geranyl linalool
3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraen-3-ol
 
Notes:
None found
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      Product(s):
      68931-30-6 GERANYL LINALOOL 92.0%
       
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      Product(s):
      G0221 Geranyl-linalool (mixture of isomers) >90.0%(GC)
       
Synonyms   Articles   Notes   Search
CAS Number: 68931-30-6Picture of molecule3D/inchi
Nikkaji Web: J354.877E
MDL: MFCD00059363
XlogP3-AA: 6.40 (est)
Molecular Weight: 290.49018000
Formula: C20 H34 O
NMR Predictor: Predict (works with chrome or firefox)
Also(can) Contains: (E)-geranyl linalool
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
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Physical Properties:
Appearance: colorless to pale yellow clear liquid (est)
Assay: 92.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 0.87300 to 0.88300 @  25.00 °C.
Pounds per Gallon - (est).: 7.264 to  7.347
Refractive Index: 1.48200 to 1.49200 @  20.00 °C.
Boiling Point: 389.87 °C. @ 760.00 mm Hg (est)
Flash Point: 230.00 °F. TCC ( 110.00 °C. )
logP (o/w): 7.351 (est)
Soluble in:
 alcohol
 water, 0.006982 mg/L @ 25 °C (est)
Insoluble in:
 water
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Organoleptic Properties:
 
Odor Type: floral
 
Odor Strength: medium
 
Substantivity: > 336 hour(s) at 100.00 %
 
 floral  rose  
Odor Description:
at 100.00 %. 
floral rose
 
Odor and/or flavor descriptions from others (if found).
 
Bedoukian Research
GERANYL LINALOOL ≥92.0%, Kosher
Odor Description: A low intensity floral (rose) aroma
Used as a fixative for rose fragrances.
 
 
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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.
GERANYL LINALOOL 92.0%
Penta International
GERANYL LINALOOL
TCI AMERICA
For experimental / research use only.
Geranyl-linalool (mixture of isomers) >90.0%(GC)
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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:
Not determined
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
 
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 68931-30-6
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 5365872
National Institute of Allergy and Infectious Diseases: Data
 3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraen-3-ol
Chemidplus: 0068931306
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References:
 3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraen-3-ol
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 5365872
Pubchem (sid): 135051186
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
CHEBI: View
KEGG (GenomeNet): C20681
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2905.22.5050
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
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Potential Blenders and core components note
 
For Odor
aldehydic
 nonanal diethyl acetalFL/FR
balsamic
 benzophenoneFR
 benzyl cinnamateFL/FR
 cinnamyl cinnamateFL/FR
alpha-methyl cinnamyl alcoholFR
 phenethyl cinnamateFL/FR
fatty
 methyl 10-undecenoateFL/FR
floral
isoamyl undecylenateFL/FR
 benzyl alcoholFL/FR
 butyl benzyl etherFL/FR
 cananga oilFL/FR
 cananga oil chinaFL/FR
 citronellyl acetoneFL/FR
 citronellyl propionateFL/FR
 cyclohexyl salicylateFR
gamma-damasconeFR
(Z)-alpha-damasconeFL/FR
(Z)-4-decen-1-yl acetateFL/FR
 dihydrocarvyl acetateFL/FR
 dihydrogeranyl linaloolFR
 ethyl phenyl acetateFL/FR
 farnesyl acetateFL/FR
 floral pyranFR
 floral undecenoneFR
 geranyl acetateFL/FR
 globulol 
 hawthorn ethanolFR
beta-ionolFL/FR
2-methyl octanalFL/FR
 musk acetateFR
 neryl acetateFL/FR
 neryl isovalerateFL/FR
 nonanolFL/FR
 phenethyl acetateFL/FR
 phenethyl anthranilateFL/FR
 phenethyl benzoateFL/FR
 phenethyl phenyl acetateFL/FR
 phenethyl salicylateFL/FR
 phenoxyethanolFL/FR
 phenyl acetaldehyde digeranyl acetalFR
1-phenyl propyl alcoholFL/FR
3-phenyl propyl propionateFL/FR
4-phenyl-3-buten-2-olFL/FR
(Z,E)-phytolFL/FR
 rose acetateFR
laevo-rose oxideFL/FR
 styralyl propionateFL/FR
(E)-2-undecen-1-olFL/FR
2-undecen-1-olFL/FR
fruity
 benzyl propionateFL/FR
 cyclohexyl crotonateFR
(E)-alpha-damasconeFL/FR
(E)-ethyl tiglateFL/FR
 geranyl methyl tiglate 
 strawberry glycidate 2FL/FR
green
isodecanalFL/FR
2-heptyl tetrahydrofuranFR
(Z)-3-hexen-1-yl benzoateFL/FR
(Z)-3-hexen-1-yl phenyl acetateFL/FR
 phenyl acetaldehydeFL/FR
honey
 methyl hydrocinnamateFL/FR
powdery
para-anisyl alcoholFL/FR
spicy
 amyl isoeugenolFR
woody
 sandal cyclopropaneFL/FR
 
For Flavor
 
No flavor group found for these
isoamyl undecylenateFL/FR
 butyl benzyl etherFL/FR
 citronellyl acetoneFL/FR
(Z)-alpha-damasconeFL/FR
isodecanalFL/FR
(Z)-4-decen-1-yl acetateFL/FR
 globulol 
 methyl hydrocinnamateFL/FR
2-methyl octanalFL/FR
 nonanal diethyl acetalFL/FR
 phenoxyethanolFL/FR
3-phenyl propyl propionateFL/FR
2-undecen-1-olFL/FR
(E)-2-undecen-1-olFL/FR
amber
 sandal cyclopropaneFL/FR
balsamic
 phenethyl cinnamateFL/FR
1-phenyl propyl alcoholFL/FR
(Z,E)-phytolFL/FR
citrus
 styralyl propionateFL/FR
fatty
(Z)-3-hexen-1-yl benzoateFL/FR
floral
 cananga oilFL/FR
 cananga oil chinaFL/FR
 citronellyl propionateFL/FR
 dihydrocarvyl acetateFL/FR
 farnesyl acetateFL/FR
beta-ionolFL/FR
pseudoiononeFL
 neryl acetateFL/FR
 phenethyl anthranilateFL/FR
 phenethyl benzoateFL/FR
laevo-rose oxideFL/FR
fruity
para-anisyl alcoholFL/FR
 benzyl alcoholFL/FR
 benzyl propionateFL/FR
(E)-alpha-damasconeFL/FR
(E)-ethyl tiglateFL/FR
 geranyl methyl tiglate 
 neryl isovalerateFL/FR
 strawberry glycidate 2FL/FR
green
 geranyl acetateFL/FR
(Z)-3-hexen-1-yl phenyl acetateFL/FR
honey
 ethyl phenyl acetateFL/FR
 phenethyl acetateFL/FR
 phenethyl phenyl acetateFL/FR
 phenyl acetaldehydeFL/FR
medicinal,
 phenethyl salicylateFL/FR
spicy
 benzyl cinnamateFL/FR
 cinnamyl cinnamateFL/FR
waxy
 methyl 10-undecenoateFL/FR
 nonanolFL/FR
4-phenyl-3-buten-2-olFL/FR
 
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Potential Uses:
 amberFR
 balsamFR
 fixer 
 floralFR
 freesiaFR
 hydrangeaFR
 muskFR
 roseFR
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Occurrence (nature, food, other): note
 picea abies
Search Trop  Picture
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Synonyms:
 geranyllinalool
 tetramethyl hexadecatetraen-3-ol
3,7,11,15-tetramethyl-1,6,10,14-hexadecatetraen-3-ol
3,7,11,15-tetramethyl-1,6,10,14-hexadecatetraene-3-ol
 tetramethyl-hexadecatetraen-3-ol
3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraen-3-ol
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Articles:
PubMed: Metabolic engineering of the C16  homoterpene TMTT in Lotus japonicus through overexpression of (E,E)-geranyllinalool synthase attracts generalist and specialist predators in different manners.
PubMed: Terpene alcohols inhibit de novo sphingolipid biosynthesis.
PubMed: Isolation and identification of ligands for the goldfish testis androgen receptor in chemical recovery condensates from a Canadian bleached kraft pulp and paper mill.
PubMed: The biochemistry of homoterpenes--common constituents of floral and herbivore-induced plant volatile bouquets.
PubMed: Herbivore-induced and floral homoterpene volatiles are biosynthesized by a single P450 enzyme (CYP82G1) in Arabidopsis.
PubMed: Identification of testosterone-dependent volatile compounds and proteins in the preputial gland of rat Rattus norvegicus.
PubMed: Two new acyclic diterpene glycosides from fruits of Habanero, Capsicum chinense.
PubMed: Fragrance material review on geranyl linalool.
PubMed: Identification and regulation of TPS04/GES, an Arabidopsis geranyllinalool synthase catalyzing the first step in the formation of the insect-induced volatile C16-homoterpene TMTT.
PubMed: Silencing geranylgeranyl diphosphate synthase in Nicotiana attenuata dramatically impairs resistance to tobacco hornworm.
PubMed: Herbivore-induced terpenoid emission in Medicago truncatula: concerted action of jasmonate, ethylene and calcium signaling.
PubMed: Induction of a leaf specific geranylgeranyl pyrophosphate synthase and emission of (E,E)-4,8,12-trimethyltrideca-1,3,7,11-tetraene in tomato are dependent on both jasmonic acid and salicylic acid signaling pathways.
PubMed: Synthesis and antimycobacterial activity of agelasine E and analogs.
PubMed: Analysis of the labial gland secretions of the male bumblebee Bombus griseocollis (Hymenoptera: Apidae).
PubMed: Novel diterpenoids and hydrocarbons in the Dufour gland of the ectoparasitoid Habrobracon hebetor (Say) (Hymenoptera: Braconidae).
PubMed: Interspecific variation in terpenoid composition of defensive secretions of European Reticulitermes termites.
PubMed: Volatile glandular secretions of three species of new world army ants,Eciton burchelli, Labidus coecus, andLabidus praedator.
PubMed: Effects of olfactory stimulation with jasmin and its component chemicals on the duration of pentobarbital-induced sleep in mice.
PubMed: Geranyllinalool (Diterpene Alcohol) : An insecticidal component of pine wood and termites (Isoptera: Rhinotermitidae) in four European ecosystems.
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