GB1571904A - Use of n-arylsulphonyl carbamates as herbicide antidotes - Google Patents
Use of n-arylsulphonyl carbamates as herbicide antidotes Download PDFInfo
- Publication number
- GB1571904A GB1571904A GB40797/76A GB4079776A GB1571904A GB 1571904 A GB1571904 A GB 1571904A GB 40797/76 A GB40797/76 A GB 40797/76A GB 4079776 A GB4079776 A GB 4079776A GB 1571904 A GB1571904 A GB 1571904A
- Authority
- GB
- United Kingdom
- Prior art keywords
- vernam
- herbicide
- ppi
- crop
- soil
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 239000003815 herbicide antidote Substances 0.000 title description 7
- 239000004009 herbicide Substances 0.000 claims abstract description 117
- 150000001875 compounds Chemical class 0.000 claims abstract description 98
- 239000000729 antidote Substances 0.000 claims abstract description 64
- 229940075522 antidotes Drugs 0.000 claims abstract description 8
- 230000002363 herbicidal effect Effects 0.000 claims description 107
- 239000002689 soil Substances 0.000 claims description 61
- 241000196324 Embryophyta Species 0.000 claims description 49
- 238000000034 method Methods 0.000 claims description 44
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 37
- 230000006378 damage Effects 0.000 claims description 35
- 208000027418 Wounds and injury Diseases 0.000 claims description 34
- 208000014674 injury Diseases 0.000 claims description 34
- GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 claims description 29
- 239000000203 mixture Substances 0.000 claims description 29
- -1 chloro, bromo, methoxy Chemical group 0.000 claims description 28
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 19
- 244000068988 Glycine max Species 0.000 claims description 18
- 235000010469 Glycine max Nutrition 0.000 claims description 17
- 239000011550 stock solution Substances 0.000 claims description 17
- 231100001184 nonphytotoxic Toxicity 0.000 claims description 16
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
- 125000003342 alkenyl group Chemical group 0.000 claims description 13
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 12
- 238000012360 testing method Methods 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 244000046052 Phaseolus vulgaris Species 0.000 claims description 10
- 230000003247 decreasing effect Effects 0.000 claims description 9
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 9
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 8
- 240000004713 Pisum sativum Species 0.000 claims description 8
- 235000010582 Pisum sativum Nutrition 0.000 claims description 8
- 125000000304 alkynyl group Chemical group 0.000 claims description 7
- 125000001246 bromo group Chemical group Br* 0.000 claims description 7
- 235000015225 Panicum colonum Nutrition 0.000 claims description 6
- 240000001592 Amaranthus caudatus Species 0.000 claims description 5
- 235000009328 Amaranthus caudatus Nutrition 0.000 claims description 5
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 5
- 235000021374 legumes Nutrition 0.000 claims description 5
- 235000010627 Phaseolus vulgaris Nutrition 0.000 claims description 4
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 235000021332 kidney beans Nutrition 0.000 claims description 4
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 claims description 3
- 125000005080 alkoxycarbonylalkenyl group Chemical group 0.000 claims description 3
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims description 3
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims description 3
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
- 244000105624 Arachis hypogaea Species 0.000 claims description 2
- 240000004658 Medicago sativa Species 0.000 claims description 2
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 claims description 2
- 108010091834 NBR-B isoenzyme Proteins 0.000 claims description 2
- 241000219793 Trifolium Species 0.000 claims description 2
- 125000005093 alkyl carbonyl alkyl group Chemical group 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 244000013123 dwarf bean Species 0.000 claims description 2
- 235000021278 navy bean Nutrition 0.000 claims description 2
- 235000020232 peanut Nutrition 0.000 claims description 2
- 238000009331 sowing Methods 0.000 claims description 2
- 238000012956 testing procedure Methods 0.000 claims 6
- QGHDLJAZIIFENW-UHFFFAOYSA-N 4-[1,1,1,3,3,3-hexafluoro-2-(4-hydroxy-3-prop-2-enylphenyl)propan-2-yl]-2-prop-2-enylphenol Chemical group C1=C(CC=C)C(O)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(O)C(CC=C)=C1 QGHDLJAZIIFENW-UHFFFAOYSA-N 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- 244000236458 Panicum colonum Species 0.000 claims 1
- 244000038559 crop plants Species 0.000 abstract description 5
- GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 abstract description 2
- 230000008654 plant damage Effects 0.000 abstract 1
- OKUGPJPKMAEJOE-UHFFFAOYSA-N S-propyl dipropylcarbamothioate Chemical compound CCCSC(=O)N(CCC)CCC OKUGPJPKMAEJOE-UHFFFAOYSA-N 0.000 description 265
- 101100084053 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) ppi-2 gene Proteins 0.000 description 76
- DEDOPGXGGQYYMW-UHFFFAOYSA-N molinate Chemical compound CCSC(=O)N1CCCCCC1 DEDOPGXGGQYYMW-UHFFFAOYSA-N 0.000 description 73
- BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 description 20
- 238000010348 incorporation Methods 0.000 description 14
- 239000007787 solid Substances 0.000 description 13
- 101100244014 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) ppi-5 gene Proteins 0.000 description 11
- 238000011282 treatment Methods 0.000 description 11
- 230000000694 effects Effects 0.000 description 10
- 244000058871 Echinochloa crus-galli Species 0.000 description 8
- 241000894007 species Species 0.000 description 8
- 101100084040 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) ppi-1 gene Proteins 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- RMRFFCXPLWYOOY-UHFFFAOYSA-N allyl radical Chemical compound [CH2]C=C RMRFFCXPLWYOOY-UHFFFAOYSA-N 0.000 description 5
- 229910014585 C2-Ce Inorganic materials 0.000 description 4
- 125000006519 CCH3 Chemical group 0.000 description 4
- 240000003461 Setaria viridis Species 0.000 description 4
- 235000002248 Setaria viridis Nutrition 0.000 description 4
- 230000009286 beneficial effect Effects 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 3
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 3
- 235000011999 Panicum crusgalli Nutrition 0.000 description 3
- 240000006394 Sorghum bicolor Species 0.000 description 3
- 230000003042 antagnostic effect Effects 0.000 description 3
- 230000001276 controlling effect Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 230000008635 plant growth Effects 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000004576 sand Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 235000007320 Avena fatua Nutrition 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- 244000299507 Gossypium hirsutum Species 0.000 description 2
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- 231100000674 Phytotoxicity Toxicity 0.000 description 2
- 229920001213 Polysorbate 20 Polymers 0.000 description 2
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 2
- 101100054666 Streptomyces halstedii sch3 gene Proteins 0.000 description 2
- 244000098338 Triticum aestivum Species 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- OCBFFGCSTGGPSQ-UHFFFAOYSA-N [CH2]CC Chemical compound [CH2]CC OCBFFGCSTGGPSQ-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- WBLIXGSTEMXDSM-UHFFFAOYSA-N chloromethane Chemical compound Cl[CH2] WBLIXGSTEMXDSM-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000012010 growth Effects 0.000 description 2
- 208000037824 growth disorder Diseases 0.000 description 2
- 230000000266 injurious effect Effects 0.000 description 2
- UJYAZVSPFMJCLW-UHFFFAOYSA-N n-(oxomethylidene)benzenesulfonamide Chemical class O=C=NS(=O)(=O)C1=CC=CC=C1 UJYAZVSPFMJCLW-UHFFFAOYSA-N 0.000 description 2
- 230000000885 phytotoxic effect Effects 0.000 description 2
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 2
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003918 triazines Chemical class 0.000 description 2
- AOSZTAHDEDLTLQ-AZKQZHLXSA-N (1S,2S,4R,8S,9S,11S,12R,13S,19S)-6-[(3-chlorophenyl)methyl]-12,19-difluoro-11-hydroxy-8-(2-hydroxyacetyl)-9,13-dimethyl-6-azapentacyclo[10.8.0.02,9.04,8.013,18]icosa-14,17-dien-16-one Chemical compound C([C@@H]1C[C@H]2[C@H]3[C@]([C@]4(C=CC(=O)C=C4[C@@H](F)C3)C)(F)[C@@H](O)C[C@@]2([C@@]1(C1)C(=O)CO)C)N1CC1=CC=CC(Cl)=C1 AOSZTAHDEDLTLQ-AZKQZHLXSA-N 0.000 description 1
- UUFQTNFCRMXOAE-UHFFFAOYSA-N 1-methylmethylene Chemical compound C[CH] UUFQTNFCRMXOAE-UHFFFAOYSA-N 0.000 description 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 1
- LJXPWUAAAAXJBX-UHFFFAOYSA-N 2-methylallyl radical Chemical compound [CH2]C(C)=C LJXPWUAAAAXJBX-UHFFFAOYSA-N 0.000 description 1
- OOHIAOSLOGDBCE-UHFFFAOYSA-N 6-chloro-4-n-cyclopropyl-2-n-propan-2-yl-1,3,5-triazine-2,4-diamine Chemical compound CC(C)NC1=NC(Cl)=NC(NC2CC2)=N1 OOHIAOSLOGDBCE-UHFFFAOYSA-N 0.000 description 1
- 241000209764 Avena fatua Species 0.000 description 1
- 244000075850 Avena orientalis Species 0.000 description 1
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical class NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 description 1
- 101100167062 Caenorhabditis elegans chch-3 gene Proteins 0.000 description 1
- 229940126657 Compound 17 Drugs 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 235000009432 Gossypium hirsutum Nutrition 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- 238000005481 NMR spectroscopy Methods 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
- 235000010086 Setaria viridis var. viridis Nutrition 0.000 description 1
- 235000007230 Sorghum bicolor Nutrition 0.000 description 1
- 235000015505 Sorghum bicolor subsp. bicolor Nutrition 0.000 description 1
- 244000062793 Sorghum vulgare Species 0.000 description 1
- 235000006923 Sorghum x drummondii Nutrition 0.000 description 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical class O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 235000005373 Uvularia sessilifolia Nutrition 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 150000008061 acetanilides Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- 230000002605 anti-dotal effect Effects 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical class OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 230000035613 defoliation Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000003054 hormonal effect Effects 0.000 description 1
- 150000002443 hydroxylamines Chemical class 0.000 description 1
- UWNADWZGEHDQAB-UHFFFAOYSA-N i-Pr2C2H4i-Pr2 Natural products CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 description 1
- 230000002147 killing effect Effects 0.000 description 1
- 230000036244 malformation Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000000051 modifying effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/04—1,3-Dioxanes; Hydrogenated 1,3-dioxanes
- C07D319/06—1,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3808—Acyclic saturated acids which can have further substituents on alkyl
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US61911475A | 1975-10-02 | 1975-10-02 | |
| US05/721,721 US4230874A (en) | 1976-09-13 | 1976-09-13 | N-(Benzenesulfonyl) carbamates-herbicidal antidotes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1571904A true GB1571904A (en) | 1980-07-23 |
Family
ID=27088427
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB40797/76A Expired GB1571904A (en) | 1975-10-02 | 1976-10-01 | Use of n-arylsulphonyl carbamates as herbicide antidotes |
| GB21016/79A Expired GB1571905A (en) | 1975-10-02 | 1976-10-01 | N-arylsulphonyl carbamates |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB21016/79A Expired GB1571905A (en) | 1975-10-02 | 1976-10-01 | N-arylsulphonyl carbamates |
Country Status (24)
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2690918B1 (fr) * | 1992-05-06 | 2001-12-28 | Poudres & Explosifs Ste Nale | Utilisation d'un arylsulfonyluréthanne comme résine garnissante dans les vernis à ongles nitrocellulosiques. Nouveaux arylsulfonyluréthannes et nouveaux vernis à ongles nitrocellulosiques. |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3799760A (en) * | 1966-05-03 | 1974-03-26 | Monsanto Co | Method for inhibiting plant growth |
-
1976
- 1976-09-30 PT PT65663A patent/PT65663B/pt unknown
- 1976-10-01 NZ NZ182204A patent/NZ182204A/xx unknown
- 1976-10-01 HU HU76SA2981A patent/HU179643B/hu unknown
- 1976-10-01 FR FR7629553A patent/FR2326414A1/fr active Granted
- 1976-10-01 DK DK442876A patent/DK442876A/da not_active Application Discontinuation
- 1976-10-01 GR GR51819A patent/GR65992B/el unknown
- 1976-10-01 CA CA262,510A patent/CA1097649A/en not_active Expired
- 1976-10-01 IT IT51532/76A patent/IT1073910B/it active
- 1976-10-01 GB GB40797/76A patent/GB1571904A/en not_active Expired
- 1976-10-01 NL NL7610893A patent/NL7610893A/xx not_active Application Discontinuation
- 1976-10-01 TR TR19020A patent/TR19020A/xx unknown
- 1976-10-01 IL IL50595A patent/IL50595A/xx unknown
- 1976-10-01 AU AU18328/76A patent/AU509009B2/en not_active Ceased
- 1976-10-01 YU YU02418/76A patent/YU241876A/xx unknown
- 1976-10-01 GB GB21016/79A patent/GB1571905A/en not_active Expired
- 1976-10-01 DE DE19762644504 patent/DE2644504A1/de not_active Withdrawn
- 1976-10-02 JP JP51118906A patent/JPS5919533B2/ja not_active Expired
- 1976-10-02 DD DD195122A patent/DD127619A5/xx unknown
- 1976-10-02 RO RO7687889A patent/RO72913A/ro unknown
- 1976-10-04 MX MX764953U patent/MX5392E/es unknown
- 1976-10-04 CH CH1253676A patent/CH629081A5/de not_active IP Right Cessation
- 1976-10-04 BR BR7606642A patent/BR7606642A/pt unknown
- 1976-10-04 AR AR264968A patent/AR217244A1/es active
- 1976-10-04 IN IN1813/CAL/76A patent/IN145026B/en unknown
- 1976-10-09 ES ES452285A patent/ES452285A1/es not_active Expired
-
1982
- 1982-04-15 YU YU01306/82A patent/YU130682A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| RO72913A (ro) | 1981-09-24 |
| BR7606642A (pt) | 1977-11-16 |
| HU179643B (en) | 1982-11-29 |
| DK442876A (da) | 1977-04-03 |
| CH629081A5 (en) | 1982-04-15 |
| JPS5265247A (en) | 1977-05-30 |
| AU1832876A (en) | 1978-04-06 |
| IN145026B (US07655688-20100202-C00548.png) | 1978-08-12 |
| GB1571905A (en) | 1980-07-23 |
| MX5392E (es) | 1983-07-08 |
| IL50595A (en) | 1981-07-31 |
| PT65663B (fr) | 1978-04-11 |
| PT65663A (fr) | 1976-10-01 |
| AU509009B2 (en) | 1980-04-17 |
| DD127619A5 (US07655688-20100202-C00548.png) | 1977-10-05 |
| YU241876A (en) | 1983-02-28 |
| IL50595A0 (en) | 1976-12-31 |
| CA1097649A (en) | 1981-03-17 |
| ES452285A1 (es) | 1978-03-01 |
| DE2644504A1 (de) | 1977-06-02 |
| AR217244A1 (es) | 1980-03-14 |
| NZ182204A (en) | 1979-07-11 |
| FR2326414A1 (fr) | 1977-04-29 |
| FR2326414B1 (US07655688-20100202-C00548.png) | 1981-05-22 |
| IT1073910B (it) | 1985-04-17 |
| NL7610893A (nl) | 1977-04-05 |
| TR19020A (tr) | 1978-02-27 |
| YU130682A (en) | 1983-01-21 |
| GR65992B (US07655688-20100202-C00548.png) | 1981-01-13 |
| JPS5919533B2 (ja) | 1984-05-07 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |