para-dimethyl hydroquinone
Notes:
Coumarin replacer.
  • Azelis
    • Azelis UK Life Sciences
      Chemical Distribution
      Azelis is a leading global distributor of speciality chemicals.
      Azelis is a leading global speciality chemicals distributor. We provide a diverse range of products and innovative services to more than 20,000 customers. Our in-depth local knowledge is supported by an international structure and value-added services including high levels of technical support and tailored solutions.
      Email: Graham Bott
      Voice: +32 3 613 01 20
      Fax: +32 3 613 01 21
      United Kingdom+44 (0) 1992 82 55 55
      United Kingdom+44 (0) 1992 82 55 66
      Product(s):
      DIMETH HYDROQUIN CRYSTALS
       
  • 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
      Product(s):
      10010 1,4-Dimethoxy benzene
       
  • Berjé
    • Berjé Inc.
      The solution is clear
      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.
      Email: For Information
      Email: For Sales
      Voice: 973-748-8980
      Fax: 973-680-9618
      Product(s):
      Dimethyl Hydroquinone
       
  • CTC Organics
    • CTC Organics
      For More Than 40 Year
      Your source for rare aroma chemicals for the flavor and fragrance industy.
      “The world is run by middle men.” The number of times I have heard Dr. Liu utter those words are innumerable. He loved reciting and recording famous quotes and had many of his own. Among his many talents, Dr. Liu had a unique genius in the area of chemistry. He had an uncanny understanding of the pulse of the chemical industry and was a superb salesman.
      US Email: Customer Service
      US Voice: (404) 524-6744
      US Fax: (404) 577-1651
      Product(s):
      W0425 p-dimethoxybenzene
       
  • 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.
      Email: Info
      Voice: 34 93 379 38 49
      Fax: 34 93 370 65 04
      Product(s):
      DIMETHYL HYDROQUINONE
       
  • 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. We warmly welcome your inquiries, come witness our solemn commitment for yourself.
      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
      Product(s):
      A0286 1,4-DIMETHOXYBENZENE, Kosher
       
  • 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):
      04-48300 DIMETHYLHYDROQUINONE, Kosher
       
  • SAFC Global
    • SAFC
      Complete Supply Chain
      The perfect blend of products and services that bring your creativity to life.
      Sigma-Aldrich is a leading Life Science and High Technology company dedicated to providing high-quality, safe and certified flavor ingredients with transparent and easily accessible documentation to customers around the globe. Sigma-Aldrich also provides a suite of analytical tools that allow food analysts to simplify sample preparation, cleanup and analysis steps, while increasing sensitivity to trace ingredients and harmful substances to meet regulations and quality standards.
      Email: Information
      US Email: Sales
      US Voice: 800-244-1173
      US Fax: 800-368-4661
      Product(s):
      W238600 1,4-Dimethoxybenzene ≥99%, Kosher
      MSDS
       
  • 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.
      Email: Info
      Email: Sales
      Voice: +44 (0) 1284 704076
      Fax: +44 (0) 1284 760819
      Product(s):
      para-DIMETHOXYBENZENE
       
 
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas
1,4-dimethoxybenzene (Click)
CAS Number: 150-78-7
ECHA EC Number: 205-771-9
FDA UNII: 24WC6T6X0G
Beilstein Number: 0774605
MDL: MFCD00008401
FEMA Number: 2386
CoE Number: 2059
XlogP3: 2.00 (est)
Molecular Weight: 138.16610000
Formula: C8 H10 O2
BioActivity Summary: listing
NMR Predictor: Predict
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
IBM Patents: Obtain
Pubchem Patents: Search
PubMed: Search
NCBI: Search
Read: Under the conditions of intended use - New developments in the FEMA GRAS program and the safety assessment of flavor ingredients
Read: A GRAS assessment program for flavor ingredients
Read: Sensory testing for flavorings with modifying properties. Food Technology
Read: Criteria for the safety evaluation of flavoring substances
Read: A procedure for the safety evaluation of natural flavor complexes used as ingredients in food: essential oils
Read: FEMA Expert Panel: 30 Years of safety evaluation for the flavor industry
Read: Consumption ratio and food predominance of flavoring materials
JECFA Food Flavoring: 1250  p-dimethoxybenzene
Flavis Number: 04.034 (Old)
EU SANCO Food Flavourings: 04.034  1,4-dimethoxybenzene

FEMA Number: 2386  p-dimethoxybenzene
FDA Mainterm: P-DIMETHOXYBENZENE
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: white crystalline solid (est)
Assay: 98.00 to 100.00 % 
Food Chemicals Codex Listed: No
Melting Point: 56.00 to  60.00 °C. @ 760.00 mm Hg
Boiling Point: 210.00 to  213.00 °C. @ 760.00 mm Hg
Boiling Point: 109.00 °C. @ 20.00 mm Hg
Vapor Pressure: 0.250000 mm/Hg @ 25.00 °C. (est)
Vapor Density: 4.8 ( Air = 1 )
Flash Point: > 212.00 °F. TCC ( > 100.00 °C. )
logP (o/w): 2.040
Shelf Life: 36.00 month(s) or longer if stored properly.
Storage: store in cool, dry place in tightly sealed containers, protected from heat and light.
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
Odor Type: green
Odor Strength: high ,
recommend smelling in a 1.00 % solution or less
Odor Description:
at 1.00 % in dipropylene glycol. 
sweet green new mown hay fennel
Luebke, William tgsc, (1981)
Odor sample from: Berjé Inc.
Taste Description:
fennel fatty mild
Substantivity: 76 Hour(s)
  
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
Augustus Oils
Dimethyl Hydro Quinone
Azelis
DIMETH HYDROQUIN CRYSTALS
Beijing Lys Chemicals
1,4-Dimethoxy benzene
Berjé
Dimethyl Hydroquinone
CG Herbals
Di Methyl Hydroquinone
Creatingperfume.com
Dimethyl Hydroquinone (1,4-Dimethoxybenzene)
Odor: Sweet, green, new mown hay, fennel, aromatic, herbaceous, earthy, tobacco note
CTC Organics
p-dimethoxybenzene
Ernesto Ventós
DIMETHYL HYDROQUINONE
Indukern F&F
DIMETHYL HYDROQUINONE
Odor: WARM, HERBAL, POWERFUL, SWEET
Kelkar Group
DIMETHYL HYDROQUINONE
Lluch Essence
DIMETHYL HYDROQUINONE
M&U International
1,4-DIMETHOXYBENZENE, Kosher
Moellhausen
DIMETHYL HYDROQUINONE
Nature-identical
Odor: sweet, aromatic, erbaceous, earthy, tobacco note
Flavor: aromatic, dusty, earthy
Penta International
DIMETHYLHYDROQUINONE, Kosher
SAFC Global
1,4-Dimethoxybenzene
≥99%, Kosher
Odor: fennel; fatty.
SRS Aromatics
para-DIMETHOXYBENZENE
The Good Scents Company
para-dimethyl hydroquinone
Odor: sweet green new mown hay fennel
Treatt
Dimethyl Hydroquinone
Synonyms   Articles   Notes   Search   Top
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 36/38 - Irritating to skin and eyes.
S 02 - Keep out of the reach of children.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 36 - Wear suitable protective clothing.
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
Skin irritation (Category 2), H315
Eye irritation (Category 2A), H319
Specific target organ toxicity - single exposure (Category 3), Respiratory system, H335
GHS Label elements, including precautionary statements
 
Pictogramexclamation-mark.jpg
 
Signal word Warning
Hazard statement(s)
H315 - Causes skin irritation
H319 - Causes serious eye irritation
H335 - May cause respiratory irritation
Precautionary statement(s)
P261 - Avoid breathing dust/fume/gas/mist/vapours/spray.
P264 - Wash skin thouroughly after handling.
P271 - Use only outdoors or in a well-ventilated area.
P280 - Wear protective gloves/protective clothing/eye protection/face protection.
P302 + P352 - IF ON SKIN: wash with plenty of soap and water.
P304 + P340 - IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305 + P351 + P338 - IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P312 - Call a POISON CENTER or doctor/physician if you feel unwell.
P332 + P313 - IF SKIN irritation occurs: Get medical advice/attention.
P337 + P313 - IF eye irritation persists: Get medical advice/attention.
P362 - Take off contaminated clothing and wash before reuse.
P403 + P233 - Store in a well-ventilated place. Keep container tightly closed.
P405 - Store locked up.
P501 - Dispose of contents/ container to an approved waste disposal plant.
Human Experience:
4 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50  3600 mg/kg
(Moreno, 1973ae)

oral-rat LD50  8500 mg/kg
(Moreno, 1973ae)

oral-mouse LD50  4000 mg/kg
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: MUSCLE CONTRACTION OR SPASTICITY)
Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 4(2), Pg. 30, 1960.

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

oral-rat LD50  3600 mg/kg
Food and Cosmetics Toxicology. Vol. 16, Pg. 715, 1978.

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 16, Pg. 715, 1978.

Inhalation Toxicity:
inhalation-rat LC50 500 mg/24hours
Food and Cosmetics Toxicology. Vol. 16, Pg. 715, 1978.

Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: flavor and fragrance agents
Recommendation for para-dimethyl hydroquinone usage levels up to:
  2.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 15.00 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 7.00 (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: -5.80000
beverages(nonalcoholic): -8.10000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -5.00000
fruit ices: -5.00000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: -4.70000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: --
sugar substitutes: --
sweet sauces: --
Synonyms   Articles   Notes   Search   Top
Safety References:
European Food Safety Athority(efsa): Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...
European Food Safety Authority (EFSA) reference(s):
Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to Flavouring Group Evaluation 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
Chemicalize.org: Calculate predicted properties
ECHA Data Sheet: View
NIOSH International Chemical Safety Cards: search
NLM Hazardous Substances Data Bank: Search
Chemical Carcinogenesis Research Information System: Search
Cancer Citations: Search
Toxicology Citations: Search
Env. Mutagen Info. Center: Search
NLM Developmental and Reproductive Toxicity: Search
National Toxicology Program: Search
EPA Substance Registry Services (TSCA): 150-78-7
EPA ACToR: Toxicology Data
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 1
 1,4-dimethoxybenzene
DTP/NCI: 7483
Chemidplus: 0000150787
EPA/NOAA CAMEO: hazardous materials
RTECS: 150-78-7
Synonyms   Articles   Notes   Search   Top
References:
 1,4-dimethoxybenzene
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 150-78-7
Pubchem (cid): 9016
Pubchem (sid): 134973236
Pherobase Floral: View
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Other Information:
(IUPAC): Atomic Weights of the Elements 2009
(IUPAC): Atomic Weights of the Elements 2009 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
FDA Everything Added to Food in the United States (EAFUS): View
CHEMBL: View
HMDB (The Human Metabolome Database): HMDB29671
Export Tariff Code: 2909.30.6000
Haz-Map: View
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
RSC Learn Chemistry: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 acetaldehyde dimethyl acetalFL/FR
 acetaldehyde ethyl phenethyl acetalFL/FR
green algae absoluteFL/FR
 allyl amyl glycolateFR
 allyl cyclohexyl propionateFL/FR
isoamyl 3-(2-furan) propionateFL/FR
 amyl benzoateFL/FR
isoamyl benzoateFL/FR
isoamyl butyrateFL/FR
alpha-amyl cinnamaldehydeFL/FR
isoamyl isovalerateFL/FR
isoamyl salicylateFL/FR
 amyris wood oilFL/FR
para-anisyl alcoholFL/FR
 anisyl propanal / methyl anthranilate schiff's baseFR
sweet basil oilFL/FR
 bay leaf oilFL/FR
 benzophenoneFL/FR
 benzyl benzoateFL/FR
 benzyl methyl etherFL/FR
 benzyl salicylateFL/FR
isobutyl benzyl carbinolFL/FR
alpha-butyl cinnamaldehydeFL/FR
isobutyl quinolineFR
isobutyl quinolineFR
isobutyl salicylateFL/FR
wild carrot seed oilFL/FR
 champaca absoluteFR
 chrysanthemum oxideFL/FR
 cinnamyl alcoholFL/FR
 cinnamyl formateFL/FR
 citral dimethyl acetalFL/FR
 citronellolFL/FR
 citronellyl acetateFL/FR
 citronellyl propionateFL/FR
 citrus carbaldehyde / methyl anthranilate schiff's baseFR
 clary sage absoluteFL/FR
 clary sage oil franceFL/FR
 clove bud oilFL/FR
 clover nitrileFR
 coriander seed oilFL/FR
 coumaneFL/FR
 coumarinFR
para-cresyl caprylateFL/FR
para-cresyl phenyl acetateFL/FR
 cumin carbinolFR
 cuminaldehydeFL/FR
 cuminyl acetaldehydeFL/FR
black currant bud absoluteFL/FR
 cypress oilFR
 decanal propylene glycol acetalFL/FR
3-decanoneFL/FR
(E)-4-decenalFL/FR
2-decenalFL/FR
 diethyl succinateFL/FR
 dihydromyrcenolFL/FR
 dimethyl benzyl carbinolFL/FR
 dimethyl benzyl carbinyl butyrateFL/FR
 dimethyl succinateFL/FR
6,8-dimethyl-2-nonanolFR
 diphenyl methaneFL/FR
 diphenyl oxideFL/FR
 earthy acetalFL/FR
 ethyl 2-benzyl butyrateFL/FR
 ethyl cinnamateFL/FR
 ethyl hydrocinnamateFL/FR
 ethyl laurateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
2-ethyl octine carbonateFL
 ethyl ortho-anisateFL/FR
 ethyl vanillinFL/FR
 eugenolFL/FR
 farnesyl acetateFL/FR
 fir balsam absoluteFR
 floral butanalFR
 floral pyranolFR
 galbasconeFR
 gardenia absoluteFR
 geranium oil bourbonFL/FR
 geranyl acetateFL/FR
 geranyl acetoneFL/FR
 geranyl benzoateFL/FR
 geranyl isobutyrateFL/FR
 grapefruit pentanolFR
 green acetateFR
 green etherFL/FR
 guaiacwood oilFL/FR
 heliotropinFL/FR
 heptyl cinnamateFL/FR
 hexanal diethyl acetalFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
 hexyl acetateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 hexyl tiglateFL/FR
 hyacinth absoluteFL/FR
 hyacinth butanalFR
 hyacinth etherFR
 hydroxycitronellal diethyl acetalFL/FR
 indoleFL/FR
 ivy carbaldehyde / methyl anthranilate schiff's baseFR
 ivy dioxolaneFR
 jasmin cyclopentanolFR
 jonquil absoluteFR
 kewda absolute 
 kewda oilCS
 labdanum resinoidFR
 lavender absolute bulgariaFL/FR
(Z)-leaf acetalFL/FR
 leafy acetalFL/FR
laevo-linaloolFL/FR
 marine hexaneFR
 melon nonenoateFL/FR
 methyl 2-undecynoateFL
para-methyl anisoleFL/FR
 methyl cinnamateFL/FR
 methyl cyclocitroneFR
 methyl dihydrojasmonateFL/FR
para-methyl hydratropaldehydeFL/FR
 methyl octine carbonateFL/FR
 methyl ortho-anisateFL/FR
4-methyl-4-phenyl pentanoneFR
 mimosa absolute franceFL/FR
 muguet undecadienalFR
 narcissus flower absoluteFR
 neroli oil bigardeFL/FR
 nerolidolFL/FR
 oakmoss absoluteFL/FR
 ocean propanalFL/FR
 ocean propanal / methyl anthranilate schiff's baseFR
 octanal dimethyl acetalFL/FR
 octyl oxyacetaldehydeFR
 orange leaf absoluteFL/FR
bitter orangeflower absolute moroccoFL/FR
 papaya isobutyrateFL/FR
 peach pivalateFR
 phenethyl alcoholFL/FR
 phenethyl formateFL/FR
 phenethyl oxyacetaldehydeFR
 phenethyl salicylateFL/FR
 phenoxyacetaldehyde 50% in benzyl alcoholFR
 phenyl acetaldehydeFL/FR
 phenyl acetaldehyde / methyl anthranilate schiff's baseFR
 phenyl acetaldehyde diisobutyl acetalFL/FR
 phenyl acetaldehyde dimethyl acetalFL/FR
 phenyl acetaldehyde ethylene glycol acetalFR
 phenyl acetic acidFL/FR
 phenyl glycol diacetateFR
2-phenyl propionaldehydeFL/FR
3-phenyl propionaldehydeFL/FR
2-phenyl propionaldehyde dimethyl acetalFL/FR
2-phenyl propionaldehyde ethylene glycol acetalFR
2-phenyl propyl acetateFL/FR
(R)-2-phenyl propyl alcoholFL/FR
2-phenyl propyl alcoholFL/FR
3-phenyl propyl alcoholFL/FR
3-phenyl propyl formateFL/FR
 phenyl propyl phenyl acetateFL/FR
3-phenyl propyl propionateFL/FR
(E)-2-phenyl-1(2)-propene-1-yl acetateFR
 prenyl benzoateFL/FR
 reseda acetalFR
 rose butanoateFL/FR
 santallFR
 styralyl acetateFL/FR
 styralyl alcoholFL/FR
 styralyl formateFL/FR
 sweet pea absoluteFR
 tea acetateFR
alpha-terpineolFL/FR
 terpinyl benzoateFR
 terpinyl isobutyrateFL/FR
 tetrahydrolinaloolFL/FR
 tonka bean absoluteFR
 verdyl acetateFR
 tuberose absolute (from concrete)FL/FR
 tuberose absolute (from pommade)FL/FR
 tuberose acetateFR
isovaleraldehyde propylene glycol acetalFL/FR
 vanilla bean absolute (vanilla planifolia)FL/FR
 vanillyl acetateFL/FR
 veramossFR
 vetiver oil haitiFL/FR
 violet leaf absoluteFL/FR
 violet methyl carbonateFR
 woody acetateFR
(Z)-woody amyleneFR
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 acorn 
 agrumen 
 algae 
 amaryllis 
 amberFR
 ambrosia 
 ash mountain ash 
 bark 
 bluebell 
 boroniaFR
 boxwood 
 boxwood blossom 
 boxwoodberry 
 calamusFR
 carrot seedFL/FR
 cassis black currant budFL/FR
 castoreumFR
 cedar forestFR
 celeryFL/FR
 chamomileFR
 champaca champakFR
 chervil 
 cilantroFL/FR
 clematisFR
 clover trefle le'trefle incarnatFR
 cognacFR
 corianderFL/FR
 coronillaFR
 cortex 
 cypressFR
 daffodil narcissusFR
 deertongueFR
 earth humusFR
 erica 
 evergreenFR
 fern fougereFR
 figFR
 fir balsamFR
 fir needle pine needleFL/FR
 flouveFR
 flouve blossom 
 foliage 
 fungus mushroomFR
 geraniumFR
 ginger whiteFR
 grass 
 greenFR
 green grassFR
 hancornia 
 hay new mown hay foin coupeFR
 heatherFR
 herbalFR
 hollyberryFR
 hugonia 
 hyacinth jacintheFR
 hydrangeaFR
 ivyFR
 jasminFR
 jonquil narcissus jonquillaFR
 kewda 
 leaf 
 autumnFR
 leatherFR
 liverwort 
 lotusFR
 marjoramFL/FR
 mateFL/FR
 meadow countryFR
 mimosaFR
 narcissus narcisseFR
 neroliFR
 nut hazelnutFR
 ocean sea 
 opoponaxFL/FR
 orange bitterFL/FR
 oreganoFL/FR
 orris irisFR
 palmarosaFL/FR
 pansyFR
 parsleyFL/FR
 passion blossomFR
 patchouliFR
 pear prickly pear 
 pine needle scotchFL/FR
 poppy 
 primrose 
 privet 
 privet blossom 
 reseda mignonetteFR
 rhubarbFR
 roseFR
 rose geraniumFR
 sandalwoodFR
 seaweedFL/FR
 stem 
 straw 
 tea 
 tobacco flowerFR
 vine 
 weedy 
 woodruff asperulaFR
 wormwood absinthiumFL/FR
 yewFR
Synonyms   Articles   Notes   Search   Top
Natural Occurrence in: note
 coffee
 hyacinth
GRIN Trop Picture
 papaya
 peppermint oil
GRIN Trop Picture
 ylang ylang oil @ 0.13%
Data  GC  GRIN Trop Picture
 ylang ylang oil CO2 extract @ 0.10%
Data  GC  GRIN Trop Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
 benzene, 1,4-dimethoxy-
 di methyl hydroquinone
1,4-dimethoxy benzene
1,4-dimethoxy-benzene
1,4-dimethoxybenzene
4-dimethoxybenzene
p-dimethoxybenzene
para-dimethoxybenzene
1,4-dimethoxybenzol
 dimethyl ether hydroquinone
 dimethyl hydroquinone
p-dimethyl hydroquinone
 dimethyl hydroquinone ether
 dimethylhydroquinone
p-dimethylhydroquinone
 hydroquinone dimethyl ether
 hydrquinone dimethyl ether
p-methoxyanisole
para-methoxyanisole
 methyl p-methoxyphenyl ether
 methyl para-methoxyphenyl ether
 quinol dimethyl ether
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: Theoretic calculation for understanding the oxidation process of 1,4-dimethoxybenzene-based compounds as redox shuttles for overcharge protection of lithium ion batteries.
PubMed: Intramolecular electronic couplings in class II/III organic mixed-valence systems of bis(1,4-dimethoxybenzene).
PubMed: Ozonolysis of lignin models in aqueous solution: anisole, 1,2-dimethoxybenzene, 1,4-dimethoxybenzene, and 1,3,5-trimethoxybenzene.
PubMed: Perception of floral volatiles involved in host-plant finding behaviour: comparison of a bee specialist and generalist.
PubMed: Highly stable high performance liquid chromatography stationary phase based on direct chemical modification of organic bridges in hybrid silica.
PubMed: 1,4-Dimethoxybenzene, a floral scent compound in willows that attracts an oligolectic bee.
PubMed: 2-Chloro-1,4-dimethoxybenzene as a mediator of lignin peroxidase catalyzed oxidations.
PubMed: 2-Chloro-1,4-dimethoxybenzene cation radical: formation and role in the lignin peroxidase oxidation of anisyl alcohol.
PubMed: Size-selected gold clusters on porous titania as the most "gold-efficient" heterogeneous catalysts.
PubMed: 2-chloro-1,4-dimethoxybenzene as a novel catalytic cofactor for oxidation of anisyl alcohol by lignin peroxidase.
PubMed: The de novo production of drosophilin A (tetrachloro-4-methoxyphenol) and drosophilin A methyl ether (tetrachloro-1,4-dimethoxybenzene) by ligninolytic basidiomycetes.
PubMed: [Antibacterial activity of secondary metabolites from Aspergillus awamori F12 isolated from rhizospheric soil of Rhizophora stylosa Griff].
PubMed: Aerobic oxidative coupling of arenes and olefins through a biomimetic approach.
PubMed: Simultaneous determination of charge number and diffusion coefficient of 2-chloro-1,4-dimethoxybenzene in acetonitrile using potential-step chronoamperometry.
PubMed: Reversible photochemically gated transformation of a hemicarcerand to a carcerand.
PubMed: Degradation and transformation products of acetaminophen in soil.
PubMed: Ecological relationship between floral thermogenesis and pollination in Nelumbo lutea (Nelumbonaceae).
PubMed: Hydrogen-bonded inclusion compounds with reversed polarity: anionic metal-complexes and cationic organic linkers.
PubMed: Quantitative preparative gas chromatography of caffeine with nuclear magnetic resonance spectroscopy.
PubMed: Halogen-substituted (C-β-D-glucopyranosyl)-hydroquinone regioisomers: synthesis, enzymatic evaluation and their binding to glycogen phosphorylase.
PubMed: Synthesis and X-ray crystal structure of a difunctionalized pillar[5]arene at A1/B2 positions by in situ cyclization and deprotection.
PubMed: Epimeric monosaccharide-quinone hybrids on gold electrodes toward the electrochemical probing of specific carbohydrate-protein recognitions.
PubMed: Regioselectivity in the nitration of dialkoxybenzenes.
PubMed: Transcriptional response of zebrafish embryos exposed to neurotoxic compounds reveals a muscle activity dependent hspb11 expression.
PubMed: Pairwise substitution effects, inter- and intramolecular hydrogen bonds in methoxyphenols and dimethoxybenzenes. Thermochemistry, calorimetry, and first-principles calculations.
PubMed: Nitration of veratryl alcohol by lignin peroxidase and tetranitromethane.
PubMed: Oxidation of dimethoxylated aromatic compounds by lignin peroxidase from Phanerochaete chrysosporium.
PubMed: Deprotonative metalation of aromatic compounds by using an amino-based lithium cuprate.
PubMed: Crystallographic, kinetic, and spectroscopic study of the first ligninolytic peroxidase presenting a catalytic tyrosine.
PubMed: Guest-induced assembly of tetracarboxyl-cavitand and tetra(3-pyridyl)-cavitand into a heterodimeric capsule via hydrogen bonds and CH-halogen and/or CH-pi interaction: control of the orientation of the encapsulated guest.
PubMed: Escherichia coli expression and in vitro activation of a unique ligninolytic peroxidase that has a catalytic tyrosine residue.
PubMed: Analysis of biogenic volatile organic compounds in zucchini flowers: identification of scent sources.
PubMed: Reactions within p-difluorobenzene/methanol heterocluster ions: a detailed experimental and theoretical investigation.
PubMed: Degradation of 2,4-dichlorophenol by the lignin-degrading fungus Phanerochaete chrysosporium.
PubMed: Application of microscale-preparative multidimensional gas chromatography with nuclear magnetic resonance spectroscopy for identification of pure methylnaphthalenes from crude oils.
PubMed: Degradation of various alkyl ethers by alkyl ether-degrading Actinobacteria isolated from activated sludge of a mixed wastewater treatment.
PubMed: Induction of forestomach lesions by butylhydroxyanisole and structurally related substances.
PubMed: Inter- and intraspecific variation in floral scent in the genus salix and its implication for pollination.
PubMed: para-Bridged symmetrical pillar[5]arenes: their Lewis acid catalyzed synthesis and host-guest property.
PubMed: Photoarylation/alkylation of bromonaphthols.
PubMed: Variability in floral scent in rewarding and deceptive orchids: the signature of pollinator-imposed selection?
PubMed: Photosensitized oxidation of sulfides: discriminating between the singlet-oxygen mechanism and electron transfer involving superoxide anion or molecular oxygen.
PubMed: Anodic oxidation of mono- and disubstituted 1,4-dimethoxybenzenes.
PubMed: One-pot synthesis of C-glycosylic compounds (C-glycosides) from D-glucal, p-tolylsulfenyl chloride and aromatic/heteroaromatic compounds in the presence of Lewis acids.
PubMed: Photochemistry of methoxyhydroquinone and methoxy-p-benzoquinone in solution related to the photoyellowing of the lignocellulosics.
PubMed: Cis-Trans Isomerization and Oxidation of Radical Cations of Stilbene Derivatives.
PubMed: Rate parameter changes by added albumin in the microsomal oxidative demethylation of deuteriated and non-deuteriated 4-methoxyanisole.
PubMed: [Quantitative analysis of tripchlorolide in pharmaceutical preparation by RP-HPLC].
PubMed: Mechanism of antitumoral activity of catechols in culture.
PubMed: The ligninase of Phanerochaete chrysosporium generates cation radicals from methoxybenzenes.
PubMed: Synthesis of new phytogrowth-inhibitory substituted aryl-p-benzoquinones.
PubMed: Selective monoiodination of aromatic compounds with electrochemically generated I+ using micromixing.
PubMed: Microbial anaerobic demethylation and dechlorination of chlorinated hydroquinone metabolites synthesized by basidiomycete fungi.
PubMed: First synthesis of a polysaccharide-supported lignin model compound and study of its oxidation promoted by lignin peroxidase.
PubMed: Role of face-to-face and edge-to-face aromatic interactions in the inclusion complexation of cyclobis(paraquat-p-phenylene): a theoretical study.
PubMed: [Studies on the chemical constituents of chloroform extract of Dracaena cochinchinensis].
PubMed: Facile oxidation of fused 1,4-dimethoxybenzenes to 1,4-quinones using NBS: fine-tuned control over bromination and oxidation reactions.
PubMed: Volatile methoxybenzene compounds in grains with off-odors.
PubMed: Effects of BHA and related phenols on the forestomach of rats.
PubMed: Decrease in glucose oxidation in isolated brown fat cells from rats due to tropolone and dimethoxybenzene.
PubMed: Reactions of N-methyl-N-(4-biphenylyl)nitrenium ion with electron-rich arenes: laser flash photolysis and product studies.
PubMed: Synthesis of indan-based unusual alpha-amino acid derivatives under phase-transfer catalysis conditions.
PubMed: Characterization of a novel manganese peroxidase-lignin peroxidase hybrid isozyme produced by Bjerkandera species strain BOS55 in the absence of manganese.
PubMed: On the mechanism of inhibition of the veratryl alcohol oxidase activity of lignin peroxidase H2 by EDTA.
PubMed: Are free radicals involved in tumor promotion?
PubMed: Metallocyclic receptors with Re(I)/Os(II)-based moieties: molecular photophysics and selective molecular sensing.
PubMed: Iodide as the mediator for the reductive reactions of peroxidases.
PubMed: Transformation of chlorinated phenolic compounds in the genusRhodococcus.
PubMed: Protective effects of butylated hydroxyanisole and its analogs on the lung toxicity of butylated hydroxytoluene in mice.
PubMed: Inhibition by 2(3)-tert-butyl-4-hydroxyanisole and other antioxidants of epidermal ornithine decarboxylase activity induced by 12-O-tetradecanoylphorbol-13-acetate.
Synonyms   Articles   Notes   Search   Top
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Picture of molecule
Soluble in:
 alcohol
 water, 1543 mg/L @ 25 °C (est)
Insoluble in:
 water
Stability:
 non-discoloring in most media
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