dextro,laevo-borneol
borneol
 
Notes:
None found
  • Advanced Biotech
    • Advanced Biotech. Inc.
      Inspired by Nature
      A diverse range of products, all meeting our stringent commitment to quality.
      Advanced Biotech is a leading manufacturer and supplier of high-quality Natural flavoring ingredients & botanical extracts for the food/beverage, cosmetic and personal care industries. With over 25 years of experience working with Fermentation processing & botanical extracts, we can help develop new innovative and functional products for today’s competitive marketplace. Our company prides itself in the ability to cater to our customer’s specific needs while maintaining our focus on integrity, honesty and the commitment to high quality product standards. We proudly offer our quality Natural ingredients to companies around the world.
      US Email: Info
      US Email: Quotes and Orders
      US Voice: 973-339-6242
      US Fax: 973-256-4101
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      Vimeo
      Product(s):
      1330 BORNEOL NATURAL 98% min.
      SDS
      1584 BORNEOL CHIRAL NATURAL
      SDS
       
  • 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.
      Email: Enquiries
      Email: Sales
      Email: web site enquiries
      Voice: +44 (0)1420 590555
      Fax: +44 (0)1420 592420
      Services
      Product(s):
      Borneol Crystals
       
  • 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.
      Email: For Information
      Email: For Sales
      Voice: 973-748-8980
      Fax: 973-680-9618
      Instagram
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      Flavor Ingredients
      Fragrance Ingredients
      Functional Ingredients
      Media
      Products List: View
      Product(s):
      Borneol Crystals
       
  • BOC Sciences
    • BOC Sciences
      Best of Chemicals Supplier
      Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
      BOC Sciences provides a wide range of services to support the pharmaceutical industry through all stages of drug discovery including Custom Synthesis of those chemicals that are not in stock, Isotope Labeling Service, Chiral Synthesis and Resolution, Bioconjugation, PEGylation services, analytical services.
      BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies.
      Email: Marketing
      US Email: Marketing
      Email: Sales
      US Email: Sales
      Voice: 1-631-485-4226
      Fax: 1-631-614-7828
      US Voice: 1-631-485-4226
      US Fax: 1-631-614-7828
      Europe44-203-286-1088
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      Product(s):
      507-70-0 dextro,laevo-Borneol
       
  • ECSA Chemicals
    • ECSA Chemicals
      Human Chemistry
      ECSA Chemicals has been active since 1913 in the trading and international commerce of raw materials. With an organisation divided into industrial segments managed by specialists, it has become one of the largest distributors worldwide.
      ECSA Chemicals is the largest Swiss-owned company in terms of warehouses for the distribution of chemical products. We have been distributing chemical products for over 100 years and we have a special interest in protecting the environment and in the safety of our facilities and collaborators.
      Established in 1913 as a small grocery store, in its over 100 years of activity ECSA Chemicals has become one of the most important Swiss-owned distributors of chemical products. The company, which is active in international distribution and trading, is organised into industrial segments that are managed by teams of specialists and experts. They guarantee professional and customised consultancy and services. With our experience, we can rapidly and safely connect you with the best suppliers on the market, providing you with a complete search, consulting and assistance service. The focus of our approach and operations is you, our customers. We strive every day to find the best products that satisfy your needs as quickly as possible. Your satisfaction is our greatest success. WHY CHOOSE ECSA? EXPERIENCE We have been working for 100 years. QUALITY We have obtained many certifications (ISO, SQAS, GDP, Responsible Care, Bio-Inspecta, RSPO, etc.). We guarantee full compliance with the current laws and continuous training for our staff. SAFETY We constantly carry out risk analyses for each infrastructure, defining safety levels and implementing corrective measures promptly wherever they are needed. WIDESPREAD DISTRIBUTION We have warehouses in strategic locations to supply goods to Switzerland and to the rest of the world. STORAGE CAPACITY The 3 ECSA-owned warehouses guarantee considerable storage area and capacity in each warehouse, with full availability of products (base chemicals and speciality chemicals). SPEED Presence all over the country, staff dedicated to sourcing raw materials and considerable storage capacity guarantee that goods are rapidly obtained and supplied. CONSULTANCY Our specialists - in-depth knowledge of the market and products allows us to provide full consulting services, from the purchase to the supply of raw materials.
      Email: Info
      Email: Sales
      Email: Trading
      Email: Maintenance
      Email: Energy
      Voice: +41 91 695 88 00
      Fax: +41 91 695 88 01
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      ECSA TRADE THE MOST UPDATED FINANCIAL PUBLICATION ON THE WORLD OF CHEMISTRY
      Products List: View
      Product(s):
      MP-024444 BORNEOL
       
  • Foreverest Resources
    • Foreverest Resources Ltd.
      Leading pine based chemicals supplier
      Supplying turpentine based and natural/extracted flavor & fragrance ingredients.
      FOREVERESTA® F&F RAW MATERIALS is a range of natural extracts and synthetic aroma chemicals based on the rich material resources and great supply network from China, which was applied for specialty chemicals industry. The markets cover application areas on food, beverage, custom fragrance, fine perfume, personal care, cosmetics, etc.
      Foreverest Resources Ltd. is a materials supplier, exporting gum turpentine based, terpene derivertives and natural/extracted monomers and intermediates from China since 1988. We offers high quality raw materials for flavors and fragrances synthetic manufacturing in the world.
      Email: Info
      Email: Sales
      Voice: +86 (0)592 5105533
      Fax: +86 (0)592 5151667
      foreverest Skype Skype
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      Products List: View
      Product(s):
      Borneol 55%
      Borneol synthetic is produced from alpha pinene.It is a mixture mainly composed of borneol and isoborneol.
       
       
  • Global Essence
    • Global Essence Inc.
      Preferred Partner
      Accommodate each customers unique needs.
      Global Essence was founded in 1993 as a two person operation servicing regional customers in the New York/ New Jersey area. In the twenty years since, it has grown into a multinational operation with offices in the US, UK, and Singapore. These offices allow Global to provide regional support to its customers worldwide. As the world continues become more connected, this approach positions Global to continue to offer the highest quality products and experience to all of its customers.
      Email: Info
      US Email: Info
      Voice: +44 (0) 1279 876666
      Fax: +44 (0)1279 876646
      US Voice: 001 732 677 1100
      US Fax: 001 732 677 1107
      Blog
      Press Release
      News
      Product(s):
      Borneol Crystals / Flakes
       
  • 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
      Linkedin
      Product(s):
      BORNEOL FLAKES
      BORNEOL NATURAL
       
  • M&U International
    • M&U International LLC
      Steady supply & demand
      Meeting customers increasing demands at home as well as abroad.
      M&U dedicates itself to the development and production of new products as well as continuously promoting those new products. We’ve maintained a steady supply&demand relationship with a large number of manufacturers at home and abroad. We’ve developed an extensive network and because of our relationships with these manufacturers, we’re able to provide a stable supply of great quality materials. We’re located in China’s largest communications hub, Shanghai and in the U.S. near one of the largest sea ports on the East Coast. The strategic locations of our facilities ensure convenient, prompt and secure delivery of our products to our customers.
      Email: Sales
      US Email: Sales
      Voice: +86-21-32515501 60762991 60762992
      Fax: +86-21-32515502 64204960
      US Voice: 908-359-9000
      US Fax: 908-359-9002
      News
      Product(s):
      A0011 Borneol Flakes, Kosher
       
  • Moellhausen
  • Penta International
    • Penta International Corporation
      Chemistry innovation
      At Penta, our products and services help businesses do business better.
      For over 30 years, Penta Manufacturing Company has played a growing role in worldwide chemistry innovations and applications. As an industry leader, Penta continues to pioneer chemistry-based solutions for practically every area of commerce. Our products and expertise have helped fuel technical advances in dozens of commercial applications including flavoring, coloring, fragrances and chemical processes.
      US Email: Technical Services
      US Email: Sales
      US Voice: (973) 740-2300
      US Fax: (973) 740-1839
      Product(s):
      02-35402 DL-BORNEOL
      02-35401 DL-BORNEOL MIXED ISOMER
       
  • PerfumersWorld
    • PerfumersWorld Ltd.
      feeeel... the smell!
      The one-stop resource for the creative perfumer.
      No minimum orders. Aroma chemicals, essential oils, isolates, pheremones, absolutes, resinoids, FleuressenceTM key bases, PWx FactorTM, solubilizers, kits, creation systems, workshops, training, distance learning, The PerfumersWorld Perfumer's Studio, The Perfumer’s Formulation Bulletin, perfumery software, bespoke creation, analysis, consultancy, project counselling, trouble-shooting, unperfumed product bases, bottles, smelling strips, scales, distillation, equipment and inspiration!
      Email: Enquiries
      Email: Sales
      Voice: +66(0)2-99-800-80
      Fax: +66(0)2-99-800-80
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      Software: Perfumer's Workbook
      Product(s):
      1BW00064 Borneol
       
  • Prodasynth
    • Prodasynth
      PRODUCTEUR PAR ESSENCE
      Chemical specialist in manufacturing, distributing and sourcing of tailor-made ingredients for the Flavour & Fragrance industry.
      Today we are also proud to say, we have created an important range of Natural Molecules which can be found in our Raw Material Compendium. The versatility of our small but efficient structure is one of our main strengths when trying to fulfill our clients' requirements.
      Email: Info:
      Email: Sales Team Prodasynth
      Voice: (33) 4 93 09 00 11
      Fax: (33) 4 22 13 07 38
      New Catalog
      Products List: View
      Product(s):
      BORNEOL 65% (60-65%; ISOBORNEOL 30-40%)
       
  • TCI AMERICA
    • TCI AMERICA
      Moving Your Chemistry Forward
      We continuously strive to advance our technology.
      With East & West Coast distribution centers, count on TCI to deliver products quickly and reliably. Over 30,000 Reagents available today in benchtop to bulk quantities. We also offer custom synthesis solutions. Sign up for a TCI account today for fast and free shipping!
      Tokyo Chemical Industry Co., Ltd. (TCI) is a leading worldwide manufacturer of specialty organic chemicals founded in 1946. TCI provides organic laboratory chemicals as well as pharmaceutical, cosmetic and functional materials. More than 70 years of synthesis experience and multi-purpose plants enable TCI to offer more than 30,000 products as well as custom synthesis.
      US Email: Sales
      Email: Technical Support
      Voice: 1-800-423-8616
      Fax: 1- 888-520-1075
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      Product(s):
      B0525 Borneol >70.0%(GC) (contains ca. 20% Isoborneol)
       
  • The John D. Walsh Company
    • The John D. Walsh Company, Inc
      Suppliers Since 1942
      Supplying the fragrance and flavor industry with high quality products.
      The John D. Walsh Company, Inc. has evolved from its beginnings as an agent/broker into a distributor of essential oils, aroma chemicals, concretes and absolutes. We currently represent the following companies, as their North American distributor: Destilerias Munoz Galvez, S.A. International Flavors & Fragrances PFW Aroma Chemicals B.V. Innospec Widnes Limited Hydrodiffusion de Guatemala, S. A. DSM Nutritional Products The John D. Walsh Company, Inc. is proud to be a founding member of IFEAT, an active member of IFRA, North America, and a corporate sponsor of the WFFC.
      Email: Information
      Email: Sales
      Email: Firmenich Flavor inquiries
      Voice: 973-962-1400
      Fax: 973-962-1557
      Firmenich Flavor Phone:973-962-1888
      Firmenich Flavor Fax:973-962-1898
      History
      Product(s):
      Borneol Crystals
       
  • The Lermond Company
    • The Lermond Company
      Your Sourcing Resource
      The Lermond family has been sourcing raw materials for the flavor and fragrance industry for nearly 7 decades.
      The Lermond Company is a women-owned distributor of raw materials primarily servicing the flavor and fragrance industry. For three generations, members of the Lermond family have been integral sourcing partners for the North American flavor and fragrance industry. We supply high quality essential oils, aroma chemicals, absolutes, concretes, resinoids and floral waters from around the world to the global industry.
      Email: Info
      Email: Tara
      Email: Erica
      Voice: 201-896-3300
      Fax: 201-623-2910
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      Product(s):
      14105 BORNEOL 60/40
       
  • Ernesto Ventós
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas
CAS Number: 507-70-0Picture of molecule3D/inchi
Other(deleted CASRN): 6627-72-1
ECHA EINECS - REACH Pre-Reg: 208-080-0
FDA UNII: M89NIB437X
Nikkaji Web: J9.305J
Beilstein Number: 2038056
MDL: MFCD00066426
CoE Number: 64
XlogP3: 2.70 (est)
Molecular Weight: 154.25266000
Formula: C10 H18 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome, Edge or firefox)
EFSA/JECFA Comments: Racemate (±) = DL-Borneol (EFFA, 2010a). CASrn refers to (1R,2S,4R)-rel. Register name to be changed to DL-Borneol (EFFA, 2011m). According to JECFA "Min. Assay value may incl. Isoborneol, other isomers of borneol, trace amounts of fenchyl alcohol & other C10H18O compounds".
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: 1385  borneol
DG SANTE Food Flavourings: 02.016  borneol
FDA Mainterm (SATF):507-70-0 ; BORNEOL
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 powder (est)
Assay: 97.00 to 100.00 % 
Food Chemicals Codex Listed: No
Melting Point: 202.00 to  208.00 °C. @ 760.00 mm Hg
Boiling Point: 212.00 to  213.00 °C. @ 760.00 mm Hg
Boiling Point: 135.00 to  136.00 °C. @ 50.00 mm Hg
Vapor Pressure: 0.035000 mmHg @ 25.00 °C.
Flash Point: 150.00 °F. TCC ( 65.56 °C. )
logP (o/w): 2.690
Soluble in:
 alcohol
 water, 738 mg/L @ 25 °C (exp)
Insoluble in:
 water
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: balsamic
 
 pine  woody  camphoreous  balsamic  
Odor Description:
at 10.00 % in dipropylene glycol. 
pine woody camphor balsamic
 
Odor and/or flavor descriptions from others (if found).
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: fragrance
perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
Advanced Biotech
BORNEOL CHIRAL NATURAL
Advanced Biotech
BORNEOL NATURAL
98% min.
Odor: Bornyl Alcohol, Camphor
Alfa Biotechnology
For experimental / research use only.
Borneol 90%
Augustus Oils
Borneol Crystals
Services
Berjé
Borneol Crystals
Media
BOC Sciences
For experimental / research use only.
dextro,laevo-Borneol
Diffusions Aromatiques
BORNEOL CRISTALLISE
ECSA Chemicals
BORNEOL
ECSA TRADE THE MOST UPDATED FINANCIAL PUBLICATION ON THE WORLD OF CHEMISTRY
Ernesto Ventós
BORNEOL 100%
Odor: DRY WOODY, SLIGHTLY CAMPHORACEOUS
Ernesto Ventós
BORNEOL 65%
Foreverest Resources
Borneol 55%
Odor: herbal
Use: Borneol synthetic is produced from alpha pinene.It is a mixture mainly composed of borneol and isoborneol.
Fuzhou Farwell
Borneol Flakes
Global Essence
Borneol Crystals / Flakes
Indenta Group
Borneol flakes
Indukern F&F
BORNEOL 60/40
Odor: CAMPHORATED, FRESH, MENTHOLATED
John Kellys (London)
Borneol Flakes
K.L. Koh Enterprise
BORNEOL
Lluch Essence
BORNEOL FLAKES
Odor: CAMPHORACEOUS, FRESH, MINTY
Lluch Essence
BORNEOL NATURAL
M&U International
Borneol Flakes, Kosher
Moellhausen
BORNEOL
Odor: camphoraceous, fresh, conifers, menthol
Flavor: fresh, menthol
Nippon Terpene Chemicals
n-Borneol
Penta International
DL-BORNEOL MIXED ISOMER
Penta International
DL-BORNEOL
PerfumersWorld
Borneol
Odor: fresh cool camphoraceous minty coniferous Natural : fresh cool herb camphor coniferous sassafras borneol
Phoenix Aromas & Essential Oils
Borneol Flakes
Prodasynth
BORNEOL 65%
(60-65%; ISOBORNEOL 30-40%)
Odor: CHARACTERISTIC, DRY, CAMPHORACEOUS
Reincke & Fichtner
Borneol
Santa Cruz Biotechnology
For experimental / research use only.
Borneol ≥70%
Sigma-Aldrich: Sigma
For experimental / research use only.
Borneol ∼75%
TCI AMERICA
For experimental / research use only.
Borneol >70.0%(GC) (contains ca. 20% Isoborneol)
The John D. Walsh Company
Borneol Crystals
The Lermond Company
BORNEOL 60/40
Vistachem
Borneol
Synonyms   Articles   Notes   Search   Top
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
R 22 - Harmful if swallowed.
S 02 - Keep out of the reach of children.
S 20/21 - When using do not eat, drink or smoke.
S 22 - Do not breath dust.
S 36/37/39 - Wear suitable clothing, gloves and eye/face protection.
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-rat LD50  500 mg/kg
French Demande Patent Document. Vol. #2448856

oral-mouse LD50  1059 mg/kg
Shika Gakuho. Journal of Dentistry. Vol. 75, Pg. 934, 1975.

oral-rabbit LDLo  2000 mg/kg
Reviews of Environmental Contamination and Toxicology. Vol. 113, Pg. 47, 1990.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: flavor and fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for dextro,laevo-borneol usage levels up to:
  3.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 130.00 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 23.00 (μg/capita/day)
Threshold of Concern:1800 (μg/person/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: -5.10000
beverages(nonalcoholic): 0.250001.40000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: -0.30000
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -1.40000
fruit ices: -1.40000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: -3.70000
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:
Flavor & Extract Manufacturers Association (FEMA) reference(s):
The FEMA GRAS assessment of alicyclic substances used as flavor ingredients. View pdf
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):
Flavouring Group Evaluation 47, (FGE.47)[1] - Bicyclic secondary alcohols, ketones and related esters from chemical group 8 - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf
Flavouring Group Evaluation 87, (FGE.87)[1] - Consideration of bicyclic secondary alcohols, ketones and related esters evaluated by JECFA (63rd meeting) structurally related to bicyclic secondary alcohols, ketones and related esters evaluated by EFSA in FGE.47 (2008) - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf
Flavouring Group Evaluation 43: Thujyl alcohol from chemical group 8
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 87 Revision 1 (FGE.87Rev1): Consideration of bicyclic secondary alcohols, ketones and related esters evaluated by JECFA (63rd meeting) structurally related to bicyclic secondary alcohols, ketones and related esters evaluated by EFSA in FGE.47 (2008)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 87, Revision 2 (FGE.87Rev2): Consideration of bicyclic secondary alcohols, ketones and related esters evaluated by JECFA (63rd meeting) structurally related to bicyclic secondary alcohols, ketones and related esters evaluated by EFSA in FGE.47Rev1 (2008)
View page or View pdf
Safety and efficacy of secondary alicyclic saturated and unsaturated alcohols, ketones, ketals and esters with ketals containing alicyclic alcohols or ketones and esters containing secondary alicyclic alcohols from chemical group 8 when used as flavourings for all animal species
View page or View pdf
EPI System: View
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 507-70-0
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 6552009
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 1312
WGK Germany: 3
 (1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
Chemidplus: 0000507700
EPA/NOAA CAMEO: hazardous materials
RTECS: ED7000000 for cas# 507-70-0
Synonyms   Articles   Notes   Search   Top
References:
Leffingwell: Chirality or Article
 (1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 507-70-0
Pubchem (cid): 6552009
Pubchem (sid): 134976836
Flavornet: 507-70-0
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
CHEBI: View
CHEMBL: View
KEGG (GenomeNet): C01411
HMDB (The Human Metabolome Database): HMDB34976
Export Tariff Code: 2906.19.5000
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
Formulations/Preparations:
grades: technical.
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
aldehydic
 dodecanal (aldehyde C-12 lauric)FL/FR
2-methyl undecanal (aldehyde C-12 mna)FL/FR
amber
 ambrette seed oilFL/FR
 angelica root oilFL/FR
 cistus ladaniferus resinoidFL/FR
balsamic
 abies alba cone oilFR
 abies alba leaf extractFR
 abies alba needle oilFL/FR
 amyris wood oilFL/FR
siam benzoin resinoidFL/FR
 benzyl salicylateFL/FR
dextro,laevo-isoborneolFL/FR
laevo-borneolFL/FR
 bornyl acetateFL/FR
isobornyl acetateFL/FR
isobornyl methyl etherFL/FR
dextro-fenchoneFL/FR
 fir balsam absoluteFR
 fir balsam fragranceFR
 myrrh oilFL/FR
camphoreous
 bornyl ethyl ether 
2,6-dimethyl-3-oxatricyclo(4.2.1.0*2,4*)nonaneFR
 fencholFL/FR
laevo-fenchoneFL/FR
chocolate
1,3,3,4,5,6-hexamethyl(2.2.2)bicyclooct-5-en-2-ol 
earthy
(-)-alpha-fencholFL/FR
scotch pine needle oilFL/FR
scotch pine needle oil estoniaFL/FR
scotch pine needle oil yugoslaviaFL/FR
floral
 acetophenoneFL/FR
alpha-amyl cinnamaldehydeFL/FR
 bois de rose oil peruFL/FR
 dimethyl benzyl carbinolFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 ho leaf oilFR
 lavender absolute replacerFR
 lavender oilFL/FR
 lavender oil replacerFR
fruity
3-allyl oxy-1,4-dimethyl bicyclo(3.2.1)octaneFR
1,3,3,5-tetramethyl-7 and 8-acetyl bicyclo(2.2.2)oct-5-ene 
herbal
1-allyl-2,2,7,7-tetramethyl cycloheptanolFR
 anthemis nobilis flower oil romanFL/FR
 daucus carota fruit oilFL/FR
 dimethyl cyclormol (IFF)FR
 geranic oxideFL/FR
 herbal dioxaneFR
 herbal specialtyFR
 lavender absolute franceFL/FR
 lavender fragranceFR
 lavender specialtyFR
 methyl cyclogeranate (Firmenich)FR
 myrtenolFL/FR
 nopyl acetateFR
 origanum oilFL/FR
 origanum oil greeceFL/FR
alpha-pineneFL/FR
 pinocarveolFL/FR
 rosemary absoluteFL/FR
 rosemary oilFL/FR
 rosemary oil africaFL/FR
 rosemary oil moroccoFL/FR
 rosemary oil replacerFR
 rosemary oil spainFL/FR
 rosemary oil tunisiaFL/FR
 terpineols (unspec.) (mixed isomers)FL/FR
honey
 methyl phenyl acetateFL/FR
 peppermint cyclohexanoneFL/FR
minty
 peppermint oil idahoFL/FR
5- and 6-isopropyl-1,3,3-trimethyl bicyclo(2.2.2)-5,7-octadien-2-one 
mossy
 veramoss (IFF)FR
pine
 cypress oil replacerFR
 evergreen fragranceFR
white pine bark oilFL/FR
powdery
para-anisyl alcoholFL/FR
spicy
 ayou wood oilFR
 cassia bark oil chinaFL/FR
 clove bud oilFL/FR
black currant bud absoluteFL/FR
 ginger fragranceFR
 ginger root oil chinaFL/FR
 ginger root oil replacerFR
 ginger specialtyFR
 outdoors specialtyFR
 pimenta acris leaf oilFL/FR
white sassafras oilFL/FR
terpenic
 frankincense oilFL/FR
 juniperus communis fruit oilFL/FR
D-(+)-beta-pineneFL/FR
thujonic
 armoise oilFR
 cedarleaf oil terpenelessFR
tonka
 tonka bean absoluteFR
vanilla
 vanillinFL/FR
waxy
 ethyl laurateFL/FR
woody
2-tert-butyl cyclohexanoneFR
atlas cedarwood oilFR
 cedarwood oil port orfordFR
 cistus twig/leaf oilFL/FR
3,7-dimethyl-1-octene 
(E+Z)-4,8-dimethyl-3,7-nonadien-2-olFL/FR
 gurjun balsam oilFR
1,2,3,3,4,5,6-heptamethyl bicyclo(2.2.2)oct-5-en-2-ol 
1,3,3,4,5,6-hexamethyl bicyclo(2.2.2)oct-5-en-2-one 
 hinoki root oilFR
 juniper berry oil terpenesFR
para-menth-3-en-1-olFL/FR
6-methoxy-1,6,7-trimethyl octahydro-4,7-methanoindene + 5-methoxy-2,4,5-trimethyl octahydro-4,7-methan 
 methyl cedryl ketoneFL/FR
 myoporum crassifolium wood oilFR
(-)-myrtenol 
 myrtenyl formateFL/FR
 myrtenyl isobutyrate 
 nopyl aldehydeFR
 patchouli ethanoneFR
 patchouli oilFL/FR
cis-2-pinanolFR
 santallFR
1,3,3,5-tetramethyl-7 and 8-cyanobicyclo(2.2.2)oct-5-ene 
 thuja occidentalis leaf oilFL/FR
 woody acetateFR
 
For Flavor
 
No flavor group found for these
isobornyl methyl etherFL/FR
 cistus ladaniferus resinoidFL/FR
3,7-dimethyl-1-octene 
(E+Z)-4,8-dimethyl-3,7-nonadien-2-olFL/FR
1,2,3,3,4,5,6-heptamethyl bicyclo(2.2.2)oct-5-en-2-ol 
1,3,3,4,5,6-hexamethyl bicyclo(2.2.2)oct-5-en-2-one 
1,3,3,4,5,6-hexamethyl(2.2.2)bicyclooct-5-en-2-ol 
para-menth-3-en-1-olFL/FR
6-methoxy-1,6,7-trimethyl octahydro-4,7-methanoindene + 5-methoxy-2,4,5-trimethyl octahydro-4,7-methan 
 myrtenyl formateFL/FR
 myrtenyl isobutyrate 
white pine bark oilFL/FR
scotch pine needle oilFL/FR
scotch pine needle oil estoniaFL/FR
scotch pine needle oil yugoslaviaFL/FR
D-(+)-beta-pineneFL/FR
5- and 6-isopropyl-1,3,3-trimethyl bicyclo(2.2.2)-5,7-octadien-2-one 
white sassafras oilFL/FR
 terpineols (unspec.) (mixed isomers)FL/FR
1,3,3,5-tetramethyl-7 and 8-acetyl bicyclo(2.2.2)oct-5-ene 
1,3,3,5-tetramethyl-7 and 8-cyanobicyclo(2.2.2)oct-5-ene 
amber
 ambrette seed oilFL/FR
balsamic
siam benzoin resinoidFL/FR
 benzyl salicylateFL/FR
 myrrh oilFL/FR
camphoreous
dextro,laevo-isoborneolFL/FR
laevo-borneolFL/FR
 bornyl acetateFL/FR
 bornyl ethyl ether 
(-)-alpha-fencholFL/FR
 fencholFL/FR
laevo-fenchoneFL/FR
 geranic oxideFL/FR
 pinocarveolFL/FR
 rosemary oil tunisiaFL/FR
cooling
dextro-fenchoneFL/FR
isomentholFL
floral
 bois de rose oil peruFL/FR
 methyl phenyl acetateFL/FR
fruity
para-anisyl alcoholFL/FR
green
 angelica root oilFL/FR
herbal
 anthemis nobilis flower oil romanFL/FR
 daucus carota fruit oilFL/FR
 lavender absolute franceFL/FR
 lavender oilFL/FR
 origanum oilFL/FR
 origanum oil greeceFL/FR
 rosemary absoluteFL/FR
 rosemary oilFL/FR
 rosemary oil africaFL/FR
 rosemary oil moroccoFL/FR
 rosemary oil spainFL/FR
medicinal
 dimethyl benzyl carbinolFL/FR
mentholic
 peppermint cyclohexanoneFL/FR
minty
(-)-myrtenol 
 myrtenolFL/FR
 peppermint oil idahoFL/FR
powdery
 acetophenoneFL/FR
soapy
 dodecanal (aldehyde C-12 lauric)FL/FR
spicy
 cassia bark oil chinaFL/FR
 clove bud oilFL/FR
black currant bud absoluteFL/FR
 ginger root oil chinaFL/FR
white pepper oleoresinFL
 pimenta acris leaf oilFL/FR
terpenic
 abies alba needle oilFL/FR
 juniperus communis fruit oilFL/FR
para-menthatrieneFL
tropical
alpha-amyl cinnamaldehydeFL/FR
vanilla
 vanillinFL/FR
waxy
 ethyl laurateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
2-methyl undecanal (aldehyde C-12 mna)FL/FR
woody
 amyris wood oilFL/FR
isobornyl acetateFL/FR
 cistus twig/leaf oilFL/FR
 frankincense oilFL/FR
 methyl cedryl ketoneFL/FR
 patchouli oilFL/FR
alpha-pineneFL/FR
 thuja occidentalis leaf oilFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 agateFR
 balsamFR
 bayberryFR
 bouquetFR
 cardamom oil replacerFR
 carrotFL
 castoreumFR
 cedarFR
 cedar forestFR
 cedarwoodFR
 christmasFR
 cinnamonFR
 citronellaFR
 corianderFL/FR
 earthFR
 fir 
 fir balsamFR
 fir needle oil replacerFR
 frankincenseFR
 geraniumFR
 gingerFR
 herbalFR
 hollyberryFR
 juniper berryFR
 lavandinFR
 lavenderFR
 lavender spike lavenderFL/FR
 maceFR
 mossFR
 myrrhFR
 nutmegFR
 peppermintFR
 pineFR
 sageFR
 spiceFR
 spruceFR
 sweet grassFR
 woodyFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 achillea tenuifolia lam. flower oil iran @ 0.50%
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 alpinia galanga oil @ trace%
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 angelica root oil @ 0.19%
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 anise seed oil star china @ 0.04%
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 armoise oil morocco @ 0.7%
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 artemisia deserti krasch. oil iran @ 0.50%
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 artemisia diffusa krasch. ex poljak oil iran @ 0.50%
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 artemisia gypsacea krasch. oil iran @ 2.60%
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 ayou wood oil @ 2.80%
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 basil absolute sweet @ 0.20%
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 calamus leaf oil @ 0.11%
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 calamus rhizome oil @ 0.11%
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 calamus root oil @ 0.04%
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 carrot seed oil spain @ trace-0.35%
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 cascarilla bark oil @ 0.94%
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 castoreum
Search  PMC Picture
 chamomile oil @ 0.20%
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 chamomile oil morocco @ 1.00%
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 champaca concrete @ 0.10%
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 cinnamon fruit oil india @ 0.3-0.4%
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 cistus oil @ 2.0%
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 citronella oil ceylon @ 5.23%
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 citronella oil china @ 0.06%
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 citronella oil java @ 0.05%
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 citronella oil zimbabwe @ 0.90%
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 clary sage oil spain @ 0.12%
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 coriander seed oil @ 0.30%
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 coriander seed oil CO2 extract @ 0.07%
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 coriander seed oil cuba @ 1.55%
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 croton cajucara benth. leaf oil brazil @ trace%
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 croton flavens l. (welensali) leaf oil curacao @ 1.20%
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 curcuma amada roxb. rhizome oil india @ 1.30%
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 cypress cone oil egypt @ 0.3%
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 cypress oil @ trace%
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 davana oil @ 0.5%
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 erigeron graveolens l. oil iran @ 60.70%
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 eucalyptus camaldulensis dehn. leaf oil jerusalem @ 3.80%
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 eucalyptus globulus bicostata oil @ 0.09%
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 eucalyptus globulus oil @ 0.06%
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 eucalyptus globulus oil burundia @ 0.20%
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 eucalyptus globulus oil pakistan @ 0.20%
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 eucalyptus globulus pseudoglobulus oil @ 0.07%
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 featherfew leaf oil @ 0.60%
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 feverfew leaf oil belgium @ 1.0%
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 fir needle oil canada @ 0.31-2.07%
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 fir needle oil siberia @ 1.66%
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 geranium rose-scented oil (pelargonium spp.) cuba @ 0.10%
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 ginger root oil brazil @ 0.70%
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 ginger root oil china @ 0.48%
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 ginger root oil CO2 extract @ 0.60%
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 ginger root oil CO2 extract australia @ 0.60%
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 glycosmis pentaphylla (cor.) seed oil india @ 0.40%
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 guava fruit headspace reunion @ 0.50%
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 hinoki leaf oil @ 1.23%
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 hinoki root oil @ 0.54%
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 hinoki wood oil @ 0.33%
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 ho leaf oil @ 0.16%
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 hypericum dogonbadanicum assadi oil iran @ 0.70%
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 kachur oil @ 4.90%
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 kewda oil @ 0.17-0.20%
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 labdanum leaf oil @ 0.80%
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 labdanum oil @ 1.45%
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 laurel leaf oil turkey @ 0.30%
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 lavandin absolute grosso @ 1.50%
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 lavandin oil abrialis @ 3.65%
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 lavandin oil china @ 0.89%
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 lavandin oil grosso @ 2.89%
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 lavandin water (lavandula hydrida) @ 1.35%
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 lavandula officinalis flower oil @ 1.60%
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 lavender oil @ 1.85%
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 lavender oil CO2 extract france @ 2.30%
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 lavender oil spike @ 2.50%
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 lavender oil spike france @ 1.69%
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 lavender oil spike spain @ 1.13%
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 lavender spike water @ 2.26%
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 lavender water bulgaria @ 2.20%
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 layana oil kenya @ 5.09%
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 layana oil wild zimbabwe @ 0.60-3.40%
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 layana oil zimbabwe @ 2.8%
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 lemon oil california @ 0.01%
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 lemongrass oil @ 0.05%
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 lime oil CO2 extract mexico @ 3.25%
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 lime oil distilled peru @ 0.82%
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 lime oil expressed florida @ trace%
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 lippia aff. gracillis h.b.k. leaf oil brazil @ 0.50%
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 mace oil east india @ 0.16%
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 mangrove bark red oil cuba @ trace%
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 marjoram oil @ 0.52%
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 marjoram oil spain @ trace%
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 marjoram oil sweet turkey @ 0.00-0.64%
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 mastic fruit oil @ 1.44%
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 mastic leaf oil @ 0.10%
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 mastic oil @ 0.12%
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 myrtle lemon scented leaf oil australia @ 0.10%
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 nutmeg extract CO2 west indian @ trace%
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 nutmeg flower oil @ 0.14%
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 nutmeg leaf oil @ 0.00-0.09%
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 nutmeg oil india @ 0.25%
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 oregano oil mexico @ 0.09%
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 origanum oil greece @ trace%
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 peppermint oil mongolia @ 0.05%
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 petitgrain bergamot oil @ 0.02%
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 phoebe oil brazil @ 0.01%
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 pine needle oil scotch siberia @ 0.4-0.7%
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 pinus sylvestris l. needle oil estonia @ 0.30%
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 pinus sylvestris l. needle oil yugoslavia @ 0.10%
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 ravintsara leaf oil @ 0.21%%
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 rosemary oil china @ 1.71%
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 rosemary oil CO2 extract @ 15.56%
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 rosemary oil corsica @ 3.20%
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 rosemary oil egypt @ 1.69%
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 rosemary oil france @ 3.24-6.53%
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 rosemary oil morocco @ 3.00-4.51%
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 rosemary oil spain @ 9.0%
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 rosemary oil turkey @ 17.50%
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 sage oil albania @ 8.70%
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 sage oil cuba @ 3.81%
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 sage oil dalmatian @ 1.20%
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 sage oil dalmatian @ 2.95%
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 sage oil dalmatian @ 8.40%
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 sage oil england @ 4.10%
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 sage oil germany @ 3.12%
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 sage oil hydrodistillation france @ 1.90%
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 sage oil lithuania @ 2.04%
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 sage oil sardinia @ 3.00%
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 sage oil spain @ 0.8%
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 sage oil spain @ 1.5-6.4%
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 sage oil spain @ 2.10%
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 salvia lavandulifolia vahl. leaf oil @ 1.50%
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 salvia lavandulifolia vahl. leaf oil spain @ 2.20%
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 salvia officinalis oil cuba @ 3.81%
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 salvia officinalis oil reunion @ 1.87%
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 salvia officinalis seed oil tunisia @ 3.54%
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 salvia plebeia oil @ 0.55%
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 salvia sclarea oil @ 0.64%
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 santolina oil @ 4.78%
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 savory oil winter @ 1.60%
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 savory oleoresin winter @ 1.60%
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 snake root oil canada @ 0.10%
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 tanacetum annum l. oil marocco @ 2.70%
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 tansy flower oil canada @ 12.49%
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 tansy oil marocco @ 2.10%
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 thyme oil portuguese @ 1.0%
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 thyme oil red CO2 extract @ 0.02%
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 thyme oil red spain @ 0.44-0.45%
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 thyme oil spain @ 1.63%
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 thyme oil spain @ 4.06%
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 thyme oil wild or creeping finland @ 0.20%
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 thyme oil wild or creeping pakistan @ 3.13%
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 thymus richardii pers. subsp. nitidus (guss.) jalas oil italy @ trace%
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 turmeric oil china @ 0.02%
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 turmeric root oil CO2 extract @ 1.08%
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 valerian root oil @ 0.1-0.6%
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 valerian root oil CO2 extract china @ 0.47%
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 wormwood oil annus france @ 0.00-0.16%
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 wormwood oil italy @ trace%
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 yarrow oil @ 2.50%
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 yarrow oil hungary @ 0.30%
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 zingiber officinale root oil china @ 0.20%
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 zingiber zerumbet (l.) sm. root oil india @ 4.90%
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Synonyms   Articles   Notes   Search   Top
Synonyms:
 bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, (1R,2S,4R)-rel-
 bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, (1R,2S,4R)-
 borneol
(1R,2S,4R)-borneol
dextro,laevo-borneol
DL-borneol
N-borneol
 borneol 60/40
 borneol crystals
 borneol flakes
 borneol natural
bhimsaim camphor
borneo camphor
dextro,laevo-1,7,7-trimethyl bicyclo(2.2.1)heptan-2-ol
DL-1,7,7-trimethyl bicyclo(2.2.1)heptan-2-ol
(1R-endo)-1,7,7-trimethylbicyclo(2.2.1)heptan-2-ol
(1R,2S,4R)-rel-1,7,7-trimethylbicyclo(2.2.1)heptan-2-ol
(1R-endo)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
(1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: Phytochemical study of Cistus libanotis L.
PubMed: Synergistic apoptosis-inducing effects on A375 human melanoma cells of natural borneol and curcumin.
PubMed: Assessment of antioxidative, chelating, and DNA-protective effects of selected essential oil components (eugenol, carvacrol, thymol, borneol, eucalyptol) of plants and intact Rosmarinus officinalis oil.
PubMed: Phytochemical and physical-chemical analysis of Polish willow (Salix spp.) honey: identification of the marker compounds.
PubMed: Mechanical, rheological and release behaviors of a poloxamer 407/ poloxamer 188/carbopol 940 thermosensitive composite hydrogel.
PubMed: Natural borneol, a monoterpenoid compound, potentiates selenocystine-induced apoptosis in human hepatocellular carcinoma cells by enhancement of cellular uptake and activation of ROS-mediated DNA damage.
PubMed: Identification of 1,8-cineole, borneol, camphor, and thujone as anti-inflammatory compounds in a Salvia officinalis L. infusion using human gingival fibroblasts.
PubMed: Chemical composition and anticancer activity of essential oils of Mediterranean sage (Salvia officinalis L.) grown in different environmental conditions.
PubMed: Chemical composition, antimicrobial, cytotoxic and antioxidant activities of the essential oil of Artemisia indica Willd.
PubMed: Synergistic combinations of high hydrostatic pressure and essential oils or their constituents and their use in preservation of fruit juices.
PubMed: Borneol alleviates oxidative stress via upregulation of Nrf2 and Bcl-2 in SH-SY5Y cells.
PubMed: Volatiles of Chrysanthemum zawadskii var. latilobum K.
PubMed: Inhibition of morphine glucuronidation in the liver microsomes of rats and humans by monoterpenoid alcohols.
PubMed: Synthesis, acute toxicity and anti-inflammatory effect of bornyl salicylate, a salicylic acid derivative.
PubMed: Preparation of natural borneol/2-hydroxypropyl-β-cyclodextrin inclusion complex and its effect on the absorption of tetramethylpyrazine phosphate in mouse.
PubMed: Velamo do campo: its volatile constituents, secretory elements, and biological activity.
PubMed: Formation of β-cyclodextrin inclusion enhances the stability and aqueous solubility of natural borneol.
PubMed: Antimicrobial Activity and Chemical Composition of Essential Oil From the Seeds of Artemisia aucheri Boiss.
PubMed: Selective extraction of oxygenated compounds from oregano with sub-critical water.
PubMed: Antibacterial activity and GC/MS analysis of the essential oils from flower, leaf and stem of Origanum vulgare ssp. viride growing wild in north-west Iran.
PubMed: Chemical composition and antimicrobial activity of Satureja kitaibelii essential oil against pathogenic microbial strains.
PubMed: Development of quality assessment method for optically active food flavor chemicals.
PubMed: Chemical composition and larvicidal effects of essential oil of Blumea martiniana against Anopheles anthropophagus.
PubMed: Chemical composition and antimicrobial activity of essential oils of Thymus algeriensis, Eucalyptus globulus and Rosmarinus officinalis from Morocco.
PubMed: Chemical composition and larvicidal activity of Blumea densiflora essential oils against Anopheles anthropophagus: a malarial vector mosquito.
PubMed: Essential oil composition and antioxidant and antimicrobial properties of the aerial parts of Salvia eremophila Boiss. from Iran.
PubMed: Chemical composition of hydrodistilled essential oil of Artemisia incana (L.) Druce and antimicrobial activity against foodborne microorganisms.
PubMed: Chemical composition and antimicrobial and antioxidant activities of Mentha (longifolia L. and viridis) essential oils.
PubMed: Investigation of anti-oxidative, cytotoxic, DNA-damaging and DNA-protective effects of plant volatiles eugenol and borneol in human-derived HepG2, Caco-2 and VH10 cell lines.
PubMed: Antimicrobial activity of the essential oil obtained from roots and chemical composition of the volatile constituents from the roots, stems, and leaves of Ballota nigra from Serbia.
PubMed: Chemical composition, antibacterial and antioxidant activities of leaf essential oil and extracts of Metasequioa glyptostroboides Miki ex Hu.
PubMed: Chemical and biomolecular characterization of Artemisia umbelliformis Lam., an important ingredient of the alpine liqueur "Genepi".
PubMed: Effects of borneol on the level of DNA damage induced in primary rat hepatocytes and testicular cells by hydrogen peroxide.
PubMed: Influence of borneol on primary mice oral fibroblasts: a penetration enhancer may be used in oral submucous fibrosis.
PubMed: Fragrance material review on l-borneol.
PubMed: Fragrance material review on borneol.
PubMed: The monoterpenoids citral and geraniol are moderate inhibitors of CYP2B6 hydroxylase activity.
PubMed: Tunisian Salvia officinalis L. and Schinus molle L. essential oils: their chemical compositions and their preservative effects against Salmonella inoculated in minced beef meat.
PubMed: Inhibition of 7,12-dimethylbenz[a]anthracene induced mouse skin carcinogenesis by Artemisia capillaris.
PubMed: Screening of antibacterial activities of twenty-one oxygenated monoterpenes.
PubMed: Bismuth subgallate/borneol (suile) is superior to bacitracin in the human forearm biopsy model for acute wound healing.
PubMed: Chemical composition and antifungal activity of Salvia macrochlamys and Salvia recognita essential oils.
PubMed: Composition, enantiomeric distribution, and antibacterial activity of the essential oil of Achillea ligustica All. from Corsica.
PubMed: Supercritical carbon dioxide extraction of compounds with antimicrobial activity from Origanum vulgare L.: determination of optimal extraction parameters.
PubMed: Chemical composition and antioxidant, antimicrobial, and antifungal activities of the essential oil of Achillea ligustica all.
PubMed: Effects of antimicrobial components of essential oils on growth of Bacillus cereus INRA L2104 in and the sensory qualities of carrot broth.
PubMed: Isolation of antioxidant compounds from the methanolic extract of the roots of Decalepis hamiltonii (Wight and Arn.).
PubMed: Harvest regimen optimization and essential oil production in five tansy (Tanacetum vulgare L.) genotypes under a northern climate.
PubMed: Chemical composition and antimicrobial activity of Rosmarinus officinalis L. essential oil obtained via supercritical fluid extraction.
PubMed: [Measurement of borneol based on near infrared spectroscopy].
PubMed: Screening of chemical composition and antifungal and antioxidant activities of the essential oils from three Turkish artemisia species.
PubMed: The effect of applying a pipe-joint lubricant to connect ductile iron pipe on off-flavors in drinking water distribution systems.
PubMed: chemical composition, plant genetic differences, antimicrobial and antifungal activity investigation of the essential oil of Rosmarinus officinalis L.
PubMed: Analysis of the essential oils of the leaves, stems, rhizomes and roots of the medicinal plant Alpinia galanga from southern India.
PubMed: Essential oils from Mediterranean lamiaceae as weed germination inhibitors.
PubMed: Chemical composition and in vitro evaluation of antioxidant effect of free volatile compounds from Satureja montana L.
PubMed: High-affinity monoclonal antibodies for detection of the microbial metabolite, 2-methylisoborneol.
PubMed: Common herbs, essential oils, and monoterpenes potently modulate bone metabolism.
PubMed: Bacterial susceptibility to and chemical composition of essential oils from Thymus kotschyanus and Thymus persicus.
PubMed: Fungicidal property of Curcuma longa L. rhizome-derived curcumin against phytopathogenic fungi in a greenhouse.
PubMed: Antimicrobial and antioxidant activity of the essential oil and methanol extracts of Thymus pectinatus Fisch. et Mey. Var. pectinatus (Lamiaceae).
PubMed: Attractiveness of 79 compounds and mixtures to wild Ceratitis capitata (Diptera: Tephritidae) in field trials.
PubMed: Composition and antimicrobial activity of the essential oils of Micromeria cristata subsp. phrygia and the enantiomeric distribution of borneol.
PubMed: Production of yarrow (Achillea millefolium L.) in Norway: essential oil content and quality.
PubMed: Volatile chemicals identified in extracts from leaves of Japanese mugwort (Artemisia princeps pamp.).
PubMed: [Stereochemical structure of d-borneol in "the Japanese Standards of Food Additives"].
PubMed: Cloning and expression of a rat liver phenobarbital-inducible UDP-glucuronosyltransferase (2B12) with specificity for monoterpenoid alcohols.
PubMed: Mutagenicity and antimutagenicity testing of six chemicals associated with the pungent properties of specific spices as revealed by the Ames Salmonella/microsomal assay.
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