[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"doc-detail-32093":3,"doc-seo-32093":28},{"code":4,"msg":5,"data":6},0,"success",{"doc_id":7,"user_id":8,"nickname":9,"user_avatar":10,"doc_module":4,"category_id":11,"category_name":12,"doc_title":13,"doc_description":14,"file_id":15,"file_url":16,"file_type":17,"file_size":18,"view_count":19,"is_deleted":4,"is_public":20,"is_downloadable":20,"audit_status":20,"page_count":21,"language":22,"language_code":23,"table_of_contents":24,"faqs":25,"seo_title":13,"seo_description":14,"update_tm":26,"read_time":27},32093,8796095360427,"Lucas Martin","https://ap-avatar.wpscdn.com/davatar_994ba38a5ba835b3df7d355c54d3ed8d",8,"Research & Report","Furfural and Derivatives","Article covering properties, production routes, and industrial uses of furfural and major derivatives derived from furfural. It outlines the commercial acid-catalyzed digestion of pentosan sugars in biomass as the key route, followed by a historical timeline of industrial milestones that shaped production capacity. It details furfural’s physical and chemical behavior, including solvent applications, azeotrope formation with water, and representative aldehyde reactions, then extends coverage to principal downstream products such as furfuryl alcohol and furans.","cbCaiix7mxSKHmVp","https://ap.wps.com/l/cbCaiix7mxSKHmVp","pdf",354551,4,1,30,"English","en","# Introduction\n# Furfural\n## Properties\n## Resources and Raw Materials\n## Production\n## Uses and Economic Aspects\n## Quality Specifications, Transportation, Toxicology\n# Furfuryl Alcohol\n# Furan\n# Tetrahydrofurfuryl Alcohol\n# Furfurylamine and Tetrahydrofurfurylamine\n# Methylfuran and Methyltetrahydrofuran\n# Furoic Acid\n# References","[{\"question\":\"What is the only commercial route to furfural described in the article?\",\"answer\":\"Commercial furfural is produced by acid-catalyzed digestion of pentosan sugars in biomass.\"},{\"question\":\"Why is furfural important in the chemical industry according to the document?\",\"answer\":\"Furfural is the sole precursor for molecules containing furyl, furfuryl, furoyl, or furfurylidene radicals in the chemical industry.\"},{\"question\":\"What key physical property of furfural is highlighted in relation to extraction and solvents?\",\"answer\":\"Furfural has an aromatic odor reminiscent of almonds and is described as an exceptional solvent/extractant for removing aromatics from lubricating oil and diesel fuels, forming an azeotrope with water at atmospheric pressure.\"}]",1780866084,76,{"code":4,"msg":29,"data":30},"ok",{"site_id":31,"language":23,"slug":32,"title":13,"keywords":33,"description":14,"schema_data":34,"social_meta":85,"head_meta":87,"extra_data":89,"updated_unix":26},105,"furfural-and-derivatives","",{"@graph":35,"@context":84},[36,52,67],{"@type":37,"itemListElement":38},"BreadcrumbList",[39,43,47,50],{"item":40,"name":41,"@type":42,"position":20},"https://docshare.wps.com","Home","ListItem",{"item":44,"name":45,"@type":42,"position":46},"https://docshare.wps.com/document/","Document",2,{"item":48,"name":12,"@type":42,"position":49},"https://docshare.wps.com/document/research-report/",3,{"item":51,"name":13,"@type":42,"position":19},"https://docshare.wps.com/document/furfural-and-derivatives/32093/",{"url":51,"name":13,"@type":53,"author":54,"headline":13,"publisher":56,"fileFormat":59,"description":14,"dateModified":60,"datePublished":61,"encodingFormat":59,"isAccessibleForFree":62,"interactionStatistic":63},"DigitalDocument",{"name":9,"@type":55},"Person",{"url":40,"name":57,"@type":58},"DocShare","Organization","application/pdf","2026-06-15","2026-06-07",true,{"@type":64,"interactionType":65,"userInteractionCount":19},"InteractionCounter",{"@type":66},"ViewAction",{"@type":68,"mainEntity":69},"FAQPage",[70,76,80],{"name":71,"@type":72,"acceptedAnswer":73},"What is the only commercial route to furfural described in the article?","Question",{"text":74,"@type":75},"Commercial furfural is produced by acid-catalyzed digestion of pentosan sugars in biomass.","Answer",{"name":77,"@type":72,"acceptedAnswer":78},"Why is furfural important in the chemical industry according to the document?",{"text":79,"@type":75},"Furfural is the sole precursor for molecules containing furyl, furfuryl, furoyl, or furfurylidene radicals in the chemical industry.",{"name":81,"@type":72,"acceptedAnswer":82},"What key physical property of furfural is highlighted in relation to extraction and solvents?",{"text":83,"@type":75},"Furfural has an aromatic odor reminiscent of almonds and is described as an exceptional solvent/extractant for removing aromatics from lubricating oil and diesel fuels, forming an azeotrope with water at atmospheric pressure.","https://schema.org",{"og:url":51,"og:type":86,"og:title":13,"og:site_name":57,"og:description":14},"article",{"robots":88,"canonical":51},"index,follow",{"doc_id":7,"site_id":31}]