http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2058661-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1d61075d73ada1c4859ec18bca37179f |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-74 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-74 |
| filingDate | 1970-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ec13547410a780462e1be511d19d16d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3f40b2339ce71ef102b069f1e226e8e2 |
| publicationDate | 1972-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | DE-2058661-A1 |
| titleOfInvention | Biocides adamantylamine derivative |
| abstract | Cpds. of formula (I):- have biocidal activity equal to that of known 2-alkylamino-6-aminopyridine but with greater colour stability and less eye- and skin irritation. It is also less sensitive to dirt, lipoids, proteins and anionic detergents than other known biocidal agents. (I) is used esp. in products which come in contact with human or animal skin or mucous membranes such as sanitary products and generally as disinfectants and preserving agents. Prepn. e.g. by reacting 1 mole adamantylbromide with 1-4 mole 2,6-diaminopyridine at 100-180 degrees C in the presence of an acid acceptor. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0174778-A1 |
| priorityDate | 1970-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 39.