{"id":727,"date":"2011-01-24T16:47:00","date_gmt":"2011-01-24T16:47:00","guid":{"rendered":"https:\/\/psiconautica.org\/wordpress\/?p=727"},"modified":"2022-01-31T12:14:54","modified_gmt":"2022-01-31T12:14:54","slug":"piperine","status":"publish","type":"post","link":"https:\/\/psiconautica.org\/wordpress\/quimica-avanzada\/piperine\/","title":{"rendered":"Piperonal from pepper"},"content":{"rendered":"<h3 align=\"left\">Piperonal from pepper<\/h3>\n<p align=\"left\">CAS: [94-62-2]<\/p>\n<p>M( C17H19NO3 ) = 285.34 g\/mol<\/p>\n<p>mp 130\u00b0C<\/p>\n<p>piperine [merck index]<\/p>\n<p>piperin [roempp]<\/p>\n<p>piperine [beilstein\/crossfire]<\/p>\n<p>piperinum [kad]<\/p>\n<p>determination of piperine &#8230; by TLC and UV absorption &#8230; [30]<\/p>\n<p>piperine forms a solid complex with 1,3,5-trinitrobenzene in a ratio 1:1,<br \/>\nin the form of red needles, mp 130\u00b0C. [06, page 235]<\/p>\n<p>IR analysis of piperine in black pepper [20]<\/p>\n<p>further references: piperine<\/p>\n<h3>References<\/h3>\n<p>[merck index]<br \/>\nTHE MERCK INDEX on CD-ROM \/ Version 12:3 \/ 1999<\/p>\n<p>[roempp]<br \/>\nroempp lexikon chemie version 2.0, cd-rom,<br \/>\nstuttgart \/ new york: georg thieme verlag 1999<\/p>\n<p>[beilstein\/crossfire]<br \/>\n<a href=\"http:\/\/www.mimas.ac.uk\/crossfire\/\" target=\"_blank\" rel=\"noopener noreferrer\">http:\/\/www.mimas.ac.uk\/crossfire\/<\/a><\/p>\n<p>[pubmed]<br \/>\n<a href=\"http:\/\/www.ncbi.nlm.nih.gov\/entrez\/query.fcgi?db=PubMed\" target=\"_blank\" rel=\"noopener noreferrer\">http:\/\/www.ncbi.nlm.nih.gov\/entrez\/query.fcgi?db=PubMed<\/a><\/p>\n<p>[kad]<br \/>\n<a href=\"http:\/\/www.ibiblio.org\/herbmed\/eclectic\/kings\/main.html\" target=\"_blank\" rel=\"noopener noreferrer\">king&#8217;s american dispensatory<\/a> 1898<br \/>\nm d harvey wickes felter, phr m ph d john uri lloyd<\/p>\n<p>[06]<br \/>\n<strong>\u00abnatural products &#8211; a laboratory guide\u00bb<\/strong> 2.edition 1991<br \/>\nraphael ikan; academic press, inc; ISBN 0-12-370551-7<\/p>\n<p>[20]<br \/>\n<a href=\"IR.analysis.piperine.pepper.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">IR Analysis of Piperine in Black Pepper<\/a><br \/>\nhttp:\/\/www.terrificscience.org\/lessonexchange\/PACTPDF\/PiperineAnalysis.pdf<\/p>\n<p>[30]<br \/>\nchromatogr 1985 338(1): 259-63<br \/>\n<strong>\u00abdetermination of piperine in biological tissues by thin-layer<br \/>\nchromatography and ultraviolet absorption densitometry.\u00bb<\/strong><br \/>\nbg bhat, n chandrasekhara<br \/>\n[<a href=\"#pubmed\">pubmed<\/a>, PMID: <a href=\"http:\/\/www.ncbi.nlm.nih.gov\/htbin-post\/Entrez\/query?db=m&amp;form=6&amp;Dopt=r&amp;uid=4019654\" target=\"_blank\" rel=\"noopener noreferrer\">4019654<\/a>]<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Piperonal from pepper CAS: [94-62-2] M( C17H19NO3 ) = 285.34 g\/mol mp 130\u00b0C piperine [merck index] piperin [roempp] piperine [beilstein\/crossfire] piperinum [kad] determination of piperine &#8230; by TLC and UV absorption &#8230; [30] piperine forms a solid complex with 1,3,5-trinitrobenzene in a ratio 1:1, in the form of red needles, mp 130\u00b0C. [06, page 235] [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":1644,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[24],"tags":[],"class_list":["post-727","post","type-post","status-publish","format-standard","has-post-thumbnail","category-quimica-avanzada"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Piperonal from pepper - Psicon\u00e1utica<\/title>\n<meta name=\"robots\" content=\"noindex, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Piperonal from pepper - Psicon\u00e1utica\" \/>\n<meta property=\"og:description\" content=\"Piperonal from pepper CAS: [94-62-2] M( C17H19NO3 ) = 285.34 g\/mol mp 130\u00b0C piperine [merck index] piperin [roempp] piperine [beilstein\/crossfire] piperinum [kad] determination of piperine &#8230; by TLC and UV absorption &#8230; [30] piperine forms a solid complex with 1,3,5-trinitrobenzene in a ratio 1:1, in the form of red needles, mp 130\u00b0C. 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