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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C11D1-72
filingDate 1968-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_467aad32dc5b1a5ff6b98e4724d11214
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_236fd3abffba6358a4155ee9d2d46267
publicationDate 1970-09-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1205721-A
titleOfInvention Aqueous solutions of reduced viscosity of ethoxylated phenols, ethoxylated long-chain alcohols, amines and mercaptants
abstract 1,205,721. Solutions of ethoxylated compounds. FARBENFABRIKEN BAYER A.G. 10 Dec., 1968 [19 Dec., 1967; 1 April, 1968], No. 58658/68. Heading C3R. The viscosities of aqueous solutions of ethoxylated phenols or ethoxylated long-chain alcohols, amines or mercaptans, are reduced by incorporating in the solutions compounds of formula where R is hydrogen, hydroxy, carboxy, carbalkoxy, carbamide, carbalkylamide, alkyl or substituted aryl, and X is hydroxy, alkoxy, aralkoxy, amino, alkylamino or arylamino. In examples the ethoxylated materials are nonylphenol, dodecylphenol, oleyl alcohol, a mixture of alkanols having 16 to 20 carbon atoms, methylstearylamine and dodecylmercaptan, and these ethoxylated materials are mixed with 4-hydroxybenzoic acid butyl ester, 4-hydroxybenzoic acid propyl ester, 4-hydroxy isophthalic acid, 3-hydroxybenzoic acid, salicylic acid amide, 2-hydroxy-5-tert.-butylbenzoic acid, 3,5 - dihydroxybenzoic acid, 4 - hydroxybenzoic acid, 4 - hydroxybenzoic acid isoamyl ester and salicylic acid, and the mixtures are dissolved in water.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5143635-A
priorityDate 1967-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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