http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-437285-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_28d7ab717e76b722f823ae4113d4ae99
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_73ee0bacab5a7576a6a3244747f6ea99
filingDate 1934-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1935-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-437285-A
titleOfInvention The manufacture of new compounds for the treatment of textiles
abstract Products stated to have emulsifying properties and to be useful as softening and cleansing agents in the textile industry are prepared by reacting a lower alkyl ester of an inorganic acid with a mercaptobenzthiazole which has an alkyl group containing at least eight carbon atoms in the 2-position and may carry substituents such as methyl, methoxy or ethoxy in the benzene nucleus. The lower alkyl ester may contain up to four carbon atoms. In examples: (1) 2-octadecylmercaptobenzthiazole, obtained by reacting octadecylbromide in butyl alcohol with the sodium mercaptobenzthiazole, is treated with dimethyl sulphate; the product may be used for softening cotton limbric; (2) 2-dodecylmercaptobenzthiazole, obtained by the interaction of dodecyl bromide and sodium mercaptobenzthiazole is treated with dimethylsulphate. The 2-alkylmercaptobenzthiazoles may also be prepared from the 2-mercaptobenzthiazoles by treating them with the sulphuric esters of higher alcohols. The following 2 - alkylmercaptobenzthiazoles are mentioned: 2-octadecyl, 2-dodecyl and 2-octadecenyl mercaptobenzthiazoles containing methyl or methoxy in the 6-position, or methyl in the 4-position.ALSO:Products stated to have emulsifying properties are obtained by reacting lower (up to C4) alkyl esters of inorganic acids with a mercaptobenzthiazole which has an alkyl group containing at least eight carbon atoms in the 2-position and may carry substitutent such as methyl, methoxy or ethoxy in the benzene nucleus. In examples 2-octadecylmercaptoand 2 - dodecylmercapto - benzthiazoles are treated with dimethylsulphate. The following 2-alkylmercapto benzthiazoles are mentioned: 2-octadecyl-, 2-dodecyl- and 2-octadecenyl-benzthiazoles containing methyl or methoxy in the 6-position or methyl in the 4-position.
priorityDate 1934-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450372608
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID153794858
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414862917
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4059537
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID153794859
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393768
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456171974
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24195611
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426013056
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID429273530
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8919
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414864238
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456987945
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID429273531
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8218
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394811
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID263
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426029679
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393787
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6497
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419524338
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID697993
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419584435
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4352104
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393636

Total number of triples: 34.