para-methyl anisole
p-methylanisole
 
Notes:
Isol. from ylang-ylang, cananga and other essential oils. Also present in tomato and Camembert cheese. Flavouring ingredient
  • ACS International
    • ACS International GmbH
      Creativity Beyond Chemistry
      Production • Distribution • Sourcing • Logistics • Consulting
      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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      Product(s):
      80005 Cresyl Methyl Ether para
       
  • 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.
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      Para Cresyl Methyl Ether
       
  • Berjé
    • Berje Inc.
      Where the world comes to its senses
      Where the world comes to its senses - Berjé is a global distributor of Essential Oils and Aromatic Chemicals.
      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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      Product(s):
      Methyl Para Cresol
       
  • BOC Sciences
    • BOC Sciences
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      Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
      BOC Sciences provides a wide range of services to support the pharmaceutical industry through all stages of drug discovery including Custom Synthesis of those chemicals that are not in stock, Isotope Labeling Service, Chiral Synthesis and Resolution, Bioconjugation, PEGylation services, analytical services.
      BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies.
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      Product(s):
      104-93-8 4-Methylanisole
       
  • Indukern F&F
  • Lluch Essence
    • Lluch Essence S.L.
      A family company dedicated to sales and distribution
      Flexibility, availability, price and quality.
      Flexibility, availability, price and quality make LLUCH ESSENCE S.L. one of Europe’s references when it comes to essential oils and aroma chemicals, and it is now well known all around the world.
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      PARA-CRESYL METHYL ETHER
       
  • Moellhausen
  • Penta International
    • Penta International Corporation
      Chemistry innovation
      At Penta, our products and services help businesses do business better.
      For over 30 years, Penta Manufacturing Company has played a growing role in worldwide chemistry innovations and applications. As an industry leader, Penta continues to pioneer chemistry-based solutions for practically every area of commerce. Our products and expertise have helped fuel technical advances in dozens of commercial applications including flavoring, coloring, fragrances and chemical processes.
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      Product(s):
      03-55500 p-CRESYL METHYL ETHER
      03-55475 P-CRESYL METHYL ETHER FCC
       
  • PerfumersWorld
    • PerfumersWorld Ltd.
      feeeel... the smell!
      The one-stop resource for the creative perfumer.
      No minimum orders. Aroma chemicals, essential oils, isolates, pheremones, absolutes, resinoids, FleuressenceTM key bases, PWx FactorTM, solubilizers, kits, creation systems, workshops, training, distance learning, The PerfumersWorld Perfumer's Studio, The Perfumer’s Formulation Bulletin, perfumery software, bespoke creation, analysis, consultancy, project counselling, trouble-shooting, unperfumed product bases, bottles, smelling strips, scales, distillation, equipment and inspiration!
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      Product(s):
      4PP00350 para-Cresyl methyl ether
      Blends-well-with - +Linalool +Isoamyl Benzyl Ether +Para-tolyl Isobutyrate +Methyl Chavicol +Dimethyl Benzyl Carbinol
       
      5PN08178 para-Cresyl methyl ether 10% in DPG
       
  • Prodasynth
    • Prodasynth
      PRODUCTEUR PAR ESSENCE
      Chemical specialist in manufacturing, distributing and sourcing of tailor-made ingredients for the Flavour & Fragrance industry.
      Today we are also proud to say, we have created an important range of Natural Molecules which can be found in our Raw Material Compendium. The versatility of our small but efficient structure is one of our main strengths when trying to fulfill our clients' requirements.
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      Product(s):
      PARA-CRESYL METHYL ETHER (> 98%)
       
  • 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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      METHYL PARA CRESOL
       
  • Taytonn
    • TAYTONN 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.
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      Product(s):
      para-Cresyl Methyl Ether
       
  • 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):
      M0149 4-Methoxytoluene >98.0%(GC)
       
  • The Good Scents Company
  • The John D. Walsh Company
    • The John D. Walsh Company, Inc
      Suppliers Since 1942
      Supplying the fragrance and flavor industry with high quality products.
      The John D. Walsh Company, Inc. has evolved from its beginnings as an agent/broker into a distributor of essential oils, aroma chemicals, concretes and absolutes. We currently represent the following companies, as their North American distributor: Destilerias Munoz Galvez, S.A. International Flavors & Fragrances PFW Aroma Chemicals B.V. Innospec Widnes Limited Hydrodiffusion de Guatemala, S. A. DSM Nutritional Products The John D. Walsh Company, Inc. is proud to be a founding member of IFEAT, an active member of IFRA, North America, and a corporate sponsor of the WFFC.
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      History
      Product(s):
      para-Cresyl Methyl Ether
      SDS
       
  • The Lermond Company
    • The Lermond Company
      Your Sourcing Resource
      The Lermond family has been sourcing raw materials for the flavor and fragrance industry for nearly 7 decades.
      The Lermond Company is a women-owned distributor of raw materials primarily servicing the flavor and fragrance industry. For three generations, members of the Lermond family have been integral sourcing partners for the North American flavor and fragrance industry. We supply high quality essential oils, aroma chemicals, absolutes, concretes, resinoids and floral waters from around the world to the global industry.
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      Product(s):
      47510 PARA CRESYL METHYL ETHER
       
  • 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.
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      para-Cresyl Methyl Ether
       
  • 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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      Product(s):
      500768 Cresyl Methyl Ether Para FCC
       
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas    Flavor Demo Formulas
CAS Number: 104-93-8Picture of molecule3D/inchi
Other(deleted CASRN): 1071687-44-9
ECHA EINECS - REACH Pre-Reg: 203-253-7
FDA UNII: 10FAI0OR9W
Nikkaji Web: J10.114A
Beilstein Number: 1237336
MDL: MFCD00008413
CoE Number: 188
XlogP3: 2.70 (est)
Molecular Weight: 122.16690000
Formula: C8 H10 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: 1243  p-methylanisole
DG SANTE Food Flavourings: 04.015  1-methoxy-4-methylbenzene
FEMA Number: 2681 p-methylanisole
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):104-93-8 ; P-METHYLANISOLE
FDA Regulation:
FDA PART 172 -- FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION
Subpart F--Flavoring Agents and Related Substances
Sec. 172.515 Synthetic flavoring substances and adjuvants.
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: colorless clear liquid (est)
Assay: 99.00 to 100.00 % 
Food Chemicals Codex Listed: Yes
Specific Gravity: 0.99600 to 1.00400 @  25.00 °C.
Pounds per Gallon - (est).: 8.288 to  8.354
Refractive Index: 1.51000 to 1.51300 @  20.00 °C.
Melting Point: -32.00 °C. @ 760.00 mm Hg
Boiling Point: 175.50 °C. @ 760.00 mm Hg
Vapor Pressure: 2.029000 mmHg @ 25.00 °C. (est)
Flash Point: 128.00 °F. TCC ( 53.33 °C. )
logP (o/w): 2.660
Shelf Life: 24.00 month(s) or longer if stored properly.
Storage: store in cool, dry place in tightly sealed containers, protected from heat and light.
Soluble in:
 alcohol
 dipropylene glycol
 fixed oils
 water, 527.1 mg/L @ 25 °C (est)
Insoluble in:
 glycerin
 propylene glycol
 water
Stability:
 non-discoloring in most media
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: naphthyl
 
Odor Strength: high ,
recommend smelling in a 1.00 % solution or less
 
Substantivity: 8 hour(s) at 100.00 %
 
 naphthyl  narcissus  ylang  powdery  nutty  
Odor Description:
at 1.00 % in dipropylene glycol. 
naphthyl cresol ylang powdery nutty
Luebke, William tgsc, (1996)
 
 naphthyl  phenolic  camphoreous  minty  powdery  nutty  
Odor Description:
Naphthyl, phenolic, camphoraceous, minty, powdery and nutty
Mosciano, Gerard P&F 15, No. 3, 51, (1990)
 
 
Flavor Type: naphthyl
 
 naphthyl  phenolic  camphoreous  cooling  woody  
Taste Description:
at 20.00 ppm.  
Naphthyl, phenolic, camphoraceous, cooling and woody
Mosciano, Gerard P&F 15, No. 3, 51, (1990)
 
Odor and/or flavor descriptions from others (if found).
 
Symrise
Cresyl methyl ether para
Odor Description: strong leather with nuances reminiscent of para-cresol
Taste Description: vanilla-, chocolate-, nut-like, slightly phenolic
Useful in: fruity red, sweet others.
 
Sigma-Aldrich
4-Methylanisole, ≥99%, FCC, FG
Odor Description: cedar; sweet; vanilla; camphoraceous
Taste Description: naphthyl phenolic camphor cooling woody
 
Moellhausen
METHYL P-CRESOL
Odor Description: floreal,camphoraceous, phenolic, in dilution Ylang Ylang, cananga
Taste Description: camphoraceous, woody, phenolic, fresh
 
PerfumersWorld
para-Cresyl methyl ether
Odor Description: aromatic-phenolic floral daffodil ylang cananga naphthyl phenolic camphor mint powdery nutty
Blends-well-with - +Linalool +Isoamyl Benzyl Ether +Para-tolyl Isobutyrate +Methyl Chavicol +Dimethyl Benzyl Carbinol
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
ACS International
Cresyl Methyl Ether para
Odor: napthyl ylang powdery nutty
Operational Capabilities
Augustus Oils
Para Cresyl Methyl Ether
Services
Berjé
Methyl Para Cresol
Media
BOC Sciences
For experimental / research use only.
4-Methylanisole
EMD Millipore
For experimental / research use only.
4-Methoxytoluene
Ernesto Ventós
para-CRESYL METHYL ETHER
Odor: YLANG YLANG, LEATHER
Flavor: VANILLA, NUTS, PHENOLIC
Indukern F&F
METHYL PARA-CRESOL
Odor: PHENOLIC, AROMATIC, CAMPHORATED
Inoue Perfumery
P-CRESYL METHYL ETHER
Keva
PARACRESYL METHYL ETHER
Odor: Pungent, sharp, sweet ylang type
Lluch Essence
PARA-CRESYL METHYL ETHER
Moellhausen
METHYL P-CRESOL 10%DPG
Moellhausen
METHYL P-CRESOL
Odor: floreal,camphoraceous, phenolic, in dilution Ylang Ylang, cananga
Flavor: camphoraceous, woody, phenolic, fresh
Pearlchem Corporation
p-Cresyl methyl ether
Penta International
P-CRESYL METHYL ETHER FCC
Penta International
p-CRESYL METHYL ETHER
PerfumersWorld
para-Cresyl methyl ether 10% in DPG
PerfumersWorld
para-Cresyl methyl ether
Odor: aromatic-phenolic floral daffodil ylang cananga naphthyl phenolic camphor mint powdery nutty
Use: Blends-well-with - +Linalool +Isoamyl Benzyl Ether +Para-tolyl Isobutyrate +Methyl Chavicol +Dimethyl Benzyl Carbinol
Prodasynth
PARA-CRESYL METHYL ETHER
(> 98%)
Odor: YLANG YLANG, LEATHER
Flavor: VANILLA, NUTS, PHENOLIC
R C Treatt & Co Ltd
para-Cresyl Methyl Ether
Reincke & Fichtner
p-Methylanisole
Sigma-Aldrich
4-Methylanisole, ≥99%, FCC, FG
Odor: cedar; sweet; vanilla; camphoraceous
Certified Food Grade Products
SRS Aromatics
METHYL PARA CRESOL
Taytonn
para-Cresyl Methyl Ether
TCI AMERICA
For experimental / research use only.
4-Methoxytoluene >98.0%(GC)
The Good Scents Company
para-methyl anisole
Odor: naphthyl cresol ylang powdery nutty
The John D. Walsh Company
para-Cresyl Methyl Ether
The Lermond Company
PARA CRESYL METHYL ETHER
The Perfumers Apprentice
para-cresyl methyl ether
Odor: naphthyl phenolic camphor mint powdery nutty
U. K. Aromatics and Chemicals
PARA CRESYL METHYL ETHER
Odor: naphthyl cresol ylang powdery nutty
Flavor: Nut, ylang ylang, jasmin
Ungerer & Company
Methyl p-Cresol
Vigon International
Cresyl Methyl Ether Para FCC
Odor: Pungent sweet, ylang, almond
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Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
R 10 - Flammable.
R 22 - Harmful if swallowed.
R 38 - Irritating to skin.
S 02 - Keep out of the reach of children.
S 16 - Keep away from sources of ignition - No Smoking.
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)
Flammable liquids (Category 3), H226
Acute toxicity, Oral (Category 4), H302
Skin irritation (Category 2), H315
Reproductive toxicity (Category 2), H361
Acute aquatic toxicity (Category 3), H402
Chronic aquatic toxicity (Category 3), H412
GHS Label elements, including precautionary statements
 
Pictogramflame.jpgexclamation-mark.jpghealth-hazard.jpg
 
Signal word Warning
Hazard statement(s)
H226 - Flammable liquid and vapour
H302 - Harmful if swallowed
H315 - Causes skin irritation
H361 - Suspected of damaging fertility or the unborn child
H402 - Harmful to aquatic life
H412 - Harmful to aquatic life with long lasting effects
Precautionary statement(s)
P201 - Obtain special instructions before use.
P202 - Do not handle until all safety precautions have been read and understood.
P210 - Keep away from heat/sparks/open flames/hot surfaces. — No smoking.
P233 - Keep container tightly closed.
P240 - Ground/bond container and receiving equipment.
P241 - Use explosion-proof electrical/ventilating/lighting/…/equipment.
P242 - Use only non-sparking tools.
P243 - Take precautionary measures against static discharge.
P264 - Wash skin thouroughly after handling.
P270 - Do not eat, drink or smoke when using this product.
P273 - Avoid release to the environment.
P280 - Wear protective gloves/protective clothing/eye protection/face protection.
P301 + P312 - IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P303 + P361 + P353 - IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P308 + P313 - IF exposed or concerned: Get medical advice/attention.
P330 - Rinse mouth.
P332 + P313 - IF SKIN irritation occurs: Get medical advice/attention.
P362 - Take off contaminated clothing and wash before reuse.
P370 + P378 - In case of fire: Use dry sand, dry chemical or alcohol-resistant foam for extinction.
P403 + P235 - Store in a well-ventilated place. Keep cool.
P405 - Store locked up.
P501 - Dispose of contents/ container to an approved waste disposal plant.
Human Experience:
2 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50  [sex: M,F] 1920 mg/kg
(Wong & Hart, 1971)

intraperitoneal-mouse LD  > 500 mg/kg
"Summary Tables of Biological Tests," National Research Council Chemical-Biological Coordination Center. Vol. 6, Pg. 214, 1954.

oral-rat LD50  1920 mg/kg
Food and Cosmetics Toxicology. Vol. 12, Pg. 393, 1974.

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 12, Pg. 393, 1974.

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
Recommendation for para-methyl anisole usage levels up to:
  2.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.49 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 15.00 (μg/capita/day)
Structure Class: I
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: -7.60000
beverages(nonalcoholic): -2.70000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: -2.00000
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -2.70000
fruit ices: -2.70000
gelatins / puddings: 0.500004.00000
granulated sugar: --
gravies: --
hard candy: -4.80000
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: --
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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 23 (FGE.23): Aliphatic, alicyclic and aromatic ethers including anisole derivatives From chemical groups 15, 16 and 26 (Commission Regulation (EC) No 1565/2000 of 18 July 2000
View page or View pdf
Flavouring Group Evaluation 59 (FGE.59): Consideration of aliphatic and aromatic ethers evaluated by JECFA (61st meeting) structurally related to aliphatic, alicyclic and aromatic ethers including anisole derivatives evaluated by EFSA in FGE.23 (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
Flavouring Group Evaluation 23, Revision 1 (FGE.23Rev1): Aliphatic, alicyclic and aromatic ethers including anisole derivatives from chemical groups 15, 16, 26 and 30[1] - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 59, Revision 1 (FGE.59Rev1): Consideration of aliphatic and aromatic ethers evaluated by JECFA (61st meeting and 63rd meeting) structurally related to aliphatic, alicyclic and aromatic ethers including anisole derivatives evaluated by EFSA in FGE.23 Rev2 (2010)
View page or View pdf
Scientific Opinion on the safety and efficacy of aromatic ethers including anisole derivatives (chemical group 26) when used as feed additives for all animal species
View page or View pdf
EPI System: View
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Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 104-93-8
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 7731
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 1993
WGK Germany: 1
 1-methoxy-4-methylbenzene
Chemidplus: 0000104938
RTECS: BZ8780000 for cas# 104-93-8
Synonyms   Articles   Notes   Search   Top
References:
 1-methoxy-4-methylbenzene
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 104-93-8
Pubchem (cid): 7731
Pubchem (sid): 134970835
Pherobase: View
Synonyms   Articles   Notes   Search   Top
Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS): View
CHEMBL: View
HMDB (The Human Metabolome Database): HMDB32076
FooDB: FDB008791
Export Tariff Code: 2909.30.6000
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
Formulations/Preparations:
grades: fcc; technical.
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
aldehydic
 dodecanal (aldehyde C-12 lauric)FL/FR
amber
 cistus ladaniferus resinoidFL/FR
animal
isobutyl quinolineFR
isobutyl quinolineFR
para-cresyl caprylateFL/FR
para-cresyl isobutyrateFL/FR
para-cresyl phenyl acetateFL/FR
anisic
para-anisaldehydeFL/FR
balsamic
 amyris wood oilFL/FR
siam benzoin resinoidFL/FR
 benzyl benzoateFL/FR
 benzyl salicylateFL/FR
isobornyl acetateFL/FR
laevo-bornyl acetateFL/FR
isobornyl formateFL/FR
isobutyl cinnamateFL/FR
 cinnamyl alcoholFL/FR
 clover nitrileFR
dextro-fenchoneFL/FR
 fir balsam absoluteFR
 geranyl benzoateFL/FR
 myrrh oilFL/FR
 peru balsam oilFL/FR
 peru balsam resinoidFL/FR
 prenyl benzoateFL/FR
 terpinyl benzoateFR
camphoreous
 bornyl isobutyrateFL/FR
beta-homocyclocitralFL/FR
 fencholFL/FR
laevo-fenchoneFL/FR
chemical
 styralyl alcoholFL/FR
citrus
 bergamot oilFL/FR
coconut
gamma-nonalactone (aldehyde C-18 (so-called))FL/FR
earthy
(-)-alpha-fencholFL/FR
floral
 acetophenoneFL/FR
alpha-amyl cinnamaldehydeFL/FR
isoamyl salicylateFL/FR
 benzaldehyde propylene glycol acetalFL/FR
 benzyl acetateFL/FR
 benzyl alcoholFL/FR
 bois de rose oil brazilFL/FR
isobutyl salicylateFL/FR
 champaca absoluteFR
 citronellolFL/FR
 coriander seed oilFL/FR
para-cresyl acetateFL/FR
para-cresyl phenyl ether 
 cyclamen aldehydeFL/FR
 cyclohexyl ethyl alcoholFL/FR
 dimethyl anthranilateFL/FR
 dimethyl benzyl carbinolFL/FR
 dimethyl benzyl carbinyl acetateFL/FR
 dimethyl benzyl carbinyl butyrateFL/FR
 ethyl ortho-anisateFL/FR
 ethyl phenyl acetateFL/FR
 floral pyranolFR
 geraniolFL/FR
 hawthorn carbinolFL/FR
 heliotropinFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 ho leaf oilFR
 hyacinth etherFR
 hydroxycitronellalFL/FR
 lilac pentanolFL/FR
 lily flower absoluteFR
laevo-linaloolFL/FR
 linaloolFL/FR
 linalool oxideFL/FR
 magnolia indeneFR
para-methyl acetophenoneFL/FR
 methyl dihydrojasmonateFL/FR
 muguet carboxaldehydeFR
 narcissus acetateFL/FR
 nerolFL/FR
 phenethyl acetateFL/FR
 phenethyl alcoholFL/FR
 phenethyl phenyl acetateFL/FR
 reseda acetalFR
 rhodinolFL/FR
 rose butanoateFL/FR
 tea acetateFR
 tetrahydrolinaloolFL/FR
 tuberose absolute (from concrete)FL/FR
 tuberose absolute (from pommade)FL/FR
 tuberose acetateFR
 wallflower absoluteFR
 ylang ylang flower oilFL/FR
fruity
 benzaldehydeFL/FR
 benzyl methyl etherFL/FR
 benzyl propionateFL/FR
 cherry oxyacetateFL/FR
 diethyl succinateFL/FR
 methyl anthranilateFL/FR
green
 phenyl acetaldehydeFL/FR
 phenyl acetaldehyde dimethyl acetalFL/FR
3-phenyl propionaldehydeFL/FR
hay
 hay absoluteFR
herbal
 clary sage oil franceFL/FR
 daucus carota fruit oilFL/FR
 geranic oxideFL/FR
 hyssop oilFL/FR
 linalyl acetateFL/FR
 methyl ortho-anisateFL/FR
 nopyl acetateFR
mentholic
laevo-mentholFL/FR
 peppermint cyclohexanoneFL/FR
mossy
 veramoss (IFF)FR
phenolic
para-cresolFL/FR
 methyl benzoateFL/FR
2,5-xylenolFL/FR
powdery
para-anisyl alcoholFL/FR
spicy
 benzyl isoeugenolFL/FR
4-carvomenthenolFL/FR
 cassia bark oil chinaFL/FR
 clove bud oilFL/FR
 cuminaldehydeFL/FR
 eugenolFL/FR
 methyl isoeugenolFL/FR
terpenic
 frankincense oilFL/FR
alpha-terpineolFL/FR
thujonic
 armoise oilFR
tonka
 coumarinFR
 tonka bean absoluteFR
vanilla
 vanilla bean absolute (vanilla planifolia)FL/FR
waxy
 ethyl laurateFL/FR
woody
(+)-campheneFL/FR
 campheneFL/FR
 cistus twig/leaf oilFL/FR
 guaiacwood oilFL/FR
 gurjun balsam oilFR
 methyl cedryl ketoneFL/FR
 patchouli ethanoneFR
 patchouli oilFL/FR
 santallFR
 santalyl acetateFL/FR
 tobacarol (IFF)FR
 vetiver oil haitiFL/FR
 woody acetateFR
(Z)-woody amyleneFR
 
For Flavor
 
No flavor group found for these
 bornyl isobutyrateFL/FR
(+)-campheneFL/FR
 cistus ladaniferus resinoidFL/FR
 ethyl ortho-anisateFL/FR
 geranyl benzoateFL/FR
 methyl ortho-anisateFL/FR
 prenyl benzoateFL/FR
animal
para-cresyl caprylateFL/FR
aromatic
para-cresyl acetateFL/FR
para-cresyl isobutyrateFL/FR
balsamic
siam benzoin resinoidFL/FR
 benzyl benzoateFL/FR
 benzyl salicylateFL/FR
laevo-bornyl acetateFL/FR
isobutyl cinnamateFL/FR
 myrrh oilFL/FR
 peru balsam oilFL/FR
 peru balsam resinoidFL/FR
camphoreous
 campheneFL/FR
(-)-alpha-fencholFL/FR
 fencholFL/FR
laevo-fenchoneFL/FR
 geranic oxideFL/FR
chemical
 styralyl alcoholFL/FR
cherry
 heliotropinFL/FR
citrus
 bergamot oilFL/FR
laevo-linaloolFL/FR
 linaloolFL/FR
 nerolFL/FR
alpha-terpineolFL/FR
coconut
gamma-nonalactone (aldehyde C-18 (so-called))FL/FR
cooling
isobutyl salicylateFL/FR
4-carvomenthenolFL/FR
beta-homocyclocitralFL/FR
dextro-fenchoneFL/FR
laevo-mentholFL/FR
creamy
para-anisaldehydeFL/FR
para-methyl acetophenoneFL/FR
floral
 bois de rose oil brazilFL/FR
 citronellolFL/FR
 dimethyl benzyl carbinyl acetateFL/FR
 dimethyl benzyl carbinyl butyrateFL/FR
 geraniolFL/FR
 linalyl acetateFL/FR
 methyl dihydrojasmonateFL/FR
 phenethyl alcoholFL/FR
 rhodinolFL/FR
 tetrahydrolinaloolFL/FR
 tuberose absolute (from concrete)FL/FR
 tuberose absolute (from pommade)FL/FR
 ylang ylang flower oilFL/FR
fruity
para-anisyl alcoholFL/FR
 benzaldehydeFL/FR
 benzaldehyde propylene glycol acetalFL/FR
 benzyl acetateFL/FR
 benzyl alcoholFL/FR
 benzyl methyl etherFL/FR
 benzyl propionateFL/FR
 cherry oxyacetateFL/FR
para-cresyl phenyl ether 
 diethyl succinateFL/FR
 dimethyl anthranilateFL/FR
 lilac pentanolFL/FR
 methyl anthranilateFL/FR
 rose butanoateFL/FR
green
isoamyl salicylateFL/FR
 cinnamyl alcoholFL/FR
 cyclamen aldehydeFL/FR
 cyclohexyl ethyl alcoholFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
 linalool oxideFL/FR
 narcissus acetateFL/FR
 phenyl acetaldehyde dimethyl acetalFL/FR
3-phenyl propionaldehydeFL/FR
isophoroneFL
herbal
 clary sage oil franceFL/FR
 coriander seed oilFL/FR
 daucus carota fruit oilFL/FR
 hyssop oilFL/FR
honey
 ethyl phenyl acetateFL/FR
 phenethyl acetateFL/FR
 phenethyl phenyl acetateFL/FR
 phenyl acetaldehydeFL/FR
medicinal
 dimethyl benzyl carbinolFL/FR
mentholic
 peppermint cyclohexanoneFL/FR
musty
2,5-xylenolFL/FR
phenolic
para-cresolFL/FR
para-cresyl phenyl acetateFL/FR
 methyl benzoateFL/FR
powdery
 acetophenoneFL/FR
soapy
 dodecanal (aldehyde C-12 lauric)FL/FR
spicy
 benzyl isoeugenolFL/FR
 cassia bark oil chinaFL/FR
 clove bud oilFL/FR
 cuminaldehydeFL/FR
 eugenolFL/FR
 hawthorn carbinolFL/FR
 methyl isoeugenolFL/FR
terpenic
para-menthatrieneFL
tropical
alpha-amyl cinnamaldehydeFL/FR
vanilla
 vanilla bean absolute (vanilla planifolia)FL/FR
waxy
 ethyl laurateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 hydroxycitronellalFL/FR
woody
 amyris wood oilFL/FR
isobornyl acetateFL/FR
isobornyl formateFL/FR
 cistus twig/leaf oilFL/FR
 frankincense oilFL/FR
 guaiacwood oilFL/FR
 methyl cedryl ketoneFL/FR
 patchouli oilFL/FR
 santalyl acetateFL/FR
 vetiver oil haitiFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 champacaFR
 cherry blossomFR
 currant black currantFR
 floralFR
 genetFR
 grapeFR
 hay new mown hayFR
 hyacinthFR
 jasminFR
 jonquilFR
 lilacFR
 lilyFR
 mulberryFR
 narcissusFR
 nutFL
 roseFR
 sandalwoodFR
 tide 
 tuberoseFR
 wallflowerFR
 walnutFL
 wisteriaFR
 ylang ylangFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 cananga
Search Trop  Picture
 cananga odorata oil java @ 2.14%
Data  GC  Search Trop  Picture
 cananga oil china @ 2.05%
Data  GC  Search Trop  Picture
 champaca concrete @ trace%
Data  GC  Search Trop  Picture
 cheese
Search  PMC Picture
 cheese gorgonzola cheese
Search  PMC Picture
 croton flavens l. (welensali) leaf oil curacao @ trace%
Data  GC  Search Trop  Picture
 hyacinthus orientalis absolute @ 0.01-0.02%
Data  GC  Search Trop  Picture
 lavender oil spike spain @ 0.009%
Data  GC  Search Trop  Picture
 tomato
Search Trop  Picture
 ylang ylang
Search Trop  Picture
 ylang ylang oil @ 0.34%
Data  GC  Search Trop  Picture
 ylang ylang oil CO2 extract @ 2.00%
Data  GC  Search Trop  Picture
 ylang ylang oil I (cananga odorata hook. f. and thomas.) @ 5.75%
Data  GC  Search Trop  Picture
 ylang ylang oil II (cananga odorata hook. f. and thomas.) @ 1.19%
Data  GC  Search Trop  Picture
 ylang ylang oil III @ 0.39%
Data  GC  Search Trop  Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
 anisole, p-methyl-
 benzene, 1-methoxy-4-methyl-
p-cresol methyl ether
para-cresol methyl ether
p-cresyl methyl ether
para-cresyl methyl ether
p-cresyl methyl ether ( p – cresol )
p-cresyl methyl ether FCC
 cresyl methyl ether para
 cresyl methyl ether para FCC
1-methoxy-4-methyl benzene
1-methoxy-4-methyl-benzene
1-methoxy-4-methylbenzene
4-methoxytoluene
p-methoxytoluene
para-methoxytoluene
 methyl 4-methyl phenyl ether
 methyl 4-methylphenyl ether
4-methyl anisole
p-methyl anisole
para-methyl anisole
para-methyl cresol
 methyl p-cresol
o-methyl p-cresol
 methyl p-cresyl ether
 methyl p-methylphenyl ether
 methyl p-tolyl ether
 methyl para cresol
ortho-methyl para-cresol
 methyl para-cresyl ether
 methyl para-methyl phenyl ether
 methyl para-tolyl ether
4-methyl phenol methyl ether
4-methyl-1-methoxybenzene
1-methyl-4-methoxybenzene
 methyl-para-cresol
4-methylanisole
p-methylanisole
para-methylanisole
4-methylcresol
p-methylcresol
4-methylphenol methyl ether
 toluene, 4-methoxy-
p-tolyl methyl ether
para-tolyl methyl ether
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: Noncovalent functionalization of graphene with a Ni(II) tetraaza[14]annulene complex.
PubMed: High resolution electronic spectroscopy of 4-methylanisole in the gas phase. Barrier height determinations for the methyl group torsional motion.
PubMed: Private channels in plant-pollinator mutualisms.
PubMed: Functionalization of the methylene bridges of the calix[6]arene scaffold.
PubMed: A concise synthesis of (+/-)-cacalol.
PubMed: Vibrations and theoretical calculations of p-methylanisole in the first electronically excited S1 and ionic ground D0 states.
PubMed: Orientational isomerism and binding ability of nonsymmetrical guests encapsulated in a self-assembling heterodimeric capsule.
PubMed: Total synthesis of (+/-)-herbertenolide by stereospecific formation of vicinal quaternary centers in a crystalline ketone.
PubMed: Individual solvent/solute interactions through social isomerism.
PubMed: Total synthesis of nucleobase-modified adenophostin A mimics.
PubMed: An assessment of the reaction energetics for cytochrome P450-mediated reactions.
PubMed: Odour-impact compounds of Gorgonzola cheese.
PubMed: Solubilization Site of Organic Perfume Molecules in Sodium Dodecyl Sulfate Micelles: New Insights from Proton NMR Studies.
PubMed: Inhibitory and noninhibitory monoclonal antibodies to human cytochrome P450 2E1.
PubMed: Studies on the mechanism of hepatotoxicity of 4-methylphenol (p-cresol): effects of deuterium labeling and ring substitution.
PubMed: Chloroperoxidase-catalyzed benzylic hydroxylation.
PubMed: Four-week toxicity study of 4-methoxytoluene in rats.
PubMed: Occurrence of aromatic methyl migration (NIH-shift) during oxidation of p-methylanisole by hemin-thiolester complex as a cytochrome P-450 model.
Synonyms   Articles   Notes   Search   Top
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