http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-189721825-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d3006be22f6ee9cdc47e1ac35ad47e40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_070b7e33e74a0cd33d18a1381a33bae2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_abbf5225510f35f440c3cf25694b45ac
filingDate 1897-09-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1898-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1898-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-189721825-A
titleOfInvention The Manufacture or Production of Paranitrobenzaldehyde-ortho-sulphonic Acid and Colouring Matters therefrom.
abstract 21,825. Green, A. G., Wahl, A. R., and Clayton Aniline Co. Sept. 23. p-Nitrobenzaldehyde-o-sulphonic acid is produced by acting upon the dinitrodiphenylethylene disulphonic acid which is described in Specification No. 5351, A.D. 1897, with oxidizing-agents. For example, the sodium salt of the dinitrodiphenylethylene disulphonic acid in aqueous solution cooled to 0‹-5‹ C. is agitated while a solution of potassium permanganate is slowly run in. The mixture is gently warmed, the precipitated manganese dioxide is filtered off, and the filtrate is neutralized, and concentrated until the very soluble sodium salt of the new acid crystallizes out. Dyes, artificial, of the triphenylmethane series are produced by condensing p-nitro-benzaldehyde-osulphonic acid with secondary or tertiary aromatic amines, for example, with benzylethylaniline sulphonic acid, and then oxidizing the leuco compound with lead peroxide and sulphuric acid. This dye yields upon wool and silk a bluish-green shade, which is fast to alkalies. Dyes of the pyrone group are obtained if p-nitro-benzaldehyde-osulphonic acid is condensed with m-amidophenol, or m-amidocresol, or their alkylated or alphylated derivatives, or sulphonic acids thereof, and the leuco products thus obtained are dehydrated and oxidized. For example, the leuco compound obtained when m-amidophenol is used is dehydrated and oxidized simultaneously by heating it with concentrated sulphuric acid at 135‹-140‹ C., and the product dyes silk a bluish-red.
priorityDate 1897-09-23-04:00^^<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/compound/CID129644538
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID153902842
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414876161
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14793
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID429410328
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1118
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14801
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453530231
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID68154
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID431918103
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID516875
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457706951
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412584819
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419516135

Total number of triples: 25.