SK408991A3 - Liquid herbicidal agent - Google Patents

Liquid herbicidal agent Download PDF

Info

Publication number: SK408991A3
Authority: SK; Slovakia
Prior art keywords: weight; ethyl; ethylene oxide; formulations; liquid herbicidal
Prior art date: 1989-06-02

Application number

SK4089-91A

Other languages

English (en)

Slovak (sk)

Inventor

Konrad Albrecht

Rudolf Heinrich

Hans Schumacher

Original Assignee

Hoechst Ag

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.)

1989-06-02

Filing date

1991-12-27

Publication date

1994-06-08

1991-12-27 Application filed by Hoechst Ag filed Critical Hoechst Ag

1994-06-08 Publication of SK408991A3 publication Critical patent/SK408991A3/sk

Links

239000007788 liquid Substances 0.000 title claims abstract description 13
239000004009 herbicide Substances 0.000 title claims abstract description 10
239000000203 mixture Substances 0.000 claims abstract description 44
239000000839 emulsion Substances 0.000 claims abstract description 12
239000004094 surface-active agent Substances 0.000 claims abstract description 12
239000004495 emulsifiable concentrate Substances 0.000 claims abstract description 9
239000010695 polyglycol Substances 0.000 claims abstract description 8
229920000151 polyglycol Polymers 0.000 claims abstract description 8
229920001400 block copolymer Polymers 0.000 claims abstract description 6
150000002191 fatty alcohols Chemical class 0.000 claims abstract description 6
150000003839 salts Chemical class 0.000 claims abstract description 6
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 5
239000002270 dispersing agent Substances 0.000 claims abstract description 4
150000002170 ethers Chemical class 0.000 claims abstract description 4
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract 3
229910052791 calcium Inorganic materials 0.000 claims abstract 3
239000011575 calcium Substances 0.000 claims abstract 3
150000001875 compounds Chemical class 0.000 claims description 18
230000002363 herbicidal effect Effects 0.000 claims description 9
239000000654 additive Substances 0.000 claims description 6
DMKKMGYBLFUGTO-UHFFFAOYSA-N 2-methyloxirane;oxirane Chemical compound C1CO1.C1CO1.CC1CO1 DMKKMGYBLFUGTO-UHFFFAOYSA-N 0.000 claims description 3
239000012141 concentrate Substances 0.000 claims description 3
238000009472 formulation Methods 0.000 abstract description 21
230000000694 effects Effects 0.000 abstract description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 9
239000013543 active substance Substances 0.000 abstract description 5
BACHBFVBHLGWSL-UHFFFAOYSA-N methyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate Chemical group C1=CC(OC(C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-UHFFFAOYSA-N 0.000 abstract description 5
238000002360 preparation method Methods 0.000 abstract description 5
BACHBFVBHLGWSL-JTQLQIEISA-N rac-diclofop methyl Natural products C1=CC(O[C@@H](C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-JTQLQIEISA-N 0.000 abstract description 5
PQKBPHSEKWERTG-UHFFFAOYSA-N Fenoxaprop ethyl Chemical group C1=CC(OC(C)C(=O)OCC)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 PQKBPHSEKWERTG-UHFFFAOYSA-N 0.000 abstract description 4
239000003795 chemical substances by application Substances 0.000 abstract description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 1
125000005037 alkyl phenyl group Chemical group 0.000 abstract 1
PQKBPHSEKWERTG-LLVKDONJSA-N ethyl (2r)-2-[4-[(6-chloro-1,3-benzoxazol-2-yl)oxy]phenoxy]propanoate Chemical group C1=CC(O[C@H](C)C(=O)OCC)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 PQKBPHSEKWERTG-LLVKDONJSA-N 0.000 abstract 1
239000004480 active ingredient Substances 0.000 description 7
-1 alkylbenzene sulfonate Chemical class 0.000 description 7
239000000126 substance Substances 0.000 description 5
150000002148 esters Chemical class 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
239000007921 spray Substances 0.000 description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
230000008901 benefit Effects 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
239000003921 oil Substances 0.000 description 3
239000000843 powder Substances 0.000 description 3
241000196324 Embryophyta Species 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
244000068988 Glycine max Species 0.000 description 2
235000010469 Glycine max Nutrition 0.000 description 2
235000013877 carbamide Nutrition 0.000 description 2
239000004359 castor oil Substances 0.000 description 2
235000019438 castor oil Nutrition 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
238000000034 method Methods 0.000 description 2
238000002156 mixing Methods 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
BTFMCMVEUCGQDX-UHFFFAOYSA-N 1-[10-[3-[4-(2-hydroxyethyl)-1-piperidinyl]propyl]-2-phenothiazinyl]ethanone Chemical compound C12=CC(C(=O)C)=CC=C2SC2=CC=CC=C2N1CCCN1CCC(CCO)CC1 BTFMCMVEUCGQDX-UHFFFAOYSA-N 0.000 description 1
XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 description 1
DXBQEHHOGRVYFF-UHFFFAOYSA-N 3-pyridin-4-ylpentane-2,4-dione Chemical group CC(=O)C(C(C)=O)C1=CC=NC=C1 DXBQEHHOGRVYFF-UHFFFAOYSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
101000891630 Arabidopsis thaliana Tubulin-folding cofactor C Proteins 0.000 description 1
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical class COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
241000233866 Fungi Species 0.000 description 1
239000005561 Glufosinate Substances 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
QUKDIMOBZWBSIM-UHFFFAOYSA-N OOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOO Chemical compound OOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOO QUKDIMOBZWBSIM-UHFFFAOYSA-N 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
241000209504 Poaceae Species 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
241000209140 Triticum Species 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
238000005054 agglomeration Methods 0.000 description 1
230000002776 aggregation Effects 0.000 description 1
150000001335 aliphatic alkanes Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
230000003373 anti-fouling effect Effects 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
238000003556 assay Methods 0.000 description 1
MCOQHIWZJUDQIC-UHFFFAOYSA-N barban Chemical compound ClCC#CCOC(=O)NC1=CC=CC(Cl)=C1 MCOQHIWZJUDQIC-UHFFFAOYSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
150000001721 carbon Chemical class 0.000 description 1
239000000969 carrier Substances 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
238000011109 contamination Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
230000002939 deleterious effect Effects 0.000 description 1
239000003599 detergent Substances 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
239000000428 dust Substances 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
DHEPLMUINOAZLH-UHFFFAOYSA-N ethyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate Chemical group C1=CC(OC(C)C(=O)OCC)=CC=C1OC1=CC=C(Cl)C=C1Cl DHEPLMUINOAZLH-UHFFFAOYSA-N 0.000 description 1
238000005189 flocculation Methods 0.000 description 1
230000016615 flocculation Effects 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
230000004927 fusion Effects 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
239000008187 granular material Substances 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
230000002209 hydrophobic effect Effects 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
229920000847 nonoxynol Polymers 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
239000010690 paraffinic oil Substances 0.000 description 1
FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000003209 petroleum derivative Substances 0.000 description 1
238000005191 phase separation Methods 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
229960004265 piperacetazine Drugs 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
XOFYZVNMUHMLCC-ZPOLXVRWSA-N prednisone Chemical compound O=C1C=C[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 XOFYZVNMUHMLCC-ZPOLXVRWSA-N 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
239000013049 sediment Substances 0.000 description 1
238000002791 soaking Methods 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
244000045561 useful plants Species 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene Substances 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
- A01N39/02—Aryloxy-carboxylic acids; Derivatives thereof
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles

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)
Agricultural Chemicals And Associated Chemicals (AREA)
Fluid-Pressure Circuits (AREA)
Fire-Extinguishing Compositions (AREA)

SK4089-91A 1989-06-02 1991-12-27 Liquid herbicidal agent SK408991A3 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE3917959A DE3917959A1 (de)	1989-06-02	1989-06-02	Fluessige herbizide mittel

Publications (1)

Publication Number	Publication Date
SK408991A3 true SK408991A3 (en)	1994-06-08

Family

ID=6381888

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK4089-91A SK408991A3 (en)	1989-06-02	1991-12-27	Liquid herbicidal agent

Country Status (15)

Country	Link
US (1)	US5821198A (fr)
EP (1)	EP0400585B1 (fr)
AT (1)	ATE161390T1 (fr)
AU (1)	AU627582B2 (fr)
CA (1)	CA2018035C (fr)
CZ (1)	CZ408991A3 (fr)
DD (1)	DD298337A5 (fr)
DE (2)	DE3917959A1 (fr)
DK (1)	DK0400585T3 (fr)
ES (1)	ES2112828T3 (fr)
GR (1)	GR3025955T3 (fr)
NZ (1)	NZ233883A (fr)
SK (1)	SK408991A3 (fr)
UA (1)	UA27691C2 (fr)
ZA (1)	ZA904202B (fr)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
ATE142422T1 (de) *	1991-05-18	1996-09-15	Hoechst Schering Agrevo Gmbh	Neue suspoemulsionen auf basis fenoxapropethyl
DE59209086D1 (de) *	1991-09-14	1998-02-05	Hoechst Schering Agrevo Gmbh	Selektive herbizide Mittel in Form konzentrierter Mikroemulsionen
CZ322292A3 (en) *	1991-11-15	1993-07-14	Ciba Geigy Ag	Synergistic gent and method of weed selective control
BR9710053A (pt) *	1996-06-28	1999-08-10	Novartis Ag	Composições pesticidas
DE19633271A1 (de) *	1996-08-19	1998-02-26	Basf Ag	Flüssige Formulierung von Ethyl-(Z)-2-chlor-3-[2-chlor-5-(4,5,6,7-tetrahydro-1,3-dioxoisoindoldion-2-yl)phenyl]acrylat
DE10258867A1 (de) *	2002-12-17	2004-07-08	Bayer Cropscience Gmbh	Mikroemulsionskonzentrate
GB202100123D0 (en) *	2021-01-06	2021-02-17	Upl Corporation Ltd	An emulsifiable concentrate composition

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4188202A (en) *	1975-11-12	1980-02-12	Fisons Limited	Composition
DE3033335A1 (de) *	1980-09-04	1982-04-22	Lentia GmbH Chem. u. pharm. Erzeugnisse - Industriebedarf, 8000 München	Verfahren zur herstellung einer lagerstabilen, konzentrierten emulsion von herbizid wirkenden phenoxyalkancarbonsaeureestern
DE3240694A1 (de) *	1982-11-04	1984-05-10	Hoechst Ag, 6230 Frankfurt	Herbizide mittel
DE3247050A1 (de) *	1982-12-20	1984-06-20	Bayer Ag, 5090 Leverkusen	Herbizide mittel
HU202052B (en) *	1983-02-11	1991-02-28	Hoechst Ag	Aqueous emulsion-based plant protective compositions
DE3304677A1 (de) *	1983-02-11	1984-08-23	Hoechst Ag, 6230 Frankfurt	Feindisperse fluessige pflanzenschutzmittel
DE3415069A1 (de) *	1983-11-19	1985-05-30	Hoechst Ag, 6230 Frankfurt	Herbizide mittel
DE3507380A1 (de) *	1985-03-02	1986-09-04	Henkel KGaA, 4000 Düsseldorf	Verdunstungshemmende mittel
DE3542439A1 (de) *	1985-11-30	1987-06-04	Hoechst Ag	Neue waessrige pflanzenschutzmittel-emulsionen
US4888041A (en) *	1987-05-18	1989-12-19	The Dow Chemical Company	Grain selective herbicides
DE3806294A1 (de) *	1988-02-27	1989-09-07	Hoechst Ag	Herbizide mittel in form von waessrigen mikroemulsionen

1989
- 1989-06-02 DE DE3917959A patent/DE3917959A1/de not_active Withdrawn
1990
- 1990-05-30 EP EP90110202A patent/EP0400585B1/fr not_active Expired - Lifetime
- 1990-05-30 DE DE59010786T patent/DE59010786D1/de not_active Expired - Lifetime
- 1990-05-30 AT AT90110202T patent/ATE161390T1/de not_active IP Right Cessation
- 1990-05-30 ES ES90110202T patent/ES2112828T3/es not_active Expired - Lifetime
- 1990-05-30 DK DK90110202T patent/DK0400585T3/da active
- 1990-05-31 NZ NZ233883A patent/NZ233883A/en unknown
- 1990-05-31 DD DD90341211A patent/DD298337A5/de unknown
- 1990-05-31 AU AU56168/90A patent/AU627582B2/en not_active Expired
- 1990-06-01 UA UA4830412A patent/UA27691C2/uk unknown
- 1990-06-01 CA CA002018035A patent/CA2018035C/fr not_active Expired - Lifetime
- 1990-06-01 ZA ZA904202A patent/ZA904202B/xx unknown
1991
- 1991-12-27 CZ CS914089A patent/CZ408991A3/cs unknown
- 1991-12-27 SK SK4089-91A patent/SK408991A3/sk unknown
1995
- 1995-05-31 US US08/455,664 patent/US5821198A/en not_active Expired - Lifetime
1998
- 1998-01-21 GR GR980400125T patent/GR3025955T3/el unknown

Also Published As

Publication number	Publication date
EP0400585A3 (fr)	1992-09-02
DE3917959A1 (de)	1990-12-06
CA2018035C (fr)	2000-08-29
AU627582B2 (en)	1992-08-27
AU5616890A (en)	1990-12-06
DK0400585T3 (da)	1998-08-31
ZA904202B (en)	1991-03-27
EP0400585A2 (fr)	1990-12-05
EP0400585B1 (fr)	1997-12-29
NZ233883A (en)	1992-07-28
UA27691C2 (uk)	2000-10-16
US5821198A (en)	1998-10-13
CZ408991A3 (en)	1993-10-13
GR3025955T3 (en)	1998-04-30
CA2018035A1 (fr)	1990-12-02
ATE161390T1 (de)	1998-01-15
DD298337A5 (de)	1992-02-20
ES2112828T3 (es)	1998-04-16
DE59010786D1 (de)	1998-02-05

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