IL44410A - Carbanilides, their preparation and preparation containing them - Google Patents

Carbanilides, their preparation and preparation containing them

Info

Publication number: IL44410A
Authority: IL; Israel
Prior art keywords: carbanilide; chloro; soap; meta; formula
Prior art date: 1973-05-23

Application number

IL44410A

Other languages

English (en)

Hebrew (he)

Other versions

IL44410A0 (en

Original Assignee

Givaudan & Cie Sa

Priority date (The priority date 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 date listed.)

1973-05-23

Filing date

1974-03-12

Publication date

1977-10-31

1974-03-12 Application filed by Givaudan & Cie Sa filed Critical Givaudan & Cie Sa

1974-06-30 Publication of IL44410A0 publication Critical patent/IL44410A0/xx

1977-10-31 Publication of IL44410A publication Critical patent/IL44410A/en

Links

239000000203 mixture Substances 0.000 title claims description 24
238000002360 preparation method Methods 0.000 title claims description 11
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
239000000344 soap Substances 0.000 claims description 39
GWEHVDNNLFDJLR-UHFFFAOYSA-N 1,3-diphenylurea Chemical compound C=1C=CC=CC=1NC(=O)NC1=CC=CC=C1 GWEHVDNNLFDJLR-UHFFFAOYSA-N 0.000 claims description 26
238000000034 method Methods 0.000 claims description 20
125000001309 chloro group Chemical group Cl* 0.000 claims description 12
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 6
125000001153 fluoro group Chemical group F* 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 6
239000000376 reactant Substances 0.000 claims description 6
239000004599 antimicrobial Substances 0.000 claims description 3
239000012948 isocyanate Substances 0.000 claims description 3
-1 para-chlorinated aromatic isocyanate Chemical class 0.000 claims description 3
239000000126 substance Substances 0.000 claims description 2
239000000022 bacteriostatic agent Substances 0.000 abstract description 2
229910052757 nitrogen Inorganic materials 0.000 abstract 1
125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 42
150000001875 compounds Chemical class 0.000 description 11
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
239000007787 solid Substances 0.000 description 9
230000003385 bacteriostatic effect Effects 0.000 description 8
239000000243 solution Substances 0.000 description 8
239000002904 solvent Substances 0.000 description 8
239000004094 surface-active agent Substances 0.000 description 8
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
238000002844 melting Methods 0.000 description 6
230000008018 melting Effects 0.000 description 6
238000001953 recrystallisation Methods 0.000 description 6
238000012360 testing method Methods 0.000 description 6
239000012043 crude product Substances 0.000 description 5
239000003599 detergent Substances 0.000 description 5
239000000047 product Substances 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
230000000844 anti-bacterial effect Effects 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
239000002537 cosmetic Substances 0.000 description 4
230000000694 effects Effects 0.000 description 4
ADAKRBAJFHTIEW-UHFFFAOYSA-N 1-chloro-4-isocyanatobenzene Chemical compound ClC1=CC=C(N=C=O)C=C1 ADAKRBAJFHTIEW-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 3
239000013543 active substance Substances 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
238000009472 formulation Methods 0.000 description 3
230000002401 inhibitory effect Effects 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
HHIRBXHEYVDUAM-UHFFFAOYSA-N 1-chloro-3-isocyanatobenzene Chemical compound ClC1=CC=CC(N=C=O)=C1 HHIRBXHEYVDUAM-UHFFFAOYSA-N 0.000 description 2
XUJFOSLZQITUOI-UHFFFAOYSA-N 4-(trifluoromethoxy)aniline Chemical compound NC1=CC=C(OC(F)(F)F)C=C1 XUJFOSLZQITUOI-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
229920001817 Agar Polymers 0.000 description 2
241000894006 Bacteria Species 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
239000000443 aerosol Substances 0.000 description 2
239000008272 agar Substances 0.000 description 2
238000013019 agitation Methods 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
238000004821 distillation Methods 0.000 description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
238000010348 incorporation Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
239000002674 ointment Substances 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
238000010992 reflux Methods 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
LWEAHXKXKDCSIE-UHFFFAOYSA-M 2,3-di(propan-2-yl)naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S([O-])(=O)=O)=C(C(C)C)C(C(C)C)=CC2=C1 LWEAHXKXKDCSIE-UHFFFAOYSA-M 0.000 description 1
XFKLCOFARDPKCT-UHFFFAOYSA-N 3,4-dibromo-2-hydroxy-n-phenylbenzamide Chemical compound OC1=C(Br)C(Br)=CC=C1C(=O)NC1=CC=CC=C1 XFKLCOFARDPKCT-UHFFFAOYSA-N 0.000 description 1
MFUVCHZWGSJKEQ-UHFFFAOYSA-N 3,4-dichlorphenylisocyanate Chemical compound ClC1=CC=C(N=C=O)C=C1Cl MFUVCHZWGSJKEQ-UHFFFAOYSA-N 0.000 description 1
MWDPEBMCVXNSPL-UHFFFAOYSA-N 3-(1,1,2,2-tetrafluoroethoxy)aniline Chemical compound NC1=CC=CC(OC(F)(F)C(F)F)=C1 MWDPEBMCVXNSPL-UHFFFAOYSA-N 0.000 description 1
VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
229930185605 Bisphenol Natural products 0.000 description 1
238000009631 Broth culture Methods 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
235000021314 Palmitic acid Nutrition 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
241000191967 Staphylococcus aureus Species 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
239000011149 active material Substances 0.000 description 1
230000002411 adverse Effects 0.000 description 1
125000002877 alkyl aryl group Chemical class 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
230000000845 anti-microbial effect Effects 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000006071 cream Substances 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
239000008121 dextrose Substances 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
239000004744 fabric Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
235000013305 food Nutrition 0.000 description 1
230000002070 germicidal effect Effects 0.000 description 1
ACGUYXCXAPNIKK-UHFFFAOYSA-N hexachlorophene Chemical compound OC1=C(Cl)C=C(Cl)C(Cl)=C1CC1=C(O)C(Cl)=CC(Cl)=C1Cl ACGUYXCXAPNIKK-UHFFFAOYSA-N 0.000 description 1
229960004068 hexachlorophene Drugs 0.000 description 1
238000000338 in vitro Methods 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
235000015110 jellies Nutrition 0.000 description 1
239000008274 jelly Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
235000020778 linoleic acid Nutrition 0.000 description 1
OYHQOLUKZRVURQ-HZJYTTRNSA-N linoleic acid group Chemical group C(CCCCCCC\C=C/C\C=C/CCCCC)(=O)O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
239000006210 lotion Substances 0.000 description 1
238000003801 milling Methods 0.000 description 1
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
235000021313 oleic acid Nutrition 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
239000003973 paint Substances 0.000 description 1
239000006072 paste Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000012545 processing Methods 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
238000013207 serial dilution Methods 0.000 description 1
239000002453 shampoo Substances 0.000 description 1
229940095696 soap product Drugs 0.000 description 1
239000008149 soap solution Substances 0.000 description 1
229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
IZWPGJFSBABFGL-GMFCBQQYSA-M sodium;2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS([O-])(=O)=O IZWPGJFSBABFGL-GMFCBQQYSA-M 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
239000011550 stock solution Substances 0.000 description 1
239000012085 test solution Substances 0.000 description 1
KVSKGMLNBAPGKH-UHFFFAOYSA-N tribromosalicylanilide Chemical compound OC1=C(Br)C=C(Br)C=C1C(=O)NC1=CC=C(Br)C=C1 KVSKGMLNBAPGKH-UHFFFAOYSA-N 0.000 description 1
229960001325 triclocarban Drugs 0.000 description 1
GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
108010050327 trypticase-soy broth Proteins 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C275/32—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms
- C07C275/34—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms having nitrogen atoms of urea groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Detergent Compositions (AREA)

IL44410A 1973-05-23 1974-03-12 Carbanilides, their preparation and preparation containing them IL44410A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US363206A US3860645A (en)	1973-05-23	1973-05-23	Bacteriostatic substituted carbanilides

Publications (2)

Publication Number	Publication Date
IL44410A0 IL44410A0 (en)	1974-06-30
IL44410A true IL44410A (en)	1977-10-31

Family

ID=23429270

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL44410A IL44410A (en)	1973-05-23	1974-03-12	Carbanilides, their preparation and preparation containing them

Country Status (13)

Country	Link
US (1)	US3860645A (de)
JP (1)	JPS5047941A (de)
AT (1)	AT336631B (de)
AU (1)	AU476065B2 (de)
BE (1)	BE815418A (de)
CA (1)	CA1026769A (de)
CH (1)	CH586194A5 (de)
DE (1)	DE2422243A1 (de)
FR (1)	FR2230627B1 (de)
GB (1)	GB1413449A (de)
IL (1)	IL44410A (de)
NL (1)	NL7405417A (de)
ZA (1)	ZA741631B (de)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2928485A1 (de) *	1979-07-14	1981-01-29	Bayer Ag	Verwendung von harnstoffderivaten als arzneimittel bei der behandlung von fettstoffwechselstoerungen
JPH0395153A (ja) *	1989-06-15	1991-04-19	Mitsubishi Kasei Corp	ジフェニル尿素誘導体
US6344476B1 (en)	1997-05-23	2002-02-05	Bayer Corporation	Inhibition of p38 kinase activity by aryl ureas
US7329670B1 (en) *	1997-12-22	2008-02-12	Bayer Pharmaceuticals Corporation	Inhibition of RAF kinase using aryl and heteroaryl substituted heterocyclic ureas
US7517880B2 (en)	1997-12-22	2009-04-14	Bayer Pharmaceuticals Corporation	Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas
US20080300281A1 (en) *	1997-12-22	2008-12-04	Jacques Dumas	Inhibition of p38 Kinase Activity Using Aryl and Heteroaryl Substituted Heterocyclic Ureas
US20080269265A1 (en) *	1998-12-22	2008-10-30	Scott Miller	Inhibition Of Raf Kinase Using Symmetrical And Unsymmetrical Substituted Diphenyl Ureas
ATE538794T1 (de) *	1999-01-13	2012-01-15	Bayer Healthcare Llc	Gamma carboxyarylsubstituierte diphenylharnstoffverbindungen als p38 kinasehemmer
EP1140840B1 (de)	1999-01-13	2006-03-22	Bayer Pharmaceuticals Corp.	-g(v)-carboxyaryl substituierte diphenyl harnstoffe als raf kinase inhibitoren
RU2319693C9 (ru)	1999-01-13	2008-08-20	Байер Копэрейшн	Производные мочевины (варианты), фармацевтическая композиция (варианты) и способ лечения заболевания, связанного с ростом раковых клеток (варианты)
US8124630B2 (en)	1999-01-13	2012-02-28	Bayer Healthcare Llc	ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US7928239B2 (en)	1999-01-13	2011-04-19	Bayer Healthcare Llc	Inhibition of RAF kinase using quinolyl, isoquinolyl or pyridyl ureas
US7235576B1 (en)	2001-01-12	2007-06-26	Bayer Pharmaceuticals Corporation	Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US7371763B2 (en) *	2001-04-20	2008-05-13	Bayer Pharmaceuticals Corporation	Inhibition of raf kinase using quinolyl, isoquinolyl or pyridyl ureas
ATE345130T1 (de) *	2001-12-03	2006-12-15	Bayer Pharmaceuticals Corp	Arylharnstoff-verbindungen in kombination mit anderen zytostatisch oder zytotoxisch wirksamen stoffen zur behandlungen menschlicher krebserkrankungen
US20080108672A1 (en) *	2002-01-11	2008-05-08	Bernd Riedl	Omega-Carboxyaryl Substituted Diphenyl Ureas As Raf Kinase Inhibitors
US20030216396A1 (en) *	2002-02-11	2003-11-20	Bayer Corporation	Pyridine, quinoline, and isoquinoline N-oxides as kinase inhibitors
US7838541B2 (en)	2002-02-11	2010-11-23	Bayer Healthcare, Llc	Aryl ureas with angiogenesis inhibiting activity
US20040023961A1 (en) *	2002-02-11	2004-02-05	Bayer Corporation	Aryl ureas with raf kinase and angiogenisis inhibiting activity
PT1580188E (pt)	2002-02-11	2012-01-25	Bayer Healthcare Llc	Aril-ureias como inibidores de cinases
UY28213A1 (es)	2003-02-28	2004-09-30	Bayer Pharmaceuticals Corp	Nuevos derivados de cianopiridina útiles en el tratamiento de cáncer y otros trastornos.
WO2004113274A2 (en) *	2003-05-20	2004-12-29	Bayer Pharmaceuticals Corporation	Diaryl ureas with kinase inhibiting activity
RS52625B (sr) *	2003-07-23	2013-06-28	Bayer Healthcare Llc	Fluoro supstituisana omega-karboksiaril difenil urea za lečenje i prevenciju bolesti i stanja bolesti

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2818930A (en) *	1948-08-07	1958-01-07	Joseph B Kucera	Three-wheeled vehicle having a high arched front frame
US2745874A (en) *	1953-06-18	1956-05-15	Geigy Ag J R	Insecticidal derivatives of diphenyl urea
US2846398A (en) *	1955-12-27	1958-08-05	Monsanto Chemicals	Antiseptic detergent composition

1973
- 1973-05-23 US US363206A patent/US3860645A/en not_active Expired - Lifetime
1974
- 1974-03-12 ZA ZA00741631A patent/ZA741631B/xx unknown
- 1974-03-12 IL IL44410A patent/IL44410A/en unknown
- 1974-03-14 AU AU66650/74A patent/AU476065B2/en not_active Expired
- 1974-03-21 CH CH393074A patent/CH586194A5/xx not_active IP Right Cessation
- 1974-04-22 NL NL7405417A patent/NL7405417A/xx unknown
- 1974-05-08 DE DE2422243A patent/DE2422243A1/de active Pending
- 1974-05-13 JP JP49053157A patent/JPS5047941A/ja active Pending
- 1974-05-21 FR FR7417631A patent/FR2230627B1/fr not_active Expired
- 1974-05-22 CA CA200,572A patent/CA1026769A/en not_active Expired
- 1974-05-22 AT AT426874A patent/AT336631B/de not_active IP Right Cessation
- 1974-05-22 BE BE144645A patent/BE815418A/xx unknown
- 1974-05-22 GB GB2289374A patent/GB1413449A/en not_active Expired

Also Published As

Publication number	Publication date
ATA426874A (de)	1976-09-15
AU6665074A (en)	1975-09-18
CH586194A5 (de)	1977-03-31
AU476065B2 (en)	1976-09-09
US3860645A (en)	1975-01-14
AT336631B (de)	1977-05-10
GB1413449A (en)	1975-11-12
ZA741631B (en)	1975-01-29
CA1026769A (en)	1978-02-21
NL7405417A (de)	1974-11-26
BE815418A (fr)	1974-11-22
JPS5047941A (de)	1975-04-28
IL44410A0 (en)	1974-06-30
FR2230627A1 (de)	1974-12-20
DE2422243A1 (de)	1974-12-12
FR2230627B1 (de)	1977-09-30

Publication	Publication Date	Title
IL44410A (en)	1977-10-31	Carbanilides, their preparation and preparation containing them
US2846398A (en)	1958-08-05	Antiseptic detergent composition
JPH02174754A (ja)	1990-07-06	スルファモイルフェニル尿素
EP0038191A1 (de)	1981-10-21	5-Acylsalicylanilid-Derivate und Verfahren zur Hemmung des Wachstums von Mikroorganismen
US3975435A (en)	1976-08-17	Substituted cinnamanilides
GB1103391A (en)	1968-02-14	(halogeno-cyano) acetyl derivatives and pesticidal preparations containing them
US2692862A (en)	1954-10-26	Cleansing compositions having antibacterial properties
US3981814A (en)	1976-09-21	Bacteriostatic substituted benzanilide compositions and methods for their use
US3800048A (en)	1974-03-26	Composition of halogenated hydroxy-diphenyl ethers
US3103467A (en)	1963-09-10	Method of controlling bacterial
US3078298A (en)	1963-02-19	3-alkyl (sulfonyl and sulfoxyl) acrylic acid esters and nitriles
US3577453A (en)	1971-05-04	Trifluoromethyl phenyl-n-(halophenyl)-carbamates and pesticidal preparations containing same
US3635997A (en)	1972-01-18	N-halophenyldichlorisothiazolones and method for their manufacture
US3904696A (en)	1975-09-09	Halogenated hydroxy-diphenyl ethers
US3651128A (en)	1972-03-21	Bacteriostatic carbamates of bisphenols
GB1561274A (en)	1980-02-20	Compositions containing beta subsituted acrylic acid amides as preservatives
US3141818A (en)	1964-07-21	Biological toxicant
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