{"id":11520,"date":"2022-11-28T04:28:21","date_gmt":"2022-11-27T20:28:21","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=11520"},"modified":"2022-11-28T04:28:21","modified_gmt":"2022-11-27T20:28:21","slug":"lakhey-nivruttis-team-published-research-in-journal-of-chemical-technology-and-biotechnology-in-95-cas-930-36-9","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=11520","title":{"rendered":"Lakhey, Nivrutti&#8217;s team published research in Journal of Chemical Technology and Biotechnology  in 95 | CAS: 930-36-9"},"content":{"rendered":"<p>Lakhey, Nivrutti published the artcile<b><i>Toxicity of azoles towards the anaerobic ammonium oxidation (anammox) process<\/i><\/b>,  <a href=\"https:\/\/www.ambeed.com\/products\/930-36-9.html\">Safety of 1-Methylpyrazole<\/a>,  the publication is  Journal of Chemical Technology and Biotechnology (2020), 95(4), 1057-1063, database is CAplus.<\/p>\n<p>Azoles are an important class of compounds that are widely used as corrosion inhibitors in aircraft de-icing agents, cooling towers, semiconductor manufacturing and household dishwashing detergents. They also are important moieties in pharmaceutical drugs and fungicides. Azoles are widespread emerging contaminants occurring frequently in water bodies. Azole compounds can potentially cause inhibition towards key biol. processes in natural ecosystems and wastewater treatment processes. Of particular concern is the inhibition of azoles to the nitrification process (aerobic oxidation of ammonium). This study investigated the acute toxicity of azole compounds towards the anaerobic ammonia oxidation (anammox) process, which is an important environmental biotechnol. gaining traction for nutrient-nitrogen removal during wastewater treatment. In this study, using batch bioassay techniques, the anammox toxicity of eight commonly occurring azole compounds was evaluated. The results show that 1H-benzotriazole and 5-methyl-1H-benzotriazole had the highest inhibitory effect on the anammox process, causing 50% decrease in anammox activity (IC<sub>50<\/sub>) at concentrations of 19.6 and 17.8 mg L<sup>-1<\/sup>, resp. 1H-imidazole caused less severe toxicity with an IC<sub>50<\/sub> of 79.4 mg L<sup>-1<\/sup>. The other azole compounds were either nontoxic (1H-pyrazole, 1H-1,2,4-triazole and 1-methyl-pyrazole) or at best mildly toxic (1H-benzotriazole-5-carboxylic acid and 3,5-dimethyl-1H-pyrazole) towards the anammox bacteria at the concentrations tested. This study showed that most azole compounds tested displayed mild to low or no toxicity towards the anammox bacteria. The anammox bacteria were found to be far less sensitive to azoles compared to nitrifying bacteria.<\/p>\n<p>Journal of Chemical Technology and Biotechnology published new progress about 930-36-9. 930-36-9 belongs to pyrazoles-derivatives, auxiliary class Pyrazole, name is 1-Methylpyrazole, and the molecular formula is C4H6N2, <a href=\"https:\/\/www.ambeed.com\/products\/930-36-9.html\">Safety of 1-Methylpyrazole<\/a>.<\/p>\n<p>Referemce:<br \/><a href=\"https:\/\/en.wikipedia.org\/wiki\/Pyrazole\">https:\/\/en.wikipedia.org\/wiki\/Pyrazole<\/a>,<br \/><a href=\"Pyrazole - Wikipedia\">Pyrazoles &#8211; an overview | ScienceDirect Topics<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Journal of Chemical Technology and Biotechnology published new progress about 930-36-9. 930-36-9 belongs to pyrazoles-derivatives, auxiliary class Pyrazole, name is 1-Methylpyrazole, and the molecular formula is C4H6N2, <a href=\"https:\/\/www.ambeed.com\/products\/930-36-9.html\">Safety of 1-Methylpyrazole<\/a>.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[245,131],"tags":[784],"class_list":["post-11520","post","type-post","status-publish","format-standard","hentry","category-930-36-9","category-pyrazoles-derivatives","tag-m-w50-100"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - 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Pyrazole derivatives play an important role in antitumor agents.\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"http:\/\/www.pyrazoles-derivatives.com\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Person\",\"@id\":\"http:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1\",\"name\":\"Jessica.F\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"http:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/image\/\",\"url\":\"https:\/\/en.cravatar.com\/avatar\/2d1cec2a99eeaad5a5b217c9cdbfb610?s=96&d=mm&r=g\",\"contentUrl\":\"https:\/\/en.cravatar.com\/avatar\/2d1cec2a99eeaad5a5b217c9cdbfb610?s=96&d=mm&r=g\",\"caption\":\"Jessica.F\"}}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Lakhey, Nivrutti's team published research in Journal of Chemical Technology and Biotechnology in 95 | CAS: 930-36-9 | pyrazoles-derivatives","description":"Lakhey, Nivrutti published the artcileToxicity of azoles towards the anaerobic ammonium oxidation (anammox) process, Safety of 1-Methylpyrazole, the publication is Journal of Chemical Technology and Biotechnology (2020), 95(4), 1057-1063, database is CAplus.","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"http:\/\/www.pyrazoles-derivatives.com\/?p=11520","og_locale":"en_US","og_type":"article","og_title":"Lakhey, Nivrutti's team published research in Journal of Chemical Technology and Biotechnology in 95 | CAS: 930-36-9 | pyrazoles-derivatives","og_description":"Lakhey, Nivrutti published the artcileToxicity of azoles towards the anaerobic ammonium oxidation (anammox) process, Safety of 1-Methylpyrazole, the publication is Journal of Chemical Technology and Biotechnology (2020), 95(4), 1057-1063, database is CAplus.","og_url":"http:\/\/www.pyrazoles-derivatives.com\/?p=11520","og_site_name":"pyrazoles-derivatives","article_published_time":"2022-11-27T20:28:21+00:00","author":"Jessica.F","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Jessica.F","Est. reading time":"2 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"http:\/\/www.pyrazoles-derivatives.com\/?p=11520","url":"http:\/\/www.pyrazoles-derivatives.com\/?p=11520","name":"Lakhey, Nivrutti's team published research in Journal of Chemical Technology and Biotechnology in 95 | CAS: 930-36-9 | pyrazoles-derivatives","isPartOf":{"@id":"http:\/\/www.pyrazoles-derivatives.com\/#website"},"datePublished":"2022-11-27T20:28:21+00:00","author":{"@id":"http:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1"},"description":"Lakhey, Nivrutti published the artcileToxicity of azoles towards the anaerobic ammonium oxidation (anammox) process, Safety of 1-Methylpyrazole, the publication is Journal of Chemical Technology and Biotechnology (2020), 95(4), 1057-1063, database is CAplus.","breadcrumb":{"@id":"http:\/\/www.pyrazoles-derivatives.com\/?p=11520#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["http:\/\/www.pyrazoles-derivatives.com\/?p=11520"]}]},{"@type":"BreadcrumbList","@id":"http:\/\/www.pyrazoles-derivatives.com\/?p=11520#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"\u9996\u9875","item":"http:\/\/www.pyrazoles-derivatives.com\/"},{"@type":"ListItem","position":2,"name":"Lakhey, Nivrutti&#8217;s team published research in Journal of Chemical Technology and Biotechnology in 95 | CAS: 930-36-9"}]},{"@type":"WebSite","@id":"http:\/\/www.pyrazoles-derivatives.com\/#website","url":"http:\/\/www.pyrazoles-derivatives.com\/","name":"pyrazoles-derivatives","description":"Several pyrazole derivatives possess important pharmacological activities and they have been proved useful materials in drug research. 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