http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DD-208535-A5

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N25-22
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N25-22
filingDate 1982-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f2bb010138a89d4cb6e1314968845896
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_25bda8d5fe306e20e50dff2580abf311
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_90e370b21ebe6ac76b3135b7d72f0d13
publicationDate 1984-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DD-208535-A5
titleOfInvention HERBICIDAL COMPOSITION
abstract Herbicide-active thiocarbamates are used in combination with certain amines of the formula in which R is high 4 and R is high 5 u. R high 5 independent of each other f. Hydrogen, a cyano group, an optional m. Zyano o. Hydroxy substituted C deep 1 ... C deep 10-Alkyl, a C deep 2 ... C deep 6-alkenyl group, a C deep 5 ... C deep 7-Cycloalkyl as well as a Phenyl-u. Benzyl-Gr. stand, where d. both latter optionally m. Halogen, cyano o. Methoxy can be substituted, and R is high 6 under hydrogen and C deep 2 ... C deep 6-alkenyl is selected o. Landwirtschaftl. usable salts of such amines used. In a typical application, the amine or amine salt is included in an amount sufficient to reduce the rate of thiocarbamate degradation in the soil. As a result, d. herbicidal activity of the thiocarbamate increased and prolonged, whereby a single administration of the herbicide remains effective over a longer period of time.
priorityDate 1981-10-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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