6-methyl coumarin
6-methylcoumarin
 
Notes:
Coumarin replacer. synthetic fragrance causing contact photoallergy. Used as a food additive [EAFUS]
  • ACS International
    • ACS International GmbH
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      Our hybrid business model, combining manufacturing with sourcing and exclusive distribution agreements, results in a superior level of purchasing power that when added to our global warehouse network with locations near all major flavor and fragrance industry compounding centers around the globe, make A.C.S. International your one-stop sourcing partner.
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      33001 Methylcoumarin-6
       
  • Advanced Biotech
    • Advanced Biotech. Inc.
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      Advanced Biotech is a leading manufacturer and supplier of high-quality Natural flavoring ingredients & botanical extracts for the food/beverage, cosmetic and personal care industries. With over 25 years of experience working with Fermentation processing & botanical extracts, we can help develop new innovative and functional products for today’s competitive marketplace. Our company prides itself in the ability to cater to our customer’s specific needs while maintaining our focus on integrity, honesty and the commitment to high quality product standards. We proudly offer our quality Natural ingredients to companies around the world.
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      2078 6 METHYL COUMARIN SYNTHETIC 99% min.
      SDS
       
  • Augustus Oils
    • Augustus Oils Ltd
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  • Berjé
    • Berje Inc.
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      Berjé is a family-owned business that has been in operation for six decades. The company's origins and strength lie in a profound understanding of the supply and the quality of the diverse raw materials consumed by the flavor and fragrance industries. This base was expanded upon more than two decades ago to include fragrance production. The company's unparalleled raw material expertise is focused on the supply of essential oils and aromatic chemicals. This is supported by our long-standing relationships with a worldwide fabric of producers ensuring the greatest prospects for uninterrupted supply in markets that are often volatile and unpredictable.
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      92-48-8 6-Methylcoumarin
       
  • Charkit Chemical
    • Charkit Chemical Corporation
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      METHYL COUMARIN, 6- FEMA 2699
       
  • Elan Inc.
    • Elan Inc.
      Legacy of Innovation
      Highest quality natural and synthetic products.
      Elan Inc. is a privately held business that has been in operation for over 30 years. Our offices and production facility are located in Newark, NJ. We are dedicated to producing the highest quality natural and synthetic products available in the flavor and fragrance industry.
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      Product(s):
      6-METHYLCOUMARIN Kosher
      SDS
       
  • H. Interdonati, Inc.
    • H. Interdonati, Inc.
      Innovative products
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      H. Interdonati, Inc. began in 1952 with the tradition of delivering quality pharmaceuticals and fine chemical ingredients at competitive prices. The mission was simple: To provide the most reliable, personal service in the industry.
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      6-Methylcoumarin Kosher
       
  • Indukern F&F
  • Jiangyin Healthway
    • Jiangyin Healthway International Trade Co., Ltd
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      Jiangyin Healthway International Trade Co., Ltd is a professional company, main engaged in manufacturing and exporting aroma chemicals ,food additives , cosmetic ingredient ,pharmaceutical intermediates & other fine chemicals; especially on aroma chemicals , as the major manufacturer of heterocyclic and sulphur aroma compounds , we are the leading independent ingredients supplier to the flavour and fragrance industries in China, can offer hundreds of different high quality aroma chemicals.
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      Product(s):
      HLK010 6-Methyl Coumarin
      HLW-FC059 6-Methylcoumarin
       
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    • Lluch Essence S.L.
      A family company dedicated to sales and distribution
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      6-METHYL COUMARIN
       
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    • M&U International LLC
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      A0108 6-Methyl Coumarin, Kosher
       
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  • Penta International
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      Product(s):
      13-35200 6-METHYLCOUMARIN POWDER
      13-35205 6-METHYLCOUMARIN CRYSTAL
       
  • PerfumersWorld
    • PerfumersWorld Ltd.
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      Product(s):
      1VD00002 6-Methyl Coumarin
      5VD07562 6-Methyl Coumarin 10% in DPG
       
  • Sigma-Aldrich
  • SRS Aromatics
    • SRS Aromatics Ltd
      For over 25 years
      Bringing flavour and fragrance into your world.
      As suppliers / distributors of ingredients to the fragrance and flavour industries, our goal is to provide high quality materials at competitive prices with an exceptional level of service. Established in 1984, SRS Aromatics Ltd is an independent family owned business which has become very well-respected within the fragrance and flavour industry as a reliable and trustworthy partner. Over the years this has allowed the company to develop strong relationships with many global manufacturers; several of whom we represent in the UK. A core aim of our business is to work extremely closely with both our suppliers and customers to maximise service levels with minimum disruption to supply.
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      6-METHYL COUMARIN
       
  • Sunaux International
    • Sunaux International
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      We have industry leading processes and procedures to ensure nothing but the most reliable product.
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      A0113 6-Methyl Coumarin
       
  • TCI AMERICA
    • TCI AMERICA
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      M0189 6-Methylcoumarin >99.0%(GC)
      SDS
       
  • R C Treatt & Co Ltd
    • R C Treatt and Co Ltd
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      6-Methylcoumarin
       
  • United International
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      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.
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      7245 6-Methylcoumarin
       
  • 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.
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      500250 Methyl-6 Coumarin
       
  • WholeChem
    • WholeChem, LLC
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      6-Methyl coumarin
       
Synonyms   Articles   Notes   Search
    Flavor Demo Formulas
CAS Number: 92-48-8Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 202-158-8
FDA UNII: EHP8W0L01A
Nikkaji Web: J3.219K
Beilstein Number: 0004222
MDL: MFCD00006875
CoE Number: 579
XlogP3: 1.80 (est)
Molecular Weight: 160.17216000
Formula: C10 H8 O2
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome, Edge 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
JECFA Food Flavoring: 1172  6-methylcoumarin
DG SANTE Food Flavourings: 13.012  6-methylcoumarin
FEMA Number: 2699 6-methylcoumarin
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):92-48-8 ; 6-METHYLCOUMARIN
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: white crystals (est)
Assay: 99.00 to 100.00 % 
Food Chemicals Codex Listed: Yes
Melting Point: 73.00 to  79.00 °C. @ 760.00 mm Hg
Boiling Point: 303.00 °C. @ 725.00 mm Hg
Congealing Point: 73.50 °C.
Vapor Pressure: 0.001000 mmHg @ 25.00 °C. (est)
Flash Point: > 230.00 °F. TCC ( > 110.00 °C. )
logP (o/w): 1.933 (est)
Soluble in:
 alcohol
 water, very slightly
 water, 1189 mg/L @ 25 °C (est)
Insoluble in:
 water
Stability:
 non-discoloring in most media
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: coconut
 
Odor Strength: medium ,
recommend smelling in a 1.00 % solution or less
 
Substantivity: 347 hour(s) at 1.00 % in dipropylene glycol
 
 coconut  creamy  powdery  coumarinic  tonka  cinnamyl  vanilla  floral  earthy  
Odor Description:
at 1.00 % in dipropylene glycol. 
coconut creamy powdery coumarinic tonka cinnamyl vanilla floral earthy
Luebke, William tgsc, (2021)
 
 sweet  coconut  vanilla  creamy  powdery  floral  
Odor Description:
Sweet coconut, vanilla, creamy with a powdery floral nuance
Mosciano, Gerard P&F 16, No. 3, 79, (1991)
 
 
Flavor Type: coconut
 
 coconut  vanilla  creamy  coumarinic  tonka  cake  
Taste Description:
coconut vanilla creamy coumarinic tonka cake
Luebke, William tgsc, (2021)
 
 sweet  coconut  vanilla  creamy  
Taste Description:
at 20.00 ppm.  
Sweet coconut, vanilla like with a creamy cake-like nuance
Mosciano, Gerard P&F 16, No. 3, 79, (1991)
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: fragrance
oral care agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
ACS International
Methylcoumarin-6
Operational Capabilities
Advanced Biotech
6 METHYL COUMARIN SYNTHETIC
99% min.
Odor: Coconut, Herbaceous
Alfa Biotechnology
For experimental / research use only.
6-Methylcoumarin 98%
Anhui Haibei
6-Methyl Coumarin
Aroma Aromatics & Flavours
6-Methyl Coumarin
Flavor: Dry herbaceous coconut
It is one of the most important constituent of coconut flavours. It is also used effectively in nut, caramel, butter, date, fig, root beer etc. Frequently used in various vanilla compositions. Its extra ordinary stability towards heat makes it excellent for flavour meant for baked goods. The concentration in finished products is usually less then 30 ppm.
Augustus Oils
6 Methyl Coumarin
Services
Berjé
6-Methyl Coumarin
Media
BOC Sciences
For experimental / research use only.
6-Methylcoumarin
Charkit Chemical
METHYL COUMARIN, 6- FEMA 2699
Diffusions Aromatiques
6-METHYLCOUMARINE
Elan Inc.
6-METHYLCOUMARIN
Kosher
Ernesto Ventós
6-METHYLCOUMARIN
Odor: CREAMY, COCONUT
Flavor: ALMOST BITTER, SWEET AT LOWER LEVEL
H. Interdonati, Inc.
6-Methylcoumarin Kosher
Featured Products
Indukern F&F
6-METHYL COUMARIN
Odor: SWEET, COCONUT, CREAMY
Jiangyin Healthway
6-Methyl Coumarin
New functional food ingredients
Jiangyin Healthway
6-Methylcoumarin
K.L. Koh Enterprise
6-METHYL COUMARIN
Lluch Essence
6-METHYL COUMARIN
M&U International
6-Methyl Coumarin, Kosher
Moellhausen
6-METHYL COUMARIN
Odor: sweet, aromatic
Flavor: sweet, cocoa, vanilla
Pearlchem Corporation
6-Methyl Coumarin
Penta International
6-METHYLCOUMARIN CRYSTAL
Penta International
6-METHYLCOUMARIN POWDER
PerfumersWorld
6-Methyl Coumarin 10% in DPG
PerfumersWorld
6-Methyl Coumarin
Odor: vanilla coconut tonka-bean sweet aromatic
Phoenix Aromas & Essential Oils
Methyl-6 Coumarin
R C Treatt & Co Ltd
6-Methylcoumarin
Reincke & Fichtner
6-Methylcoumarin
Sigma-Aldrich
6-Methylcoumarin, ≥99%, FCC, FG
Odor: anise; coconut; creamy; herbaceous; vanilla; balsamic
Certified Food Grade Products
SRS Aromatics
6-METHYL COUMARIN
Sunaux International
6-Methyl Coumarin
TCI AMERICA
For experimental / research use only.
6-Methylcoumarin >99.0%(GC)
United International
6-Methylcoumarin
Vigon International
Methyl-6 Coumarin
Odor: COCONUT-LIKE
WholeChem
6-Methyl coumarin
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Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
R 22 - Harmful if swallowed.
R 42/43 - May cause sensitization by inhalation and skin contact.
S 02 - Keep out of the reach of children.
S 20/21 - When using do not eat, drink or smoke.
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 37/39 - Wear suitable gloves and eye/face protection.
 
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.
Human Experience:
4 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50  1680 mg/kg
Food and Cosmetics Toxicology. Vol. 14, Pg. 605, 1976.

Dermal Toxicity:
subcutaneous-mouse LD50 253 mg/kg
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
Yakugaku Zasshi. Journal of Pharmacy. Vol. 76, Pg. 186, 1956.

skin-rabbit LD50 > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 14, Pg. 605, 1976.

Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: flavoring agents
IFRA Critical Effect: Photosensitization
IFRA: View Standard
Recommendation for 6-methyl coumarin usage levels up to:
 PROHIBITED: Should not be used as a fragrance ingredient.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 250.00 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 96.00 (μg/capita/day)
NOEL (No Observed Effect Level): 150.00 (mg/kg bw per day)
Structure Class: III
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: 3
Click here to view publication 3
 average usual ppmaverage maximum ppm
baked goods: -24.00000
beverages(nonalcoholic): -5.20000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: 0.8000015.00000
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -4.80000
fruit ices: -4.80000
gelatins / puddings: -39.00000
granulated sugar: --
gravies: --
hard candy: -21.00000
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:
Flavor & Extract Manufacturers Association (FEMA) reference(s):
The FEMA GRAS assessment of lactones used as flavor ingredients. View pdf
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):
Flavouring Group Evaluation 217: alpha,beta-Unsaturated ketones and precursors from chemical subgroup 4.1 of FGE.19: Lactones[1]
View page or View pdf
Flavouring Group Evaluation 80, Revision 1 (FGE.80Rev1): Consideration of alicyclic, alicyclic-fused and aromatic-fused ring lactones evaluated by JECFA (61st meeting) structurally related to a aromatic lactone evaluated by EFSA in FGE.27 (2008)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 217, Revision 1 (FGE.217Rev1). Consideration of genotoxic potential for a,ß-unsaturated ketones and precursors from chemical subgroup 4.1 of FGE.19: Lactones
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 217 Revision 2 (FGE.217Rev2), consideration of genotoxic potential for a,ß-unsaturated ketones and precursors from chemical subgroup 4.1 of FGE.19: lactones
View page or View pdf
EPI System: View
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA GENetic TOXicology: Search
EPA Substance Registry Services (TSCA): 92-48-8
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 7092
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 6-methylchromen-2-one
Chemidplus: 0000092488
EPA/NOAA CAMEO: hazardous materials
RTECS: GN7792000 for cas# 92-48-8
Synonyms   Articles   Notes   Search   Top
References:
 6-methylchromen-2-one
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 92-48-8
Pubchem (cid): 7092
Pubchem (sid): 134972192
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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
CHEBI: View
CHEMBL: View
HMDB (The Human Metabolome Database): HMDB32394
FooDB: FDB009822
Export Tariff Code: 2932.20.0500
ChemSpider: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
aldehydic
aldehydic
 acetyl nonyrylFL/FR
animal
 costus valerolactoneFR
6-methyl quinolineFL/FR
anisic
para-acetanisoleFL/FR
para-anisaldehydeFL/FR
balsamic
 benzyl cinnamateFL/FR
 pine needle absoluteFL/FR
black poplar bud oleoresinFL/FR
buttery
 acetoinFL/FR
 acetyl butyrylFL/FR
 acetyl isobutyrylFL/FR
 acetyl propionylFL/FR
 butyl butyryl lactateFL/FR
caramellic
2-oxobutyric acidFL/FR
 fenugreek absoluteFL/FR
 immortelle absoluteFL/FR
 levulinic acidFL/FR
 strawberry furanone acetateFL/FR
cheesy
 butyric acidFL/FR
2-heptanoneFL/FR
chocolate
 vanillyl ethyl etherFL/FR
citrus
 lime oil expressed floridaFL/FR
coconut
alpha-angelica lactoneFL/FR
 coconut decanone methylFR
 coconut naphthalenoneFL/FR
delta-decalactoneFL/FR
delta-2-dodecenolactoneFL/FR
delta-heptalactoneFL/FR
gamma-heptalactoneFL/FR
delta-nonalactoneFL/FR
gamma-nonalactone (aldehyde C-18 (so-called))FL/FR
delta-octalactoneFL/FR
gamma-octalactoneFL/FR
 propyl octanoateFL/FR
 tetrahydrojasmoneFR
delta-undecalactoneFL/FR
 wine lactoneFL/FR
coumarinic
 coumaneFL/FR
 phthalideFL/FR
 tonka furanoneFL/FR
 tonka ketoneFR
 tonkavertFR
creamy
gamma-butyrolactoneFL/FR
 creamy lactoneFL/FR
3-heptyl dihydro-5-methyl-2(3H)-furanoneFL/FR
para-vanillic acidFL/FR
para-vanillyl alcoholFL/FR
earthy
1-nonen-3-olFL/FR
fatty
(Z)-dairy lactoneFL/FR
 ethyl undecylenateFL/FR
 lauric acidFL/FR
4-methyl octanoic acidFL/FR
fermented
 butyl laevo-lactateFL/FR
floral
para-anisyl nitrileFR
 dihydrojasmone lactoneFL/FR
 dimethyl anthranilateFL/FR
 heliotropinFL/FR
 hexenyl cyclopentanoneFR
(E)-beta-iononeFL/FR
 jasmin lactone (IFF)FL/FR
para-methyl acetophenoneFL/FR
alpha-isomethyl ionone (50% min.)FL/FR
 orris rhizome resinoid (iris pallida)FL/FR
2-pentyl cyclopentanoneFR
 petitgrain mandarin oil terpenelessFL/FR
 rhodinyl acetateFL/FR
fruity
 acetoin acetateFL/FR
bitter almond oilFL/FR
 amyl heptanoateFL/FR
isoamyl octanoateFL/FR
 cherry propanolFL/FR
gamma-decalactoneFL/FR
 farnesyl acetoneFL/FR
4-hydroxybenzyl alcoholFL/FR
 methyl (Z)-5-octenoateFL/FR
 octyl butyrateFL/FR
isopropyl octanoateFL/FR
 tolualdehydes (mixed o,m,p)FL/FR
gamma-undecalactone (aldehyde C-14 (so-called))FL/FR
green
isobutyl benzyl carbinolFL/FR
 butyl lactateFL/FR
alpha-decalactoneFL/FR
(Z)-4-hepten-1-olFL/FR
(Z)-4-heptenalFL/FR
(Z)-4-heptenal diethyl acetalFL/FR
(E)-2-hexen-1-yl propionateFL/FR
 syringaldehydeFL/FR
hay
 hay absoluteFR
 immortelle flower oilFL/FR
mushroom
3-octen-2-olFL/FR
musty
2-acetyl pyrroleFL/FR
nutty
2-acetyl-5-methyl furanFL/FR
orris
beta-methyl iononeFL/FR
powdery
para-anisyl acetateFL/FR
para-anisyl alcoholFL/FR
soapy
 ethyl undecanoateFL/FR
 methyl heptadienoneFL/FR
 myrtenalFL/FR
sweet
 vanilla oleoresin baliFL/FR
tonka
6-amyl-alpha-pyroneFL/FR
 coumarinFR
 deertongue absoluteFR
 deertongue concreteFR
 deertongue oleoresinFR
 dihydrocoumarinFL/FR
 flouve absoluteFR
gamma-hexalactoneFL/FR
 melilot absoluteFR
7-methyl coumarinCS
 mint lactoneFL/FR
 octahydrocoumarinFL/FR
 tonka undecanoneFR
 whiskey lactoneFL/FR
tropical
delta-dodecalactoneFL/FR
 glyceryl 5-hydroxydecanoateFL/FR
 glyceryl 5-hydroxydodecanoateFL/FR
vanilla
ortho-dimethyl hydroquinoneFL/FR
 ethyl vanillinFL/FR
 ethyl vanillin isobutyrateFL/FR
 ethyl vanillin propylene glycol acetalFL/FR
 heliotropyl alcoholFL/FR
 propenyl guaetholFL/FR
 vanillinFL/FR
 vanillyl acetateFL/FR
 vanillyl isobutyrateFL/FR
 vanillylidene acetoneFL/FR
vegetable
 methionalFL/FR
waxy
 allyl nonanoateFL/FR
1-dodecanolFL/FR
 ethyl palmitateFL/FR
 methyl laurateFL/FR
 myristyl alcoholFL/FR
2-nonanolFL/FR
 octyl isobutyrateFL/FR
delta-tetradecalactoneFL/FR
2-tridecanoneFL/FR
 undecanoic acidFL/FR
 
For Flavor
 
No flavor group found for these
 allyl methyl trisulfideFL
 coconut naphthalenoneFL/FR
 coumaneFL/FR
alpha-decalactoneFL/FR
6-decenoic acidFL
(S)-dihydroactinidiolideFL
 dimethyl benzofuranoneFL
ortho-dimethyl hydroquinoneFL/FR
delta-2-dodecenolactoneFL/FR
4-ethoxy-3-anisaldehydeFL
 farnesyl acetoneFL/FR
 fig leaf absoluteFL
 heliotropyl alcoholFL/FR
 jasmin lactone (IFF)FL/FR
 lauric acidFL/FR
 melilot oleoresinFL
7-methoxycoumarinFL
 myristyl alcoholFL/FR
4-octen-3-oneFL
 pine needle absoluteFL/FR
black poplar bud oleoresinFL/FR
 propyl octanoateFL/FR
 tonka furanoneFL/FR
(R)-tonka furanoneFL
 wine lactoneFL/FR
acidic
 levulinic acidFL/FR
aldehydic
 acetyl nonyrylFL/FR
amber
isobutyl benzyl carbinolFL/FR
animal
6-methyl quinolineFL/FR
anisic
para-acetanisoleFL/FR
balsamic
 vanillylidene acetoneFL/FR
brown
2-oxobutyric acidFL/FR
buttery
 butter cream frosting flavorFL
 butyl laevo-lactateFL/FR
 diacetylFL
cabbage
 methyl 2-thiofuroateFL
caramellic
 fenugreek absoluteFL/FR
 strawberry furanone acetateFL/FR
cheesy
2-heptanoneFL/FR
cherry
 heliotropinFL/FR
chocolate
 chocolate vanilla flavorFL
citrus
 lime oil expressed floridaFL/FR
cocoa
 syringaldehydeFL/FR
coconut
delta-decalactoneFL/FR
(R)-massoia lactoneFL
gamma-nonalactone (aldehyde C-18 (so-called))FL/FR
 octahydrocoumarinFL/FR
delta-octalactoneFL/FR
coumarinic
 phthalideFL/FR
creamy
 acetoinFL/FR
 acetyl butyrylFL/FR
 acetyl isobutyrylFL/FR
6-amyl-alpha-pyroneFL/FR
alpha-angelica lactoneFL/FR
para-anisaldehydeFL/FR
 butyl butyryl lactateFL/FR
 creamy lactoneFL/FR
5,5-dibutyl dihydrofuran-2(3H)-oneFL
 dihydrocoumarinFL/FR
delta-dodecalactoneFL/FR
 glyceryl 5-hydroxydecanoateFL/FR
 glyceryl 5-hydroxydodecanoateFL/FR
gamma-hexalactoneFL/FR
para-methyl acetophenoneFL/FR
 mint lactoneFL/FR
delta-nonalactoneFL/FR
 octyl isobutyrateFL/FR
delta-undecalactoneFL/FR
gamma-undecalactone (aldehyde C-14 (so-called))FL/FR
para-vanillic acidFL/FR
para-vanillyl alcoholFL/FR
dairy
 methyl (Z)-5-octenoateFL/FR
earthy
1-nonen-3-olFL/FR
fatty
(Z)-dairy lactoneFL/FR
 ethyl undecylenateFL/FR
4-methyl octanoic acidFL/FR
2,4-octadien-1-olFL
2-tridecanoneFL/FR
floral
beta-methyl iononeFL/FR
alpha-isomethyl ionone (50% min.)FL/FR
 orris rhizome resinoid (iris pallida)FL/FR
 rhodinyl acetateFL/FR
fruity
 acetoin acetateFL/FR
 acetyl isovalerylFL
bitter almond oilFL/FR
 amyl heptanoateFL/FR
isoamyl octanoateFL/FR
para-anisyl acetateFL/FR
para-anisyl alcoholFL/FR
 apricot vanilla flavorFL
 cherry propanolFL/FR
gamma-decalactoneFL/FR
 dimethyl anthranilateFL/FR
3-heptyl dihydro-5-methyl-2(3H)-furanoneFL/FR
4-hydroxybenzyl alcoholFL/FR
 petitgrain mandarin oil terpenelessFL/FR
isopropyl octanoateFL/FR
 tolualdehydes (mixed o,m,p)FL/FR
green
 butyl lactateFL/FR
 heptanal 2,3-butane diol acetalFL
(Z)-4-hepten-1-olFL/FR
(Z)-4-heptenalFL/FR
(Z)-4-heptenal diethyl acetalFL/FR
(E)-2-hexen-1-yl propionateFL/FR
 immortelle absoluteFL/FR
 methyl heptadienoneFL/FR
herbal
 immortelle flower oilFL/FR
 massoia bark oilFL
lactonic
gamma-heptalactoneFL/FR
delta-heptalactoneFL/FR
gamma-octalactoneFL/FR
meaty
4-allyl-2,6-dimethoxyphenolFL
milky
gamma-butyrolactoneFL/FR
minty
 myrtenalFL/FR
mushroom
3-octen-2-olFL/FR
nutty
2-acetyl pyrroleFL/FR
2-acetyl-5-methyl furanFL/FR
powdery
 powdery ketoneFL
rummy
 vanillyl ethyl etherFL/FR
soapy
1-dodecanolFL/FR
sour
 butyric acidFL/FR
spicy
 benzyl cinnamateFL/FR
 benzylidene acetoneFL
 cinnamon vanilla cream flavorFL
 levisticum officinale oleoresinFL
 root beer float flavorFL
sweet
 ethyl 3-(2-hydroxyphenyl) propionateFL
 orange vanilla cream flavorFL
 vanilla oleoresin baliFL/FR
toasted
 acetyl propionylFL/FR
tomato
 methionalFL/FR
vanilla
 ethyl vanillinFL/FR
 ethyl vanillin isobutyrateFL/FR
 ethyl vanillin propylene glycol acetalFL/FR
vanilla ice cream flavorFL
 propenyl guaetholFL/FR
 vanillinFL/FR
 vanillyl acetateFL/FR
 vanillyl isobutyrateFL/FR
waxy
 allyl nonanoateFL/FR
 dihydrojasmone lactoneFL/FR
 ethyl palmitateFL/FR
 ethyl undecanoateFL/FR
 methyl laurateFL/FR
2-nonanolFL/FR
 octyl 2-furoateFL
 octyl butyrateFL/FR
delta-tetradecalactoneFL/FR
 undecanoic acidFL/FR
woody
(E)-beta-iononeFL/FR
 whiskey lactoneFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 amberFR
 balsamFR
 caramelFL
 coconutFL
 dateFL
 fernFR
 figFL
 hay new mown hayFR
 incenseFR
 labdanumFR
 lavenderFR
 mimosaFL
 mossFR
 myrrhFR
 oral care agents 
 orientalFR
 tonka beanFR
 vanillaFL
 woodyFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 not found in nature
Synonyms   Articles   Notes   Search   Top
Synonyms:
2H-1-benzopyran-2-one, 6-methyl-
 cocodescol
 coumarin, 6-methyl-
6-methyl benzopyrone
6-methyl coumarin synthetic
6-methyl coumarine
6-methyl-1,2-benzopyrone
5-methyl-2-hydroxyphenyl propenoic acid lactone
5-methyl-2-hydroxyphenylpropenoic acid lactone
6-methyl-2H-1-benzopyran-2-one
6-methyl-2H-chromen-2-one
 methyl-6 coumarin
6-methyl-cis-o-coumarinic lactone
6-methyl-cis-ortho-coumarinic lactone
6-methylbenzopyrone
6-methylchromen-2-one
6-methylcoumarin
6-methylcoumarin crystal
6-methylcoumarin powder
 pralina
 toncair
 toncarine
Synonyms   Articles   Notes   Search   Top
Articles:
Info: EVALUATION OF CERTAIN FOOD ADDITIVES AND CONTAMINANTS
PubMed: Aquatic toxicity assessment of the additive 6-methylcoumarine using four experimental systems.
PubMed: Comparison of the hepatic effects of coumarin, 3,4-dimethylcoumarin, dihydrocoumarin and 6-methylcoumarin in the rat.
PubMed: A predictive mouse ear-swelling model for investigating topical photoallergy.
PubMed: Use of the occlusive patch to evaluate the photosensitive properties of chemicals in guinea-pigs.
PubMed: Regulatory issues concerning AETT and 6-MC.
PubMed: Insight into the Functional and Structural Properties of 3-Arylcoumarin as an Interesting Scaffold in Monoamine Oxidase B Inhibition.
PubMed: Supramolecular photocatalysis: insights into cucurbit[8]uril catalyzed photodimerization of 6-methylcoumarin.
PubMed: Photomicronucleus assay of phototoxic and pseudophotoclastogenic chemicals in human keratinocyte NCTC2544 cells.
PubMed: Phosphorylation of histone H2AX is a powerful tool for detecting chemical photogenotoxicity.
PubMed: Vibrational and ab initio studies of 3-acetyl-6-bromocoumarin and 3-acetyl-6-methylcoumarin.
PubMed: Supramolecular photocatalysis by confinement--photodimerization of coumarins within cucurbit[8]urils.
PubMed: Development of an in vitro photosensitization assay using human monocyte-derived cells.
PubMed: Complete reduction of 2H-pyran-2-one moiety of coumarin and 6-methyl coumarin by Colletotrichum capsici.
PubMed: Simultaneous determination of 6-methylcoumarin and 7-methoxycoumarin in cosmetics using three-dimensional excitation-emission matrix fluorescence coupled with second-order calibration methods.
PubMed: Aquatic toxicity assessment of the additive 6-methylcoumarine using four experimental systems.
PubMed: Infrared study of 6-methylcoumarin in binary solvent mixtures.
PubMed: In vitro phototoxicity test using artificial skin with melanocytes.
PubMed: Induction of keratinocyte apoptosis by photosensitizing chemicals plus UVA.
PubMed: Causal agents of photoallergic contact dermatitis diagnosed in the national institute of dermatology of Colombia.
PubMed: Fourier transform-infrared and Raman spectra, ab initio calculations and assignments for 6-methyl-4-bromomethylcoumarin.
PubMed: Photoallergic contact sensitization to 6-methylcoumarin in poikiloderma of Civatte.
PubMed: Selectivity in the photodimerization of 6-alkylcoumarins.
PubMed: Use of human reconstituted epidermis Episkin for assessment of weak phototoxic potential of chemical compounds.
PubMed: Development of a highly sensitive in vitro phototoxicity assay using the SkinEthic reconstructed human epidermis.
PubMed: Photochemical formation of singlet molecular oxygen ((1)O2) in illuminated 6-methylcoumarin solutions.
PubMed: Comparison of the hepatic effects of coumarin, 3,4-dimethylcoumarin, dihydrocoumarin and 6-methylcoumarin in the rat.
PubMed: Photoallergic contact dermatitis. Results of photopatch testing in New York, 1985 to 1990.
PubMed: The phototoxicity of 8-methoxythionepsoralen and 6-methylthionecoumarin.
PubMed: A predictive mouse ear-swelling model for investigating topical photoallergy.
PubMed: Use of UVB and UVA to induce and elicit contact photoallergy in the mouse.
PubMed: Use of the occlusive patch to evaluate the photosensitive properties of chemicals in guinea-pigs.
PubMed: Perfume dermatitis.
PubMed: Mechanisms of contact photosensitivity in mice. III. Predictive testing of chemicals with photoallergenic potential in mice.
PubMed: [New data on photoallergy].
PubMed: Determination of coumarin and 6-methylcoumarin in cosmetics by high-performance liquid chromatography.
PubMed: Experimental photoallergic contact dermatitis: a mouse model.
PubMed: The guinea pig as a model for predicting photoallergic contact dermatitis.
PubMed: Perfume dermatitis. Part II. Photodermatitis to Musk Ambrette and 6-methylcoumarin.
PubMed: Evaluation of the photocontact allergenic potential of 6-methylcoumarin in the guinea pig.
PubMed: Photomaximization test for identifying photoallergic contact sensitizers.
PubMed: Regulatory issues concerning AETT and 6-MC.
PubMed: Contact photoallergy to 6-methylcoumarin in proprietary sunscreens.
PubMed: Photocontact allergy to 6-methylcoumarin.
PubMed: Caffeine, caffeine derivatives and chromosomal aberrations. II. Different responses of Allium root tips and Chinese hamster cells to treatments with caffeine, 8-ethoxycaffeine and 6-methylcoumarin.
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