2,5-furan dicarboxylic acid
dehydromucic acid

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  CODE143579 CODE143579
  Product(s):
  3238-40-2 2,5-Furandicarboxylic acid 98%

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  Product(s):
  F0710 2,5-Furandicarboxylic Acid >98.0%(HPLC)(T)
  SDS

Name: furan-2,5-dicarboxylic acid CAS Number: 3238-40-2 3D/inchi ECHA EINECS - REACH Pre-Reg: 221-800-8 FDA UNII: 73C4JJ695C Nikkaji Web: J7.694E MDL: MFCD00016582 XlogP3-AA: 0.70 (est) Molecular Weight: 156.09388000 Formula: C6 H4 O5 BioActivity Summary: listing NMR Predictor: Predict (works with chrome, Edge or firefox) Category:indirect food additives: adhesives and components of coatings   US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information: Google Scholar: Search Google Books: Search Google Scholar: with word "volatile" Search Google Scholar: with word "flavor" Search Google Scholar: with word "odor" Search Google Patents: Search US Patents: Search EU Patents: Search Pubchem Patents: Search PubMed: Search NCBI: Search   Physical Properties: Assay: 95.00 to 100.00 Food Chemicals Codex Listed: No Melting Point: 342.00 °C. @ 760.00 mm Hg Boiling Point: 419.20 °C. @ 760.00 mm Hg (est) Flash Point: 405.00 °F. TCC ( 207.30 °C. ) (est) logP (o/w): -0.020 (est) Soluble in:   water, 1000 mg/L @ 18C (exp)   water, 1.269e+004 mg/L @ 25 °C (est)   Organoleptic Properties: Odor and/or flavor descriptions from others (if found).   Cosmetic Information: None found   Suppliers: AVA Biochem 2,5-Furandicarboxylic Acid Odor: characteristic Use: 2,5-furandicarboxylic acid (FDCA) is listed in a 2004 US Department of Energy National Renewable Energy Laboratory (NREL) report as one of the top twelve building blocks that can be subsequently converted to a number of high-value bio-based chemicals or materials. Derivatives of furan produced from renewable carbohydrates are the main types of next generation platform chemicals. FDCA made from bio-based 5-HMF (5-hydroxymethylfurfural) plays a particularly important role and opens, amongst others, the door to the multi-billion bio-based packaging market. FDCA is the oxidation product of both primary alcohol and aldehyde groups of 5-HMF to carboxylic acid groups and is considered to be the most important derivative of 5-HMF. This sugar based compound is a potential replacement of terephthalic acid, which is a monomer, used in polyethylene terephthalate (PET) plastics. Amongst others, FDCA is the basis for 100% bio-based PEF (polyethylene furanoate) bottles, fibres or films. BOC Sciences For experimental / research use only. 2,5-Furandicarboxylic acid 98% Carbosynth For experimental / research use only. 2,5-Furandicarboxylic Acid Santa Cruz Biotechnology For experimental / research use only. 2,5-Furandicarboxylic Acid Sigma-Aldrich: Aldrich For experimental / research use only. 2,5-Furandicarboxylic Acid 97% sds TCI AMERICA For experimental / research use only. 2,5-Furandicarboxylic Acid >98.0%(HPLC)(T) sds   Safety Information: Preferred SDS: View   Hazards identification   Classification of the substance or mixture GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) None found. GHS Label elements, including precautionary statements   Pictogram   Hazard statement(s) None found. Precautionary statement(s) None found. Oral/Parenteral Toxicity: Not determined Dermal Toxicity: Not determined Inhalation Toxicity: Not determined   Safety in Use Information: Category: indirect food additives: adhesives and components of coatings Recommendation for 2,5-furan dicarboxylic acid usage levels up to:   not for fragrance use.   Recommendation for 2,5-furan dicarboxylic acid flavor usage levels up to:   not for flavor use.   Safety References: European Food Safety Authority (EFSA) reference(s): Scientific Opinion on the safety assessment of the substance, furan-2,5-dicarboxylic acid, CAS No 3238-40-2, for use in food contact materials View page or View pdf EPI System: View AIDS Citations:Search Cancer Citations:Search Toxicology Citations:Search EPA Substance Registry Services (TSCA):3238-40-2 EPA ACToR:Toxicology Data EPA Substance Registry Services (SRS):Registry Laboratory Chemical Safety Summary :76720 National Institute of Allergy and Infectious Diseases:Data WGK Germany:3 furan-2,5-dicarboxylic acid Chemidplus:0003238402   References:   furan-2,5-dicarboxylic acid NIST Chemistry WebBook: Search Inchi Pubchem (cid): 76720 Pubchem (sid): 135036134   Other Information: (IUPAC): Atomic Weights of the Elements 2011 (pdf) Videos: The Periodic Table of Videos tgsc: Atomic Weights use for this web site (IUPAC): Periodic Table of the Elements FDA Indirect Additives used in Food Contact Substances: View CHEBI: View KEGG (GenomeNet): C20450 HMDB (The Human Metabolome Database): HMDB04812 FooDB: FDB023423 Export Tariff Code: 2918.99.4700 ChemSpider: View EFSA Update of results on the monitoring of furan levels in food: Read Report EFSA Previous report: Results on the monitoring of furan levels in food: Read Report EFSA Report of the CONTAM Panel on provisional findings on furan in food: Read Report   Potential Blenders and core components note None Found   Potential Uses: None Found   Occurrence (nature, food, other):note   not found in nature   Synonyms:   dehydromucic acid   furan-2,5-dicarboxylic acid   furan-alpha,alpha'-dicarboxylic acid 2,5- furandicarboxylic acid   furane-alpha,alpha'-dicarboxylic acid   Articles:   None found yet. Try the PubMed Search.

Notes: 2,5-Furandicarboxylic acid is a normal urinary metabolite in humans. (PMIDs 14708889, 8087979, 2338430, 3711221) Dietary studies show that the furan derivatives or their precursors are of exogenous origin. They are originated from furan derivatives found in food prepared by strong heating. This may explain the absence of 2,5-furandicarboxylic acid in urine of breastfed children, and the absence of these acids in the urine of rat, pig, cow, ox, rabbit, and monkey. (PMID 4630229) [HMDB]