2,3,6-trimethyl phenol
2,3,6-trimethylphenol
 
Notes:
Flavouring ingredient
  • BOC Sciences
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      Product(s):
      2416-94-6 2,3,6-Trimethylphenol
       
  • Penta International
    • Penta International Corporation
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      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.
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      Product(s):
      20-83700 2,3,6-TRIMETHYLPHENOL
       
  • 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.
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      Product(s):
      W2032 2,3,6-trimethylphenol
       
  • TCI AMERICA
    • TCI AMERICA
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      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.
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      Product(s):
      T0877 2,3,6-Trimethylphenol >98.0%(GC)
       
Synonyms   Articles   Notes   Search
CAS Number: 2416-94-6Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 219-330-3
FDA UNII: 05WKL2L5LJ
Nikkaji Web: J116.743J
Beilstein Number: 2042207
MDL: MFCD00002229
XlogP3-AA: 2.70 (est)
Molecular Weight: 136.19384000
Formula: C9 H12 O
BioActivity Summary: listing
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: 737  2,3,6-trimethylphenol
DG SANTE Food Flavourings: 04.085  2,3,6-trimethylphenol
DG SANTE Food Contact Materials: 2,3,6-trimethylphenol
FEMA Number: 3963 2,3,6-trimethylphenol
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):2416-94-6 ; 2,3,6-TRIMETHYLPHENOL
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Physical Properties:
Appearance: white to pale yellow crystalline solid (est)
Assay: 98.00 to 100.00 % 
Food Chemicals Codex Listed: No
Melting Point: 63.00 to  64.00 °C. @ 760.00 mm Hg
Boiling Point: 226.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.066000 mmHg @ 25.00 °C. (est)
Flash Point: 212.00 °F. TCC ( 100.00 °C. )
logP (o/w): 2.670
Soluble in:
 alcohol
 water, 1732 mg/L @ 25 °C (est)
 water, 1580 mg/L @ 25 °C (exp)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
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Suppliers:
Axsyn
For experimental / research use only.
Phenol,2,3,6-trimethyl-
BOC Sciences
For experimental / research use only.
2,3,6-Trimethylphenol
Parchem
2,3,6-trimethyl phenol
Penta International
2,3,6-TRIMETHYLPHENOL
Santa Cruz Biotechnology
For experimental / research use only.
2,3,6-Trimethylphenol
Synerzine
2,3,6-trimethylphenol
TCI AMERICA
For experimental / research use only.
2,3,6-Trimethylphenol >98.0%(GC)
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Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
C - Corrosive.
R 34 - Causes burns.
R 36/37/38 - Irritating to eyes, respiratory system, and skin.
S 01/02 - Keep locked up and 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 36/37/39 - Wear suitable clothing, gloves and eye/face protection.
S 45 - In case of accident or if you feel unwell seek medical advice immediately.
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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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
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.24 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 0.30 (μg/capita/day)
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: 19
Click here to view publication 19
 average usual ppmaverage maximum ppm
baked goods: 1.000003.00000
beverages(nonalcoholic): 0.020000.20000
beverages(alcoholic): 0.100000.50000
breakfast cereal: 0.020000.10000
cheese: 0.040000.40000
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: 0.100000.50000
fats / oils: 0.100000.50000
fish products: --
frozen dairy: 0.100000.50000
fruit ices: --
gelatins / puddings: --
granulated sugar: --
gravies: 0.100000.50000
hard candy: 0.200001.00000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: 0.100000.50000
milk products: 0.020000.20000
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: 0.100000.50000
snack foods: 0.200001.00000
soft candy: --
soups: 0.020000.20000
sugar substitutes: --
sweet sauces: --
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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 22 (FGE.22): Ring-substituted phenolic substances from chemical groups 21 and 25 (Commission Regulation (EC) No 1565/2000 of 18 July 2000)
View page or View pdf
Flavouring Group Evaluation 58 (FGE.58) Consideration of phenol derivatives evaluated by JECFA (55th meeting) structurally related to ring substituted phenolic substances evaluated by EFSA in FGE.22 (2006) (Commission Regulation (EC) No 1565/2000 of 18 July 2000) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)
View page or View pdf
25th list of substances for food contact materials
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 22, Revision 1 (FGE.22Rev1): Ring-substituted phenolic substances from chemical groups 21 and 25
View page or View pdf
EPI System: View
EPA Substance Registry Services (TSCA): 2416-94-6
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 17016
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 2430
WGK Germany: 1
 2,3,6-trimethylphenol
Chemidplus: 0002416946
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References:
 2,3,6-trimethylphenol
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 2416-94-6
Pubchem (cid): 17016
Pubchem (sid): 134982872
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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
FDA Indirect Additives used in Food Contact Substances:View
CHEMBL: View
HMDB (The Human Metabolome Database): HMDB29667
FooDB: FDB000850
Export Tariff Code: 2907.19.2000
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 coffee
Search  PMC Picture
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Synonyms:
1-hydroxy-2,3,6-trimethyl benzene
1-hydroxy-2,3,6-trimethylbenzene
3-hydroxypseudocumene
 phenol, 2,3,6-trimethyl-
2,3,6-trimethylphenol
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Articles:
Google Patents: Production of 2,3,6-trimethylphenol
PubMed: Me3(OMe)tBuXPhos: a surrogate ligand for Me4tBuXPhos in palladium-catalyzed C-N and C-O bond-forming reactions.
PubMed: Hierarchical mesoporous TS-1 zeolite: a highly active and extraordinarily stable catalyst for the selective oxidation of 2,3,6-trimethylphenol.
PubMed: Magnetic and catalytic properties of copper ferrite nanopowders prepared by combustion process.
PubMed: Zr(IV)-monosubstituted Keggin-type dimeric polyoxometalates: synthesis, characterization, catalysis of H2O2-based oxidations, and theoretical study.
PubMed: FTIR spectroscopic study of titanium-containing mesoporous silicate materials.
PubMed: Synthesis, characterization, and reactivity of Ti(IV)-monosubstituted Keggin polyoxometalates.
PubMed: Aerobic oxidation of 2,3,6-trimethylphenol to trimethyl-1,4-benzoquinone with copper(II) chloride as catalyst in ionic liquid and structure of the active species.
PubMed: First isolated active titanium peroxo complex: characterization and theoretical study.
PubMed: Synthesis and anti lipid-peroxidation activity of hydroquinone monoalkyl ethers.
PubMed: Suppression of intestinal smooth muscle contraction by phenolic compounds.
PubMed: Bacterial metabolism of 2,6-xylenol.
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