{"query":{"product_cat":"agrochemical-reference-standards"},"query_vars":{"product_cat":"agrochemical-reference-standards","error":"","m":"","p":0,"post_parent":"","subpost":"","subpost_id":"","attachment":"","attachment_id":0,"name":"","pagename":"","page_id":0,"second":"","minute":"","hour":"","day":0,"monthnum":0,"year":0,"w":0,"category_name":"","tag":"","cat":"","tag_id":"","author":"","author_name":"","feed":"","tb":"","paged":0,"meta_key":"","meta_value":"","preview":"","s":"","sentence":"","title":"","fields":"all","menu_order":"","embed":"","category__in":[],"category__not_in":[],"category__and":[],"post__in":[],"post__not_in":[],"post_name__in":[],"tag__in":[],"tag__not_in":[],"tag__and":[],"tag_slug__in":[],"tag_slug__and":[],"post_parent__in":[],"post_parent__not_in":[],"author__in":[],"author__not_in":[],"search_columns":[],"orderby":"menu_order title","order":"ASC","meta_query":[],"tax_query":{"relation":"AND","0":{"taxonomy":"product_visibility","field":"term_taxonomy_id","terms":[36],"operator":"NOT IN"}},"wc_query":"product_query","posts_per_page":12,"ignore_sticky_posts":false,"suppress_filters":false,"cache_results":true,"update_post_term_cache":true,"update_menu_item_cache":false,"lazy_load_term_meta":true,"update_post_meta_cache":true,"post_type":"","nopaging":false,"comments_per_page":"50","no_found_rows":false,"taxonomy":"product_cat","term":"agrochemical-reference-standards"},"tax_query":{"queries":{"relation":"AND","0":{"taxonomy":"product_visibility","terms":[36],"field":"term_taxonomy_id","operator":"NOT IN","include_children":true},"1":{"taxonomy":"product_cat","terms":["agrochemical-reference-standards"],"field":"slug","operator":"IN","include_children":true}},"relation":"AND","queried_terms":{"product_cat":{"terms":["agrochemical-reference-standards"],"field":"slug"}},"primary_table":"wp_posts","primary_id_column":"ID"},"meta_query":{"queries":[],"relation":null,"meta_table":null,"meta_id_column":null,"primary_table":null,"primary_id_column":null},"date_query":false,"queried_object":{"term_id":99,"name":"Agrochemical Standards","slug":"agrochemical-reference-standards","term_group":0,"term_taxonomy_id":99,"taxonomy":"product_cat","description":"","parent":0,"count":48,"filter":"raw"},"queried_object_id":99,"request":"SELECT SQL_CALC_FOUND_ROWS wp_posts.ID\n\t\t\t\t\t FROM wp_posts LEFT JOIN wp_term_relationships ON (wp_posts.ID = wp_term_relationships.object_id)\n\t\t\t\t\t WHERE 1=1 AND ( \n wp_posts.ID NOT IN (\n\t\t\t\tSELECT object_id\n\t\t\t\tFROM wp_term_relationships\n\t\t\t\tWHERE term_taxonomy_id IN (36)\n\t\t\t) \n AND \n wp_term_relationships.term_taxonomy_id IN (99,100,107,109,110,111)\n) AND ((wp_posts.post_type = 'product' AND (wp_posts.post_status = 'publish')))\n\t\t\t\t\t GROUP BY wp_posts.ID\n\t\t\t\t\t ORDER BY wp_posts.menu_order ASC, wp_posts.post_title ASC\n\t\t\t\t\t LIMIT 0, 12","posts":[{"ID":5066,"post_author":"5","post_date":"2023-11-16 09:30:22","post_date_gmt":"2023-11-16 09:30:22","post_content":"Azadirachta indica <\/em><\/a>is commonly referred to as the neem tree or simply neem. It serves as a rich source for triterpenoids (limonoids). Limonoids are of profound interest to humans due to their diverse medicinal properties, including antioxidant, anti-inflammatory, and anticancer activities. 14,15-Epoxyazadiradione (CAS 58525-91-0) is a naturally occurring metabolite isolated from A. indica<\/em>. It is one of the 11 major limonoids found in neem extracts. Oils extracted from neem fruits and seeds are used as one of the most popular natural insecticides, miticides, and fungicides. Moreover, in traditional medicine, all parts of the neem tree were utilized for treatment of inflammation, infections, fevers, skin diseases, and dental disorders.\r\n\r\nNeem reference standards are broken up into two classes, azadirachtin and non-azadirachtin neem limonoids. The list of the most common standards includes: Azadirachtin A, Azadirachtin B, Azadirachtin D, Azadirachtin H, Azadiradione, 14,15-Epoxyazadiradione, Nimbin, Salannin, 3-Deacetylsalannin, 6-Deacetylnimbin, and Ohchinolide. You can follow this link<\/a> for our entire collection of neem reference standards.","post_title":"14,15-Epoxyazadiradione","post_excerpt":"[wc_measurement_price_calculator_pricing_table]","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"epoxyazadiradione","to_ping":"","pinged":"","post_modified":"2026-03-20 16:53:21","post_modified_gmt":"2026-03-20 20:53:21","post_content_filtered":"","post_parent":0,"guid":"http:\/\/159.69.28.184\/product\/1415-epoxyazadiradione-2\/","menu_order":0,"post_type":"product","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":5057,"post_author":"5","post_date":"2023-11-16 09:30:18","post_date_gmt":"2023-11-16 09:30:18","post_content":"3-Deacetylsalannin (CAS 1110-56-1) is a naturally occurring metabolite isolated from <\/span>A. indica<\/em>.\u00a0<\/span>Azadirachta indica <\/em><\/a>is commonly referred to as the neem tree or simply neem. It serves as a rich source for triterpenoids (limonoids). Limonoids are of profound interest to humans due to their diverse medicinal properties, including antioxidant, anti-inflammatory, and anticancer activities. It is one of the 11 major limonoids found in neem extracts. Oils extracted from neem fruits and seeds are used as one of the most popular natural insecticides, miticides, and fungicides. Moreover, in traditional medicine, all parts of the neem tree were utilized for treatment of inflammation, infections, fevers, skin diseases, and dental disorders.\r\n\r\nNeem reference standards are broken up into two classes, azadirachtin and non-azadirachtin neem limonoids. The list of the most common standards includes: Azadirachtin A, Azadirachtin B, Azadirachtin D, Azadirachtin H, Azadiradione, 14,15 Epoxyazadiradione, Nimbin, Salannin, 3-Deacetylsalannin, 6-Deacetylnimbin, and Ohchinolide. You can follow this link<\/a> for our entire collection of neem reference standards.","post_title":"3-deacetylsalannin","post_excerpt":"[wc_measurement_price_calculator_pricing_table]","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"3-deacetylsalannin","to_ping":"","pinged":"","post_modified":"2026-03-20 16:59:42","post_modified_gmt":"2026-03-20 20:59:42","post_content_filtered":"","post_parent":0,"guid":"http:\/\/159.69.28.184\/product\/3-deacetylsalannin\/","menu_order":0,"post_type":"product","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":5078,"post_author":"7","post_date":"2023-11-16 09:30:27","post_date_gmt":"2023-11-16 09:30:27","post_content":"4-OH-8a-Oxo-Avermectin B1a is one of the Avermectin soil metabolites monitored by regulatory bodies. Avermectins are a group of 16-membered macrocyclic lactone derivatives with potent anthelmintic and insecticidal properties. These naturally occurring compounds are generated as fermentation products of the soil actinomycete Streptomyces avermitilis<\/em>. In invertebrates, avermectins effect the nerve and muscle cells by enhancing the effects of glutamate and the glutamate-gated chloride channel. This results in an in influx of chloride ions and subsequent paralysis of the invertebrate.\r\n\r\nAvermectins<\/a> are isolated in four pairs of homologous compounds (A1, A2, B1, B2). Avermectin B1 comprises Avermectin B1a and Avermectin B2a and is marketed as abamectin. 4-OH-8a-Oxo-Avermectin B1a is one of several soil metabolites resulting from avermectin B1a degradation. This standard, along with our other avermectin metabolite reference standards, are used to monitor fate of avermectin products in soil in the presence of microbes and exposure to sunlight. Please find the entire collection here<\/a>.\r\n\r\n ","post_title":"4-OH-8a-Oxo-Avermectin B1a","post_excerpt":"[wc_measurement_price_calculator_pricing_table]","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"4-oh-8a-oxo-avermectin-b1a","to_ping":"","pinged":"","post_modified":"2026-03-20 16:59:54","post_modified_gmt":"2026-03-20 20:59:54","post_content_filtered":"","post_parent":0,"guid":"http:\/\/159.69.28.184\/product\/4-oh-8a-oxo-avermectin-b1a\/","menu_order":0,"post_type":"product","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":5079,"post_author":"5","post_date":"2023-11-16 09:30:28","post_date_gmt":"2023-11-16 09:30:28","post_content":"4,8a-diOH-Avermectin B1a\u00a0is one of the Avermectin soil metabolites monitored by regulatory bodies. Avermectins are a group of 16-membered macrocyclic lactone derivatives with potent anthelmintic and insecticidal properties. These naturally occurring compounds are generated as fermentation products of the soil actinomycete Streptomyces avermitilis<\/em>. In invertebrates, avermectins effect the nerve and muscle cells by enhancing the effects of glutamate and the glutamate-gated chloride channel. This results in an in influx of chloride ions and subsequent paralysis of the invertebrate.\r\n\r\nAvermectins<\/a> are isolated in four pairs of homologous compounds (A1, A2, B1, B2). Avermectin B1 comprises Avermectin B1a and Avermectin B2a and is marketed as abamectin. 4,8a-diOH-Avermectin B1a is one of several soil metabolites resulting from avermectin B1a degradation. This standard, along with our other avermectin metabolite reference standards, are used to monitor fate of avermectin products in soil in the presence of microbes and exposure to sunlight. Please find the entire collection here<\/a>.\r\n\r\n ","post_title":"4,8a-diOH-Avermectin B1a","post_excerpt":"[wc_measurement_price_calculator_pricing_table]","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"48a-dioh-avermectin-b1a","to_ping":"","pinged":"","post_modified":"2026-03-20 17:00:17","post_modified_gmt":"2026-03-20 21:00:17","post_content_filtered":"","post_parent":0,"guid":"http:\/\/159.69.28.184\/product\/48a-dioh-avermectin-b1a\/","menu_order":0,"post_type":"product","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":5046,"post_author":"7","post_date":"2023-11-16 09:30:07","post_date_gmt":"2023-11-16 09:30:07","post_content":"4\"-Oxo-Avermectin B1a is one of the Avermectin soil metabolites monitored by regulatory bodies. Avermectins are a group of 16-membered macrocyclic lactone derivatives with potent anthelmintic and insecticidal properties. These naturally occurring compounds are generated as fermentation products of the soil actinomycete Streptomyces avermitilis<\/em>. In invertebrates, avermectins effect the nerve and muscle cells by enhancing the effects of glutamate and the glutamate-gated chloride channel. This results in an in influx of chloride ions and subsequent paralysis of the invertebrate.\r\n\r\nAvermectins<\/a> are isolated in four pairs of homologous compounds (A1, A2, B1, B2). Avermectin B1 comprises Avermectin B1a and Avermectin B2a and is marketed as abamectin. 4\"-Oxo-Avermectin B1a is one of several soil metabolites resulting from avermectin B1a degradation. This standard, along with our other avermectin metabolite reference standards, are used to monitor fate of avermectin products in soil in the presence of microbes and exposure to sunlight. Please find the entire collection here<\/a>.\r\n\r\n ","post_title":"4\"-Oxo-Avermectin B1a","post_excerpt":"[wc_measurement_price_calculator_pricing_table]","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"4-oxo-avermectin-b1a","to_ping":"","pinged":"","post_modified":"2026-03-20 17:00:26","post_modified_gmt":"2026-03-20 21:00:26","post_content_filtered":"","post_parent":0,"guid":"http:\/\/159.69.28.184\/product\/4-oxo-avermectin-b1a\/","menu_order":0,"post_type":"product","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":5058,"post_author":"5","post_date":"2023-11-16 09:30:19","post_date_gmt":"2023-11-16 09:30:19","post_content":"Azadirachta indica <\/em><\/a>is commonly referred to as the neem tree or simply neem. It serves as a rich source for triterpenoids (limonoids). Limonoids are of profound interest to humans due to their diverse medicinal properties, including antioxidant, anti-inflammatory, and anticancer activities. 6-deacetylnimbin (CAS 18609-16-0) is a naturally occurring metabolite isolated from A. indica<\/em>. It is one of the 11 major limonoids found in neem extracts. Oils extracted from neem fruits and seeds are used as one of the most popular natural insecticides, miticides, and fungicides. Moreover, in traditional medicine, all parts of the neem tree were utilized for treatment of inflammation, infections, fevers, skin diseases, and dental disorders.\r\n\r\nNeem reference standards are broken up into two classes, azadirachtin and non-azadirachtin neem limonoids. The list of the most common standards includes: Azadirachtin A, Azadirachtin B, Azadirachtin D, Azadirachtin H, Azadiradione, 14,15 Epoxyazadiradione, Nimbin, Salannin, 3-deacaetylsalnnin, 6-deacetylnimbin, and Ohchinolide. You can follow this link<\/a> for our entire collection of neem reference standards.","post_title":"6-deacetylnimbin","post_excerpt":"[wc_measurement_price_calculator_pricing_table]","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"6-deacetylnimbin","to_ping":"","pinged":"","post_modified":"2026-03-20 17:00:55","post_modified_gmt":"2026-03-20 21:00:55","post_content_filtered":"","post_parent":0,"guid":"http:\/\/159.69.28.184\/product\/6-deacetylnimbin\/","menu_order":0,"post_type":"product","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":5080,"post_author":"7","post_date":"2023-11-16 09:30:28","post_date_gmt":"2023-11-16 09:30:28","post_content":"8,9-Z-Avermectin B1a is one of the Avermectin soil metabolites monitored by regulatory bodies. Avermectins are a group of 16-membered macrocyclic lactone derivatives with potent anthelmintic and insecticidal properties. These naturally occurring compounds are generated as fermentation products of the soil actinomycete Streptomyces avermitilis<\/em>. In invertebrates, avermectins effect the nerve and muscle cells by enhancing the effects of glutamate and the glutamate-gated chloride channel. This results in an in influx of chloride ions and subsequent paralysis of the invertebrate.\r\n\r\nAvermectins<\/a> are isolated in four pairs of homologous compounds (A1, A2, B1, B2). Avermectin B1 comprises Avermectin B1a and Avermectin B2a and is marketed as abamectin. 8,9-Z-Avermectin B1a is one of several soil metabolites resulting from avermectin B1a degradation. This standard, along with our other avermectin metabolite reference standards, are used to monitor fate of avermectin products in soil in the presence of microbes and exposure to sunlight. Please find the entire collection here<\/a>.\r\n\r\n ","post_title":"8,9-Z-Avermectin B1a","post_excerpt":"[wc_measurement_price_calculator_pricing_table]","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"89-z-avermectin-b1a","to_ping":"","pinged":"","post_modified":"2026-03-20 17:01:36","post_modified_gmt":"2026-03-20 21:01:36","post_content_filtered":"","post_parent":0,"guid":"http:\/\/159.69.28.184\/product\/89-z-avermectin-b1a\/","menu_order":0,"post_type":"product","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":10080,"post_author":"3","post_date":"2026-01-16 16:12:24","post_date_gmt":"2026-01-16 21:12:24","post_content":"<\/span>\r\n
\r\n
\r\n
\r\n
8,9 Z Methylamino Avermectin B1a, also known as 8,9 Z Emamectin B1a, is used in agrochemical residue analysis, method validation, and environmental fate research. The isomer forms when emamectin B1a undergoes UV driven conversion, making it essential for laboratories that monitor real world residue profiles.<\/p>\r\n
Regulatory residue definitions often include emamectin B1a, B1b, and their 8,9 isomers, which increases the need for accurate quantification. A reliable 8,9 Z MAB1a reference standard supports compliance focused residue chemistry, stability studies, and multi residue method development across agricultural and environmental testing programs.<\/p>\r\n
The compound retains the 16 membered macrocyclic lactone scaffold characteristic of avermectins. It originates from Streptomyces avermitilis fermentation followed by semi synthetic installation of the methylamino group. The 8,9 Z configuration appears as an isomerization product that laboratories track in soil, plant, and complex environmental matrices.<\/p>\r\n
Emamectin related compounds act on glutamate gated chloride channels in invertebrates, increasing chloride influx and disrupting neurotransmission. This mode of action explains the neuromuscular paralysis seen in susceptible pests and supports the importance of monitoring emamectin isomers in environmental risk assessments.<\/p>\r\n
Related emamectin and avermectin standards, impurities, and metabolites are available to support QC and comparability studies. <\/span>View the related products <\/span>here<\/a>.<\/span><\/p>\r\n\r\n<\/div>\r\n<\/div>\r\n<\/div>","post_title":"8,9-Z-Methylamino Avermectin b1a","post_excerpt":"[wc_measurement_price_calculator_pricing_table]","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"8-9-z-methylamino-avermectin-b1a","to_ping":"","pinged":"","post_modified":"2026-03-20 16:06:35","post_modified_gmt":"2026-03-20 20:06:35","post_content_filtered":"","post_parent":0,"guid":"https:\/\/plantaanalytica.com\/?post_type=product&p=10080","menu_order":0,"post_type":"product","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":5044,"post_author":"7","post_date":"2023-11-16 09:30:06","post_date_gmt":"2023-11-16 09:30:06","post_content":"8a-OH-Avermectin B1a is one of the Avermectin soil metabolites monitored by regulatory bodies. Avermectins are a group of 16-membered macrocyclic lactone derivatives with potent anthelmintic and insecticidal properties. These naturally occurring compounds are generated as fermentation products of the soil actinomycete Streptomyces avermitilis<\/em>. In invertebrates, avermectins effect the nerve and muscle cells by enhancing the effects of glutamate and the glutamate-gated chloride channel. This results in an in influx of chloride ions and subsequent paralysis of the invertebrate.\r\n\r\nAvermectins<\/a> are isolated in four pairs of homologous compounds (A1, A2, B1, B2). Avermectin B1 comprises Avermectin B1a and Avermectin B2a and is marketed as abamectin. 8a-OH-Avermectin B1a is one of several soil metabolites resulting from avermectin B1a degradation. This standard, along with our other avermectin metabolite reference standards, are used to monitor fate of avermectin products in soil in the presence of microbes and exposure to sunlight. Please find the entire collection here<\/a>.\r\n\r\n \r\n\r\n ","post_title":"8a-OH-Avermectin B1a","post_excerpt":"[wc_measurement_price_calculator_pricing_table]","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"8a-hydroxy-avermectin-b1a","to_ping":"","pinged":"","post_modified":"2024-03-28 12:07:14","post_modified_gmt":"2024-03-28 16:07:14","post_content_filtered":"","post_parent":0,"guid":"http:\/\/159.69.28.184\/product\/8a-hydroxy-avermectin-b1a\/","menu_order":0,"post_type":"product","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":5045,"post_author":"7","post_date":"2023-11-16 09:30:07","post_date_gmt":"2023-11-16 09:30:07","post_content":"8a-Oxo-Avermectin B1a is one of the Avermectin soil metabolites monitored by regulatory bodies. Avermectins are a group of 16-membered macrocyclic lactone derivatives with potent anthelmintic and insecticidal properties. These naturally occurring compounds are generated as fermentation products of the soil actinomycete Streptomyces avermitilis<\/em>. In invertebrates, avermectins effect the nerve and muscle cells by enhancing the effects of glutamate and the glutamate-gated chloride channel. This results in an in influx of chloride ions and subsequent paralysis of the invertebrate.\r\n\r\nAvermectins<\/a> are isolated in four pairs of homologous compounds (A1, A2, B1, B2). Avermectin B1 comprises Avermectin B1a and Avermectin B2a and is marketed as abamectin. 8a-Oxo-Avermectin B1a is one of several soil metabolites resulting from avermectin B1a degradation. This standard, along with our other avermectin metabolite reference standards, are used to monitor fate of avermectin products in soil in the presence of microbes and exposure to sunlight. Please find the entire collection here<\/a>.","post_title":"8a-Oxo-Avermectin B1a","post_excerpt":"[wc_measurement_price_calculator_pricing_table]","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"8a-oxo-avermectin-b1a","to_ping":"","pinged":"","post_modified":"2024-03-28 12:37:51","post_modified_gmt":"2024-03-28 16:37:51","post_content_filtered":"","post_parent":0,"guid":"http:\/\/159.69.28.184\/product\/8a-oxo-avermectin-b1a\/","menu_order":0,"post_type":"product","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":10072,"post_author":"3","post_date":"2026-01-16 14:28:22","post_date_gmt":"2026-01-16 19:28:22","post_content":"Amino Avermectin B1a is a high purity reference standard used in residue analysis, method development, and environmental fate studies. As a member of the avermectin family of 16 membered macrocyclic lactones, it provides a relevant comparator for avermectin and emamectin profiling programs.\r\n\r\nProduced through Streptomyces avermitilis fermentation, the compound retains the natural macrocyclic scaffold with a 4 double prime amino, 4 double prime deoxy substitution on the sugar group. This modification makes it useful for tracking transformation pathways and confirming impurity identities in complex matrices.\r\n\r\nIts structural similarity to commercial avermectins supports laboratories developing selective and reliable analytical methods. In invertebrates, avermectin class compounds act on glutamate gated chloride channels, increasing chloride influx and disrupting neurotransmission. This mode of action underlines the need for accurate profiling of related compounds in environmental evaluations.\r\n
\r\n\r\nRelated avermectin and emamectin standards, impurities, and metabolites are available to support QC and comparability studies. View the related products <\/span>here<\/a>.<\/span>\r\n\r\n<\/div>","post_title":"Amino avermectin B1a","post_excerpt":"[wc_measurement_price_calculator_pricing_table]","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"amino-avermectin-b1a-121064-68-4","to_ping":"","pinged":"","post_modified":"2026-03-20 16:06:43","post_modified_gmt":"2026-03-20 20:06:43","post_content_filtered":"","post_parent":0,"guid":"https:\/\/plantaanalytica.com\/?post_type=product&p=10072","menu_order":0,"post_type":"product","post_mime_type":"","comment_count":"0","filter":"raw"},{"ID":3134,"post_author":"1","post_date":"2023-10-19 15:15:35","post_date_gmt":"2023-10-19 15:15:35","post_content":"Avermectin A1a is one of the primary avermectin metabolites. Avermectins are a group of 16-membered macrocyclic lactone derivatives with potent anthelmintic and insecticidal properties. These naturally occurring compounds are generated as fermentation products of the soil actinomycete Streptomyces avermitilis<\/em>. In invertebrates, avermectins effect the nerve and muscle cells by enhancing the effects of glutamate and the glutamate-gated chloride channel. This results in an in influx of chloride ions and subsequent paralysis of the invertebrate.\r\n\r\nAvermectins<\/a> are isolated in four pairs of homologous compounds (A1, A2, B1, B2). Avermectin B1 comprises Avermectin B1a and Avermectin B2a and is marketed as abamectin. Avermectin A1a standard, along with our other avermectin metabolite reference standards, are used to monitor fate of avermectin products in soil in the presence of microbes and exposure to sunlight. Please find the entire collection here<\/a>.","post_title":"Avermectin A1a","post_excerpt":"[wc_measurement_price_calculator_pricing_table]","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"avermectin-a1a","to_ping":"","pinged":"","post_modified":"2026-03-20 17:08:33","post_modified_gmt":"2026-03-20 21:08:33","post_content_filtered":"","post_parent":0,"guid":"http:\/\/159.69.28.184\/?post_type=product&p=3134","menu_order":0,"post_type":"product","post_mime_type":"","comment_count":"0","filter":"raw"}],"post_count":12,"current_post":-1,"before_loop":true,"in_the_loop":false,"post":{"ID":5066,"post_author":"5","post_date":"2023-11-16 09:30:22","post_date_gmt":"2023-11-16 09:30:22","post_content":"Azadirachta indica <\/em><\/a>is commonly referred to as the neem tree or simply neem. It serves as a rich source for triterpenoids (limonoids). Limonoids are of profound interest to humans due to their diverse medicinal properties, including antioxidant, anti-inflammatory, and anticancer activities. 14,15-Epoxyazadiradione (CAS 58525-91-0) is a naturally occurring metabolite isolated from A. indica<\/em>. It is one of the 11 major limonoids found in neem extracts. Oils extracted from neem fruits and seeds are used as one of the most popular natural insecticides, miticides, and fungicides. Moreover, in traditional medicine, all parts of the neem tree were utilized for treatment of inflammation, infections, fevers, skin diseases, and dental disorders.\r\n\r\nNeem reference standards are broken up into two classes, azadirachtin and non-azadirachtin neem limonoids. The list of the most common standards includes: Azadirachtin A, Azadirachtin B, Azadirachtin D, Azadirachtin H, Azadiradione, 14,15-Epoxyazadiradione, Nimbin, Salannin, 3-Deacetylsalannin, 6-Deacetylnimbin, and Ohchinolide. You can follow this link<\/a> for our entire collection of neem reference standards.","post_title":"14,15-Epoxyazadiradione","post_excerpt":"[wc_measurement_price_calculator_pricing_table]","post_status":"publish","comment_status":"closed","ping_status":"closed","post_password":"","post_name":"epoxyazadiradione","to_ping":"","pinged":"","post_modified":"2026-03-20 16:53:21","post_modified_gmt":"2026-03-20 20:53:21","post_content_filtered":"","post_parent":0,"guid":"http:\/\/159.69.28.184\/product\/1415-epoxyazadiradione-2\/","menu_order":0,"post_type":"product","post_mime_type":"","comment_count":"0","filter":"raw"},"comment_count":0,"current_comment":-1,"found_posts":50,"max_num_pages":5,"max_num_comment_pages":0,"is_single":false,"is_preview":false,"is_page":false,"is_archive":true,"is_date":false,"is_year":false,"is_month":false,"is_day":false,"is_time":false,"is_author":false,"is_category":false,"is_tag":false,"is_tax":true,"is_search":false,"is_feed":false,"is_comment_feed":false,"is_trackback":false,"is_home":false,"is_privacy_policy":false,"is_404":false,"is_embed":false,"is_paged":false,"is_admin":false,"is_attachment":false,"is_singular":false,"is_robots":false,"is_favicon":false,"is_posts_page":false,"is_post_type_archive":false,"thumbnails_cached":false}

Agrochemical Standards

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14,15-Epoxyazadiradione

3-deacetylsalannin

4-OH-8a-Oxo-Avermectin B1a

4,8a-diOH-Avermectin B1a

4″-Oxo-Avermectin B1a

6-deacetylnimbin

8,9-Z-Avermectin B1a

8,9-Z-Methylamino Avermectin b1a

8a-OH-Avermectin B1a

8a-Oxo-Avermectin B1a

Amino avermectin B1a

Avermectin A1a