thymyl methyl ether
1-methyl-3-methoxy-4-isopropylbenzene
 
Notes:
Naturally occurring, e.g. in oil of sea fennel (Crithmum maritimum) and Citrus spp.
  • 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):
      THYMOL METHYL ETHER
       
  • 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):
      10439 Thymol methyl ether
       
  • BOC Sciences
    • BOC Sciences
      Best of Chemicals Supplier
      Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
      BOC Sciences provides a wide range of services to support the pharmaceutical industry through all stages of drug discovery including Custom Synthesis of those chemicals that are not in stock, Isotope Labeling Service, Chiral Synthesis and Resolution, Bioconjugation, PEGylation services, analytical services.
      BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies.
      Email: Marketing
      US Email: Marketing
      Email: Sales
      US Email: Sales
      Voice: 1-631-485-4226
      Fax: 1-631-614-7828
      US Voice: 1-631-485-4226
      US Fax: 1-631-614-7828
      Europe44-203-286-1088
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      Product(s):
      1076-56-8 Benzene,2-methoxy-4-methyl-1-(1-methylethyl)-
       
  • 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
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      Products List: View
      Product(s):
      THYMOL METHYL ETHER T0510 FEMA 3436
       
  • Frutarom
    • FRUTAROM USA INC,
      Flavor & Specialty Ingredients
      Your preferred partner for flavour and fragrance success.
      Our broad and diverse product portfolio is designed to provide and cater for every flavor and taste profile required by our customer base and incorporates historic, and iconic, market leading products.
      Email: Info
      US Email: Info- USA
      Email: Sales
      Voice: +44 (0) 1429 863 222
      CBD Offering
      Products List: View
      Product(s):
      441T051000 THYMOL METHYL ETHER KOSHER
       
  • M&U International
    • M&U International LLC
      Steady supply & demand
      Meeting customers increasing demands at home as well as abroad.
      M&U dedicates itself to the development and production of new products as well as continuously promoting those new products. We’ve maintained a steady supply&demand relationship with a large number of manufacturers at home and abroad. We’ve developed an extensive network and because of our relationships with these manufacturers, we’re able to provide a stable supply of great quality materials. We’re located in China’s largest communications hub, Shanghai and in the U.S. near one of the largest sea ports on the East Coast. The strategic locations of our facilities ensure convenient, prompt and secure delivery of our products to our customers.
      Email: Sales
      US Email: Sales
      Voice: +86-21-32515501 60762991 60762992
      Fax: +86-21-32515502 64204960
      US Voice: 908-359-9000
      US Fax: 908-359-9002
      News
      Product(s):
      A0396 THYMOL METHYL ETHER, Kosher
       
  • 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.
      US Email: Technical Services
      US Email: Sales
      US Voice: (973) 740-2300
      US Fax: (973) 740-1839
      Product(s):
      13-54550 1-METHYL-3-METHOXY-4-ISOPROPYLBENZENE
       
  • Sigma-Aldrich
  • 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):
      Thymol Methyl Ether
       
  • 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
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      Product(s):
      I0996 2-Isopropyl-5-methylanisole >96.0%(GC)
      SDS
       
Synonyms   Articles   Notes   Search
CAS Number: 1076-56-8Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 214-063-9
FDA UNII: VTE0C4390U
Nikkaji Web: J217.197J
Beilstein Number: 2042889
MDL: MFCD01674973
CoE Number: 11245
XlogP3: 3.80 (est)
Molecular Weight: 164.24772000
Formula: C11 H16 O
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: 1246  1-methyl-3-methoxy-4-isopropylbenzene
DG SANTE Food Flavourings: 04.043  1-isopropyl-2-methoxy-4-methylbenzene
FEMA Number: 3436 1-methyl-3-methoxy-4-isopropylbenzene
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):1076-56-8 ; 1-METHYL-3-METHOXY-4-ISOPROPYLBENZENE
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: colorless clear liquid (est)
Assay: 98.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 0.93600 to 0.94000 @  25.00 °C.
Pounds per Gallon - (est).: 7.788 to  7.822
Refractive Index: 1.50400 to 1.50800 @  20.00 °C.
Boiling Point: 214.00 to  216.00 °C. @ 760.00 mm Hg
Boiling Point: 94.00 to  96.00 °C. @ 15.00 mm Hg
Vapor Pressure: 0.083000 mmHg @ 25.00 °C. (est)
Flash Point: 197.00 °F. TCC ( 91.67 °C. )
logP (o/w): 4.347 (est)
Soluble in:
 alcohol
 water, 21.57 mg/L @ 25 °C (est)
Insoluble in:
 water
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: herbal
 
 woody  smoky  burnt  
Odor Description:
at 1.00 % in dipropylene glycol. 
woody smoky burnt
 
 
Flavor Type: musty
 
 musty  green  earthy  coffee  beany  
Taste Description:
musty green earthy coffee beany
 
Odor and/or flavor descriptions from others (if found).
 
Alfrebro
THYMOL METHYL ETHER
Odor Description: Woody, Smoky, Slightly Burnt
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
Alfrebro
THYMOL METHYL ETHER
Odor: Woody, Smoky, Slightly Burnt
Beijing Lys Chemicals
Thymol methyl ether
BOC Sciences
For experimental / research use only.
Benzene,2-methoxy-4-methyl-1-(1-methylethyl)-
Charkit Chemical
THYMOL METHYL ETHER T0510 FEMA 3436
Frutarom
THYMOL METHYL ETHER
KOSHER
CBD Offering
IFF
THYMOL METHYL ETHER
KOSHER
Flavor: musty green earthy coffee beany
M&U International
THYMOL METHYL ETHER, Kosher
Moellhausen
METHYL THYMOL
Odor: aromatic, herbal, slightly phenolic; somewhat reminiscent of green roots
Penta International
1-METHYL-3-METHOXY-4-ISOPROPYLBENZENE
Sigma-Aldrich
1-Methyl-3-methoxy-4-isopropylbenzene, 98%
Odor: chocolate; musty; nutty; herbaceous; vegetable; earthy; green; coffee; spicy
Certified Food Grade Products
Taytonn ASCC
Thymol Methyl Ether
Odor: Citrus, Green, Herbal/ Herbaceous, Spicy
TCI AMERICA
For experimental / research use only.
2-Isopropyl-5-methylanisole >96.0%(GC)
Synonyms   Articles   Notes   Search   Top
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
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 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.
Oral/Parenteral Toxicity:
intravenous-dog LDLo  1850 mg/kg
LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Therapie. Vol. 3, Pg. 109, 1948.

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 thymyl methyl ether usage levels up to:
  0.5000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 1.70 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 0.10 (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: 8
Click here to view publication 8
 average usual ppmaverage maximum ppm
baked goods: -3.00000
beverages(nonalcoholic): -2.00000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: -2.00000
confectionery froastings: -3.00000
egg products: --
fats / oils: --
fish products: --
frozen dairy: --
fruit ices: --
gelatins / puddings: --
granulated sugar: --
gravies: -2.00000
hard candy: --
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: -2.00000
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: -2.00000
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 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
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 1076-56-8
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 14104
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 1993
WGK Germany: 3
 2-methoxy-4-methyl-1-propan-2-ylbenzene
Chemidplus: 0001076568
RTECS: BZ8770000 for cas# 1076-56-8
Synonyms   Articles   Notes   Search   Top
References:
 2-methoxy-4-methyl-1-propan-2-ylbenzene
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 1076-56-8
Pubchem (cid): 14104
Pubchem (sid): 134980439
Pherobase: View
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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
CHEMBL: View
HMDB (The Human Metabolome Database): HMDB35989
FooDB: FDB014797
Export Tariff Code: 2909.30.6000
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
No odor group found for these
2,5-dimethyl-3,6-diethyl pyrazine 
 gentiana lutea root extractFL/FR
2,5-lutidine 
2-(pyridyl-2)-methyl methyl sulfide 
para-menth-1-en-9-alFL/FR
aldehydic
 agrumen nitrileFR
animal
2-isobutyl quinolineFR
balsamic
 abies alba needle oilFL/FR
cheesy
2-heptanoneFL/FR
citrus
2-heptanolFL/FR
earthy
3-octen-2-oneFL/FR
fatty
2-(methyl thio) benzothiazole 
floral
 dimethyl benzyl carbinyl butyrateFL/FR
 rhubarb pyranFR
green
 carrot leaf oil (daucus carota ssp.maximus)FR
 galbanum oilFL/FR
 galbanum oil replacerFR
(Z)-3-hexen-1-yl isovalerateFL/FR
 privet dioxaneFR
 solanum lycopersicum leaf absoluteFL/FR
 coriander seed concreteFR
T-muurololFL/FR
1-octen-3-yl acetateFL/FR
 origanum oilFL/FR
2-pentyl acetateFL/FR
 safranalFL/FR
white thyme oilFL/FR
 thyme oil CO2 extract spainFL/FR
red thyme oil spainFL/FR
 thyme oil wild or creeping pakistanFL/FR
 thyme undecaneFR
licorice
 glycyrrhiza glabra root extractFL/FR
naphthyl
1-methyl naphthaleneFL/FR
nutty
2-methyl-3-propyl pyrazineFL/FR
rooty
 vetiveryl propionateFR
smoky
 beech wood creosoteFL/FR
 birch tar oilFL/FR
 cade oilFR
 cade oil replacerFR
 propyl parabenCS
 pyroligneous acidsFL/FR
spicy
isobutyl (E,E)-2,4-decadienamideFL/FR
 carvacryl ethyl etherFL/FR
 cinnamaldehyde dimethyl acetalFL/FR
(-)-cubenolFL/FR
black currant bud absoluteFL/FR
 origanum majorana oilFL/FR
 origanum majorana oil cubaFL/FR
waxy
2-nonanolFL/FR
woody
 bruyere root oilFR
 juniper berry oleoresinFL/FR
 patchouli absoluteFR
 thyme oil portugueseFR
 vetiver oil acetylatedFR
 vetiver resinoidFR
yeasty
2-octen-4-oneFL/FR
 
For Flavor
 
No flavor group found for these
 benzyl disulfideFL
 birch tar oilFL/FR
isobutyl (E,E)-2,4-decadienamideFL/FR
delta-cadineneFL
 carvacryl ethyl etherFL/FR
 elecampane root absoluteFL
 elecampane root oilFL
 fleabane oil (erigeron canadensis)FL
para-menth-1-en-9-alFL/FR
1-methyl pyrroleFL
2-(methyl thio) benzothiazole 
T-muurololFL/FR
 hexyl 3-mercaptobutanoateFL
bitter
2-(pyridyl-2)-methyl methyl sulfide 
cheesy
2-heptanoneFL/FR
coffee
 coffee distillatesFL
2,5-dimethyl-3,6-diethyl pyrazine 
creamy
3-octen-2-oneFL/FR
dairy
2-pentyl acetateFL/FR
earthy
2-methyl-3-propyl pyrazineFL/FR
floral
 dimethyl benzyl carbinyl butyrateFL/FR
fruity
2-heptanolFL/FR
 galbanum oilFL/FR
 gentiana lutea root extractFL/FR
(Z)-3-hexen-1-yl isovalerateFL/FR
3-methyl pyridineFL
1-octen-3-yl acetateFL/FR
 propylene glycol acetone ketalFL
 solanum lycopersicum leaf absoluteFL/FR
herbal
 origanum majorana oilFL/FR
 origanum oilFL/FR
white thyme oilFL/FR
 thyme oil CO2 extract spainFL/FR
red thyme oil spainFL/FR
 thyme oil wild or creeping pakistanFL/FR
licorice
 glycyrrhiza glabra root extractFL/FR
naphthyl
1-methyl naphthaleneFL/FR
roasted
2,5-lutidine 
smoky
 beech wood creosoteFL/FR
 prosopis juliflora wood extractFL
 pyroligneous acidsFL/FR
dextro-xyloseFL
spicy
 cinnamaldehyde dimethyl acetalFL/FR
(-)-cubenolFL/FR
black currant bud absoluteFL/FR
 origanum majorana oil cubaFL/FR
terpenic
 abies alba needle oilFL/FR
vegetable
2-octen-4-oneFL/FR
waxy
2-nonanolFL/FR
woody
 juniper berry oleoresinFL/FR
 safranalFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 citrusFR
 cranberryFR
 gooseberryFR
 herbalFR
 marjoramFL/FR
 spiceFR
 thyme oil white replacerFR
 tobaccoFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 basil plant
Search Trop  Picture
 cascarilla bark oil @ 0.02%
Data  GC  Search Trop  Picture
 chenopodium ambrosioides oil @ 2.8%
Data  GC  Search Trop  Picture
 coffee
Search  PMC Picture
 crithmum maritimum l. oil turkey @ 0.30%
Data  GC  Search Trop  Picture
 croton flavens l. (welensali) leaf oil curacao @ trace%
Data  GC  Search Trop  Picture
 fennel sea fennel
Search Trop  Picture
 lavender oil france @ trace%
Data  GC  Search Trop  Picture
 lime fruit
Search Trop  Picture
 lippia aff. gracillis h.b.k. leaf oil brazil @ 6.00%
Data  GC  Search Trop  Picture
 mandarin fruit
Search Trop  Picture
 oregano plant
Search Trop  Picture
 oregano shoot
Search Trop  Picture
 oregano shoot oil
Search Trop  Picture
 potato fried potato
Search Trop  Picture
 snake root oil canada @ trace%
Data  GC  Search Trop  Picture
 thyme oil red CO2 extract @ 0.32%
Data  GC  Search Trop  Picture
 thyme oil red spain @ 1.43-1.52%
Data  GC  Search Trop  Picture
 thyme plant
Search Trop  Picture
 thymus richardii pers. subsp. nitidus (guss.) jalas oil italy @ 12.40%
Data  GC  Search Trop  Picture
 valerian root oil @ trace-0.4%
Data  GC  Search Trop  Picture
 valerian root oil china @ 0.28%
Data  GC  Search Trop  Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
 anisole, 2-isopropyl-5-methyl-
 benzene, 2-methoxy-4-methyl-1- (1-methylethyl)-
 benzene, 2-methoxy-4-methyl-1-(1-methylethyl)-
 ether, methyl thymyl
2-methoxy-4-methyl-1-(1-methyl ethyl) benzene
2-methoxy-4-methyl-1-(1-methylethyl)-benzene
2-methoxy-4-methyl-1-(1-methylethyl)benzene
2-methoxy-4-methyl-1-(propan-2-yl)benzene
2-methoxy-4-methyl-1-propan-2-ylbenzene
3-methoxy-p-cymene
3-methoxy-para-cymene
 methyl 5-methyl-2-(propan-2-yl)phenyl ether
 methyl thymol
o-methyl thymol
ortho-methyl thymol
 methyl thymol ether
 methyl thymyl ether
1-methyl-3-methoxy-4-isopropyl benzene
1-methyl-3-methoxy-4-isopropylbenzene
o-methylthymol
ortho-methylthymol
 methylthymol, o-
1-isopropyl-2-methoxy-4-methyl benzene
1-isopropyl-2-methoxy-4-methylbenzene
4-isopropyl-3-methoxytoluene
2-isopropyl-5-methyl anisole
2-isopropyl-5-methylanisole
2-isopropyl-5-methylphenyl methyl ether
 thymol methyl ether
 thymyl methyl ether
Synonyms   Articles   Notes   Search   Top
Synonyms   Articles   Notes   Search   Top
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