IL45060A - Herbicidal compositions containing a dinitroaniline derivative and a carbamate thiolcarbamate or dithiocarbamate and/or a pyridazone derivative - Google Patents
Herbicidal compositions containing a dinitroaniline derivative and a carbamate thiolcarbamate or dithiocarbamate and/or a pyridazone derivativeInfo
- Publication number
- IL45060A IL45060A IL45060A IL4506074A IL45060A IL 45060 A IL45060 A IL 45060A IL 45060 A IL45060 A IL 45060A IL 4506074 A IL4506074 A IL 4506074A IL 45060 A IL45060 A IL 45060A
- Authority
- IL
- Israel
- Prior art keywords
- spp
- per hectare
- substituted
- halogen
- dinitro
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 28
- 230000002363 herbicidal effect Effects 0.000 title claims description 11
- 239000012990 dithiocarbamate Substances 0.000 title description 2
- WLRLSNCGSKQYFH-UHFFFAOYSA-N carbamic acid thiophen-2-ylcarbamic acid Chemical compound S1C(=CC=C1)NC(=O)O.C(N)(O)=O WLRLSNCGSKQYFH-UHFFFAOYSA-N 0.000 title 1
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 title 1
- LZGUHMNOBNWABZ-UHFFFAOYSA-N n-nitro-n-phenylnitramide Chemical class [O-][N+](=O)N([N+]([O-])=O)C1=CC=CC=C1 LZGUHMNOBNWABZ-UHFFFAOYSA-N 0.000 title 1
- 229910052736 halogen Inorganic materials 0.000 claims description 26
- 125000005843 halogen group Chemical group 0.000 claims description 26
- 125000000217 alkyl group Chemical group 0.000 claims description 20
- -1 tetrahydrofurfuryl Chemical group 0.000 claims description 20
- 125000003545 alkoxy group Chemical group 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 14
- 125000003342 alkenyl group Chemical group 0.000 claims description 8
- 125000000304 alkynyl group Chemical group 0.000 claims description 8
- 125000001188 haloalkyl group Chemical group 0.000 claims description 6
- 239000004009 herbicide Substances 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 239000011593 sulfur Substances 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 150000001602 bicycloalkyls Chemical group 0.000 claims description 2
- 125000001246 bromo group Chemical group Br* 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 2
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 1
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- 235000002634 Solanum Nutrition 0.000 description 1
- 241000207763 Solanum Species 0.000 description 1
- 241000488874 Sonchus Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- 244000062793 Sorghum vulgare Species 0.000 description 1
- 241000960310 Spergula Species 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 235000012308 Tagetes Nutrition 0.000 description 1
- 241000736851 Tagetes Species 0.000 description 1
- 241000245665 Taraxacum Species 0.000 description 1
- 241000722118 Thlaspi Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 241000819233 Tribulus <sea snail> Species 0.000 description 1
- 241000249864 Tussilago Species 0.000 description 1
- 241000145124 Uniola Species 0.000 description 1
- 239000005659 Urtica spp. Substances 0.000 description 1
- 241000218215 Urticaceae Species 0.000 description 1
- 240000005592 Veronica officinalis Species 0.000 description 1
- 241000219873 Vicia Species 0.000 description 1
- 241000405217 Viola <butterfly> Species 0.000 description 1
- 241001106476 Violaceae Species 0.000 description 1
- 241001506766 Xanthium Species 0.000 description 1
- 241000159213 Zygophyllaceae Species 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 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
- 239000013011 aqueous formulation Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 244000030166 artemisia Species 0.000 description 1
- 235000009052 artemisia Nutrition 0.000 description 1
- 210000000081 body of the sternum Anatomy 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical class OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 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 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N heptadecan-1-ol Chemical class CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical class CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- SLFVYFOEHHLHDW-UHFFFAOYSA-N n-(trifluoromethyl)aniline Chemical compound FC(F)(F)NC1=CC=CC=C1 SLFVYFOEHHLHDW-UHFFFAOYSA-N 0.000 description 1
- HLLYDGVOMRCOFR-UHFFFAOYSA-N n-butyl-n-ethyl-2,6-dinitro-4-(trifluoromethyl)aniline;2,6-dinitro-n,n-dipropyl-4-(trifluoromethyl)aniline Chemical compound CCCCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O.CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O HLLYDGVOMRCOFR-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 229960003903 oxygen Drugs 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical class CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 229940047183 tribulus Drugs 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
- G03H1/00—Holographic processes or apparatus using light, infrared or ultraviolet waves for obtaining holograms or for obtaining an image from them; Details peculiar thereto
- G03H1/04—Processes or apparatus for producing holograms
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19732334563 DE2334563A1 (de) | 1973-07-07 | 1973-07-07 | Herbizid |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL45060A0 IL45060A0 (en) | 1974-09-10 |
| IL45060A true IL45060A (en) | 1977-10-31 |
Family
ID=5886189
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL45060A IL45060A (en) | 1973-07-07 | 1974-06-18 | Herbicidal compositions containing a dinitroaniline derivative and a carbamate thiolcarbamate or dithiocarbamate and/or a pyridazone derivative |
Country Status (24)
| Country | Link |
|---|---|
| JP (1) | JPS5036636A (de) |
| AR (1) | AR217032A1 (de) |
| BE (1) | BE817305A (de) |
| BG (2) | BG25636A3 (de) |
| BR (1) | BR7405534D0 (de) |
| CH (1) | CH585005A5 (de) |
| CS (1) | CS189658B2 (de) |
| DD (1) | DD111778A5 (de) |
| DE (1) | DE2334563A1 (de) |
| DK (1) | DK137742C (de) |
| ES (1) | ES428035A1 (de) |
| FR (1) | FR2235645B1 (de) |
| GB (1) | GB1471772A (de) |
| HU (1) | HU169820B (de) |
| IL (1) | IL45060A (de) |
| IT (1) | IT1049296B (de) |
| LU (1) | LU70472A1 (de) |
| NL (1) | NL7409071A (de) |
| NO (1) | NO742394L (de) |
| PL (1) | PL94007B1 (de) |
| RO (1) | RO69333A (de) |
| SE (1) | SE7408882L (de) |
| SU (1) | SU579844A3 (de) |
| ZA (1) | ZA744217B (de) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5520919A (en) * | 1978-07-31 | 1980-02-14 | Nihon Radiator Co | Parts connecting method to aluminium pipe |
| DE2909158A1 (de) * | 1979-03-08 | 1980-09-11 | Basf Ag | Herbizide mischungen |
| PT82293B (en) * | 1985-04-08 | 1988-01-11 | Stauffer Chemical Co | Process for the preparation of synergetic herbicide compositions containing a tiolcarbamate and a by product with benzene |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3449111A (en) * | 1966-12-08 | 1969-06-10 | Lilly Co Eli | Method of eliminating weeds |
| US3518076A (en) * | 1967-05-17 | 1970-06-30 | Lilly Co Eli | Method of fliminating weed species with herbicidal combination |
-
1973
- 1973-07-07 DE DE19732334563 patent/DE2334563A1/de not_active Withdrawn
-
1974
- 1974-06-17 BG BG028827A patent/BG25636A3/xx unknown
- 1974-06-17 AR AR254225A patent/AR217032A1/es active
- 1974-06-17 BG BG26996A patent/BG22056A3/xx unknown
- 1974-06-18 IL IL45060A patent/IL45060A/en unknown
- 1974-06-25 JP JP49071970A patent/JPS5036636A/ja active Pending
- 1974-06-28 RO RO7479338A patent/RO69333A/ro unknown
- 1974-07-01 ZA ZA00744217A patent/ZA744217B/xx unknown
- 1974-07-01 NO NO742394A patent/NO742394L/no unknown
- 1974-07-04 FR FR7423307A patent/FR2235645B1/fr not_active Expired
- 1974-07-04 NL NL7409071A patent/NL7409071A/xx not_active Application Discontinuation
- 1974-07-04 BR BR5534/74A patent/BR7405534D0/pt unknown
- 1974-07-05 CS CS744807A patent/CS189658B2/cs unknown
- 1974-07-05 DD DD179738A patent/DD111778A5/xx unknown
- 1974-07-05 SU SU7402042434A patent/SU579844A3/ru active
- 1974-07-05 SE SE7408882A patent/SE7408882L/xx unknown
- 1974-07-05 HU HUBA3109A patent/HU169820B/hu unknown
- 1974-07-05 DK DK361174A patent/DK137742C/da not_active IP Right Cessation
- 1974-07-05 IT IT51942/74A patent/IT1049296B/it active
- 1974-07-05 CH CH926774A patent/CH585005A5/xx not_active IP Right Cessation
- 1974-07-05 BE BE146264A patent/BE817305A/xx unknown
- 1974-07-05 PL PL1974172460A patent/PL94007B1/pl unknown
- 1974-07-05 GB GB2987074A patent/GB1471772A/en not_active Expired
- 1974-07-05 LU LU70472A patent/LU70472A1/xx unknown
- 1974-07-06 ES ES428035A patent/ES428035A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| IL45060A0 (en) | 1974-09-10 |
| NO742394L (de) | 1975-02-03 |
| FR2235645B1 (de) | 1978-07-07 |
| ES428035A1 (es) | 1977-02-01 |
| AR217032A1 (es) | 1980-02-29 |
| NL7409071A (nl) | 1975-01-09 |
| DK361174A (de) | 1975-02-24 |
| GB1471772A (en) | 1977-04-27 |
| BR7405534D0 (pt) | 1975-05-06 |
| RO69333A (ro) | 1980-06-15 |
| PL94007B1 (de) | 1977-07-30 |
| JPS5036636A (de) | 1975-04-05 |
| BG22056A3 (de) | 1976-11-25 |
| DK137742C (da) | 1978-10-09 |
| ZA744217B (en) | 1975-08-27 |
| SE7408882L (de) | 1975-01-08 |
| BG25636A3 (bg) | 1978-11-10 |
| FR2235645A1 (de) | 1975-01-31 |
| BE817305A (fr) | 1975-01-06 |
| CS189658B2 (en) | 1979-04-30 |
| CH585005A5 (de) | 1977-02-28 |
| AU7028774A (en) | 1976-01-08 |
| DK137742B (da) | 1978-05-01 |
| IT1049296B (it) | 1981-01-20 |
| DD111778A5 (de) | 1975-03-12 |
| SU579844A3 (ru) | 1977-11-05 |
| DE2334563A1 (de) | 1975-01-30 |
| LU70472A1 (de) | 1974-11-28 |
| HU169820B (de) | 1977-02-28 |
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