http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CS-259795-B1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6776a22bbd1c5291714a1a209dc98c86
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5823ae01234cec7ca914fe569ec50857
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08B11-16
filingDate 1986-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8072e8ddda3ff4b7ef5bfa95277bca50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c13fe12404a92a9b9d7ed0d63e11089d
publicationDate 1988-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CS-259795-B1
titleOfInvention Pearl Cellulose Phenylether and its Preparation
abstract The solution falls within the field of macromolecules!nchemistry and relates to the preparation of phenyl ethernbead cellulose as sorbent for purposenhydrophobic Interaction ohromatography eventuallyn; As an intermediate for further transformations.nSo far prepared by aganose-based sorbentsnand dextrate (Pharmacia FINE-CHMICAL.nLtd., Sweden) show low mechanicalnstrength, phenylether pearl cellulose hasna high strength in conservationnmacroporous character of the matrix. Phenylethernbead cellulose according to the general formulanI, where Cel is the remainder of the pearl cellulose,nn is 0 or 1, R is a phenyl radicalnPrepare by tosylate pearl cellulosenor a tosylate of a hydroxyalkyl derivativenreacts the pearl cellulose with phenolnin an environment of water, organic solventnmiscible with water; and / orntheir mixtures preferably include ethanol,nacetone, 1,4-dioxane in the presence of hydroxidenalkali metal at 40 to 100 ° Cnfor 1 to 7 hours.
priorityDate 1986-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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