GB1572348A

GB1572348A – Method of regulating plant growth
– Google Patents

GB1572348A – Method of regulating plant growth
– Google Patents
Method of regulating plant growth

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Publication number
GB1572348A

GB1572348A
GB14728/76A
GB1472876A
GB1572348A
GB 1572348 A
GB1572348 A
GB 1572348A
GB 14728/76 A
GB14728/76 A
GB 14728/76A
GB 1472876 A
GB1472876 A
GB 1472876A
GB 1572348 A
GB1572348 A
GB 1572348A
Authority
GB
United Kingdom
Prior art keywords
optionally substituted
compound
comprises applying
carbon atoms
imidazole
Prior art date
1976-04-10
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
GB14728/76A
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.)

Boots Co PLC

Original Assignee
Boots Co PLC
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.)
1976-04-10
Filing date
1976-04-10
Publication date
1980-07-30

1976-04-10
Application filed by Boots Co PLC
filed
Critical
Boots Co PLC

1976-04-10
Priority to GB14728/76A
priority
Critical
patent/GB1572348A/en

1977-03-29
Priority to ZA00771887A
priority
patent/ZA771887B/en

1977-03-31
Priority to US05/783,084
priority
patent/US4139365A/en

1977-04-05
Priority to BR7702138A
priority
patent/BR7702138A/en

1977-04-05
Priority to AR267117A
priority
patent/AR217072A1/en

1977-04-08
Priority to JP4027077A
priority
patent/JPS52125628A/en

1977-04-09
Priority to EG207/77A
priority
patent/EG12748A/en

1977-04-12
Priority to AU24192/77A
priority
patent/AU2419277A/en

1980-07-30
Publication of GB1572348A
publication
Critical
patent/GB1572348A/en

Status
Expired
legal-status
Critical
Current

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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

A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid

A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms

A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof Description PATENT SPECIFICATION ( 11) 1 572 348 O O ( 21) Application No 14728/76 ( 22) Filed 10 April 1976 ( 23) Complete Specification filed 31 March 1977 ( 19) ( 44) Complete Specification published 30 July 1980 ( 51) INT CL 3 AOIN 43/50 U ( 52) Index at acceptance CIB 3 F 1 ( 72) Inventors LEONARD GEORGE COPPING and JOHN FREDERICK GARROD ( 54) METHOD OF REGULATING PLANT GROWTH ( 71) We, THE BOOTS COMPANY LIMITED, a British Company, of 1 Thane Road West, Nottingham, do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement:- This invention relates to the regulation of the growth of plants 5 A method according to the invention of regulating plant growth comprises applying to the plant a growth-regulating amount of a compound having the formula N N I CON in which RI is alkyl containing up to 10 carbon atoms, alkenyl, optionally 10 substituted phenyl or optionally substituted benzyl and R 2 is alkyl containing up to carbon atoms, alkenyl, optionally substituted phenyl, optionally substituted benzyl, optionally substituted 2-phenethyl or optionally substituted phenoxyalkyl of the formula Ph O(CH,), where N is 2 or 3 The compound is generally provided in the form of a plant growth regulating composition comprising the compound and 15 a carrier, and these compositions form a further part of the invention. These compounds show growth regulating activity on a variety of plants, notably sugar cane, rice, tomatoes, sunflowers, sorghum, maize and pot plants for example chrysanthemums and carnations In one method they are of special use in the improvement of sugar cane In another method they are of special use in the 20 improvement of rice crops. The active compound can be applied directly to the plant or to the locus of the plant, in any convenient way that allows uptake by the plant, for instance, by spraying, application of granules to the soil or, when appropriate, by irrigation methods Treatment takes place at a stage when growth regulation, generally a 25 retardation effect, results in a corresponding increase in crop yield or a convenient reduction in plant size A reduction in plant size is often an advantage with crops such as rice, sunflowers, sorghum and maize Under such conditions plant height is reduced which results in a sturdier crop less susceptible to lodging The size of pot plants and tomatoes can also conveniently be controlled by use of the compounds 30 of formula I It is often best to apply the active compound to a crop during the early vegetative stage of growth for example at a rate of from -1 to 20 kilograms per hectare, more preferably at a rate of from 1 to 10 kilograms per hectare. A preferred method of the invention is one for increasing the sucrose content of sugar cane by applying to the sugar cane a compound of formula I In this 35 instance the active compound is preferably applied to the crop by addition to the water supply irrigating the land, but other methods can be used such as for example foliar spray treatment or the application of granules to the crop The active compound has the effect of ripening the crop by increasing the proportion of sucrose in the cane and so it is preferably supplied to the maturing sugar cane 40 shortly before harvest, for example within 10 weeks of harvest and most suitably between 2 and 8 weeks of harvest The active compound is applied in an amount 2 1,572,348 2 that results in an increased yield of sucrose and is such as to avoid severe phytotoxic damage to the crop Amounts depend on the method of application, the stage of growth of the sugar cane and climatic conditions, but in many instances a suitable rate of application of from 1 to 10 kilograms per hectare and preferably from 2 to 8 kilograms per hectare 5 A further preferred method of the invention is one for the treatment of rice crops to prevent lodging which comprises applying to the crop a compound of formula I Most suitably the active compound is supplied to the paddy field in the form of granules or spray, preferably before heading An application rate of from, to 10 kilograms per hectare is preferred and an especially suitable rate is from I to 8 10 kilograms per hectare. In formula I above, R' and R 2 can be straight or branched chain alkyl groups. An alkyl group contains up to 10 carbon atoms and typical examples include methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec butyl, tert butyl, pentyl, hexyl, octyl, nonyl and decyl An especially suitable alkyl group contains 1 to 5 carbon 15 atoms. When R' or R 2 is alkenyl it can be straight or branched chain and preferably contains 3 to 5 carbon atoms Examples include allyl, 2-methylallyl and 1propenyl, the most suitable group being allyl. The groups R' and R 2 can be optionally substituted phenyl or benzyl and also 20 in the case of R 2, optionally substituted 2-phenethyl, or phenoxyalkyl of the formula Ph O(CH 2)A where N is 2 or 3 When the group is substituted it includes a phenyl nucleus with one or more, for example 1 to 4, substituents which are the same or different and which include halo (fluorine, chlorine, bromine and iodine), alkoxy, alkyl, trihalomethyl and cyano Preferably there are 1 to 3 substituents 25 which are the same or different and are halo, alkoxy containing I or 2 carbon atoms and alkyl containing 1 to 4 carbon atoms preferably methyl Amongst these substituents methyl and halo groups are preferred In particular halo, especially chloro, is the most preferred substituent, one or more of the substituents often being in the 2 or 4 position on the phenyl nucleus 30 A group of compounds for use in the method of the invention is one in which RI is alkyl, alkenyl, optionally substituted phenyl or optionally substituted benzyl and R 2 is optionally substituted phenyl, optionally substituted benzyl, optionally substituted 2-phenethyl or optionally substituted 2-phenoxyethyl. A further group of compounds is one in which RI is alkyl and R 2 is optionally 35 substituted benzyl or optionally substituted 2-phenoxyethyl In particular R' contains 1 to 5 carbon atoms and when the benzyl or 2-phenoxyethyl group is substituted there are preferably 1 to 3 halo or methyl substituents, which can be the same or different, on the phenyl nucleus Especially preferred examples are 1 (N 2 phenoxyethyl N propylcarbamoyl) imidazole and 1 (N 2,4 40 dichlorobenzyl N isopropylcarbamoyl) imidazole. The active compound can be employed as a wide variety of formulations, for example, a solution, a dispersion, an aqueous emulsion, a dispersible powder, an emulsifiable concentrate or granules Moreover it can be in a form for direct application or as a concentrate which requires dilution with a suitable quantity of 45 water or other diluent before application, for example a concentrate for addition to irrigation water. As a dispersion, the composition comprises an active compound dispersed in a liquid medium, preferably water It is often convenient to supply the consumer with a primary composition which can be diluted with water to form a dispersion having 50 the desired concentration The primary composition can be provided in any one of the following forms It can be a dispersible solution which comprises the active compound dissolved in a water-miscible solvent with the addition of a dispersing agent Alternatively it can be a dispersible powder which comprises an active compound and a dispersing agent A further alternative comprises the active 55 compound in the form of a finely ground powder in association with a dispersing agent and intimately mixed with water to give a paste or cream which can if desired be added to an emulsion of oil in water to give a dispersion of active ingredient in an aqueous oil emulsion. An emulsion comprises an active compound dissolved in a water-immiscible 60 solvent which is formed into an emulsion with water in the presence of an emulsifying agent An emulsion of the desired concentration can be formed from a primary composition of the following types A concentrated stock emulsion can be supplied comprising the active compound in combination with an emulsifying agent, water and a water-immiscible solvent Alternatively an emulsifiable 65 3 1,572,3483 concentrate can be supplied to the user comprising a solution of the active compound in a water-immiscible solvent containing an emulsifying agent. A granular solid comprises an active compound associated with a solid pulverulent diluent, for example kaolin, and the mixture is granulated by known methods Alternatively it comprises the active ingredient absorbed, adsorbed or 5 coated in a preformed granular diluent, for example, fuller's earth, attapulgite or limestone grit. More than one active compound can, of course, be included in the composition In addition the composition can comprise one or more additional plant growth regulator or other active ingredients, with herbicidal, fungicidal, 10 insecticidal or acaricidal properties. Many of the active ingredients used in the invention and fungicidal compositions thereof are generically disclosed and claimed in British Patent 1,469,772 They can be prepared by a process that comprises reacting imidazole with a carbamoyl halide of the formula Z-CONR 1 R 2 (II) in which R' and R 2 are as 15 defined in formula I and Z is halogen, for example, chlorine or bromine and preferably chlorine The reaction is suitably effected in the presence of an inert organic liquid as the reaction medium, which is preferably a solvent for the reactants Preferably the reaction is carried out in the presence of a suitable acid binding agent, for example a tertiary amine such as triethylamine or pyridine or an 20 excess of imidazole reactant, in order to absorb the hydrogen halide produced in the reaction Alternatively the reaction can be carried out by first forming an alkali metal derivative of imidazole, for example an N-sodio-derivative, and subsequently reacting it with carbamoyl halide The reaction can be performed at a temperature of for example from O C to 2000 C, and preferably within the range of 50 to 1500 C 25 The carbamoyl halide of the formula II can be prepared by reacting a secondary amine of the formula HNR 1 R 2 with a carbonyl halide of the formula COZ 2 The secondary amine HNRIR 2 can, in its turn, be prepared in accordance with any of the methods known in the art For example it can be made by reacting a primary amine of the formula R'NH 2 or R 2 NH 2 with the respective alkyl halide of 30 the formula R 2 Q or R'Q, in which Q is halogen, preferably bromine. The method of the invention is illustrated by the following Examples. EXAMPLE 1 a) Sugar cane sets were grown under controlled conditions in pots containing compost The plants were allowed to develop for six weeks and the soil surrounding 35 the canes was then treated with aqueous dispersions of the compounds 1 (N 2,4 dichlorobenzyl N isopropylcarbamoyl)imidazole (compound A) and I (N 2 phenoxyethyl N propylcarbamoyl)imidazole (compound B) at rates equivalent to 4 and 8 kilograms per hectare After a further six weeks the plants were harvested and measurements of the length in centimetres of the first six 40 internodes recorded A significant retardation of growth was observed in plants treated with compounds A and B. compound A compound B control 4 kg 8 kg 4 kg 8 kg length 14 90 12 40 12 43 11 77 18 13 45 (cm) b) Samples of compounds A and B were also evaluated on field growth sugar cane to determine their ripening properties The compounds were applied at a rate of 4 lb per acre through a simulated irrigation system Harvests were made at intervals after application and sucrose concentration determined (per cent cane as 50 determined by polarimetry). Sucrose Concentration Weeks after application compound A compound B control 0 5 6 55 4 10 58 10 27 7 12 7 11 29 11 22 10 58 The above results clearly indicate that a significant improvement in the concentration of sucrose occurs when compounds A and B were applied to the sugar cane 60 1,572,348 EXAMPLE 2 In a field trial, sugar cane was treated at a rate of 4 lb per acre by sub-surface irrigation with the compound 1 (N 2 phenoxyethyl N propylcarbamoyl)imidazole Samples of cane were taken at regular intervals and _juice purity and sucrose concentration determined. The former quantity is a measure of the amount of sucrose present, being the percentage sucrose in the total soluble solids in the juice expressed from the sample of sugar cane It is calculated by determining the total soluble solid content by means of refractometry and with a knowledge of sucrose concentration determined by polarimetry 10 Sucrose concentration is the percentage of sucrose per unit weight of fresh cane. Time after application Sucrose (weeks) Treatment Juice purity concentration 15 0 active compound 73 90 8 04 control 72 33 7 49 2 active compound 71 63 6 90 control 69 19 6 40 3 active compound 77 54 8 69 20 control 74 51 7 83 4 active compound 73 32 7 65 control 66 54 6 17 The above observations demonstrate that the active compound increases the sucrose content of sugar cane It improves the crop in two important respects by 25 increasing the proportion of sucrose in the extracted juice and by increasing the quantity of sucrose produced An improvement in juice purity also aids processing and extraction of sucrose from the sugar cane. EXAMPLE 3 In an experiment to demonstrate the crop regulating activity of compounds on 30 rice, rice plants were grown in pots containing low organic content compost The temperature conditions were controlled with a daytime temperature of 280 C and a temperature of 180 C at night Approximately 15 days before heading out, the plants were treated with the two compounds I (N 2,4 dichlorobenzyl N isopropylcarbamoyl)imidazole (compound A) and 1 (N 2 phenoxyethyl N 35 propylcarbamoyl)imidazole (compound B) as a soil drench at rates of 4, 2, 1 and lb/acre The height of the plants was recorded two and four weeks after treatment and the following results obtained: Plant height (centimetres) control compound A compound B 40 41 b 21 b 1 lb +lb 41 b 21 b 1 lb +lb 2 weeks 35 2 25 7 31 5 31 2 33 5 21 5 23 0 26 0 28 2 4 weeks 45 2 26 7 35 7 37 0 40 5 372 40 0 37 0 39 7 No adverse effect on the yield of the rice plants was observed. EXAMPLE 4 45 Young sunflower seedlings were supported above aqueous solutions of active compounds at concentration of 100 mg/litre in small plastic pots The seedlings were covered with a layer of vermiculite and incubated in a controlled environment for 10 days at 250 C At the end of the growing period an assessment of the reduction in plant height was made 50 All of the following compounds reduced the height of the seedlings at least 50 percent by comparison with the control. 1 lN 3 ( 4 bromophenoxy)propyl N isopropylcarbamoyllimidazole I lN butyl N 2 ( 2,4,6 trichlorophenoxy)ethylcarbamoyllimidazole 1 lN pentyl N 2 ( 2,4,6 trichlorophenoxy)ethylcarbamoyllimidazole 55 1,572,348 1 lN 2 ( 4 iodophenoxy)ethyl N propylcarbamoyllimidazole I lN allyl N 2 ( 2,4 dichloro 6 methylphenoxy)ethylcarbamoyllimidazole 1 lN 2 ( 2,6 dibromo 4 fluorophenoxy)ethyl N propylcarbamoyllimidazole 5 EXAMPLE 5 Sorghum plants were grown in 3 + inch diameter pots in compost containing a low proportion of organic matter The environmental conditions were controlled at a temperature of 27 C during the day and 18 C at night Aqueous drenches were applied to the pots at rates equivalent to 4, 2, 1 and + lb/acre of active compound, 10 with the following results. The height of the plants was measured in comparison with that of controls at two and four weeks after treatment. Plant height (centimetres) control compound A compound B 15 4 lb 2 lb 1 lb + lb 4 lb 2 lb 1 lb lb 2 weeks 52 2 27 7 46 2 44 0 48 7 35 0 43 2 42 0 45 0 4 weeks 62 7 47 0 55 0 57 2 63 7 56 0 60 7 56 0 56 7 Compound A was 1 (N 2,4 dichlorobenzyl N isopropylcarbamoyl)imidazole 20 Compound B was 1 (N 2 phenoxyethyl N propylcarbamoyl)imidazole. EXAMPLE 6 Tests were carried out to demonstrate the growth regulating properties of compounds on tomato plants 25 Tomato plants were grown in a low organic matter compost in pots in the glasshouse At the 4 leaf stage plants were selected for uniformity of growth and active compounds applied as an aqeous drench to the soil at 15 mg/pot Four replicates were carried out for each treatment and after periods of 2 and 4 weeks from the time of application the height of plants was assessed in comparison with 30 controls. The following compounds all reduced the height of plants by more than 25 per cent (R' and R 2 refer to formula I above). RI R 2 phenyl 4-fluorophenyl 35 methyl 4-bromophenyl propyl phenyl methyl 4-chlorophenyl propyl 2-chlorophenyl butyl butyl 40 isopropyl isopropyl propyl propyl allyl allyl methyl hexyl hexyl hexyl 45 butyl allyl propyl 2-propynyl benzyl 2-( 2,4-dichlorophenoxy)ethyl benzyl 2-phenoxyethyl methyl 4-methoxy 50 methyl 4-chlorobenzyl ethyl 4-chlorobenzyl ethyl benzyl isopropyl benzyl allyl 4-chlorobenzyl 55 isopropyl 4-chlorobenzyl 1,572,348 s R' R 2 allyl 2-methylphenyl methyl 2-phenethyl benzyl 2-phenethyl phenyl 2,4-dichlorobenzyl 5 phenyl benzyl benzyl 4-methylbenzyl Claims (17) WHAT WE CLAIM IS:- 1 A method of regulating plant growth which comprises applying to the plant a growth-regulating amount of a compound having the formula 10 /NJ j R' CON R 2 in which R' is alkyl containing up to 10 carbon atoms, alkenyl, optionally substituted phenyl or optionally substituted benzyl and R 2 is alkyl containing up to carbon atoms, alkenyl, optionally substituted phenyl, optionally substituted benzyl, optionally substituted 2-phenethyl or optionally substituted phenoxyalkyl 15 of the formula Ph O(CH 2)n where N is 2 or 3. 2 A method according to Claim 1 in which the plant is selected from sugar cane, rice, tomatoes, sunflowers, sorghum, maize and pot plants. 3 A method according to Claim 1 in which the plant is selected from sugar cane and rice 20 4 A method according to Claim 1 in which R 2 is optionally substituted phenyl, optionally substituted benzyl, optionally substituted 2-phenethyl or optionally substituted 2-phenoxyethyl. A method according to any of Claims I to 4 in which R' is alkyl containing 1 to 5 carbon atoms 25 6 A method according to any of Claims I to 5 in which R 2 is optionally substituted benzyl or optionally substituted 2-phenoxyethyl, in which the phenyl nucleus is optionally substituted with 1 to 3 substituents which are the same or different and are halo or methyl. 7 A method for increasing the sucrose content of sugar cane by applying to 30 the sugar cane a compound as defined in either of Claim 4 and 5. 8 A method according to Claim 7 in which R' is alkyl containing I to 5 carbon atoms and R 2 is optionally substituted benzyl or optionally substituted 2phenoxyethyl, in which the phenyl nucleus is optionally substituted with 1 to 3 substituents which are the same or different and are halo or methyl 35 9 A method according to Claim 8 which comprises applying I (N 2 phenoxyethyl N propylcarbamoyl)imidazole. A method according to Claim 8 which comprises applying I (N 2,4 dichlorobenzyl N isopropylcarbamoyl)imidazole. 11 A method according to any of Claims 7 to 10 which comprises applying the 40 compound between 2 and 8 weeks of harvest. 12 A method according to Claim 11 which comprises applying the compound at a rate of 2 to 8 kilograms per hectare. 13 A method for the treatment of rice crops to prevent lodging which comprises applying to the crop a compound as defined in either of Claims 4 and 5 45 14 A method according to Claim 13 in which R' is alkyl containing 1 to 5 carbon atoms and R 2 is optionally substituted benzyl or optionally substituted 2phenoxyethyl, in which the phenyl nucleus is optionally substituted with I to 3 substituents which are the same or different and are halo or methyl. 15 A method according to Claim 14 which comprises applying I (N 2 50 phenoxyethyl N propylcarbamoyl)imidazole. 16 A method according to Claim 14 which comprises applying 1 (N 2,4 dichlorobenzyl N isopropylcarbamoyl)imidazole. 17 A method according to any of Claims 13 to 18 which comprises applying the compound at a rate of I to 8 kilograms per hectare 55 18 A method according to Claim 1 substantially as described in Examples 1 and 2. 1,572,348 19 A plant growth regulating composition comprising a carrier and a compound having the formula N N /R CON/ \R 2 in which R' is alkyl containing up to 10 carbon atoms, alkenyl, optionally substituted phenyl or optionally substituted benzyl and R 2 is alkyl containing up to 5 carbon atoms, alkenyl optionally substituted phenyl, optionally substituted benzyl, optionally substituted 2-phenethyl or optionally substituted phenoxyalkyl of the formula Ph O(CH 2)n where N is 2 or 3. A composition according to Claim 19 comprising a carrier and 1 (N 2 phenoxyethyl N propylcarbamoyl)imidazole or 1 (N 2,4 dichlorobenzyl 10 N isopropylcarbamoyl)imidazole. For the Applicants, GILL, JENNINGS & EVERY, Chartered Patent Agents, 53/64 Chancery Lane, London, WC 2 A l HN. Printed for Her Majesty's Stationery Office, by the Courier Press, Leamington Spa 1980 Published by The Patent Office, 25 Southampton Buildings, London WC 2 A l AY, from which copies may be obtained. 1,572,348 GB14728/76A 1976-04-10 1976-04-10 Method of regulating plant growth Expired GB1572348A (en) Priority Applications (8) Application Number Priority Date Filing Date Title GB14728/76A GB1572348A (en) 1976-04-10 1976-04-10 Method of regulating plant growth ZA00771887A ZA771887B (en) 1976-04-10 1977-03-29 Method of regulating plant growth US05/783,084 US4139365A (en) 1976-04-10 1977-03-31 Method of regulating plant growth BR7702138A BR7702138A (en) 1976-04-10 1977-04-05 PLANT GROWTH REGULATORY COMPOSITION; PROCESS FOR REGULATING PLANT GROWTH; PROCESS TO INCREASE SUGARCANE SUCHAROSE CONTENT; AND PROCESS FOR TREATING RICE HARVESTS AR267117A AR217072A1 (en) 1976-04-10 1977-04-05 COMPOSITIONS CONTAINING COMPOUNDS OF 1-CARBAMOIL IMIDAZOL N, N-DISSTITUTED TO REGULATE THE GROWTH OF PLANTS JP4027077A JPS52125628A (en) 1976-04-10 1977-04-08 Plant growth controlling composition EG207/77A EG12748A (en) 1976-04-10 1977-04-09 Method of regulating plant growth AU24192/77A AU2419277A (en) 1976-04-10 1977-04-12 Imidazole carbamate plant growth regulants Applications Claiming Priority (1) Application Number Priority Date Filing Date Title GB14728/76A GB1572348A (en) 1976-04-10 1976-04-10 Method of regulating plant growth Publications (1) Publication Number Publication Date GB1572348A true GB1572348A (en) 1980-07-30 Family ID=10046434 Family Applications (1) Application Number Title Priority Date Filing Date GB14728/76A Expired GB1572348A (en) 1976-04-10 1976-04-10 Method of regulating plant growth Country Status (8) Country Link US (1) US4139365A (en) JP (1) JPS52125628A (en) AR (1) AR217072A1 (en) AU (1) AU2419277A (en) BR (1) BR7702138A (en) EG (1) EG12748A (en) GB (1) GB1572348A (en) ZA (1) ZA771887B (en) Families Citing this family (5) * Cited by examiner, † Cited by third party Publication number Priority date Publication date Assignee Title US4239526A (en) * 1979-09-04 1980-12-16 W. R. Grace & Co. Substituted ureas as sugarcane ripeners DE3411388A1 (en) * 1984-03-28 1985-10-10 Basf Ag, 6700 Ludwigshafen VINYL AZOLYL UREAS AND FUNGICIDES CONTAINING THEM DE3415138A1 (en) * 1984-04-21 1985-10-31 Basf Ag, 6700 Ludwigshafen N- (AZOLYLCARBAMOYL) HYDROXYLAMINE AND FUNGICIDES CONTAINING THEM US4565875A (en) * 1984-06-27 1986-01-21 Fmc Corporation Imidazole plant growth regulators DE3435944A1 (en) * 1984-09-29 1986-04-10 Basf Ag, 6700 Ludwigshafen VINYL-CARBAMOYL-IMIDAZOLE CONTAINERS FOR REGULATING PLANT GROWTH Family Cites Families (3) * Cited by examiner, † Cited by third party Publication number Priority date Publication date Assignee Title US3875180A (en) * 1968-08-13 1975-04-01 Bayer Ag Herbicidally active imidazolidin-2-one-1-carboxylic acid isobutyl amide US3937626A (en) * 1971-09-30 1976-02-10 Ciba-Geigy Corporation Agents for regulating plant metabolism GB1469772A (en) 1973-06-21 1977-04-06 Boots Co Ltd Fungicidal imidazole derivatives 1976 1976-04-10 GB GB14728/76A patent/GB1572348A/en not_active Expired 1977 1977-03-29 ZA ZA00771887A patent/ZA771887B/en unknown 1977-03-31 US US05/783,084 patent/US4139365A/en not_active Expired - Lifetime 1977-04-05 AR AR267117A patent/AR217072A1/en active 1977-04-05 BR BR7702138A patent/BR7702138A/en unknown 1977-04-08 JP JP4027077A patent/JPS52125628A/en active Pending 1977-04-09 EG EG207/77A patent/EG12748A/en active 1977-04-12 AU AU24192/77A patent/AU2419277A/en not_active Expired Also Published As Publication number Publication date US4139365A (en) 1979-02-13 JPS52125628A (en) 1977-10-21 ZA771887B (en) 1978-02-22 AU2419277A (en) 1978-10-19 BR7702138A (en) 1978-01-10 AR217072A1 (en) 1980-02-29 EG12748A (en) 1979-12-31 Similar Documents Publication Publication Date Title JPS6248649A (en) 1987-03-03 Acrylic acid ester derivative, manufacture and fungicidal or plant growth regulant composition US4492597A (en) 1985-01-08 1,5-Diphenyl derivative of 1,2,4-triazole-3-carboxamide and herbicide containing the same KR920000050B1 (en) 1992-01-06 2-substituted phenyl-3-chlorotetra hydro-2h-indazoles and their production and use US4139365A (en) 1979-02-13 Method of regulating plant growth US4150967A (en) 1979-04-24 Agents for regulating plant growth US4250179A (en) 1981-02-10 Metal complex imidazole fungicides, and methods of controlling fungi with them CS208456B2 (en) 1981-09-15 Fungicide means and method of making the active substances US4049418A (en) 1977-09-20 Method of regulating plant growth EP0013873B1 (en) 1982-01-20 N-azolyl acetic acid anilides, process for their preparation and their use as herbicides US4189483A (en) 1980-02-19 Pesticidal compounds, compositions and processes US4385069A (en) 1983-05-24 Combating fungi with N-allenyl-acetanilides US4261731A (en) 1981-04-14 Alpha-isocyano-carboxylic acid amide compounds and plant growth regulant compositions US4969950A (en) 1990-11-13 Triazole compounds and methods for regulating plant growth US4181518A (en) 1980-01-01 Method of regulating plant growth using triazole and imidazole compounds US3989525A (en) 1976-11-02 H-isopropyl-2-chloroethane-(thiono)-phosphonic acid ester amide compounds and herbicidal compositions US4596801A (en) 1986-06-24 4H-3,1-benzoxazine derivatives, process for producing the same and agricultural or horticultural fungicide containing the same US4350520A (en) 1982-09-21 Plant growth regulant compositions JPS60233075A (en) 1985-11-19 Substituted phenylhydantoin and herbicide containing the same as an active ingredient JPS6127962A (en) 1986-02-07 N-substituted dicarboximide and herbicide comprising it as active ingredient JPH02229191A (en) 1990-09-11 Heterocyclic compound, preparation thereof and herbicide containing same compound as active ingredient JPH03193765A (en) 1991-08-23 Alkanoic acid derivative and herbicide IE51555B1 (en) 1987-01-07 A composition for increasing plant productivity protein nitrogen level and anion uptake US4076517A (en) 1978-02-28 Method of inhibiting the growth of plants with phospholenium salts KR840000194B1 (en) 1984-02-28 Process for preparing pyrazole derivatives JPS60260560A (en) 1985-12-23 Azolylvinyl ether Legal Events Date Code Title Description 1980-10-15 PS Patent sealed [section 19, patents act 1949] 1981-11-04 PCNP Patent ceased through non-payment of renewal fee
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