GB1564387A - Germicidal herbicide compositions for use in agriculture and horticulture containing active ingredients amides of alkylthioalkylsulphinyl and alkylsulphonyl-acrylic acids - Google Patents
Germicidal herbicide compositions for use in agriculture and horticulture containing active ingredients amides of alkylthioalkylsulphinyl and alkylsulphonyl-acrylic acids Download PDFInfo
- Publication number
- GB1564387A GB1564387A GB23425/77A GB2342577A GB1564387A GB 1564387 A GB1564387 A GB 1564387A GB 23425/77 A GB23425/77 A GB 23425/77A GB 2342577 A GB2342577 A GB 2342577A GB 1564387 A GB1564387 A GB 1564387A
- Authority
- GB
- United Kingdom
- Prior art keywords
- germicidal
- chconh
- herbicide composition
- sch
- formula
- 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
- 239000000203 mixture Substances 0.000 title claims description 25
- 230000002070 germicidal effect Effects 0.000 title claims description 21
- 239000004009 herbicide Substances 0.000 title claims description 19
- 230000002363 herbicidal effect Effects 0.000 title claims description 17
- 239000004480 active ingredient Substances 0.000 title claims description 15
- 238000003898 horticulture Methods 0.000 title claims description 8
- 150000001408 amides Chemical class 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims description 26
- -1 2-sulphoethyl group Chemical group 0.000 claims description 19
- 239000000843 powder Substances 0.000 claims description 8
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 125000000143 2-carboxyethyl group Chemical group [H]OC(=O)C([H])([H])C([H])([H])* 0.000 claims description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 125000005702 oxyalkylene group Chemical group 0.000 claims description 2
- 150000003839 salts Chemical group 0.000 claims description 2
- 241000196324 Embryophyta Species 0.000 description 20
- 230000000694 effects Effects 0.000 description 18
- 230000000855 fungicidal effect Effects 0.000 description 10
- 230000002401 inhibitory effect Effects 0.000 description 8
- 239000011734 sodium Substances 0.000 description 8
- 230000000885 phytotoxic effect Effects 0.000 description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 239000000969 carrier Substances 0.000 description 6
- 231100000208 phytotoxic Toxicity 0.000 description 6
- 239000002689 soil Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 244000025254 Cannabis sativa Species 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- 230000009931 harmful effect Effects 0.000 description 5
- 230000005764 inhibitory process Effects 0.000 description 5
- 238000005507 spraying Methods 0.000 description 4
- 240000001592 Amaranthus caudatus Species 0.000 description 3
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 3
- 244000058871 Echinochloa crus-galli Species 0.000 description 3
- 241000283903 Ovis aries Species 0.000 description 3
- 244000046052 Phaseolus vulgaris Species 0.000 description 3
- 241000219053 Rumex Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 239000003905 agrochemical Substances 0.000 description 3
- 235000013339 cereals Nutrition 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 235000005822 corn Nutrition 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000000417 fungicide Substances 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 239000004563 wettable powder Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 241001450781 Bipolaris oryzae Species 0.000 description 2
- 241000222235 Colletotrichum orbiculare Species 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- 240000004472 Dopatrium junceum Species 0.000 description 2
- 241000634867 Eleocharis uniglumis Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 241000282414 Homo sapiens Species 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 240000000178 Monochoria vaginalis Species 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 241000588702 Pectobacterium carotovorum subsp. carotovorum Species 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- 241000209504 Poaceae Species 0.000 description 2
- 241000341978 Rotala Species 0.000 description 2
- 244000155504 Rotala indica Species 0.000 description 2
- 241001408202 Sagittaria pygmaea Species 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 241000208041 Veronica Species 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
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 239000004495 emulsifiable concentrate Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 238000011081 inoculation Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical compound [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 1
- CZWJCQXZZJHHRH-YCRXJPFRSA-N 2-[(1r,2r,3s,4r,5r,6s)-3-(diaminomethylideneamino)-4-[(2r,3r,4r,5s)-3-[(2s,3s,4s,5r,6s)-4,5-dihydroxy-6-(hydroxymethyl)-3-(methylamino)oxan-2-yl]oxy-4-hydroxy-4-(hydroxymethyl)-5-methyloxolan-2-yl]oxy-2,5,6-trihydroxycyclohexyl]guanidine;sulfuric acid Chemical compound OS(O)(=O)=O.OS(O)(=O)=O.OS(O)(=O)=O.CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](CO)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](N=C(N)N)[C@H](O)[C@@H](N=C(N)N)[C@H](O)[C@H]1O.CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](CO)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](N=C(N)N)[C@H](O)[C@@H](N=C(N)N)[C@H](O)[C@H]1O CZWJCQXZZJHHRH-YCRXJPFRSA-N 0.000 description 1
- YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 description 1
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 244000036890 Amaranthus blitum Species 0.000 description 1
- 235000010149 Brassica rapa subsp chinensis Nutrition 0.000 description 1
- 235000000536 Brassica rapa subsp pekinensis Nutrition 0.000 description 1
- 241000499436 Brassica rapa subsp. pekinensis Species 0.000 description 1
- 240000006122 Chenopodium album Species 0.000 description 1
- 235000011498 Chenopodium album var missouriense Nutrition 0.000 description 1
- 235000013328 Chenopodium album var. album Nutrition 0.000 description 1
- 235000014052 Chenopodium album var. microphyllum Nutrition 0.000 description 1
- 235000014050 Chenopodium album var. stevensii Nutrition 0.000 description 1
- 235000013012 Chenopodium album var. striatum Nutrition 0.000 description 1
- 101150065749 Churc1 gene Proteins 0.000 description 1
- 240000008067 Cucumis sativus Species 0.000 description 1
- 235000009849 Cucumis sativus Nutrition 0.000 description 1
- 241000817048 Cyperus microiria Species 0.000 description 1
- 244000075634 Cyperus rotundus Species 0.000 description 1
- 240000003176 Digitaria ciliaris Species 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 239000004129 EU approved improving agent Substances 0.000 description 1
- 241000759118 Eleocharis kuroguwai Species 0.000 description 1
- 244000025670 Eleusine indica Species 0.000 description 1
- 235000014716 Eleusine indica Nutrition 0.000 description 1
- 235000014820 Galium aparine Nutrition 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 240000005178 Oxalis martiana Species 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- 241000205407 Polygonum Species 0.000 description 1
- 244000234609 Portulaca oleracea Species 0.000 description 1
- 235000001855 Portulaca oleracea Nutrition 0.000 description 1
- 102100038239 Protein Churchill Human genes 0.000 description 1
- 244000189123 Rumex japonicus Species 0.000 description 1
- 235000005247 Rumex japonicus Nutrition 0.000 description 1
- 241000759139 Schoenoplectiella hotarui Species 0.000 description 1
- 240000003461 Setaria viridis Species 0.000 description 1
- 235000002248 Setaria viridis Nutrition 0.000 description 1
- 235000010086 Setaria viridis var. viridis Nutrition 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 239000004280 Sodium formate Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 229940064004 antiseptic throat preparations Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229960001162 dihydrostreptomycin sulfate Drugs 0.000 description 1
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- AWZOLILCOUMRDG-UHFFFAOYSA-N edifenphos Chemical compound C=1C=CC=CC=1SP(=O)(OCC)SC1=CC=CC=C1 AWZOLILCOUMRDG-UHFFFAOYSA-N 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000002917 insecticide Substances 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
- 150000002576 ketones Chemical class 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- UORVCLMRJXCDCP-UHFFFAOYSA-N propynoic acid Chemical compound OC(=O)C#C UORVCLMRJXCDCP-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts 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
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 244000082735 tidal marsh flat sedge Species 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D33/00—Details of, or accessories for, sacks or bags
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7719676A JPS533523A (en) | 1976-06-30 | 1976-06-30 | Agri-horticultural fungicide |
| JP7719576A JPS533522A (en) | 1976-06-30 | 1976-06-30 | Herbicide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1564387A true GB1564387A (en) | 1980-04-10 |
Family
ID=26418305
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB23425/77A Expired GB1564387A (en) | 1976-06-30 | 1977-06-02 | Germicidal herbicide compositions for use in agriculture and horticulture containing active ingredients amides of alkylthioalkylsulphinyl and alkylsulphonyl-acrylic acids |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US4115103A (enExample) |
| CH (1) | CH604498A5 (enExample) |
| DE (1) | DE2729672C2 (enExample) |
| FR (1) | FR2356369A1 (enExample) |
| GB (1) | GB1564387A (enExample) |
| NL (1) | NL180165C (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5300672A (en) * | 1990-01-05 | 1994-04-05 | Rohm And Haas Company | S-substituted carbonyl substituted beta-thioacrylamide biocides and fungicides |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4429333A (en) | 1982-03-08 | 1984-01-31 | The Mead Corporation | Document scanning system |
| US5151447A (en) * | 1989-07-28 | 1992-09-29 | Rohm And Haas Company | S-substituted beta-thioacrylamide biocides and fungicides |
| US5302592A (en) * | 1990-08-17 | 1994-04-12 | Rohm And Haas Company | Use of substituted 3-thioacryloyl compounds as antimicrobial agents |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2634262A (en) * | 1950-10-19 | 1953-04-07 | Bayer Ag | Pyrazolone monoazo dyestuffs |
| NL106983C (enExample) * | 1957-05-24 | |||
| US3227542A (en) * | 1962-04-18 | 1966-01-04 | Union Carbide Corp | Method for controlling plant growth |
| GB1170269A (en) * | 1965-12-27 | 1969-11-12 | Sanitized Inc | Method of Producing Unsaturated Sulfones. |
| GB1182151A (en) * | 1966-04-28 | 1970-02-25 | Sanitized Inc | Bioactive Sulfones |
| IL31647A (en) * | 1968-03-25 | 1972-09-28 | Bayer Ag | Beta-alkoxyacrylic acid amides,their preparation and use for combating pests |
| FR2201035B1 (enExample) * | 1972-09-26 | 1980-04-25 | Roussel Uclaf | |
| CH569410A5 (en) * | 1973-08-02 | 1975-11-28 | Ciba Geigy Ag | 1-Chloro-2-alkyl sulphonyl or sulphinyl acrylic amides - microbiocides prepd. from a dichloro acrylic amide and a thiol |
| JPS5082372A (enExample) * | 1973-11-27 | 1975-07-03 | ||
| JPS5426947B2 (enExample) * | 1973-11-30 | 1979-09-06 | ||
| JPS5084944A (enExample) * | 1973-11-30 | 1975-07-09 | ||
| GB1528853A (en) * | 1975-07-04 | 1978-10-18 | Kao Corp | Betathio acrylic acid compounds and process of preparing same |
| GB1557225A (en) * | 1975-07-10 | 1979-12-05 | Kao Corp | Sulphinyl compounds and processes ofr preparing same |
| JPS5234923A (en) * | 1975-09-11 | 1977-03-17 | Kao Corp | Novel antimicrobial agents for non-medical use |
-
1977
- 1977-06-02 GB GB23425/77A patent/GB1564387A/en not_active Expired
- 1977-06-16 US US05/807,148 patent/US4115103A/en not_active Expired - Lifetime
- 1977-06-17 NL NLAANVRAGE7706686,A patent/NL180165C/xx not_active IP Right Cessation
- 1977-06-20 FR FR7718864A patent/FR2356369A1/fr active Granted
- 1977-06-28 CH CH794977A patent/CH604498A5/xx not_active IP Right Cessation
- 1977-06-30 DE DE2729672A patent/DE2729672C2/de not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5300672A (en) * | 1990-01-05 | 1994-04-05 | Rohm And Haas Company | S-substituted carbonyl substituted beta-thioacrylamide biocides and fungicides |
Also Published As
| Publication number | Publication date |
|---|---|
| NL180165B (nl) | 1986-08-18 |
| DE2729672C2 (de) | 1987-03-05 |
| NL180165C (nl) | 1987-01-16 |
| US4115103A (en) | 1978-09-19 |
| CH604498A5 (enExample) | 1978-09-15 |
| FR2356369A1 (fr) | 1978-01-27 |
| FR2356369B1 (enExample) | 1983-12-16 |
| NL7706686A (nl) | 1978-01-03 |
| DE2729672A1 (de) | 1978-01-12 |
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