http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105478054-B

Outgoing Links

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K23-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C231-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C237-08
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C237-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-12
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filingDate 2015-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2017-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105478054-B
titleOfInvention A kind of naphthol derivative quaternary cationics and preparation method thereof
abstract A kind of naphthol derivative quaternary cationics and preparation method thereof; it is related to quaternary cationics and preparation method thereof; it is that to solve the technical problem that existing quaternary cationics critical micelle concentration is high, surface-active is low; the chemical name of the naphthol derivative quaternary cationics of the present invention is N alkyl acyls methyl N [2 (2 ethylnaphthalene oxygen acetyl group) ethyl] N; N dimethy lammonium chlorides, its structural formula are: Preparation method:By solvent, N acetyl group (2 ethylnaphthalene epoxide) N; N dimethyl-ethylenediamines and halogen acetyl pheynylalkylamine are added in reactor; produced after heating stirring reaction; its critical micelle concentration is 0.005~0.28mmol/L; surface-active is high; and preparation method is simple, reaction condition is easily controllable, and product is easily isolated, purified.Available for cosmetics, sterilization, pharmacy, petrochemical industry.
priorityDate 2015-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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