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. Augustus has invested in modern, well equipped laboratories to provide unparalleled control of quality, and a development environment that continues to produce innovative ranges of natural ingredients. The strength of the company is built on both its comprehensive knowledge base, and extensive stocks of raw materials for both fragrance and flavour use. To complement its range of conventional and Organic Essential Oils and Aroma Chemicals, Augustus also offers a steadily increasing range of its own, UK manufactured Natural Extracts, Absolutes, Resinoids and Natural Chemicals. These again are fully tested and certificated, and very tightly quality controlled. Augustus is committed to promoting the use of natural ingredients, wherever the potential lies and to provide an environment of support and trust to both our customers and suppliers.
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      Product(s):
      Dimethyl Hydro Quinone
       
  • 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
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      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
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      Product(s):
      10010 1,4-Dimethoxy benzene
       
  • Berjé
    • Berje 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
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      Voice: 973-748-8980
      Fax: 973-680-9618
      Flavor Ingredients
      Fragrance Ingredients
      Functional Ingredients
      Happening at Berje
      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
      Resources
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      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
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      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
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      Voice: +86-21-32515501 60762991 60762992
      Fax: +86-21-32515502 64204960
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      Product(s):
      A0286 1,4-DIMETHOXYBENZENE, Kosher
       
  • Moellhausen
    • Moellhausen S.P.A.
      THE CHEMISTRY OF EMOTIONS
      Innovation and commitment in the name of excellence.
      After 50 years in business, Moellhausen stands out as one of the world’s leading family-run companies in the industry of flavors and fragrances, raw materials, and specialties. My personal history is inextricably bound to that of the company, and I continue to dedicate all my energy to it along with our partners and collaborators who have supported us thus far with dedication, passion, love, and experience. Continuous investments and a professionalism aimed at achieving the highest levels of performance in service and quality, along with that same dedication, passion, love, and experience, have together enabled us to reach the absolute avant-garde level that characterizes Moellhausen today, recognized worldwide for its modernity, innovation, creativity, and respect for the environment and the safety and rights of those who work with us. As President and CEO of the company for 32 years, I offer a well-deserved thank you to all of our numerous customers, suppliers, employees, and company friends for helping to sustain our unstoppable and honorable growth. And it is with the support of all of our stakeholders that we will confidently continue to pursue our commitment to further advancing the excellence that our industry demands.
      Voice: +39 039.685.6262
      Fax: +39 039.685.6263
      Linkedin
      A network of knowledge to grow together
      Sustainability is at the foundation of a
      Pervasive technology and total control
      Product(s):
      108226 DIMETHYL HYDROQUINONE
       
  • 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. If you’re looking for something even more exclusive our bespoke fragrance design service could be what you’re looking for: we design custom fragrances for individuals, other perfume brands, hotels, corporations and organisations.
      Email: Info
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      Voice: +44 1630 652546
      Mobile+44 7792 580511
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      Product(s):
      Dimethyl Hydroquinone
       
  • 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
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      US Voice: (973) 740-2300
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      Product(s):
      04-48300 DIMETHYLHYDROQUINONE, Kosher
       
  • Sigma-Aldrich
    • Sigma-Aldrich
      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
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      US Fax: 800-368-4661
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      Certified Food Grade Products
      Product(s):
      W238600 1,4-Dimethoxybenzene, 99%, FG
      SDS
       
  • 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
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      Voice: +44 (0) 1284 704076
      Fax: +44 (0) 1284 760819
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      Product(s):
      para-DIMETHOXYBENZENE
       
  • TCI AMERICA
    • TCI AMERICA
      Moving Your Chemistry Forward
      We continuously strive to advance our technology.
      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 60 years of synthesis experience and multi-purpose plants enable TCI to offer more than 27,000 products as well as custom synthesis. TCI established overseas facilities in North America, Europe, China and India to serve customers worldwide.
      Email: Sales
      US Email: Sales
      Email: Global Business
      Voice: +81-3-5640-8878
      Fax: +81-3-5640-8902
      US Voice: 800-423-8616
      US Fax: 888-520-1075
      Tokyo Tel:03-5640-8851
      Tokyo Fax:03-5640-8865
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      Product(s):
      D0629 1.4-Dimethoxybenzene >99.0%(GC)
       
  • Treatt
    • Treatt PLC
      Innovative ingredient solutions
      World-leading innovative ingredient solutions provider for the flavour, fragrance and FMCG industries.
      We offer innovative and trend-setting product concepts for our customers, collaborating with them to create true value for their products.
      Email: Enquiries
      US Email: Enquiries
      Voice: +44 (0) 1284 702500
      Fax: +44 (0) 1284 703809
      US Voice: +1 863 668 9500
      US Fax: +1 863 668 3388
      News
      Product(s):
      Dimethyl Hydroquinone
       
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas
1,4-dimethoxybenzene (Click)
CAS Number: 150-78-7Picture of molecule
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 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
Flavis Number: 04.034 (Old)
DG SANTE 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.
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
 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)
 fennel  fatty  green  
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
Services
Azelis
DIMETH HYDROQUIN CRYSTALS
Services
Beijing Lys Chemicals
1,4-Dimethoxy benzene
Berjé
Dimethyl Hydroquinone
Happening at Berje
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
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
CROP CALENDAR
Keva
DIMETHYL HYDROQUINONE
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
DIMETHYLHYDROQUINONE, Kosher
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
para-DIMETHOXYBENZENE
TCI AMERICA
For experimental / research use only.
1.4-Dimethoxybenzene >99.0%(GC)
Treatt
Dimethyl Hydroquinone
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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
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
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 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
FooDB: FDB000855
Export Tariff Code: 2909.30.6000
Haz-Map: View
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
RSC Learn Chemistry: View
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
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 resinoidFR
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
 benzophenoneFL/FR
 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
(E)-2-nonen-1-olFL/FR
(Z)-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
2-phenyl propionaldehydeFL/FR
3-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
sweet
 vanilla bean absolute (vanilla planifolia)FL/FR
terpenic
 cypress leaf oilFR
D-(+)-beta-pineneFL/FR
alpha-terpineolFL/FR
tonka
 coumarinFR
 tonka bean absoluteFR
vanilla
 ethyl vanillinFL/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
 benzyl methyl etherFL/FR
 chrysanthemum oxideFL/FR
 coumaneFL/FR
para-cresyl caprylateFL/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
 green etherFL/FR
 heptyl cinnamateFL/FR
 hexanal diethyl acetalFL/FR
 hyacinth absoluteFL/FR
 kewda absolute 
 methyl ortho-anisateFL/FR
 phenethyl salicylateFL/FR
2-phenyl propyl acetateFL/FR
(R)-2-phenyl propyl alcoholFL/FR
2-phenyl propyl alcoholFL/FR
3-phenyl propyl formateFL/FR
3-phenyl propyl propionateFL/FR
D-(+)-beta-pineneFL/FR
laevo-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
 indoleFL/FR
aromatic
para-cresyl phenyl acetateFL/FR
 diphenyl methaneFL/FR
 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
(Z)-2-nonen-1-olFL/FR
2-nonen-1-olFL/FR
2-nonenalFL/FR
floral
 citronellolFL/FR
 citronellyl acetateFL/FR
 citronellyl propionateFL/FR
 dimethyl benzyl carbinyl butyrateFL/FR
 diphenyl oxideFL/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
 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
geranium
 benzophenoneFL/FR
green
 acetaldehyde ethyl phenethyl acetalFL/FR
isoamyl isovalerateFL/FR
isoamyl salicylateFL/FR
 cinnamyl alcoholFL/FR
 clary sage absoluteFL/FR
 cucumber distillatesFL
 cuminyl acetaldehydeFL/FR
 dihydromyrcenolFL/FR
2,5-dimethyl-3,6-dihexyl pyrazine 
 geranyl acetateFL/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 dimethyl acetalFL/FR
2-phenyl propionaldehydeFL/FR
3-phenyl propionaldehydeFL/FR
 violet leaf absoluteFL/FR
herbal
 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
 phenyl acetaldehyde diisobutyl acetalFL/FR
medicinal
 dimethyl benzyl carbinolFL/FR
melon
 hydroxycitronellal diethyl acetalFL/FR
minty
 spearmint absoluteFL/FR
naphthyl
para-methyl anisoleFL/FR
oily
 olive oil absoluteFL/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
sweet
 vanilla bean absolute (vanilla planifolia)FL/FR
tropical
alpha-amyl cinnamaldehydeFL/FR
vanilla
 ethyl vanillinFL/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:
 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
Occurrence (nature, food, other): note
 coffee
Search  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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