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<!--Generated by Squarespace V5 Site Server v5.13.546-352 (http://www.squarespace.com) on Mon, 23 Sep 2019 20:26:04 GMT--><rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:rss="http://purl.org/rss/1.0/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:sy="http://purl.org/rss/1.0/modules/syndication/" xmlns:admin="http://webns.net/mvcb/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:cc="http://web.resource.org/cc/"><rss:channel rdf:about="http://chemicaloftheday.squarespace.com/todays-chemical/"><rss:title>*Today's Chemical</rss:title><rss:link>http://chemicaloftheday.squarespace.com/todays-chemical/</rss:link><rss:description></rss:description><dc:language>en-US</dc:language><dc:date>2019-09-23T20:26:04Z</dc:date><admin:generatorAgent rdf:resource="http://www.squarespace.com/">Squarespace V5 Site Server v5.13.546-352 (http://www.squarespace.com)</admin:generatorAgent><rss:items><rdf:Seq><rdf:li rdf:resource="http://chemicaloftheday.squarespace.com/todays-chemical/2016/4/14/12-hexylene-glycol.html"/><rdf:li rdf:resource="http://chemicaloftheday.squarespace.com/todays-chemical/2016/4/5/sodium-coceth-sulfate.html"/><rdf:li rdf:resource="http://chemicaloftheday.squarespace.com/todays-chemical/2016/3/15/peg-100-stearate.html"/><rdf:li rdf:resource="http://chemicaloftheday.squarespace.com/todays-chemical/2016/3/3/propanediol.html"/><rdf:li rdf:resource="http://chemicaloftheday.squarespace.com/todays-chemical/2014/9/29/methylisothiazolinone.html"/><rdf:li rdf:resource="http://chemicaloftheday.squarespace.com/todays-chemical/2014/8/25/trolamine.html"/><rdf:li rdf:resource="http://chemicaloftheday.squarespace.com/todays-chemical/2014/8/25/guar-hydroxypropyltrimonium-chloride.html"/><rdf:li rdf:resource="http://chemicaloftheday.squarespace.com/todays-chemical/2014/8/13/potassium-sorbate.html"/><rdf:li rdf:resource="http://chemicaloftheday.squarespace.com/todays-chemical/2014/8/5/benzisothiazolinone.html"/><rdf:li rdf:resource="http://chemicaloftheday.squarespace.com/todays-chemical/2014/6/10/selenium-sulfide.html"/></rdf:Seq></rss:items></rss:channel><rss:item rdf:about="http://chemicaloftheday.squarespace.com/todays-chemical/2016/4/14/12-hexylene-glycol.html"><rss:title>1,2-Hexylene Glycol</rss:title><rss:link>http://chemicaloftheday.squarespace.com/todays-chemical/2016/4/14/12-hexylene-glycol.html</rss:link><dc:creator>[Stephanie Greenwood]</dc:creator><dc:date>2016-04-14T11:47:14Z</dc:date><dc:subject></dc:subject><content:encoded><![CDATA[<p><strong>Today's Chemical:</strong></p>
<p>1,2-Hexylene Glycol</p>
<p><strong>EWG Risk Score:</strong></p>
<p><a href="https://www.ewg.org/skindeep/ingredient/702849/HEXYLENE_GLYCOL/">1</a></p>
<p><strong>What is it?</strong></p>
<p>1,2-Hexylene glycol is a chemical relative to the more-known propylene glycol. It's a clear viscous liquid used as a humectant, filler, thickener, and conditioning agent.&nbsp;</p>
<p><strong>What are its risks?&nbsp;</strong></p>
<p>
<ul>
<li>1,2-Hexylene glycol is a penetration enhancer, meaning that it has the ability to cross the skin's barrier and also bring other chemicals in to the body. (<a href="http://www.alegesanatos.ro/dbimg/files/1,2-Glycols.pdf">Source</a>)</li>
<li>While it's considered to have a low-toxicity (ie it doesn't make you sick or immediately kill you upon ingestion) it is broken down in the body through oxidation, a process that releases free radicals. (<a href="http://www.alegesanatos.ro/dbimg/files/1,2-Glycols.pdf">Source</a>)</li>
<li>1,2-Hexylene glycol can be a skin irritant. (<a href="https://www.ewg.org/skindeep/ingredient/702849/HEXYLENE_GLYCOL/">Source</a>)&nbsp;</li>
</ul>
</p>
<p><strong>Bottom line:&nbsp;</strong></p>
<p>While 1,2-Hexylene glycol isn't acutely toxic, it certainly isn't a beneficial ingredient that would nourish or benefit the body in any way, and only creates free radical damage as its absorbed in the body and broken down.&nbsp;</p>]]></content:encoded></rss:item><rss:item rdf:about="http://chemicaloftheday.squarespace.com/todays-chemical/2016/4/5/sodium-coceth-sulfate.html"><rss:title>Sodium Coceth Sulfate</rss:title><rss:link>http://chemicaloftheday.squarespace.com/todays-chemical/2016/4/5/sodium-coceth-sulfate.html</rss:link><dc:creator>[Stephanie Greenwood]</dc:creator><dc:date>2016-04-05T13:56:45Z</dc:date><dc:subject></dc:subject><content:encoded><![CDATA[<p><strong>Today's Chemical:</strong></p>
<p>Sodium Coceth Sulfate</p>
<p><strong>EWG Risk Score:</strong></p>
<p><a href="http://www.ewg.org/skindeep/ingredient/706030/SODIUM_COCETH_SULFATE/">1</a> (Should be higher)</p>
<p><strong>What is it?</strong></p>
<p>Sodium coceth sulfate is a surfactant/detergent similar to sodium laureth sulfate. Instead of isolated lauric acid (used in sodium laureth sulfate) it uses the full spectrum of coconut fatty acids.</p>
<p><strong>What are its risks?</strong>&nbsp;</p>
<ul>
<li>Sodium coceth sulfate is created with the carcinogen ethylene oxide, traces of which and its carcinogenic by-product 1,4-dioxane can remain in the finished product.&nbsp;</li>
</ul>
<ul>
<li>Generally milder, but a potential irritant. (<a href="https://www.ncbi.nlm.nih.gov/pubmed/20634505">Source</a>)</li>
</ul>
<ul>
</ul>
<p><strong>Bottom line:</strong></p>
<p>Sodium coceth sulfate is to sodium laureth sulfate as sodium coco sulfate is to sodium lauryl sulfate. Sodium coceth sulfate may be more gentle on skin than sodium laureth sulfate, but it poses the same contamination risks. &nbsp;</p>]]></content:encoded></rss:item><rss:item rdf:about="http://chemicaloftheday.squarespace.com/todays-chemical/2016/3/15/peg-100-stearate.html"><rss:title>PEG-100 Stearate</rss:title><rss:link>http://chemicaloftheday.squarespace.com/todays-chemical/2016/3/15/peg-100-stearate.html</rss:link><dc:creator>[Stephanie Greenwood]</dc:creator><dc:date>2016-03-15T16:53:47Z</dc:date><dc:subject></dc:subject><content:encoded><![CDATA[<p><strong>Today's Chemical:</strong></p>
<p>PEG -100 stearate</p>
<p><strong>EWG Risk Score:</strong></p>
<p><a href="http://www.ewg.org/skindeep/ingredient/721388/PEG-100_STEARATE/">3</a></p>
<p><strong>What is it?</strong></p>
<p>PEG-100 stearate, also known as polywax, is used primarily as an emulsifier in cosmetics and foods.&nbsp;</p>
<p><strong>What are its risks?</strong>&nbsp;</p>
<ul>
<li>PEG-100 stearate is an ethoxylated chemical, meaning that it's been created using the carcinogen ethylene oxide, traces of which, and its carcinogenic by-product 1-4,dioxane can remain in the product.&nbsp;</li>
</ul>
<ul>
<li>Can be a skin irritant when used on broken skin. (<strong>Source</strong>)</li>
</ul>
<p><strong>Bottom line:</strong></p>
<p>May be listed as "made from coconut" but don't believe that this ingredient is "natural."&nbsp;</p>
<p>&nbsp;</p>
<p>&nbsp;</p>]]></content:encoded></rss:item><rss:item rdf:about="http://chemicaloftheday.squarespace.com/todays-chemical/2016/3/3/propanediol.html"><rss:title>Propanediol</rss:title><rss:link>http://chemicaloftheday.squarespace.com/todays-chemical/2016/3/3/propanediol.html</rss:link><dc:creator>[Stephanie Greenwood]</dc:creator><dc:date>2016-03-03T12:51:27Z</dc:date><dc:subject></dc:subject><content:encoded><![CDATA[<p><strong>Today's Chemical:</strong></p>
<p>Propanediol</p>
<p><span class="ssNonEditable full-image-block"><strong>EWG Risk Score:</strong></span></p>
<p><a href="http://www.ewg.org/skindeep/ingredient/723043/PROPANEDIOL/">1</a></p>
<p><strong>What is it?</strong></p>
<p><strong></strong>Propanediol is a clear, thick liquid used in formulas to control viscosity. Also known as 1,3 propylene glycol, it is an isomer of the more widely-used chemical, propylene glycol.&nbsp;</p>
<p><strong>Is it a risk?</strong></p>
<p>Propanediol does not appear to pose any significant risks when used diluted in a cosmetic formula, based on current research. However, the manufacturing of propanediol does pose potential environmental and health concerns. It can be produced from acrolein, a compound found in cigarette smoke that may contribute to lung cancer. (<a href="http://www.pnas.org/content/103/42/15404.full.pdf">Source</a>) While this wouldn't pose a risk in the finished product of propanediol, there may be exposures to workers and the environment, especially if produced in countries with less-than-stringent working and environmental regulations.&nbsp;</p>
<p>You may also see propanediol created from "natural" sources. The most widely-distributed form is made by DuPont Chemical, created from (most likely GMO) corn syrup and a genetically-modified strain of e coli bacteria. (<a href="http://brew.geo.uu.nl/BREWsymposiumWiesbaden11mei2005/WEBSITEBrewPresentations51105.PDF">Source</a>)</p>
<p>It can also be produced from fermenting glycerol with genetically modified bacteria. (<a href="https://www.ncbi.nlm.nih.gov/pubmed/10531640">Source</a>)</p>
<p>Can be a skin allergen. (<a href="https://www.ncbi.nlm.nih.gov/pubmed/23474444">Source</a>)</p>
<p><strong>Steph's Opinion:</strong></p>
<p>Propanediol as a finished ingredient doesn't pose significant health risks unless you have an allergy to the ingredient. However, when you see propanediol in a product marketed as "natural," think GMOs because it has most likely been created with either genetically-modified bacteria or from GMO corn (or both.)&nbsp;</p>]]></content:encoded></rss:item><rss:item rdf:about="http://chemicaloftheday.squarespace.com/todays-chemical/2014/9/29/methylisothiazolinone.html"><rss:title>Methylisothiazolinone</rss:title><rss:link>http://chemicaloftheday.squarespace.com/todays-chemical/2014/9/29/methylisothiazolinone.html</rss:link><dc:creator>[Stephanie Greenwood]</dc:creator><dc:date>2014-09-30T02:59:44Z</dc:date><dc:subject></dc:subject><content:encoded><![CDATA[<p><strong>Today's Chemical:</strong></p>
<p>Methylisothiazolinone</p>
<p><span class="full-image-block ssNonEditable"><strong>EWG Risk Score:</strong></span></p>
<p><a href="http://www.cosmeticsdatabase.com/ingredient/703935/METHYLISOTHIAZOLINONE/ ">6</a></p>
<p><strong>What is it?</strong></p>
<p><strong></strong>Methylisothiazolinone &nbsp;is a synthetic cosmetic preservative.</p>
<p><strong>Why is it a risk?</strong></p>
<ul>
<li>Methylisothiazolinone is a known&nbsp;neurotoxin.&nbsp; In 2004, the European Scientific Committee on Cosmetic Products and Non-Food Products Intended for Consumers (SCCNFP)&nbsp;suggested that companies limit the&nbsp;maximum concentration to 0.01% (100 ppm).&nbsp; However, US companies are not required to follow this guideline.</li>
</ul>
<ul>
<li>It is known to be absorbed through skin.&nbsp; A study at the Pittsburgh School of Medicine concluded that "Prolonged exposure to low levels of MIT and related compounds may have damaging consequences to the developing nervous system."&nbsp;</li>
</ul>
<ul>
<li>Is a developmental toxin. &nbsp;(<a href="http://www.ncbi.nlm.nih.gov/pubmed/22245758">Source</a>)&nbsp;</li>
</ul>
<ul>
<li>Is a known contact allergen. &nbsp;(<a href="http://www.ncbi.nlm.nih.gov/pubmed/21901563">Source</a>)</li>
</ul>
<p><strong>Steph's Opinion:</strong></p>
<p>Although concentrations of this ingredient are typically very low in a formulation, I personally suggest avoiding this ingredient.&nbsp;</p>]]></content:encoded></rss:item><rss:item rdf:about="http://chemicaloftheday.squarespace.com/todays-chemical/2014/8/25/trolamine.html"><rss:title>Trolamine</rss:title><rss:link>http://chemicaloftheday.squarespace.com/todays-chemical/2014/8/25/trolamine.html</rss:link><dc:creator>[Stephanie Greenwood]</dc:creator><dc:date>2014-08-25T22:59:27Z</dc:date><dc:subject></dc:subject><content:encoded><![CDATA[<p>Trolamine is another name for Triethanolamine, or TEA, which you can read about <a href="http://chemicaloftheday.squarespace.com/todays-chemical/2009/10/24/triethanolamine-tea-or-teoa.html?SSScrollPosition=273">here</a>.</p>]]></content:encoded></rss:item><rss:item rdf:about="http://chemicaloftheday.squarespace.com/todays-chemical/2014/8/25/guar-hydroxypropyltrimonium-chloride.html"><rss:title>Guar Hydroxypropyltrimonium Chloride</rss:title><rss:link>http://chemicaloftheday.squarespace.com/todays-chemical/2014/8/25/guar-hydroxypropyltrimonium-chloride.html</rss:link><dc:creator>[Stephanie Greenwood]</dc:creator><dc:date>2014-08-25T22:57:40Z</dc:date><dc:subject></dc:subject><content:encoded><![CDATA[<p>No data available for this ingredient. It is, however, a quaternary ammonium compound, a class of chemicals used commonly in conditioners and other hair products to impart "slip." You can read about this class of chemicals&nbsp;<a href="http://chemicaloftheday.squarespace.com/most-controversial/2011/8/31/quaternary-ammonium-compounds.html">here</a>.&nbsp;</p>]]></content:encoded></rss:item><rss:item rdf:about="http://chemicaloftheday.squarespace.com/todays-chemical/2014/8/13/potassium-sorbate.html"><rss:title>Potassium Sorbate</rss:title><rss:link>http://chemicaloftheday.squarespace.com/todays-chemical/2014/8/13/potassium-sorbate.html</rss:link><dc:creator>[Stephanie Greenwood]</dc:creator><dc:date>2014-08-13T18:23:20Z</dc:date><dc:subject></dc:subject><content:encoded><![CDATA[<p><strong>EWG Risk Score:</strong></p>
<p><a href="http://www.ewg.org/skindeep/ingredient/705225/POTASSIUM_SORBATE/">3</a></p>
<p><strong>What is it?</strong></p>
<p>Potassium sorbate is the potassium salt of sorbic acid and is used as a preservative in cosmetic items as well as food.&nbsp;</p>
<p><strong>What are its risks:</strong></p>
<ul>
<li>Potassium sorbate can cause allergic reaction in repeated high amounts or in certain individuals. (<a href="http://www.ncbi.nlm.nih.gov/pubmed/22570031">Source</a>)</li>
<li>Can be a skin or eye irritant when used in high concentrations.</li>
<li>Found to be genotoxic to human lymphocytes. In other words, it has been found to alter or destroy the DNA within human white blood cells. (<a href="http://www.ncbi.nlm.nih.gov/pubmed/20036729">Source</a>)</li>
<li>Derived from petroleum (<a href="http://standards.nsf.org/apps/group_public/download.php/23627/OPC-2014-4%20-%20Potassium%20Sorbate.pdf">Source</a>) This itself doesn't make it harmful, unless there are impurities that are not filtered out in processing (polyaromatic hydrocarbons.)&nbsp;</li>
</ul>
<p><strong>Steph's Opinion:&nbsp;</strong></p>
<p>Potassium sorbate has longbeen considered one of the "safer" options when it comes to preservatives, with the biggest risk it was thought to carry being potential for allergy. However, with new information shedding light on its genotoxicity, it is now on my "avoid" list. &nbsp;</p>
<p><iframe width="640" height="390" src="http://chemicaloftheday.squarespace.com//www.youtube.com/embed/5mKik9sVHKc" frameborder="0" allowfullscreen></iframe></p>]]></content:encoded></rss:item><rss:item rdf:about="http://chemicaloftheday.squarespace.com/todays-chemical/2014/8/5/benzisothiazolinone.html"><rss:title>Benzisothiazolinone</rss:title><rss:link>http://chemicaloftheday.squarespace.com/todays-chemical/2014/8/5/benzisothiazolinone.html</rss:link><dc:creator>[Stephanie Greenwood]</dc:creator><dc:date>2014-08-05T18:14:00Z</dc:date><dc:subject></dc:subject><content:encoded><![CDATA[<p><strong>Today's Chemical:</strong></p>
<p>Benzisothiazolinone</p>
<p><strong>EWG Risk Score:</strong></p>
<p><a href="http://www.ewg.org/skindeep/ingredient/716930/BENZISOTHIAZOLINONE/">3-4</a></p>
<p><strong>What is it?</strong></p>
<p>Beznisothiazolinone is used in cosmetic items as a preservative. It is used on an industrial level as a biocide on buildings (to kill fungus on roofs and buildings) as well as a preservative in paints and cleaning products.&nbsp;</p>
<p><strong>What type of products is it found in?</strong></p>
<p>Hand wash, sunblock, air freshener</p>
<p><strong>What are its risks?</strong></p>
<ul>
<li>Has been found that when used in air freshener products, benzisothiazolinone is cytotoxic to lung cells, creating free radical damage to these cells. (<a href="http://www.ncbi.nlm.nih.gov/pubmed/24273871">Source</a>)</li>
<li>Exposure can lead to allergic contact dermatitis and skin sensitization. (<a href="http://www.ncbi.nlm.nih.gov/pubmed/23429043">Source</a>)</li>
<li>The Scientific Committee on Consumer Safety (EU) has advised that it not be used in personal care items due to lack of data as well as its potential for skin sensitization. (<a href="http://ec.europa.eu/health/scientific_committees/consumer_safety/docs/sccs_o_099.pdf">Source</a>)</li>
<li>Animal studies have observed reproductive effects when administered orally at high doses. (Concentrations in household/personal care products are thought not to be high enough to have an effect on human reproduction, however.) (<a href="http://ec.europa.eu/health/scientific_committees/consumer_safety/docs/sccs_o_099.pdf">Source</a>)</li>
</ul>]]></content:encoded></rss:item><rss:item rdf:about="http://chemicaloftheday.squarespace.com/todays-chemical/2014/6/10/selenium-sulfide.html"><rss:title>Selenium Sulfide</rss:title><rss:link>http://chemicaloftheday.squarespace.com/todays-chemical/2014/6/10/selenium-sulfide.html</rss:link><dc:creator>[Stephanie Greenwood]</dc:creator><dc:date>2014-06-10T16:10:20Z</dc:date><dc:subject></dc:subject><content:encoded><![CDATA[<p><strong>Today's Chemical:</strong><br />Selenium Sulfide<br /><br /><strong>EWG Risk Score:</strong><br /><a href="http://www.ewg.org/skindeep/ingredient/705878/SELENIUM_SULFIDE/">8</a><br /><br /><strong>What is it?</strong><br />This selenium compound is used as a hair conditioning and anti-dandruff agent.</p>
<p><strong>What type of products is it found in?</strong><br />Shampoos and conditioners</p>
<p><br /><strong>Why is it a risk?</strong></p>
<ul>
<li>Selenium sulfide is a suspected carcinogen. (<a href="http://oehha.ca.gov/prop65/policy_procedure/pdf_zip/Feb2001StatRpt.pdf">Source</a>)(<a href="http://www.epa.gov/iris/subst/0458.htm">Source</a>)</li>
<li>Considered by OSHA to be a hazardous material. (<a href="http://www.ecfr.gov/cgi-bin/text-idx?SID=08c968b099a77798be76dd386b13e959&amp;node=29:6.1.1.1.1&amp;rgn=div5">Source</a>)</li>
<li>Respiratory toxin / dust breathing hazard. (<a href="http://nj.gov/health/eoh/rtkweb/documents/fs/1653.pdf">Source</a>)</li>
<li>Some selenium compounds have been found to be reproductive toxins, that may affect fertility in women and development of fetuses. (<a href="http://nj.gov/health/eoh/rtkweb/documents/fs/1653.pdf">Source</a>)&nbsp;</li>
<li>"Repeated exposure can cause pallor, nervousness, and mood changes." (<a href="http://nj.gov/health/eoh/rtkweb/documents/fs/1653.pdf">Source</a>)</li>
<li>May cause damage to liver and kidneys. (<a href="http://nj.gov/health/eoh/rtkweb/documents/fs/1653.pdf">Source</a>)&nbsp;</li>
</ul>]]></content:encoded></rss:item></rdf:RDF>