http://rdf.ncbi.nlm.nih.gov/pubchem/patent/IL-46125-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0e5e37c55ff492dd0f59ba7e84e2346c
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S534-03
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A23L5-47
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B69-10
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B69-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A23L1-275
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B69-10
filingDate 1974-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1977-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber IL-46125-A
titleOfInvention Non-toxic paint mixture, process for its preparation and a food substance mixed with it
abstract 1485846 Food colourings DYNAPOL 19 Nov 1974 [30 Nov 1973] 50124/74 Heading C3P [Also in Divisions A2 and C6] Non-toxic food colourings have the general structure M-(NR-SO 2 -K) z in which M is a non-degradable, non-digestable organic polymer backbone of M.W. at least 10,000 and of such molecular dimensions that the colouring does not pass through the mucosa of the gastrointestinal tract, K is an optically chromophore group, z is a positive integer, R is H or a C 1-6 hydrocarbon group, and NR-SO 2 is a sulphonamido group linking M to K and which is oriented with its NR group pendant from, but attached to, M. In the examples, the polymer backbone is derived from polyacrylic acid, and the following reaction sequence is used: (i) polyacrylic acid is treated with hydrazoic acid to effect, via the Schmidt rearrangement, production of an acrylic acid/vinyl amine copolymer, which is (ii) reacted with either N-acetylsulphanilyl chloride or 4-acetamido-1-naphthalene sulphonyl chloride, the product being (iii) hydrolysed to release free amine groups, (iv) diazotized, and (v) linked with a colouring substance selected from the following: Schaeffer's salt (orange), Pyrazolone T (yelloworange), 2-naphthol-3,6-disulphonic acid (red) or 1,8 - dihydroxynaphthalene - 3,6 - disulphonic acid (deep violet).n[GB1485846A]
priorityDate 1973-11-30-04:00^^<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/CID1099
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3935589
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24530
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5284479
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419525471
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453047454
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454105947
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425193155
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409140283
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456171974
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453047453
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID164825
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID783
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67045
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID418699117
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426011937
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11513733
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11642
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67221
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10614
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID75496
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419502284
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6326
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419519989
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458392451
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457781088
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8481
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID17730
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4025596
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID86607863
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450459896
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID297
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID447734460
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419526217
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559581
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419588021
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421243469
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6581
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8000
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420827622
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5333
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422062388
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8640
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414863512
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419474364
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID421846
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID452913088
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559546
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415735615
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451346688

Total number of triples: 65.