http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8884053-B2

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_94f11f78f9b720c7591e032727d81fbf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d270c6541cde81f6ceb0b43ae9e20c09
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-3817
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-38
filingDate 2009-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0e38185bb7512d00760a4a7d23e11447
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1cb96ed0eb78e1006026568d30431514
publicationDate 2014-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8884053-B2
titleOfInvention Method for the manufacture of aminoalkylene phosphonic acid
abstract A method for the manufacture of amino alkylene phosphonic acids is disclosed. Pure P 4 O 6 is hydrolyzed in the presence of a homogeneous Broensted acid catalyst whereby the pH of the reaction medium is maintained below 5 and the free water content of said reaction medium is, after the P 4 O 6 hydrolysis has been completed, from 0 to 40%. The required amine component can be added before, during, or in one preferred execution, after the P 4 O 6 hydrolysis has been completed. Formaldehyde is then added and the reaction mixture containing the P 4 O 6 hydrolysate, the amine and the formaldehyde is reacted in presence of a Broensted acid catalyst selected from homogeneous and heterogeneous species. The amino alkylene phosphonic acid reaction product can then be recovered in a manner known per sé.
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priorityDate 2008-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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