BE471422A - - Google Patents
Info
- Publication number
- BE471422A BE471422A BE471422DA BE471422A BE 471422 A BE471422 A BE 471422A BE 471422D A BE471422D A BE 471422DA BE 471422 A BE471422 A BE 471422A
- Authority
- BE
- Belgium
- Prior art keywords
- chlorine
- diphenyl
- solution
- products
- chlorinated
- Prior art date
Links
- 239000000047 product Substances 0.000 claims description 33
- 239000000460 chlorine Substances 0.000 claims description 30
- 229910052801 chlorine Inorganic materials 0.000 claims description 29
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 28
- 125000006267 biphenyl group Chemical group 0.000 claims description 18
- 239000004305 biphenyl Substances 0.000 claims description 16
- 235000010290 biphenyl Nutrition 0.000 claims description 16
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 16
- 239000002904 solvent Substances 0.000 claims description 11
- 238000006243 chemical reaction Methods 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 238000005660 chlorination reaction Methods 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- 238000010521 absorption reaction Methods 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 4
- 230000005855 radiation Effects 0.000 claims description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 2
- 230000000996 additive effect Effects 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 239000012295 chemical reaction liquid Substances 0.000 claims 2
- 238000004821 distillation Methods 0.000 claims 2
- FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical compound OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 238000010924 continuous production Methods 0.000 claims 1
- 238000001640 fractional crystallisation Methods 0.000 claims 1
- 238000005194 fractionation Methods 0.000 claims 1
- 238000006386 neutralization reaction Methods 0.000 claims 1
- 230000003472 neutralizing effect Effects 0.000 claims 1
- 230000003071 parasitic effect Effects 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 241000607479 Yersinia pestis Species 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 230000002141 anti-parasite Effects 0.000 description 5
- 230000000749 insecticidal effect Effects 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- 241000238631 Hexapoda Species 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- 239000003096 antiparasitic agent Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 241000254173 Coleoptera Species 0.000 description 2
- 241000258916 Leptinotarsa decemlineata Species 0.000 description 2
- 241000238814 Orthoptera Species 0.000 description 2
- 229940125687 antiparasitic agent Drugs 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- -1 fuller's earth Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000009965 odorless effect Effects 0.000 description 2
- 230000000590 parasiticidal effect Effects 0.000 description 2
- 239000002297 parasiticide Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 241001136249 Agriotes lineatus Species 0.000 description 1
- 241000902876 Alticini Species 0.000 description 1
- 241001124076 Aphididae Species 0.000 description 1
- 206010004194 Bed bug infestation Diseases 0.000 description 1
- 241001338801 Chlorus Species 0.000 description 1
- 241001414835 Cimicidae Species 0.000 description 1
- 241000238424 Crustacea Species 0.000 description 1
- 241000254171 Curculionidae Species 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 241000282414 Homo sapiens Species 0.000 description 1
- 101100005911 Mus musculus Cer1 gene Proteins 0.000 description 1
- 241000131095 Oniscidea Species 0.000 description 1
- CXOFVDLJLONNDW-UHFFFAOYSA-N Phenytoin Chemical compound N1C(=O)NC(=O)C1(C=1C=CC=CC=1)C1=CC=CC=C1 CXOFVDLJLONNDW-UHFFFAOYSA-N 0.000 description 1
- 102000016941 Rho Guanine Nucleotide Exchange Factors Human genes 0.000 description 1
- 108010053823 Rho Guanine Nucleotide Exchange Factors Proteins 0.000 description 1
- 241001168761 Rhynchites Species 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 241000615724 Sucra Species 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052925 anhydrite Inorganic materials 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000010575 fractional recrystallization Methods 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 244000000011 human parasite Species 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 201000008585 noma Diseases 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 239000010454 slate Substances 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000563 toxic property Toxicity 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE471422A true BE471422A (cs) |
Family
ID=121297
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE471422D BE471422A (cs) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE471422A (cs) |
-
0
- BE BE471422D patent/BE471422A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| FR2492376A1 (fr) | Polymethylene-4,5 isothiazoline-4 ones-3, leur procede de preparation et leurs utilisation comme agents bactericides et fongicides | |
| FR2597472A1 (fr) | Composes difluorohalogenomethoxyphenyle et compositions acaricides les contenant. | |
| EP0003708A1 (fr) | Nouveau procédé de préparation stéréosélectif de phéromones sexuelles et phéromones sexuelles obtenues | |
| Gunther | Aspects of the chemistry of DDT | |
| Ruzo et al. | Environmental chemistry of flame retardants. 4. Photodegradation of polybromobiphenyls (PBB) | |
| DE968171C (de) | Mittel zur Bekaempfung von schaedlichen Insekten | |
| BE471422A (cs) | ||
| DE69525434T2 (de) | Verfahren zur keimungshemmenden Behandlung von Knollen oder Zwiebeln | |
| US2579434A (en) | Parasiticidal composition | |
| CH427400A (fr) | Composition fongicide | |
| EP0135432A1 (fr) | Dérivés de l'acide benzoique, procédé de préparation et application à titre de médicaments désinfectants ou de conservateurs | |
| DE2635545C3 (de) | S^-Dimethyl-S-hydroxy-octannitril, seine Herstellung und Verwendung als Duftstoff | |
| LU84091A1 (fr) | Derives n-carbamoyl d'isothiazolo-(5,4b)pyridine one-3,leur procede de preparation et leurs utilisations comme agents bactericides et fongicides | |
| DE69020377T2 (de) | Verfahren zur Herstellung von für die Umwelt unbedenklichem Dicofol und dessen Formulierungen. | |
| FR2737085A1 (fr) | Associations insecticides d'un oxime carbamate avec un insecticide a groupe pyrazole ou phenylimidazole | |
| DE1493366C3 (de) | 1 eckige Klammer auf p (2',3' Dihydroxypropoxy) phenyl eckige Klammer zu 2 phenyl 6 methoxy 1,2,3,4 tetra hydronaphthahn, Verfahren zu seiner Herstellung und diese Verbindung ent haltende therapeutische Zubereitung | |
| US3336401A (en) | Ar-nitro-alpha-(2, 2, 2-trichloroethyl) styrene compounds | |
| DE2533172C3 (de) | Herbizides Mittel auf Basis von Nitrophenolätherderivaten | |
| BE565945A (cs) | ||
| JPH0692281B2 (ja) | アミノ酸メチルエステルを有効成分とするコガネムシ類の誘引剤 | |
| US3154399A (en) | Synergistic herbicidal composition and method employing a trichlorobenzyloxyalkanol and a chlorinated aliphatic acid or ester thereof | |
| DER0015335MA (cs) | ||
| JPS6075445A (ja) | ２、２−ジメチル−３−〔２−フルオル−３−オキソ−３−（１、１−ジメチルエトキシ）−１−プロペニル〕シクロプロパンカルボン酸の新誘導体 | |
| CH178448A (de) | Mittel zum Vertreiben von Schädlingen. | |
| DE2157601A1 (cs) |