beta-terpineol
p-menth-8-en-1-ol
 
Notes:
Flavouring ingredient Terpineol is a naturally occurring monoterpene alcohol that has been isolated from a variety of sources such as cajuput oil, pine oil, and petitgrain oil. There are three isomers, alpha-, beta-, and gamma-terpineol, the last two differing only by the location of the double bond. Terpineol is usually a mixture of these isomers with alpha-terpineol as the major constituent. (Wikipedia)
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      Product(s):
      138-87-4 beta-Terpineol
       
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    • Penta International Corporation
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      Product(s):
      20-07850 BETA-TERPINEOL
       
Synonyms   Articles   Notes   Search
CAS Number: 138-87-4Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 205-342-6
FDA UNII: XS86XKC2VT
Nikkaji Web: J5.638C
Beilstein Number: 2205072
CoE Number: 10254
XlogP3-AA: 2.50 (est)
Molecular Weight: 154.25266000
Formula: C10 H18 O
NMR Predictor: Predict (works with chrome 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: 374  p-menth-8-en-1-ol
DG SANTE Food Flavourings: 02.097  beta-terpineol
FEMA Number: 3564 p-menth-8-en-1-ol
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):138-87-4 ; BETA-TERPINEOL
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 liquid (est)
Assay: 96.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 0.93000 to 0.93600 @  25.00 °C.
Pounds per Gallon - (est).: 7.739 to  7.788
Refractive Index: 1.48200 to 1.48500 @  20.00 °C.
Melting Point: 32.00 to  33.00 °C. @ 760.00 mm Hg
Boiling Point: 209.00 to  210.00 °C. @ 760.00 mm Hg
Congealing Point: 24.00 °C.
Vapor Pressure: 0.034000 mmHg @ 25.00 °C. (est)
Flash Point: 189.00 °F. TCC ( 87.22 °C. )
logP (o/w): 2.837 (est)
Soluble in:
 alcohol
 oils
 water, 2200 mg/L @ 15 °C (exp)
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Organoleptic Properties:
 
Odor Type: woody
 
 pungent  earthy  woody  pungent  
Odor Description:
at 10.00 % in dipropylene glycol. 
pungent earthy woody
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
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Suppliers:
BOC Sciences
For experimental / research use only.
beta-Terpineol
DRT Terpenes
TERPINEOL OR
Beta Terpineol content (%) : 15 - 20
Penta International
BETA-TERPINEOL
Chemical Sources Association
Need This Item for Flavor/Food?: You can contact the CSA
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Safety Information:
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.
Oral/Parenteral Toxicity:
oral-rat LD50  4300 mg/kg
Reported for a mixture of alpha- and beta-terpineol.
(Moreno, 1971)

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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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
maximum skin levels for fine fragrances:
  0.0200 %  and are based on the assumption that the fragrance mixture is used at 20% in a consumer product (IFRA Use Level Survey).
Recommendation for beta-terpineol usage levels up to:
  3.0000 % in the fragrance concentrate.
use level in formulae for use in cosmetics:
  0.0200 %
Dermal Systemic Exposure in Cosmetic Products:
 0.0005 mg/kg/day
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 1.30 (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: 11
Click here to view publication 11
 average usual ppmaverage maximum ppm
baked goods: -47.50000
beverages(nonalcoholic): -14.60000
beverages(alcoholic): -10.00000
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -20.00000
fruit ices: --
gelatins / puddings: -20.00000
granulated sugar: --
gravies: --
hard candy: --
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: -10.00000
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: -37.50000
soups: --
sugar substitutes: --
sweet sauces: --
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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 18 (FGE.18): Aliphatic, alicyclic and aromatic saturated and unsaturated tertiary alcohols, aromatic tertiary alcohols and their esters from chemical group 6
View page or View pdf
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
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 138-87-4
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 8748
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 2
 1-methyl-4-prop-1-en-2-ylcyclohexan-1-ol
Chemidplus: 0000138874
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References:
 1-methyl-4-prop-1-en-2-ylcyclohexan-1-ol
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 138-87-4
Pubchem (cid): 8748
Pubchem (sid): 134974072
Flavornet: 138-87-4
Pherobase: View
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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
CHEBI: View
CHEMBL: View
KEGG (GenomeNet): C17517
HMDB (The Human Metabolome Database): HMDB36996
FooDB: FDB015970
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
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Potential Blenders and core components note
 
For Odor
balsamic
isobornyl formateFL/FR
isobornyl isobutyrateFL/FR
dextro-fenchoneFL/FR
 fir needle oil siberiaFL/FR
camphoreous
 fencholFL/FR
laevo-fenchoneFL/FR
citrus
(E+Z)-4,8-dimethyl-3,7-nonadien-2-yl acetateFL/FR
earthy
(-)-alpha-fencholFL/FR
 pogostemon cablin leaf extractFR
floral
 bois de rose oil terpenelessFL/FR
 dihydro-alpha-iononeFL/FR
 linalool oxideFL/FR
green
isocyclocitral (IFF)FL/FR
 fern absolute 
 galbanum absoluteFL/FR
 galbanum oilFL/FR
 lawsonia inermis leaf oil CO2 extractFR
 oakmoss oilFR
herbal
 arnica flower absoluteFR
 guava leaf oil cubaFR
6-hydroxydihydrotheaspirane (mixture of isomers)FL/FR
alpha-pineneFL/FR
mossy
 oakmoss absoluteFL/FR
spicy
4-carvomenthenolFL/FR
 ginger root oil chinaFL/FR
terpenic
 cypress leaf oilFR
tropical
 patchwoodFR
woody
 cyperus root oil (cyperus scariosus)FR
 cypriol oil (cyperus scariosus)FR
 dihydro-beta-iononeFL/FR
 dihydro-gamma-iononeFL/FR
3(or 2),4-dimethyl-5-vinyl octahydro-4,7-methanoinden-5-ol 
 dryopteris filix-mas oleoresinFR
 germacrene B 
 herbal norbornaneFR
5,5a,6,7,8,8a-hexahydro-6,6,7,8,8-pentamethyl-4H-indeno[5,4-D]isoxazole 
 octahydro-3(or 2),4-dimethyl-4,7-methanoinden-5-one 
 orris hexanoneFR
terpeneless patchouli oilFL/FR
 patchouli oil chinaFL/FR
 pelargonium radula oilFR
 pinacolFR
 pogostemon cablin leaf oilFR
3(or 2),4,5-trimethyl octahydro-4,7-methanoinden-5-olFR
3(or 2),4,5-trimethyl-3a,4,5,6,7,7a-hexahydro-4,7-methanoinden-5-ol 
1,3,5,7-undecatetraeneFL/FR
 vetiver oil CO2 extractFL/FR
 vetiver oil fractionsFR
 vetiver oil haitiFL/FR
 vetiveria zizanioides root oilFL/FR
 
For Flavor
 
No flavor group found for these
 dihydro-gamma-iononeFL/FR
(E+Z)-4,8-dimethyl-3,7-nonadien-2-yl acetateFL/FR
3(or 2),4-dimethyl-5-vinyl octahydro-4,7-methanoinden-5-ol 
 fern absolute 
 germacrene B 
5,5a,6,7,8,8a-hexahydro-6,6,7,8,8-pentamethyl-4H-indeno[5,4-D]isoxazole 
 octahydro-3(or 2),4-dimethyl-4,7-methanoinden-5-one 
3-propyl pyridineFL
3(or 2),4,5-trimethyl-3a,4,5,6,7,7a-hexahydro-4,7-methanoinden-5-ol 
1,3,5,7-undecatetraeneFL/FR
 vitispiraneFL
balsamic
isobornyl isobutyrateFL/FR
 fir needle oil siberiaFL/FR
berry
 dihydro-alpha-iononeFL/FR
camphoreous
(-)-alpha-fencholFL/FR
 fencholFL/FR
laevo-fenchoneFL/FR
6-hydroxydihydrotheaspirane (mixture of isomers)FL/FR
cooling
4-carvomenthenolFL/FR
dextro-fenchoneFL/FR
floral
 bois de rose oil terpenelessFL/FR
green
isocyclocitral (IFF)FL/FR
 galbanum absoluteFL/FR
 galbanum oilFL/FR
 linalool oxideFL/FR
 oakmoss absoluteFL/FR
spicy
 ginger root oil chinaFL/FR
 turmeric oleoresinFL
woody
isobornyl formateFL/FR
 dihydro-beta-iononeFL/FR
terpeneless patchouli oilFL/FR
 patchouli oil chinaFL/FR
alpha-pineneFL/FR
 vetiver oil CO2 extractFL/FR
 vetiver oil haitiFL/FR
 vetiveria zizanioides root oilFL/FR
 
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Potential Uses:
 earthFR
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Occurrence (nature, food, other): note
 boldo leaf oil italy @ 0.13%
Data  GC  Search Trop  Picture
 boldus leaf oil chile @ 0.07%
Data  GC  Search Trop  Picture
 cardamom seed oil
Search Trop  Picture
 cascarilla bark oil @ trace%
Data  GC  Search Trop  Picture
 clove oil
Search Trop  Picture
 cornmint oil india @ 0.01%
Data  GC  Search Trop  Picture
 dill plant
Search Trop  Picture
 dill seed
Search Trop  Picture
 lavandin oil china @ 0.45%
Data  GC  Search Trop  Picture
 lemongrass oil @ 0.17%
Data  GC  Search Trop  Picture
 lime fruit
Search Trop  Picture
 mace oil east india @ 0.32%
Data  GC  Search Trop  Picture
 mandarin fruit
Search Trop  Picture
 nutmeg flower oil @ 0.36%
Data  GC  Search Trop  Picture
 nutmeg leaf oil @ 0.00-0.21%
Data  GC  Search Trop  Picture
 nutmeg seed oil
Search Trop  Picture
 orange peel oil bitter china @ 0.02%
Data  GC  Search Trop  Picture
 oregano shoot
Search Trop  Picture
 pepper black pepper fruit oil
Search Trop  Picture
 pepper black pepper seed oil
Search Trop  Picture
 pine oils
Search  PMC Picture
 sage oil dalmatian @ 0.30%
Data  GC  Search Trop  Picture
 salvia sclarea oil @ 1.19%
Data  GC  Search Trop  Picture
 thyme oil
Search Trop  Picture
 thyme oil red CO2 extract @ 0.22%
Data  GC  Search Trop  Picture
 thyme plant
Search Trop  Picture
 wine
Search  PMC Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
 cyclohexanol, 1-methyl-4-(1-methylethenyl)-
p-menth-8-en-1-ol
para-menth-8-en-1-ol
1-methyl-4-(1-methyl ethenyl) cyclohexanol
1-methyl-4-(1-methyl vinyl) cyclohexan-1-ol
1-methyl-4-(1-methylethenyl)cyclohexanol
1-methyl-4-(1-methylvinyl)cyclohexan-1-ol
1-methyl-4-(prop-1-en-2-yl)cyclohexanol
1-methyl-4-isopropenyl cyclohexan-1-ol
1-methyl-4-isopropenylcyclohexan-1-ol
1-methyl-4-methyl vinyl cyclohexanol
1-methyl-4-prop-1-en-2-ylcyclohexan-1-ol
4-isopropenyl-1-methyl-1-cyclohexanol
4-isopropenyl-1-methylcyclohexanol
 terpin-1-ol
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: Induction of defensive response in Eucalyptus globulus plants and its persistence in vegetative propagation.
PubMed: Volatile oil constituents of different parts of Artemisia chamaemelifolia and the composition and antibacterial activity of the aerial parts of A. turcomanica from Iran.
PubMed: Chemical compositions and antioxidant/antimicrobial activities of various samples prepared from Schinus terebinthifolius leaves cultivated in Egypt.
PubMed: Effect of pulp reduction and pasteurization on the release of aroma compounds in industrial orange juice.
PubMed: Chemical composition and antimicrobial activity of essential oil from the rhizomes of Amomum cannicarpum.
PubMed: [Analysis of terpineol and improvement of technology process in terpineol production].
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