CH521707A - Verfahren und Mittel zum Regulieren des Pflanzenwachstums - Google Patents

Verfahren und Mittel zum Regulieren des Pflanzenwachstums

Info

Publication number: CH521707A
Authority: CH; Switzerland
Prior art keywords: active ingredient; phosphonic acid; chloroethyl; acid; ingredient used
Prior art date: 1967-02-23

Application number

CH261568A

Other languages

German (de)

English (en)

Inventor

David Fritz Charles

Fell Evans Wilbur

Original Assignee

Amchem Prod

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.)

1967-02-23

Filing date

1968-02-23

Publication date

1972-04-30

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=27088113&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CH521707(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1968-02-23 Application filed by Amchem Prod filed Critical Amchem Prod

1972-04-30 Publication of CH521707A publication Critical patent/CH521707A/de

Links

239000005648 plant growth regulator Substances 0.000 title claims description 7
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 title description 3
-1 vinyl- Chemical group 0.000 claims abstract description 72
150000003007 phosphonic acid derivatives Chemical class 0.000 claims abstract description 65
229940042400 direct acting antivirals phosphonic acid derivative Drugs 0.000 claims abstract description 49
239000002253 acid Substances 0.000 claims abstract description 19
230000008635 plant growth Effects 0.000 claims abstract description 17
150000008064 anhydrides Chemical class 0.000 claims abstract description 9
125000000623 heterocyclic group Chemical group 0.000 claims abstract description 8
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims abstract description 7
125000003118 aryl group Chemical group 0.000 claims abstract description 7
150000005690 diesters Chemical class 0.000 claims abstract description 7
150000003839 salts Chemical class 0.000 claims abstract description 6
125000004969 haloethyl group Chemical group 0.000 claims abstract description 5
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims abstract description 4
UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 claims description 121
238000000034 method Methods 0.000 claims description 68
239000004480 active ingredient Substances 0.000 claims description 53
238000011282 treatment Methods 0.000 claims description 46
239000007864 aqueous solution Substances 0.000 claims description 35
238000002360 preparation method Methods 0.000 claims description 22
230000012010 growth Effects 0.000 claims description 19
YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
239000004009 herbicide Substances 0.000 claims description 10
230000001105 regulatory effect Effects 0.000 claims description 10
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 8
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 7
229920006395 saturated elastomer Polymers 0.000 claims description 7
229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 7
125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 claims description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 6
150000007513 acids Chemical class 0.000 claims description 6
239000007788 liquid Substances 0.000 claims description 6
150000003009 phosphonic acids Chemical class 0.000 claims description 6
229930195734 saturated hydrocarbon Natural products 0.000 claims description 6
239000007787 solid Substances 0.000 claims description 6
230000006870 function Effects 0.000 claims description 5
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
125000005002 aryl methyl group Chemical group 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
150000001768 cations Chemical class 0.000 claims description 4
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239000002270 dispersing agent Substances 0.000 claims description 4
150000002148 esters Chemical class 0.000 claims description 4
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 4
229960004889 salicylic acid Drugs 0.000 claims description 4
NGADBMHGWDBFSS-UHFFFAOYSA-N 2-iodoethylphosphonic acid Chemical compound OP(O)(=O)CCI NGADBMHGWDBFSS-UHFFFAOYSA-N 0.000 claims description 3
UDBZUFZWXJJBAL-UHFFFAOYSA-N 4-chloro-5-methylpyrimidin-2-amine Chemical compound CC1=CN=C(N)N=C1Cl UDBZUFZWXJJBAL-UHFFFAOYSA-N 0.000 claims description 3
150000001555 benzenes Chemical class 0.000 claims description 3
125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 claims description 3
229910052801 chlorine Inorganic materials 0.000 claims description 3
125000001309 chloro group Chemical group Cl* 0.000 claims description 3
239000003995 emulsifying agent Substances 0.000 claims description 3
125000005843 halogen group Chemical group 0.000 claims description 3
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
239000003960 organic solvent Substances 0.000 claims description 3
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125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 claims description 3
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239000003381 stabilizer Substances 0.000 claims description 3
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RRBMVWQICIXSEO-UHFFFAOYSA-N tetrachlorocatechol Chemical compound OC1=C(O)C(Cl)=C(Cl)C(Cl)=C1Cl RRBMVWQICIXSEO-UHFFFAOYSA-N 0.000 claims description 3
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
229920002554 vinyl polymer Polymers 0.000 claims description 3
ZHNLTTJSGOZSMN-UHFFFAOYSA-N 2-fluoroethylphosphonic acid Chemical compound OP(O)(=O)CCF ZHNLTTJSGOZSMN-UHFFFAOYSA-N 0.000 claims description 2
125000004208 3-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C([H])C(*)=C1[H] 0.000 claims description 2
WWOBYPKUYODHDG-UHFFFAOYSA-N 4-chlorocatechol Chemical compound OC1=CC=C(Cl)C=C1O WWOBYPKUYODHDG-UHFFFAOYSA-N 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
239000002612 dispersion medium Substances 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
125000001476 phosphono group Chemical group [H]OP(*)(=O)O[H] 0.000 claims description 2
125000005499 phosphonyl group Chemical group 0.000 claims description 2
239000003352 sequestering agent Substances 0.000 claims description 2
125000003107 substituted aryl group Chemical group 0.000 claims description 2
125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
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230000002378 acidificating effect Effects 0.000 description 1
239000013543 active substance Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000032683 aging Effects 0.000 description 1
239000003905 agrochemical Substances 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
SOIFLUNRINLCBN-UHFFFAOYSA-N ammonium thiocyanate Chemical compound [NH4+].[S-]C#N SOIFLUNRINLCBN-UHFFFAOYSA-N 0.000 description 1
238000012443 analytical study Methods 0.000 description 1
230000003042 antagnostic effect Effects 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
230000003796 beauty Effects 0.000 description 1
125000002619 bicyclic group Chemical group 0.000 description 1
230000033228 biological regulation Effects 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
235000014633 carbohydrates Nutrition 0.000 description 1
150000001720 carbohydrates Chemical class 0.000 description 1
230000032823 cell division Effects 0.000 description 1
230000008859 change Effects 0.000 description 1
235000020971 citrus fruits Nutrition 0.000 description 1
238000004040 coloring Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
230000003111 delayed effect Effects 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
235000004879 dioscorea Nutrition 0.000 description 1
235000021186 dishes Nutrition 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
238000009826 distribution Methods 0.000 description 1
230000002255 enzymatic effect Effects 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
235000019197 fats Nutrition 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
235000015203 fruit juice Nutrition 0.000 description 1
230000004345 fruit ripening Effects 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
235000002532 grape seed extract Nutrition 0.000 description 1
235000021021 grapes Nutrition 0.000 description 1
230000009422 growth inhibiting effect Effects 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
230000001976 improved effect Effects 0.000 description 1
230000006872 improvement Effects 0.000 description 1
238000007689 inspection Methods 0.000 description 1
230000003993 interaction Effects 0.000 description 1
229940039717 lanolin Drugs 0.000 description 1
235000019388 lanolin Nutrition 0.000 description 1
235000014666 liquid concentrate Nutrition 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
230000004060 metabolic process Effects 0.000 description 1
125000002950 monocyclic group Chemical group 0.000 description 1
SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Chemical compound CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
235000016709 nutrition Nutrition 0.000 description 1
239000011022 opal Substances 0.000 description 1
239000003973 paint Substances 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
125000003367 polycyclic group Chemical group 0.000 description 1
239000000843 powder Substances 0.000 description 1
235000013324 preserved food Nutrition 0.000 description 1
230000002265 prevention Effects 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
RZKYDQNMAUSEDZ-UHFFFAOYSA-N prop-2-enylphosphonic acid Chemical compound OP(O)(=O)CC=C RZKYDQNMAUSEDZ-UHFFFAOYSA-N 0.000 description 1
235000018102 proteins Nutrition 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
238000013138 pruning Methods 0.000 description 1
230000026267 regulation of growth Effects 0.000 description 1
238000011160 research Methods 0.000 description 1
230000000284 resting effect Effects 0.000 description 1
239000011555 saturated liquid Substances 0.000 description 1
230000008117 seed development Effects 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
238000002791 soaking Methods 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
238000005507 spraying Methods 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
230000001629 suppression Effects 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
210000002105 tongue Anatomy 0.000 description 1
230000001960 triggered effect Effects 0.000 description 1
230000007306 turnover Effects 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
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1

Classifications

- 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
- C07F9/3839—Polyphosphonic acids
- 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)]
- 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
- 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
- C07F9/3826—Acyclic unsaturated acids

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)

CH261568A 1967-02-23 1968-02-23 Verfahren und Mittel zum Regulieren des Pflanzenwachstums CH521707A (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US61786067A	1967-02-23	1967-02-23
US69369867A	1967-12-27	1967-12-27

Publications (1)

Publication Number	Publication Date
CH521707A true CH521707A (de)	1972-04-30

Family

ID=27088113

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH261568A CH521707A (de)	1967-02-23	1968-02-23	Verfahren und Mittel zum Regulieren des Pflanzenwachstums

Country Status (14)

Country	Link
AT (1)	AT343694B (fr)
BE (1)	BE711222A (fr)
CH (1)	CH521707A (fr)
CY (1)	CY570A (fr)
DE (2)	DE1792797C2 (fr)
DK (1)	DK130131B (fr)
ES (1)	ES350866A1 (fr)
FR (1)	FR1555173A (fr)
GB (1)	GB1194433A (fr)
IL (1)	IL29492A (fr)
MY (1)	MY7100071A (fr)
NL (1)	NL144816B (fr)
PL (1)	PL79299B1 (fr)
SE (3)	SE366903B (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3713805A (en) *	1969-12-23	1973-01-30	Gaf Corp	Plant growth method and composition using 2-chloro-ethyl phosphonic diamide
JPS4861259A (fr) *	1971-12-02	1973-08-28
US4135909A (en) *	1974-05-10	1979-01-23	Basf Aktiengesellschaft	Salts of phosphonic acids
US4042370A (en) *	1974-09-18	1977-08-16	Sandoz Ltd.	Di-(acyloxyalkyl)-β-haloethane-phosphonates and dithiophosphonates and use as plant growth regulators
HU179142B (en) *	1977-09-28	1982-08-28	Chinoin Gyogyszer Es Vegyeszet	Process for improving defoliation and cutting fruits with treating plants withsynergistic composition of plant-ascission-improving activity,containing two active agents
HU184066B (en) *	1979-12-28	1984-06-28	Chinoin Gyogyszer Es Vegyeszet	Plant growth regulating substance and process for preparing such compound
DE3111238A1 (de) *	1981-03-21	1982-10-07	Bayer Ag, 5090 Leverkusen	Substituierte triazolylmethyl-oxirane, verfahren zu ihrer herstellung sowie ihre verwendung als zwischenprodukte
ZA828650B (en) *	1981-12-01	1983-09-28	Hunt Chem Corp Philip A	Herbicidal compositions and method using phosphonalkanoic acids, esters and salts thereof
PL1653805T5 (pl) *	2003-08-08	2012-01-31	Basf Se	Zastosowanie pochodnych acylocykloheksanodionu wraz z etefonem do traktowania drzew ziarnkowych
NL2017598B1 (en) *	2016-10-10	2018-04-16	Melinda Meulenberg Van Niekerk	Potted plants, and methods for their manufacture.
CN117859859A (zh) *	2023-12-22	2024-04-12	浙江大学	3-氨基-1,2,4-三唑在促进红梨果皮着色中的应用

1968
- 1968-02-18 IL IL2949268A patent/IL29492A/xx unknown
- 1968-02-20 DE DE19681792797 patent/DE1792797C2/de not_active Expired
- 1968-02-20 DE DE1968A0058241 patent/DE1667968B2/de active Granted
- 1968-02-22 PL PL12541168A patent/PL79299B1/pl unknown
- 1968-02-23 DK DK71768A patent/DK130131B/da not_active IP Right Cessation
- 1968-02-23 ES ES350866A patent/ES350866A1/es not_active Expired
- 1968-02-23 AT AT175068A patent/AT343694B/de not_active IP Right Cessation
- 1968-02-23 GB GB885968A patent/GB1194433A/en not_active Expired
- 1968-02-23 NL NL6802633A patent/NL144816B/xx not_active IP Right Cessation
- 1968-02-23 CH CH261568A patent/CH521707A/de not_active IP Right Cessation
- 1968-02-23 FR FR1555173D patent/FR1555173A/fr not_active Expired
- 1968-02-23 BE BE711222D patent/BE711222A/fr not_active IP Right Cessation
- 1968-02-23 SE SE238968A patent/SE366903B/xx unknown
1970
- 1970-12-05 CY CY57070A patent/CY570A/xx unknown
1971
- 1971-06-03 SE SE716671A patent/SE393992B/xx unknown
- 1971-07-09 SE SE892671A patent/SE393918B/xx unknown
- 1971-12-31 MY MY7100071A patent/MY7100071A/xx unknown

Also Published As

Publication number	Publication date
SE393918B (sv)	1977-05-31
IL29492A (en)	1974-05-16
NL6802633A (fr)	1968-08-26
MY7100071A (en)	1971-12-31
NL144816B (nl)	1975-02-17
PL79299B1 (en)	1975-06-30
FR1555173A (fr)	1969-01-24
BE711222A (fr)	1968-07-01
ES350866A1 (es)	1969-12-01
DE1792797C2 (de)	1982-07-29
AT343694B (de)	1978-06-12
SE366903B (fr)	1974-05-13
DE1667968B2 (de)	1977-06-23
GB1194433A (en)	1970-06-10
DE1667968A1 (de)	1972-03-16
DK130131C (fr)	1975-06-09
SE393992B (sv)	1977-05-31
DK130131B (da)	1974-12-30
CY570A (en)	1970-12-05

Legal Events

Date	Code	Title	Description
1988-04-29	PL	Patent ceased

Publication	Publication Date	Title
DE2211489C3 (de)	1976-01-02	Verfahren zur Regulierung des natürlichen Wachstums oder der Entwicklung von Pflanzen unter Verwendung organischer Phosphorverbindungen
US3879188A (en)	1975-04-22	Growth regulation process
Bowling et al.	1966	The effect of insecticides on the selectivity of propanil on rice
US4361436A (en)	1982-11-30	Composition for plant growth regulation
DE2843722A1 (de)	1979-04-19	N- (2-chlor-4-pyridyl)-harnstoffe, verfahren zu deren herstellung sowie diese enthaltende pflanzenwachsregulatoren
DE2716832A1 (de)	1977-10-27	Verfahren zur pflanzenwachstumsregulierung, dafuer geeignete mittel sowie neue pyridin-n-oxide
US4374661A (en)	1983-02-22	Growth regulation process
DE1642239A1 (de)	1971-04-22	Verfahren zur Foerderung des Wachstums von Kulturpflanzen
MATSUDA	1982	STUDIES ON THE EARLY PHASE OF THE REGENERATION OF A KONARA OAK (QUERCUS SERRATA THUNB.) SECONDARY FOREST: I. DEVELOPMENT AND PREMATURE ABSCISSIONS OF KONARA OAK ACORNS
Crane et al.	1970	Growth and Maturation of Fig Fruits Stimulated by 2-Chloroethylphosphonic Acid1
CH521707A (de)	1972-04-30	Verfahren und Mittel zum Regulieren des Pflanzenwachstums
DE2349745B2 (de)	1979-09-13	Pflanzenwuchsregelnde Mittel
US4401454A (en)	1983-08-30	Growth regulation methods
EP0133155A2 (fr)	1985-02-13	Agent et procédé pour augmenter le rendement de la récolte
Kolo et al.	2000	Control of termites in sugarcane using insecticides
DE2907783C2 (de)	1984-05-03	Äthylen-freisetzende Komplexverbindungen, Verfahren zu deren Herstellung sowie diese enthaltende Pflanzenbehandlungsmittel
DD250453A5 (de)	1987-10-14	Verfhren zur behandlung von pflanzen
EA004305B1 (ru)	2004-02-26	Применение регулятора роста растений на основе семикарбазона для раннего останавливания роста культурных растений
DE1642330A1 (de)	1971-06-03	Mittel zur Beeinflussung des Pflanzenwachstums
DE1667968C3 (fr)	1978-02-09
EP0481407A1 (fr)	1992-04-22	Procédé pour augmenter la production des carbohydrates dans les plantes
Bruinsma	1962	Chemical control of crop growth and development.
Kavitha et al.	2021	Evaluation of bio efficacy and phyto toxicity evaluation of Indaziflam 500 SC in acid lime.
LU83596A1 (de)	1982-01-20	Cytochininartiges membranaktives praeparat zur steigerung der pflanzlichen produktivitaet,des eiweissstickstoffniveaus und der anionenaufnahme
AT355604B (de)	1980-03-10	Verfahren zur regulierung des pflanzen- wachstums