fr) | Sulfobétaines fluorées et applications de leurs propriétés tensio-actives à des compositions extinctrices | |
| WO2000040550A1 (fr) | Procede de preparation de nitroxydes | |
| BE560641A (ca) | ||
| CH626061A5 (ca) | ||
| FR2786483A1 (fr) | Procede de preparation de 4-hydroxyquinoleines et/ou formes tautomeres | |
| CH394247A (fr) | Procédé de préparation de nouveaux aminoesters | |
| EP0025620B1 (fr) | Procédé pour la fabrication d'anthraquinones substituées | |
| CA1305712C (fr) | Procede de preparation de sulfates cycliques | |
| EP0098783B1 (fr) | Procédé de préparation de halogéno anilines | |
| EP0037781B1 (fr) | Phényl alcoxy propanolamines, leur préparation et leur application en tant que médicaments | |
| JP3202236B2 (ja) | 界面活性剤が改良されたｐ−アミノフェノールの製造法 | |
| JPH03153664A (ja) | 芳香族ジチオールの製造方法 | |
| EP0888318A1 (fr) | Procede ameliore pour la preparation de derives de l'acide 3-(10-phenothiazyl)propanoique ou 3-(10-phenoxazyl)propanoique | |
| FR2505327A1 (fr) | Procede d'halogenation en meta de n-(o,o'-dialkyl phenyl) alaninates et homologues | |
| JPH0336829B2 (ca) | ||
| CN116478704B (zh) | 一种不含氯的有机反离子季铵盐双子表面活性剂及其制备方法与应用 | |
| EP0382641B1 (fr) | Procédé de préparation de dicarbonate de ditertioalcoyle | |
| EP0376801B1 (fr) | Acétates, thioacétates et acétamides de polyfluoroalkyle substitués, leur procédé de préparation et leurs applications | |
| FR2579592A1 (fr) | Procede de preparation de derives aromatiques 1,1 difluoro perhalogenoalcoxyles ou 1,1 difluoro perhalogenothioalkyles | |
| CH587795A5 (en) | 2-Aminoalkyl amino indanes - anti-arrhythmic,orally active, long-acting, not myocardial depressant | |
| MC939A1 (fr) | Procédé de préparation de dérivés de benzamide | |
| JPS60100552A (ja) | スルホン類およびスルホキシド類の製造方法 | |
| BE386506A (ca) | ||
| BE454551A (ca) | ||
| CH639085A5 (en) | Process for the preparation of xanthone derivatives |