DD262791A5 - Herbizides mittel auf der basis eines herbizids vom typ glyphosat und eines herbizides vom typ phenoxybenzoesaeure und dessen verwendung - Google Patents
Herbizides mittel auf der basis eines herbizids vom typ glyphosat und eines herbizides vom typ phenoxybenzoesaeure und dessen verwendung Download PDFInfo
- Publication number
- DD262791A5 DD262791A5 DD30861587A DD30861587A DD262791A5 DD 262791 A5 DD262791 A5 DD 262791A5 DD 30861587 A DD30861587 A DD 30861587A DD 30861587 A DD30861587 A DD 30861587A DD 262791 A5 DD262791 A5 DD 262791A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- herbicide
- group
- glyphosate
- groups
- lower alkyl
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 52
- 239000004009 herbicide Substances 0.000 title claims abstract description 49
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- 239000005562 Glyphosate Substances 0.000 title claims abstract description 38
- 229940097068 glyphosate Drugs 0.000 title claims abstract description 38
- 239000002253 acid Substances 0.000 title description 8
- 239000000203 mixture Substances 0.000 claims abstract description 33
- PKRSYEPBQPFNRB-UHFFFAOYSA-N 2-phenoxybenzoic acid Chemical compound OC(=O)C1=CC=CC=C1OC1=CC=CC=C1 PKRSYEPBQPFNRB-UHFFFAOYSA-N 0.000 claims abstract description 13
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- 239000011734 sodium Substances 0.000 claims abstract description 9
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- GNOGEOVZOOFKIA-UHFFFAOYSA-N ethyl(dimethyl)sulfanium Chemical compound CC[S+](C)C GNOGEOVZOOFKIA-UHFFFAOYSA-N 0.000 description 1
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- ZEKANFGSDXODPD-UHFFFAOYSA-N glyphosate-isopropylammonium Chemical compound CC(C)N.OC(=O)CNCP(O)(O)=O ZEKANFGSDXODPD-UHFFFAOYSA-N 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
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- 150000002576 ketones Chemical class 0.000 description 1
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- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- SRLHDBRENZFCIN-UHFFFAOYSA-N n,n-di(butan-2-yl)butan-2-amine Chemical compound CCC(C)N(C(C)CC)C(C)CC SRLHDBRENZFCIN-UHFFFAOYSA-N 0.000 description 1
- OOHAUGDGCWURIT-UHFFFAOYSA-N n,n-dipentylpentan-1-amine Chemical compound CCCCCN(CCCCC)CCCCC OOHAUGDGCWURIT-UHFFFAOYSA-N 0.000 description 1
- QHCCDDQKNUYGNC-UHFFFAOYSA-N n-ethylbutan-1-amine Chemical compound CCCCNCC QHCCDDQKNUYGNC-UHFFFAOYSA-N 0.000 description 1
- IUZZLNVABCISOI-UHFFFAOYSA-N n-ethylheptan-1-amine Chemical compound CCCCCCCNCC IUZZLNVABCISOI-UHFFFAOYSA-N 0.000 description 1
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- NJWMENBYMFZACG-UHFFFAOYSA-N n-heptylheptan-1-amine Chemical compound CCCCCCCNCCCCCCC NJWMENBYMFZACG-UHFFFAOYSA-N 0.000 description 1
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- SZEGKVHRCLBFKJ-UHFFFAOYSA-N n-methyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCNC SZEGKVHRCLBFKJ-UHFFFAOYSA-N 0.000 description 1
- CNCBAEHAEKNSPZ-UHFFFAOYSA-N n-methylpentadecan-1-amine Chemical compound CCCCCCCCCCCCCCCNC CNCBAEHAEKNSPZ-UHFFFAOYSA-N 0.000 description 1
- JACMPVXHEARCBO-UHFFFAOYSA-N n-pentylpentan-1-amine Chemical compound CCCCCNCCCCC JACMPVXHEARCBO-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 125000000018 nitroso group Chemical group N(=O)* 0.000 description 1
- FJDUDHYHRVPMJZ-UHFFFAOYSA-N nonan-1-amine Chemical compound CCCCCCCCCN FJDUDHYHRVPMJZ-UHFFFAOYSA-N 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 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
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 150000003142 primary aromatic amines Chemical class 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 229960000278 theophylline Drugs 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
- 239000002562 thickening agent Substances 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- ABVVEAHYODGCLZ-UHFFFAOYSA-N tridecan-1-amine Chemical compound CCCCCCCCCCCCCN ABVVEAHYODGCLZ-UHFFFAOYSA-N 0.000 description 1
- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 description 1
- RKBCYCFRFCNLTO-UHFFFAOYSA-N triisopropylamine Chemical compound CC(C)N(C(C)C)C(C)C RKBCYCFRFCNLTO-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- OOLZXLYYPCOPQZ-UHFFFAOYSA-N tripropylsulfanium Chemical compound CCC[S+](CCC)CCC OOLZXLYYPCOPQZ-UHFFFAOYSA-N 0.000 description 1
- QFKMMXYLAPZKIB-UHFFFAOYSA-N undecan-1-amine Chemical compound CCCCCCCCCCCN QFKMMXYLAPZKIB-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US92707086A | 1986-11-04 | 1986-11-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD262791A5 true DD262791A5 (de) | 1988-12-14 |
Family
ID=25454123
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD30861587A DD262791A5 (de) | 1986-11-04 | 1987-11-03 | Herbizides mittel auf der basis eines herbizids vom typ glyphosat und eines herbizides vom typ phenoxybenzoesaeure und dessen verwendung |
Country Status (16)
| Country | Link |
|---|---|
| CN (1) | CN1025142C (fr) |
| CS (1) | CS268540B2 (fr) |
| DD (1) | DD262791A5 (fr) |
| EG (1) | EG18496A (fr) |
| ES (1) | ES2007741A6 (fr) |
| GR (1) | GR871682B (fr) |
| IE (1) | IE61109B1 (fr) |
| IL (1) | IL84166A (fr) |
| MA (1) | MA21092A1 (fr) |
| MY (1) | MY101947A (fr) |
| PH (1) | PH23765A (fr) |
| PL (1) | PL152636B1 (fr) |
| PT (1) | PT86064B (fr) |
| TR (1) | TR25883A (fr) |
| YU (1) | YU46084B (fr) |
| ZA (1) | ZA878216B (fr) |
-
1987
- 1987-10-12 PH PH35919A patent/PH23765A/en unknown
- 1987-10-13 IL IL84166A patent/IL84166A/xx not_active IP Right Cessation
- 1987-10-26 MA MA21333A patent/MA21092A1/fr unknown
- 1987-10-28 CN CN 87107479 patent/CN1025142C/zh not_active Expired - Fee Related
- 1987-11-02 MY MYPI87003004A patent/MY101947A/en unknown
- 1987-11-02 PL PL26856087A patent/PL152636B1/pl unknown
- 1987-11-02 ZA ZA878216A patent/ZA878216B/xx unknown
- 1987-11-02 CS CS877847A patent/CS268540B2/cs unknown
- 1987-11-02 YU YU199187A patent/YU46084B/sh unknown
- 1987-11-02 IE IE294987A patent/IE61109B1/en not_active IP Right Cessation
- 1987-11-03 DD DD30861587A patent/DD262791A5/de not_active IP Right Cessation
- 1987-11-03 GR GR871682A patent/GR871682B/el unknown
- 1987-11-03 ES ES8703135A patent/ES2007741A6/es not_active Expired
- 1987-11-03 PT PT8606487A patent/PT86064B/pt not_active IP Right Cessation
- 1987-11-03 EG EG63387A patent/EG18496A/xx active
- 1987-11-04 TR TR77187A patent/TR25883A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PH23765A (en) | 1989-11-03 |
| YU46084B (sh) | 1992-12-21 |
| IL84166A (en) | 1992-06-21 |
| GR871682B (en) | 1988-03-04 |
| MA21092A1 (fr) | 1988-07-01 |
| CN1025142C (zh) | 1994-06-29 |
| ZA878216B (en) | 1989-06-28 |
| CS268540B2 (en) | 1990-03-14 |
| PT86064A (fr) | 1987-12-01 |
| PT86064B (pt) | 1990-11-07 |
| IE872949L (en) | 1988-05-04 |
| CS784787A2 (en) | 1989-06-13 |
| CN87107479A (zh) | 1988-08-10 |
| PL268560A1 (en) | 1988-08-18 |
| ES2007741A6 (es) | 1989-07-01 |
| IL84166A0 (en) | 1988-03-31 |
| MY101947A (en) | 1992-02-15 |
| PL152636B1 (en) | 1991-01-31 |
| TR25883A (tr) | 1993-09-02 |
| YU199187A (en) | 1990-06-30 |
| IE61109B1 (en) | 1994-10-05 |
| EG18496A (en) | 1993-02-28 |
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| Date | Code | Title | Description |
|---|---|---|---|
| ENJ | Ceased due to non-payment of renewal fee |