para-dimethyl hydroquinone
p-dimethoxybenzene
 
Notes:
Coumarin replacer. Flavouring ingredient
  • 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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  • 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.
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  • 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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      150-78-7 para-Dimethyl Hydroquinone
       
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    • 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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  • M&U International
    • M&U International LLC
      Steady supply & demand
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      A0286 1,4-DIMETHOXYBENZENE, Kosher
       
  • Moellhausen
  • Pell Wall Perfumes
    • Pell Wall Perfumes
      Hand-made fragrances
      Pell Wall maintains a broad palette of ingredients & in order to keep stocks fresh & the options wide we also sell from our own stock.
      Pell Wall was founded by perfumer Chris Bartlett to provide exclusive hand-made fragrances to a select few people who love them. All our products are created using fine quality ingredients, many of which we also offer for sale to other perfumers and enthusiasts. Pell Wall make fragrances for men, for women and for the home.
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      For over 30 years, Penta Manufacturing Company has played a growing role in worldwide chemistry innovations and applications. As an industry leader, Penta continues to pioneer chemistry-based solutions for practically every area of commerce. Our products and expertise have helped fuel technical advances in dozens of commercial applications including flavoring, coloring, fragrances and chemical processes.
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  • 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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    • Synerzine, Inc.
      Innovation. Customization. Aroma Ingredients.
      Synerzine is a leading supplier of flavor and fragrance ingredients.
      Synerzine expresses what we have grown to embody as an organization - the synergy and connection between raw ingredients, science, technology, and the final product. Our experienced team is passionate about bringing our customers high-quality innovative ingredients that they can trust.
      Building upon our 44 year history, the Synerzine team provides customers around the globe with convenient access to over 1200 high-quality aroma ingredients. We actively engage with customers to add a wide array of new products and services on a regular basis. Our aim is to delight every customer with our exceptional services, large product selection, customization and the highest quality and safety standards. We provide our customers with true value designed to help them bring their products to market faster.
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      Tianjin danjun international trade co., LTD. is an organic chemicals trading company approved by the relevant state authorities to register. We have about 300 kinds of products (natural aroma chemicals, synthetic aroma chemicals and pharmaceutical intermediates). Most of the products are used in flavor and fragrance industry. We know the Chinese chemical market well and we have close relationship with many of the main manufacturers, and to provide our customers with quality goods together with comprehensive service.
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Synonyms   Articles   Notes   Search
Fragrance Demo Formulas
CAS Number: 150-78-7Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 205-771-9
FDA UNII: 24WC6T6X0G
Nikkaji Web: J5.858K
Beilstein Number: 0774605
MDL: MFCD00008401
CoE Number: 2059
XlogP3: 2.00 (est)
Molecular Weight: 138.16610000
Formula: C8 H10 O2
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: 1250  p-dimethoxybenzene
DG SANTE Food Flavourings: 04.034  1,4-dimethoxybenzene
FEMA Number: 2386 p-dimethoxybenzene
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):150-78-7 ; 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 mmHg @ 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.
Soluble in:
 alcohol
 water, 1543 mg/L @ 25 °C (est)
Insoluble in:
 water
Stability:
 non-discoloring in most media
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: green
 
Odor Strength: high ,
recommend smelling in a 1.00 % solution or less
 
Substantivity: 76 hour(s) at 100.00 %
 
 sweet  green  hay new mown hay  fennel  
Odor Description:
at 1.00 % in dipropylene glycol. 
sweet green new mown hay fennel
Luebke, William tgsc, (1981)
 
 
Flavor Type: green
 
 green  hawthorn  hay new mown hay  anisic  anise  fennel  powdery  fatty  
Taste Description:
sweet green hawthorn new mown hay anisic anise fennel powdery fatty
Luebke, William tgsc, (1981)
 
Odor and/or flavor descriptions from others (if found).
 
Moellhausen
DIMETHYL HYDROQUINONE
Odor Description: sweet, aromatic, erbaceous, earthy, tobacco note
Taste Description: aromatic, dusty, earthy
 
 
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
Services
Beijing Lys Chemicals
1,4-Dimethoxy benzene
Berjé
Dimethyl Hydroquinone
Media
BOC Sciences
For experimental / research use only.
para-Dimethyl Hydroquinone
Creatingperfume.com
Dimethyl Hydroquinone (1,4-Dimethoxybenzene)
Odor: Sweet, green, new mown hay, fennel, aromatic, herbaceous, earthy, tobacco note
Diffusions Aromatiques
1.4-DIMETHOXYBENZENE
EMD Millipore
For experimental / research use only.
Hydroquinone dimethyl ether
Ernesto Ventós
DIMETHYL HYDROQUINONE
Indukern F&F
DIMETHYL HYDROQUINONE
Odor: WARM, HERBAL, POWERFUL, SWEET
Keva
DIMETHYL HYDROQUINONE
Odor: Warm, herbaceous sweet
Lluch Essence
DIMETHYL HYDROQUINONE
M&U International
1,4-DIMETHOXYBENZENE, Kosher
Moellhausen
DIMETHYL HYDROQUINONE
Odor: sweet, aromatic, erbaceous, earthy, tobacco note
Flavor: aromatic, dusty, earthy
Pell Wall Perfumes
Dimethyl Hydroquinone
Penta International
DIMETHYL HYDROQUINONE
R C Treatt & Co Ltd
Dimethyl Hydroquinone
Santa Cruz Biotechnology
For experimental / research use only.
1.4-Dimethoxybenzene 98%
Sigma-Aldrich
1,4-Dimethoxybenzene, 99%, FG
Odor: fennel; fatty.
Certified Food Grade Products
SRS Aromatics
DIMETHYL HYDROQUINONE
Synerzine
p-Dimethoxybenzene
TCI AMERICA
For experimental / research use only.
1.4-Dimethoxybenzene >99.0%(GC)
Tianjin Danjun International
1,4-Dimethoxy benzene
WholeChem
1,4-Dimethoxy benzene
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
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
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
NIOSH International Chemical Safety Cards: search
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 150-78-7
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 9016
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 1
 1,4-dimethoxybenzene
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: 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): HMDB29671
FooDB: FDB000855
Export Tariff Code: 2909.30.6000
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
No odor group found for these
2-acetonyl-5-methyl furan 
1-amyl-pyrrole-3-aldehyde 
2,5-dimethyl-3,6-dihexyl pyrazine 
2-(pyridyl-2)-ethyl ethyl sulfide 
para-thiocresol 
aldehydic
 muguet undecadienalFR
2-tridecenalFL/FR
amber
 cistus ladaniferus resinoidFL/FR
animal
isobutyl quinolineFR
isobutyl quinolineFR
para-cresyl caprylateFL/FR
para-cresyl phenyl acetateFL/FR
 indoleFL/FR
anisic
 ocimum basilicum herb oilFL/FR
balsamic
isoamyl benzoateFL/FR
 amyris wood oilFL/FR
 benzophenoneFR
 benzyl benzoateFL/FR
 benzyl salicylateFL/FR
 cinnamyl alcoholFL/FR
 cinnamyl formateFL/FR
 clover nitrileFR
 ethyl cinnamateFL/FR
 fir balsam absoluteFR
 geranyl benzoateFL/FR
 methyl cinnamateFL/FR
2-phenyl propyl alcoholFL/FR
3-phenyl propyl alcoholFL/FR
 prenyl benzoateFL/FR
 terpinyl benzoateFR
brown
sec-heptyl acetateFL/FR
chemical
 styralyl alcoholFL/FR
citrus
 citral dimethyl acetalFL/FR
(E)-4-decenalFL/FR
 dihydromyrcenolFL/FR
 grapefruit pentanolFR
coumarinic
 coumaneFL/FR
ethereal
 acetaldehyde dimethyl acetalFL/FR
isovaleraldehyde propylene glycol acetalFL/FR
fatty
 decanolFL/FR
2-decenalFL/FR
2-nonen-1-olFL/FR
2-nonenalFL/FR
fermented
 hexanal diethyl acetalFL/FR
floral
 amyl benzoateFL/FR
alpha-amyl cinnamaldehydeFL/FR
isoamyl salicylateFL/FR
 anisyl propanal / methyl anthranilate schiff's baseFR
alpha-butyl cinnamaldehydeFL/FR
isobutyl salicylateFL/FR
 champaca absoluteFR
 citronellolFL/FR
 citronellyl acetateFL/FR
 citronellyl propionateFL/FR
 coriander seed oilFL/FR
 cumin carbinolFR
 cuminyl acetaldehydeFL/FR
 dimethyl benzyl carbinolFL/FR
 dimethyl benzyl carbinyl butyrateFL/FR
6,8-dimethyl-2-nonanolFR
 ethyl 2-benzyl butyrateFL/FR
 ethyl hydrocinnamateFL/FR
 ethyl ortho-anisateFL/FR
 farnesyl acetateFL/FR
 floral butanalFR
 floral pyranolFR
 gardenia absoluteFR
 geranium oil bourbonFL/FR
 geranyl acetateFL/FR
(E)-geranyl acetoneFL/FR
 geranyl acetoneFL/FR
 geranyl isobutyrateFL/FR
 geranyl phenyl acetateFL/FR
 heliotropinFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 hyacinth etherFR
 hydroxycitronellal diethyl acetalFL/FR
 jasmin cyclopentanolFR
 jonquil absoluteFR
 kewda absolute 
 kewda oilCS
laevo-linaloolFL/FR
 methyl dihydrojasmonateFL/FR
 mimosa absolute franceFL/FR
 neroli oil bigardeFL/FR
 nerolidolFL/FR
 ocean propanalFL/FR
 ocean propanal / methyl anthranilate schiff's baseFR
 orange leaf absoluteFL/FR
bitter orangeflower absolute moroccoFL/FR
 papaya isobutyrateFL/FR
 phenethyl alcoholFL/FR
 phenethyl formateFL/FR
 phenethyl salicylateFL/FR
 phenyl acetaldehyde / methyl anthranilate schiff's baseFR
 phenyl acetaldehyde diisobutyl acetalFL/FR
 phenyl glycol diacetateFR
2-phenyl propionaldehyde dimethyl acetalFL/FR
2-phenyl propionaldehyde ethylene glycol acetalFR
2-phenyl propyl acetateFL/FR
(R)-2-phenyl propyl alcoholFL/FR
3-phenyl propyl formateFL/FR
 phenyl propyl phenyl acetateFR
3-phenyl propyl propionateFL/FR
(E)-2-phenyl-1(2)-propene-1-yl acetateFR
 reseda acetalFR
 rose butanoateFL/FR
 styralyl formateFL/FR
 sweet pea absoluteFR
 tea acetateFR
 terpinyl isobutyrateFL/FR
 tetrahydrolinaloolFL/FR
 tuberose absolute (from concrete)FL/FR
 tuberose absolute (from pommade)FL/FR
 tuberose acetateFR
 verdyl acetateFR
 violet methyl carbonateFR
fruity
 allyl amyl glycolateFR
 allyl cyclohexyl propionateFL/FR
isoamyl butyrateFL/FR
isoamyl isobutyrateFL/FR
isoamyl isovalerateFL/FR
 benzyl methyl etherFL/FR
 diethyl succinateFL/FR
 dimethyl succinateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
 green acetateFR
2-hexen-1-olFL/FR
 hexyl acetateFL/FR
 peach pivalateFR
green
 acetaldehyde ethyl phenethyl acetalFL/FR
isoamyl 3-(2-furan) propionateFL/FR
isobutyl benzyl carbinolFL/FR
 chrysanthemum oxideFL/FR
 citrus carbaldehyde / methyl anthranilate schiff's baseFR
 decanal propylene glycol acetalFL/FR
 diphenyl methaneFL/FR
 diphenyl oxideFL/FR
 earthy acetalFL/FR
 galbascone (IFF)FR
 green etherFL/FR
1-heptanolFL/FR
 heptyl acetateFL/FR
 heptyl cinnamateFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
 hexyl tiglateFL/FR
 hyacinth absoluteFL/FR
 hyacinth butanalFR
 ivy carbaldehyde / methyl anthranilate schiff's baseFR
 ivy dioxolaneFR
(Z)-leaf acetalFL/FR
 leafy acetalFL/FR
 melon nonenoateFL/FR
 methyl cyclocitrone (IFF)FR
para-methyl hydratropaldehydeFL/FR
 methyl octine carbonateFL/FR
4-methyl-4-phenyl pentanoneFR
 narcissus flower absoluteFR
(Z)-2-nonen-1-olFL/FR
(E)-2-nonen-1-olFL/FR
 octanal dimethyl acetalFL/FR
(E)-2-octen-1-yl acetateFL/FR
 octyl oxyacetaldehydeFR
 olive oil absoluteFL/FR
 phenethyl oxyacetaldehydeFR
 phenoxyacetaldehyde 50% in benzyl alcoholFR
 phenyl acetaldehydeFL/FR
 phenyl acetaldehyde dimethyl acetalFL/FR
 phenyl acetaldehyde ethylene glycol acetalFR
3-phenyl propionaldehydeFL/FR
2-phenyl propionaldehydeFL/FR
 styralyl acetateFL/FR
 violet leaf absoluteFL/FR
herbal
 clary sage absoluteFL/FR
 clary sage oil franceFL/FR
 daucus carota fruit oilFL/FR
 lavender absolute bulgariaFL/FR
 methyl ortho-anisateFL/FR
beta-pineneFL/FR
laevo-beta-pineneFL/FR
honey
 phenyl acetic acidFL/FR
marine
green algae absoluteFL/FR
 marine hexaneFR
melon
(Z)-6-nonen-1-yl acetateFL/FR
minty
 spearmint absoluteFL/FR
2,4,4,6-tetramethyl cyclohexa-2,5-diene-1-oneFR
mossy
 oakmoss absoluteFL/FR
 veramoss (IFF)FR
naphthyl
para-methyl anisoleFL/FR
powdery
para-anisyl alcoholFL/FR
spicy
 clove bud oilFL/FR
 cuminaldehydeFL/FR
black currant bud absoluteFL/FR
 eugenolFL/FR
 pimenta acris leaf oilFL/FR
terpenic
 cypress leaf oilFR
D-(+)-beta-pineneFL/FR
alpha-terpineolFL/FR
tonka
 coumarinFR
 tonka bean absoluteFR
vanilla
 ethyl vanillinFL/FR
 vanilla bean absolute (vanilla planifolia)FL/FR
 vanillyl acetateFL/FR
waxy
3-decanoneFL/FR
 ethyl laurateFL/FR
woody
 guaiacwood oilFL/FR
 santallFR
 vetiver oil haitiFL/FR
 woody acetateFR
(Z)-woody amyleneFR
 
For Flavor
 
No flavor group found for these
green algae absoluteFL/FR
 amyl benzoateFL/FR
 cistus ladaniferus resinoidFL/FR
 coumaneFL/FR
 decanal propylene glycol acetalFL/FR
3-decanoneFL/FR
 earthy acetalFL/FR
 ethyl 2-benzyl butyrateFL/FR
 ethyl hydrocinnamateFL/FR
 ethyl ortho-anisateFL/FR
 geranyl benzoateFL/FR
 heptyl cinnamateFL/FR
 hexanal diethyl acetalFL/FR
 hyacinth absoluteFL/FR
 kewda absolute 
 methyl ortho-anisateFL/FR
2-phenyl propyl acetateFL/FR
(R)-2-phenyl propyl alcoholFL/FR
3-phenyl propyl formateFL/FR
3-phenyl propyl propionateFL/FR
laevo-beta-pineneFL/FR
D-(+)-beta-pineneFL/FR
 prenyl benzoateFL/FR
 styralyl formateFL/FR
 terpinyl isobutyrateFL/FR
isoamyl 3-(2-furan) propionateFL/FR
alpha-butyl cinnamaldehydeFL/FR
aldehydic
2-tridecenalFL/FR
amber
isobutyl benzyl carbinolFL/FR
animal
para-cresyl caprylateFL/FR
 indoleFL/FR
aromatic
 leafy acetalFL/FR
astringent
2-(pyridyl-2)-ethyl ethyl sulfide 
balsamic
 benzyl benzoateFL/FR
 benzyl salicylateFL/FR
 ethyl cinnamateFL/FR
burnt
para-thiocresol 
chemical
 styralyl alcoholFL/FR
cherry
 heliotropinFL/FR
citrus
 citral dimethyl acetalFL/FR
laevo-linaloolFL/FR
alpha-terpineolFL/FR
cooling
isobutyl salicylateFL/FR
cucumber
2-ethyl octine carbonateFL
ethereal
 acetaldehyde dimethyl acetalFL/FR
fatty
2-acetonyl-5-methyl furan 
1-amyl-pyrrole-3-aldehyde 
2-decenalFL/FR
(E,E)-2,4-heptadienalFL
sec-heptyl acetateFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
2-nonen-1-olFL/FR
(Z)-2-nonen-1-olFL/FR
2-nonenalFL/FR
floral
 citronellolFL/FR
 citronellyl acetateFL/FR
 citronellyl propionateFL/FR
 dimethyl benzyl carbinyl butyrateFL/FR
 farnesyl acetateFL/FR
 geranium oil bourbonFL/FR
(E)-geranyl acetoneFL/FR
 geranyl acetoneFL/FR
 geranyl isobutyrateFL/FR
 geranyl phenyl acetateFL/FR
 methyl dihydrojasmonateFL/FR
 neroli oil bigardeFL/FR
 ocean propanalFL/FR
 orange leaf absoluteFL/FR
bitter orangeflower absolute moroccoFL/FR
 phenethyl alcoholFL/FR
 phenyl acetic acidFL/FR
 tetrahydrolinaloolFL/FR
 tuberose absolute (from concrete)FL/FR
 tuberose absolute (from pommade)FL/FR
fruity
 allyl cyclohexyl propionateFL/FR
isoamyl benzoateFL/FR
isoamyl isobutyrateFL/FR
para-anisyl alcoholFL/FR
 benzyl methyl etherFL/FR
 diethyl succinateFL/FR
 dimethyl succinateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
2-hexen-1-olFL/FR
 hexyl acetateFL/FR
2-phenyl propionaldehyde dimethyl acetalFL/FR
 rose butanoateFL/FR
 styralyl acetateFL/FR
isovaleraldehyde propylene glycol acetalFL/FR
green
 acetaldehyde ethyl phenethyl acetalFL/FR
isoamyl isovalerateFL/FR
isoamyl salicylateFL/FR
 chrysanthemum oxideFL/FR
 cinnamyl alcoholFL/FR
 cucumber distillatesFL
 cuminyl acetaldehydeFL/FR
 dihydromyrcenolFL/FR
2,5-dimethyl-3,6-dihexyl pyrazine 
 diphenyl methaneFL/FR
 diphenyl oxideFL/FR
 geranyl acetateFL/FR
 green etherFL/FR
 heptyl acetateFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
 hexyl tiglateFL/FR
(Z)-leaf acetalFL/FR
3,5-lutidineFL
 melon nonenoateFL/FR
 methyl 2-undecynoateFL
para-methyl hydratropaldehydeFL/FR
 methyl octine carbonateFL/FR
 nerolidolFL/FR
(E)-2-nonen-1-olFL/FR
(Z)-6-nonen-1-yl acetateFL/FR
 oakmoss absoluteFL/FR
 octanal dimethyl acetalFL/FR
(E)-2-octen-1-yl acetateFL/FR
 papaya isobutyrateFL/FR
 phenethyl formateFL/FR
 phenyl acetaldehyde diisobutyl acetalFL/FR
 phenyl acetaldehyde dimethyl acetalFL/FR
2-phenyl propionaldehydeFL/FR
3-phenyl propionaldehydeFL/FR
2-phenyl propyl alcoholFL/FR
 violet leaf absoluteFL/FR
herbal
 clary sage absoluteFL/FR
 clary sage oil franceFL/FR
 coriander seed oilFL/FR
 daucus carota fruit oilFL/FR
 lavender absolute bulgariaFL/FR
 ocimum basilicum herb oilFL/FR
honey
 phenyl acetaldehydeFL/FR
medicinal
 dimethyl benzyl carbinolFL/FR
 phenethyl salicylateFL/FR
melon
 hydroxycitronellal diethyl acetalFL/FR
minty
 spearmint absoluteFL/FR
naphthyl
para-methyl anisoleFL/FR
oily
 olive oil absoluteFL/FR
phenolic
para-cresyl phenyl acetateFL/FR
pine
beta-pineneFL/FR
ripe
(E)-4-decenalFL/FR
solvent
1-heptanolFL/FR
spicy
 cinnamyl formateFL/FR
 clove bud oilFL/FR
 cuminaldehydeFL/FR
black currant bud absoluteFL/FR
 eugenolFL/FR
 methyl cinnamateFL/FR
3-phenyl propyl alcoholFL/FR
 pimenta acris leaf oilFL/FR
tropical
alpha-amyl cinnamaldehydeFL/FR
vanilla
 ethyl vanillinFL/FR
 vanilla bean absolute (vanilla planifolia)FL/FR
 vanillyl acetateFL/FR
waxy
isoamyl butyrateFL/FR
 decanolFL/FR
 ethyl laurateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 mimosa absolute franceFL/FR
woody
 amyris wood oilFL/FR
 guaiacwood oilFL/FR
 vetiver oil haitiFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 acornFR
 agrumen aldehydeFR
 algaeFR
 amaryllisFR
 amberFR
 ambrosiaFR
 ash mountain ashFR
 autumnFR
 barkFR
 bluebellFR
 boroniaFR
 boxwoodFR
 boxwood blossomFR
 boxwood berryFR
 calamus oil replacerFR
 carrot seedFL/FR
 castoreumFR
 cedar forestFR
 celeryFR
 chamomileFR
 champacaFR
 chervilFL
 cilantroFL/FR
 clematisFR
 cloverFR
 cognacFR
 corianderFL/FR
 coronillaFR
 cortexFR
 country meadowFR
 currant bud absolute replacerFL/FR
 cypress oil replacerFR
 daffodilFR
 deertongue absolute replacerFR
 earthFR
 erica 
 evergreenFR
 fernFR
 figFR
 fir balsamFR
 fir needle oil replacerFR
 flouveFR
 flouve blossomFR
 foliageFR
 fungusFR
 geraniumFR
 ginger white gingerFR
 grass 
 greenFR
 green grassFR
 hancorniaFR
 hay new mown hayFR
 hazelnutFR
 heatherFR
 herbalFR
 hollyberryFR
 hugoniaFR
 hyacinthFR
 hydrangeaFR
 ivyFR
 jasminFR
 jonquilFR
 kewdaFR
 leaf 
 leatherFR
 liverwort 
 lotusFR
 marjoramFL/FR
 mimosaFR
 narcissusFR
 neroliFR
 ocean seaFR
 opoponaxFR
 orange bitter orange peelFL/FR
 oreganoFR
 orrisFR
 palmarosa oil replacerFR
 pansyFR
 parsley leafFL/FR
 passion blossomFR
 patchouliFR
 pear prickly pearFL
 pine scotch pineFL/FR
 poppyFR
 primroseFR
 privetFR
 privet blossomFR
 resedaFR
 rhubarbFR
 roseFR
 rose geraniumFR
 sandalwoodFR
 seaweed absolute replacerFR
 stem 
 straw 
 teaFL
 tobacco flowerFR
 vine 
 weedy 
 woodruffFR
 wormwood oil replacerFR
 yerba mateFL/FR
 yewFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 coffee
Search  PMC Picture
 hyacinth
Search Trop  Picture
 papaya fruit
Search Trop  Picture
 peppermint leaf
Search Trop  Picture
 peppermint oil
Search Trop  Picture
 ylang ylang oil @ 0.13%
Data  GC  Search Trop  Picture
 ylang ylang oil CO2 extract @ 0.10%
Data  GC  Search 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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