http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-862863-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2b8b744d430e252fa21c14c2b8dee176
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N37-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N37-34
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-48
filingDate 1958-11-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1961-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-862863-A
titleOfInvention Improvements in or relating to preparations for influencing the growth of plants
abstract 2,6 diethyl benzonitrile (B.P. 111 DEG -114 DEG C. at 12 mm. Hg) may be prepared by conventional methods. It may be used in plant growth controlling compositions (see Group VI).ALSO:A preparation for controlling the growth of plants is prepared by mixing or dissolving one or more compounds of formula <FORM:0862863/VI/1> in which Y represents a halogen atom, a C1-5 alkyl group (preferably methyl) or a nitro group, and X represents a halogen atom, a C1-5 alkyl group (preferably methyl) or a nitro group or Xn represents a plurality of such groups or atoms being the same as or different from one another, each individually linked to the benzene ring and n is 0-4 if both X and Y are halogen atoms, or n is 0, 1 or 2 if at least one alkyl group or at least one nitro group is linked to the benzene ring, with an inert solid or liquid carrier material, if desired with the addition of surface-active materials, dispersion agents and/or adhesives. Preferably the halogen is chlorine. The preferred compounds contain substituents on both ortho-positions to the nitrile group such as 2-chloro-, 2-methyl-, 2-ethyl- and 2-nitrobenzonitrile; 2,6 - dichlorobenzonitrile; 2,6 - dimethyl- and 2,6 - diethyl - benzonitrile; 2,4,6-trichloro- and 2,4,5-trichlorobenzonitrile; 2 - chloro - 6 - methyl and 2,3,5,6 - tetrachlorobenzonitrile. Other active compounds include 2,4 - dichloro-, 2,5 - dichloro-, 2,4,5 - trichloro-, 2 - chloro - 5 - nitro- and 2 - methyl - 5 - nitrobenzonitrile. The active ingredient may be compounded as (a) a wettable powder with a wetting agent such as a fatty alcohol sulphate or an alkyl aryl sulphonate or a dispersing agent such as lignin sulphonate and a carrier such as kaolin, chalk, pipe clay, magnesium marlstone or attapulgite; (b) a miscible oil earth 5-10% of ionic or non-ionic emulsifier and a solvent (benzene, toluene, xylene or other aromatic hydrocarbon mixed with ketones such as acetone or cyclohexanone); (c) a dust in which the active substance may be ground with a carrier such as a mixture of kieselguhr and magnesium marlstone and, if desired, a wetting agent; or (d) a solution in an organic solvent such as an aromatic hydrocarbon or an aliphatic or aromatic ketone or a mixture of them. The preparations may be used for controlling the growth of both mono- and di-cetyledonous plants and the premature sprouting of tubers during storage.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3401191-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5101061-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3303092-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5214187-A
priorityDate 1957-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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