Crystalline mixtures of capillary active salts and processes for preparing same
A mixture of salts of formula RO(C2H4O)nCH2COOM where R is C8- 14 alkylene, M is a cation and n is 1-5 is prepared either by treating a polyether mixture of general formula RO(C2H4O)nH (A) with chloroacetic acid or oxidizing a polyether mixture of formula RO(C2H4O)n+1H (B) and neutralizing the acid...
Gespeichert in:
Hauptverfasser: | , |
---|---|
Format: | Patent |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | |
container_start_page | |
container_title | |
container_volume | |
creator | BRENKMAN JACOBUS ADRIANUS AALBERS JOHAN GERHARD |
description | A mixture of salts of formula RO(C2H4O)nCH2COOM where R is C8- 14 alkylene, M is a cation and n is 1-5 is prepared either by treating a polyether mixture of general formula RO(C2H4O)nH (A) with chloroacetic acid or oxidizing a polyether mixture of formula RO(C2H4O)n+1H (B) and neutralizing the acid so produced. (A) and (B) may be prepared from an alcohol having 8-14 carbon atoms, e.g. lauryl alcohol, and 2-3 moles of ethylene oxide. The oxyethylated product may be fractionally distilled optionally under reduced pressure to remove any unchanged alcohol and products in which n is greater than 5. The unchanged alcohol may be reused. M may be an alkali metal. The product may be recrystallized from ethanol. In the examples the following alcohols are disclosed: lauryl alcohol containing 30% myristyl alcohol, decyl alcohol, dodecyl alcohol and dodecyl alcohol containing 30% myristyl alcohol. After treatment with ethylene oxide, distillation and treatment with chloroacetic acid, these are acidified with HCl and neutralized with NaOH, KOH or NH4OH. |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_GB1027481A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>GB1027481A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_GB1027481A3</originalsourceid><addsrcrecordid>eNqFyj0KAjEQQOE0FqKewbmA4KqgrS7-dDb2yxAnS2A2CTOjuLc3hb3V48E3dfdWRjVkjolgiB97CSnkAB5LZEYZAb3FN4EimwKmJxTJnlSrC1nqUUGJqa9ioLmbBGSlxa8zt7ycH-1tRSV3pAU9JbLuemrWm_3u0By3_8UXz1g2kw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Crystalline mixtures of capillary active salts and processes for preparing same</title><source>esp@cenet</source><creator>BRENKMAN JACOBUS ADRIANUS ; AALBERS JOHAN GERHARD</creator><creatorcontrib>BRENKMAN JACOBUS ADRIANUS ; AALBERS JOHAN GERHARD</creatorcontrib><description>A mixture of salts of formula RO(C2H4O)nCH2COOM where R is C8- 14 alkylene, M is a cation and n is 1-5 is prepared either by treating a polyether mixture of general formula RO(C2H4O)nH (A) with chloroacetic acid or oxidizing a polyether mixture of formula RO(C2H4O)n+1H (B) and neutralizing the acid so produced. (A) and (B) may be prepared from an alcohol having 8-14 carbon atoms, e.g. lauryl alcohol, and 2-3 moles of ethylene oxide. The oxyethylated product may be fractionally distilled optionally under reduced pressure to remove any unchanged alcohol and products in which n is greater than 5. The unchanged alcohol may be reused. M may be an alkali metal. The product may be recrystallized from ethanol. In the examples the following alcohols are disclosed: lauryl alcohol containing 30% myristyl alcohol, decyl alcohol, dodecyl alcohol and dodecyl alcohol containing 30% myristyl alcohol. After treatment with ethylene oxide, distillation and treatment with chloroacetic acid, these are acidified with HCl and neutralized with NaOH, KOH or NH4OH.</description><language>eng</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1966</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=19660427&DB=EPODOC&CC=GB&NR=1027481A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76418</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19660427&DB=EPODOC&CC=GB&NR=1027481A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>BRENKMAN JACOBUS ADRIANUS</creatorcontrib><creatorcontrib>AALBERS JOHAN GERHARD</creatorcontrib><title>Crystalline mixtures of capillary active salts and processes for preparing same</title><description>A mixture of salts of formula RO(C2H4O)nCH2COOM where R is C8- 14 alkylene, M is a cation and n is 1-5 is prepared either by treating a polyether mixture of general formula RO(C2H4O)nH (A) with chloroacetic acid or oxidizing a polyether mixture of formula RO(C2H4O)n+1H (B) and neutralizing the acid so produced. (A) and (B) may be prepared from an alcohol having 8-14 carbon atoms, e.g. lauryl alcohol, and 2-3 moles of ethylene oxide. The oxyethylated product may be fractionally distilled optionally under reduced pressure to remove any unchanged alcohol and products in which n is greater than 5. The unchanged alcohol may be reused. M may be an alkali metal. The product may be recrystallized from ethanol. In the examples the following alcohols are disclosed: lauryl alcohol containing 30% myristyl alcohol, decyl alcohol, dodecyl alcohol and dodecyl alcohol containing 30% myristyl alcohol. After treatment with ethylene oxide, distillation and treatment with chloroacetic acid, these are acidified with HCl and neutralized with NaOH, KOH or NH4OH.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1966</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqFyj0KAjEQQOE0FqKewbmA4KqgrS7-dDb2yxAnS2A2CTOjuLc3hb3V48E3dfdWRjVkjolgiB97CSnkAB5LZEYZAb3FN4EimwKmJxTJnlSrC1nqUUGJqa9ioLmbBGSlxa8zt7ycH-1tRSV3pAU9JbLuemrWm_3u0By3_8UXz1g2kw</recordid><startdate>19660427</startdate><enddate>19660427</enddate><creator>BRENKMAN JACOBUS ADRIANUS</creator><creator>AALBERS JOHAN GERHARD</creator><scope>EVB</scope></search><sort><creationdate>19660427</creationdate><title>Crystalline mixtures of capillary active salts and processes for preparing same</title><author>BRENKMAN JACOBUS ADRIANUS ; AALBERS JOHAN GERHARD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_GB1027481A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1966</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>BRENKMAN JACOBUS ADRIANUS</creatorcontrib><creatorcontrib>AALBERS JOHAN GERHARD</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>BRENKMAN JACOBUS ADRIANUS</au><au>AALBERS JOHAN GERHARD</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Crystalline mixtures of capillary active salts and processes for preparing same</title><date>1966-04-27</date><risdate>1966</risdate><abstract>A mixture of salts of formula RO(C2H4O)nCH2COOM where R is C8- 14 alkylene, M is a cation and n is 1-5 is prepared either by treating a polyether mixture of general formula RO(C2H4O)nH (A) with chloroacetic acid or oxidizing a polyether mixture of formula RO(C2H4O)n+1H (B) and neutralizing the acid so produced. (A) and (B) may be prepared from an alcohol having 8-14 carbon atoms, e.g. lauryl alcohol, and 2-3 moles of ethylene oxide. The oxyethylated product may be fractionally distilled optionally under reduced pressure to remove any unchanged alcohol and products in which n is greater than 5. The unchanged alcohol may be reused. M may be an alkali metal. The product may be recrystallized from ethanol. In the examples the following alcohols are disclosed: lauryl alcohol containing 30% myristyl alcohol, decyl alcohol, dodecyl alcohol and dodecyl alcohol containing 30% myristyl alcohol. After treatment with ethylene oxide, distillation and treatment with chloroacetic acid, these are acidified with HCl and neutralized with NaOH, KOH or NH4OH.</abstract><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | eng |
recordid | cdi_epo_espacenet_GB1027481A |
source | esp@cenet |
subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS CHEMISTRY METALLURGY ORGANIC CHEMISTRY |
title | Crystalline mixtures of capillary active salts and processes for preparing same |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T17%3A24%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=BRENKMAN%20JACOBUS%20ADRIANUS&rft.date=1966-04-27&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EGB1027481A%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |