http://rdf.ncbi.nlm.nih.gov/pubchem/patent/PL-171259-B1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B62-04
filingDate 1993-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0508adb8ff9f49904d4e9f276078fcdd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9c7b21bc7038f24f239321ea8c464b22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9b946e193e4e12630a4a50343df36a22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_43b7e0349c7bb1217c532829bbc95036
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dabf9e34a1b1c049d3ae47719aba016c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_78595fd56be3814a2a89cd7c28fda3e5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b52c80f2d52484367709e73746fa99ec
publicationDate 1997-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PL-171259-B1
titleOfInvention The method of producing reactive dyes of s-triazine derivatives
abstract The method of producing reactive derivative dyesns-triazine in general formula 1, in which R is a diazov remainder57)nin an aromatic amine, at least they will be gnipp sulnin tone, aX means differentinfeeyleeovw> which ee ^^ eemphiheeaa ^ eernan alkyl substituent of 1-4 carbon atoms or sPOone groups,nconsisting in the condensation of the sodium salt of 1-amino-S-hydroxy-3,6-disploic acidnwith cyanpi-p chloride in a 1: 1 molar ratio in an aqueous environment at 0-10 ° C,nI will add a mixture of an equivalent amount of the oenyl-acid acid orn-naphthalene-mono-or -disulOne new in solid form, diranwrnipnsodium nitrite solution and coupling to obtainndichloyotriazyanwegn dye, followed by condensation with the derivativenphenyl diamininaviCakp added as an aqueous formnsolution in a molar ratio of 2: 1, that tonthe obtained cyanum acid H at a temperature of 3 - 5 ° C is addedn30% hydrochloric acid is obtained in an amount of S5 -150 part No. 1 g / mol of acidnrmmoOeayl- or -naphthalene-mono- or -displonic, followed bynthe qurs rmianOeaclo- or -aroίaleao-monn- orn-disulfonic acid and the reaction mixture is mixed with the reaction mixturenat 0-10 ° C, followed by the introduction of chloridensodium in the amount of 50 - SO parts / dcm3 of meat and rlcalalizesnaddition of sodium bicarbonate to pH 6.5 - S, stirring toncompletion of the coupling reaction, r then the resulting dyendichlorotriaacic acid of the general formula 2, wherein R mr aboventhe given discs are separated from the post-reaction mixture,nor undergoes direct condensation with a phenyl derivativendirminnzwicakp at 20 - 50 ° C in the presence of thiosirrcaraunsodium, which is added as a solid in an amount of S-12nparts or pieces of 35% aqueous solution in the amount of 20 - 30 parts No. 0.5ng / molr dirminoawlczkp, then the basic factors are introducednpH 6.6 - S, 0 and the resulting reactive dyes in the general formulan1, in which the symbols have the meaning given above, distinguishesnfrom the reaction mixture or is directly subjected to itnstabilization, drying
priorityDate 1993-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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