EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

geranyl linalool
3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraen-3-ol

Supplier Sponsors

Name:3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraen-3-ol
CAS Number: 68931-30-6Picture of molecule3D/inchi
FDA UNII: Search
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, Edge 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
 
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
 
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.
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: perfuming agents
 
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)
 
Safety Information:
Preferred SDS: View
 
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
 
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
 
 
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
 
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
 
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
 
Potential Blenders and core components note
For Odor
aldehydic
nonanal diethyl acetal
FL/FR
balsamic
benzophenone
FR
benzyl cinnamate
FL/FR
cinnamyl cinnamate
FL/FR
alpha-
methyl cinnamyl alcohol
FR
phenethyl cinnamate
FL/FR
fatty
methyl 10-undecenoate
FL/FR
floral
iso
amyl undecylenate
FL/FR
benzyl alcohol
FL/FR
butyl benzyl ether
FL/FR
cananga oil
FL/FR
cananga oil china
FL/FR
citronellyl acetone
FL/FR
citronellyl propionate
FL/FR
cyclohexyl salicylate
FR
(Z)-alpha-
damascone
FL/FR
gamma-
damascone
FR
(Z)-4-
decen-1-yl acetate
FL/FR
dihydrocarvyl acetate
FL/FR
dihydrogeranyl linalool
FR
ethyl phenyl acetate
FL/FR
farnesyl acetate
FL/FR
floral pyran
FR
floral undecenone
FR
geranyl acetate
FL/FR
hawthorn ethanol
FR
beta-
ionol
FL/FR
2-
methyl octanal
FL/FR
musk acetate
FR
neryl acetate
FL/FR
neryl isovalerate
FL/FR
nonanol
FL/FR
phenethyl acetate
FL/FR
phenethyl anthranilate
FL/FR
phenethyl benzoate
FL/FR
phenethyl phenyl acetate
FL/FR
phenethyl salicylate
FL/FR
phenoxyethanol
FL/FR
phenyl acetaldehyde digeranyl acetal
FR
1-
phenyl propyl alcohol
FL/FR
3-
phenyl propyl propionate
FL/FR
4-
phenyl-3-buten-2-ol
FL/FR
(Z,E)-
phytol
FL/FR
rose acetate
FR
laevo-
rose oxide
FL/FR
styralyl propionate
FL/FR
(E)-2-
undecen-1-ol
FL/FR
2-
undecen-1-ol
FL/FR
fruity
benzyl propionate
FL/FR
cyclohexyl crotonate
FR
(E)-alpha-
damascone
FL/FR
(E)-
ethyl tiglate
FL/FR
strawberry glycidate 2
FL/FR
green
iso
decanal
FL/FR
2-
heptyl tetrahydrofuran
FR
(Z)-3-
hexen-1-yl benzoate
FL/FR
(Z)-3-
hexen-1-yl phenyl acetate
FL/FR
phenyl acetaldehyde
FL/FR
honey
methyl hydrocinnamate
FL/FR
powdery
para-
anisyl alcohol
FL/FR
spicy
amyl isoeugenol
FR
woody
sandal cyclopropane
FL/FR
For Flavor
No flavor group found for these
iso
amyl undecylenate
FL/FR
butyl benzyl ether
FL/FR
citronellyl acetone
FL/FR
(Z)-alpha-
damascone
FL/FR
iso
decanal
FL/FR
(Z)-4-
decen-1-yl acetate
FL/FR
methyl hydrocinnamate
FL/FR
2-
methyl octanal
FL/FR
nonanal diethyl acetal
FL/FR
phenoxyethanol
FL/FR
3-
phenyl propyl propionate
FL/FR
2-
undecen-1-ol
FL/FR
(E)-2-
undecen-1-ol
FL/FR
amber
amber
sandal cyclopropane
FL/FR
balsamic
phenethyl cinnamate
FL/FR
1-
phenyl propyl alcohol
FL/FR
(Z,E)-
phytol
FL/FR
citrus
styralyl propionate
FL/FR
fatty
(Z)-3-
hexen-1-yl benzoate
FL/FR
floral
cananga oil
FL/FR
cananga oil china
FL/FR
citronellyl propionate
FL/FR
dihydrocarvyl acetate
FL/FR
farnesyl acetate
FL/FR
beta-
ionol
FL/FR
pseudo
ionone
FL
neryl acetate
FL/FR
phenethyl anthranilate
FL/FR
phenethyl benzoate
FL/FR
laevo-
rose oxide
FL/FR
fruity
para-
anisyl alcohol
FL/FR
benzyl alcohol
FL/FR
benzyl propionate
FL/FR
(E)-alpha-
damascone
FL/FR
(E)-
ethyl tiglate
FL/FR
neryl isovalerate
FL/FR
strawberry glycidate 2
FL/FR
green
geranyl acetate
FL/FR
(Z)-3-
hexen-1-yl phenyl acetate
FL/FR
honey
ethyl phenyl acetate
FL/FR
phenethyl acetate
FL/FR
phenethyl phenyl acetate
FL/FR
phenyl acetaldehyde
FL/FR
medicinal,
phenethyl salicylate
FL/FR
spicy
benzyl cinnamate
FL/FR
cinnamyl cinnamate
FL/FR
waxy
methyl 10-undecenoate
FL/FR
nonanol
FL/FR
4-
phenyl-3-buten-2-ol
FL/FR
 
Potential Uses:
FRamber
FRbalsam
 fixer
FRfloral
FRfreesia
FRhydrangea
FRmusk
FRrose
 
Occurrence (nature, food, other):note
 picea abies
Search Trop Picture
 
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
 

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.
 
Notes:
None found
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