DE2833582C2 - Verfahren zur Steigerung der Wurzelausbeute und des Zuckergehalts von Zuckerrüben - Google Patents

Verfahren zur Steigerung der Wurzelausbeute und des Zuckergehalts von Zuckerrüben

Info

Publication number: DE2833582C2
Authority: DE; Germany
Prior art keywords: triazine; sugar; methylthio; sugar content; yield
Prior art date: 1977-08-01
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

Application number

DE19782833582

Other languages

German (de)

English (en)

Other versions

DE2833582A1 (de

Inventor

Emanuel Dipl.-Ing. Beska

Ján Dipl.-Ing. Dr.Sc. Suchá nad Parmou Královic

Pavel Dipl.-Ing. Rapos

Stefan Dipl.-Ing. Bratislava Truchlik

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

URAD PREDSEDNIC SLOVENSK VIED

Original Assignee

URAD PREDSEDNIC SLOVENSK VIED

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.)

1977-08-01

Filing date

1978-07-31

Publication date

1986-07-10

1978-07-31 Application filed by URAD PREDSEDNIC SLOVENSK VIED filed Critical URAD PREDSEDNIC SLOVENSK VIED

1979-02-15 Publication of DE2833582A1 publication Critical patent/DE2833582A1/de

1986-07-10 Application granted granted Critical

1986-07-10 Publication of DE2833582C2 publication Critical patent/DE2833582C2/de

Status Expired legal-status Critical Current

Links

241000219310 Beta vulgaris subsp. vulgaris Species 0.000 title claims description 12
235000021536 Sugar beet Nutrition 0.000 title claims description 12
238000000034 method Methods 0.000 title claims description 5
JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical class C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 claims description 9
241000196324 Embryophyta Species 0.000 description 23
-1 methoxyamino Chemical group 0.000 description 16
230000000052 comparative effect Effects 0.000 description 13
239000004480 active ingredient Substances 0.000 description 10
239000003995 emulsifying agent Substances 0.000 description 6
238000002474 experimental method Methods 0.000 description 6
239000002904 solvent Substances 0.000 description 6
239000004009 herbicide Substances 0.000 description 5
239000000243 solution Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
238000012360 testing method Methods 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
239000000843 powder Substances 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
SQROAKSRUALIEJ-UHFFFAOYSA-N 4-methylsulfanyl-1,3,5-triazin-2-amine Chemical compound CSC1=NC=NC(N)=N1 SQROAKSRUALIEJ-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
238000011161 development Methods 0.000 description 2
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
239000000344 soap Substances 0.000 description 2
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
DFUGJTBMQKRCPI-UHFFFAOYSA-N 2,4,6-trimethoxy-1,3,5-triazine Chemical compound COC1=NC(OC)=NC(OC)=N1 DFUGJTBMQKRCPI-UHFFFAOYSA-N 0.000 description 1
WOPHAXVWACNHPM-UHFFFAOYSA-N 2-(methylthio)-1,3,5-triazine Chemical compound CSC1=NC=NC=N1 WOPHAXVWACNHPM-UHFFFAOYSA-N 0.000 description 1
HTSVYUUXJSMGQC-UHFFFAOYSA-N 2-chloro-1,3,5-triazine Chemical compound ClC1=NC=NC=N1 HTSVYUUXJSMGQC-UHFFFAOYSA-N 0.000 description 1
NCMONXLWVRSCBP-UHFFFAOYSA-N 2-methoxy-1,3,5-triazine Chemical compound COC1=NC=NC=N1 NCMONXLWVRSCBP-UHFFFAOYSA-N 0.000 description 1
LNCCBHFAHILMCT-UHFFFAOYSA-N 2-n,4-n,6-n-triethyl-1,3,5-triazine-2,4,6-triamine Chemical compound CCNC1=NC(NCC)=NC(NCC)=N1 LNCCBHFAHILMCT-UHFFFAOYSA-N 0.000 description 1
NAIYJWUIKVAZPK-UHFFFAOYSA-N 4-tert-butylimino-6-chloro-N-ethyl-1,3-dihydrotriazin-2-amine Chemical compound C(C)NN1NC(=CC(=N1)NC(C)(C)C)Cl NAIYJWUIKVAZPK-UHFFFAOYSA-N 0.000 description 1
QHXDTLYEHWXDSO-UHFFFAOYSA-N 6-chloro-2-n,2-n,4-n,4-n-tetraethyl-1,3,5-triazine-2,4-diamine Chemical compound CCN(CC)C1=NC(Cl)=NC(N(CC)CC)=N1 QHXDTLYEHWXDSO-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
AFIIBUOYKYSPKB-UHFFFAOYSA-N Aziprotryne Chemical compound CSC1=NC(NC(C)C)=NC(N=[N+]=[N-])=N1 AFIIBUOYKYSPKB-UHFFFAOYSA-N 0.000 description 1
VZBGLJPBALZWPS-UHFFFAOYSA-N CN(C)C1=NC(=NC(=N1)NCCCOC)SC Chemical compound CN(C)C1=NC(=NC(=N1)NCCCOC)SC VZBGLJPBALZWPS-UHFFFAOYSA-N 0.000 description 1
HCRWJJJUKUVORR-UHFFFAOYSA-N Desmetryn Chemical compound CNC1=NC(NC(C)C)=NC(SC)=N1 HCRWJJJUKUVORR-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
239000004471 Glycine Substances 0.000 description 1
BGRDGMRNKXEXQD-UHFFFAOYSA-N Maleic hydrazide Chemical compound OC1=CC=C(O)N=N1 BGRDGMRNKXEXQD-UHFFFAOYSA-N 0.000 description 1
239000005983 Maleic hydrazide Substances 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
HFBWPRKWDIRYNX-UHFFFAOYSA-N Trietazine Chemical compound CCNC1=NC(Cl)=NC(N(CC)CC)=N1 HFBWPRKWDIRYNX-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000013543 active substance Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000001447 alkali salts Chemical class 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 description 1
239000010775 animal oil Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
229910000389 calcium phosphate Inorganic materials 0.000 description 1
235000011010 calcium phosphates Nutrition 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000011280 coal tar Substances 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
235000011389 fruit/vegetable juice Nutrition 0.000 description 1
238000003306 harvesting Methods 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
239000000463 material Substances 0.000 description 1
230000004060 metabolic process Effects 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
239000000203 mixture Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000011837 pasties Nutrition 0.000 description 1
230000035515 penetration Effects 0.000 description 1
230000035790 physiological processes and functions Effects 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
238000012545 processing Methods 0.000 description 1
AAEVYOVXGOFMJO-UHFFFAOYSA-N prometryn Chemical compound CSC1=NC(NC(C)C)=NC(NC(C)C)=N1 AAEVYOVXGOFMJO-UHFFFAOYSA-N 0.000 description 1
WJNRPILHGGKWCK-UHFFFAOYSA-N propazine Chemical compound CC(C)NC1=NC(Cl)=NC(NC(C)C)=N1 WJNRPILHGGKWCK-UHFFFAOYSA-N 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000004576 sand Substances 0.000 description 1
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
150000003460 sulfonic acids Chemical class 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
IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
229940055764 triaz Drugs 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000002023 wood 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
- A01N43/70—Diamino—1,3,5—triazines with only one oxygen, sulfur or halogen atom or only one cyano, thiocyano (—SCN), cyanato (—OCN) or azido (—N3) group directly attached to a ring carbon atom

Landscapes

Life Sciences & Earth Sciences (AREA)
Dentistry (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

DE19782833582 1977-08-01 1978-07-31 Verfahren zur Steigerung der Wurzelausbeute und des Zuckergehalts von Zuckerrüben Expired DE2833582C2 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CS506577A CS197620B1 (en)	1977-08-01	1977-08-01	Agent for enhancement of root yield and sugar content of sugar beet

Publications (2)

Publication Number	Publication Date
DE2833582A1 DE2833582A1 (de)	1979-02-15
DE2833582C2 true DE2833582C2 (de)	1986-07-10

Family

ID=5394796

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE19782833582 Expired DE2833582C2 (de)	1977-08-01	1978-07-31	Verfahren zur Steigerung der Wurzelausbeute und des Zuckergehalts von Zuckerrüben

Country Status (5)

Country	Link
CH (1)	CH635303A5 (cs)
CS (1)	CS197620B1 (cs)
DE (1)	DE2833582C2 (cs)
FR (1)	FR2399206A1 (cs)
GB (1)	GB2002339B (cs)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3222147A1 (de) *	1982-06-11	1983-12-15	Chemische Werke Hüls AG, 4370 Marl	Verwendung gegebenenfalls substituierter thiomethylcycloalkylamino-s-triazine als selektive mittel gegen unkraeuter und schadgraeser
WO2002036578A2 (en) *	2000-10-31	2002-05-10	Lynn Bonham	Triazine derivatives as lpaat-b inhibitors and uses thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE793112A (fr) *	1971-12-22	1973-06-21	Ciba Geigy	Pyridinium-s-triazines agissant sur la croissance des plantes

1977
- 1977-08-01 CS CS506577A patent/CS197620B1/cs unknown
1978
- 1978-07-27 GB GB7831360A patent/GB2002339B/en not_active Expired
- 1978-07-28 CH CH817178A patent/CH635303A5/de not_active IP Right Cessation
- 1978-07-31 DE DE19782833582 patent/DE2833582C2/de not_active Expired
- 1978-07-31 FR FR7822594A patent/FR2399206A1/fr active Granted

Also Published As

Publication number	Publication date
FR2399206A1 (fr)	1979-03-02
DE2833582A1 (de)	1979-02-15
FR2399206B1 (cs)	1983-04-01
CS197620B1 (en)	1980-05-30
CH635303A5 (de)	1983-03-31
GB2002339B (en)	1982-04-28
GB2002339A (en)	1979-02-21

Legal Events

Date	Code	Title	Description
1982-10-07	8110	Request for examination paragraph 44
1983-01-13	8128	New person/name/address of the agent	Representative=s name: BEETZ SEN., R., DIPL.-ING. BEETZ JUN., R., DIPL.-I
1986-07-10	D2	Grant after examination
1987-01-15	8364	No opposition during term of opposition
1990-07-05	8339	Ceased/non-payment of the annual fee

Publication	Publication Date	Title
DE2433410C2 (de)	1985-10-31	Carbaminsäure-3-jodpropinyl-2- bzw. 4-jodbutinyl-3- bzw. 5-jodpentinyl-4-ester und fungicides Mittel
DD246245A5 (de)	1987-06-03	Herbizide zusammensetzung
DE4422025A1 (de)	1995-01-05	Gegen Pilzbefall geschütztes Pflanzen-Vermehrungsgut und seine Herstellung unter Verwendung eines Wirkstoffs auf der Basis der Phosphorigen Säure
DE1287358B (de)	1969-01-16	Herbizide Mittel
DE1213665B (de)	1966-03-31	Selektive Herbicide
DE1217695B (de)	1966-05-26	Insekticide Mittel mit acaricider Wirkung
EP0132512A1 (de)	1985-02-13	Verwendung von in 2-Stellung mit (substituierten) Aminogruppen substituierten 4-DL-Alkylester-alpha-alaninyl-6-chlor-s-Triazinen als Herbizide, insbesondere gegen Flughafer
DE2265029C3 (de)	1979-12-20	Verfahren zur Bekämpfung von pflanzenpathogenen Pilzen
DE2525383A1 (de)	1975-12-18	Addukte von carbamoylsulfoxyden und harnstoff
CH337019A (de)	1959-03-15	Verfahren und Mittel zur Beeinflussung des Pflanzenwachstums, insbesondere zur Bekämpfung von Unkraut
EP0626808B1 (de)	1997-03-12	Fungizide zusammensetzungen
DE2833582A1 (de)	1979-02-15	Mittel und verfahren zur steigerung der wurzelausbeute und des zuckergehalts von zuckerrueben
DE1140396B (de)	1962-11-29	Unkrautvertilgungsmittel
DE1542896A1 (de)	1972-04-06	Selektives Herbizid
DE951181C (de)	1956-10-25	Unkrautvertilgungsmittel
DE1072814C2 (de)	1960-06-30	Verfahren zur Herstellung höhermolekularer, metallarmcr Organo-Zinnverbindungen
DE2323021C3 (de)	1980-07-31	2-Substituierte 4-Alkylamino-6( a , a -dimethyl--acetyl- äthylamino)-13>5-triazine sowie ihre Verwendung als Herbizide und Verfahren zur Herstellung derselben
DE1545755C (cs)
DE1255982B (de)	1967-12-07	Herbizides Mittel
DE1695023B1 (de)	1972-03-23	Substituierte 2-Chlor-4-cyclopropylamino-6-amino-s-triazin und deren Verwendung als Unkrautbekaempfungsmittel
CH335570A (de)	1959-01-15	Verfahren und Mittel zur Beeinflussung des Pflanzenwachstums, insbesondere zur Bekämpfung von Unkraut
DE1567006C3 (de)	1974-08-08	Unkrautbekämpfungsmittel
EP0084767A2 (de)	1983-08-03	Verwendung von Chlor-s-triazinen, die mit ein oder zwei Cyclohexylamino-Gruppen mit mindestens 3 einwertigen Substituenten oder mit Cyclopentylamino-Gruppen substituiert sind, als selektive Mittel gegen Unkräuter und Schadgräser
AT203799B (de)	1959-06-10	Fungizide Mittel
DE4032465A1 (de)	1992-04-16	Pflanzenschuetzende mittel auf basis von benfuresate und dymrone