5-hydroxymethyl furfural
hydroxymethylfurfuralaldehyde
 
Notes:
hmf is the causative component in honey that affects the presystemic metabolism and pharmacokinetics of gz in-vivo. Obtainable from various carbohydrates. Present in tomatoes, tobacco oil etc. Constit. of numerous plant spp.. Used as an index of heat treatment and deterioration in food such as tomato paste, honey and fruit juices. Also an indicator of adulteration with acid-converted invert sugars
  • Beijing Lys Chemicals
    • Beijing Lys Chemicals Co, LTD.
      From Grams to Tons
      Fine chemical high-tech company which contains R&D, production, and sales.
      BEIJING LYS CHEMICALS CO, LTD, established in 2004, is a fine chemical high-tech company which contains R&D, production, and sales. We mainly engaged in export and technology development of flavor and fragrance materials and pharmaceutical intermediates. We have nearly 500 kinds of products, from grams to tons, exported to USA, Europe, South Asia and etc. And we custom manufacture new products according to customers’ needs, and serve good quality products and service. Our goal is to become a fine chemical enterprise which could provide special products and services.
      Email: Mr. Jia
      Email: Mr. Guo
      Voice: 86-10-68418738
      Fax: 86-10-68418739
      Mr. Guo86-10-68483445
      Mr. Guo86-10-68418739
      News
      Product(s):
      10210 5-(Hydroxymethyl)furfural
       
  • BOC Sciences
    • BOC Sciences
      Best of Chemicals Supplier
      Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
      BOC Sciences provides a wide range of services to support the pharmaceutical industry through all stages of drug discovery including Custom Synthesis of those chemicals that are not in stock, Isotope Labeling Service, Chiral Synthesis and Resolution, Bioconjugation, PEGylation services, analytical services.
      BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies.
      Email: Marketing
      US Email: Marketing
      Email: Sales
      US Email: Sales
      Voice: 1-631-485-4226
      Fax: 1-631-614-7828
      US Voice: 1-631-485-4226
      US Fax: 1-631-614-7828
      Europe44-203-286-1088
      Facebook
      Twitter
      Linkedin
      Blog
      Get the App!
      Product(s):
      67-47-0 5-Hydroxymethylfurfural
       
  • ECSA Chemicals
    • ECSA Chemicals
      Human Chemistry
      ECSA Chemicals has been active since 1913 in the trading and international commerce of raw materials. With an organisation divided into industrial segments managed by specialists, it has become one of the largest distributors worldwide.
      ECSA Chemicals is the largest Swiss-owned company in terms of warehouses for the distribution of chemical products. We have been distributing chemical products for over 100 years and we have a special interest in protecting the environment and in the safety of our facilities and collaborators.
      Established in 1913 as a small grocery store, in its over 100 years of activity ECSA Chemicals has become one of the most important Swiss-owned distributors of chemical products. The company, which is active in international distribution and trading, is organised into industrial segments that are managed by teams of specialists and experts. They guarantee professional and customised consultancy and services. With our experience, we can rapidly and safely connect you with the best suppliers on the market, providing you with a complete search, consulting and assistance service. The focus of our approach and operations is you, our customers. We strive every day to find the best products that satisfy your needs as quickly as possible. Your satisfaction is our greatest success. WHY CHOOSE ECSA? EXPERIENCE We have been working for 100 years. QUALITY We have obtained many certifications (ISO, SQAS, GDP, Responsible Care, Bio-Inspecta, RSPO, etc.). We guarantee full compliance with the current laws and continuous training for our staff. SAFETY We constantly carry out risk analyses for each infrastructure, defining safety levels and implementing corrective measures promptly wherever they are needed. WIDESPREAD DISTRIBUTION We have warehouses in strategic locations to supply goods to Switzerland and to the rest of the world. STORAGE CAPACITY The 3 ECSA-owned warehouses guarantee considerable storage area and capacity in each warehouse, with full availability of products (base chemicals and speciality chemicals). SPEED Presence all over the country, staff dedicated to sourcing raw materials and considerable storage capacity guarantee that goods are rapidly obtained and supplied. CONSULTANCY Our specialists - in-depth knowledge of the market and products allows us to provide full consulting services, from the purchase to the supply of raw materials.
      Email: Info
      Email: Sales
      Email: Trading
      Email: Maintenance
      Email: Energy
      Voice: +41 91 695 88 00
      Fax: +41 91 695 88 01
      Linkedin
      Youtube
      RSS Feed
      ECSA Trade
      ECSA TRADE THE MOST UPDATED FINANCIAL PUBLICATION ON THE WORLD OF CHEMISTRY
      Products List: View
      Product(s):
      MP-026205 5-HYDROXYMETHYL-FURFURAL
       
  • Endeavour Specialty Chemicals
    • Endeavour Specialty Chemicals Ltd
      Expertise in high impact aroma chemicals
      Endeavour Speciality Chemicals offers high-impact aroma chemicals, at small to medium scale.
      Speciality Chemical has more than 25 years experience of manufacturing high-impact aroma chemicals. With our core expertise in sulfur and heterocyclic chemistries, Endeavours products have applications in a range of industry sectors including flavours and fragrances, pharmaceutical research and material sciences. Endeavour also offer custom synthesis and contract manufacturing services at their UK manufacturing site.
      Email: Info
      Email: Sales
      Voice: +44 (0)1327 310 079
      Fax: +44 (0)1327 310 701
      Twitter
      Linkedin
      News
      Speciality Chemical Product Groups
      Product(s):
      AL0150 5-(Hydroxymethyl)furfural
       
  • M&U International
    • M&U International LLC
      Steady supply & demand
      Meeting customers increasing demands at home as well as abroad.
      M&U dedicates itself to the development and production of new products as well as continuously promoting those new products. We’ve maintained a steady supply&demand relationship with a large number of manufacturers at home and abroad. We’ve developed an extensive network and because of our relationships with these manufacturers, we’re able to provide a stable supply of great quality materials. We’re located in China’s largest communications hub, Shanghai and in the U.S. near one of the largest sea ports on the East Coast. The strategic locations of our facilities ensure convenient, prompt and secure delivery of our products to our customers.
      Email: Sales
      US Email: Sales
      Voice: +86-21-32515501 60762991 60762992
      Fax: +86-21-32515502 64204960
      US Voice: 908-359-9000
      US Fax: 908-359-9002
      News
      Product(s):
      H0095 5-HYDROXYMETHYL FURFURAL, Kosher
       
  • Penta International
    • Penta International Corporation
      Chemistry innovation
      At Penta, our products and services help businesses do business better.
      For over 30 years, Penta Manufacturing Company has played a growing role in worldwide chemistry innovations and applications. As an industry leader, Penta continues to pioneer chemistry-based solutions for practically every area of commerce. Our products and expertise have helped fuel technical advances in dozens of commercial applications including flavoring, coloring, fragrances and chemical processes.
      US Email: Technical Services
      US Email: Sales
      US Voice: (973) 740-2300
      US Fax: (973) 740-1839
      Product(s):
      08-65100 5-(HYDROXYMETHYL) FURFURAL
       
  • Robinson Brothers
  • Sigma-Aldrich
  • Sunaux International
    • Sunaux International
      Buy With Confidence
      We have industry leading processes and procedures to ensure nothing but the most reliable product.
      Sunaux International was founded in 2012 by the owner Mr.John Felton after spending 18 years involved in developing global business in the aromatic chemicals, fragrance and flavour compounds business.
      Email: John Felton
      Email: Stephen Zhou (Sales)
      Voice: 0512-57995626
      Fax: 0512-57570299
      Sales0512-57995626
      Sales0512-57570299
      News
      Product(s):
      H0095 5-Hydroxymethyl Furfural
       
  • Synerzine
    • Synerzine, Inc.
      Innovation. Customization. Aroma Ingredients.
      Synerzine is a leading supplier of flavor and fragrance ingredients.
      Synerzine expresses what we have grown to embody as an organization - the synergy and connection between raw ingredients, science, technology, and the final product. Our experienced team is passionate about bringing our customers high-quality innovative ingredients that they can trust.
      Building upon our 44 year history, the Synerzine team provides customers around the globe with convenient access to over 1200 high-quality aroma ingredients. We actively engage with customers to add a wide array of new products and services on a regular basis. Our aim is to delight every customer with our exceptional services, large product selection, customization and the highest quality and safety standards. We provide our customers with true value designed to help them bring their products to market faster.
      US Email: Customer Service
      US Email: Sales
      US Voice: (404) 524-6744
      US Fax: (404) 577-1651
      Inquiry
      Products List: View
      Product(s):
      W089 5-(Hydroxymethyl) Furfural
       
  • TCI AMERICA
    • TCI AMERICA
      Moving Your Chemistry Forward
      We continuously strive to advance our technology.
      With East & West Coast distribution centers, count on TCI to deliver products quickly and reliably. Over 30,000 Reagents available today in benchtop to bulk quantities. We also offer custom synthesis solutions. Sign up for a TCI account today for fast and free shipping!
      Tokyo Chemical Industry Co., Ltd. (TCI) is a leading worldwide manufacturer of specialty organic chemicals founded in 1946. TCI provides organic laboratory chemicals as well as pharmaceutical, cosmetic and functional materials. More than 70 years of synthesis experience and multi-purpose plants enable TCI to offer more than 30,000 products as well as custom synthesis.
      US Email: Sales
      Email: Technical Support
      Voice: 1-800-423-8616
      Fax: 1- 888-520-1075
      Facebook
      Twitter
      Instagram
      Linkedin
      Product(s):
      H0269 5-Hydroxymethyl-2-furaldehyde (stabilized with Water) >95.0%(GC)
       
  • Tianjin Danjun International
    • Tianjin Danjun International Trade Co., LTD.
      Quality Products
      We know the Chinese chemical market well.
      Tianjin danjun international trade co., LTD. is an organic chemicals trading company approved by the relevant state authorities to register. We have about 300 kinds of products (natural aroma chemicals, synthetic aroma chemicals and pharmaceutical intermediates). Most of the products are used in flavor and fragrance industry. We know the Chinese chemical market well and we have close relationship with many of the main manufacturers, and to provide our customers with quality goods together with comprehensive service.
      Email: Info
      Email: Sales
      Voice: +86-15822601686
      Products List: View
      Product(s):
      B-055 5-(Hydroxymethyl)furfural
       
  • R C Treatt & Co Ltd
    • R C Treatt and Co Ltd
      Innovative ingredient solutions
      World-leading innovative ingredient solutions provider for the flavour, fragrance and FMCG industries.
      We offer innovative and trend-setting product concepts for our customers, collaborating with them to create true value for their products.
      Email: Enquiries
      US Email: Enquiries
      Voice: +44 (0) 1284 702500
      Fax: +44 (0) 1284 703809
      US Voice: +1 863 668 9500
      US Fax: +1 863 668 3388
      Twitter
      Linkedin
      Youtube
      News
      Product(s):
      5-(Hydroxymethyl)furfural Kosher
       
  • United International
    • Qingdao Free Trade Zone United International Co Ltd
      Quality Products
      A partner in your supply chain solution.
      Qingdao Free Trade Zone United International Trade Co., Ltd.was founded in 1996, specializing in the production and import and export of food additives,flavor raw materials and pharmaceutical and chemical raw materials. The company has experienced R&D and business personnel,product quality, low price, efficient service and fast insight and grasp the latest market information.
      Email: Info
      Email: Sales
      Voice: +86-532-83893699
      Fax: +86-532-83893695
      Product(s):
      7129 5-Hydroxymethyl furfural
       
  • WholeChem
    • WholeChem, LLC
      Connecting Innovators To the Building Blocks Of the Universe
      Custom manufacturer and distributor of specialty ingredients. We make global local.
      SQF-Certified Supplier
      We owe our success to our integrity, our dedication to the industry, and our commitment to our clients. We invite your inquiries regarding our current product list and any other products you may be having trouble sourcing.
      Email: Info
      Email: Orders
      Voice: +1 (262) 995.8668
      Certification
      Our Services
      Products List: View
      Product(s):
      5-(Hydroxymethyl)furfural
       
Synonyms   Articles   Notes   Search
CAS Number: 67-47-0Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 200-654-9
FDA UNII: 70ETD81LF0
Nikkaji Web: J4.850J
Beilstein Number: 0110889
MDL: MFCD00003234
CoE Number: 11112
XlogP3: -0.60 (est)
Molecular Weight: 126.11142000
Formula: C6 H6 O3
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: flavoring agents
 
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
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
DG SANTE Food Flavourings: 13.139  hydroxymethylfurfuralaldehyde
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 1.24300 @  25.00 °C.
Refractive Index: 1.56200 @  20.00 °C.
Melting Point: 32.00 to  35.00 °C. @ 760.00 mm Hg
Boiling Point: 114.00 to  116.00 °C. @ 1.00 mm Hg
Boiling Point: 291.00 to  292.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.001000 mmHg @ 25.00 °C. (est)
Flash Point: 175.00 °F. TCC ( 79.44 °C. )
logP (o/w): -0.778 (est)
Soluble in:
 alcohol
 water, 3.643e+005 mg/L @ 25 °C (est)
Insoluble in:
 water
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: fatty
 
 fatty  buttery  musty  waxy  caramellic  
Odor Description:
at 0.10 % in dipropylene glycol. 
fatty buttery musty waxy caramellic
 
 
Flavor Type: herbal
 
 herbal  hay  tobacco  
Taste Description:
herbal hay tobacco
 
Odor and/or flavor descriptions from others (if found).
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
None found
Synonyms   Articles   Notes   Search   Top
Suppliers:
Alfa Biotechnology
For experimental / research use only.
5-Hydroxymethylfurfural 98%
Ambles Nature et Chimie
5-HYDROXYMETHYL FURFURAL
AVA Biochem
5-Hydroxymethylfurfural
Odor: characteristic
Use: Among the organic compounds that can be obtained from biomass, 5-Hydroxymethylfurfural (5-HMF) is one of the most interesting ones. 5-HMF is an organic compound derived from dehydration of certain sugars (hexoses). This yellow, low-melting solid is highly water-soluble. The molecule consists of a furan ring, containing both aldehyde and alcohol functional groups. HMF as natural substance has been identified in a wide variety of heat-processed foods including milk, fruit juices, spirits, honey, etc. HMF, which is derived from cellulose, is a potential "carbon-neutral" feedstock for a number of chemical substances. AVA Biochem offers 5-HMF in various purities in crystalline form or in aqueous solution to its customers in the research and fine chemical industry.
Beijing Lys Chemicals
5-(Hydroxymethyl)furfural
BOC Sciences
For experimental / research use only.
5-Hydroxymethylfurfural
Connect Chemicals
5-(Hydroxymethyl)furan-2-carbaldehyde
ECSA Chemicals
5-HYDROXYMETHYL-FURFURAL
ECSA TRADE THE MOST UPDATED FINANCIAL PUBLICATION ON THE WORLD OF CHEMISTRY
Endeavour Specialty Chemicals
5-(Hydroxymethyl)furfural
Speciality Chemical Product Groups
Jalor-Chem
For experimental / research use only.
5-Hydroxymethylfurfural
Jinan Enlighten Chemical Technology(Wutong Aroma )
5-Hydroxymethyl furfural Kosherk
M&U International
5-HYDROXYMETHYL FURFURAL, Kosher
Penta International
5-(HYDROXYMETHYL) FURFURAL
R C Treatt & Co Ltd
5-(Hydroxymethyl)furfural
Kosher
Robinson Brothers
5-(Hydroxymethyl)furfural F&F
https://www.robinsonbrothers.uk/chemistry-competences
Santa Cruz Biotechnology
For experimental / research use only.
5-Hydroxymethyl-2-furaldehyde
Sigma-Aldrich
5-(Hydroxymethyl)furfural, ≥99%, FG
Odor: butter; caramel; musty
Certified Food Grade Products
Sunaux International
5-Hydroxymethyl Furfural
Synerzine
5-(Hydroxymethyl) Furfural
TCI AMERICA
For experimental / research use only.
5-Hydroxymethyl-2-furaldehyde (stabilized with Water) >95.0%(GC)
Tengzhou Jitian Aroma Chemiclal
5-Hydroxymethyl Furfural
Tianjin Danjun International
5-(Hydroxymethyl)furfural
United International
5-Hydroxymethyl furfural
WholeChem
5-(Hydroxymethyl)furfural
Synonyms   Articles   Notes   Search   Top
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi N - Irritant, Dangerous for the environment.
R 36/37/38 - Irritating to eyes, respiratory system, and skin.
R 51/53 - Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 36 - Wear suitable protective clothing.
S 61 - Avoid release to the environment. Refer to special instructions/safety data sheet.
 
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:
oral-rat LD50  3100 mg/kg
(Simonyan, 1969)

gavage-rat LD50  [sex: M,F] 2500 mg/kg
(Warf Institute, 1977)

oral-mouse LD50  1910 mg/kg
(Simonyan, 1969)

oral-mouse LD50  > 2000 mg/kg
(Czok, 1970)

oral-rat LD50  2500 mg/kg
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
National Technical Information Service. Vol. OTS0544683

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: flavoring agents
Recommendation for 5-hydroxymethyl furfural usage levels up to:
 not for fragrance use.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.39 (μg/capita/day)
Modified Theoretical Added Maximum Daily Intake (mTAMDI): 1600 (μg/person/day)
Threshold of Concern:540 (μg/person/day)
Structure Class: II
 
Food categories according to Commission Regulation EC No. 1565/2000 (EC, 2000) in FGE.06 (EFSA, 2002a). According to the Industry the "normal" use is defined as the average of reported usages and "maximum use" is defined as the 95th percentile of reported usages (EFSA, 2002i).
Note: mg/kg = 0.001/1000 = 0.000001 = 1/1000000 = ppm.
 average usage mg/kgmaximum usage mg/kg
Dairy products, excluding products of category 02.0 (01.0): 3.0000015.00000
Fats and oils, and fat emulsions (type water-in-oil) (02.0): 2.0000010.00000
Edible ices, including sherbet and sorbet (03.0): 3.0000015.00000
Processed fruit (04.1): 2.0000010.00000
Processed vegetables (incl. mushrooms & fungi, roots & tubers, pulses and legumes), and nuts & seeds (04.2): --
Confectionery (05.0): 4.0000020.00000
Chewing gum (05.0): --
Cereals and cereal products, incl. flours & starches from roots & tubers, pulses & legumes, excluding bakery (06.0): 2.0000010.00000
Bakery wares (07.0): 5.0000025.00000
Meat and meat products, including poultry and game (08.0): 1.000005.00000
Fish and fish products, including molluscs, crustaceans and echinoderms (MCE) (09.0): 1.000005.00000
Eggs and egg products (10.0): --
Sweeteners, including honey (11.0): --
Salts, spices, soups, sauces, salads, protein products, etc. (12.0): 2.0000010.00000
Foodstuffs intended for particular nutritional uses (13.0): 3.0000015.00000
Non-alcoholic ("soft") beverages, excl. dairy products (14.1): 2.0000010.00000
Alcoholic beverages, incl. alcohol-free and low-alcoholic counterparts (14.2): 4.0000020.00000
Ready-to-eat savouries (15.0): 5.0000025.00000
Composite foods (e.g. casseroles, meat pies, mincemeat) - foods that could not be placed in categories 01.0 - 15.0 (16.0): 2.0000010.00000
Synonyms   Articles   Notes   Search   Top
Safety References:
European Food Safety Athority(EFSA): Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...
European Food Safety Authority (EFSA) reference(s):
Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to Flavouring Group Evaluation 13 (FGE.13); Furfuryl and furan derivatives with and without additional side-chain substituents and heteroatoms from chemical group 14 (Commission Regulation (EC) No 1565/2000 of 18
View page or View pdf
Flavouring Group Evaluation 66 (FGE.66)[1]:Consideration of furfuryl alcohol and related flavouring substances evaluated by JECFA (55th meeting) structurally related to Furfuryl and furan derivatives with and without additional side chain substituents and heteroatoms evaluated by EFSA in FGE.13 (2005)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 13Rev1: Furfuryl and furan derivatives with and without additional side-chain substituents and heteroatoms from chemical group 14
View page or View pdf
Consideration of sulfur-substituted furan derivatives used as flavouring agents evaluated by JECFA (59th meeting) structurally related to a subgroup of substances within the group of “Furfuryl and furan derivatives with and without additional side-chain substituents and heteroatoms from chemical group 14” evaluated by EFSA in FGE.13Rev1 (2009)
View page or View pdf
Flavouring Group Evaluation 67 (FGE.67): Consideration of 40 furan-substituted aliphatic hydrocarbons, alcohols, aldehydes, ketones, carboxylic acids and related esters, sulfides, disulfides and ethers evaluated by JECFA at the 65th meeting (JECFA, 2006b) and re-evaluated at the 69th meeting (JECFA, 2009c)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 13, Revision 2 (FGE.13Rev2): Furfuryl and furan derivatives with and without additional side-chain substituents and heteroatoms from chemical group 14
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 67, Revision 1 (FGE.67Rev.1): Consideration of 40 furan-substituted aliphatic hydrocarbons, alcohols, aldehydes, ketones, carboxylic acids and related esters, sulfides, disulfides and ethers evaluated by JECFA at the 65th meeting (JECFA, 2006b) and re-evaluated at the 69th meeting (JECFA, 2009c)
View page or View pdf
Extensive literature search on grayanotoxins and 5-hydroxymethylfurfural
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 13 Revision 3 (FGE.13Rev3): furfuryl and furan derivatives with and without additional side-chain substituents and heteroatoms from chemical group 14
View page or View pdf
EPI System: View
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 67-47-0
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 237332
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 2
 5-(hydroxymethyl)furan-2-carbaldehyde
Chemidplus: 0000067470
RTECS: LT7031100 for cas# 67-47-0
Synonyms   Articles   Notes   Search   Top
References:
 5-(hydroxymethyl)furan-2-carbaldehyde
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 67-47-0
Pubchem (cid): 237332
Pubchem (sid): 134970717
Flavornet: 67-47-0
Pherobase: View
Synonyms   Articles   Notes   Search   Top
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
CHEBI: View
CHEMBL: View
KEGG (GenomeNet): C11101
HMDB (The Human Metabolome Database): HMDB34355
FooDB: FDB012717
Export Tariff Code: 2932.19.5100
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: 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
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
acidic
 cyclohexyl acetic acidFL/FR
aldehydic
 dodecanal (aldehyde C-12 lauric)FL/FR
balsamic
2-acetyl furanFL/FR
buttery
 acetoin propylene glycol acetalFL/FR
 acetyl propionylFL/FR
3,4-hexane dioneFL/FR
2-oxobutyric acidFL/FR
 caramel pentadioneFL/FR
 cycloteneFL/FR
 cyclotene hydrateFL/FR
alpha,alpha-dimethyl anisyl acetoneFL/FR
 ethyl 2-hydroxy-2-methyl butyrateFL/FR
 ethyl cyclopentenoloneFL/FR
 ethyl maltolFL/FR
5-ethyl-2,3,4,5-tetramethyl-2-cyclohexen-1-oneFL/FR
 fenugreek absoluteFL/FR
 immortelle absoluteFL/FR
 levulinic acidFL/FR
 maltolFL/FR
 maltyl propionateFL/FR
 maple furanoneFL/FR
 menthone lactoneFL/FR
5-methyl furfuralFL/FR
 rosefuranFL/FR
 shoyu furanoneFL/FR
 strawberry furanoneFL/FR
 strawberry furanone acetateFL/FR
 toffee furanoneFL/FR
coconut
gamma-heptalactoneFL/FR
creamy
gamma-butyrolactoneFL/FR
delta-tridecalactoneFL/FR
ethereal
 ethyl 4-pentenoateFL/FR
 ethyl pyruvateFL/FR
fatty
 allyl octanoateFL/FR
(Z)-dairy lactoneFL/FR
2,4-decadien-1-olFL/FR
(E)-2-decen-1-olFL/FR
7-decen-4-olideFL/FR
(E)-2-decenalFL/FR
 ethyl undecylenateFL/FR
 methyl 10-undecenoateFL/FR
4-methyl octanoic acidFL/FR
(Z)-2-nonenalCS
 octanoic acidFL/FR
(Z)-oleic acidFL/FR
fermented
 ethyl (E)-2-crotonateFL/FR
floral
 benzyl lactateFL/FR
 jasmin absolute (from pommade)FL/FR
fruity
 allyl cyclohexyl propionateFL/FR
(S)-delta-decalactoneFL/FR
 ethyl hexanoateFL/FR
(E)-ethyl tiglateFL/FR
2-methyl butyl butyrateFL/FR
 tetrahydrofurfuryl acetateFL/FR
green
isoamyl 3-(2-furan) propionateFL/FR
 manzanate (Givaudan)FL/FR
herbal
 butyl levulinateFL/FR
 clary sage oil franceFL/FR
 salvia sclarea oilFL/FR
musty
3-acetyl-2,5-dimethyl furanFL/FR
nutty
2-acetyl-3,5(or 6)-dimethyl pyrazineFL/FR
2,3-dimethyl pyrazineFL/FR
 nutty cyclohexenoneFL/FR
phenolic
4-methyl-2,6-dimethoxyphenolFL/FR
soapy
 benzyl laurateFL/FR
 ethyl undecanoateFL/FR
 methyl eugenolFR
(E)-tiglic acidFL/FR
sweet
 vanilla oleoresin baliFL/FR
tonka
6-amyl-alpha-pyroneFL/FR
tropical
 genet absoluteFL/FR
vanilla
 ethyl vanillinFL/FR
 vanillyl isobutyrateFL/FR
vegetable
 tetrahydrofurfuryl alcoholFL/FR
waxy
isoamyl laurateFL/FR
(Z)-5-decen-1-ol 
(E)-2-decen-1-yl acetateFL/FR
1-dodecanolFL/FR
 ethyl octanoateFL/FR
 methyl myristateFL/FR
 myristic acidFL/FR
2,4-nonadien-1-olFL/FR
 palmitic acidFR
 tetradecanalFL/FR
 
For Flavor
 
No flavor group found for these
2-acetyl-3,4,5,6-tetrahydropyridineFL
 allyl 2-furoateFL
 benzyl disulfideFL
 benzyl lactateFL/FR
(S)-delta-decalactoneFL/FR
(E)-2-decen-1-olFL/FR
(Z)-5-decen-1-ol 
(E)-2-decen-1-yl acetateFL/FR
7-decen-4-olideFL/FR
2,5-diethyl tetrahydrofuranFL
alpha,alpha-dimethyl anisyl acetoneFL/FR
 ethyl 2-hydroxy-2-methyl butyrateFL/FR
 ethyl 4-pentenoateFL/FR
5-ethyl-2,3,4,5-tetramethyl-2-cyclohexen-1-oneFL/FR
 furfuryl acetoneFL
 furfuryl hexanoateFL
 menthone lactoneFL/FR
 methyl myristateFL/FR
4,5-octane dioneFL
 rosefuranFL/FR
isoamyl 3-(2-furan) propionateFL/FR
acidic
 levulinic acidFL/FR
bready
 mango furanoneFL
brown
2-oxobutyric acidFL/FR
5-methyl furfuralFL/FR
 tetrahydrofurfuryl acetateFL/FR
(E)-tiglic acidFL/FR
burnt
 furfuryl alcoholFL
buttery
 acetoin propylene glycol acetalFL/FR
 diacetylFL
3,4-hexane dioneFL/FR
caramellic
 caramel dioneFL
 caramel furanoneFL
 caramel pentadioneFL/FR
 cycloteneFL/FR
 cyclotene hydrateFL/FR
 ethyl maltolFL/FR
5-ethyl-3,4,5,6-tetramethyl cyclohexen-2-oneFL
 fenugreek absoluteFL/FR
 maltolFL/FR
 maltyl propionateFL/FR
 maple furanoneFL/FR
3-methyl butyl 2-furyl butyrateFL
 shoyu furanoneFL/FR
 strawberry furanoneFL/FR
 strawberry furanone acetateFL/FR
 toffee furanoneFL/FR
coffee
2-thiophene thiolFL
cooling
 manzanate (Givaudan)FL/FR
creamy
6-amyl-alpha-pyroneFL/FR
delta-tridecalactoneFL/FR
ethereal
 benzyl laurateFL/FR
fatty
 allyl octanoateFL/FR
isoamyl laurateFL/FR
(Z)-dairy lactoneFL/FR
2,4-decadien-1-olFL/FR
 ethyl undecylenateFL/FR
4-methyl octanoic acidFL/FR
2,4-nonadien-1-olFL/FR
(E)-2-octenoic acidFL
(Z)-oleic acidFL/FR
 tetradecanalFL/FR
(E,E)-2,4-undecadienalFL
2,4-undecadienalFL
floral
 jasmin absolute (from pommade)FL/FR
fruity
 allyl cyclohexyl propionateFL/FR
 ethyl (E)-2-octenoateFL
 ethyl hexanoateFL/FR
(E)-ethyl tiglateFL/FR
 furfuryl valerateFL
2-methyl butyl butyrateFL/FR
2-pentanoyl furanFL
green
 immortelle absoluteFL/FR
hay
 genet absoluteFL/FR
herbal
 butyl levulinateFL/FR
 clary sage oil franceFL/FR
 salvia sclarea oilFL/FR
jammy
 ethyl cyclopentenoloneFL/FR
lactonic
gamma-heptalactoneFL/FR
milky
gamma-butyrolactoneFL/FR
musty
 ethyl (E)-2-crotonateFL/FR
nutty
2-acetyl furanFL/FR
3-acetyl-2,5-dimethyl furanFL/FR
2-acetyl-3,5(or 6)-dimethyl pyrazineFL/FR
2,3-dimethyl pyrazineFL/FR
 nutty cyclohexenoneFL/FR
 peanut oxazoleFL
 tetrahydrofurfuryl alcoholFL/FR
phenolic
4-methyl-2,6-dimethoxyphenolFL/FR
rummy
 ethyl pyruvateFL/FR
soapy
 dodecanal (aldehyde C-12 lauric)FL/FR
1-dodecanolFL/FR
 octanoic acidFL/FR
sweet
 cyclohexyl acetic acidFL/FR
dextro-sorbitolFL
 vanilla oleoresin baliFL/FR
toasted
 acetyl propionylFL/FR
vanilla
 ethyl vanillinFL/FR
 vanillyl isobutyrateFL/FR
waxy
(E)-2-decenalFL/FR
 ethyl octanoateFL/FR
 ethyl undecanoateFL/FR
 furfuryl octanoateFL
 methyl 10-undecenoateFL/FR
 myristic acidFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 breadFL
 fatFL
 honeyFR
 tobaccoFR
 waxy 
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 almond roasted almond - 9 mg/kg
Search Trop  Picture
 apple juice
Search  PMC Picture
 barley roasted barley
Search Trop  Picture
 beer - up to 8 mg/kg
Search  PMC Picture
 brandy - up to 11.6 mg/kg
Search  PMC Picture
 bread wheat bread - up to 19.1 mg/kg
Search  PMC Picture
 caulifiower
Search Trop  Picture
 chicory
Search Trop  Picture
 cichorium intybus l. root extract @ 4.27%
Data  GC  Search Trop  Picture
 cloudberry fruit - 0.2 mg/kg
Search Trop  Picture
 coffee - up to 35 mg/kg
PbMd  Search  PMC Picture
 cognac
Search  PMC Picture
 fruit canned
Search  PMC Picture
 honey
Search  PMC Picture
 milk - 0.03 mg/kg
Search  PMC Picture
 onion
Search Trop  Picture
 onion roasted onion
Search Trop  Picture
 pineapple fruit
Search Trop  Picture
 popcorn
Search  PMC Picture
 prune - up to 450 mg/kg
Search  PMC Picture
 sherry - up to 680 mg/kg
Search  PMC Picture
 strawberry jam
Search  Picture
 vanilla
Search  Picture
 whiskey - up to 10.1 mg/kg
Search  Picture
 wine - up to 27.3 mg/kg
Search  Picture
 wine port wine - up to 63 mg/kg
Search  Picture
 wine white wine
Search  Picture
 wood smoke
Search  Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
2-furaldehyde, 5-(hydroxymethyl)-
2-furaldehyde, 5-hydroxymethyl-
2-furancarboxaldehyde, 5-(hydroxymethyl)-
5-HMF
5-hydroxymethyl furaldehyde
 hydroxymethyl furfurole
5-hydroxymethyl-2-formyl furan
5-hydroxymethyl-2-formylfuran
5-hydroxymethyl-2-furaldehyde
5-hydroxymethyl-2-furancarboxaldehyde
5-hydroxymethyl-2-furfural
2-hydroxymethyl-5-furfural
5-hydroxymethyl-furfural
5-(hydroxymethyl) furfural
5-(hydroxymethyl)-2-furaldehyde
5-(hydroxymethyl)-2-furan carbonal
5-(hydroxymethyl)-2-furan carboxaldehyde
5-(hydroxymethyl)-2-furancarbonal
5-(hydroxymethyl)-2-furancarboxaldehyde
5-(hydroxymethyl)-2-furfural
5-(hydroxymethyl)-furfural
5-(hydroxymethyl)furan-2-carbaldehyde
5-(hydroxymethyl)furan-2-carboxaldehyde
5-(hydroxymethyl)furfural
5-hydroxymethylfuraldehyde
5-hydroxymethylfuran-2-aldehyde
5-hydroxymethylfurfural
 hydroxymethylfurfuralaldehyde
 hydroxymethylfurfurole
5-oxymethyl furfurole
5-oxymethylfurfurole
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: Non-targeted metabolomic reveals the effect of salt stress on global metabolite of halotolerant yeast Candida versatilis and principal component analysis.
PubMed: Effect of roasting conditions on color and volatile profile including HMF level in sweet almonds (Prunus dulcis).
PubMed: Honey collected from different floras of Chandigarh Tricity: a comparative study involving physicochemical parameters and biochemical activities.
PubMed: Decrease of aged beer aroma by the reducing activity of brewing yeast.
PubMed: Role of roasting conditions in the profile of volatile flavor chemicals formed from coffee beans.
PubMed: 3-Hydroxy-4,5-dimethyl-2(5H)-furanone levels in fortified Madeira wines: relationship to sugar content.
PubMed: Generation of Maillard compounds from inulin during the thermal processing of Agave tequilana Weber Var. azul.
PubMed: Separation and determination of 4-methylimidazole, 2-methylimidazole and 5-hydroxymethylfurfural in beverages by amino trap column coupled with pulsed amperometric detection.
PubMed: Tolerance of the Nanocellulose-Producing Bacterium Gluconacetobacter xylinus to Lignocellulose-Derived Acids and Aldehydes.
PubMed: Advanced glycation end products, physico-chemical and sensory characteristics of cooked lamb loins affected by cooking method and addition of flavour precursors.
PubMed: Non-targeted metabolomic reveals the effect of salt stress on global metabolite of halotolerant yeast Candida versatilis and principal component analysis.
PubMed: Determination of caramel colorants' by-products in liquid foods by ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS).
PubMed: Nutritional and physicochemical characteristic of commercial Spanish citrus juices.
PubMed: Volatile profile of Madeira wines submitted to traditional accelerated ageing.
PubMed: 5-HMF and carbohydrates content in stingless bee honey by CE before and after thermal treatment.
PubMed: Properties and catalytic activity of magnetic and acidic ionic liquids: experimental and molecular simulation.
PubMed: Validation of a HPLC method for determination of hydroxymethylfurfural in crude palm oil.
PubMed: Tolerance of S. cerevisiae and Z. mobilis to inhibitors produced during dilute acid hydrolysis of soybean meal.
PubMed: Enhancing the organoleptic and functional properties of jujube by a quick aging process.
PubMed: Acrylamide, 5-hydroxymethylfurfural and N(ε)-carboxymethyl-lysine in coffee substitutes and instant coffees.
PubMed: Kinetics of browning, phenolics, and 5-hydroxymethylfurfural in commercial sparkling wines.
PubMed: Toxic compounds in honey.
PubMed: Hydroxymethylfurfural: a possible emergent cause of honey bee mortality?
PubMed: In vitro antioxidant and antiproliferative activities of 5-hydroxymethylfurfural.
PubMed: Comparison of an HPTLC method with the Reflectoquant assay for rapid determination of 5-hydroxymethylfurfural in honey.
PubMed: Application of a high-throughput process analytical technology metabolomics pipeline to Port wine forced ageing process.
PubMed: New approaches to determination of HMF.
PubMed: Developing an effective means to reduce 5-hydroxymethyl-2-furfural from caramel colour.
PubMed: Isolation, structural elucidation, and biological evaluation of a 5-hydroxymethyl-2-furfural derivative, asfural, from enzyme-treated asparagus extract.
PubMed: Impacts of selected dietary polyphenols on caramelization in model systems.
PubMed: Physicochemical properties of the Harenna forest honey, Bale, Ethiopia.
PubMed: Identification of 5-hydroxymethyl-2-furfural (5-HMF) in Cava sparkling wines by LC-DAD-MS/MS and NMR spectrometry.
PubMed: Study of hydroxymethylfurfural and furfural formation in cakes during baking in different ovens, using a validated multiple-stage extraction-based analytical method.
PubMed: Changes of antioxidant activity and formation of 5-hydroxymethylfurfural in honey during thermal and microwave processing.
PubMed: Impact of flavour solvent (propylene glycol or triacetin) on vanillin, 5-(hydroxymethyl)furfural, 2,4-decadienal, 2,4-heptadienal, structural parameters and sensory perception of shortcake biscuits over accelerated shelf life testing.
PubMed: Identification of bitter compounds in whole wheat bread.
PubMed: Indirect competitive ELISA based on monoclonal antibody for the detection of 5-hydroxymethyl-2-furfural in milk, compared with HPLC.
PubMed: Effect of concentration temperature on some bioactive compounds and antioxidant proprieties of date syrup.
PubMed: Effects of extrusion, infrared and microwave processing on Maillard reaction products and phenolic compounds in soybean.
PubMed: Industrially applicable strategies for mitigating acrylamide, furan, and 5-hydroxymethylfurfural in food.
PubMed: Effect of 5-hydroxymethylfurfural derived from processed Cornus officinalis on the prevention of high glucose-induced oxidative stress in human umbilical vein endothelial cells and its mechanism.
PubMed: Congeners in sugar cane spirits aged in casks of different woods.
PubMed: Rapid determination of 5-hydroxymethylfurfural by DART ionization with time-of-flight mass spectrometry.
PubMed: Short communication: possible mechanism for inhibiting the formation of polymers originated from 5-hydroxymethyl-2-furaldehyde by sulfite groups in the dairy thermal process.
PubMed: Jujube honey from China: physicochemical characteristics and mineral contents.
PubMed: Physicochemical and antioxidant properties of Malaysian honeys produced by Apis cerana, Apis dorsata and Apis mellifera.
PubMed: Reactivity of thermally treated α-dicarbonyl compounds.
PubMed: Untangling the chemistry of port wine aging with the use of GC-FID, multivariate statistics, and network reconstruction.
PubMed: Thermal stability of anthocyanins and colourless phenolics in pomegranate (Punica granatum L.) juices and model solutions.
PubMed: Determination of metabolites of 5-hydroxymethylfurfural in human urine after oral application.
PubMed: Impact of cooking and handling conditions on furanic compounds in breaded fish products.
PubMed: Effect of adulteration versus storage on volatiles in unifloral honeys from different floral sources and locations.
PubMed: A comparison of different dilute solution explosions pretreatment for conversion of distillers' grains into ethanol.
PubMed: Controlling the Maillard reaction by reactant encapsulation: sodium chloride in cookies.
PubMed: Physicochemical and antioxidant properties of Bangladeshi honeys stored for more than one year.
PubMed: Reporter gene mutation in the livers of gpt delta mice treated with 5-(hydroxymethyl)-2-furfural, a contaminant of various foods.
PubMed: Okara promoted acrylamide and carboxymethyl-lysine formation in bakery products.
PubMed: Short communication: simultaneous analysis of reducing sugars and 5-hydroxymethyl-2-furaldehyde at a low concentration by high performance anion exchange chromatography with electrochemical detector, compared with HPLC with refractive index detector.
PubMed: Identification and mode of action of 5-hydroxymethyl-2-furfural (5-hmf) and 1-methyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid (MTCA) as potent xanthine oxidase inhibitors in vinegars.
PubMed: Riboflavin and lumichrome in Dalmatian sage honey and other unifloral honeys determined by LC-DAD technique.
PubMed: Development and validation of an HPLC method to determine metabolites of 5-hydroxymethylfurfural (5-HMF).
PubMed: Volatile constituents of roasted tigernut oil (Cyperus esculentus L.).
PubMed: Micellar electrokinetic chromatography method for the simultaneous determination of furanic compounds in honey and vegetable oils.
PubMed: In depth study of acrylamide formation in coffee during roasting: role of sucrose decomposition and lipid oxidation.
PubMed: Determination of very low levels of 5-(hydroxymethyl)-2-furaldehyde (HMF) in natural honey: comparison between the HPLC technique and the spectrophotometric white method.
PubMed: 1,2-dicarbonyl compounds in commonly consumed foods.
PubMed: Mutagenicity of 5-hydroxymethylfurfural in V79 cells expressing human SULT1A1: identification and mass spectrometric quantification of DNA adducts formed.
PubMed: Effect of roasting conditions on color and volatile profile including HMF level in sweet almonds (Prunus dulcis).
PubMed: Survey of 1,2-dicarbonyl compounds in commercial honey of different floral origin.
PubMed: Effect of temperature and some added compounds on the stability of blood orange marmalade.
PubMed: Kinetics of 3-deoxy-D-erythro-hexos-2-ulose in unifloral honeys.
PubMed: Study of 5-hydroxymethylfurfural and its metabolite 5-sulfooxymethylfurfural on induction of colonic aberrant crypt foci in wild-type mice and transgenic mice expressing human sulfotransferases 1A1 and 1A2.
PubMed: Optimization of furfural and 5-hydroxymethylfurfural production from wheat straw by a microwave-assisted process.
PubMed: Simultaneous quantitation of 2-acetyl-4-tetrahydroxybutylimidazole, 2- and 4-methylimidazoles, and 5-hydroxymethylfurfural in beverages by ultrahigh-performance liquid chromatography-tandem mass spectrometry.
PubMed: Analysis of roasted and unroasted Pistacia terebinthus volatiles using direct thermal desorption-GCxGC-TOF/MS.
PubMed: The potential of biodetoxification activity as a probiotic property of Lactobacillus reuteri.
PubMed: Degradation of 5-hydroxymethylfurfural during yeast fermentation.
PubMed: Maillard reaction and protein cross-linking in relation to the solubility of milk powders.
PubMed: Intestinal carcinogenesis of two food processing contaminants, 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine and 5-hydroxymethylfurfural, in transgenic FVB min mice expressing human sulfotransferases.
PubMed: Development of an enzyme-linked immunosorbent assay for the determination of 5-hydroxymethyl-2-furfural in food.
PubMed: Biological pretreatment with a cellobiose dehydrogenase-deficient strain of Trametes versicolor enhances the biofuel potential of canola straw.
PubMed: Mead production: tradition versus modernity.
PubMed: Thermal decomposition of 5-(hydroxymethyl)-2-furaldehyde (HMF) and its further transformations in the presence of glycine.
PubMed: Hydroxymethyl-substituted furans: mutagenicity in Salmonella typhimurium strains engineered for expression of various human and rodent sulphotransferases.
PubMed: Identification of Hâ‚‚Oâ‚‚ as a major antimicrobial component in coffee.
PubMed: Fructo-oligosaccharide production from inulin through partial citric or phosphoric acid hydrolyses.
PubMed: 5-Hydroxymethylfurfural content in foodstuffs determined by micellar electrokinetic chromatography.
PubMed: Fast quantitation of 5-hydroxymethylfurfural in honey using planar chromatography.
PubMed: Kinetic study of the thermal hydrolysis of Agave salmiana for mezcal production.
PubMed: Reversible and covalent binding of 5-(hydroxymethyl)-2-furaldehyde (HMF) with lysine and selected amino acids.
PubMed: Vitamin C and sugar levels as simple markers for discriminating Spanish honey sources.
PubMed: Characterization of a wild strain of Alicyclobacillus acidoterrestris: heat resistance and implications for tomato juice.
PubMed: Effect of antibrowning agents on browning and intermediate formation in the glucose-glutamic acid model.
PubMed: Toxicology and risk assessment of 5-Hydroxymethylfurfural in food.
PubMed: Effects of aldehydes on the growth and lipid accumulation of oleaginous yeast Trichosporon fermentans.
PubMed: Thermal degradation characteristics and antioxidant activity of fructose solution with heating temperature and time.
PubMed: nematicidal carboxylic acids and aldehydes from Melia azedarach fruits.
PubMed: Use of green rooibos (Aspalathus linearis) extract and water-soluble nanomicelles of green rooibos extract encapsulated with ascorbic acid for enhanced aspalathin content in ready-to-drink iced teas.
PubMed: Characterization of artisanal honey produced on the Northwest of Portugal by melissopalynological and physico-chemical data.
PubMed: Optimization of extraction of apple pomace phenolics with water by response surface methodology.
PubMed: Determination of some chemical parameters and antimicrobial activity of traditional food: mesir paste.
PubMed: High 5-hydroxymethylfurfural concentrations are found in Malaysian honey samples stored for more than one year.
PubMed: Glucose reversion reaction kinetics.
PubMed: Determination of furan precursors and some thermal damage markers in baby foods: ascorbic acid, dehydroascorbic acid, hydroxymethylfurfural and furfural.
PubMed: Does the pelleting process affect the nutritive value of a pre-starter diet for suckling piglets? Ex vivo studies on mineral absorption.
PubMed: Quantitative determination of caffeine, formic acid, trigonelline and 5-(hydroxymethyl)furfural in soluble coffees by 1H NMR spectrometry.
PubMed: Decrease of aged beer aroma by the reducing activity of brewing yeast.
PubMed: Analysis, distribution, and dietary exposure of glyoxal and methylglyoxal in cookies and their relationship with other heat-induced contaminants.
PubMed: Sucrose: A prospering and sustainable organic raw material.
PubMed: Estimation of dietary intake of 5-hydroxymethylfurfural and related substances from coffee to Spanish population.
PubMed: In vitro antioxidant activity of 5-HMF isolated from marine red alga Laurencia undulata in free-radical-mediated oxidative systems.
PubMed: Physico-chemical studies on adulteration of honey in Nigeria.
PubMed: Genotoxic activities of the food contaminant 5-hydroxymethylfurfural using different in vitro bioassays.
PubMed: Effect of L-asparaginase on acrylamide mitigation in a fried-dough pastry model.
PubMed: Simultaneous determination of melamine and 5-hydroxymethylfurfural in milk by capillary electrophoresis with diode array detection.
PubMed: Assessment of hydroxymethylfurfural intake in the Spanish diet.
PubMed: [Studies on chemical constituents from bee-collected rape pollen].
PubMed: Role of roasting conditions in the profile of volatile flavor chemicals formed from coffee beans.
PubMed: 5-Hydroxymethylfurfural and 5-sulfooxymethylfurfural increase adenoma and flat ACF number in the intestine of Min/+ mice.
PubMed: Improved method to measure aldehyde adducts to N-terminal valine in hemoglobin using 5-hydroxymethylfurfural and 2,5-furandialdehyde as model compounds.
PubMed: Identification of an interfering substrate in apple juice and improvement for determination of patulin with high-performance liquid chromatography analyses.
PubMed: Determination of 5-hydroxymethylfurfural using derivatization combined with polymer monolith microextraction by high-performance liquid chromatography.
PubMed: Conversion of the common food constituent 5-hydroxymethylfurfural into a mutagenic and carcinogenic sulfuric acid ester in the mouse in vivo.
PubMed: Development and validation of an HPLC method to quantify 3,4-dideoxyglucosone-3-ene in peritoneal dialysis fluids.
PubMed: Evaluation of the DNA damaging effect of the heat-induced food toxicant 5-hydroxymethylfurfural (HMF) in various cell lines with different activities of sulfotransferases.
PubMed: Influence of roasting on the antioxidant activity and HMF formation of a cocoa bean model systems.
PubMed: Wheat straw autohydrolysis: process optimization and products characterization.
PubMed: Evaluation of antioxidant activity, colour and some nutritional characteristics of pomegranate (Punica granatum L.) juice and its sour concentrate processed by conventional evaporation.
PubMed: Degradation of 5-hydroxymethylfurfural in honey.
PubMed: Simple gas chromatographic method for furfural analysis.
PubMed: Dietary exposure to 5-hydroxymethylfurfural from Norwegian food and correlations with urine metabolites of short-term exposure.
PubMed: Quality evaluation of different honey samples produced in Peshawar valley.
PubMed: Isotope labeling studies on the formation of 5-(hydroxymethyl)-2-furaldehyde (HMF) from sucrose by pyrolysis-GC/MS.
PubMed: Changes in the chemical composition of reduced cooked musts during the heating process.
PubMed: Impact of caramelization on the glass transition temperature of several caramelized sugars. Part II: Mathematical modeling.
PubMed: Comparative study of pulsed electric field and thermal processing of apple juice with particular consideration of juice quality and enzyme deactivation.
PubMed: Estimation of hydroxymethylfurfural availability in breakfast cereals. Studies in Caco-2 cells.
PubMed: Liquid chromatography multi-stage mass spectrometry for the analysis of 5-hydroxymethylfurfural in foods.
PubMed: Evolution of hydroxymethylfurfural content of honeys from different climates: influence of induced granulation.
PubMed: Investigation of acrylamide in curries made from coconut milk.
PubMed: SULT1C3, an orphan sequence of the human genome, encodes an enzyme activating various promutagens.
PubMed: The effect of various drying techniques on apricot volatiles analysed using direct thermal desorption-GC-TOF/MS.
PubMed: Determination of patulin in commercial apple juice by micellar electrokinetic chromatography.
PubMed: The potential antimutagenic and antioxidant effects of Maillard reaction products used as "natural antibrowning" agents.
PubMed: Formation of 5-hydroxymethyl-2-furfural (HMF) and 5-hydroxymethyl-2-furoic acid during roasting of coffee.
PubMed: Inhibition of polyphenoloxidase activity by mixtures of heated cysteine derivatives with carbonyl compounds.
PubMed: Isolation and identification of potential cancer chemopreventive agents from methanolic extracts of green onion (Allium cepa).
PubMed: Maillard reaction indicators in diets usually consumed by adolescent population.
PubMed: Analysis of 5-hydroxymethylfurfural in foods by gas chromatography-mass spectrometry.
PubMed: Analysis of 5-hydroxymethylfurfual in coffee, dried fruits and urine.
PubMed: Study on fluorescence of Maillard reaction compounds in breakfast cereals.
PubMed: Relationship between acrylamide and thermal-processing indexes in commercial breakfast cereals: a survey of Spanish breakfast cereals.
PubMed: Identification and urinary excretion of metabolites of 5-(hydroxymethyl)-2-furfural in human subjects following consumption of dried plums or dried plum juice.
PubMed: Diets rich in Maillard reaction products affect protein digestibility in adolescent males aged 11-14 y.
PubMed: Improved method for the determination of hydroxymethylfurfural in baby foods using liquid chromatography-mass spectrometry.
PubMed: Analysis of amino acids and carbohydrates in green coffee.
PubMed: 5-(Hydroxymethyl)-2-furfural: a selective inhibitor of DNA polymerase lambda and terminal deoxynucleotidyltransferase.
PubMed: Browning of model orange juice solution: factors affecting the formation of decomposition products.
PubMed: Amla (Emblica officinalis Gaertn.) extracts reduce oxidative stress in streptozotocin-induced diabetic rats.
PubMed: Honey in combination with vacuum impregnation to prevent enzymatic browning of fresh-cut apples.
PubMed: Effect of storage period under variable conditions on the chemical and physical composition and colour of Spanish refrigerated orange juices.
PubMed: Single laboratory validation of a method for the determination of hydroxymethylfurfural in honey by using solid-phase extraction cleanup and liquid chromatography.
PubMed: Quality evaluation of honey harvested from selected areas in Tanzania with special emphasis on hydroxymethyl furfural (HMF) levels.
PubMed: 3-Hydroxy-4,5-dimethyl-2(5H)-furanone levels in fortified Madeira wines: relationship to sugar content.
PubMed: A benzenoid from the stem of Acanthopanax senticosus.
PubMed: 1H NMR studies on Italian balsamic and traditional balsamic vinegars.
PubMed: Browning and decomposed products of model orange juice.
PubMed: Influence of distillation system, oak wood type, and aging time on composition of cider brandy in phenolic and furanic compounds.
PubMed: 2-Furoylmethyl amino acids and hydroxymethylfurfural as indicators of honey quality.
PubMed: Influence of seasonal variation on kinetics of time temperature integrators for thermally processed milk.
PubMed: Thermal decomposition of specifically phosphorylated D-glucoses and their role in the control of the Maillard reaction.
PubMed: Kinetics of hydroxymethylfurfural, lactulose and furosine formation in milk with different fat content.
PubMed: Phytochemical composition and antioxidant stability of fortified yellow passion fruit (Passiflora edulis).
PubMed: Identification and quantification of antioxidant components of honeys from various floral sources.
PubMed: Interactions between cyanidin 3-O-glucoside and furfural derivatives and their impact on food color changes.
PubMed: Role of aldehydic derivatives in the condensation of phenolic compounds with emphasis on the sensorial properties of fruit-derived foods.
PubMed: Antioxidant effects of isorhamnetin 3,7-di-O-beta-D-glucopyranoside isolated from mustard leaf (Brassica juncea) in rats with streptozotocin-induced diabetes.
PubMed: Erythritol attenuates the diabetic oxidative stress through modulating glucose metabolism and lipid peroxidation in streptozotocin-induced diabetic rats.
PubMed: Generation of Maillard compounds from inulin during the thermal processing of Agave tequilana Weber Var. azul.
PubMed: Formation kinetics of hydroxymethylfurfural, lactulose and furosine in milk heated under isothermal and non-isothermal conditions.
PubMed: Supercritical fluid extraction of 5-hydroxymethyl-2-furaldehyde from raisins.
PubMed: Derivative spectrophotometric determination of 5-(hydroxymethyl)-2-furaldehyde (HMF) and furfural in Locust bean extract.
PubMed: Effects of some hydrocolloids and water activity on nonenzymic browning of concentrated orange juice.
PubMed: Study of the reactions between (+)-catechin and furfural derivatives in the presence or absence of anthocyanins and their implication in food color change.
PubMed: Use of 2-furoylmethyl derivatives of GABA and arginine as indicators of the initial steps of maillard reaction in orange juice.
PubMed: 5-Hydroxymethylfurfural: assessment of mutagenicity, DNA-damaging potential and reactivity towards cellular glutathione.
PubMed: Effects of Ca(OH)(2) treatments ("overliming") on the composition and toxicity of bagasse hemicellulose hydrolysates.
PubMed: Confirmation of patulin and 5-hydroxymethylfurfural in apple juice by gas chromatography/mass spectrometry.
PubMed: Effect of hexanal and iron on color development in a glucose/phenylalanine model system.
PubMed: Hydroxymethylfurfural and furosine reaction kinetics in tomato products.
PubMed: Study of the formation mechanisms of some volatile compounds during the aging of sweet fortified wines.
PubMed: Effects of L-cysteine and N-acetyl-L-cysteine on 4-hydroxy-2, 5-dimethyl-3(2H)-furanone (furaneol), 5-(hydroxymethyl)furfural, and 5-methylfurfural formation and browning in buffer solutions containing either rhamnose or glucose and arginine.
PubMed: Phenolic constituents, furans, and total antioxidant status of distilled spirits.
PubMed: Analysis of furanone, pyranone, and new heterocyclic colored compounds from sugar-glycine model Maillard systems.
PubMed: Effect of selected aldehydes on the growth and fermentation of ethanologenic Escherichia coli.
PubMed: Simultaneous determination of 5-hydroxymethylfurfural and patulin in apple juice by reversed-phase liquid chromatography.
PubMed: Distribution and metabolism of (5-hydroxymethyl)furfural in male F344 rats and B6C3F1 mice after oral administration.
PubMed: Rapid reversed-phase liquid chromatographic determination of patulin in apple juice.
PubMed: Bioactivation of 5-hydroxymethyl-2-furaldehyde to an electrophilic and mutagenic allylic sulfuric acid ester.
PubMed: Semiautomatic determination of furanic aldehydes in food and pharmaceutical samples by a stopped-flow injection analysis method.
PubMed: Detection and determination of interfering 5-hydroxymethylfurfural in the analysis of caramel-coloured pharmaceutical syrups.
PubMed: Toxicity potential of compounds found in parenteral solutions with rubber stoppers.
PubMed: Reversed-phase high-performance liquid chromatographic method for the quantification of 5-hydroxymethylfurfural as the major degradation product of glucose in infusion fluids.
PubMed: Influence of water activity and reaction temperature of ribose-lysine and glucose-lysine Maillard systems on mutagenicity, absorbance and content of furfurals.
PubMed: [Formation of hydroxymethylfurfural during the storage and processing of food products].
PubMed: Desmutagenic effect of alpha-dicarbonyl and alpha-hydroxycarbonyl compounds against mutagenic heterocyclic amines.
PubMed: Rapid and complete urinary elimination of [14C]-5-hydroxymethyl-2-furaldehyde administered orally or intravenously to rats.
PubMed: High performance liquid chromatography of furfural and hydroxymethylfurfural in spirits and honey.
PubMed: Hydroxymethylfurfural and honey adulteration.
PubMed: [Hygienic significance of patulin in foods. 1. Analytical detection of patulin].
Synonyms   Articles   Notes   Search   Top
Please share your Comments.
Email Address:
 
 
 
 
Top of Page Home
Copyright © 1980-2021 Perflavory ™ Disclaimer Privacy Policy