alpha-ambrinol
1,2,3,4,4a,5,6,7-octahydro-2,2,5-trimethyl-2-naphthalenol
 
Notes:
None found
  • Azelis UK
    • Azelis UK Ltd.
      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: Info
      Email: Gaynor Cowan
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      United Kingdom+44 1858 545 837
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      Product(s):
      12334 AMBRINOL 95
      908930 Ambrinol
       
  • 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
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      Product(s):
      41199-19-3 Ambrinol S
       
  • Firmenich
    • Firmenich Inc.
      We Create
      We create perfumes and flavors for the World's most desirable brands.
      Firmenich is the largest privately-owned company in the perfume and flavor business. Swiss and family owned, we have created many of the world’s favorite perfumes for over 100 years and produced a number of the most well known flavors we enjoy each day.
      US Email: Fred Keifer
      US Voice: +1 609 452 1000
      US Fax: +1 609 452 6077
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      Product(s):
      908930 AMBRINOL for fragrance
      This ingredient is best used in small amounts. It can be used in all perfume types to add depth, complexity and texture; in particular to woody, oriental and floral creations.
       
       
  • 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):
      AMBRINOL S
       
  • Moellhausen
  • Pell Wall Perfumes
    • Pell Wall Perfumes
      Hand-made fragrances
      Pell Wall maintains a broad palette of ingredients & in order to keep stocks fresh & the options wide we also sell from our own stock.
      Pell Wall was founded by perfumer Chris Bartlett to provide exclusive hand-made fragrances to a select few people who love them. All our products are created using fine quality ingredients, many of which we also offer for sale to other perfumers and enthusiasts. Pell Wall make fragrances for men, for women and for the home.
      Email: Info
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      Product(s):
      Ambrinol 95 (at 10% in ethanol)
      IFF describe it like this: “Possesses the elegant tonalities of aged natural ambergris tincture. Tobacco, leathery nuances and the power of oceanic seaweed notes supported with a warm animalic, musky dry down“. Traces of Ambrinol 95 can be used in all perfume types to add naturalness, depth, complexity and texture; it can be particularly interesting in woody, oriental, Chypre and floral creations. A touch of Ambrinol 95 can transform a labdanum-based amber accord into a natural ambergris note. Writing in the 1960s Arctander had this to say about the potential of a material not yet part of the palette: “The title materials are briefly mentioned in this work because of their potential interest to the perfumer. They are natural components of Ambregris, and they are considered of major importance to the olfactory properties of natural Ambregris and Ambregris tincture. Although the materials have been synthesized, and also obtained as isolates from natural Ambregris, they are not yet commercially available under the name Ambrinol. Closely related chemicals are made syntheically at lower cost, but not of the same attractive olfactory eflect …When the title materials become commercially available at an attractive price, they will undoubtedly find their way into perfumery as part of Ambre bases, new perfume types, specialities etc.“ He was of course right and Ambrinols have been used in bases such as Ambergris Oliffac (an IFF product, recently discontinued) for many years.
       
       
  • 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):
      Ambrinol 95 PRG
      SDS
       
  • Ernesto Ventós
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas
CAS Number: 41199-19-3Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 255-256-8
FDA UNII: Search
Nikkaji Web: J320.020E
CoE Number: 10173
XlogP3-AA: 2.80 (est)
Molecular Weight: 194.31754000
Formula: C13 H22 O
NMR Predictor: Predict (works with chrome, Edge or firefox)
EFSA/JECFA Comments: Mixture of diastereo isomers (EFFA, 2010). Stereoisomeric composition to be specified.
Category: cosmetic, 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
DG SANTE Food Flavourings: 02.197  1,2,3,4,4a,5,6,7-octahydro-2,2,5-trimethyl-2-naphthalenol
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: colorless to pale yellow clear liquid to solid (est)
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 0.93600 to 0.94800 @  20.00 °C.
Pounds per Gallon - (est).: 7.798 to  7.898
Refractive Index: 1.48300 to 1.49100 @  20.00 °C.
Boiling Point: 280.00 to  281.00 °C. @ 760.00 mm Hg
Acid Value: 1.00 max. KOH/g
Vapor Pressure: 0.000500 mmHg @ 25.00 °C. (est)
Flash Point: > 200.00 °F. TCC ( > 93.33 °C. )
logP (o/w): 3.785 (est)
Shelf Life: 18.00 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, 71.04 mg/L @ 25 °C (est)
Stability:
 APC: -
 candle: -
 detergent: traces - 1%
 fine fragrances: traces - 0.1%
 shampoo: traces - 0.1%
 shower gel: traces - 0.1%
 soap: traces - 0.1%
 softener: traces - 1%
Similar Items: note
ambrinol
ambrinol alpha
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: amber
 
Odor Strength: high ,
recommend smelling in a 10.00 % solution or less
 
Substantivity: 72 hour(s) at 100.00 %
 
 amber  natural  musk  animal  musty  earthy  ambergris  seaweed  
Odor Description:
at 10.00 % in dipropylene glycol. 
amber natural musk animal
Luebke, William tgsc, (1993)
 
 
Flavor Type: amber
 
 amber  woody  earthy  rooty  herbal  animal  woody old wood  humus  tea  
Taste Description:
amber woody earthy rooty herbal animal old wood humus tea
Luebke, William tgsc, (1993)
 
Odor and/or flavor descriptions from others (if found).
 
Firmenich
AMBRINOL for fragrance
Odor Description: A very strong and powerful note with a natural ambergris quality; somewhat musky, animal and earthy
This ingredient is best used in small amounts. It can be used in all perfume types to add depth, complexity and texture; in particular to woody, oriental and floral creations.
 
IFF
Ambrinol 95
Odor Description: Possesses the elegant tonalities of aged natural ambergris tincture. Tobacco, leathery nuances and the power of oceanic seaweed notes supported with a warm animalic, musky dry down
 
Pell Wall Perfumes
Ambrinol 95 (at 10% in ethanol)
Odor Description: Ambergris, natural, musky, animalic, tobacco
IFF describe it like this: “Possesses the elegant tonalities of aged natural ambergris tincture. Tobacco, leathery nuances and the power of oceanic seaweed notes supported with a warm animalic, musky dry down“. Traces of Ambrinol 95 can be used in all perfume types to add naturalness, depth, complexity and texture; it can be particularly interesting in woody, oriental, Chypre and floral creations. A touch of Ambrinol 95 can transform a labdanum-based amber accord into a natural ambergris note. Writing in the 1960s Arctander had this to say about the potential of a material not yet part of the palette: “The title materials are briefly mentioned in this work because of their potential interest to the perfumer. They are natural components of Ambregris, and they are considered of major importance to the olfactory properties of natural Ambregris and Ambregris tincture. Although the materials have been synthesized, and also obtained as isolates from natural Ambregris, they are not yet commercially available under the name Ambrinol. Closely related chemicals are made syntheically at lower cost, but not of the same attractive olfactory eflect …When the title materials become commercially available at an attractive price, they will undoubtedly find their way into perfumery as part of Ambre bases, new perfume types, specialities etc.“ He was of course right and Ambrinols have been used in bases such as Ambergris Oliffac (an IFF product, recently discontinued) for many years.
 
Azelis UK
Ambrinol
Odor Description: A very strong and powerful note with a natural ambergris quality; somewhat musky, animal and earthy
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
Azelis UK
AMBRINOL 95
Azelis UK
Ambrinol
BOC Sciences
For experimental / research use only.
Ambrinol S
Ernesto Ventós
AMBRINOL 95 PRG IFF
Odor: AMBER, ANIMALIC, TOBACCO, LEATHER
Ernesto Ventós
AMBRINOL FIRMENICH 908930
Odor: EXTREMELY POWERFUL AMBER NOTE
Fine Fragrances Pvt Ltd
Ambrinol 95
Firmenich
AMBRINOL
for fragrance
Odor: A very strong and powerful note with a natural ambergris quality; somewhat musky, animal and earthy
Use: This ingredient is best used in small amounts. It can be used in all perfume types to add depth, complexity and texture; in particular to woody, oriental and floral creations.
IFF
Ambrinol 95
Odor: Possesses the elegant tonalities of aged natural ambergris tincture. Tobacco, leathery nuances and the power of oceanic seaweed notes supported with a warm animalic, musky dry down
Indukern F&F
AMBRINOL F
Indukern F&F
AMBRINOL
Lluch Essence
AMBRINOL S
Moellhausen
AMBRINOL
Pell Wall Perfumes
Ambrinol 95 (at 10% in ethanol)
Odor: Ambergris, natural, musky, animalic, tobacco
Use: IFF describe it like this: “Possesses the elegant tonalities of aged natural ambergris tincture. Tobacco, leathery nuances and the power of oceanic seaweed notes supported with a warm animalic, musky dry down“. Traces of Ambrinol 95 can be used in all perfume types to add naturalness, depth, complexity and texture; it can be particularly interesting in woody, oriental, Chypre and floral creations. A touch of Ambrinol 95 can transform a labdanum-based amber accord into a natural ambergris note. Writing in the 1960s Arctander had this to say about the potential of a material not yet part of the palette: “The title materials are briefly mentioned in this work because of their potential interest to the perfumer. They are natural components of Ambregris, and they are considered of major importance to the olfactory properties of natural Ambregris and Ambregris tincture. Although the materials have been synthesized, and also obtained as isolates from natural Ambregris, they are not yet commercially available under the name Ambrinol. Closely related chemicals are made syntheically at lower cost, but not of the same attractive olfactory eflect …When the title materials become commercially available at an attractive price, they will undoubtedly find their way into perfumery as part of Ambre bases, new perfume types, specialities etc.“ He was of course right and Ambrinols have been used in bases such as Ambergris Oliffac (an IFF product, recently discontinued) for many years.
Perfumery Laboratory
AMBRINOL 95® IFF 10% DPG
Odor: amber, animal musk, old tree. Powerful, reminiscent of the smell of damp earth after the rain
The John D. Walsh Company
Ambrinol 95 PRG
Synonyms   Articles   Notes   Search   Top
Safety Information:
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.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: cosmetic, 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 alpha-ambrinol usage levels up to:
  1.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.026 (μg/capita/day)
Modified Theoretical Added Maximum Daily Intake (mTAMDI): 1600 (μg/person/day)
Threshold of Concern:540 (μg/person/day)
Structure Class: II
 
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): --
Fats and oils, and fat emulsions (type water-in-oil) (02.0): --
Edible ices, including sherbet and sorbet (03.0): --
Processed fruit (04.1): --
Processed vegetables (incl. mushrooms & fungi, roots & tubers, pulses and legumes), and nuts & seeds (04.2): --
Confectionery (05.0): --
Chewing gum (05.0): --
Cereals and cereal products, incl. flours & starches from roots & tubers, pulses & legumes, excluding bakery (06.0): --
Bakery wares (07.0): --
Meat and meat products, including poultry and game (08.0): --
Fish and fish products, including molluscs, crustaceans and echinoderms (MCE) (09.0): --
Eggs and egg products (10.0): --
Sweeteners, including honey (11.0): --
Salts, spices, soups, sauces, salads, protein products, etc. (12.0): --
Foodstuffs intended for particular nutritional uses (13.0): --
Non-alcoholic ("soft") beverages, excl. dairy products (14.1): 5.0000025.00000
Alcoholic beverages, incl. alcohol-free and low-alcoholic counterparts (14.2): --
Ready-to-eat savouries (15.0): --
Composite foods (e.g. casseroles, meat pies, mincemeat) - foods that could not be placed in categories 01.0 - 15.0 (16.0): --
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 18, Revision 1 (FGE. 18 Rev1)[1] : Aliphatic, alicyclic and aromatic saturated and unsaturated tertiary alcohols, aromatic tertiary alcohols and their esters from chemical groups 6 and 8
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 90 (FGE.90): Consideration of Aliphatic, acyclic and alicyclic terpenoid tertiary alcohols and structurally related substances evaluated by JECFA (68th meeting)FGE.18Rev1 (2009)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 18, Revision 2 (FGE.18Rev2): Aliphatic, alicyclic and aromatic saturated and unsaturated tertiary alcohols, aromatic tertiary alcohols and their esters from chemical groups 6 and 8.
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 18, Revision 3 (FGE.18Rev3): Aliphatic, alicyclic and aromatic saturated and unsaturated tertiary alcohols, aromatic tertiary alcohols and their esters from chemical groups 6 and 8.
View page or View pdf
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 41199-19-3
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 162452
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 2
 2,5,5-trimethyl-1,3,4,4a,6,7-hexahydronaphthalen-2-ol
Chemidplus: 0041199193
Synonyms   Articles   Notes   Search   Top
References:
Leffingwell: Chirality or Article
 2,5,5-trimethyl-1,3,4,4a,6,7-hexahydronaphthalen-2-ol
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 41199-19-3
Pubchem (cid): 162452
Pubchem (sid): 135116670
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
HMDB (The Human Metabolome Database): Search
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
No odor group found for these
2-methyl-3-isobutyl quinoxaline 
black pepper distillatesFL/FR
aldehydic
9-decenalFL/FR
 dodecanal (aldehyde C-12 lauric)FL/FR
10-undecenal (aldehyde C-11 undecylenic)FL/FR
amber
 ambergris naphtholFR
 ambrette seed oilFL/FR
 ambrinolFR
 ambroxanFL/FR
 angelica root oilFL/FR
 cistus ladaniferus resinoidFL/FR
animal
 animal carbolactoneFR
 animal specialtyFR
isobutyl quinolineFR
para-cresyl caprylateFL/FR
 musk indenofuranFR
 procavia capensis excrete absoluteFR
anisic
para-anisaldehydeFL/FR
balsamic
isoamyl benzoateFL/FR
 amyris wood oilFL/FR
siam benzoin resinoidFL/FR
 benzophenoneFR
 benzyl cinnamateFL/FR
 benzyl salicylateFL/FR
dextro,laevo-isoborneolFL/FR
laevo-bornyl acetateFL/FR
isobutyl cinnamateFL/FR
 cinnamyl alcoholFL/FR
 clover nitrileFR
 ethyl cinnamateFL/FR
 fir balsam absoluteFR
 juniper berry oil terpenelessFL/FR
 methyl (E)-cinnamateFL/FR
 peru balsam absoluteFL/FR
3-phenyl propyl alcoholFL/FR
berry
 raspberry ketoneFL/FR
 raspberry ketone acetateFL/FR
 raspberry ketone methyl etherFL/FR
caramellic
 ethyl maltolFL/FR
citrus
 bergamot oil bergaptene reduced italyFL/FR
 grapefruit pentanolFR
blood orange oil italyFL/FR
cocoa
2-isobutyl-3,5-(and 3,6)-dimethyl pyrazineFL/FR
earthy
(+)-geosmin 
(-)-geosmin 
 geosminFL/FR
 muscogeneFR
1-octen-3-oneFL/FR
fatty
 decanolFL/FR
floral
alpha-amyl cinnamaldehydeFL/FR
isoamyl salicylateFL/FR
 benzyl acetateFL/FR
 bois de rose oil brazilFL/FR
isobutyl salicylateFL/FR
laevo-citronellolFL/FR
 citronellolFL/FR
 coriander seed oilFL/FR
 cyclamen aldehydeFL/FR
 cyclohexyl ethyl alcoholFL/FR
9-decen-1-olFL/FR
 dimethyl benzyl carbinolFL/FR
 ethyl phenyl acetateFL/FR
 floral pyranolFR
 gardenia oxideFR
 geraniolFL/FR
 geranyl acetateFL/FR
 heliotropinFL/FR
 heliotropyl diethyl acetalFR
(Z)-3-hexen-1-yl salicylateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 hyacinth etherFR
 hydroxycitronellalFL/FR
 leerallFR
 lilyallFR
 linaloolFL/FR
laevo-linaloolFL/FR
 linalool oxideFL/FR
para-methyl acetophenoneFL/FR
 methyl dihydrojasmonateFL/FR
2-methyl-4-phenyl butanalFL/FR
 muguet carboxaldehydeFR
 muguet octadienolFR
 muguet shiseolFL/FR
 nerolFL/FR
 neroli oil bigardeFL/FR
 nerolidolFL/FR
 nonanolFL/FR
 ocean propanalFL/FR
 orris pyridine 25% IPMFR
 peony alcoholFR
 phenethyl alcoholFL/FR
 phenethyl isobutyrateFL/FR
 phenethyl phenyl acetateFL/FR
 phenethyl propionateFL/FR
 phenethyl salicylateFL/FR
 rhodinolFL/FR
 rose butanoateFL/FR
 tetrahydrolinaloolFL/FR
 violet methyl carbonateFR
fresh
10-undecen-1-yl acetateFL/FR
fruity
 allyl amyl glycolateFR
 artemisia pallens herb oilFL/FR
 benzyl propionateFL/FR
(E)-alpha-damasconeFL/FR
(E)-beta-damasconeFL/FR
gamma-decalactoneFL/FR
 green acetateFR
 osmanthus flower absoluteFL/FR
gamma-undecalactone (aldehyde C-14 (so-called))FL/FR
green
isocyclocitral (IFF)FL/FR
(Z)-3-hexen-1-yl acetateFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
(Z)-3-hexen-1-yl propionateFL/FR
(Z)-leaf acetalFL/FR
 melon nonenoateFL/FR
 violet leaf absoluteFL/FR
hay
 beeswax absoluteFL/FR
 hay absoluteFR
herbal
 clary sage oil franceFL/FR
 daucus carota fruit oilFL/FR
alpha-dihydroterpineolFL/FR
 lavender absolute bulgariaFL/FR
 linalyl acetateFL/FR
honey
 methyl phenyl acetateFL/FR
melon
 watermelon ketoneFR
mossy
 oakmoss absoluteFL/FR
 oakmoss distillatesFL/FR
 veramoss (IFF)FR
musk
(Z)-ambrettolideFL/FR
(E)-3-methyl-5-cyclotetradecen-1-oneFR
delta-muscenoneFR
dextro,laevo-musconeFL/FR
 musk cyclopentenyl propionateFR
 musk dimethyl indaneFL/FR
(Z)-musk pentaneFR
omega-pentadecalactoneFL/FR
naphthyl
ortho-methyl anisoleFL/FR
beta-naphthyl ethyl etherFL/FR
powdery
para-anisyl acetateFL/FR
para-anisyl alcoholFL/FR
spicy
4-carvomenthenolFL/FR
 clove bud oilFL/FR
black currant bud absoluteFL/FR
 ginger oleoresinFL/FR
 methyl isoeugenolFL/FR
black pepper oilFL/FR
terpenic
 frankincense oilFL/FR
alpha-terpineolFL/FR
thujonic
 armoise oilFR
tonka
 coumarinFR
 tonka bean absoluteFR
vanilla
 ethyl vanillinFL/FR
 vanilla bean absolute (vanilla planifolia)FL/FR
 vanillyl acetateFL/FR
waxy
 decyl acetateFL/FR
1-dodecanolFL/FR
 ethyl laurateFL/FR
1-undecanolFL/FR
woody
 amber carbinolFR
 cedrolFL/FR
 cistus twig/leaf oilFL/FR
 guaiacwood oilFL/FR
 gurjun balsam oilFR
 leptospermum scoparium branch/leaf oil new zealandFR
 longifoleneFL/FR
 methyl cedryl ketoneFL/FR
 patchouli ethanoneFR
 patchouli oilFL/FR
 patchouli oil decolorizedFL/FR
 patchouli oil molecular distilledFL/FR
 santallFR
 tobacarol (IFF)FR
 vetiver oil haitiFL/FR
 woody acetateFR
(Z)-woody amyleneFR
 woody propanolFR
 
For Flavor
 
No flavor group found for these
(Z)-ambrettolideFL/FR
2-isobutyl-3,5-(and 3,6)-dimethyl pyrazineFL/FR
 cistus ladaniferus resinoidFL/FR
9-decenalFL/FR
 geosminFL/FR
(+)-geosmin 
(-)-geosmin 
 methyl (E)-cinnamateFL/FR
2-methyl-4-phenyl butanalFL/FR
aldehydic
1-undecanolFL/FR
amber
 ambrette seed oilFL/FR
animal
para-cresyl caprylateFL/FR
balsamic
siam benzoin resinoidFL/FR
 benzyl salicylateFL/FR
laevo-bornyl acetateFL/FR
isobutyl cinnamateFL/FR
 ethyl cinnamateFL/FR
 peru balsam absoluteFL/FR
berry
 raspberry ketoneFL/FR
 raspberry ketone acetateFL/FR
 raspberry ketone methyl etherFL/FR
bitter
2-methyl-3-isobutyl quinoxaline 
brown
 beeswax absoluteFL/FR
camphoreous
dextro,laevo-isoborneolFL/FR
ortho-methyl anisoleFL/FR
caramellic
 ethyl maltolFL/FR
cherry
 heliotropinFL/FR
citrus
 bergamot oil bergaptene reduced italyFL/FR
laevo-linaloolFL/FR
 linaloolFL/FR
 nerolFL/FR
blood orange oil italyFL/FR
alpha-terpineolFL/FR
cooling
isobutyl salicylateFL/FR
4-carvomenthenolFL/FR
creamy
para-anisaldehydeFL/FR
para-methyl acetophenoneFL/FR
gamma-undecalactone (aldehyde C-14 (so-called))FL/FR
earthy
 chrysanthemum distillatesFL
1-octen-3-oneFL/FR
fatty
(Z)-3-hexen-1-yl benzoateFL/FR
10-undecenal (aldehyde C-11 undecylenic)FL/FR
floral
 bois de rose oil brazilFL/FR
 citronellolFL/FR
laevo-citronellolFL/FR
 geraniolFL/FR
 linalyl acetateFL/FR
 methyl dihydrojasmonateFL/FR
 methyl phenyl acetateFL/FR
 muguet shiseolFL/FR
 neroli oil bigardeFL/FR
 ocean propanalFL/FR
 phenethyl alcoholFL/FR
 phenethyl propionateFL/FR
 rhodinolFL/FR
 tetrahydrolinaloolFL/FR
fruity
isoamyl benzoateFL/FR
para-anisyl acetateFL/FR
para-anisyl alcoholFL/FR
 artemisia pallens herb oilFL/FR
 benzyl acetateFL/FR
 benzyl propionateFL/FR
 cherry guarana flavorFL
(E)-beta-damasconeFL/FR
(E)-alpha-damasconeFL/FR
gamma-decalactoneFL/FR
 osmanthus flower absoluteFL/FR
 rose butanoateFL/FR
greasy
10-undecen-1-yl acetateFL/FR
green
isoamyl salicylateFL/FR
 angelica root oilFL/FR
 cinnamyl alcoholFL/FR
 cyclamen aldehydeFL/FR
isocyclocitral (IFF)FL/FR
 cyclohexyl ethyl alcoholFL/FR
 geranyl acetateFL/FR
(Z)-3-hexen-1-yl acetateFL/FR
(Z)-3-hexen-1-yl propionateFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
(Z)-leaf acetalFL/FR
 linalool oxideFL/FR
 melon nonenoateFL/FR
 nerolidolFL/FR
 oakmoss absoluteFL/FR
 violet leaf absoluteFL/FR
herbal
 chrysanthemum flavorFL
 clary sage oil franceFL/FR
 coriander seed oilFL/FR
 daucus carota fruit oilFL/FR
 lavender absolute bulgariaFL/FR
honey
 ethyl phenyl acetateFL/FR
 phenethyl isobutyrateFL/FR
 phenethyl phenyl acetateFL/FR
medicinal
 dimethyl benzyl carbinolFL/FR
 phenethyl salicylateFL/FR
mossy
 oakmoss distillatesFL/FR
musk
dextro,laevo-musconeFL/FR
 musk dimethyl indaneFL/FR
peppery
black pepper flavorFL
powdery
beta-naphthyl ethyl etherFL/FR
soapy
 dodecanal (aldehyde C-12 lauric)FL/FR
1-dodecanolFL/FR
spicy
 benzyl cinnamateFL/FR
 clove bud oilFL/FR
black currant bud absoluteFL/FR
 ginger oleoresinFL/FR
 methyl isoeugenolFL/FR
black pepper distillatesFL/FR
black pepper oilFL/FR
3-phenyl propyl alcoholFL/FR
 turmeric oleoresinFL
tropical
alpha-amyl cinnamaldehydeFL/FR
vanilla
 ethyl vanillinFL/FR
omega-pentadecalactoneFL/FR
 vanilla bean absolute (vanilla planifolia)FL/FR
 vanillyl acetateFL/FR
waxy
 decanolFL/FR
9-decen-1-olFL/FR
 decyl acetateFL/FR
 ethyl laurateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 hydroxycitronellalFL/FR
 nonanolFL/FR
woody
 ambroxanFL/FR
 amyris wood oilFL/FR
 cedrolFL/FR
 cistus twig/leaf oilFL/FR
alpha-dihydroterpineolFL/FR
 frankincense oilFL/FR
 guaiacwood oilFL/FR
 juniper berry oil terpenelessFL/FR
 longifoleneFL/FR
 methyl cedryl ketoneFL/FR
 patchouli oilFL/FR
 patchouli oil decolorizedFL/FR
 patchouli oil molecular distilledFL/FR
 vetiver oil haitiFL/FR
 yerba mate concentrateFL
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 acaciaFR
 amberFR
 ambergrisFR
 ambrette oil replacerFR
 angelicaFL/FR
 animalFR
 autumnFR
 balsamFR
 barkFR
 bayberryFR
 beeswax absolute replacerFR
 boroniaFR
 bouquetFR
 cabreuva woodFR
 carnationFR
 cassia blossomFR
 cedarFR
 cedar forestFR
 champacaFR
 chocolate cacaoFL
 chypreFR
 cistusFL/FR
 civetFR
 clean 
 cloverFR
 coloniaFR
 country meadowFR
 cyclamenFR
 daffodilFR
 daphneFR
 dogwoodFR
 dusty 
 earthFR
 fantasy blends 
 fernFR
 figFR
 fir balsamFR
 fir needle oil replacerFR
 fixer 
 floralFR
 flouveFR
 flouve blossomFR
 foliageFR
 frangipani plumeriaFR
 freesiaFR
 fungusFR
 genetFR
 ginger white gingerFR
 guaiacwoodFL/FR
 gurjun balsamFR
 hawthornFR
 hay new mown hayFR
 heatherFR
 herbalFR
 hinoki oil replacerFR
 hollyberryFR
 hugoniaFR
 immortelleFL/FR
 incenseFR
 jasminFR
 kiwi blossomFR
 labdanumFR
 lavenderFR
 leatherFR
 lilyFR
 lily of the valleyFR
 lotusFR
 millefleursFR
 mimosaFR
 mossFR
 muskFR
 muskrat 
 narcissusFR
 oakwoodFR
 ocean seaFR
 orange blossomFR
 orchidFR
 orientalFR
 pansyFR
 passion blossomFR
 patchouliFR
 petuniaFR
 phloxFR
 pineFR
 pine forestFR
 poppyFR
 powderFR
 privet blossomFR
 rainFR
 resedaFR
 roseFR
 rose d'orientFR
 rose red roseFR
 rose tea roseFR
 rose white roseFR
 rose wild rose 
 sandalwoodFR
 soapy sandalwood mossFR
 spiceFR
 spring rainFR
 stephanotisFR
 sweet grassFR
 timber 
 tobaccoFR
 tonka beanFR
 tulipFR
 vanillaFR
 wisteriaFR
 woodruffFR
 woodyFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 cistus oil @ 0.2%
Data  GC  Search Trop  Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
 amber naphthalenol
alpha-ambrinol
 ambrinol 95 (IFF)
 ambrinol 95 PRG
2-hydroxy-2,5,5-trimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalene
2-naphthalenol, 1,2,3,4,4a,5,6,7-octahydro-2,5,5-trimethyl-
2-naphthalenol, octahydro-2,5,5-trimethyl-
1,2,3,4,4a,5,6,7-octahydro-2,2,5-trimethyl-2-naphthalenol
1,2,3,4,4a,5,6,7-octahydro-2,5,5-trimethyl-2-naphthol
2,5,5-trimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-2-ol
2,5,5-trimethyl-1,3,4,4a,6,7-hexahydronaphthalen-2-ol
2,5,5-trimethyl-octahydro-2-naphthalenol
Synonyms   Articles   Notes   Search   Top
Synonyms   Articles   Notes   Search   Top
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