{"id":7180,"date":"2023-09-18T09:02:42","date_gmt":"2023-09-18T08:02:42","guid":{"rendered":"https:\/\/pakistan-cosmetics.com\/?post_type=product&#038;p=7180"},"modified":"2023-09-18T09:02:42","modified_gmt":"2023-09-18T08:02:42","slug":"phenoxyethanol","status":"publish","type":"product","link":"https:\/\/pakistan-cosmetics.com\/index.php\/phenoxyethanol\/","title":{"rendered":"Phenoxyethanol"},"content":{"rendered":"<div class=\"vector-sitenotice-container\">\n<div id=\"siteNotice\">\n<div id=\"centralNotice\" class=\"cn-wlm_2023_pk\">\n<div id=\"wlm_2023_pk\" class=\"cbnnr\">\n<div class=\"cbnnr-main\">\n<div class=\"cbnnr-close\">\n<div class=\"cbnnr-close-icon\" title=\"Hide\"><\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"mw-content-container\"><main id=\"content\" class=\"mw-body\" role=\"main\"><\/p>\n<header class=\"mw-body-header vector-page-titlebar\">\n<h1 id=\"firstHeading\" class=\"firstHeading mw-first-heading\"><span class=\"mw-page-title-main\">Phenoxyethanol<\/span><\/h1>\n<div id=\"p-lang-btn\" class=\"vector-dropdown mw-portlet mw-portlet-lang\"><input id=\"p-lang-btn-checkbox\" class=\"vector-dropdown-checkbox mw-interlanguage-selector\" role=\"button\" type=\"checkbox\" aria-haspopup=\"true\" data-event-name=\"ui.dropdown-p-lang-btn\" aria-label=\"Go to an article in another language. Available in 21 languages\" \/><label id=\"p-lang-btn-label\" class=\"vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet cdx-button--action-progressive mw-portlet-lang-heading-21\" for=\"p-lang-btn-checkbox\" aria-hidden=\"true\"><span class=\"vector-dropdown-label-text\">21 languages<\/span><\/label><\/div>\n<\/header>\n<div class=\"vector-page-toolbar\">\n<div class=\"vector-page-toolbar-container\">\n<div id=\"left-navigation\">\n<nav aria-label=\"Namespaces\">\n<div id=\"p-associated-pages\" class=\"vector-menu vector-menu-tabs mw-portlet mw-portlet-associated-pages\">\n<div class=\"vector-menu-content\">\n<ul class=\"vector-menu-content-list\">\n<li id=\"ca-nstab-main\" class=\"selected vector-tab-noicon mw-list-item\"><a accesskey=\"c\" title=\"View the content page [alt-shift-c]\" href=\"https:\/\/en.wikipedia.org\/wiki\/Phenoxyethanol\" target=\"_blank\" rel=\"noopener\">Article<\/a><\/li>\n<li id=\"ca-talk\" class=\"vector-tab-noicon mw-list-item\"><a accesskey=\"t\" title=\"Discuss improvements to the content page [alt-shift-t]\" href=\"https:\/\/en.wikipedia.org\/wiki\/Talk:Phenoxyethanol\" rel=\"discussion noopener\" target=\"_blank\">Talk<\/a><\/li>\n<\/ul>\n<\/div>\n<\/div>\n<\/nav>\n<\/div>\n<div id=\"right-navigation\" class=\"vector-collapsible\">\n<nav aria-label=\"Views\">\n<div id=\"p-views\" class=\"vector-menu vector-menu-tabs mw-portlet mw-portlet-views\">\n<div class=\"vector-menu-content\">\n<ul class=\"vector-menu-content-list\">\n<li id=\"ca-view\" class=\"selected vector-tab-noicon mw-list-item\"><a href=\"https:\/\/en.wikipedia.org\/wiki\/Phenoxyethanol\" target=\"_blank\" rel=\"noopener\">Read<\/a><\/li>\n<li id=\"ca-edit\" class=\"vector-tab-noicon mw-list-item\"><a accesskey=\"e\" title=\"Edit this page [alt-shift-e]\" href=\"https:\/\/en.wikipedia.org\/w\/index.php?title=Phenoxyethanol&amp;action=edit\" target=\"_blank\" rel=\"noopener\">Edit<\/a><\/li>\n<li id=\"ca-history\" class=\"vector-tab-noicon mw-list-item\"><a accesskey=\"h\" title=\"Past revisions of this page [alt-shift-h]\" href=\"https:\/\/en.wikipedia.org\/w\/index.php?title=Phenoxyethanol&amp;action=history\" target=\"_blank\" rel=\"noopener\">View history<\/a><\/li>\n<\/ul>\n<\/div>\n<\/div>\n<\/nav>\n<nav class=\"vector-page-tools-landmark\" aria-label=\"Page tools\">\n<div id=\"vector-page-tools-dropdown\" class=\"vector-dropdown vector-page-tools-dropdown\">\n<div class=\"vector-dropdown-content\">\n<div id=\"vector-page-tools-unpinned-container\" class=\"vector-unpinned-container\">\n<div id=\"vector-page-tools\" class=\"vector-page-tools vector-pinnable-element\">\n<div class=\"vector-pinnable-header vector-page-tools-pinnable-header vector-pinnable-header-unpinned\" data-feature-name=\"page-tools-pinned\" data-pinnable-element-id=\"vector-page-tools\" data-pinned-container-id=\"vector-page-tools-pinned-container\" data-unpinned-container-id=\"vector-page-tools-unpinned-container\" data-saved-pinned-state=\"false\"><\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/nav>\n<\/div>\n<\/div>\n<\/div>\n<div id=\"bodyContent\" class=\"vector-body ve-init-mw-desktopArticleTarget-targetContainer\" aria-labelledby=\"firstHeading\" data-mw-ve-target-container=\"\">\n<div class=\"vector-body-before-content\">\n<div id=\"siteSub\" class=\"noprint\"><\/div>\n<\/div>\n<div id=\"contentSub\">\n<div id=\"mw-content-subtitle\"><\/div>\n<\/div>\n<div id=\"mw-content-text\" class=\"mw-body-content mw-content-ltr\" dir=\"ltr\" lang=\"en\">\n<div class=\"mw-parser-output\">\n<table class=\"infobox ib-chembox\">\n<caption>Phenoxyethanol<sup id=\"cite_ref-a_1-0\" class=\"reference\"><a href=\"https:\/\/en.wikipedia.org\/wiki\/Phenoxyethanol#cite_note-a-1\" target=\"_blank\" rel=\"noopener\">[1]<\/a><\/sup><sup id=\"cite_ref-2\" class=\"reference\"><a href=\"https:\/\/en.wikipedia.org\/wiki\/Phenoxyethanol#cite_note-2\" target=\"_blank\" rel=\"noopener\">[2]<\/a><\/sup><sup id=\"cite_ref-3\" class=\"reference\"><a href=\"https:\/\/en.wikipedia.org\/wiki\/Phenoxyethanol#cite_note-3\" target=\"_blank\" rel=\"noopener\">[3]<\/a><\/sup><\/caption>\n<tbody>\n<tr>\n<td colspan=\"2\"><a class=\"mw-file-description\" href=\"https:\/\/en.wikipedia.org\/wiki\/File:2-phenoxyethanol-Line-Structure.svg\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"mw-file-element\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/f\/ff\/2-phenoxyethanol-Line-Structure.svg\/220px-2-phenoxyethanol-Line-Structure.svg.png\" srcset=\"\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/f\/ff\/2-phenoxyethanol-Line-Structure.svg\/330px-2-phenoxyethanol-Line-Structure.svg.png 1.5x, \/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/f\/ff\/2-phenoxyethanol-Line-Structure.svg\/440px-2-phenoxyethanol-Line-Structure.svg.png 2x\" width=\"220\" height=\"89\" data-file-width=\"441\" data-file-height=\"178\" \/><\/a><\/td>\n<\/tr>\n<tr>\n<td colspan=\"2\"><a class=\"mw-file-description\" href=\"https:\/\/en.wikipedia.org\/wiki\/File:Phenoxyethanol_3d_structure.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"mw-file-element\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/4\/47\/Phenoxyethanol_3d_structure.png\/220px-Phenoxyethanol_3d_structure.png\" srcset=\"\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/4\/47\/Phenoxyethanol_3d_structure.png\/330px-Phenoxyethanol_3d_structure.png 1.5x, \/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/4\/47\/Phenoxyethanol_3d_structure.png\/440px-Phenoxyethanol_3d_structure.png 2x\" width=\"220\" height=\"249\" data-file-width=\"1006\" data-file-height=\"1138\" \/><\/a><\/td>\n<\/tr>\n<tr>\n<th colspan=\"2\">Names<\/th>\n<\/tr>\n<tr>\n<td colspan=\"2\"><a title=\"Preferred IUPAC name\" href=\"https:\/\/en.wikipedia.org\/wiki\/Preferred_IUPAC_name\" target=\"_blank\" rel=\"noopener\">Preferred IUPAC name<\/a><\/p>\n<div>\n<div>2-Phenoxyethan-1-ol<\/div>\n<\/div>\n<\/td>\n<\/tr>\n<tr>\n<td colspan=\"2\">Other names<\/p>\n<div>Phenoxyethanol<br \/>\nEthylene glycol monophenyl ether<br \/>\nPhenoxytolarosol<br \/>\nDowanol EP \/ EPH<br \/>\nProtectol PE<br \/>\nEmery 6705<br \/>\nRose ether<br \/>\n1-Hydroxy-2-phenoxyethane<br \/>\n\u03b2-hydroxyethyl phenyl ether<br \/>\nPhenyl cellosolve<\/div>\n<\/td>\n<\/tr>\n<tr>\n<th colspan=\"2\">Identifiers<\/th>\n<\/tr>\n<tr>\n<td>\n<div><a title=\"CAS Registry Number\" href=\"https:\/\/en.wikipedia.org\/wiki\/CAS_Registry_Number\" target=\"_blank\" rel=\"noopener\">CAS Number<\/a><\/div>\n<\/td>\n<td>\n<div class=\"plainlist\">\n<ul>\n<li><span title=\"commonchemistry.cas.org\"><a class=\"external text\" href=\"https:\/\/commonchemistry.cas.org\/detail?cas_rn=122-99-6\" rel=\"nofollow noopener\" target=\"_blank\">122-99-6<\/a><\/span><sup><img loading=\"lazy\" decoding=\"async\" class=\"mw-file-element\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/f\/fb\/Yes_check.svg\/7px-Yes_check.svg.png\" srcset=\"\/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/f\/fb\/Yes_check.svg\/11px-Yes_check.svg.png 1.5x, \/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/f\/fb\/Yes_check.svg\/14px-Yes_check.svg.png 2x\" alt=\"check\" width=\"7\" height=\"7\" data-file-width=\"600\" data-file-height=\"600\" \/><\/sup><\/li>\n<\/ul>\n<\/div>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<div>3D model (<a class=\"mw-redirect\" title=\"JSmol\" href=\"https:\/\/en.wikipedia.org\/wiki\/JSmol\" target=\"_blank\" rel=\"noopener\">JSmol<\/a>)<\/div>\n<\/td>\n<td>\n<div class=\"plainlist\">\n<ul>\n<li><span title=\"chemapps.stolaf.edu (3D interactive model)\"><a class=\"external text\" href=\"https:\/\/chemapps.stolaf.edu\/jmol\/jmol.php?model=c1ccc%28cc1%29OCCO\" rel=\"nofollow noopener\" target=\"_blank\">Interactive image<\/a><\/span><\/li>\n<\/ul>\n<\/div>\n<\/td>\n<\/tr>\n<tr>\n<td><a title=\"ChEBI\" href=\"https:\/\/en.wikipedia.org\/wiki\/ChEBI\" target=\"_blank\" rel=\"noopener\">ChEBI<\/a><\/td>\n<td>\n<div class=\"plainlist\">\n<ul>\n<li><span title=\"www.ebi.ac.uk\"><a class=\"external text\" href=\"https:\/\/www.ebi.ac.uk\/chebi\/searchId.do?chebiId=64275\" rel=\"nofollow noopener\" target=\"_blank\">CHEBI:64275<\/a><\/span><sup><img loading=\"lazy\" decoding=\"async\" class=\"mw-file-element\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/a\/a2\/X_mark.svg\/7px-X_mark.svg.png\" srcset=\"\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/a\/a2\/X_mark.svg\/11px-X_mark.svg.png 1.5x, \/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/a\/a2\/X_mark.svg\/14px-X_mark.svg.png 2x\" alt=\"\u2612\" width=\"7\" height=\"8\" data-file-width=\"525\" data-file-height=\"600\" \/><\/sup><\/li>\n<\/ul>\n<\/div>\n<\/td>\n<\/tr>\n<tr>\n<td><a title=\"ChEMBL\" href=\"https:\/\/en.wikipedia.org\/wiki\/ChEMBL\" target=\"_blank\" rel=\"noopener\">ChEMBL<\/a><\/td>\n<td>\n<div class=\"plainlist\">\n<ul>\n<li><span title=\"www.ebi.ac.uk\"><a class=\"external text\" href=\"https:\/\/www.ebi.ac.uk\/chembldb\/index.php\/compound\/inspect\/ChEMBL1229846\" rel=\"nofollow noopener\" target=\"_blank\">ChEMBL1229846<\/a><\/span><sup><img loading=\"lazy\" decoding=\"async\" class=\"mw-file-element\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/a\/a2\/X_mark.svg\/7px-X_mark.svg.png\" srcset=\"\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/a\/a2\/X_mark.svg\/11px-X_mark.svg.png 1.5x, \/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/a\/a2\/X_mark.svg\/14px-X_mark.svg.png 2x\" alt=\"\u2612\" width=\"7\" height=\"8\" data-file-width=\"525\" data-file-height=\"600\" \/><\/sup><\/li>\n<\/ul>\n<\/div>\n<\/td>\n<\/tr>\n<tr>\n<td><a title=\"ChemSpider\" href=\"https:\/\/en.wikipedia.org\/wiki\/ChemSpider\" target=\"_blank\" rel=\"noopener\">ChemSpider<\/a><\/td>\n<td>\n<div class=\"plainlist\">\n<ul>\n<li><span title=\"www.chemspider.com\"><a class=\"external text\" href=\"https:\/\/www.chemspider.com\/Chemical-Structure.13848467.html\" rel=\"nofollow noopener\" target=\"_blank\">13848467<\/a><\/span><sup><img loading=\"lazy\" decoding=\"async\" class=\"mw-file-element\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/f\/fb\/Yes_check.svg\/7px-Yes_check.svg.png\" srcset=\"\/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/f\/fb\/Yes_check.svg\/11px-Yes_check.svg.png 1.5x, \/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/f\/fb\/Yes_check.svg\/14px-Yes_check.svg.png 2x\" alt=\"check\" width=\"7\" height=\"7\" data-file-width=\"600\" data-file-height=\"600\" \/><\/sup><\/li>\n<\/ul>\n<\/div>\n<\/td>\n<\/tr>\n<tr>\n<td><a class=\"mw-redirect\" title=\"ECHA InfoCard\" href=\"https:\/\/en.wikipedia.org\/wiki\/ECHA_InfoCard\" target=\"_blank\" rel=\"noopener\"><span title=\"echa.europa.eu\">ECHA InfoCard<\/span><\/a><\/td>\n<td><a class=\"external text\" href=\"https:\/\/echa.europa.eu\/substance-information\/-\/substanceinfo\/100.004.173\" rel=\"nofollow noopener\" target=\"_blank\">100.004.173<\/a>\u00a0<span class=\"mw-valign-text-top noprint\"><a title=\"Edit this at Wikidata\" href=\"https:\/\/www.wikidata.org\/wiki\/Q418038#P2566\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"mw-file-element\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/8\/8a\/OOjs_UI_icon_edit-ltr-progressive.svg\/10px-OOjs_UI_icon_edit-ltr-progressive.svg.png\" srcset=\"\/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/8\/8a\/OOjs_UI_icon_edit-ltr-progressive.svg\/15px-OOjs_UI_icon_edit-ltr-progressive.svg.png 1.5x, \/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/8\/8a\/OOjs_UI_icon_edit-ltr-progressive.svg\/20px-OOjs_UI_icon_edit-ltr-progressive.svg.png 2x\" alt=\"Edit this at Wikidata\" width=\"10\" height=\"10\" data-file-width=\"20\" data-file-height=\"20\" \/><\/a><\/span><\/td>\n<\/tr>\n<tr>\n<td>\n<div><a title=\"PubChem\" href=\"https:\/\/en.wikipedia.org\/wiki\/PubChem\" target=\"_blank\" rel=\"noopener\">PubChem<\/a>\u00a0<abbr title=\"Compound ID\">CID<\/abbr><\/div>\n<\/td>\n<td>\n<div class=\"plainlist\">\n<ul>\n<li><span title=\"pubchem.ncbi.nlm.nih.gov\"><a class=\"external text\" href=\"https:\/\/pubchem.ncbi.nlm.nih.gov\/compound\/31236\" rel=\"nofollow noopener\" target=\"_blank\">31236<\/a><\/span><\/li>\n<\/ul>\n<\/div>\n<\/td>\n<\/tr>\n<tr>\n<td><a title=\"Unique Ingredient Identifier\" href=\"https:\/\/en.wikipedia.org\/wiki\/Unique_Ingredient_Identifier\" target=\"_blank\" rel=\"noopener\">UNII<\/a><\/td>\n<td>\n<div class=\"plainlist\">\n<ul>\n<li><span title=\"precision.fda.gov\"><a class=\"external text\" href=\"https:\/\/precision.fda.gov\/uniisearch\/srs\/unii\/HIE492ZZ3T\" rel=\"nofollow noopener\" target=\"_blank\">HIE492ZZ3T<\/a><\/span><sup><img loading=\"lazy\" decoding=\"async\" class=\"mw-file-element\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/f\/fb\/Yes_check.svg\/7px-Yes_check.svg.png\" srcset=\"\/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/f\/fb\/Yes_check.svg\/11px-Yes_check.svg.png 1.5x, \/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/f\/fb\/Yes_check.svg\/14px-Yes_check.svg.png 2x\" alt=\"check\" width=\"7\" height=\"7\" data-file-width=\"600\" data-file-height=\"600\" \/><\/sup><\/li>\n<\/ul>\n<\/div>\n<\/td>\n<\/tr>\n<tr>\n<td>\n<div><a title=\"CompTox Chemicals Dashboard\" href=\"https:\/\/en.wikipedia.org\/wiki\/CompTox_Chemicals_Dashboard\" target=\"_blank\" rel=\"noopener\">CompTox Dashboard<\/a>\u00a0(<abbr title=\"U.S. Environmental Protection Agency\">EPA<\/abbr>)<\/div>\n<\/td>\n<td>\n<div class=\"plainlist\">\n<ul>\n<li><span title=\"comptox.epa.gov\"><a class=\"external text\" href=\"https:\/\/comptox.epa.gov\/dashboard\/chemical\/details\/DTXSID9021976\" rel=\"nofollow noopener\" target=\"_blank\">DTXSID9021976<\/a><span class=\"mw-valign-text-top noprint\"><a title=\"Edit this at Wikidata\" href=\"https:\/\/www.wikidata.org\/wiki\/Q418038#P3117\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"mw-file-element\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/8\/8a\/OOjs_UI_icon_edit-ltr-progressive.svg\/10px-OOjs_UI_icon_edit-ltr-progressive.svg.png\" srcset=\"\/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/8\/8a\/OOjs_UI_icon_edit-ltr-progressive.svg\/15px-OOjs_UI_icon_edit-ltr-progressive.svg.png 1.5x, \/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/8\/8a\/OOjs_UI_icon_edit-ltr-progressive.svg\/20px-OOjs_UI_icon_edit-ltr-progressive.svg.png 2x\" alt=\"Edit this at Wikidata\" width=\"10\" height=\"10\" data-file-width=\"20\" data-file-height=\"20\" \/><\/a><\/span><\/span><\/li>\n<\/ul>\n<\/div>\n<\/td>\n<\/tr>\n<tr>\n<td colspan=\"2\">\n<div class=\"collapsible-list mw-collapsible mw-collapsed mw-made-collapsible\"><button class=\"mw-collapsible-toggle mw-collapsible-toggle-default mw-collapsible-toggle-collapsed\" tabindex=\"0\" type=\"button\" aria-expanded=\"false\"><span class=\"mw-collapsible-text\">show<\/span><\/button><\/p>\n<div>\n<div><a title=\"International Chemical Identifier\" href=\"https:\/\/en.wikipedia.org\/wiki\/International_Chemical_Identifier\" target=\"_blank\" rel=\"noopener\">InChI<\/a><\/div>\n<\/div>\n<\/div>\n<\/td>\n<\/tr>\n<tr>\n<td colspan=\"2\">\n<div class=\"collapsible-list mw-collapsible mw-collapsed mw-made-collapsible\"><button class=\"mw-collapsible-toggle mw-collapsible-toggle-default mw-collapsible-toggle-collapsed\" tabindex=\"0\" type=\"button\" aria-expanded=\"false\"><span class=\"mw-collapsible-text\">show<\/span><\/button><\/p>\n<div>\n<div><a title=\"Simplified molecular-input line-entry system\" href=\"https:\/\/en.wikipedia.org\/wiki\/Simplified_molecular-input_line-entry_system\" target=\"_blank\" rel=\"noopener\">SMILES<\/a><\/div>\n<\/div>\n<\/div>\n<\/td>\n<\/tr>\n<tr>\n<th colspan=\"2\">Properties<\/th>\n<\/tr>\n<tr>\n<td>\n<div><a title=\"Chemical formula\" href=\"https:\/\/en.wikipedia.org\/wiki\/Chemical_formula\" target=\"_blank\" rel=\"noopener\">Chemical formula<\/a><\/div>\n<\/td>\n<td><span title=\"Carbon\">C<\/span><sub>8<\/sub><span title=\"Hydrogen\">H<\/span><sub>10<\/sub><span title=\"Oxygen\">O<\/span><sub>2<\/sub><\/td>\n<\/tr>\n<tr>\n<td><a title=\"Molar mass\" href=\"https:\/\/en.wikipedia.org\/wiki\/Molar_mass\" target=\"_blank\" rel=\"noopener\">Molar mass<\/a><\/td>\n<td><span class=\"nowrap\">138.166<\/span>\u00a0g\u00b7mol<sup>\u22121<\/sup><\/td>\n<\/tr>\n<tr>\n<td>Appearance<\/td>\n<td>Colorless oily liquid<\/td>\n<\/tr>\n<tr>\n<td><a title=\"Odor\" href=\"https:\/\/en.wikipedia.org\/wiki\/Odor\" target=\"_blank\" rel=\"noopener\">Odor<\/a><\/td>\n<td>faint rose-like<\/td>\n<\/tr>\n<tr>\n<td><a title=\"Density\" href=\"https:\/\/en.wikipedia.org\/wiki\/Density\" target=\"_blank\" rel=\"noopener\">Density<\/a><\/td>\n<td>1.102 g\/cm<sup>3<\/sup><\/td>\n<\/tr>\n<tr>\n<td><a title=\"Melting point\" href=\"https:\/\/en.wikipedia.org\/wiki\/Melting_point\" target=\"_blank\" rel=\"noopener\">Melting point<\/a><\/td>\n<td>\u22122\u00a0\u00b0C (28\u00a0\u00b0F; 271\u00a0K)<\/td>\n<\/tr>\n<tr>\n<td><a title=\"Boiling point\" href=\"https:\/\/en.wikipedia.org\/wiki\/Boiling_point\" target=\"_blank\" rel=\"noopener\">Boiling point<\/a><\/td>\n<td>247\u00a0\u00b0C (477\u00a0\u00b0F; 520\u00a0K)<\/td>\n<\/tr>\n<tr>\n<td>\n<div><a title=\"Aqueous solution\" href=\"https:\/\/en.wikipedia.org\/wiki\/Aqueous_solution\" target=\"_blank\" rel=\"noopener\">Solubility in water<\/a><\/div>\n<\/td>\n<td>26 g\/kg<\/td>\n<\/tr>\n<tr>\n<td><a title=\"Solubility\" href=\"https:\/\/en.wikipedia.org\/wiki\/Solubility\" target=\"_blank\" rel=\"noopener\">Solubility<\/a><\/td>\n<td><a title=\"Chloroform\" href=\"https:\/\/en.wikipedia.org\/wiki\/Chloroform\" target=\"_blank\" rel=\"noopener\">Chloroform<\/a>,\u00a0<a title=\"Alkali\" href=\"https:\/\/en.wikipedia.org\/wiki\/Alkali\" target=\"_blank\" rel=\"noopener\">Alkali<\/a>,\u00a0<a title=\"Diethyl ether\" href=\"https:\/\/en.wikipedia.org\/wiki\/Diethyl_ether\" target=\"_blank\" rel=\"noopener\">diethyl ether<\/a>: soluble<\/td>\n<\/tr>\n<tr>\n<td><a title=\"Solubility\" href=\"https:\/\/en.wikipedia.org\/wiki\/Solubility\" target=\"_blank\" rel=\"noopener\">Solubility<\/a>\u00a0in\u00a0<a title=\"Peanut oil\" href=\"https:\/\/en.wikipedia.org\/wiki\/Peanut_oil\" target=\"_blank\" rel=\"noopener\">peanut oil<\/a><\/td>\n<td>slightly<\/td>\n<\/tr>\n<tr>\n<td><a title=\"Solubility\" href=\"https:\/\/en.wikipedia.org\/wiki\/Solubility\" target=\"_blank\" rel=\"noopener\">Solubility<\/a>\u00a0in\u00a0<a title=\"Olive oil\" href=\"https:\/\/en.wikipedia.org\/wiki\/Olive_oil\" target=\"_blank\" rel=\"noopener\">olive oil<\/a><\/td>\n<td>slightly<\/td>\n<\/tr>\n<tr>\n<td><a title=\"Solubility\" href=\"https:\/\/en.wikipedia.org\/wiki\/Solubility\" target=\"_blank\" rel=\"noopener\">Solubility<\/a>\u00a0in\u00a0<a title=\"Acetone\" href=\"https:\/\/en.wikipedia.org\/wiki\/Acetone\" target=\"_blank\" rel=\"noopener\">acetone<\/a><\/td>\n<td>miscible<\/td>\n<\/tr>\n<tr>\n<td><a title=\"Solubility\" href=\"https:\/\/en.wikipedia.org\/wiki\/Solubility\" target=\"_blank\" rel=\"noopener\">Solubility<\/a>\u00a0in\u00a0<a title=\"Ethanol\" href=\"https:\/\/en.wikipedia.org\/wiki\/Ethanol\" target=\"_blank\" rel=\"noopener\">ethanol<\/a><\/td>\n<td>miscible<\/td>\n<\/tr>\n<tr>\n<td><a title=\"Solubility\" href=\"https:\/\/en.wikipedia.org\/wiki\/Solubility\" target=\"_blank\" rel=\"noopener\">Solubility<\/a>\u00a0in\u00a0<a title=\"Glycerol\" href=\"https:\/\/en.wikipedia.org\/wiki\/Glycerol\" target=\"_blank\" rel=\"noopener\">glycerol<\/a><\/td>\n<td>miscible<\/td>\n<\/tr>\n<tr>\n<td><a title=\"Vapor pressure\" href=\"https:\/\/en.wikipedia.org\/wiki\/Vapor_pressure\" target=\"_blank\" rel=\"noopener\">Vapor pressure<\/a><\/td>\n<td>0.001\u00a0kPa (0.00015\u00a0psi)<\/td>\n<\/tr>\n<tr>\n<td><a title=\"Thermal conductivity\" href=\"https:\/\/en.wikipedia.org\/wiki\/Thermal_conductivity\" target=\"_blank\" rel=\"noopener\">Thermal conductivity<\/a><\/td>\n<td>0.169 W\/(m\u22c5K)<\/td>\n<\/tr>\n<tr>\n<td>\n<div><a title=\"Refractive index\" href=\"https:\/\/en.wikipedia.org\/wiki\/Refractive_index\" target=\"_blank\" rel=\"noopener\">Refractive index<\/a>\u00a0(<i>n<\/i><sub>D<\/sub>)<\/div>\n<\/td>\n<td>1.534 (20 \u00b0C)<\/td>\n<\/tr>\n<tr>\n<th colspan=\"2\"><\/th>\n<\/tr>\n<tr>\n<td colspan=\"2\"><b><a title=\"Occupational safety and health\" href=\"https:\/\/en.wikipedia.org\/wiki\/Occupational_safety_and_health\" target=\"_blank\" rel=\"noopener\">Occupational safety and health<\/a><\/b>\u00a0(OHS\/OSH):<\/td>\n<\/tr>\n<tr>\n<td>\n<div>Main hazards<\/div>\n<\/td>\n<td>Harmful if swallowed<br \/>\nCauses serious eye irritation<\/td>\n<\/tr>\n<tr>\n<td colspan=\"2\"><a title=\"Globally Harmonized System of Classification and Labelling of Chemicals\" href=\"https:\/\/en.wikipedia.org\/wiki\/Globally_Harmonized_System_of_Classification_and_Labelling_of_Chemicals\" target=\"_blank\" rel=\"noopener\"><b>GHS<\/b>\u00a0labelling<\/a>:<\/td>\n<\/tr>\n<tr>\n<td>\n<div><a title=\"GHS hazard pictograms\" href=\"https:\/\/en.wikipedia.org\/wiki\/GHS_hazard_pictograms\" target=\"_blank\" rel=\"noopener\">Pictograms<\/a><\/div>\n<\/td>\n<td><a class=\"mw-file-description\" title=\"GHS07: Exclamation mark\" href=\"https:\/\/en.wikipedia.org\/wiki\/File:GHS-pictogram-exclam.svg\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"mw-file-element\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/c\/c3\/GHS-pictogram-exclam.svg\/50px-GHS-pictogram-exclam.svg.png\" srcset=\"\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/c\/c3\/GHS-pictogram-exclam.svg\/75px-GHS-pictogram-exclam.svg.png 1.5x, \/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/c\/c3\/GHS-pictogram-exclam.svg\/100px-GHS-pictogram-exclam.svg.png 2x\" alt=\"GHS07: Exclamation mark\" width=\"50\" height=\"50\" data-file-width=\"512\" data-file-height=\"512\" \/><\/a><\/td>\n<\/tr>\n<tr>\n<td>\n<div><a title=\"Globally Harmonized System of Classification and Labelling of Chemicals\" href=\"https:\/\/en.wikipedia.org\/wiki\/Globally_Harmonized_System_of_Classification_and_Labelling_of_Chemicals#Signal_word\" target=\"_blank\" rel=\"noopener\">Signal word<\/a><\/div>\n<\/td>\n<td><b>Warning<\/b><\/td>\n<\/tr>\n<tr>\n<td><a title=\"NFPA 704\" href=\"https:\/\/en.wikipedia.org\/wiki\/NFPA_704\" target=\"_blank\" rel=\"noopener\"><b>NFPA 704<\/b><\/a>\u00a0(fire\u00a0diamond)<\/td>\n<td>\n<div class=\"nfpa-704-diamond\">\n<div class=\"nfpa-704-diamond-container\">\n<div class=\"nfpa-704-diamond-images nounderlines\">\n<div class=\"nfpa-704-diamond-map\">\n<figure class=\"noresize\"><img loading=\"lazy\" decoding=\"async\" class=\"mw-file-element\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/6\/6f\/NFPA_704.svg\/80px-NFPA_704.svg.png\" srcset=\"\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/6\/6f\/NFPA_704.svg\/120px-NFPA_704.svg.png 1.5x, \/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/6\/6f\/NFPA_704.svg\/160px-NFPA_704.svg.png 2x\" alt=\"NFPA 704 four-colored diamond\" usemap=\"#ImageMap_d51ef1fd76621882\" width=\"80\" height=\"80\" data-file-width=\"512\" data-file-height=\"512\" \/><\/p>\n<map name=\"ImageMap_d51ef1fd76621882\">\n<area title=\"Health 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gas\" alt=\"Health 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gas\" coords=\"23,23,47,47,23,70,0,47\" shape=\"poly\" href=\"https:\/\/en.wikipedia.org\/wiki\/NFPA_704#Blue\" \/>\n<area title=\"Flammability 1: Must be pre-heated before ignition can occur. Flash point over 93 \u00b0C (200 \u00b0F). E.g. canola oil\" alt=\"Flammability 1: Must be pre-heated before ignition can occur. Flash point over 93 \u00b0C (200 \u00b0F). E.g. canola oil\" coords=\"47,0,70,23,47,47,23,23\" shape=\"poly\" href=\"https:\/\/en.wikipedia.org\/wiki\/NFPA_704#Red\" \/>\n<area title=\"Instability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogen\" alt=\"Instability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogen\" coords=\"70,23,94,47,70,70,47,47\" shape=\"poly\" href=\"https:\/\/en.wikipedia.org\/wiki\/NFPA_704#Yellow\" \/>\n<area title=\"Special hazards (white): no code\" alt=\"Special hazards (white): no code\" coords=\"47,47,70,70,47,94,23,70\" shape=\"poly\" href=\"https:\/\/en.wikipedia.org\/wiki\/NFPA_704#White\" \/><\/map>\n<\/figure>\n<\/div>\n<div class=\"nfpa-704-diamond-code nfpa-704-diamond-blue\"><a title=\"NFPA 704\" href=\"https:\/\/en.wikipedia.org\/wiki\/NFPA_704#Blue\" target=\"_blank\" rel=\"noopener\"><span title=\"Health 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gas\">3<\/span><\/a><\/div>\n<div class=\"nfpa-704-diamond-code nfpa-704-diamond-red\"><a title=\"NFPA 704\" href=\"https:\/\/en.wikipedia.org\/wiki\/NFPA_704#Red\" target=\"_blank\" rel=\"noopener\"><span title=\"Flammability 1: Must be pre-heated before ignition can occur. Flash point over 93 \u00b0C (200 \u00b0F). E.g. canola oil\">1<\/span><\/a><\/div>\n<div class=\"nfpa-704-diamond-code nfpa-704-diamond-yellow\"><a title=\"NFPA 704\" href=\"https:\/\/en.wikipedia.org\/wiki\/NFPA_704#Yellow\" target=\"_blank\" rel=\"noopener\"><span title=\"Instability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogen\">0<\/span><\/a><\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/td>\n<\/tr>\n<tr>\n<td><a title=\"Flash point\" href=\"https:\/\/en.wikipedia.org\/wiki\/Flash_point\" target=\"_blank\" rel=\"noopener\">Flash point<\/a><\/td>\n<td>126\u00a0\u00b0C (259\u00a0\u00b0F; 399\u00a0K)<\/td>\n<\/tr>\n<tr>\n<td>\n<div><a title=\"Autoignition temperature\" href=\"https:\/\/en.wikipedia.org\/wiki\/Autoignition_temperature\" target=\"_blank\" rel=\"noopener\">Autoignition<br \/>\ntemperature<\/a><\/div>\n<\/td>\n<td>430\u00a0\u00b0C (806\u00a0\u00b0F; 703\u00a0K)<\/td>\n<\/tr>\n<tr>\n<td colspan=\"2\"><b>Lethal dose<\/b>\u00a0or concentration (LD, LC):<\/td>\n<\/tr>\n<tr>\n<td>\n<div>LD<sub>50<\/sub>\u00a0(<a title=\"Lethal dose\" href=\"https:\/\/en.wikipedia.org\/wiki\/Lethal_dose#LD50\" target=\"_blank\" rel=\"noopener\">median dose<\/a>)<\/div>\n<\/td>\n<td>1850 mg\/kg (rat, oral)<\/td>\n<\/tr>\n<tr>\n<th colspan=\"2\">Related compounds<\/th>\n<\/tr>\n<tr>\n<td>\n<div>Related compounds<\/div>\n<\/td>\n<td><a class=\"mw-redirect\" title=\"Phenetole\" href=\"https:\/\/en.wikipedia.org\/wiki\/Phenetole\" target=\"_blank\" rel=\"noopener\">phenetole<\/a><\/td>\n<\/tr>\n<tr>\n<td colspan=\"2\">\n<div>Except where otherwise noted, data are given for materials in their\u00a0<a title=\"Standard state\" href=\"https:\/\/en.wikipedia.org\/wiki\/Standard_state\" target=\"_blank\" rel=\"noopener\">standard state<\/a>\u00a0(at 25\u00a0\u00b0C [77\u00a0\u00b0F], 100\u00a0kPa).<\/div>\n<div>\n<div><img loading=\"lazy\" decoding=\"async\" class=\"mw-file-element\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/a\/a2\/X_mark.svg\/12px-X_mark.svg.png\" srcset=\"\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/a\/a2\/X_mark.svg\/18px-X_mark.svg.png 1.5x, \/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/a\/a2\/X_mark.svg\/24px-X_mark.svg.png 2x\" alt=\"\u2612\" width=\"12\" height=\"14\" data-file-width=\"525\" data-file-height=\"600\" \/>\u00a0<span class=\"reflink plainlinks nourlexpansion\"><a class=\"external text\" href=\"https:\/\/en.wikipedia.org\/w\/index.php?title=Special:ComparePages&amp;rev1=464200667&amp;page2=Phenoxyethanol\" target=\"_blank\" rel=\"noopener\">verify<\/a><\/span>\u00a0(<a title=\"Wikipedia:WikiProject Chemicals\/Chembox validation\" href=\"https:\/\/en.wikipedia.org\/wiki\/Wikipedia:WikiProject_Chemicals\/Chembox_validation\" target=\"_blank\" rel=\"noopener\">what is<\/a>\u00a0<sup><img loading=\"lazy\" decoding=\"async\" class=\"mw-file-element\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/f\/fb\/Yes_check.svg\/7px-Yes_check.svg.png\" srcset=\"\/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/f\/fb\/Yes_check.svg\/11px-Yes_check.svg.png 1.5x, \/\/upload.wikimedia.org\/wikipedia\/en\/thumb\/f\/fb\/Yes_check.svg\/14px-Yes_check.svg.png 2x\" alt=\"check\" width=\"7\" height=\"7\" data-file-width=\"600\" data-file-height=\"600\" \/><img loading=\"lazy\" decoding=\"async\" class=\"mw-file-element\" src=\"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/a\/a2\/X_mark.svg\/7px-X_mark.svg.png\" srcset=\"\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/a\/a2\/X_mark.svg\/11px-X_mark.svg.png 1.5x, \/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/a\/a2\/X_mark.svg\/14px-X_mark.svg.png 2x\" alt=\"\u2612\" width=\"7\" height=\"8\" data-file-width=\"525\" data-file-height=\"600\" \/><\/sup>\u00a0?)<\/div>\n<\/div>\n<div><a title=\"Wikipedia:Chemical infobox\" href=\"https:\/\/en.wikipedia.org\/wiki\/Wikipedia:Chemical_infobox#References\" target=\"_blank\" rel=\"noopener\">Infobox references<\/a><\/div>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><b>Phenoxyethanol<\/b>\u00a0is the\u00a0<a title=\"Organic compound\" href=\"https:\/\/en.wikipedia.org\/wiki\/Organic_compound\" target=\"_blank\" rel=\"noopener\">organic compound<\/a>\u00a0with the formula C<sub>6<\/sub>H<sub>5<\/sub>OC<sub>2<\/sub>H<sub>4<\/sub>OH. It is a colorless oily liquid. It can be classified as a\u00a0<a class=\"mw-redirect\" title=\"Glycol ether\" href=\"https:\/\/en.wikipedia.org\/wiki\/Glycol_ether\" target=\"_blank\" rel=\"noopener\">glycol ether<\/a>\u00a0and a\u00a0<a title=\"Phenol ether\" href=\"https:\/\/en.wikipedia.org\/wiki\/Phenol_ether\" target=\"_blank\" rel=\"noopener\">phenol ether<\/a>. It is a common preservative in vaccine formulations.<sup id=\"cite_ref-4\" class=\"reference\"><a href=\"https:\/\/en.wikipedia.org\/wiki\/Phenoxyethanol#cite_note-4\" target=\"_blank\" rel=\"noopener\">[4]<\/a><\/sup><\/p>\n<h2><span id=\"Use\" class=\"mw-headline\">Use<\/span><span class=\"mw-editsection\"><span class=\"mw-editsection-bracket\">[<\/span><a title=\"Edit section: Use\" href=\"https:\/\/en.wikipedia.org\/w\/index.php?title=Phenoxyethanol&amp;action=edit&amp;section=1\" target=\"_blank\" rel=\"noopener\">edit<\/a><span class=\"mw-editsection-bracket\">]<\/span><\/span><\/h2>\n<p>Phenoxyethanol has\u00a0<a class=\"mw-redirect\" title=\"Germicidal\" href=\"https:\/\/en.wikipedia.org\/wiki\/Germicidal\" target=\"_blank\" rel=\"noopener\">germicidal<\/a>\u00a0and\u00a0<a title=\"Bacteriostatic agent\" href=\"https:\/\/en.wikipedia.org\/wiki\/Bacteriostatic_agent\" target=\"_blank\" rel=\"noopener\">germistatic<\/a>\u00a0properties.<sup id=\"cite_ref-5\" class=\"reference\"><a href=\"https:\/\/en.wikipedia.org\/wiki\/Phenoxyethanol#cite_note-5\" target=\"_blank\" rel=\"noopener\">[5]<\/a><\/sup>\u00a0It is often used together with\u00a0<a class=\"mw-redirect\" title=\"Quaternary ammonium compound\" href=\"https:\/\/en.wikipedia.org\/wiki\/Quaternary_ammonium_compound\" target=\"_blank\" rel=\"noopener\">quaternary ammonium compounds<\/a>.<\/p>\n<p>Phenoxyethanol is used as a\u00a0<a title=\"Fixative (perfumery)\" href=\"https:\/\/en.wikipedia.org\/wiki\/Fixative_(perfumery)\" target=\"_blank\" rel=\"noopener\">perfume fixative<\/a>; an\u00a0<a title=\"Insect repellent\" href=\"https:\/\/en.wikipedia.org\/wiki\/Insect_repellent\" target=\"_blank\" rel=\"noopener\">insect repellent<\/a>; an\u00a0<a title=\"Antiseptic\" href=\"https:\/\/en.wikipedia.org\/wiki\/Antiseptic\" target=\"_blank\" rel=\"noopener\">antiseptic<\/a>;<sup id=\"cite_ref-6\" class=\"reference\"><a href=\"https:\/\/en.wikipedia.org\/wiki\/Phenoxyethanol#cite_note-6\" target=\"_blank\" rel=\"noopener\">[6]<\/a><\/sup>\u00a0a\u00a0<a title=\"Solvent\" href=\"https:\/\/en.wikipedia.org\/wiki\/Solvent\" target=\"_blank\" rel=\"noopener\">solvent<\/a>\u00a0for\u00a0<a title=\"Cellulose acetate\" href=\"https:\/\/en.wikipedia.org\/wiki\/Cellulose_acetate\" target=\"_blank\" rel=\"noopener\">cellulose acetate<\/a>, dyes, inks, and resins; a preservative for pharmaceuticals, cosmetics and lubricants;<sup id=\"cite_ref-7\" class=\"reference\"><a href=\"https:\/\/en.wikipedia.org\/wiki\/Phenoxyethanol#cite_note-7\" target=\"_blank\" rel=\"noopener\">[7]<\/a><\/sup>\u00a0an\u00a0<a title=\"Anesthetic\" href=\"https:\/\/en.wikipedia.org\/wiki\/Anesthetic\" target=\"_blank\" rel=\"noopener\">anesthetic<\/a>\u00a0in fish aquaculture;<sup id=\"cite_ref-8\" class=\"reference\"><a href=\"https:\/\/en.wikipedia.org\/wiki\/Phenoxyethanol#cite_note-8\" target=\"_blank\" rel=\"noopener\">[8]<\/a><\/sup><sup id=\"cite_ref-9\" class=\"reference\"><a href=\"https:\/\/en.wikipedia.org\/wiki\/Phenoxyethanol#cite_note-9\" target=\"_blank\" rel=\"noopener\">[9]<\/a><\/sup>\u00a0and in\u00a0<a title=\"Organic synthesis\" href=\"https:\/\/en.wikipedia.org\/wiki\/Organic_synthesis\" target=\"_blank\" rel=\"noopener\">organic synthesis<\/a>.<\/p>\n<p>Phenoxyethanol is an alternative to\u00a0<a title=\"Formaldehyde releaser\" href=\"https:\/\/en.wikipedia.org\/wiki\/Formaldehyde_releaser\" target=\"_blank\" rel=\"noopener\">formaldehyde-releasing preservatives<\/a>.<sup id=\"cite_ref-10\" class=\"reference\"><a href=\"https:\/\/en.wikipedia.org\/wiki\/Phenoxyethanol#cite_note-10\" target=\"_blank\" rel=\"noopener\">[10]<\/a><\/sup>\u00a0In Japan and the European Union, its concentration in cosmetics is restricted to 1%.<sup id=\"cite_ref-11\" class=\"reference\"><a href=\"https:\/\/en.wikipedia.org\/wiki\/Phenoxyethanol#cite_note-11\" target=\"_blank\" rel=\"noopener\">[11]<\/a><\/sup><\/p>\n<\/div>\n<p><strong>contact. 03154497759.\u00a0 \u00a0 \u00a003074568939<\/strong><\/p>\n<\/div>\n<\/div>\n<p><\/main><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Phenoxy ethanol, other name ethelene glycol mono phenyl ether,\u00a0Phenoxy ethanol is a preservative used in many cosmetics and personal care products. In perfumes, fragrances, soaps, and cleansers, phenoxy ethanol works as a stabilizer. In other cosmetics, it\u2019s used as an antibacterial and\/or a preservative to prevent products from losing their potency or spoiling<\/p>\n<p><strong>contact. 03154497759.\u00a0 \u00a0 \u00a003074568939<\/strong><\/p>\n","protected":false},"featured_media":7181,"comment_status":"open","ping_status":"closed","template":"","meta":{"_acf_changed":false},"product_brand":[],"product_cat":[73,32,37],"product_tag":[],"class_list":{"0":"post-7180","1":"product","2":"type-product","3":"status-publish","4":"has-post-thumbnail","6":"product_cat-raw-materials","7":"product_cat-essential-oils","8":"product_cat-soap","10":"first","11":"instock","12":"shipping-taxable","13":"product-type-simple"},"acf":[],"_links":{"self":[{"href":"https:\/\/pakistan-cosmetics.com\/index.php\/wp-json\/wp\/v2\/product\/7180","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pakistan-cosmetics.com\/index.php\/wp-json\/wp\/v2\/product"}],"about":[{"href":"https:\/\/pakistan-cosmetics.com\/index.php\/wp-json\/wp\/v2\/types\/product"}],"replies":[{"embeddable":true,"href":"https:\/\/pakistan-cosmetics.com\/index.php\/wp-json\/wp\/v2\/comments?post=7180"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/pakistan-cosmetics.com\/index.php\/wp-json\/wp\/v2\/media\/7181"}],"wp:attachment":[{"href":"https:\/\/pakistan-cosmetics.com\/index.php\/wp-json\/wp\/v2\/media?parent=7180"}],"wp:term":[{"taxonomy":"product_brand","embeddable":true,"href":"https:\/\/pakistan-cosmetics.com\/index.php\/wp-json\/wp\/v2\/product_brand?post=7180"},{"taxonomy":"product_cat","embeddable":true,"href":"https:\/\/pakistan-cosmetics.com\/index.php\/wp-json\/wp\/v2\/product_cat?post=7180"},{"taxonomy":"product_tag","embeddable":true,"href":"https:\/\/pakistan-cosmetics.com\/index.php\/wp-json\/wp\/v2\/product_tag?post=7180"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}