phenethyl tiglate
phenethyl 2-methylcrotonate
 
Notes:
Fixer blender in floral and herbal types. Flavouring ingredient
  • Alfrebro
    • Alfrebro LLC/ Archer Daniels Midland Company
      Let's get reacquainted
      Building great taste with aroma chemicals, extracts, and distillates
      The Alfrebro brand was established in the early 1900s by Alex Fries & Brothers, a Cincinnati Flavor Company. In 1980, the brand was re-launched as an aroma chemical manufacturer. Since its inception, Alfrebro’s primary focus has been to provide quality natural and high value synthetic chemicals.
      Email: Sarah Forbis
      Email: Sales
      Voice: 513-539-3021
      Fax: 513-539-7372
      US Voice: 513-539-7373
      Newsroom
      Product(s):
      PHENETHYL TIGLATE NATURAL
       
  • Bedoukian Research
  • 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):
      55719-85-2 PHENETHYL TIGLATE 98.0%
       
  • 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):
      PHENYL ETHYL TIGLATE
       
  • 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):
      16-36800 PHENYLETHYL TIGLATE
       
  • 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):
      PHENYLETHYL TIGLATE (> 98%)
       
  • Sigma-Aldrich
  • Synerzine
    • Synerzine, Inc.
      Innovation. Customization. Aroma Ingredients.
      Synerzine is a leading supplier of flavor and fragrance ingredients.
      Synerzine expresses what we have grown to embody as an organization - the synergy and connection between raw ingredients, science, technology, and the final product. Our experienced team is passionate about bringing our customers high-quality innovative ingredients that they can trust.
      Building upon our 44 year history, the Synerzine team provides customers around the globe with convenient access to over 1200 high-quality aroma ingredients. We actively engage with customers to add a wide array of new products and services on a regular basis. Our aim is to delight every customer with our exceptional services, large product selection, customization and the highest quality and safety standards. We provide our customers with true value designed to help them bring their products to market faster.
      US Email: Customer Service
      US Email: Sales
      US Voice: (404) 524-6744
      US Fax: (404) 577-1651
      Inquiry
      Products List: View
      Product(s):
      W1655 Phenethyl Tiglate
       
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas
CAS Number: 55719-85-2Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 259-774-5
FDA UNII: 121LO7146V
Nikkaji Web: J60.242F
Beilstein Number: 2523411
MDL: MFCD00036576
CoE Number: 2186
XlogP3-AA: 3.30 (est)
Molecular Weight: 204.26892000
Formula: C13 H16 O2
NMR Predictor: Predict (works with chrome, Edge or firefox)
Category: flavor and fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
JECFA Food Flavoring: 997  phenethyl tiglate
DG SANTE Food Flavourings: 09.496  phenethyl 2-methylcrotonate
FEMA Number: 2870 phenethyl tiglate
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):55719-85-2 ; PHENETHYL TIGLATE
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 clear oily liquid (est)
Assay: 96.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 1.01000 to 1.01700 @  25.00 °C.
Pounds per Gallon - (est).: 8.404 to  8.462
Refractive Index: 1.51000 to 1.51600 @  20.00 °C.
Boiling Point: 139.00 to  140.00 °C. @ 7.00 mm Hg
Boiling Point: 259.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.001000 mmHg @ 25.00 °C. (est)
Flash Point: 215.00 °F. TCC ( 101.67 °C. )
logP (o/w): 3.540 (est)
Soluble in:
 alcohol
 water, slightly
 water, 19.95 mg/L @ 25 °C (est)
Similar Items: note
allyl tiglate
amyl tiglate
isoamyl tiglate
benzyl methyl tiglate
benzyl tiglate
butyl tiglate
isobutyl tiglate
cinnamyl tiglate
(E)-citronellyl tiglate
(E)-ethyl tiglate
geranyl methyl tiglate
geranyl tiglate
(Z)-3-hexen-1-yl tiglate
hexyl tiglate
methyl tiglate
3-octyl tiglate
propyl tiglate
isopropyl tiglate
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: green
 
Odor Strength: medium
 
Substantivity: 240 hour(s) at 100.00 %
 
 green  sweet  rose  natural  oily  leafy  herbal  
Odor Description:
at 100.00 %. 
green sweet rose natural oily leaf herbal
Luebke, William tgsc, (1997)
 
 
Flavor Type: green
 
 sweet  green  leafy  cortex  rose  geranium  
Taste Description:
sweet green leafy cortex rose geranium
Luebke, William tgsc, (1997)
 
Odor and/or flavor descriptions from others (if found).
 
Bedoukian Research
PHENYL ETHYL TIGLATE ≥98.0%, Kosher
Odor Description: heavy rose note
Used in hyacinth compositions and for a fresh outdoors type fragrance.
Taste Description: Sweet, green, slightly rosy
Sweet, green notes for fruits, especially cherry, kiwi, and other fruits.
 
Alfrebro
PHENETHYL TIGLATE NATURAL
Odor Description: Floral, Leafy, Vegetable, Wine
 
Moellhausen
TIGLATO FENILETILE
Odor Description: aromatic floral, warm herbal, reminiscent of roses
Taste Description: rose note, slightly aromatic fruity
 
Tadimety Aromatics
Phenyl Ethyl Tiglate
Odor Description: Green Sweet rose natural oily leaf herbal
Taste Description: sweet, green, slightly rosy
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
Alfrebro
PHENETHYL TIGLATE NATURAL
Odor: Floral, Leafy, Vegetable, Wine
Bedoukian Research
PHENYL ETHYL TIGLATE, NO ANTIOXIDANT
≥98.0%, Special Order
Odor: heavy rose note
Use: Used in hyacinth compositions and for a fresh outdoors type fragrance.
Flavor: Sweet, green, slightly rosy
Sweet, green notes for fruits, especially cherry, kiwi, and other fruits.
Bedoukian Research
PHENYL ETHYL TIGLATE
≥98.0%, Kosher
Odor: heavy rose note
Use: Used in hyacinth compositions and for a fresh outdoors type fragrance.
Flavor: Sweet, green, slightly rosy
Sweet, green notes for fruits, especially cherry, kiwi, and other fruits.
BOC Sciences
For experimental / research use only.
PHENETHYL TIGLATE 98.0%
Ernesto Ventós
PHENYL ETHYL TIGLATE
Odor: PLEASANT, WARM, ROSE-LIKE
Flavor: SWEET, WINY
Indukern F&F
PHENYL ETHYL TIGLATE
Odor: SWEET, GREEN
Inoue Perfumery
PHENETHYL TIGLATE
Liaison Carbone
PHENYLETHYL TIGLATE N°426
Lluch Essence
PHENYL ETHYL TIGLATE
Moellhausen
TIGLATO FENILETILE
Odor: aromatic floral, warm herbal, reminiscent of roses
Flavor: rose note, slightly aromatic fruity
Organica Aromatics
PHENYL ETHYL TIGLATE
NLT 98%
PCW France
Phenyl Ethyl Tiglate
Steps to a fragranced product
Penta International
PHENYLETHYL TIGLATE
Prodasynth
PHENYLETHYL TIGLATE
(> 98%)
Odor: PLEASANT, WARM, ROSE-LIKE
Reincke & Fichtner
Phenethyl Tiglate
Sigma-Aldrich
Phenethyl tiglate, ≥95%, stabilized, FG
Odor: herbaceous; raspberry; rose; strawberry; green
Certified Food Grade Products
Synerzine
Phenethyl Tiglate
Tadimety Aromatics
Phenyl Ethyl Tiglate
Odor: Green Sweet rose natural oily leaf herbal
Synonyms   Articles   Notes   Search   Top
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 36/38 - Irritating to skin and eyes.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
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:
6 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50  > 5000 mg/kg
(Levenstein, 1974e)

oral-rat LD50  > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 13, Pg. 909, 1975.

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 13, Pg. 909, 1975.

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 phenethyl tiglate usage levels up to:
  6.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.24 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 1.00 (μg/capita/day)
Structure Class: I
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 3
Click here to view publication 3
 average usual ppmaverage maximum ppm
baked goods: -10.00000
beverages(nonalcoholic): 0.800000.90000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -4.30000
fruit ices: -4.30000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: -10.00000
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 phenethyl alcohol, aldehydes, acids, and related acetals and esters 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):
Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to: Flavouring Group Evaluation 14 (FGE.14): Phenethyl alcohol, aldehyde, esters, and related phenylacetic acid esters from chemical group 15 (Commission Regulation (EC) No 1565/2000 of 18 July 2000)
View page or View pdf
Flavouring Group Evaluation 53 (FGE.53): Consideration of phenethyl alcohol, aldehyde, acid and related acetals and esters evaluated by JECFA (59th meeting) structurally related to phenethyl alcohol, aldehyde, esters and related phenylacetic acid esters evaluated by EFSA in FGE.14 (2005) and one phenoxyethyl ester evaluated in FGE.23 (2006) (Commission Regulation (EC) No 1565/2000 of 18 July 2000) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)
View page or View pdf
Flavouring Group Evaluation 14, Revision 1 (FGE.14Rev1): Phenethyl alcohol, aldehyde, acetals, carboxylic acid and related esters from chemical group 15 and 22 [1] - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf
Flavouring Group Evaluation 53, Revision 1 (FGE.53Rev1): Consideration of phenethyl alcohol, aldehyde, acid and related acetals and esters evaluated by JECFA (59th meeting) FGE.23Rev1 (2008)
View page or View pdf
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 55719-85-2
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 5357002
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 2
 2-cyclohexylethyl (E)-2-methylbut-2-enoate
Chemidplus: 0055719852
RTECS: EM9255000 for cas# 55719-85-2
Synonyms   Articles   Notes   Search   Top
References:
 2-cyclohexylethyl (E)-2-methylbut-2-enoate
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 55719-85-2
Pubchem (cid): 5357002
Pubchem (sid): 135003326
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): HMDB37628
FooDB: FDB016742
Export Tariff Code: 2916.19.6000
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
 tea leaf oilCS
aldehydic
 undecenal mixture (aldehyde C-11 mixed)FL/FR
alliaceous
 dibutyl sulfideFL/FR
animal
 methyl (E)-2-octenoateFL/FR
balsamic
 benzophenoneFR
citrus
 bergamot oil bergaptene reduced italyFL/FR
 petitgrain combava oilFR
(E)-2-tetradecenalFL/FR
 valenceneFL/FR
coconut
delta-heptalactoneFL/FR
creamy
3-heptyl dihydro-5-methyl-2(3H)-furanoneFL/FR
dairy
 methyl butyl phenyl acetateFL/FR
earthy
1-octen-3-olFL/FR
ethereal
 ethyl formateFL/FR
(E)-2-octenalFL/FR
(Z)-2-octenal 
floral
 acetaldehyde dibutyl acetalFL/FR
 allyl anthranilateFL/FR
 citronellalFL/FR
 citronellolFL/FR
(R)-(+)-beta-citronellolFL/FR
laevo-citronellolFL/FR
 citronellyl acetateFL/FR
(E)-citronellyl tiglateFL/FR
isocyclodimethyl octanolFR
 cyclohexyl propanolFR
 cymbopogon validus leaf oilFR
gamma-damasconeFR
 dihydrorose oxideFR
 dimethyl benzyl carbinolFL/FR
 floral pyranFR
white frangipani concreteFR
 gardenia amideFR
 gardenia pentyl acetateFR
 geranium dihydropyranFR
 geranium nitrileFR
 geranium oil africaFL/FR
 geranium oil egyptFL/FR
 geranium pyranFR
 geranyl formateFL/FR
 geranyl hexanoateFL/FR
 geranyl nonanoateCS
 geranyl tiglateFL/FR
 glycoacetalFR
(Z)-3-hexen-1-yl salicylateFL/FR
 hydroxycitronellal dimethyl acetalFL/FR
southern magnolia leaf oil fractionsFR
(3-methoxy-2-methyl propyl) benzeneFR
 methyl citronellateFL/FR
(Z)-methyl epi-jasmonateFL/FR
 methyl jasmonateFL/FR
 muguet butanolFR
 muguet carbinolFL/FR
 musk acetateFR
 narcissus acetateFL/FR
 peony acetonitrileFR
 phenethyl acetateFL/FR
 phenethyl formateFL/FR
 phenethyl phenyl acetateFL/FR
 phenethyl pivalateFL/FR
 phenyl acetaldehyde digeranyl acetalFR
 phenyl propyl phenyl acetateFR
 rhodinyl propionateFL/FR
 rose butanoateFL/FR
laevo-rose oxideFL/FR
(Z)-rose oxideFL/FR
 rose pyranFR
 styralyl propionateFL/FR
fried
(E,Z)-2,4-decadienal 
fruity
isobutyl 2-butenoateFL/FR
isobutyl isovalerateFL/FR
 citronellyl isobutyrateFL/FR
 ethyl 3-hexenoateFL/FR
(E,E)-ethyl sorbateFL/FR
 geranyl acetoacetateFL/FR
(E)-2-hexen-1-olFL/FR
2-hexen-1-olFL/FR
 nerolidyl isobutyrateFR
 neryl isobutyrateFL/FR
 octyl butyrateFL/FR
 prenyl acetateFL/FR
isopropyl 2-methyl butyrateFL/FR
green
 acetaldehyde butyl phenethyl acetalFL/FR
 acetaldehyde di-(Z)-3-hexen-1-yl acetalFL/FR
 acetaldehyde dipropyl acetalFL/FR
 acetaldehyde ethyl phenethyl acetalFL/FR
 artichoke leaf 
 bark carbaldehydeFR
 benzhydrolFR
 biphenyl 
 coriander heptenolFL/FR
3,5,6-neocyclocitralFR
 diphenyl methaneFL/FR
 diphenyl oxideFL/FR
 galbanum oil terpenelessFL/FR
 geranium absoluteFL/FR
 geranium thiazoleFL/FR
1-hepten-3-olFL/FR
 heptyl cinnamateFL/FR
3-hexen-1-olFL/FR
(Z)-2-hexen-1-olFL/FR
(E)-2-hexen-1-yl acetateFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
(Z)-3-hexen-1-yl lactateFL/FR
(Z)-3-hexen-1-yl methyl carbonateFL/FR
(Z)-3-hexen-1-yl phenyl acetateFL/FR
(Z)-3-hexen-1-yl pyruvateFL/FR
(E)-2-hexenalFL/FR
3-hexenalFL/FR
 hexoxyacetaldehyde dimethyl acetalFR
 hexyl isobutyrateFL/FR
 hexyl tiglateFL/FR
2,4-ivy carbaldehydeFL/FR
(Z)-leaf acetalFL/FR
 leafy acetalFL/FR
 magnolia leaf oilFL/FR
 methyl heptine carbonateFL/FR
 methyl R-3-acetoxyhexanoate 
(E,Z)-2,6-nonadien-1-yl acetateFL/FR
 octanal dimethyl acetalFL/FR
(Z)-5-octen-1-yl propionateFL/FR
 phenethyl isopropyl etherFR
 phenethyl oxyacetaldehydeFR
3-phenyl propionaldehydeFL/FR
 privet dioxaneFR
isopropyl phenyl propionaldehydeFR
 rose leaf absolute (rosa centifolia)FL/FR
 styralyl acetateFL/FR
 violet decenolFR
 violet leaf absoluteFL/FR
 violet leaf absolute egyptFL/FR
 violet leaf oil (viola odorata)FL/FR
herbal
sweet basil absoluteFL/FR
 clary sage absoluteFL/FR
 geranium cyclohexaneFR
 herbal carbonateFR
 herbal heptaneFR
laevo-menthyl isobutyrate 
(E)-6-methyl-3-hepten-2-oneFL/FR
4,4,6-trimethyl-2-phenyl-1,3-dioxaneFR
honey
 methyl phenyl acetateFL/FR
leathery
 leather cyclohexanolFR
minty
 peppermint absoluteFL/FR
isopulegyl formateFL/FR
musty
ketoisophoroneFL/FR
pine
 plectranthus glandulosus hook f. leaf oil cameroonFR
spicy
 methyl heptadienoneFL/FR
tea
 camellia oleifera leaf extractFL/FR
waxy
 heptyl octanoateFL/FR
woody
(E)-ethyl geranateFR
 
For Flavor
 
No flavor group found for these
 acetaldehyde di-(Z)-3-hexen-1-yl acetalFL/FR
 acetaldehyde dibutyl acetalFL/FR
 allyl anthranilateFL/FR
(R)-(+)-beta-citronellolFL/FR
 coriander heptenolFL/FR
(E,Z)-2,4-decadienal 
 heptyl cinnamateFL/FR
3-hexen-1-olFL/FR
2-hexenalFL
(E)-2-hexenalFL
 magnolia leaf oilFL/FR
laevo-menthyl isobutyrate 
(E)-6-methyl-3-hepten-2-oneFL/FR
3-methyl-3-pentanolFL
(Z)-2-octenal 
isopulegyl formateFL/FR
 tiglyl alcoholFL
 undecenal mixture (aldehyde C-11 mixed)FL/FR
aromatic
 leafy acetalFL/FR
balsamic
 phenethyl pivalateFL/FR
citrus
 bergamot oil bergaptene reduced italyFL/FR
ketoisophoroneFL/FR
 styralyl propionateFL/FR
 valenceneFL/FR
dairy
 methyl butyl phenyl acetateFL/FR
ethereal
 ethyl formateFL/FR
fatty
(E,E)-2,4-heptadienalFL
(Z)-3-hexen-1-yl benzoateFL/FR
(E)-2-octenalFL/FR
floral
 biphenyl 
 citronellalFL/FR
 citronellolFL/FR
laevo-citronellolFL/FR
 citronellyl acetateFL/FR
 geranium oil africaFL/FR
 geranium oil egyptFL/FR
 geranyl tiglateFL/FR
 methyl citronellateFL/FR
(Z)-methyl epi-jasmonateFL/FR
 methyl jasmonateFL/FR
 methyl phenyl acetateFL/FR
 muguet carbinolFL/FR
laevo-rose oxideFL/FR
fruity
 citronellyl isobutyrateFL/FR
 ethyl 3-hexenoateFL/FR
 ethyl 3-oxohexanoateFL
(E,E)-ethyl sorbateFL/FR
 geranyl hexanoateFL/FR
3-heptyl dihydro-5-methyl-2(3H)-furanoneFL/FR
2-hexen-1-olFL/FR
 methyl (E)-2-octenoateFL/FR
 neryl isobutyrateFL/FR
 prenyl acetateFL/FR
isopropyl 2-methyl butyrateFL/FR
 rhodinyl propionateFL/FR
 rose butanoateFL/FR
 styralyl acetateFL/FR
green
 acetaldehyde butyl phenethyl acetalFL/FR
 acetaldehyde dipropyl acetalFL/FR
 acetaldehyde ethyl phenethyl acetalFL/FR
 artichoke leaf 
isobutyl 2-butenoateFL/FR
isobutyl isovalerateFL/FR
(E)-citronellyl tiglateFL/FR
 dibutyl sulfideFL/FR
 diphenyl methaneFL/FR
 diphenyl oxideFL/FR
2-ethyl-5-methyl thiopheneFL
 galbanum oil terpenelessFL/FR
 geranium absoluteFL/FR
 geranium thiazoleFL/FR
 geranyl formateFL/FR
1-hepten-3-olFL/FR
(E)-2-heptenalFL
(E)-2-hexen-1-olFL/FR
(Z)-2-hexen-1-olFL/FR
(E)-2-hexen-1-yl acetateFL/FR
(Z)-3-hexen-1-yl lactateFL/FR
(Z)-3-hexen-1-yl methyl carbonateFL/FR
(Z)-3-hexen-1-yl phenyl acetateFL/FR
(Z)-3-hexen-1-yl pyruvateFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
3-hexenalFL/FR
(E)-2-hexenalFL/FR
 hexyl isobutyrateFL/FR
 hexyl tiglateFL/FR
2,4-ivy carbaldehydeFL/FR
(Z)-leaf acetalFL/FR
 methyl heptadienoneFL/FR
 methyl heptine carbonateFL/FR
 methyl R-3-acetoxyhexanoate 
 narcissus acetateFL/FR
(E,Z)-2,6-nonadien-1-yl acetateFL/FR
 octanal dimethyl acetalFL/FR
(Z)-5-octen-1-yl propionateFL/FR
 phenethyl formateFL/FR
3-phenyl propionaldehydeFL/FR
 rose leaf absolute (rosa centifolia)FL/FR
(Z)-rose oxideFL/FR
 sorbyl acetateFL
 violet leaf absoluteFL/FR
 violet leaf absolute egyptFL/FR
 violet leaf oil (viola odorata)FL/FR
herbal
sweet basil absoluteFL/FR
 clary sage absoluteFL/FR
honey
 phenethyl acetateFL/FR
 phenethyl phenyl acetateFL/FR
lactonic
delta-heptalactoneFL/FR
medicinal
 dimethyl benzyl carbinolFL/FR
minty
 peppermint absoluteFL/FR
mushroom
 methional diethyl acetalFL
1-octen-3-olFL/FR
musty
 geranyl acetoacetateFL/FR
sweet
 acetone alcoholFL
tea
 camellia oleifera leaf extractFL/FR
waxy
 heptyl octanoateFL/FR
 hydroxycitronellal dimethyl acetalFL/FR
 octyl butyrateFL/FR
(E)-2-tetradecenalFL/FR
 
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Potential Uses:
 greenFR
 hyacinthFR
 modifier 
 nutFL
 fresh outdoorsFR
 raspberryFR
 roseFR
 strawberryFR
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Occurrence (nature, food, other): note
 champaca concrete @ 0.02%
Data  GC  Search Trop  Picture
 geranium leaf oil india @ 0.77%
Data  GC  Search Trop  Picture
 geranium oil africa @ 0.76%
Data  GC  Search Trop  Picture
 geranium oil bourbon @ 0.43%
Data  GC  Search Trop  Picture
 geranium oil bourbon @ 0.77%
Data  GC  Search Trop  Picture
 geranium oil china @ 0.6%
Data  GC  Search Trop  Picture
 geranium oil egypt @ 0.65%
Data  GC  Search Trop  Picture
 geranium oil moroccan @ 1.04%
Data  GC  Search Trop  Picture
 geranium oil rwanda @ 1.15%
Data  GC  Search Trop  Picture
 geranium petiole oil india @ 1.45%
Data  GC  Search Trop  Picture
 geranium stem oil india @ 1.09%
Data  GC  Search Trop  Picture
 hyacinthus orientalis absolute @ 0.02-0.05%
Data  GC  Search Trop  Picture
 tagete oil egypt @ 0.14%
Data  GC  Search Trop  Picture
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Synonyms:
 benzyl carbinyl tiglate
 benzylcarbinyl tiglate
2-butenoic acid, 2-methyl-, 2-phenylethyl ester, (2E)-
2-butenoic acid, 2-methyl-, 2-phenylethyl ester, (E)-
2-cyclohexylethyl (E)-2-methylbut-2-enoate
(E)-2-methyl-2-butenoic acid 2-phenethyl ester
(E)-2-methyl-2-butenoic acid 2-phenyl ethyl ester
 phenethyl 2-methyl crotonate
(E)-2-phenethyl 2-methyl-2-butenoate
 phenethyl 2-methylcrotonate
 phenethyl-alpha-methyl butenoate
 phenyl ethyl (2E)-2-methyl-2-butenoate
(E)-2-phenyl ethyl 2-methyl-2-butenoate
 phenyl ethyl tiglate
2-phenyl ethyl tiglate
 phenyl ethyl tiglate, no antioxidant
2-phenyl ethyl trans-2-methyl butenoate
2-phenyl ethyl trans-2,3-dimethyl acrylate
 phenyl ethyl-alpha-methyl butenoate
2-phenylethyl (2E)-2-methylbut-2-enoate
2-phenylethyl 2-methyl-2-butenoate, (E)-
2-phenylethyl trans-2-methylbutenoate
2-phenylethyl trans-2,3-dimethylacrylate
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Synonyms   Articles   Notes   Search   Top
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