AROMATIC ALCOHOL P-STYRENESULFONIC ACID ESTER
NEW MATERIAL:An aromatic alcohol p-styrenesulfonic acid ester. EXAMPLE:Citronellyl p-styrenesulfonate. USE:An aromatic alcohol releasing agent, keeping aroma for a long period. PREPARATION:An aromatic alcohol is reacted with p-styrenesulfonyl chloride to give the titled compound. A terpene alcohol s...
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creator | KAMOGAWA HIROMI |
description | NEW MATERIAL:An aromatic alcohol p-styrenesulfonic acid ester. EXAMPLE:Citronellyl p-styrenesulfonate. USE:An aromatic alcohol releasing agent, keeping aroma for a long period. PREPARATION:An aromatic alcohol is reacted with p-styrenesulfonyl chloride to give the titled compound. A terpene alcohol such as citronellol, l-menthol, borneol, etc., an aromatic ring-containing alcohol such as eugenol, p-anisyl alcohol, cinnamyl alcohol, etc., may be cited as the aromatic alcohol. The copolymer of this compound can change the degree of hydrophilic nature depending upon a monomer to be copolymerized, and regulate a hydrolysis rate, so strength of aroma and durability can be controlled. |
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PREPARATION:An aromatic alcohol is reacted with p-styrenesulfonyl chloride to give the titled compound. A terpene alcohol such as citronellol, l-menthol, borneol, etc., an aromatic ring-containing alcohol such as eugenol, p-anisyl alcohol, cinnamyl alcohol, etc., may be cited as the aromatic alcohol. The copolymer of this compound can change the degree of hydrophilic nature depending upon a monomer to be copolymerized, and regulate a hydrolysis rate, so strength of aroma and durability can be controlled.</description><language>eng</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1986</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19860901&DB=EPODOC&CC=JP&NR=S61197552A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19860901&DB=EPODOC&CC=JP&NR=S61197552A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>KAMOGAWA HIROMI</creatorcontrib><title>AROMATIC ALCOHOL P-STYRENESULFONIC ACID ESTER</title><description>NEW MATERIAL:An aromatic alcohol p-styrenesulfonic acid ester. EXAMPLE:Citronellyl p-styrenesulfonate. USE:An aromatic alcohol releasing agent, keeping aroma for a long period. PREPARATION:An aromatic alcohol is reacted with p-styrenesulfonyl chloride to give the titled compound. A terpene alcohol such as citronellol, l-menthol, borneol, etc., an aromatic ring-containing alcohol such as eugenol, p-anisyl alcohol, cinnamyl alcohol, etc., may be cited as the aromatic alcohol. The copolymer of this compound can change the degree of hydrophilic nature depending upon a monomer to be copolymerized, and regulate a hydrolysis rate, so strength of aroma and durability can be controlled.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1986</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZNB1DPL3dQzxdFZw9HH29_D3UQjQDQ6JDHL1cw0O9XHz9wPJOHu6KLgGh7gG8TCwpiXmFKfyQmluBkU31xBnD93Ugvz41OKCxOTUvNSSeK-AYDNDQ0tzU1MjR2Ni1AAA0HMl5A</recordid><startdate>19860901</startdate><enddate>19860901</enddate><creator>KAMOGAWA HIROMI</creator><scope>EVB</scope></search><sort><creationdate>19860901</creationdate><title>AROMATIC ALCOHOL P-STYRENESULFONIC ACID ESTER</title><author>KAMOGAWA HIROMI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_JPS61197552A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1986</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>KAMOGAWA HIROMI</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>KAMOGAWA HIROMI</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>AROMATIC ALCOHOL P-STYRENESULFONIC ACID ESTER</title><date>1986-09-01</date><risdate>1986</risdate><abstract>NEW MATERIAL:An aromatic alcohol p-styrenesulfonic acid ester. EXAMPLE:Citronellyl p-styrenesulfonate. USE:An aromatic alcohol releasing agent, keeping aroma for a long period. PREPARATION:An aromatic alcohol is reacted with p-styrenesulfonyl chloride to give the titled compound. A terpene alcohol such as citronellol, l-menthol, borneol, etc., an aromatic ring-containing alcohol such as eugenol, p-anisyl alcohol, cinnamyl alcohol, etc., may be cited as the aromatic alcohol. The copolymer of this compound can change the degree of hydrophilic nature depending upon a monomer to be copolymerized, and regulate a hydrolysis rate, so strength of aroma and durability can be controlled.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS CHEMISTRY METALLURGY ORGANIC CHEMISTRY |
title | AROMATIC ALCOHOL P-STYRENESULFONIC ACID ESTER |
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