http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-651194-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2b8b744d430e252fa21c14c2b8dee176
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-07
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-07
filingDate 1946-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1951-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-651194-A
titleOfInvention Improvements in or relating to methods of preparing emulsions, in water or an aqueous medium, of vitamins, provitamins and vitamin or provitamin concentrations, soluble i n fat
abstract Aqueous emulsions of fat-soluble vitamins, provitamines, or their concentrates are prepared with an emulsifying agent constituted by a sterol having an aliphatic side-chain of at least 4 carbon atoms at carbon atom 17, said sterol having had introduced into it one or more hydrophile groups by esterifying or alkoxylating its hydroxyl group by means of suitable compounds. Examples describe the emulsification of (1) a crude irradiation product containing vitamin D3 by means of the trisodium salt of butane-1,2,3,4-tetracarboxylic mono-cholesteryl ester; (2) a solution of vitamin D2 in arachis oil by means of cholesteroxy-methyl-triethyl ammonium chloride; (3) an alcoholic solution of ergosterol by means of the sodium salt of phthalic mono-cholesteryl ester, and (4) an acetone solution of a carotene concentrate by means of the trisodium salt of butane-1,2,3,4-tetra carboxylic monocholesteryl ester. Other emulsifying agents specified are the sodium salt of acetylcitric acid mono-cholesteryl ester, the sodium salt of succinic mono-cholesteryl ester, the ethyl chloride quaternary salt of diethylamine acetoxy cholesterol, the potassium salt of cyclohexane - 4 - dicarboxylic - 1,2 - mono-chlesteryl ester, the a -glycerol phosphoric mono-cholesteryl ester, the sodium salt of the latter, and the sodium salt of the phthalic monoester of a sterol mixture from the unsaponifiable part of the fat of the mussel (mytilus eculis).ALSO:Aqueous emulsions of fat-soluble vitamins, provitamines, or their concentrates are prepared with an emulsifying agent constituted by a sterol having an aliphatic side-chain of at least 4 carbon atoms at carbon atom 17, said sterol having had introduced into it one or more hydrophile groups by esterifying or alkoxylating its hydroxyl group by means of suitable compounds. Examples describe the emulsification of (1) a crude irradiation product containing vitamin D3 by means of the trisodium salt of butane-1, 2, 3, 4 tetracarboxylic mono-cholesteryl ester, (2) a solution of vitamin D2 in arachis oil by means of cholesteroxy-methyl-triethyl ammoonium chloride, (3) an alcoholic solution of ergosterol by means of the sodium salt of phthalic mono-cholesteryl ester, and (4) an acetone solution of carotene concentrate by means of the tri-sodium salt of butane-1, 2, 3, 4-tetra carboxylic conocholesteryl ester. Other emulsifying agents specified are the sodium salt of acetyl-citric acid mono-cholesteryl ester, the sodium salt of succinic mono-cholesteryl ester, the ethyl chloride quaternary salt of diethylamino acetoxy cholesterol, the potassium salt of cyclohexane-4-dicarboxylic-1, 2,-mono-chlesteryl ester, the a-glycerol phosphoric mono-cholesteryl ester, the sodium salt of the latter, and the sodium salt of the phthalic mono-ester of a sterol mixture from the unsaponifiable part of the fat of the mussel (mytilus eculis). The resulting emulsions may be added to foodstuffs or milk, or may be administered by injection.
priorityDate 1943-03-04-04:00^^<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/SID456171974
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID408794676
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419537701
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5997
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6337
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID6550
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419520471
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419548902
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID154496532
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397310
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419507953
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12303103
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID312
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID444679
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419553004
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5280793
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393647
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419484729
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559517
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID6550
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID753
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID433322227
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419483452
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID180
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419547105
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419552862
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID452729134
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15560
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8078
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8021
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5280795
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID962
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410437395
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID17904700
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419512635
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID160899
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426586890

Total number of triples: 47.