alpha-cedrene
(1S,2R,5S)-2,6,6,8-tetramethyl tricyclo(5.3.1.01.5)undec-8-ene
 
Notes:
None found
  • 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
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      US Email: Sales
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      Fax: 1-631-614-7828
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      Product(s):
      469-61-4 alpha-Cedrene =>99%
       
  • Fleurchem
    • Fleurchem, Inc.
      Have A Flavorful Day
      A leading global manufacturer and supplier of ingredients for Flavors, Fragrances, AromaTherapy, Foods, Beverages, Personal Care Products, and other uses.
      Operating out of the 200,000 sq. ft., former Hercules/PFW facility in Middletown, NY; Fleurchem produces a full range of natural isolates, synthetic chemicals & specialities, essential oils and flavors. Additionally, the company performs toll manufacturing, as well as custom chemical synthesis for a wide range of clients.
      Email: Information
      US Voice: 845-341-2100
      US Fax: 845-341-2121
      Product(s):
      cedrene
       
  • 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
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      Voice: +86 (0)592 5105533
      Fax: +86 (0)592 5151667
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      Products List: View
      Product(s):
      alpha-Cedrene 90%
      Cedrene is from Cedar oil, has two kind of isomer, Alpha-cedrene and beta-cedrene. It can be used to synthetic Acetyl cedrene, Cedryl ketone, Epoxy cedrane, Cedryl aldehyde and other important perfume. Alpha-Cedrene has been widely used as solvent, intermediate to perfume, medicine production.
       
       
  • 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):
      ALPHA-CEDRENE NATURAL
       
  • 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
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      US Voice: (973) 740-2300
      US Fax: (973) 740-1839
      Product(s):
      03-16300 CEDRENE
      03-16305 CEDRENE NATURAL
       
  • United International
    • Qingdao Free Trade Zone United International Co Ltd
      Quality Products
      A partner in your supply chain solution.
      Qingdao Free Trade Zone United International Trade Co., Ltd.was founded in 1996, specializing in the production and import and export of food additives,flavor raw materials and pharmaceutical and chemical raw materials. The company has experienced R&D and business personnel,product quality, low price, efficient service and fast insight and grasp the latest market information.
      Email: Info
      Email: Sales
      Voice: +86-532-83893699
      Fax: +86-532-83893695
      Product(s):
      7209 Cedrene
       
  • Vigon International
    • Vigon International
      Passion for Simplicity
      Manufacturer and supplier of high quality flavor and fragrance ingredients.
      The growth and success of Vigon is due in large part to a unique corporate concept that Vigon has developed and established within the industry: Creative Partnerships. This partnership concept has been and continues to be the foundation and guiding principle for all of Vigon's activities.
      US Email: Sales
      US Voice: 570-476-6300
      US Fax: 570-476-1110
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      Product(s):
      508305 CEDRENE ALPHA NATURAL
       
Synonyms   Articles   Notes   Search
CAS Number: 469-61-4Picture of molecule3D/inchi
Other(deleted CASRN): 1224161-35-6
ECHA EINECS - REACH Pre-Reg: 207-418-4
FDA UNII: 50D4A81G8T
Beilstein Number: 3196861
MDL: MFCD00063003
CoE Number: 10985
XlogP3-AA: 4.60 (est)
Molecular Weight: 204.35628000
Formula: C15 H24
NMR Predictor: Predict (works with chrome or firefox)
EFSA/JECFA Comments: Register name to be changed to (-)-alpha-Cedrene. No longer supported by Industry (DG SANCO, 2012).
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
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: colorless clear oily liquid (est)
Assay: 95.00 to 100.00 % sum of isomers
Food Chemicals Codex Listed: No
Specific Gravity: 0.92600 to 0.93700 @  25.00 °C.
Pounds per Gallon - (est).: 7.705 to  7.797
Refractive Index: 1.50000 to 1.50300 @  20.00 °C.
Boiling Point: 261.00 to  262.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.018000 mmHg @ 25.00 °C. (est)
Flash Point: 219.00 °F. TCC ( 103.89 °C. )
logP (o/w): 6.308 (est)
Soluble in:
 alcohol
 water, 0.1504 mg/L @ 25 °C (est)
Insoluble in:
 water
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: woody
 
Odor Strength: medium
 
Substantivity: 112 hour(s) at 100.00 %
 
 woody  cedar  sweet  fresh  
Odor Description:
at 100.00 %. 
woody cedar sweet fresh
Luebke, William tgsc, (1987)
 
Odor and/or flavor descriptions from others (if found).
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
BOC Sciences
For experimental / research use only.
alpha-Cedrene =>99%
Diffusions Aromatiques
CEDRENE
ExtraSynthese
For experimental / research use only.
alpha-Cedrene (GC) ≥98% (sum of enantiomers)
Fleurchem
cedrene
Foreverest Resources
alpha-Cedrene 90%
Odor: characteristic
Use: Cedrene is from Cedar oil, has two kind of isomer, Alpha-cedrene and beta-cedrene. It can be used to synthetic Acetyl cedrene, Cedryl ketone, Epoxy cedrane, Cedryl aldehyde and other important perfume. Alpha-Cedrene has been widely used as solvent, intermediate to perfume, medicine production.
Fuzhou Farwell
Cedrene 78%min
Fuzhou Farwell
Cedrene CAS#469-61-4
Indukern F&F
ALPHA CEDRENE 35% NATURAL
Indukern F&F
ALPHA CEDRENE 60% NATURAL
Odor: WOODY, CEDAR
Lluch Essence
ALPHA-CEDRENE NATURAL
Moellhausen
CEDRENE Natural
Odor: mild woody, cedar-note
Penta International
CEDRENE NATURAL
Penta International
CEDRENE
Reincke & Fichtner
alpha-Cedrene natural
Reincke & Fichtner
alpha-Cedrene
Santa Cruz Biotechnology
For experimental / research use only.
(-)-a-Cedrene ≥95%
Sigma-Aldrich: Aldrich
For experimental / research use only.
(-)-a-Cedrene ≥95.0% (sum of enantiomers, GC)
United International
Cedrene
Vigon International
CEDRENE ALPHA NATURAL
Synonyms   Articles   Notes   Search   Top
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 36/37/38 - Irritating to eyes, respiratory system, and skin.
S 02 - Keep out of the reach of children.
S 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)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Human Experience:
5 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
Not determined
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
IFRA Critical Effect: Dermal sensitization
IFRA: View Standard
View IFRA Standards Library for complete information.
Please review Amendment 49 IFRA documentation for complete information.
IFRA RESTRICTION LIMITS IN THE FINISHED PRODUCT (%):
Category 1: Products applied to the lips
0.27 %
Category 2: Products applied to the axillae
0.080 %
Category 3: Products applied to the face/body using fingertips
1.60 %
Category 4: Products related to fine fragrance
1.50 %
 Category 5: Products applied to the face and body using the hands (palms), primarily leave-on
Category 5A: Body lotion products applied to the body using the hands (palms), primarily leave-on
0.38 %
Category 5B: Face moisturizer products applied to the face using the hands (palms), primarily leave-on
0.38 %
Category 5C: Hand cream products applied to the hands using the hands (palms), primarily leave-on
0.38 %
Category 5D: Baby Creams, baby Oils and baby talc
0.38 %
Category 6: Products with oral and lip exposure
0.88 %
 Category 7: Products applied to the hair with some hand contact
Category 7A: Rinse-off products applied to the hair with some hand contact
3.10 %
Category 7B: Leave-on products applied to the hair with some hand contact
3.10 %
Category 8: Products with significant anogenital exposure
0.16 %
Category 9: Products with body and hand exposure, primarily rinse off
2.90 %
 Category 10: Household care products with mostly hand contact
Category 10A: Household care excluding aerosol products (excluding aerosol/spray products)
11.00 %
Category 10B: Household aerosol/spray products
11.00 %
 Category 11: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate
Category 11A: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate without UV exposure
5.80 %
Category 11B: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate with potential UV exposure
5.80 %
Category 12: Products not intended for direct skin contact, minimal or insignificant transfer to skin
No Restriction
 Notes:
IFRA FLAVOR REQUIREMENTS:

Due to the possible ingestion of small amounts of fragrance ingredients from their use in products in Categories 1 and 6, materials must not only comply with IFRA Standards but must also be recognized as safe as a flavoring ingredient as defined by the IOFI Code of Practice (www.iofi.org). For more details see chapter 1 of the Guidance for the use of IFRA Standards.

 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.012 (μg/capita/day)
Modified Theoretical Added Maximum Daily Intake (mTAMDI): 3900 (μg/person/day)
Threshold of Concern:1800 (μg/person/day)
Structure Class: I
 
Food categories according to Commission Regulation EC No. 1565/2000 (EC, 2000) in FGE.06 (EFSA, 2002a). According to the Industry the "normal" use is defined as the average of reported usages and "maximum use" is defined as the 95th percentile of reported usages (EFSA, 2002i).
Note: mg/kg = 0.001/1000 = 0.000001 = 1/1000000 = ppm.
 average usage mg/kgmaximum usage mg/kg
Dairy products, excluding products of category 02.0 (01.0): 7.0000035.00000
Fats and oils, and fat emulsions (type water-in-oil) (02.0): 5.0000025.00000
Edible ices, including sherbet and sorbet (03.0): 10.0000050.00000
Processed fruit (04.1): 7.0000035.00000
Processed vegetables (incl. mushrooms & fungi, roots & tubers, pulses and legumes), and nuts & seeds (04.2): --
Confectionery (05.0): 10.0000050.00000
Chewing gum (05.0): --
Cereals and cereal products, incl. flours & starches from roots & tubers, pulses & legumes, excluding bakery (06.0): 5.0000025.00000
Bakery wares (07.0): 10.0000050.00000
Meat and meat products, including poultry and game (08.0): 2.0000010.00000
Fish and fish products, including molluscs, crustaceans and echinoderms (MCE) (09.0): 2.0000010.00000
Eggs and egg products (10.0): --
Sweeteners, including honey (11.0): --
Salts, spices, soups, sauces, salads, protein products, etc. (12.0): 5.0000025.00000
Foodstuffs intended for particular nutritional uses (13.0): 10.0000050.00000
Non-alcoholic ("soft") beverages, excl. dairy products (14.1): 5.0000025.00000
Alcoholic beverages, incl. alcohol-free and low-alcoholic counterparts (14.2): 10.0000050.00000
Ready-to-eat savouries (15.0): 20.00000100.00000
Composite foods (e.g. casseroles, meat pies, mincemeat) - foods that could not be placed in categories 01.0 - 15.0 (16.0): 5.0000025.00000
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):
Flavouring Group Evaluation 25, (FGE.25)[1] - Aliphatic and aromatic hydrocarbons from chemical group 31 - 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 78 (FGE.78)[1] - Consideration of Aliphatic and alicyclic and aromatic hydrocarbons evaluated by JECFA (63rd meeting) structurally related to aliphatic and aromatic hydrocarbons evaluated by EFSA in FGE.25 - Scientific Opinion of the Panel on Food Additives,Flavourings, Processing Aids and Materials in Contact with Food (AFC)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 25Rev1: Aliphatic and aromatic hydrocarbons from chemical group 31
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 78, Revision 1 (FGE.78Rev1): Consideration of aliphatic and alicyclic and aromatic hydrocarbons evaluated by JECFA (63rd meeting) structurally related to aliphatic and aromatic hydrocarbons evaluated by EFSA in FGE.25Rev2
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 25, Revision 2 (FGE.25Rev2): Aliphatic and aromatic hydrocarbons from chemical group 31
View page or View pdf
Scientific opinion on Flavouring Group Evaluation 25, Revision 3 (FGE.25Rev3): Aliphatic hydrocarbons from chemical group 31
View page or View pdf
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 469-61-4
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 10099
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 3082
WGK Germany: 2
 (3R-(3a,3ab,7b,8aa))-2,3,4,7,8,8a-hexahydro-3,6,8,8-tetramethyl-1H-3a,7-methanoazulene
Chemidplus: 0000469614
RTECS: PB7725000 for cas# 469-61-4
Synonyms   Articles   Notes   Search   Top
References:
 (3R-(3a,3ab,7b,8aa))-2,3,4,7,8,8a-hexahydro-3,6,8,8-tetramethyl-1H-3a,7-methanoazulene
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 469-61-4
Pubchem (cid): 10099
Pubchem (sid): 134975160
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
KEGG (GenomeNet): C09630
HMDB (The Human Metabolome Database): Search
FooDB: FDB003904
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
aldehydic
 dodecanal (aldehyde C-12 lauric)FL/FR
10-undecenal (aldehyde C-11 undecylenic)FL/FR
amber
 amber decaneFR
 ambrette seed oilFL/FR
 angelica root oilFL/FR
 cistus ladaniferus resinoidFL/FR
animal
 animal carbolactoneFR
 costus valerolactoneFR
 indoleFL/FR
balsamic
 amyris wood oilFL/FR
siam benzoin resinoidFL/FR
 benzyl salicylateFL/FR
isobornyl acetateFL/FR
 cedar forest fragranceFR
 cinnamyl alcoholFL/FR
 copaiba balsam oilFL/FR
 ethyl cinnamateFL/FR
 fir balsam absoluteFR
 fir needle oil siberiaFL/FR
 hemlock western oil (tsuga heterophylla) canadaFR
3-phenyl propyl alcoholFL/FR
fatty
 decanolFL/FR
floral
isoamyl salicylateFL/FR
 bois de rose oil brazilFL/FR
 cananga oilFL/FR
 coriander seed oilFL/FR
 floral pyranolFR
 heliotropyl acetoneFL/FR
alpha-hexyl cinnamaldehydeFL/FR
laevo-linaloolFL/FR
 nerolidolFL/FR
 ocean propanalFL/FR
 orris rhizome absolute (iris pallida)FL/FR
 phenethyl alcoholFL/FR
fruity
gamma-decalactoneFL/FR
 green acetateFR
beta-ionyl ethyl etherFR
herbal
 carum carvi fruit oilFL/FR
 clary sage oil franceFL/FR
 daucus carota fruit oilFL/FR
abrialis lavandin oilFL/FR
 lavender absolute bulgariaFL/FR
spike lavender oilFL/FR
(1S,5R)-myrtenyl acetateFL/FR
 nopyl acetateFR
 origanum oil greeceFL/FR
 rosemary oil spainFL/FR
alpha-terpinyl acetateFL/FR
 tricyclo(5.2.1.02,6)dec-3-enyl acetateFR
leathery
 castoreum absoluteFL/FR
melon
 watermelon ketoneFR
mossy
 treemoss absoluteFR
 veramoss (IFF)FR
powdery
para-anisyl alcoholFL/FR
rooty
 vetiveryl propionateFR
spicy
 anona squamosa leaf oilFR
 cassia bark oil chinaFL/FR
 elettaria cardamomum seed oilFL/FR
isoeugenyl acetateFL/FR
 ginger root oil chinaFL/FR
 machilus kusanoi leaf oilFR
terpenic
 cypress leaf oilFR
 frankincense oilFL/FR
 juniperus communis fruit oilFL/FR
thujonic
 sage oil dalmatianFL/FR
tonka
 tonka bean absoluteFR
vanilla
 vanillinFL/FR
waxy
1-dodecanolFL/FR
 ethyl laurateFL/FR
woody
 acetyl cedreneFR
 amber decatrieneFR
 ambrene acetalFR
 amyris acetateFR
 caryophyllene alcohol acetateFR
 cedar cyclododecatrieneFR
 cedarwood oil alcoholsFL/FR
 cedarwood oil himalayaFR
 cedarwood oil terpenesFL/FR
 cedarwood oil texasFR
 cedarwood oil virginiaFR
 cedarwood oil whiteFR
 cedrela wood oilFR
 cedreneFR
 cedrenyl acetateFR
 cedrolFL/FR
 cedryl acetateFL/FR
 cistus twig/leaf oilFL/FR
4-(3,3-dimethyl bicyclo(2.2.1)hept-2-yl)-2-oxabicyclo(2.2.2)octaneFR
 guaiacwood oilFL/FR
 gurjun balsam oilFR
 juniperus deppeana wood oilFR
 juniperus mexicana extractFR
 methyl cedryl ketoneFL/FR
 methyl cedryl ketone replacerFR
 patchouli ethanoneFR
 patchouli oilFL/FR
 sandal pentanolFR
 santallFR
 spruce needle oil canadaFL/FR
 sugi wood oilFR
2,6,10,10-tetramethyl-1-oxa-spiro[4.5]dec-3-en-6-yl acetate 
 thuja occidentalis leaf oilFL/FR
 vetiver oil haitiFL/FR
 violet propanolFR
 woody acetateFR
 woody dodecaneFR
 woody epoxideFR
 
For Flavor
 
No flavor group found for these
 cedarwood oil alcoholsFL/FR
 cistus ladaniferus resinoidFL/FR
 elecampane root absoluteFL
2,6,10,10-tetramethyl-1-oxa-spiro[4.5]dec-3-en-6-yl acetate 
amber
 ambrette seed oilFL/FR
animal
 indoleFL/FR
balsamic
siam benzoin resinoidFL/FR
 benzyl salicylateFL/FR
 copaiba balsam oilFL/FR
 ethyl cinnamateFL/FR
 fir needle oil siberiaFL/FR
berry
 heliotropyl acetoneFL/FR
citrus
laevo-linaloolFL/FR
cooling
spike lavender oilFL/FR
fatty
10-undecenal (aldehyde C-11 undecylenic)FL/FR
floral
 bois de rose oil brazilFL/FR
 cananga oilFL/FR
 ocean propanalFL/FR
 phenethyl alcoholFL/FR
fruity
para-anisyl alcoholFL/FR
gamma-decalactoneFL/FR
green
isoamyl salicylateFL/FR
 angelica root oilFL/FR
 cinnamyl alcoholFL/FR
 nerolidolFL/FR
herbal
 carum carvi fruit oilFL/FR
 clary sage oil franceFL/FR
 coriander seed oilFL/FR
 daucus carota fruit oilFL/FR
abrialis lavandin oilFL/FR
 lavender absolute bulgariaFL/FR
 origanum oil greeceFL/FR
 rosemary oil spainFL/FR
leathery
 castoreum absoluteFL/FR
soapy
 dodecanal (aldehyde C-12 lauric)FL/FR
1-dodecanolFL/FR
spicy
 benzylidene acetoneFL
 cassia bark oil chinaFL/FR
 elettaria cardamomum seed oilFL/FR
isoeugenyl acetateFL/FR
 ginger root oil chinaFL/FR
3-phenyl propyl alcoholFL/FR
sweet
 orris rhizome absolute (iris pallida)FL/FR
terpenic
 juniperus communis fruit oilFL/FR
thujonic
 sage oil dalmatianFL/FR
vanilla
 vanillinFL/FR
waxy
 decanolFL/FR
 ethyl laurateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
woody
 amyris wood oilFL/FR
isobornyl acetateFL/FR
 cedarwood oil terpenesFL/FR
 cedrolFL/FR
 cedryl acetateFL/FR
 cistus twig/leaf oilFL/FR
 frankincense oilFL/FR
 guaiacwood oilFL/FR
 methyl cedryl ketoneFL/FR
(1S,5R)-myrtenyl acetateFL/FR
 patchouli oilFL/FR
 spruce needle oil canadaFL/FR
alpha-terpinyl acetateFL/FR
 thuja occidentalis leaf oilFL/FR
 vetiver oil haitiFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 balsamFR
 cedarFR
 cedarwoodFR
 clary sage oil replacerFR
 costusFR
 herbalFR
 juniperFR
 lavenderFR
 sandalwoodFR
 sassafrasFR
 topnotes 
 woodyFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 artichoke - 0.0007 mg/kg
Search Trop  Picture
 ayou wood oil @ 0.10%
Data  GC  Search Trop  Picture
 basil oil
Search Trop  Picture
 blueberry plant
Search Trop  Picture
 calamus root oil @ 0.61%
Data  GC  Search Trop  Picture
 cedarwood oil atlanta @ 20.50%
Data  GC  Search Trop  Picture
 cedarwood oil china @ 26.40%
Data  GC  Search Trop  Picture
 cedarwood oil lebanon @ 0.20%
Data  GC  Search Trop  Picture
 cedarwood oil texas @ 30.70%
Data  GC  Search Trop  Picture
 cedarwood oil virginia @ 21.10%
Data  GC  Search Trop  Picture
 cedarwood oils
Search  PMC Picture
 celery seed
Search Trop  Picture
 clary sage oil spain @ 0.14%
Data  GC  Search Trop  Picture
 costus
Search Trop  Picture
 cypress cone oil egypt @ 0.2%
Data  GC  Search Trop  Picture
 cypress oil @ trace-0.19%
Data  GC  Search Trop  Picture
 fir needle oil canada @ 0.00-0.27%
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 ginger root oil china @ 3.39%
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 guava leaf oil cuba @ 0.20%
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 lavender
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 lavender oil france @ 0.05%
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 lemon verbena oil morocco @ 0.4%
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 lemon verbena oil turkey @ 0.43%
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 peppermint oil
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 phoebe oil brazil @ 0.11%
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 pinus laricio poiret branch oil italy @ 0.50%
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 safflower flower
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 sage clary sage
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 sage leaf oil
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 sage plant
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 tarragon plant
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 verbena oil france @ 0.20%
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 ylang ylang oil CO2 extract @ 0.21%
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 zingiber officinale root oil china @ 0.19%
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Synonyms:
(-)-a-cedrene
(-)-alpha-cedrene
L-alpha-cedrene
laevo-alpha-cedrene
levo-a-cedrene
alpha-cedrene 60% natural
(3R- (3alpha,3abeta, 7beta,8aalpha))- 2,3,4,7,8,8a-hexahydro-3,6,8,8-tetramethyl-1H-3a,7-methanoazulene
1H-3a,7-methanoazulene, 2,3,4,7,8,8a-hexahydro-3,6,8,8-tetramethyl-, (3R,3aS,7S,8aS)-
(1S,2R,5S)-2,6,6,8-tetramethyl tricyclo(5.3.1.01.5)undec-8-ene
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Articles:
PubMed: [Analysis of Volatile Oils from Different Processed Products of Zingiber officinale Rhizome by GC-MS].
PubMed: Metabolite Profiling and Comparison of Bioactivity in Antrodia cinnamomea and Antrodia salmonea Fruiting Bodies.
PubMed: Terpenoids Preserved in Fossils from Miocene-aged Japanese Conifer Wood.
PubMed: Complete (1)H NMR assignment of cedranolides.
PubMed: Role of the reaction of stabilized Criegee intermediates with peroxy radicals in particle formation and growth in air.
PubMed: Gas-phase rate coefficients of the reaction of ozone with four sesquiterpenes at 295 ± 2 K.
PubMed: In vivo absorption and disposition of α-cedrene, a sesquiterpene constituent of cedarwood oil, in female and male rats.
PubMed: Coriander (Coriandrum sativum L.) and its bioactive constituents.
PubMed: Constituents of essential oils from the leaf and flower of Plumeria alba grown in Nigeria.
PubMed: Role of sterically demanding chiral dirhodium catalysts in site-selective C-H functionalization of activated primary C-H bonds.
PubMed: Essential oils and crude extracts from Chrysanthemum trifurcatum leaves, stems and roots: chemical composition and antibacterial activity.
PubMed: Sesquiterpene acids from Shellac and their bioactivities evaluation.
PubMed: Hepatoprotection of sesquiterpenoids: a quantitative structure-activity relationship (QSAR) approach.
PubMed: GC-MS/MS method for the quantification of α-cedrene in rat plasma and its pharmacokinetic application.
PubMed: Identification of insecticidal constituents of the essential oil of Acorus calamus rhizomes against Liposcelis bostrychophila Badonnel.
PubMed: Composition, anticancer, and antimicrobial activities in vitro of the heartwood essential oil of Cunninghamia lanceolata var. konishii from Taiwan.
PubMed: Pyrolytic formation of polycyclic aromatic hydrocarbons from sesquiterpenes.
PubMed: Phytochemical analysis of the essential oils of 10 endemic Cephalaria species from Turkey.
PubMed: Chemical composition, antimicrobial and antitumor activities of the essential oils and crude extracts of Euphorbia macrorrhiza.
PubMed: Determination of gas-phase ozonolysis rate coefficients of a number of sesquiterpenes at elevated temperatures using the relative rate method.
PubMed: Essential oils of Cupressus funebris, Juniperus communis, and J. chinensis (Cupressaceae) as repellents against ticks (Acari: Ixodidae) and mosquitoes (Diptera: Culicidae) and as toxicants against mosquitoes.
PubMed: Chemical composition and antioxidant activity of essential oil from berries of Schisandra chinensis (Turcz.) Baill.
PubMed: Changes in volatile compound composition of Antrodia camphorata during solid state fermentation.
PubMed: Acaricidal activity against Tetranychus urticae and essential oil composition of four Croton species from Caatinga biome in northeastern Brazil.
PubMed: Biosynthesis of sesquiterpenes by the fungus Fusarium verticillioides.
PubMed: Chemical composition of the essential oil of Croton gossypiifolius from Venezuela.
PubMed: Persistency assessment and aerobic biodegradation of selected cyclic sesquiterpenes present in essential oils.
PubMed: An oxidative dearomatization-induced [5 + 2] cascade enabling the syntheses of α-cedrene, α-pipitzol, and sec-cedrenol.
PubMed: Bisabolyl-derived sesquiterpenes from tobacco 5-epi-aristolochene synthase-catalyzed cyclization of (2Z,6E)-farnesyl diphosphate.
PubMed: [Studies on the chemical constituents of Coleus forskohlii].
PubMed: Identification of organic hydroperoxides and hydroperoxy acids in secondary organic aerosol formed during the ozonolysis of different monoterpenes and sesquiterpenes by on-line analysis using atmospheric pressure chemical ionization ion trap mass spectrometry.
PubMed: Flowerhead volatile oil composition of soilless culture-grown Chrysanthemum balsamita L.
PubMed: Essential Oil Composition and Antibacterial Studies of Vitex negundo Linn. Extracts.
PubMed: Contribution to the analysis of the essential oil of Helichrysum italicum (Roth) G. Don. Determination of ester bonded acids and phenols.
PubMed: Remote position substituents as modulators of conformational and reactive properties of quinones. Relevance of the pi/pi intramolecular interaction.
PubMed: From alpha-cedrene to crinipellin B and onward: 25 years of the alkene-arene meta-photocycloaddition reaction in natural product synthesis.
PubMed: New woody and ambery notes from cedarwood and turpentine oil.
PubMed: Analysis of atmospheric sesquiterpenes: sampling losses and mitigation of ozone interferences.
PubMed: Aroma evaluation of an aquatic herb, Changpo (Acorus calamus Var. angustatus Bess), by AEDA and SPME.
PubMed: Orientation and feeding responses of the pollen beetle, Meligethes aeneus, to candytuft, Iberis amara.
PubMed: Volatile sesquiterpene hydrocarbons characteristic for Penicillium roqueforti strains producing PR toxin.
PubMed: Key tricyclic synthetic intermediates for the preparation of the sesquiterpenes alpha- and beta-cedrene.
PubMed: Selective oviposition by Aedes aegypti (Diptera: culicidae) in response to Mesocyclops longisetus (Copepoda: Cyclopoidea) under laboratory and field conditions.
PubMed: Cloning, expression, and characterization of epi-cedrol synthase, a sesquiterpene cyclase from Artemisia annua L.
PubMed: Analysis of the essential oil of Juniperus procera Endl. growing in Kenya.
PubMed: Novel Allylic Oxidation of alpha-Cedrene to sec-Cedrenol by a Rhodococcus Strain.
PubMed: The Essential Oil of Perilla ocimoides: A Rich Source of Rosefuran.
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