furfuryl mercaptan
2-furanmethanethiol
 
Notes:
major flavoring agent in coffee. Flavour ingredient used in coffee aroma. Formed by thermal treatment of cysteine/ribose mixtures. Present in cooked meats, popcorn, wheat bread, roasted coffee and roasted sesame seed oil
  • Advanced Biotech
  • Alfrebro
    • Alfrebro LLC/ Archer Daniels Midland Company
      Let's get reacquainted
      Building great taste with aroma chemicals, extracts, and distillates
      The Alfrebro brand was established in the early 1900s by Alex Fries & Brothers, a Cincinnati Flavor Company. In 1980, the brand was re-launched as an aroma chemical manufacturer. Since its inception, Alfrebro’s primary focus has been to provide quality natural and high value synthetic chemicals.
      Email: Sarah Forbis
      Email: Sales
      Voice: 513-539-3021
      Fax: 513-539-7372
      US Voice: 513-539-7373
      Newsroom
      Product(s):
      Furfuryl Mercaptan, Natural
       
  • Augustus Oils
    • Augustus Oils Ltd
      The Premier Supplier
      Augustus Oils Ltd, in harmony with nature - to present it at its best...
      A wealth of experience, expertise and knowledge has allowed Augustus to bridge the gulf in expectation and trust between growers and users of natural ingredients. The Company works in partnership with customers on the one hand, and growers, farmers and distillers on the other. Both users and producers can then focus on exactly what they do best, while skilled Augustus technicians closely monitor and control the delivered product. This ensures users can have the confidence that they will receive the best raw materials suited to their requirements.
      Email: Enquiries
      Email: Sales
      Email: web site enquiries
      Voice: +44 (0)1420 590555
      Fax: +44 (0)1420 592420
      Services
      Product(s):
      Furfuryl Mercaptan
      Furfuryl Mercaptan Natural
       
  • Axxence Aromatic
    • Axxence Aromatic GmbH
      We bring nature to your flavour
      Dedicated to provide the best possible quality and supply service of natural aroma ingredients.
      Axxence Aromatic is entirely dedicated to provide the best possible quality and supply service of natural aroma ingredients to the Flavour & Fragrance Industry worldwide.
      Email: Service
      Voice: +49.2822.68561.0
      Fax: +49.2822.68561.39
      Sustainability
      Products List: View
      Product(s):
      249300 FURFURYL MERCAPTAN Natural Kosher
       
  • 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):
      10325 Furfuryl mercaptan
       
  • Charkit Chemical
    • Charkit Chemical Corporation
      The Specialty Chemical Specialists
      Explore this website to discover the products and services that Charkit provides for your industry and please contact us directly to find out how we can be of service to you.
      about: Since 1982, Charkit has been committed to expanding the markets we serve as our roster of products and services continues to grow with us. Our substantial portfolio of personal care ingredients now include a wide array of luxury and exotic components to compliment the key products we have always offered. We have expanded our offerings to the nutraceutical, industrial, and resin markets with a growing roster of versatile and unique ingredients. We continue to lead the way in our traditional markets such as Metal and Water Treatment, Imaging, Flavor & Fragrance, Aroma and Food. Our Pharmaceutical offerings continue to expand, still anchored by the Boronic Derivatives that meet the demands of Suzuki coupling reactions. Please contact us to learn how we can help you reach your goals.
      Email: Sales
      Voice: 203-299-3220
      Fax: 203-299-1355
      Facebook
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      Events
      Blog
      Products List: View
      Product(s):
      FURFURYL MERCAPTAN FEMA 2493
       
  • Endeavour Specialty Chemicals
  • Excellentia International
    • Excellentia International
      Ingredients by Nature
      Exceptional quality and excellence in meeting our customers requirements.
      Excellentia International was founded in 2010 through the merger of Excellentia Flavors LLC and Polarome International. Collectively, these companies account for more than one hundred years of industry experience, and are recognized for exceptional quality and excellence in meeting our customers’ requirements.
      Email: Info
      Email: Sales
      Email: Regulatory
      Voice: 732.749.9840
      Our Services
      Product(s):
      Furfuryl Mercaptan Natural
       
  • FCI SAS
    • FCI SAS
      Inspired by Nature
      At FCI customer service is not a department it’s an attitude.
      Our team is composed of motivated professionals with great experience in the flavours and fragrances market. Our company has been serving this industry for more than 40 years and is ISO 9001 certified since 2009 . Whatever your question on flavour and fragrance ingredients: commercial, technical or regulatory – we will answer it very quickly.
      Email: Info
      Email: Philippe Faucher
      US Email: USA Sales
      Email: Germany Sales
      Email: Italy Sales
      Email: Japan Sales
      Voice: +33 (0)1 34 25 58 10
      Fax: + 33 1 34 25 58 18
      About Us
      Product(s):
      50037 FURFURYL MERCAPTAN
       
  • Fleurchem
    • Fleurchem, Inc.
      Have A Flavorful Day
      A leading global manufacturer and supplier of ingredients for Flavors, Fragrances, AromaTherapy, Foods, Beverages, Personal Care Products, and other uses.
      Operating out of the 200,000 sq. ft., former Hercules/PFW facility in Middletown, NY; Fleurchem produces a full range of natural isolates, synthetic chemicals & specialities, essential oils and flavors. Additionally, the company performs toll manufacturing, as well as custom chemical synthesis for a wide range of clients.
      Email: Information
      US Voice: 845-341-2100
      US Fax: 845-341-2121
      Product(s):
      furfuryl mercaptan natural
      furfuryl mercaptan
       
  • Natural Advantage
  • OQEMA
    • OQEMA
      With a focus on providing the highest level of service
      OQEMA has established itself at the forefront of the global chemical industry.
      The guiding principles of OQEMA have always been to establish long term relationships with customers and suppliers alike to build sustainable and profitable business for all parties. Through OQEMA’s business divisions the company tailors products and services to better support and service our customers requirements. This structure also allows the company to focus its marketing campaigns more effectively to certain industries. Over the last decade OQEMA has achieved strong growth as a result of the expansion of our business model. Going forward, the company will be expanding this business model into existing and new strategic territories.
      Email: Contact Us:
      US Email: Dean Matienzo
      Email: Sales
      US Email: Dean Matienzo - Sales Manager
      Voice: +44 1993 843081
      Fax: +44 1993 841261
      US Voice: +1 973 886 3778
      US Fax: +1 973 346 1106
      Linkedin
      Website
      Global Distribution
      Product(s):
      Furfural Mercaptan
       
  • Penta International
  • Riverside Aromatics
    • Riverside Aromatics Ltd.
      Speciality Aroma Chemicals, Naturals and Synthetics
      A specialist supplier of raw materials to the flavour industry.
      Peter Cannon & David Rowe established Riverside Aromatics in 2006 in Poole, UK, to offer a new type of specialist raw material supplier to the Flavour & Fragrance Industry. We bring together over 40 years of commercial & technical experience in the F&F industry which allows us to understand the needs of the Global F&F business and especially that of the West European Market.
      Email: Info
      Email: Peter Cannon (sales)
      Voice: +44 (0) 1202 679532
      Fax: +44 (0) 1202 679532
      Products List: View
      Product(s):
      NF1000 FURFURYL MERCAPTAN NATURAL
       
  • Robertet
  • 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):
      H0136 Furfuryl Mercaptan
       
  • 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):
      W063 Furfuryl Mercaptan
       
  • Taytonn ASCC
    • Taytonn ASCC Pte Ltd
      Supplying Asia Pacific
      We fully understand the demands of the F&F industry and we endeavour to supply quality products, with ready availability and a personalised service.
      Since 2001 TAYTONN has been distributing key ingredients to the Fragrance and Flavor industry in Asia. We work closely with customers, principals and vendors. Together we forecast demand and match it with supply of aroma chemicals, essential oils and natural isolates & extracts. Sourced from around the world, our F&F ingredient inventory in Singapore is ready to ship to any location in Asia and beyond. Time and again, we help our principals introduce new discoveries to the F&F market - stimulating creativity and bringing value added proposition to our customers.
      Email: Info
      Email: Sales
      Voice: + 65 - 6861 8113
      Fax: + 65 - 6861 8115
      Linkedin
      Product(s):
      Furfuryl Mercaptan
       
  • 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
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      Linkedin
      Product(s):
      F0077 Furfuryl Mercaptan >98.0%(GC)
      SDS
       
  • 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
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      News
      Product(s):
      Furfuryl Mercaptan Halal, Kosher
      Odor threshold in water: 0.005 ppb.
      Flavor threshold in water: 0.04 ppb. Found as a natural constituent in Roasted offee in 1926, it has long been used as the character impact compound in Artificial Coffee flavors. At 0.1-1 ppb this material is coffee-like, but at 5-10 ppb it has a stale coffee & sulphury character (Tressl, 1989). Mosciano, et. al. (1997) describe the odor as "sulphurous, coffee, savory and meaty with a pungent nuance" and the taste (at 1.0 ppm) as "Sulphurous, roasted, onion, garlic, coffee and sesame". Used in Coffee, Chocolate, Meat, Smoke, Nut, Toffee and Caramel flavors. Normal use levels in finished consumer product: 0.0001-0.5 ppm. Council of Europe limits: Foods (30 ppm); Beverages (1 ppm).
       
       
  • 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):
      3007 Furfuryl Mercaptan
      3007N Furfuryl mercaptan Nat.
       
  • Ernesto Ventós
  • Vigon International
    • Vigon International
      Passion for Simplicity
      Manufacturer and supplier of high quality flavor and fragrance ingredients.
      The growth and success of Vigon is due in large part to a unique corporate concept that Vigon has developed and established within the industry: Creative Partnerships. This partnership concept has been and continues to be the foundation and guiding principle for all of Vigon's activities.
      US Email: Sales
      US Voice: 570-476-6300
      US Fax: 570-476-1110
      Facebook
      Twitter
      Linkedin
      Newsletter
      Blog
      Products List: View
      Product(s):
      508070 FURFURYL MERCAPTAN 1% IN TEC
       
  • 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):
      Furfuryl mercaptan
       
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas    Flavor Demo Formulas
CAS Number: 98-02-2Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 202-628-2
FDA UNII: 29W096TCPG
Nikkaji Web: J21.666F
Beilstein Number: 0383594
MDL: MFCD00003254
CoE Number: 2202
XlogP3: 1.30 (est)
Molecular Weight: 114.16702000
Formula: C5 H6 O S
NMR Predictor: Predict (works with chrome, Edge or firefox)
Category: flavor and fragrance 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
JECFA Food Flavoring: 1072  furfuryl mercaptan
DG SANTE Food Flavourings: 13.026  2-furanmethanethiol
FEMA Number: 2493 furfuryl mercaptan
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):98-02-2 ; FURFURYL MERCAPTAN
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: colorless to pale yellow clear oily liquid (est)
Assay: 97.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 1.12500 to 1.13500 @  20.00 °C.
Pounds per Gallon - (est).: 9.372 to  9.455
Refractive Index: 1.52700 to 1.54200 @  20.00 °C.
Boiling Point: 154.00 to  155.00 °C. @ 760.00 mm Hg
Boiling Point: 147.00 °C. @ 12.00 mm Hg
Vapor Pressure: 3.980000 mmHg @ 25.00 °C. (est)
Vapor Density: 3.9 ( Air = 1 )
Flash Point: 113.00 °F. TCC ( 45.00 °C. )
logP (o/w): 1.727 (est)
Soluble in:
 alcohol
 water, 2216 mg/L @ 25 °C (est)
Insoluble in:
 water
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Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: coffee
 
 sulfurous  coffee roasted coffee  oily  fatty  burnt  smoky  
Odor Description:
at 0.10 % in dipropylene glycol. 
sulfury roasted coffee oily fatty burnt smoky
 
 coffee roasted coffee  sulfurous  burnt  savory  meaty  chicken  onion cooked onion  
Odor Description:
at 0.10 % in propylene glycol.  
Roasted coffee, sulfurous, with a burnt match note. It is savory meaty with chicken and fried onion nuances.
Mosciano, Gerard P&F 26, No. 5, 68, (2001)
 
 
Flavor Type: coffee
 
 sulfurous  roasted  coffee  burnt  rubbery  nutty  eggy  savory  meaty  
Taste Description:
at 1.00 ppm.  
Sulfurous roasted coffee, burnt match-like, rubbery, and slightly nutty with eggy and savory meaty nuances.
Mosciano, Gerard P&F 26, No. 5, 68, (2001)
 
Odor and/or flavor descriptions from others (if found).
 
Sigma-Aldrich
Furfuryl mercaptan, ≥97%, FG
Odor Description: caramel; chocolate; oily; smoky; herbaceous; nutty; sulfurous; meaty; waxy; fishy; coffee; alliaceous (onion, garlic)
 
R C Treatt & Co Ltd
Furfuryl Mercaptan Halal, Kosher
Odor Description: Powerful; burnt, coffee-like aroma on dilution
Odor threshold in water: 0.005 ppb.
Taste Description: burnt
Flavor threshold in water: 0.04 ppb. Found as a natural constituent in Roasted offee in 1926, it has long been used as the character impact compound in Artificial Coffee flavors. At 0.1-1 ppb this material is coffee-like, but at 5-10 ppb it has a stale coffee & sulphury character (Tressl, 1989). Mosciano, et. al. (1997) describe the odor as "sulphurous, coffee, savory and meaty with a pungent nuance" and the taste (at 1.0 ppm) as "Sulphurous, roasted, onion, garlic, coffee and sesame". Used in Coffee, Chocolate, Meat, Smoke, Nut, Toffee and Caramel flavors. Normal use levels in finished consumer product: 0.0001-0.5 ppm. Council of Europe limits: Foods (30 ppm); Beverages (1 ppm).
 
Nagar Haveli Perfumes & Aromatics
Furfuryl Mercaptan
Odor Description: Roasted coffee, sulfurous, with a burnt match note. It is savory meaty with chicken and fried onion nuances.
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
Advanced Biotech
FURFURYL MERCAPTAN 1% IN ETOH NATURAL
Advanced Biotech
FURFURYL MERCAPTAN 1% IN PG NATURAL
Advanced Biotech
FURFURYL MERCAPTAN EEC NATURAL
98% min.
Odor: Coffee, Roasted
Advanced Biotech
FURFURYL MERCAPTAN NATURAL
98% min.
Odor: Coffee, Roasted
Advanced Biotech
FURFURYL MERCAPTAN
Alfrebro
Furfuryl Mercaptan, Natural
Odor: Sulfury Roasted Coffee Oily Fatty Burnt Smoky
Ambles Nature et Chimie
FURFURYL MERCAPTAN NAT
Anhui Haibei
Furfuryl Mercaptan
Odor: Sulfury roasted coffee oily fatty burnt smoky
Anhui Suzhou Jinli Aromatic Chemicals
Furfuryl Mercaptan
Odor: coke, coffee
Augustus Oils
Furfuryl Mercaptan Natural
Services
Augustus Oils
Furfuryl Mercaptan
Aurochemicals
FURFURYL MERCAPTAN 1% IN ETOH, Natural
Aurochemicals
FURFURYL MERCAPTAN 1% IN PG, Natural
Aurochemicals
FURFURYL MERCAPTAN 1% IN TRIGLYCERIDE, Natural
Aurochemicals
FURFURYL MERCAPTAN, Natural
Axxence Aromatic
FURFURYL MERCAPTAN Natural
Kosher
Sustainability
Beijing Lys Chemicals
Furfuryl mercaptan
Charkit Chemical
FURFURYL MERCAPTAN FEMA 2493
DeLong Chemicals America
Furfuryl mercaptan, Kosher
Endeavour Specialty Chemicals
Furfuryl mercaptan 98% F&F
Speciality Chemical Product Groups
Endeavour Specialty Chemicals
Furfuryl mercaptan PG acetal
Ernesto Ventós
FURFURYL MERCAPTAN
Odor: ROAST BURNT, COFFEE
Excellentia International
Furfuryl Mercaptan Natural
FCI SAS
FURFURYL MERCAPTAN
Odor: Roasted coffee
Fleurchem
furfuryl mercaptan natural
Fleurchem
furfuryl mercaptan
Frutarom
FURFURYL MERCAPTAN
KOSHER
Flavor: Burnt, Coffee, Oily, Roasted, Sulfurous
CBD Offering
IFF
FURFURYL MERCAPTAN
KOSHER
Flavor: Burnt, Coffee, Oily, Roasted, Sulfurous
Indukern F&F
FURFURYL MERCAPTAN NATURAL
Odor: SULFUROUS, POWERFUL, COFFEE
Indukern F&F
FURFURYL MERCAPTAN
Odor: SULFUROUS, POWERFUL, COFFEE
Jinan Enlighten Chemical Technology(Wutong Aroma )
Furfuryl mercaptan, Kosherk
Kingchem Laboratories
FURFURYL MERCAPTAN
Odor: Charred coffee
Lluch Essence
ALPHA-FURFURYL MERCAPTANE NATURAL
Lluch Essence
ALPHA-FURFURYL MERCAPTANE
M&U International
Furfuryl Mercaptan, Kosher
M&U International
Nat. Furfuryl Mercaptan
Moellhausen
FURFURYL MERCAPTAN
Nagar Haveli Perfumes & Aromatics
Furfuryl Mercaptan
Odor: Roasted coffee, sulfurous, with a burnt match note. It is savory meaty with chicken and fried onion nuances.
Natural Advantage
Furfuryl Mercaptan Nat
Flavor: burnt, caramellic, coffee, meaty, savory
Riverside Aromatics LTD.is the exclusive distributor for Europe in UK for any non-US based inquiries
OQEMA
Furfural Mercaptan
Penta International
FURFURYL MERCAPTAN NATURAL 0.1% IN P.G.
Penta International
FURFURYL MERCAPTAN NATURAL 1.0% IN P.G.
Penta International
FURFURYL MERCAPTAN NATURAL
Penta International
FURFURYL MERCAPTAN
R C Treatt & Co Ltd
Furfuryl Mercaptan
Halal, Kosher
Odor: Powerful; burnt, coffee-like aroma on dilution
Use: Odor threshold in water: 0.005 ppb.
Flavor: burnt
Flavor threshold in water: 0.04 ppb. Found as a natural constituent in Roasted offee in 1926, it has long been used as the character impact compound in Artificial Coffee flavors. At 0.1-1 ppb this material is coffee-like, but at 5-10 ppb it has a stale coffee & sulphury character (Tressl, 1989). Mosciano, et. al. (1997) describe the odor as "sulphurous, coffee, savory and meaty with a pungent nuance" and the taste (at 1.0 ppm) as "Sulphurous, roasted, onion, garlic, coffee and sesame". Used in Coffee, Chocolate, Meat, Smoke, Nut, Toffee and Caramel flavors. Normal use levels in finished consumer product: 0.0001-0.5 ppm. Council of Europe limits: Foods (30 ppm); Beverages (1 ppm).
Reincke & Fichtner
Furfuryl Mercaptan natural
Reincke & Fichtner
Furfuryl Mercaptan
Riverside Aromatics
FURFURYL MERCAPTAN NATURAL
Robertet
FURFURYL MERCAPTAN
Pure & Nat (EU)
Seasons and Harvest / Crop calendar
Robinson Brothers
Furfuryl mercaptan F&F
https://www.robinsonbrothers.uk/chemistry-competences
Robinson Brothers
Furfuryl mercaptan PG acetal
Santa Cruz Biotechnology
For experimental / research use only.
2-Furanmethanethiol
Sigma-Aldrich
Furfuryl mercaptan, ≥97%, FG
Odor: caramel; chocolate; oily; smoky; herbaceous; nutty; sulfurous; meaty; waxy; fishy; coffee; alliaceous (onion, garlic)
Certified Food Grade Products
Sigma-Aldrich
Furfuryl mercaptan, natural, 98%, FG
Odor: roasted
Sunaux International
Furfuryl Mercaptan
Synerzine
Furfuryl Mercaptan
Taytonn ASCC
Furfuryl Mercaptan
Odor: Burnt, Coffee, Oily, Roast, Sulphurous
TCI AMERICA
For experimental / research use only.
Furfuryl Mercaptan >98.0%(GC)
Tengzhou Jitian Aroma Chemiclal
Furfuryl Mercaptan
Tengzhou Xiang Yuan Aroma Chemicals
Furfuryl Mercaptan
United International
Furfuryl mercaptan Nat.
United International
Furfuryl Mercaptan
Vigon International
FURFURYL MERCAPTAN 1% IN TEC
WholeChem
Furfuryl mercaptan
Synonyms   Articles   Notes   Search   Top
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 10 - Flammable.
R 36/37/38 - Irritating to eyes, respiratory system, and skin.
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.
 
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:
intraperitoneal-mouse LD50  [sex: M] 100 - 200 mg/kg
(Doull et al., 1962)

intraperitoneal-mouse LD50  100 mg/kg
National Technical Information Service. Vol. AD277-689

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: flavor and fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for furfuryl mercaptan usage levels up to:
  0.0500 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 29.00 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 11.00 (μg/capita/day)
NOEL (No Observed Effect Level): 3.00 (mg/kg bw per day)
Structure Class: II
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 2
Click here to view publication 2
 average usual ppmaverage maximum ppm
baked goods: -2.10000
beverages(nonalcoholic): -0.52000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: -0.50000
egg products: --
fats / oils: --
fish products: --
frozen dairy: -0.78000
fruit ices: -0.78000
gelatins / puddings: -0.10000
granulated sugar: --
gravies: --
hard candy: -2.00000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: --
sugar substitutes: --
sweet sauces: --
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
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
Scientific Opinion on Flavouring Group Evaluation 65, Revision 1 (FGE.65Rev1): 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.13Rev2 (2011)
View page or View pdf
Safety and efficacy of furfuryl and furan derivatives belonging to chemical group 14 when used as flavourings for all animal species and categories
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
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 98-02-2
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 7363
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 3336
WGK Germany: 3
 furan-2-ylmethanethiol
Chemidplus: 0000098022
RTECS: LU2100000 for cas# 98-02-2
Synonyms   Articles   Notes   Search   Top
References:
 furan-2-ylmethanethiol
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 98-02-2
Pubchem (cid): 7363
Pubchem (sid): 134970963
Flavornet: 98-02-2
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
FDA Substances Added to Food (formerly EAFUS): View
CHEMBL: View
HMDB (The Human Metabolome Database): HMDB32915
FooDB: FDB010898
YMDB (Yeast Metabolome Database): YMDB01433
Export Tariff Code: 2932.19.5100
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
No odor group found for these
 chicory root 
roasted robusta coffee bean 
roasted congo coffee bean 
roasted coffea coffee bean 
roasted bengal coffee bean 
roasted liberian coffee bean 
roasted arabica coffee bean 
3,6-dimethyl pyrazine-2-thiol 
2,5-dimethyl-3-furfurylthio-pyrazine 
2,5-dimethyl-3,6-diethyl pyrazine 
2,6-dimethyl-gamma-thiopyrone 
2,6-dimethyl-thio-gamma-pyrone 
2-hydroxymethyl-6-methyl-pyridine 
4-hydroxymethyl-pyridine 
2-methyl-3-pentyl pyrazine 
(2-methylpyrazinyl-3, -5 and-6) furfuryl sulfide 
2-pentenyl furan 
2-(1-propenyl) pyridine 
2-(thienyl-2)-ethanethiol 
2,3,5-trimethyl phenolFR
 methyl furfuryl disulfideFL/FR
balsamic
2-acetyl furanFL/FR
(R)-2-methyl butyraldehyde 
 caramel furanone solutionFL/FR
 coffee dioneFL/FR
 cycloteneFL/FR
 fenugreek absoluteFL/FR
 fenugreek oleoresinFL/FR
5-methyl furfuralFL/FR
isopropenyl pyrazineFL/FR
cheesy
2-methyl hexanoic acidFL/FR
chocolate
 cocoa hexenalFL/FR
2,6-dimethyl pyrazineFL/FR
2,4,5-trimethyl thiazoleFL/FR
 vanillyl ethyl etherFL/FR
cocoa
2-methyl butyraldehydeFL/FR
coffee
 cappuccino fragranceFR
 cichorium intybus root extractFL/FR
 cichorium intybus root solid extractFL/FR
 coffea arabica fruit extractFL/FR
roasted coffea arabica seed extractFL/FR
 coffea arabica seed extractFL/FR
 coffea arabica seed oilFL/FR
 coffee absoluteFL/FR
arabica coffee bean butterFL/FR
roasted arabica coffee bean essenceFL/FR
roasted coffee bean extractFL/FR
roasted arabica coffee bean oilFL/FR
roasted arabica coffee bean oil CO2 extractFL/FR
 coffee bean oil extractFL/FR
 coffee difuranFL/FR
 coffee fragranceFR
 coffee resinoidFL/FR
1-hydroxy-2-butanoneFL/FR
2-methyl-3-,5 or 6-(furfuryl thio) pyrazineFL/FR
creamy
gamma-butyrolactoneFL/FR
 nutty pyrazineFL/FR
fatty
 butter estersFL/FR
(Z)-ethyl oleateFL/FR
1-ethyl propyl 2-butenoate 
 perilla seed oilFL/FR
 sorbitan oleateCS
(E,Z,Z)-2,4,7-tridecatrienalFL/FR
 octanal / methyl anthranilate schiff's baseFR
2-pentadecanoneFL/FR
fruity
 butyl 2-decenoateFL/FR
 dodecyl isobutyrateFL/FR
 ethyl 3-hydroxyhexanoateFL/FR
(R)-(-)-2-heptanolFL/FR
(S)-2-methyl butyraldehyde 
 tropical thiazoleFL/FR
green
3,7-dimethyl-6-octenoic acidFL/FR
(Z)-3-hepten-1-olFL/FR
(Z)-4-hepten-1-olFL/FR
(Z)-4-heptenalFL/FR
 neryl butyrateFL/FR
herbal
 thymyl methyl etherFL/FR
 wormwood oil americaFL/FR
 wormwood oil italyFL/FR
 wormwood oil polandFL/FR
leathery
 castoreum absoluteFL/FR
marine
5-sec-butyl-2,3-dimethyl pyrazineFL/FR
medicinal
2,6-xylenolFL/FR
moldy
 strawberry furanone methyl etherFL/FR
mushroom
(S)-(+)-2-heptanolFL/FR
(S)-(+)-2-octanol 
 menthofuranFL/FR
nutty
3-acetyl pyridineFL/FR
3,6-cocoa pyrazineFL/FR
3,5-cocoa pyrazineFL/FR
2,3-dimethyl pyrazineFL/FR
4,5-dimethyl-2-ethyl-3-thiazolineFL/FR
2-ethyl pyrazineFL/FR
2-ethyl-4-methyl thiazoleFL/FR
 filbert heptenoneFL/FR
 filbert heptenone BFL/FR
2,6-lutidineFL/FR
5-methyl quinoxalineFL/FR
2-methyl thio-3,5 or 6-methyl pyrazineFL/FR
 sesame absoluteFL/FR
 sesame absolute CO2 extractFL/FR
2,3,5,6-tetramethyl pyrazineFL/FR
oily
 amyl laurateFL/FR
 butter acidsFL/FR
 glyceryl tripropanoate 
phenolic
2,3-dimethyl benzofuranFL/FR
para-alpha-dimethyl styreneFL/FR
ortho-guaiacolFL/FR
4-methyl-2,6-dimethoxyphenolFL/FR
 piper betle leaf oilFR
2-propyl phenolFL/FR
2-isopropyl phenolFL/FR
2,5-xylenolFL/FR
popcorn
2-acetyl pyrazineFL/FR
 fenugreek resinoidFL/FR
 trigonella foenum-graecum seed oil CO2 extractFL/FR
2,6-dimethoxyphenolFL/FR
alpha-ethoxy-ortho-cresolFL/FR
4-ethyl phenolFL/FR
 phoebe oil brazil 
 propyl parabenCS
 pyroligneous acidsFL/FR
 pyroligneous acids hickoryFL/FR
 cubeb oilFL/FR
4-ethyl guaiacolFL/FR
 pepper tree berry oilFL/FR
sulfurous
 benzothiazoleFL/FR
 cocoa essenceFL/FR
 ethyl 3-mercaptobutyrateFL/FR
 fish thiolFL/FR
 furfuryl thioacetateFL/FR
S-furfuryl thioformateFL/FR
4-methyl 4-mercaptopentan-2-one 1% solutionFL/FR
2-methyl 5-(methyl thio) furanFL/FR
O-methyl S-1-methoxyhexan-3-yl carbonothioateFL/FR
3-thiohexanolFL/FR
sweet
2-hydroxy-3,4,5-trimethyl-2-cyclopenten-1-oneFL/FR
vegetable
1-furfuryl pyrroleFL/FR
 tetrahydrofurfuryl alcoholFL/FR
waxy
delta-tetradecalactoneFL/FR
woody
 guaiacyl acetateFL/FR
 juniper berry oleoresinFL/FR
2-methyl-3-isopropyl pyrazine 
 nopyl aldehydeFR
 
For Flavor
 
No flavor group found for these
2-acetyl-6-methyl pyrazineFL
 amyl laurateFL/FR
 benzyl disulfideFL
 benzyl methyl sulfideFL
1,2-butane dithiolFL
2-butenoic acidFL
5-sec-butyl-2,3-dimethyl pyrazineFL/FR
2-isobutyl-4,5-dimethyl oxazoleFL
 coffea arabica fruit extractFL/FR
 dimethyl dihydrocyclopentapyrazineFL
(Z+E)-2,5-dimethyl-3-tetrahydrofuran thiolFL
(Z+E)-2,5-dimethyl-3-thioacetoxytetrahydrofuranFL
2,5-dimethyl-3-thiofuroyl furanFL
 dodecyl isobutyrateFL/FR
alpha-ethoxy-ortho-cresolFL/FR
 ethyl 3-mercaptobutyrateFL/FR
 ethyl 4-(acetyl thio) butyrateFL
1-ethyl propyl 2-butenoate 
2-formyl pyrroleFL
(R)-(-)-2-heptanolFL/FR
(S)-(+)-2-heptanolFL/FR
2-hydroxy-3,4,5-trimethyl-2-cyclopenten-1-oneFL/FR
3-mercapto-3-methyl butyl formateFL
4-methyl 4-mercaptopentan-2-one 1% solutionFL/FR
(S)-2-methyl butyraldehyde 
(R)-2-methyl butyraldehyde 
 methyl dihydrofuran thiolFL
 methyl methane thiosulfonateFL
1-methyl pyrroleFL
2-methyl-3-,5 or 6-(furfuryl thio) pyrazineFL/FR
2-methyl-3-furyl tetrasulfideFL
1,9-nonane dithiolFL
(S)-(+)-2-octanol 
 perilla seed oilFL/FR
 phoebe oil brazil 
 prenyl mercaptanFL
2-propyl phenolFL/FR
 pyrazines mixtureFL
absinthe
 absinthe flavorFL
alliaceous
 benzyl mercaptanFL
1,3-butane dithiolFL
 dicyclohexyl disulfideFL
 tropical thiazoleFL/FR
bitter
2-hydroxymethyl-6-methyl-pyridine 
(E,Z,Z)-2,4,7-tridecatrienalFL/FR
brown
 fenugreek oleoresinFL/FR
1-hydroxy-2-butanoneFL/FR
5-methyl furfuralFL/FR
burnt
 bacon dithiazineFL
 furfuryl alcoholFL
1-(2-furfuryl thio) propanoneFL
2-methyl quinoxalineFL
isopropenyl pyrazineFL/FR
 tea pyrroleFL
2-(thienyl-2)-ethanethiol 
2,6-xylenolFL/FR
caramellic
 caramel furanoneFL
 caramel furanone solutionFL/FR
 cycloteneFL/FR
 fenugreek absoluteFL/FR
 fenugreek resinoidFL/FR
chemical
2,3-dimethyl benzofuranFL/FR
chocolate
 cocoa essenceFL/FR
 mocha cream flavorFL
cocoa
 cocoa hexenalFL/FR
coffee
 cappuccino flavorFL
 chicory flavorFL
 chicory root 
 chicory root distillatesFL
 chicory root essenceFL
roasted chicory root oilFL
 chicory tinctureFL
 cichorium intybus root extractFL/FR
 cichorium intybus root solid extractFL/FR
 coffea arabica seed extractFL/FR
roasted coffea arabica seed extractFL/FR
 coffea arabica seed oilFL/FR
 coffea canephora seed extractFL
 coffee absoluteFL/FR
roasted congo coffee bean 
roasted liberian coffee bean 
roasted robusta coffee bean 
roasted coffea coffee bean 
roasted bengal coffee bean 
roasted arabica coffee bean 
arabica coffee bean butterFL/FR
roasted coffee bean concentrateFL
roasted coffee bean essenceFL
roasted robusta coffee bean essenceFL
roasted arabica coffee bean essenceFL/FR
roasted coffee bean extractFL/FR
dried roasted coffee bean extractFL
roasted robusta coffee bean extractFL
roasted arabica coffee bean oil CO2 extractFL/FR
 coffee bean oil extractFL/FR
 coffee creme brulee flavorFL
 coffee difuranFL/FR
 coffee dioneFL/FR
espresso coffee distillatesFL
 coffee distillatesFL
 coffee enhancersFL
espresso coffee essenceFL
espresso coffee extractFL
 coffee flavorFL
irish coffee flavorFL
dark roast coffee flavorFL
espresso coffee flavorFL
 coffee liqueur flavorFL
 coffee pyrazineFL
 coffee resinoidFL/FR
 coffee royale flavorFL
 difurfuryl etherFL
 diisoamyl thiomalateFL
3,6-dimethyl pyrazine-2-thiol 
2,4-dimethyl thiazoleFL
2,5-dimethyl-3-furfurylthio-pyrazine 
2,5-dimethyl-3,6-diethyl pyrazine 
2-ethyl-4-methyl thiazoleFL/FR
 methyl furfuryl disulfideFL/FR
 methyl furfuryl mercaptopropionateFL
 methyl furfuryl thiolFL
2-methyl-5-vinyl pyrazineFL
2-isopropyl pyrazineFL
2-thiophene thiolFL
creamy
 butter estersFL/FR
dairy
 creme brulle coffee flavorFL
earthy
 difurfuryl sulfideFL
2-methyl-3-isopropyl pyrazine 
1,8-octane dithiolFL
fatty
 butter acidsFL/FR
 dimethyl sulfoxideFL
4,5-dimethyl-2-propyl oxazoleFL
(Z)-ethyl oleateFL/FR
2-pentadecanoneFL/FR
floral
3,7-dimethyl-6-octenoic acidFL/FR
fruity
 butyl 2-decenoateFL/FR
 ethyl 3-hydroxyhexanoateFL/FR
 furfuryl isobutyrateFL
 furfuryl isovalerateFL
 furfuryl propionateFL
fusel
2-methyl butyraldehydeFL/FR
garlic
 garlic oleoresinFL
green
3,4-dimethoxystyreneFL
2,5-dimethyl-4-ethyl oxazoleFL
2,6-dimethyl-gamma-thiopyrone 
(Z)-4-hepten-1-olFL/FR
(Z)-3-hepten-1-olFL/FR
(E)-2-heptenalFL
(Z)-4-heptenalFL/FR
2-methyl-5-isopropyl pyrazineFL
 neryl butyrateFL/FR
2,4-octadienalFL
2-(1-propenyl) pyridine 
hazelnut
4-hydroxymethyl-pyridine 
herbal
 wormwood oil americaFL/FR
 wormwood oil italyFL/FR
 wormwood oil polandFL/FR
leathery
 castoreum absoluteFL/FR
meaty
4-allyl-2,6-dimethoxyphenolFL
 benzothiazoleFL/FR
2,6-dimethyl pyrazineFL/FR
2,6-dimethyl thiophenolFL
2,5-dimethyl-3-furan thiolFL
3-mercapto-2-butanoneFL
(R,S)-2-mercapto-3-butanolFL
2-methyl 3-(methyl thio) furanFL
bis(2-methyl-3-furyl) disulfideFL
S-(2-methyl-3-furyl) ethane thioateFL
2-methyl-3-thioacetoxytetrahydrofuranFL
 phenyl mercaptanFL
 pyrazinyl ethane thiolFL
medicinal
2,6-dimethoxyphenolFL/FR
metallic
2,5-dihydroxy-1,4-dithianeFL
milky
gamma-butyrolactoneFL/FR
molasses
 molasses blackstrapFL
moldy
 strawberry furanone methyl etherFL/FR
mustard
 furfuryl methyl etherFL
musty
2-ethoxythiazoleFL
 menthofuranFL/FR
2-methyl 5-(methyl thio) furanFL/FR
 thymyl methyl etherFL/FR
2,5-xylenolFL/FR
nutty
2-acetyl furanFL/FR
3-acetyl pyridineFL/FR
3-acetyl-2,5-dimethyl thiopheneFL
 arachis hypogaea fruit extractFL
3,5(6)-cocoa pyrazineFL
3,6-cocoa pyrazineFL/FR
3,5-cocoa pyrazineFL/FR
2,3-dimethyl pyrazineFL/FR
4,5-dimethyl-2-ethyl-3-thiazolineFL/FR
2-ethyl pyrazineFL/FR
1-ethyl-2-acetyl pyrroleFL
 filbert heptenoneFL/FR
 filbert heptenone BFL/FR
2,6-lutidineFL/FR
5-methyl quinoxalineFL/FR
2-methyl thio-3,5 or 6-methyl pyrazineFL/FR
2-methyl-3-pentyl pyrazine 
 nutty pyrazineFL/FR
 nutty thiazoleFL
 sesame absoluteFL/FR
 sesame absolute CO2 extractFL/FR
 tetrahydrofurfuryl alcoholFL/FR
2,3,5,6-tetramethyl pyrazineFL/FR
2,4,5-trimethyl thiazoleFL/FR
oily
 glyceryl tripropanoate 
2-methyl hexanoic acidFL/FR
onion
 furfuryl isopropyl sulfideFL
2-methyl-1,3-dithiolaneFL
phenolic
2-ethyl benzene thiolFL
4-methyl-2,6-dimethoxyphenolFL/FR
2-pentenyl furan 
roasted
2-acetyl pyrazineFL/FR
roasted arabica coffee bean oilFL/FR
2,6-dimethyl-thio-gamma-pyrone 
 ethyl 3-(furfuryl thio) propionateFL
 furfuryl thioacetateFL/FR
 hexyl mercaptanFL
O-methyl S-1-methoxyhexan-3-yl carbonothioateFL/FR
(2-methylpyrazinyl-3, -5 and-6) furfuryl sulfide 
 trigonella foenum-graecum seed oil CO2 extractFL/FR
rummy
 vanillyl ethyl etherFL/FR
smoky
4-ethyl phenolFL/FR
 pyroligneous acidsFL/FR
 pyroligneous acids hickoryFL/FR
dextro-xyloseFL
solvent
2-ethyl furanFL
 methyl phenyl sulfideFL
2-isopropyl phenolFL/FR
spicy
 chipotle chili oleoresinFL
 cinnamon hazelnut cappuccino flavorFL
 cubeb oilFL/FR
para-alpha-dimethyl styreneFL/FR
 pepper tree berry oilFL/FR
sulfurous
2,3-butane dithiolFL
 butyl mercaptanFL
 ethyl methyl sulfideFL
O-ethyl S-1-methoxyhexan-3-yl carbonothioateFL
S-ethyl thioacetateFL
 fish thiolFL/FR
S-furfuryl thioformateFL/FR
 furfuryl thiopropionateFL
 methyl 2-methyl-3-furyl disulfideFL
2-methyl thiopheneFL
3-methyl-2-butane thiolFL
 roasted butanolFL
2-thienyl mercaptanFL
3-thiohexanolFL/FR
vegetable
1-furfuryl pyrroleFL/FR
waxy
delta-tetradecalactoneFL/FR
woody
4-ethyl guaiacolFL/FR
ortho-guaiacolFL/FR
 guaiacyl acetateFL/FR
 juniper berry oleoresinFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 butterscotchFR
 caramelFL
 chocolate cocoaFL
 coffeeFR
 eggFL
 garlicFL
 meatFL
 nutFL
 onionFL
 smokeFL
 toffeeFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 beef cooked beef
Search  PMC Picture
 bread wheat bread
Search  PMC Picture
 chicken cooked chicken
Search  PMC Picture
 coffee roasted coffee
Search  PMC Picture
 popcorn
Search  PMC Picture
 pork
Search  PMC Picture
 sesame seed oil roasted
Search Trop  Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
 coffee mercaptan
2-furan methane thiol
 furan-2-methanethiol
 furan-2-ylmethanethiol
2-furanmethanethiol
(2-furanyl) methyl mercaptan
(2-furanyl)methylmercaptan
 furfuryl mercaptan
2-furfuryl mercaptan
a-furfuryl mercaptan
alpha-furfuryl mercaptan
nat.furfuryl mercaptan
natural furfuryl mercaptan
 furfuryl mercaptan 1% in benzyl benoate
 furfuryl mercaptan 1% in ETOH natural
 furfuryl mercaptan EEC natural
 furfuryl mercaptan natural
 furfuryl mercaptan natural 1% in grain alcohol
 furfuryl mercaptan, natural
 furfuryl mercaptan, natural 0.1% in P.G.
 furfuryl mercaptan, natural 1.0% in P.G.
 furfuryl thiol
2-furfuryl thiol
 furfurylmercaptan
2-furfurylmercaptan
2-furyl methane thiol
2-furyl methyl mercaptan
2-furyl-2-thienyl methane
2-furyl-2-thienylmethane
2-furylmethane-1-thiol
2-furylmethanethiol
2-furylmethyl mercaptan
2-(mercaptomethyl) furan
2-(mercaptomethyl)furan
Synonyms   Articles   Notes   Search   Top
Articles:
US Patents: 3,931,166 - Certain 2,5-dimethyl-3-thiopyrazines
PubMed: Formation of cysteine-S-conjugates in the Maillard reaction of cysteine and xylose.
US Patents: 3,993,792 - Flavoring agent
PubMed: Evaluation of process parameters governing the aroma generation in three hazelnut cultivars (Corylus avellana L.) by correlating quantitative key odorant profiling with sensory evaluation.
PubMed: Identification of aroma active compounds of cereal coffee brew and its roasted ingredients.
PubMed: Characterization of the key odorants in raw Italian hazelnuts ( Corylus avellana L. var. Tonda Romana) and roasted hazelnut paste by means of molecular sensory science.
PubMed: Color, lipid oxidation, sensory quality, and aroma compounds of beef steaks displayed under different levels of oxygen in a modified atmosphere package.
PubMed: Metabolomic approach for determination of key volatile compounds related to beef flavor in glutathione-Maillard reaction products.
PubMed: Theoretical studies on iron surface coating: adsorption of furan derivatives over Fe(n) clusters (n = 1-4).
PubMed: Analysis, occurrence, and potential sensory significance of five polyfunctional mercaptans in white wines.
PubMed: Identification of novel aroma-active thiols in pan-roasted white sesame seeds.
PubMed: Changes in the key odorants of Italian Hazelnuts ( Coryllus avellana L. Var. Tonda Romana) induced by roasting.
PubMed: New factor characterizing the in-mouth release of odorants (volatile thiols): compositional changes in odorants exhaled from the human nose during drinking.
PubMed: Odor detection of mixtures of homologous carboxylic acids and coffee aroma compounds by humans.
PubMed: Study on the role of precursors in coffee flavor formation using in-bean experiments.
PubMed: Selective preconcentration of volatile mercaptans in small SPE cartridges: quantitative determination of trace odor-active polyfunctional mercaptans in wine.
PubMed: Improved solid-phase extraction procedure for the isolation and in-sorbent pentafluorobenzyl alkylation of polyfunctional mercaptans. Optimized procedure and analytical applications.
PubMed: Effect of type of oil and addition of delta-tocopherol on model flavor compound stability during storage.
PubMed: Quantitative studies on the formation of phenol/2-furfurylthiol conjugates in coffee beverages toward the understanding of the molecular mechanisms of coffee aroma staling.
PubMed: Quantitative determination of wine polyfunctional mercaptans at nanogram per liter level by gas chromatography-negative ion mass spectrometric analysis of their pentafluorobenzyl derivatives.
PubMed: Effect of pH on the Maillard reaction of [13C5]xylose, cysteine, and thiamin.
PubMed: Synthesis and structure determination of covalent conjugates formed from the sulfury-roasty-smelling 2-furfurylthiol and di- or trihydroxybenzenes and their identification in coffee brew.
PubMed: Interactions between volatile and nonvolatile coffee components. 2. Mechanistic study focused on volatile thiols.
PubMed: Screening of raw coffee for thiol binding site precursors using "in bean" model roasting experiments.
PubMed: Alpha-mercaptoketone formation during the maillard reaction of cysteine and [1-(13)C]ribose.
PubMed: Studies on the metabolism of the thiofurans furfuryl mercaptan and 2-methyl-3-furanthiol in rat liver.
PubMed: Generation of thiols by biotransformation of cysteine-aldehyde conjugates with baker's yeast.
PubMed: Formation of aroma compounds from ribose and cysteine during the Maillard reaction.
PubMed: Investigation of the change in the flavor of a coffee drink during heat processing.
PubMed: Flavor composition of cashew (Anacardium occidentale) and marmeleiro (Croton species) honeys.
PubMed: Lipase-assisted generation of 2-methyl-3-furanthiol and 2-furfurylthiol from thioacetates.
PubMed: Influence of human salivary enzymes on odorant concentration changes occurring in vivo. 1. Esters and thiols.
PubMed: Furfural-cysteine model reaction in food grade nonionic oil/water microemulsions for selective flavor formation.
PubMed: Effects of carnosine on volatile generation from Maillard reaction of ribose and cysteine.
PubMed: Degradation of the coffee flavor compound furfuryl mercaptan in model Fenton-type reaction systems.
PubMed: Characterization of the most odor-active compounds of Iberian ham headspace.
PubMed: Chemical interactions between odor-active thiols and melanoidins involved in the aroma staling of coffee beverages.
PubMed: Stability of thiols in an aqueous process flavoring.
PubMed: Model studies on the influence of coffee melanoidins on flavor volatiles of coffee beverages.
PubMed: Quantitative Model Studies on the Effectiveness of Different Precursor Systems in the Formation of the Intense Food Odorants 2-Furfurylthiol and 2-Methyl-3-furanthiol.
PubMed: Structured fluids as microreactors for flavor formation by the Maillard reaction.
PubMed: Sensory study on the character impact odorants of roasted arabica coffee.
PubMed: Olfactory transduction mechanisms in sheep.
PubMed: Short-term toxicity of furfuryl mercaptan in rats.
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