http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1301780-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S8-927 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/D06P1-66 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/D06P3-76 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/D06P3-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/D06P1-66 |
| filingDate | 1971-09-10^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1973-01-04^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-1301780-A |
| abstract | 1301780 Dyeing polyacrylonitrile BAYER AG 10 Sept 1971 [11 Sept 1970] 42362/71 Heading D1B Polyacrylonitrile and acrylo-nitrile copolymers are dyed with cationic dyes in presence of a salt derived from a free ammonium base of formula I in which R is a C 6 -C 20 alkyl, C 6 -C 20 alkenyl or an optionally substituted aralkyl radical, R 1 and R 2 are each independantly C 1 -C 4 alkyl or C 1 -C 4 hydroxyalkyl radicals or form together with the nitrogen atom a heterocyclic ring, A is an optionally substituted naphthyl or tetrahydronaphthyl radical. Preferably 0.25 to 2.5% by weight of the compound on weight of the fabric is used, and may be applied in a pre-treatment bath. Examples of hetero cyclic rings formed by R 1 and R 2 are pyrrolidine, piperidine and morpholine. |
| priorityDate | 1970-09-11^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Showing number of triples: 1 to 20 of 20.