(S)-campholene acetate
(S)-trimenal acetate (IFF)
 
Notes:
Flavouring ingredient. Constit. of Juniperus communis (juniper)
  • BOC Sciences
    • BOC Sciences
      Best of Chemicals Supplier
      Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
      BOC Sciences provides a wide range of services to support the pharmaceutical industry through all stages of drug discovery including Custom Synthesis of those chemicals that are not in stock, Isotope Labeling Service, Chiral Synthesis and Resolution, Bioconjugation, PEGylation services, analytical services.
      BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies.
      Email: Marketing
      US Email: Marketing
      Email: Sales
      US Email: Sales
      Voice: 1-631-485-4226
      Fax: 1-631-614-7828
      US Voice: 1-631-485-4226
      US Fax: 1-631-614-7828
      Europe44-203-286-1088
      Facebook
      Twitter
      Linkedin
      Blog
      Get the App!
      Product(s):
      36789-59-0 (S)-2,2,3-trimethylcyclopent-3-ene-1-ethyl acetate
       
  • 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):
      03-03500 CAMPHOLENE ACETATE
       
Synonyms   Articles   Notes   Search
CAS Number: 36789-59-0Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 253-212-2
FDA UNII: 450PNS9Q6I
Nikkaji Web: J332.359E
XlogP3-AA: 2.70 (est)
Molecular Weight: 196.28980000
Formula: C12 H20 O2
NMR Predictor: Predict (works with chrome or firefox)
EFSA/JECFA Comments: JECFA evaluated campholene acetate (CASrn as in Register). CASrn in Register refers to the (S)-enantiomer. Commercial product (S)-enantiomer (EFFA, 2010a). Synonym (-)-campholenyl acetate (EFFA, 2010a). Register name to be changed to (-)-campholenyl acetate or (S)-campholenyl acetate. (EFFA, 2010a)
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: 969  (S)-campholene acetate
DG SANTE Food Flavourings: 09.289  (S)-campholene acetate
FEMA Number: 3657 (S)-campholene acetate
FDA:No longer provide for the use of these seven synthetic flavoring substances
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: colorless to pale yellow clear liquid (est)
Assay: 98.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 0.80200 to 0.82200 @  20.00 °C.
Pounds per Gallon - (est).: 6.681 to  6.848
Specific Gravity: 0.94300 to 0.94900 @  25.00 °C.
Pounds per Gallon - est.: 7.847 to 7.897
Refractive Index: 1.36000 to 1.37000 @  20.00 °C.
Refractive Index: 1.45300 to 1.46000 @  20.00 °C.
Boiling Point: 226.00 to  227.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.059000 mmHg @ 25.00 °C. (est)
Flash Point: 62.00 °F. TCC ( 16.67 °C. )
logP (o/w): 3.944 (est)
Shelf Life: 12.00 month(s) or longer if stored properly.
Storage: refrigerate in tightly sealed containers.
Soluble in:
 alcohol
 water, 9.035 mg/L @ 25 °C (est)
Insoluble in:
 water
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: herbal
 
 lavender  floral  berry  woody  
Odor Description:
at 100.00 %. 
sweet fresh lavender, floral, berry note with fine woody undertone
 
 
Flavor Type: jammy
 
 jammy  raspberry  fruity  
Taste Description:
jammy raspberry
 
Odor and/or flavor descriptions from others (if found).
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
None found
Synonyms   Articles   Notes   Search   Top
Suppliers:
BOC Sciences
For experimental / research use only.
(S)-2,2,3-trimethylcyclopent-3-ene-1-ethyl acetate
Organica Aromatics
NATURANATE
NLT 90%(sum of isomers)
Odor: Sweet fresh lavender, floral, Berry note with fine woody undertone
Use: Can be used to create floral, lavender, woody, fresh and fruity fragrances. Improves the Organoleptic properties of tobacco products
Parchem
campholene acetate
Penta International
CAMPHOLENE ACETATE
Synonyms   Articles   Notes   Search   Top
Safety Information:
 
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:
gavage-rat LD50  [sex: M,F] 4640 - 5270 mg/kg
The study is considered valid.
(Piccirillo et al., 1979)

gavage-rat LD50  [sex: F] 3000 mg/kg
(Piccirillo et al., 1979)

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: flavor and fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for (S)-campholene acetate usage levels up to:
  0.5000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.061 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): ND (μg/capita/day)
Threshold of Concern:1800 (μg/person/day)
Structure Class: I
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 13
Click here to view publication 13
 average usual ppmaverage maximum ppm
baked goods: --
beverages(nonalcoholic): -3.00000
beverages(alcoholic): -3.00000
breakfast cereal: --
cheese: --
chewing gum: -3.00000
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: --
fruit ices: --
gelatins / puddings: -3.00000
granulated sugar: --
gravies: --
hard candy: -3.00000
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: -3.00000
soups: --
sugar substitutes: --
sweet sauces: --
 
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): --
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:
Flavor & Extract Manufacturers Association (FEMA) reference(s):
The FEMA GRAS assessment of alicyclic substances used as flavor ingredients. View pdf
European Food Safety Athority(EFSA): Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...
European Food Safety Authority (EFSA) reference(s):
Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to Flavouring Group Evaluation 12 (FGE.12); Primary saturated or unsaturated alicyclic alcohol, aldehyde, and esters from chemical group 7 (Commission Regulation (EC) No 1565/2000 of 18 July 2000)
View page or View pdf
Primary saturated or unsaturated alicyclic alcohol, aldehyde, and esters from chemical group 7 - Flavouring Group Evaluation 12, Revision 1 - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)
View page or View pdf
Flavouring Group Evaluation 73, (FGE.73)[1] - Consideration of alicyclic primary alcohols, aldehydes, acids and related esters evaluated by JECFA (59th meeting) structurally related to primary saturated or unsaturated alicyclic alcohol, aldehyde and esters evaluated by EFSA in FGE.12 (2005) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 73, Revision 1 (FGE.73Rev1): Consideration of alicyclic primary alcohols, aldehydes, acids and related esters evaluated by JECFA (59th meeting) structurally related to primary saturated or unsaturated alicyclic alcohol, aldehyde, and esters evaluated by EFSA in FGE.12Rev2 (2011)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 73, Revision 2 (FGE.73Rev2): Consideration of alicyclic primary alcohols, aldehydes, acids and related esters evaluated by JECFA (59th meeting) structurally related to primary saturated or unsaturated alicyclic alcohols, aldehydes, acids and esters evaluated by EFSA in FGE.12Rev3 (2012)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 73, Revision 3 (FGE.73Rev3): Consideration of alicyclic alcohols, aldehydes, acids and related esters evaluated by JECFA (59th and 63rd meeting) structurally related to primary saturated or unsaturated alicyclic alcohols, aldehydes, acids and esters evaluated by EFSA in FGE.12Rev4 (2013)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 73, Revision 4 (FGE.73Rev4): consideration of alicyclic alcohols, aldehydes, acids and related esters evaluated by JECFA (59th and 63rd meeting) structurally related to primary saturated or unsaturated alicyclic alcohols, aldehydes, acids and esters evaluated by EFSA in FGE.12Rev5
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 73, Revision 5 (FGE.73Rev5): consideration of alicyclic alcohols, aldehydes, acids and related esters evaluated by JECFA (59th, 63rd and 86th meeting) and structurally related to substances evaluated in FGE.12Rev5
View page or View pdf
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 21149427
National Institute of Allergy and Infectious Diseases: Data
 2-[(1S)-2,2,3-trimethylcyclopent-3-en-1-yl]ethyl acetate
Chemidplus: 0036789590
Synonyms   Articles   Notes   Search   Top
References:
 2-[(1S)-2,2,3-trimethylcyclopent-3-en-1-yl]ethyl acetate
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 36789-59-0
Pubchem (cid): 21149427
Pubchem (sid): 135213768
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): HMDB32193
FooDB: FDB014897
Export Tariff Code: 2915.39.9050
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
anisic
anisic
para-anisyl propanalFR
balsamic
 conifer acetateFR
 fir balsam absolute replacerFL/FR
 fir balsam concreteFR
berry
sec-butyl ethyl etherFL/FR
 raspberry ketoneFL/FR
 raspberry ketone acetateFL/FR
 raspberry ketone methyl etherFL/FR
citrus
 myrcenyl acetateFL/FR
earthy
 orris specialtyFR
floral
 cyclohexyl ethyl acetateFL/FR
beta-damascenoneFL/FR
 dihydro-alpha-iononeFL/FR
 ethyl ortho-anisateFL/FR
 heliotropyl acetoneFL/FR
 hibiscus sabdariffa flower extractFL/FR
 hyacinth etherFR
beta-ionyl acetateFL/FR
beta-ironeFL/FR
alpha-ironeFL/FR
 jasmopyrane (Givaudan)FR
 linaloe wood oil mexicoFL/FR
 myrcenolFL/FR
beta-naphthyl anthranilateFL/FR
 orris fragranceFR
 orris rhizome absolute (iris germanica)FL/FR
 orris rhizome absolute (iris pallida)FL/FR
 orris rhizome absolute replacerFR
 orris rhizome oil (iris germanica)FL/FR
 rose carboxylateFR
 terpinyl formateFL/FR
 tetrahydroionyl acetateFR
fruity
isoamyl isovalerateFL/FR
red apple fragranceFR
3-benzyl-4-heptanoneFL/FR
 berry hexanoateFR
 butyl 2-naphthyl etherFL/FR
isobutyl anthranilateFL/FR
isobutyl isovalerateFL/FR
 butyl valerateFL/FR
(E)-beta-damasconeFL/FR
 dihydroactinidolideFL/FR
 ethyl para-methyl-beta-phenyl glycidateFR
(E)-ethyl tiglateFL/FR
 geranyl butyrateFL/FR
beta-ionone epoxideFL/FR
 neryl isobutyrateFL/FR
 octyl propionateFL/FR
3-phenyl propyl isovalerateFL/FR
 propyl acetateFL/FR
 prune glycidateFR
4-(para-tolyl)-2-butanoneFL/FR
herbal
 geranium cyclohexaneFR
 herbal undecanoneFR
 terpineol acetateFL/FR
sulfurous
 mango thiolFL/FR
waxy
 orris rhizome oil CO2 extractFL/FR
 
For Flavor
 
No flavor group found for these
 butyl 2-naphthyl etherFL/FR
sec-butyl ethyl etherFL/FR
 dihydroactinidolideFL/FR
 ethyl ortho-anisateFL/FR
beta-ionone epoxideFL/FR
 linaloe wood oil mexicoFL/FR
 myrcenolFL/FR
3-phenyl propyl isovalerateFL/FR
 terpineol acetateFL/FR
balsamic
 fir balsam absolute replacerFL/FR
berry
 blackberry raspberry flavorFL
 dihydro-alpha-iononeFL/FR
 heliotropyl acetoneFL/FR
 hibiscus sabdariffa flower extractFL/FR
 prunus spinosa extractFL
 raspberry ketoneFL/FR
 raspberry ketone acetateFL/FR
 raspberry ketone methyl etherFL/FR
 sloeberry flavorFL
citrus
 myrcenyl acetateFL/FR
estery
 octyl propionateFL/FR
 propyl acetateFL/FR
beta-ironeFL/FR
 orris rhizome oil (iris germanica)FL/FR
fruity
 apple raspberry flavorFL
3-benzyl-4-heptanoneFL/FR
 brambleberry flavorFL
isobutyl anthranilateFL/FR
 butyl valerateFL/FR
(E)-beta-damasconeFL/FR
(E)-ethyl tiglateFL/FR
 geranyl butyrateFL/FR
beta-naphthyl anthranilateFL/FR
 neryl isobutyrateFL/FR
 terpinyl formateFL/FR
4-(para-tolyl)-2-butanoneFL/FR
green
isoamyl isovalerateFL/FR
isobutyl isovalerateFL/FR
 cyclohexyl ethyl acetateFL/FR
sulfurous
 mango thiolFL/FR
sweet
 orris rhizome absolute (iris germanica)FL/FR
 orris rhizome absolute (iris pallida)FL/FR
woody
beta-damascenoneFL/FR
beta-ionyl acetateFL/FR
alpha-ironeFL/FR
 orris rhizome oil CO2 extractFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 berryFR
 raspberryFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 juniper
Search Trop  Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
3-cyclopentene-1-ethanol, 2,2,3-trimethyl-, acetate, (S)-
(S)-trimenal acetate (IFF)
(S)-2,2,3-trimethyl cyclopent-3-ene-1-ethyl acetate
2-[(1S)-2,2,3-trimethylcyclopent-3-en-1-yl]ethyl acetate
(S)-2,2,3-trimethylcyclopent-3-ene-1-ethyl acetate
Synonyms   Articles   Notes   Search   Top
Synonyms   Articles   Notes   Search   Top
Please share your Comments.
Email Address:
 
 
 
 
Top of Page Home
Copyright © 1980-2021 Perflavory ™ Disclaimer Privacy Policy