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

hyacinth ether
phenafleur (IFF)

Sponsors

Name:2-cyclohexyloxyethylbenzene
CAS Number: 80858-47-5Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:279-576-2
Nikkaji Web:J320.325E
XlogP3-AA:3.80 (est)
Molecular Weight:204.31260000
Formula:C14 H20 O
NMR Predictor:Predict (works with chrome or firefox)
Category: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
 
Physical Properties:
Appearance:colorless to pale yellow clear liquid (est)
Assay: 97.00 to 100.00
Food Chemicals Codex Listed: No
Specific Gravity:0.96600 to 0.97400 @ 25.00 °C.
Pounds per Gallon - (est).: 8.038 to 8.105
Specific Gravity:0.96700 to 0.97500 @ 20.00 °C.
Pounds per Gallon - est.: 8.056 to 8.122
Refractive Index:1.50800 to 1.51300 @ 20.00 °C.
Boiling Point: 289.54 °C. @ 760.00 mm Hg (est)
Vapor Pressure:0.004000 mm/Hg @ 25.00 °C. (est)
Flash Point:> 212.00 °F. TCC ( > 100.00 °C. )
logP (o/w): 4.099 (est)
Shelf Life: 24.00 month(s) or longer if stored properly.
Storage:store in cool, dry place in tightly sealed containers, protected from heat and light.
Soluble in:
 alcohol
 paraffin oil
 water, 5.566 mg/L @ 25 °C (est)
Insoluble in:
 water
Stability:
 acid cleaner
 alcoholic lotion
 antiperspirant
 bleach
 deo stick
 detergent
 fabric softener
 hard surface cleaner
 shampoo
 soap
 
Organoleptic Properties:
Odor Type: floral
Odor Strength:medium
Substantivity:168 hour(s) at 100.00 %
floral hyacinth green metallic fruity raspberry balsamic
Odor Description:at 100.00 %. floral hyacinth green metallic fruity raspberry balsam
Luebke, William tgsc, (1992)
Odor sample from: International Flavors & Fragrances Inc.
Odor and/or flavor descriptions from others (if found).
IFF
Phenafleur®
Odor Description:Refined floral note with hyacinth associations and a modifying fruity (raspberry) effect. Excellent stability
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: perfuming agents
 
Suppliers:
Associate Allied Chemicals
Phenafleur
About
Azelis UK
PHENAFLEUR
Services
BOC Sciences
For experimental / research use only.
[2-(Cyclohexyloxy)ethyl]benzene
CG Herbals
Phenafleur
Odor: Refined floral note with hyacinth associations and a modifying fruity (raspberry) effect
Ernesto Ventós
PHENAFLEUR IFF
IFF
Phenafleur®
Odor: Refined floral note with hyacinth associations and a modifying fruity (raspberry) effect. Excellent stability
Penta International
PHENYLETHYL CYCLOHEXYL ETHER
Taytonn
Phenafleur®
Odor: Floral, Fruity, Hyacinth
The Good Scents Company
hyacinth ether
Odor: floral hyacinth green metallic fruity raspberry balsam
The John D. Walsh Company
Phenafleur
 
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:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category: fragrance agents
Recommendation for hyacinth ether usage levels up to:
  20.0000 % in the fragrance concentrate.
 
Recommendation for hyacinth ether flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
EPA Substance Registry Services (TSCA):80858-47-5
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :166527
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:2
2-cyclohexyloxyethylbenzene
Chemidplus:0080858475
 
References:
 2-cyclohexyloxyethylbenzene
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:80858-47-5
Pubchem (cid):166527
Pubchem (sid):135120590
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2009
(IUPAC):Atomic Weights of the Elements 2009 (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):Search
Export Tariff Code:2909.30.9090
ChemSpider:View
 
Potential Blenders and core components note
For Odor
aldehydic
citrus carbaldehyde
FR
iso
freshal
FR
muguet undecadienal
FR
animal
iso
butyl quinoline
FR
costus valerolactone
FR
balsamic
clover nitrile
FR
citrus
grapefruit pentanol
FR
lime oil fractions
FR
floral
cyclohexyl salicylate
FR
floral pyran
FR
floral pyranol
FR
gardenia oxide
FR
heliotropyl diethyl acetal
FR
leerall
FR
muguet carboxaldehyde
FR
muguet octadienol
FR
orris pyridine 25% IPM
FR
peony alcohol
FR
phenethyl butyl ether
FR
phenyl acetaldehyde / methyl anthranilate schiff's base
FR
(E)-2-
phenyl-1(2)-propene-1-yl acetate
FR
tea acetate
FR
violet methyl carbonate
FR
fruity
allyl amyl glycolate
FR
berry hexanoate
FR
dimethyl benzyl carbinyl isobutyrate
FR
green acetate
FR
prune glycidate
FR
raspberry dicarboxylate
FR
green
phenethyl oxyacetaldehyde
FR
marine
marine pyridine
FR
melon
watermelon ketone
FR
mossy
veramoss (IFF)
FR
tonka
tonka bean absolute
FR
waxy
cyclododecyl acetate
FR
woody
amber carbinol
FR
patchouli ethanone
FR
santall
FR
tobacarol (IFF)
FR
woody acetate
FR
(Z)-
woody amylene
FR
For Flavor
 
Potential Uses:
 agrumen
FRaldehydic
 algae
 almond blossom
 apple crabapple
FRapple red
FRapricot
FRbalsam
 bark
FRblackberry
FRblueberry
 blueberry whortleberry red whortleberry
FRbouquet
 boxwood
FRboysenberry
 bramble arctic bramble blackberry
 brandy
FRbutterscotch
FRcalamus
FRcarnation dianthus oeillet
FL/FRcassis black currant bud
FRcedar forest
FRcherry black
FRcherry blossom
 chocolate cacao
FRchypre
 cloudberry bakeapple
FRclover trefle le'trefle incarnat
FRcolonia
 cortex
FRcrabapple blossom
FRcucumber
FRcurrant
FRdaffodil narcissus
FRdillenia
 durian
FReglantine sweet briar
FRelder berry
FRelder flower
 exotic
 fantasy blends
FRfig
FRfir balsam
FL/FRfir needle pine needle
FRfloral
 foliage
FRfrangipanni plumeria
FRfreesia
FRfungus mushroom
FRgardenia
FRgeranium
FRginger white
FRgrape
FRgrass sweet
FRgreen
FRguava
FRhibiscus
FL/FRhops houblon
FRhuckleberry bilberry
 hugonia
FRhyacinth jacinthe
FRhydrangea
 iris blossom
FRivy
FRjonquil narcissus jonquilla
 kewda
 kiwi blossom
FRkumquat
FRlinden blossom limeflower tilleul
 liverwort
FRloganberry dewberry
FRlotus
FRlychee
FRmandarin
FRmango
FRmango flower
FRmaple
FRmeadow country
 metallic
 millefleurs
FRmulberry
 nectarine
 nut
FRoakmoss mousse de chene moss
FRorchid
FRpansy
FRpapaya
FL/FRparsley
FRpassion blossom
FRpassion fruit
FRpeach
FRpeach blossom
FRpear
FRpear blossom
 pear prickly pear
FRpeony
FRpeppermint
FRpine
FRpineapple
FRplum
 plum blossom
FRpomegranate
 praline
FRquince
FRraspberry
FRreseda mignonette
FRrose d'orient
FRrose tea rose
 sap
FRspearmint
FL/FRspruce
 starfruit
FRstock evening scented
FRstrawberry
FRsweet pea
FRtangerine
 tea
FRtoffee
 tomato
FRtuberose
FRtulip
 wasabi
FRwintergreen
FRwisteria wistaria glycine
FL/FRwormwood absinthium
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
 benzene, (2-(cyclohexyloxy)ethyl)-
(2-(cyclohexyl oxy)ethyl) benzene
 cyclohexyl phenethyl ether
 cyclohexyl phenethylether
 cyclohexyl phenyl ethyl ether
(2-(cyclohexyloxy)ethyl)benzene
[2-(cyclohexyloxy)ethyl]benzene
2-cyclohexyloxyethylbenzene
 hyacinth ether
 phenafleur (IFF)
 phenethyl cyclohexyl ether
 phenyl ethyl cyclohexyl ether
 phenylethyl cyclohexyl ether
 

Articles:

US Patents:Cyclohexyl phenethylether
US Patents:Cyclohexyl phenethylether derivative
US Patents:Process for augmenting or enhancing the aroma of detergents using cyclohexyl phenethylether
US Patents:Use of cyclohexyl phenethylether in augmenting or enhancing the aroma of perfumes and colognes
US Patents:Cyclohexyl phenethylether derivatives for combatting tobacco beetles
US Patents:Cyclohexyl phenethylether used for combatting tobacco beetles
US Patents:Cyclohexyl phenethylether and uses thereof in combatting tobacco beetles and in augmenting or enhancing the aroma of perfumes, colognes and perfumed articles
US Patents:Use of cyclohexyl phenethylether derivative in augmenting or enhancing the aromas of perfumes and colognes
US Patents:Process for preparing cyclohexyl phenethylether derivatives
US Patents:Cyclohexyl phenethylether derivatives, process for preparing same and uses thereof in combatting tobacco beetles and in augmenting or enhancing the aroma of perfumes, colognes and perfumed articles
 
Notes:
Blends well with damascones.
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