FORFARANDE FOR FRAMSTELLNING AV STERISKT HINDRADE BIS- ELLER POLYFENOLER
Sterically hindered bisphenols or polyphenols of the general formula wherein the substituents are defined in Claim 1, are obtained by reacting sterically hindered 2,4,6-trialkylphenols with acetals or with aldehydes or with cyclic or linear polymers of these aldehydes at a temperature of 60 to 200 D...
Gespeichert in:
Hauptverfasser: | , , , , , , , , |
---|---|
Format: | Patent |
Sprache: | swe |
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 | 8)V K GUSEV 4)O F STARIKOVA 5)G I RUTMAN 6)J I MICHUROV 1)E L STYSKIN 9)A G LIAKUMOVICH 2)Y A GURVICH 3)S T KUMOK 7)V A YANSHEVSKY |
description | Sterically hindered bisphenols or polyphenols of the general formula wherein the substituents are defined in Claim 1, are obtained by reacting sterically hindered 2,4,6-trialkylphenols with acetals or with aldehydes or with cyclic or linear polymers of these aldehydes at a temperature of 60 to 200 DEG C in the presence of an acid catatlyst. The sterically hindered bisphenols or polyphenols may be used, for example, as effective, non-staining, non-toxic and low-volatility stabilisers for natural and synthetic rubbers, plastics and other organic products. |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_SE442632B</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>SE442632B</sourcerecordid><originalsourceid>FETCH-epo_espacenet_SE442632B3</originalsourceid><addsrcrecordid>eNrjZPBw8w9ycwxy9HNxVQAyFdyCHH2DQ1x9fPw8_dwVHMMUgJwgz2DvEAUPTz-XIEegMifPYF0FoArXIIUAf59IN1c_fyCbh4E1LTGnOJUXSnMzyLm5hjh76KYW5MenFhckJqfmpZbEB7uamBiZGRs5GRNUAAAK5yu1</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>FORFARANDE FOR FRAMSTELLNING AV STERISKT HINDRADE BIS- ELLER POLYFENOLER</title><source>esp@cenet</source><creator>8)V K GUSEV ; 4)O F STARIKOVA ; 5)G I RUTMAN ; 6)J I MICHUROV ; 1)E L STYSKIN ; 9)A G LIAKUMOVICH ; 2)Y A GURVICH ; 3)S T KUMOK ; 7)V A YANSHEVSKY</creator><creatorcontrib>8)V K GUSEV ; 4)O F STARIKOVA ; 5)G I RUTMAN ; 6)J I MICHUROV ; 1)E L STYSKIN ; 9)A G LIAKUMOVICH ; 2)Y A GURVICH ; 3)S T KUMOK ; 7)V A YANSHEVSKY</creatorcontrib><description>Sterically hindered bisphenols or polyphenols of the general formula wherein the substituents are defined in Claim 1, are obtained by reacting sterically hindered 2,4,6-trialkylphenols with acetals or with aldehydes or with cyclic or linear polymers of these aldehydes at a temperature of 60 to 200 DEG C in the presence of an acid catatlyst. The sterically hindered bisphenols or polyphenols may be used, for example, as effective, non-staining, non-toxic and low-volatility stabilisers for natural and synthetic rubbers, plastics and other organic products.</description><edition>4</edition><language>swe</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; APPARATUS THEREFOR ; CHEMISTRY ; COMPOSITIONS BASED THEREON ; COMPOSITIONS OF MACROMOLECULAR COMPOUNDS ; GENERAL METHODS OF ORGANIC CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY ; ORGANIC MACROMOLECULAR COMPOUNDS ; THEIR PREPARATION OR CHEMICAL WORKING-UP ; USE OF INORGANIC OR NON-MACROMOLECULAR ORGANIC SUBSTANCES ASCOMPOUNDING INGREDIENTS</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=19860120&DB=EPODOC&CC=SE&NR=442632B$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,777,882,25545,76296</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19860120&DB=EPODOC&CC=SE&NR=442632B$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>8)V K GUSEV</creatorcontrib><creatorcontrib>4)O F STARIKOVA</creatorcontrib><creatorcontrib>5)G I RUTMAN</creatorcontrib><creatorcontrib>6)J I MICHUROV</creatorcontrib><creatorcontrib>1)E L STYSKIN</creatorcontrib><creatorcontrib>9)A G LIAKUMOVICH</creatorcontrib><creatorcontrib>2)Y A GURVICH</creatorcontrib><creatorcontrib>3)S T KUMOK</creatorcontrib><creatorcontrib>7)V A YANSHEVSKY</creatorcontrib><title>FORFARANDE FOR FRAMSTELLNING AV STERISKT HINDRADE BIS- ELLER POLYFENOLER</title><description>Sterically hindered bisphenols or polyphenols of the general formula wherein the substituents are defined in Claim 1, are obtained by reacting sterically hindered 2,4,6-trialkylphenols with acetals or with aldehydes or with cyclic or linear polymers of these aldehydes at a temperature of 60 to 200 DEG C in the presence of an acid catatlyst. The sterically hindered bisphenols or polyphenols may be used, for example, as effective, non-staining, non-toxic and low-volatility stabilisers for natural and synthetic rubbers, plastics and other organic products.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>APPARATUS THEREFOR</subject><subject>CHEMISTRY</subject><subject>COMPOSITIONS BASED THEREON</subject><subject>COMPOSITIONS OF MACROMOLECULAR COMPOUNDS</subject><subject>GENERAL METHODS OF ORGANIC CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>ORGANIC MACROMOLECULAR COMPOUNDS</subject><subject>THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><subject>USE OF INORGANIC OR NON-MACROMOLECULAR ORGANIC SUBSTANCES ASCOMPOUNDING INGREDIENTS</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1986</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZPBw8w9ycwxy9HNxVQAyFdyCHH2DQ1x9fPw8_dwVHMMUgJwgz2DvEAUPTz-XIEegMifPYF0FoArXIIUAf59IN1c_fyCbh4E1LTGnOJUXSnMzyLm5hjh76KYW5MenFhckJqfmpZbEB7uamBiZGRs5GRNUAAAK5yu1</recordid><startdate>19860120</startdate><enddate>19860120</enddate><creator>8)V K GUSEV</creator><creator>4)O F STARIKOVA</creator><creator>5)G I RUTMAN</creator><creator>6)J I MICHUROV</creator><creator>1)E L STYSKIN</creator><creator>9)A G LIAKUMOVICH</creator><creator>2)Y A GURVICH</creator><creator>3)S T KUMOK</creator><creator>7)V A YANSHEVSKY</creator><scope>EVB</scope></search><sort><creationdate>19860120</creationdate><title>FORFARANDE FOR FRAMSTELLNING AV STERISKT HINDRADE BIS- ELLER POLYFENOLER</title><author>8)V K GUSEV ; 4)O F STARIKOVA ; 5)G I RUTMAN ; 6)J I MICHUROV ; 1)E L STYSKIN ; 9)A G LIAKUMOVICH ; 2)Y A GURVICH ; 3)S T KUMOK ; 7)V A YANSHEVSKY</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_SE442632B3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>swe</language><creationdate>1986</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>APPARATUS THEREFOR</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS BASED THEREON</topic><topic>COMPOSITIONS OF MACROMOLECULAR COMPOUNDS</topic><topic>GENERAL METHODS OF ORGANIC CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>ORGANIC MACROMOLECULAR COMPOUNDS</topic><topic>THEIR PREPARATION OR CHEMICAL WORKING-UP</topic><topic>USE OF INORGANIC OR NON-MACROMOLECULAR ORGANIC SUBSTANCES ASCOMPOUNDING INGREDIENTS</topic><toplevel>online_resources</toplevel><creatorcontrib>8)V K GUSEV</creatorcontrib><creatorcontrib>4)O F STARIKOVA</creatorcontrib><creatorcontrib>5)G I RUTMAN</creatorcontrib><creatorcontrib>6)J I MICHUROV</creatorcontrib><creatorcontrib>1)E L STYSKIN</creatorcontrib><creatorcontrib>9)A G LIAKUMOVICH</creatorcontrib><creatorcontrib>2)Y A GURVICH</creatorcontrib><creatorcontrib>3)S T KUMOK</creatorcontrib><creatorcontrib>7)V A YANSHEVSKY</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>8)V K GUSEV</au><au>4)O F STARIKOVA</au><au>5)G I RUTMAN</au><au>6)J I MICHUROV</au><au>1)E L STYSKIN</au><au>9)A G LIAKUMOVICH</au><au>2)Y A GURVICH</au><au>3)S T KUMOK</au><au>7)V A YANSHEVSKY</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>FORFARANDE FOR FRAMSTELLNING AV STERISKT HINDRADE BIS- ELLER POLYFENOLER</title><date>1986-01-20</date><risdate>1986</risdate><abstract>Sterically hindered bisphenols or polyphenols of the general formula wherein the substituents are defined in Claim 1, are obtained by reacting sterically hindered 2,4,6-trialkylphenols with acetals or with aldehydes or with cyclic or linear polymers of these aldehydes at a temperature of 60 to 200 DEG C in the presence of an acid catatlyst. The sterically hindered bisphenols or polyphenols may be used, for example, as effective, non-staining, non-toxic and low-volatility stabilisers for natural and synthetic rubbers, plastics and other organic products.</abstract><edition>4</edition><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | swe |
recordid | cdi_epo_espacenet_SE442632B |
source | esp@cenet |
subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS APPARATUS THEREFOR CHEMISTRY COMPOSITIONS BASED THEREON COMPOSITIONS OF MACROMOLECULAR COMPOUNDS GENERAL METHODS OF ORGANIC CHEMISTRY METALLURGY ORGANIC CHEMISTRY ORGANIC MACROMOLECULAR COMPOUNDS THEIR PREPARATION OR CHEMICAL WORKING-UP USE OF INORGANIC OR NON-MACROMOLECULAR ORGANIC SUBSTANCES ASCOMPOUNDING INGREDIENTS |
title | FORFARANDE FOR FRAMSTELLNING AV STERISKT HINDRADE BIS- ELLER POLYFENOLER |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T17%3A26%3A01IST&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=8)V%20K%20GUSEV&rft.date=1986-01-20&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ESE442632B%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 |