cyclamen aldehyde
3-(p-cumenyl)-2-methylpropionaldehyde
 
Notes:
jasmin accord - cyclamen aldehyde and benzyl alcohol. rain accord - cyclamen aldehyde and hexyl cinnamaldehyde. Used as a food additive [EAFUS]
  • Augustus Oils
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      Arctander describes it as “Diffusive and powerful floral-green, floral-stem like odor with pronounced vegetable Cucumber-Melon-like notes. Overall resembling the odor of Lindenblossom. Extensively used in perfumery for floral effects, fresh-green-floral topnotes (of lasting fragrance), Useful in Lilac, Lily, Peony, Magnolia, Orangeblossom, Alpine Violet, etc. Blends well with the Ionones and all Rose notes.”
       
       
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      Blends-well-with - +Galbanum +Orris +Lime +Ivy Absolute +Ho
       
       
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      I0377 3-(4-isopropylphenyl)isobutyraldehyde >92.0%(GC)
       
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Synonyms   Articles   Notes   Search
Fragrance Demo Formulas    Flavor Demo Formulas
CAS Number: 103-95-7Picture of molecule3D/inchi
Other(deleted CASRN): 80949-77-5
ECHA EINECS - REACH Pre-Reg: 203-161-7
FDA UNII: 4U37UX0E1E
Nikkaji Web: J4.429F
Beilstein Number: 2047689
MDL: MFCD00024160
CoE Number: 133
XlogP3-AA: 3.30 (est)
Molecular Weight: 190.28566000
Formula: C13 H18 O
NMR Predictor: Predict (works with chrome, Edge or firefox)
EFSA/JECFA Comments: At least 90%; secondary component 5% 3-(p-cumenyl)-2-methylpropionic acid. (EFSA)
Category: 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: 1465  2-methyl-3-(p-isopropylphenyl)propionaldehyde
DG SANTE Food Flavourings: 05.045  3-(p-cumenyl)-2-methylpropionaldehyde
FEMA Number: 2743 cyclamen aldehyde
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):103-95-7 ; 2-METHYL-3-(P-ISOPROPYLPHENYL) PROPIONALDEHYDE
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: colorless to pale yellow clear liquid (est)
Assay: 94.00 to 100.00 % 
Food Chemicals Codex Listed: Yes
Specific Gravity: 0.94500 to 0.95500 @  25.00 °C.
Pounds per Gallon - (est).: 7.863 to  7.947
Refractive Index: 1.50200 to 1.51200 @  20.00 °C.
Boiling Point: 270.00 °C. @ 760.00 mm Hg
Acid Value: 5.00 max. KOH/g
Vapor Pressure: 0.009000 mmHg @ 25.00 °C. (est)
Flash Point: 228.00 °F. TCC ( 109.00 °C. )
logP (o/w): 3.428 (est)
Shelf Life: 24.00 month(s) or longer if stored properly.
Storage: store in cool, dry place in tightly sealed containers, protected from heat and light.
Soluble in:
 dipropylene glycol
 fixed oils
 paraffin oil
 water, 22.59 mg/L @ 25 °C (est)
Insoluble in:
 water
 propylene glycol
 glycerin
Stability:
 bath foam
 hair spray
 non-discoloring in most media
 soap
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: floral
 
Odor Strength: medium
 
Substantivity: 72 hour(s) at 100.00 %
 
 floral  cyclamen  fresh  rhubarb  musty  green  
Odor Description:
at 100.00 %. 
floral cyclamen fresh rhubarb musty green
Luebke, William tgsc, (1983)
 
 
Flavor Type: green
 
 green  tropical  rhubarb  watery  oily  cyclamen  cortex  phenolic  
Taste Description:
green tropical rhubarb watery oily cyclamen cortex phenolic
Luebke, William tgsc, (1986)
 
Odor and/or flavor descriptions from others (if found).
 
Givaudan
Cyclamen Aldehyde Extra
Odor Description: Floral, Green, Powerful
Cyclamen Aldehyde Extra can be used in many floral, green, fresh and marine accords. Its stability and substantivity are especially useful for functional perfumery.
 
PerfumersWorld
Cyclamen Aldehyde
Odor Description: cyclamen fresh rhubarb musty green sweet floral aromatic cyclamen
Blends-well-with - +Galbanum +Orris +Lime +Ivy Absolute +Ho
 
Pell Wall Perfumes
Cyclamen Aldehyde
Odor Description: floral-cyclamen, fresh, Linden-blossom, green, rhubarb
Arctander describes it as “Diffusive and powerful floral-green, floral-stem like odor with pronounced vegetable Cucumber-Melon-like notes. Overall resembling the odor of Lindenblossom. Extensively used in perfumery for floral effects, fresh-green-floral topnotes (of lasting fragrance), Useful in Lilac, Lily, Peony, Magnolia, Orangeblossom, Alpine Violet, etc. Blends well with the Ionones and all Rose notes.”
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: fragrance
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Suppliers:
Augustus Oils
Cyclamen Aldehyde
Services
BOC Sciences
For experimental / research use only.
3-p-Cumenyl-2-methylpropionaldehyde
Creatingperfume.com
Cyclamen Aldehyde Extra (Givaudan)
Odor: Floral, Green, Powerful, Fresh
Diffusions Aromatiques
ALDEHYDE CYCLAMEN
ECSA Chemicals
CYCLAMEN ALDEHYDE FLAVOUR USE
ECSA TRADE THE MOST UPDATED FINANCIAL PUBLICATION ON THE WORLD OF CHEMISTRY
ECSA Chemicals
CYCLAMEN ALDEHYDE
Ernesto Ventós
CYCLAMEN ALDEHYDE EXTRA
Odor: FLORAL, FRESH, LILY OF THE VALLEY
Ernesto Ventós
CYCLAMEN ALDEHYDE
Eternis Fine Chemicals
Cyclamen Aldehyde-Pure
Odor: characteristic
Use: Cyclamen Aldehyde is a very powerful, floral, green note used in many perfumery applications to blend into fresh, floral, green or ozonic/marine accords. It is an ingredient with growing use and importance in helping to build replacement accords for materials disappearing from the Perfumers’ palette. Cyclamen has good overall stability except in extremes of pH. It has good tenacity and substantivity and represents very good value for money in new creations.
Givaudan
Cyclamen Aldehyde Extra
Odor: Floral, Green, Powerful
Use: Cyclamen Aldehyde Extra can be used in many floral, green, fresh and marine accords. Its stability and substantivity are especially useful for functional perfumery.
Indukern F&F
CYCLAMEN ALDEHYDE
Odor: FLORAL, SWEET
Inoue Perfumery
CYCLAMEN ALDEHYDE
Jiangyin Healthway
Cyclamen Aldehyde
New functional food ingredients
Kun Shan P&A
Cyclamen Aldehyde
Lluch Essence
CYCLAMEN ALDEHYDE
M&U International
Cyclamen Aldehyde
Moellhausen
CYCLAMEN ALDEHYDE
OQEMA
Cyclamen Aldehyde
Pell Wall Perfumes
Cyclamen Aldehyde
Odor: floral-cyclamen, fresh, Linden-blossom, green, rhubarb
Use: Arctander describes it as “Diffusive and powerful floral-green, floral-stem like odor with pronounced vegetable Cucumber-Melon-like notes. Overall resembling the odor of Lindenblossom. Extensively used in perfumery for floral effects, fresh-green-floral topnotes (of lasting fragrance), Useful in Lilac, Lily, Peony, Magnolia, Orangeblossom, Alpine Violet, etc. Blends well with the Ionones and all Rose notes.”
Penta International
CYCLAMEN ALDEHYDE
Perfumer Supply House
Cyclamen Aldehyde
Odor: powerful floral green, marine-like
PerfumersWorld
Cyclamen Aldehyde
Odor: cyclamen fresh rhubarb musty green sweet floral aromatic cyclamen
Use: Blends-well-with - +Galbanum +Orris +Lime +Ivy Absolute +Ho
Perfumery Laboratory
CYCLAMENE ALDEHYDE (Cyclamen aldehyde)
Odor: Aroma of cyclamen colors, a little green, transparent, powerful with a thin shade of rhubarb
Phoenix Aromas & Essential Oils
Cyclamen Aldehyde
R C Treatt & Co Ltd
Cyclamen Aldehyde
Reincke & Fichtner
Cyclamen Aldehyde
Santa Cruz Biotechnology
For experimental / research use only.
2-Methyl-3-(p-isopropylphenyl)propionaldehyde
Sigma-Aldrich
2-Methyl-3-(p-isopropylphenyl)propionaldehyde, ≥95%, FCC, FG
Odor: vegetable; floral
Certified Food Grade Products
SRS Aromatics
CYCLAMEN ALDEHYDE
Stort Chemicals
Cyclamen Aldehyde
TCI AMERICA
For experimental / research use only.
3-(4-isopropylphenyl)isobutyraldehyde >92.0%(GC)
The Good Scents Company
cyclamen aldehyde
Odor: floral cyclamen fresh rhubarb musty green
The John D. Walsh Company
Cyclamen Aldehyde
The Lermond Company
CYCLAMEN ALDEHYDE
The Perfumers Apprentice
Cyclamen Aldehyde
Odor: Diffusive powerful floral green stem like
Vigon International
Cyclamen Aldehyde Extra
Odor: STRONG, FLOWERY ODOR WITH A LILY CHARACTER
Zanos
Cyclamen Aldehyde
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Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi N - Irritant, Dangerous for the environment.
R 38 - Irritating to skin.
R 51/53 - Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.
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.
S 61 - Avoid release to the environment. Refer to special instructions/safety data sheet.
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
Skin irritation (Category 2), H315
GHS Label elements, including precautionary statements
 
Pictogramexclamation-mark.jpg
 
Signal word Warning
Hazard statement(s)
H315 - Causes skin irritation
Precautionary statement(s)
P264 - Wash skin thouroughly after handling.
P280 - Wear protective gloves/protective clothing/eye protection/face protection.
P302 + P352 - IF ON SKIN: wash with plenty of soap and water.
P321 - Specific treatment (see supplemental first aid instructions on this label).
P332 + P313 - IF SKIN irritation occurs: Get medical advice/attention.
P362 - Take off contaminated clothing and wash before reuse.
Human Experience:
3 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50  3810 mg/kg
BEHAVIORAL: ATAXIA BEHAVIORAL: COMA SKIN AND APPENDAGES (SKIN): HAIR: OTHER
Food and Cosmetics Toxicology. Vol. 2, Pg. 327, 1964.

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) SKIN AND APPENDAGES (SKIN): HAIR: OTHER
National Technical Information Service. Vol. OTS0535055

Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: 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 and systemic toxicity
IFRA Purity Specification: < 1.5% free cyclamen alcohol
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
0.11 %
Category 2: Products applied to the axillae
0.14 %
Category 3: Products applied to the face/body using fingertips
0.038 %
Category 4: Products related to fine fragrance
0.95 %
 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
0.45 %
Category 5B: Face moisturizer products applied to the face using the hands (palms), primarily leave-on
0.076 %
Category 5C: Hand cream products applied to the hands using the hands (palms), primarily leave-on
0.076 %
Category 5D: Baby Creams, baby Oils and baby talc
0.025 %
Category 6: Products with oral and lip exposure
0.076 %
 Category 7: Products applied to the hair with some hand contact
Category 7A: Rinse-off products applied to the hair with some hand contact
0.076 %
Category 7B: Leave-on products applied to the hair with some hand contact
0.075 %
Category 8: Products with significant anogenital exposure
0.025 %
Category 9: Products with body and hand exposure, primarily rinse off
0.23 %
 Category 10: Household care products with mostly hand contact
Category 10A: Household care excluding aerosol products (excluding aerosol/spray products)
0.23 %
Category 10B: Household aerosol/spray products
0.72 %
 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
0.025 %
Category 11B: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate with potential UV exposure
0.025 %
Category 12: Products not intended for direct skin contact, minimal or insignificant transfer to skin
16.00 %
 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): 18.00 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 343.00 (μg/capita/day)
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: -1.20000
beverages(nonalcoholic): -0.30000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -0.45000
fruit ices: -0.45000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: -0.99000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: --
sugar substitutes: --
sweet sauces: --
Synonyms   Articles   Notes   Search   Top
Safety References:
European Food Safety Athority(EFSA): Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...
European Food Safety Authority (EFSA) reference(s):
Flavouring Group Evaluation 55 (FGE.55): Consideration of phenyl-substituted aliphatic alcohols and related aldehydes and esters evaluated by JECFA (63rd meeting) structurally related to phenethyl alcohol, aldehyde, esters and related phenylacetic acid esters evaluated by EFSA in FGE.14 (2005) and aryl-substituted saturated and unsaturated primary alcohol/aldehyde/acid/ester derivatives evaluated by EFSA in FGE.15 (2005) (Commission Regulation (EC) No 1565/2000 of 18 July 2000) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)
View page or View pdf
Safety and efficacy of aryl-substituted primary alcohol, aldehyde, acid, ester and acetal derivatives belonging to chemical group 22 when used as flavourings for all animal species
View page or View pdf
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 103-95-7
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 7687
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 2
 2-methyl-3-(4-propan-2-ylphenyl)propanal
Chemidplus: 0000103957
RTECS: MW4900000 for cas# 103-95-7
Synonyms   Articles   Notes   Search   Top
References:
Leffingwell: Chirality or Article
 2-methyl-3-(4-propan-2-ylphenyl)propanal
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 103-95-7
Pubchem (cid): 7687
Pubchem (sid): 134972568
Pherobase: View
Synonyms   Articles   Notes   Search   Top
Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS): View
CHEMBL: View
HMDB (The Human Metabolome Database): HMDB37763
FooDB: FDB019240
Export Tariff Code: 2912.19.5000
ChemSpider: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
No odor group found for these
 dihydrofarnesolFL/FR
 satinaldehydeFL/FR
acidic
 cyclohexyl acetic acidFL/FR
aldehydic
 citrus carbaldehydeFR
 dodecanal (aldehyde C-12 lauric)FL/FR
 muguet undecadienalFR
 nonanal (aldehyde C-9)FL/FR
10-undecenal (aldehyde C-11 undecylenic)FL/FR
animal
 costus valerolactoneFR
anisic
para-anisaldehydeFL/FR
 ocimum basilicum herb oilFL/FR
balsamic
isoamyl benzoateFL/FR
 amyris wood oilFL/FR
siam benzoin resinoidFL/FR
 benzyl benzoateFL/FR
 benzyl salicylateFL/FR
isobornyl acetateFL/FR
isobutyl cinnamateFL/FR
 cinnamyl alcoholFL/FR
 cinnamyl formateFL/FR
 clover nitrileFR
 ethyl cinnamateFL/FR
 fir needle oil siberiaFL/FR
 methyl cinnamateFL/FR
3-phenyl propyl alcoholFL/FR
berry
 raspberry ketone acetateFL/FR
chemical
 propyl propionateFL/FR
citrus
 citral dimethyl acetalFL/FR
(E)-4-decenalFL/FR
 grapefruit oil c.p. californiaFL/FR
 grapefruit pentanolFR
 lime oil distilled mexicoFL/FR
 methyl heptenoneFL/FR
blood orange oil italyFL/FR
sweet orange peel oil c.p. brazilFL/FR
 rhubafuranFR
 tangerine nitrileFR
earthy
(S)-1-octen-3-olFL/FR
ethereal
isovaleraldehyde propylene glycol acetalFL/FR
fatty
 coconut absoluteFL/FR
 decanolFL/FR
2-decenalFL/FR
 hexyl pivalateFR
floral
 amyl benzoateFL/FR
alpha-amyl cinnamaldehydeFL/FR
isoamyl salicylateFL/FR
 anisyl propanal / methyl anthranilate schiff's baseFR
 benzyl alcoholFL/FR
alpha-butyl cinnamaldehydeFL/FR
 cananga oilFL/FR
 cassie absoluteFL/FR
 citronellolFL/FR
 citronellyl acetateFL/FR
 citronellyl propionateFL/FR
 coriander seed oilFL/FR
 cumin carbinolFR
 cuminyl acetaldehydeFL/FR
 cyclamen fragranceFR
 cyclamen propanalFR
 cyclamen specialtyFR
4-cyclohexyl cyclohexanoneFR
 cyclohexyl ethyl alcoholFL/FR
alpha-damasconeFL/FR
9-decen-1-olFL/FR
 dihydrojasmoneFL/FR
 dimethyl anthranilateFL/FR
 dimethyl benzyl carbinolFL/FR
 dimethyl benzyl carbinyl acetateFL/FR
 dimethyl benzyl carbinyl butyrateFL/FR
6,8-dimethyl-2-nonanolFR
 ethyl 2-benzyl butyrateFL/FR
 ethyl phenyl acetateFL/FR
 farnesyl acetateFL/FR
 floral butanalFR
 floral pyranolFR
 floral specialtyFR
 gardenia oxideFR
 geraniolFL/FR
 geranium oil bourbonFL/FR
 geranyl acetoneFL/FR
 geranyl isobutyrateFL/FR
 heliotropinFL/FR
 heliotropyl acetoneFL/FR
 heliotropyl diethyl acetalFR
(Z)-3-hexen-1-yl salicylateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 ho leaf oilFR
 hyacinth acetalsFL/FR
 hyacinth etherFR
 hydroxycitronellalFL/FR
 hydroxycitronellal diethyl acetalFL/FR
 jasmin cyclopentanolFR
 jonquil absoluteFR
 leerallFR
 lilyallFR
laevo-linaloolFL/FR
 linalool oxideFL/FR
 magnolia decadienalFR
 methyl dihydrojasmonateFL/FR
 mimosa absolute franceFL/FR
 muguet carboxaldehydeFR
 muguet octadienolFR
 nerolFL/FR
 neroli oil bigardeFL/FR
 nerolidolFL/FR
 nonanolFL/FR
(R)-ocean propanal 
 ocean propanalFL/FR
 ocean propanal / methyl anthranilate schiff's baseFR
beta-ocimeneFL/FR
(Z)-beta-ocimeneFL/FR
 orange leaf absoluteFL/FR
bitter orangeflower water absoluteFL/FR
 orris pyridine 25% IPMFR
 orris rhizome absolute (iris pallida)FL/FR
 papaya isobutyrateFL/FR
 peony alcoholFR
 petitgrain oil paraguayFL/FR
 phenethyl acetateFL/FR
 phenethyl alcoholFL/FR
 phenethyl butyrateFL/FR
 phenyl acetaldehyde diisobutyl acetalFL/FR
2-phenyl propionaldehyde ethylene glycol acetalFR
 rose butanoateFL/FR
 styralyl formateFL/FR
 terpinyl isobutyrateFL/FR
 tetrahydrolinaloolFL/FR
 verdyl acetateFR
fresh
10-undecen-1-yl acetateFL/FR
fruity
 allyl amyl glycolateFR
 allyl butyrateFL/FR
 allyl cyclohexyl propionateFL/FR
 benzyl isovalerateFL/FR
 benzyl methyl etherFL/FR
isobutyl hexanoateFL/FR
beta-damasconeFL/FR
gamma-decalactoneFL/FR
1,8-dimethoxy-para-menthane 
 dimethyl succinateFL/FR
 ethyl levulinateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
 green acetateFR
 peach pivalateFR
 propyl hexanoateFL/FR
 rhubarb pyranFR
 rhubarb undecaneFR
 strawberry glycidate 1 (aldehyde C-16 (so-called))FL/FR
 tetrahydrofurfuryl butyrateFL/FR
gamma-undecalactone (aldehyde C-14 (so-called))FL/FR
green
isoamyl 3-(2-furan) propionateFL/FR
isobutyl benzyl carbinolFL/FR
 chrysanthemum oxideFL/FR
 cortex pyridineFL/FR
 decanal propylene glycol acetalFL/FR
 earthy acetalFL/FR
 galbanum oilFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
 hexyl 2-methyl butyrateFL/FR
 hexyl hexanoateFL/FR
 hyacinth absoluteFL/FR
 ivy carbaldehyde / methyl anthranilate schiff's baseFR
 ivy dioxolaneFR
(Z)-leaf acetalFL/FR
 melon nonenoateFL/FR
 methyl cyclocitrone (IFF)FR
 methyl heptine carbonateFL/FR
para-methyl hydratropaldehydeFL/FR
 methyl octine carbonateFL/FR
4-methyl-4-phenyl pentanoneFR
 octanal dimethyl acetalFL/FR
(Z)-5-octen-1-olFL/FR
 octyl oxyacetaldehydeFR
 phenyl acetaldehydeFL/FR
 styralyl acetateFL/FR
hay
 beeswax absoluteFL/FR
herbal
 carum carvi fruit oilFL/FR
 clary sage absoluteFL/FR
 clary sage oil franceFL/FR
2-cyclohexyl cyclohexanoneFR
 daucus carota fruit oilFL/FR
 lavender absolute bulgariaFL/FR
 linalyl octanoateFL/FR
marine
 marine hexaneFR
 marine pyridineFR
melon
 melon heptenalFL/FR
 watermelon ketoneFR
mossy
 veramoss (IFF)FR
2,3,5-trimethyl pyrazineFL/FR
powdery
para-anisyl alcoholFL/FR
 midnight passion fragranceFR
spicy
 benzyl isoeugenolFL/FR
 cassia bark oil chinaFL/FR
 cuminaldehydeFL/FR
black currant bud absoluteFL/FR
isoeugenyl acetateFL/FR
sulfurous
 buchu mercaptanFL/FR
terpenic
 frankincense oilFL/FR
gamma-terpineneFL/FR
alpha-terpineolFL/FR
tonka
 tonka bean absoluteFR
vanilla
 ethyl vanillinFL/FR
 vanilla bean absolute (vanilla planifolia)FL/FR
 vanillyl acetateFL/FR
waxy
3-decanoneFL/FR
 decyl acetateFL/FR
1-dodecanolFL/FR
 ethyl laurateFL/FR
 heptyl octanoateFL/FR
 octyl 2-methyl butyrateFL/FR
1-undecanolFL/FR
woody
 cedryl methyl etherFR
 patchouli ethanoneFR
 rhubarb oxiraneFR
 santallFR
 woody acetateFR
 
For Flavor
 
No flavor group found for these
 amyl benzoateFL/FR
 cyclohexyl methyl pyrazineFL
 decanal propylene glycol acetalFL/FR
3-decanoneFL/FR
 dihydrofarnesolFL/FR
 earthy acetalFL/FR
 ethyl 2-benzyl butyrateFL/FR
 hyacinth absoluteFL/FR
(R)-ocean propanal 
(S)-1-octen-3-olFL/FR
3-propyl pyridineFL
 styralyl formateFL/FR
 terpinyl isobutyrateFL/FR
isoamyl 3-(2-furan) propionateFL/FR
alpha-butyl cinnamaldehydeFL/FR
beta-damasconeFL/FR
aldehydic
 nonanal (aldehyde C-9)FL/FR
1-undecanolFL/FR
amber
isobutyl benzyl carbinolFL/FR
aromatic
 hyacinth acetalsFL/FR
balsamic
siam benzoin resinoidFL/FR
 benzyl benzoateFL/FR
 benzyl salicylateFL/FR
isobutyl cinnamateFL/FR
 ethyl cinnamateFL/FR
 fir needle oil siberiaFL/FR
berry
 heliotropyl acetoneFL/FR
 raspberry ketone acetateFL/FR
brown
 beeswax absoluteFL/FR
cherry
 heliotropinFL/FR
citrus
 citral dimethyl acetalFL/FR
 grapefruit oil c.p. californiaFL/FR
 lime oil distilled mexicoFL/FR
laevo-linaloolFL/FR
 nerolFL/FR
blood orange oil italyFL/FR
sweet orange peel oil c.p. brazilFL/FR
alpha-terpineolFL/FR
cocoa
 butyraldehydeFL
creamy
para-anisaldehydeFL/FR
gamma-undecalactone (aldehyde C-14 (so-called))FL/FR
cucumber
2-ethyl octine carbonateFL
fatty
 coconut absoluteFL/FR
2-decenalFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
10-undecenal (aldehyde C-11 undecylenic)FL/FR
floral
 cananga oilFL/FR
 citronellolFL/FR
 citronellyl acetateFL/FR
 citronellyl propionateFL/FR
 dihydrojasmoneFL/FR
 dimethyl benzyl carbinyl acetateFL/FR
 dimethyl benzyl carbinyl butyrateFL/FR
 farnesyl acetateFL/FR
 geraniolFL/FR
 geranium oil bourbonFL/FR
 geranyl acetoneFL/FR
 geranyl isobutyrateFL/FR
 methyl dihydrojasmonateFL/FR
 neroli oil bigardeFL/FR
 ocean propanalFL/FR
 orange leaf absoluteFL/FR
bitter orangeflower water absoluteFL/FR
 phenethyl alcoholFL/FR
 satinaldehydeFL/FR
 tetrahydrolinaloolFL/FR
fruity
 allyl cyclohexyl propionateFL/FR
isoamyl benzoateFL/FR
para-anisyl alcoholFL/FR
 benzyl alcoholFL/FR
 benzyl isovalerateFL/FR
 benzyl methyl etherFL/FR
isobutyl hexanoateFL/FR
alpha-damasconeFL/FR
gamma-decalactoneFL/FR
 dimethyl anthranilateFL/FR
 dimethyl succinateFL/FR
 ethyl levulinateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
2,4-hexadien-1-olFL
 hexyl hexanoateFL/FR
 linalyl octanoateFL/FR
(Z)-3-nonen-1-yl acetateFL
 phenethyl butyrateFL/FR
 propyl hexanoateFL/FR
 rose butanoateFL/FR
 strawberry glycidate 1 (aldehyde C-16 (so-called))FL/FR
 styralyl acetateFL/FR
 tetrahydrofurfuryl butyrateFL/FR
isovaleraldehyde propylene glycol acetalFL/FR
greasy
10-undecen-1-yl acetateFL/FR
green
 allyl butyrateFL/FR
isoamyl salicylateFL/FR
 chrysanthemum oxideFL/FR
 cinnamyl alcoholFL/FR
 cortex pyridineFL/FR
 cuminyl acetaldehydeFL/FR
 cyclohexyl ethyl alcoholFL/FR
 galbanum oilFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
 hexyl 2-methyl butyrateFL/FR
(Z)-leaf acetalFL/FR
 linalool oxideFL/FR
 melon heptenalFL/FR
 melon nonenoateFL/FR
 methyl 2-undecynoateFL
 methyl heptenoneFL/FR
 methyl heptine carbonateFL/FR
para-methyl hydratropaldehydeFL/FR
 methyl octine carbonateFL/FR
3-(5-methyl-2-furyl) butanalFL
 nerolidolFL/FR
(Z)-beta-ocimeneFL/FR
beta-ocimeneFL/FR
 octanal dimethyl acetalFL/FR
(Z)-5-octen-1-olFL/FR
 papaya isobutyrateFL/FR
 phenyl acetaldehyde diisobutyl acetalFL/FR
herbal
 carum carvi fruit oilFL/FR
 clary sage absoluteFL/FR
 clary sage oil franceFL/FR
 coriander seed oilFL/FR
 daucus carota fruit oilFL/FR
 lavender absolute bulgariaFL/FR
 ocimum basilicum herb oilFL/FR
 petitgrain oil paraguayFL/FR
honey
 ethyl phenyl acetateFL/FR
 phenethyl acetateFL/FR
 phenyl acetaldehydeFL/FR
medicinal
 dimethyl benzyl carbinolFL/FR
melon
 hydroxycitronellal diethyl acetalFL/FR
musty
2,3,5-trimethyl pyrazineFL/FR
nutty
1,8-dimethoxy-para-menthane 
ripe
(E)-4-decenalFL/FR
soapy
 dodecanal (aldehyde C-12 lauric)FL/FR
1-dodecanolFL/FR
spicy
 benzyl isoeugenolFL/FR
 benzylidene acetoneFL
 cassia bark oil chinaFL/FR
 cassie absoluteFL/FR
 cinnamyl formateFL/FR
 cuminaldehydeFL/FR
black currant bud absoluteFL/FR
isoeugenyl acetateFL/FR
 methyl cinnamateFL/FR
3-phenyl propyl alcoholFL/FR
sulfurous
 buchu mercaptanFL/FR
sweet
 cyclohexyl acetic acidFL/FR
 orris rhizome absolute (iris pallida)FL/FR
terpenic
gamma-terpineneFL/FR
tropical
alpha-amyl cinnamaldehydeFL/FR
 propyl propionateFL/FR
vanilla
 ethyl vanillinFL/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
 heptyl octanoateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 hydroxycitronellalFL/FR
 mimosa absolute franceFL/FR
 nonanolFL/FR
 octyl 2-methyl butyrateFL/FR
woody
 amyris wood oilFL/FR
isobornyl acetateFL/FR
 frankincense oilFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 acaciaFR
 aimant 
 aldehydicFR
 alpine bouquetFR
 amberFR
 angel essenceFR
 appleFR
 apple blossomFR
 apple green appleFR
 cedarFR
 cherryFR
 cherry blossomFR
 citrusFR
 clean linenFR
 cloverFR
 coconut tropical coconutFR
 cortexFR
 crabapple blossomFR
 cucumberFR
 cyclamenFR
 diorissimo 
 earthFR
 fishFL
 floralFR
 florida breezeFR
 freesiaFR
 ginger white gingerFR
 grapefruitFR
 green leafFR
 greenhouseFR
 heatherFR
 heliotropeFR
 herbalFR
 hyacinthFR
 hydrangeaFR
 jasminFR
 jonquilFR
 joy 
 kiwiFR
 lilacFR
 lilyFR
 lily of the valleyFR
 limeFR
 lux beauty shower soap 
 melonFR
 mintFR
 nutmegFR
 ocean seaFR
 sea breezeFR
 orchidFR
 orrisFR
 potpourriFR
 powderFR
 rainFR
 rhubarbFR
 roseFR
 rose white roseFR
 sea breezeFR
 spring rainFR
 strawberryFR
 sweet grassFR
 tropicalFL
 violetFR
 vol de nuit 
 watery 
 woodyFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 not found in nature
Synonyms   Articles   Notes   Search   Top
Synonyms:
 benzenepropanal, a-methyl-4-(1-methylethyl)-
3-p-cumenyl-2-methyl propionaldehyde
3-para-cumenyl-2-methyl propionaldehyde
3-p-cumenyl-2-methylpropionaldehyde
3-para-cumenyl-2-methylpropionaldehyde
3-(p-cumenyl)-2-methylpropionaldehyde
 cyclamen aldehyde extra
 cyclamen aldehyde FCC
 cyclemen aldehyde
2-methyl-3-(4-propan-2-ylphenyl)propanal
2-methyl-3-(p-isopropyl phenyl) propionaldehyde
2-methyl-3-(p-isopropylphenyl)propionaldehyde
2-methyl-3-(para-isopropyl phenyl) propionaldehyde
2-methyl-3-(para-isopropylphenyl)propionaldehyde
2-methyl-3-[4-(propan-2-yl)phenyl]propanal
alpha-methyl-4-(1-methyl ethyl) benzene propanal
a-methyl-4-(1-methylethyl)benzenepropanal
alpha-methyl-4-(1-methylethyl)benzenepropanal
alpha-methyl-p-isopropyl hydrocinnamaldehyde
alpha-methyl-p-isopropylhydrocinnamaldehyde
alpha-methyl-p-isopropylphenylpropyl aldehyde
alpha-methyl-para-isopropyl hydrocinnamaldehyde
alpha-methyl-para-isopropyl phenyl propyl aldehyde
3-(4-propan-2-ylphenyl)butanal
isopropyl methyl hydrocinnamaldehyde
3-(4-isopropyl phenyl)-2-methyl propanal
4-isopropyl-a-methylhydrocinnamaldehyde
para-isopropyl-alpha-methyl hydrocinnamaldehyde
4-isopropyl-alpha-methyl hydrocinnamic aldehyde
p-isopropyl-alpha-methyl hydrocinnamic aldehyde
para-isopropyl-alpha-methyl hydrocinnamic aldehyde
p-isopropyl-alpha-methylhydrocinnamaldehyde
3-(4-isopropylphenyl)-2-methylpropanal
3-(4-isopropylphenyl)-2-methylpropionaldehyde
3-(p-isopropylphenyl)-2-methylpropionaldehyde
Synonyms   Articles   Notes   Search   Top
Synonyms   Articles   Notes   Search   Top
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