http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-509739-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8efbae6056f7ee0275c50b0f1e7243be
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-92
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-90
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N55-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-92
filingDate 1965-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c1d101d42181eec6e14be8eda1cab191
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_47b6c04769b891d91296d5a401da9601
publicationDate 1971-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-509739-A
titleOfInvention Process for protecting textiles not containing keratin against microorganisms
abstract Use of cpds. RnSbX3-n (I) where R = alkyl, alkenyl, alkynyl, aryl, cycloalkyl or cycloalkenyl. X = halogen, carboxylate, alkoxide, oxide, hydroxide, sulphide or mercaptide n = 1-3 When X is divalent (e.g. oxide) cpds. of formula (II) are also included R2Sb-X-sbR2 (II) Bactericides and fungicides esp. of use in the treatment of plastics, textiles, papers and paints. 27.2 g. (C4H9)2 SbCl in 500 ml. dry benzene treated with 22.5 g. sodium lauryl mercaptide. Refluxed 5 hours, filtered hot and filtrate evaporated to give di-n-butyl antimony lauryl mercaptide.
priorityDate 1964-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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