http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1501318-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2b02345350a179a77bd5b1c9e042e65f http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bf41bac2b1f75d4f3b3e8e729f76b7ee |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-66 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B62-04 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B62-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-66 |
filingDate | 1976-10-20^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 1978-02-15^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | GB-1501318-A |
titleOfInvention | Method of producing a bactericidal active monochlorotriazine dye |
abstract | 1501318 Preparation of bactericidal monochlorotriazine dyes NI INST PO PERERA ISKUSSTVEN I SINTETICHE VOLOKON and INST KHIM AKAD NAUK TADZHIX SSR 20 Oct 1976 43500/76 Heading C4P Bactericidal active monochlorotriazine dyes are prepared by reacting a dichlorotriazine dye with a bactericidal compound containing one or more hydroxyl or amino groups at 20-40‹ C. in an aqueous, organic, or aqueous-organic medium whereby one chlorine atom in the triazine ring is replaced by the bactericidal compound. Preferred bactericidal compounds include 2,2' - hydroxy - 3,3',5,5',6,6' - hexachloro - diphenylmethane, leromycetin, the sodium salts of p-aminobenzenesulphamide or sulphacetamide. The products may be salted out from aqueous medium or reprecipitated from a dimethylformamide reaction medium. The dyes are applied to stockings, socks, shoe cloth, filters and medical personnel clothing. |
priorityDate | 1976-02-02^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
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