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

lilyall
lilial

Sponsors

Fragrance Demo Formulas
Name:3-(4-tert-butylphenyl)butanal
CAS Number: 80-54-6Picture of molecule3D/inchi
Other:39390-70-0
ECHA EINECS - REACH Pre-Reg:201-289-8
FDA UNII:T7540GJV69
Nikkaji Web:J560.043J
Beilstein Number:0880140
MDL:MFCD00047655
XlogP3-AA:3.60 (est)
Molecular Weight:204.31260000
Formula:C14 H20 O
BioActivity Summary:listing
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
PubMed:Search
NCBI:Search
 
Physical Properties:
Appearance:colorless to pale yellow clear oily liquid (est)
Assay: 93.00 to 100.00
Food Chemicals Codex Listed: No
Specific Gravity:0.94200 to 0.94700 @ 25.00 °C.
Pounds per Gallon - (est).: 7.838 to 7.880
Refractive Index:1.50300 to 1.50600 @ 20.00 °C.
Boiling Point: 250.00 to 251.00 °C. @ 750.00 mm Hg
Boiling Point: 126.00 to 127.00 °C. @ 6.00 mm Hg
Acid Value: 2.00 max. KOH/g
Vapor Pressure:0.005000 mm/Hg @ 25.00 °C. (est)
Flash Point: 210.00 °F. TCC ( 98.89 °C. )
logP (o/w): 4.216 (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. store under nitrogen.
Storage:store under nitrogen.
Soluble in:
 alcohol
 paraffin oil
 water, 38 mg/L @ 20 °C (exp)
Insoluble in:
 water
Stability:
 detergent
 soap
 
Organoleptic Properties:
Odor Type: floral
Odor Strength:medium
Substantivity:236 hour(s) at 100.00 %
floral muguet watery green powdery cumin
Odor Description:at 100.00 %. floral muguet watery green powdery cumin
Luebke, William tgsc, (1986)
Odor sample from: Givaudan Corporation
Odor and/or flavor descriptions from others (if found).
Moellhausen
ALDEHYDE MBDC PURE
Odor Description:fresh, green, floreal
Taste Description:lime tree flowers, lily of valley
Indukern F&F
LILESTRALIS PURE
Odor Description:FRESH, GREEN, FLORAL, LILAC
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: perfuming agents
 
Suppliers:
BASF
Lysmeral Extra®
Odor: Floral, muguet, powdery
BOC Sciences
For experimental / research use only.
3-(4-tert-Butylphenyl)-2-methylpropionaldehyde
CG Herbals
Lilial
Odor: Powerful, Floral-Muguet, Fresh
Use: Lilial is used in a wide variety of compositions where it confers a particularly recommended for floral notes such as muguet, linden-blossom and cyclamen.
CG Herbals
Lysmeral
Odor: Fresh, Light, Floral, Muguet, Powdery
Creatingperfume.com
Lilestralis / Lysmeral
Odor: Fresh, light, green floral, reminiscent of lily
ECSA Chemicals
Lilial
Company Profile
Emerald Kalama Chemical
Lilestralis® Pure
meta-Lilestralis < 0.1%; total Lilestralis > 99.0%
Odor: Fresh, light, green, floral, lily
Ernesto Ventós
LILY ALDEHYDE EXTRA
Odor: FRESH, LIGHT, FLORAL,MUGUET,POWDERY
Ernesto Ventós
LYSMERAL EXTRA BASF
Odor: FRESH, LIGHT, FLORAL,MUGUET,POWDERY
Ernesto Ventós
LYSMERAL/LYRAL SUBSTITUTE-LILIAL BASE
Odor: FRESH,LIGHT,FLORAL,MUGUET,POWDERY
Indenta Group
Lilyal
Indukern F&F
LILESTRALIS PURE
Odor: FRESH, GREEN, FLORAL, LILAC
Indukern F&F
LILIALDEHYDE
Odor: FRESH, GREEN, FLORAL, LILAC
Indukern F&F
MEFLORAL
Odor: FRESH, FLORAL, GREEN
Inoue Perfumery
LILY ALDEHYDE PURE
Lluch Essence
LILIAL
MG International Fragrance
Liligul N 743 CLP
Odor: Allergen free Lilial Oil replacement
Moellhausen
ALDEHYDE MBDC PURE
Moellhausen
ALDEHYDE MBDC PURE
Odor: fresh, green, floreal
Flavor: lime tree flowers, lily of valley
Pell Wall Perfumes
Lilial
Penta International
LILIAL
PerfumersWorld
Lilial
Odor: fresh light green floral lily notes muguet lindenblossom
Perfumery Laboratory
LILIAL
Odor: Sweet, floral fragrance of the lily of the valley
Phoenix Aromas & Essential Oils
Lilial
Prinova
Lilialdehyde
Prodasynth
LILYALL
> 99%, META-LYSMERAL < 0,1%
Odor: FRESH, LIGHT, FLORAL,MUGUET,POWDERY
Santa Cruz Biotechnology
For experimental / research use only.
2-(4-tert-Butylbenzyl)propionaldehyde ≥95%
Sigma-Aldrich
For experimental / research use only.
2-(4-tert-Butylbenzyl)propionaldehyde analytical standard
SRS Aromatics
LILIALDEHYDE
Taytonn
Lilestralis®
Odor: Floral, Fresh, Green
TCI AMERICA
For experimental / research use only.
3-(4-tert-Butylphenyl)isobutyraldehyde >96.0%(GC)
The Good Scents Company
lilyall
Odor: floral muguet watery green powdery cumin
The John D. Walsh Company
Lilestralis
The John D. Walsh Company
Mefloral
The Lermond Company
Lilial
The Perfumers Apprentice
Lilial a.k.a Lilestralis
Odor: fresh slightly green lily watery
Vigon International
Lysmeral Extra (Lilial)
 
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
R 22 - Harmful if swallowed.
R 36/38 - Irritating to skin and eyes.
R 43 - May cause sensitisation by skin contact.
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 37 - Wear suitable gloves.
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
Acute toxicity, Oral (Category 4), H302
Skin irritation (Category 2), H315
Skin sensitisation (Category 1), H317
Reproductive toxicity (Category 2), H361
Acute aquatic toxicity (Category 2), H401
Chronic aquatic toxicity (Category 2), H411
GHS Label elements, including precautionary statements
 
Pictogramhealth-hazard.jpgexclamation-mark.jpgenvironment.jpg
 
Signal word Warning
Hazard statement(s)
H302 - Harmful if swallowed
H315 - Causes skin irritation
H317 - May cause an allergic skin reaction
H361 - Suspected of damaging fertility or the unborn child
H401 - Toxic to aquatic life
H411 - Toxic to aquatic life with long lasting effects
Precautionary statement(s)
P201 - Obtain special instructions before use.
P202 - Do not handle until all safety precautions have been read and understood.
P261 - Avoid breathing dust/fume/gas/mist/vapours/spray.
P264 - Wash skin thouroughly after handling.
P270 - Do not eat, drink or smoke when using this product.
P272 - Contaminated work clothing should not be allowed out of the workplace.
P273 - Avoid release to the environment.
P280 - Wear protective gloves/protective clothing/eye protection/face protection.
P281 - Use personal protective equipment as required.
P301 + P312 - IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P302 + P352 - IF ON SKIN: wash with plenty of soap and water.
P308 + P313 - IF exposed or concerned: Get medical advice/attention.
P330 - Rinse mouth.
P333 + P313 - IF SKIN irritation or rash occurs: Get medical advice/attention.
P362 - Take off contaminated clothing and wash before reuse.
P391 - Collect spillage. Hazardous to the aquatic environment
P405 - Store locked up.
P501 - Dispose of contents/container in accordance with local/regional/national/international regulations.
Human Experience:
4 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50 1390 mg/kg
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) LUNGS, THORAX, OR RESPIRATION: DYSPNEA
National Technical Information Service. Vol. OTS0535449

intraperitoneal-mouse LD50 700 mg/kg
National Technical Information Service. Vol. OTS0535449

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
National Technical Information Service. Vol. OTS0535449

Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category: fragrance agents
IFRA Critical Effect: Dermal sensitization
IFRA: View Standard
Fragrance usage is IFRA RESTRICTED. View Standard for complete information.
Please review all IFRA documents for complete information.
IFRA categories: limits in the finished product: (For a description of the categories, refer to the IFRA QRA Information Booklet.)
Category 1:
See Note (1)
0.12 % (1)
Category 2:  0.15 %
Category 3:  0.62 %
Category 4:  1.86 %
Category 5:  0.98 %
Category 6:  2.97 % (1)
Category 7:  0.31 %
Category 8:  2.00 %
Category 9:  5.00 %
Category 10:  2.50 %
Category 11: See Note (2)
 Notes:
 

For this material, for pragmatic reasons, restrictive levels allowed by the QRA for certain categories but actually being higher than those already in place before applying the QRA, will temporarily not be implemented until the end of a 5 year monitoring phase. At the end of the 5 years the position will be reevaluated again.

 

(1) IFRA would recommend that any material used to impart perfume or flavour in products intended for human ingestion should consist of ingredients that are in compliance with appropriate regulations for foods and food flavourings in the countries of planned distribution and, where these are lacking, with the recommendations laid down in the Code of Practice of IOFI (International Organisation of the Flavor Industry). Further information about IOFI can be found on its website (www.iofi.org).

 

(2) Category 11 includes all non-skin contact or incidental skin contact products. Due to the negligible skin contact from these types of products there is no justification for a restriction of the concentration of this fragrance ingredient in the finished product.

 
Recommendation for lilyall flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):80-54-6
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :6652
National Institute of Allergy and Infectious Diseases:Data
SCCNFP:opinion
WISER:UN 3082
WGK Germany:3
3-(4-tert-butylphenyl)butanal
Chemidplus:0000080546
RTECS:MW4895000 for cas# 80-54-6
 
References:
Leffingwell:Chirality or Article
 3-(4-tert-butylphenyl)butanal
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:80-54-6
Pubchem (cid):6652
Pubchem (sid):134972321
 
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:2912.49.2600
ChemSpider:View
Wikipedia:View
RSC Learn Chemistry:View
 
Potential Blenders and core components note
For Odor
aldehydic
adoxal (Givaudan)
FL/FR
citronellyl oxyacetaldehyde
FL/FR
citrus carbaldehyde
FR
decanal (aldehyde C-10)
FL/FR
9-
decenal
FL/FR
dodecanal (aldehyde C-12 lauric)
FL/FR
lily pentanal
FR
nonanal (aldehyde C-9)
FL/FR
10-
undecenal (aldehyde C-11 undecylenic)
FL/FR
animal
para-
cresyl isobutyrate
FL/FR
anisic
para-
anisaldehyde
FL/FR
balsamic
amyris wood oil
FL/FR
siam
benzoin resinoid
FL/FR
benzyl salicylate
FL/FR
iso
butyl cinnamate
FL/FR
cinnamyl alcohol
FL/FR
(E)-
cinnamyl alcohol
FL/FR
clover nitrile
FR
ethyl cinnamate
FL/FR
fir balsam absolute
FR
linalyl cinnamate
FL/FR
3-
phenyl propyl alcohol
FL/FR
berry
raspberry ketone
FL/FR
raspberry ketone acetate
FL/FR
raspberry ketone methyl ether
FL/FR
citrus
benzyl anthranilate
FR
citrus ocimenol
FR
iso
decyl acetate
FR
lime oil distilled mexico
FL/FR
methyl indole-1-carboxylate
FR
myrmac aldehyde
FR
tetrahydromyrcenol
FR
fatty
decanol
FL/FR
floral
aeolanthus graveolens oil
FR
alpha-
amyl cinnamaldehyde
FL/FR
alpha-
amyl cinnamaldehyde dimethyl acetal
FL/FR
iso
amyl salicylate
FL/FR
bois de rose oil brazil
FL/FR
alpha-
butyl cinnamaldehyde
FL/FR
4-iso
butyl cyclohexane propanal
FR
iso
butyl salicylate
FL/FR
citronellol
FL/FR
citronellyl (R)-lactate
FR
citronellyl acetate
FL/FR
citronellyl ethoxalate
FR
citrus propanol
FR
coriander seed oil
FL/FR
corps popinal
FR
cumin carbinol
FR
cuminyl acetaldehyde
FL/FR
cyclamen aldehyde
FL/FR
cyclamen homoaldehyde
FR
cyclohexyl ethyl alcohol
FL/FR
cyclohexyl propanol
FR
2-
decalinol
FR
dihydrojasmone
FL/FR
dimethyl anthranilate
FL/FR
dimethyl benzyl carbinol
FL/FR
dimethyl benzyl carbinyl acetate
FL/FR
2,5-
dimethyl-2-indan methanol
FR
4-
ethyl cyclohexane propanal
FR
ethyl linalyl acetal
FR
(E,E)-
farnesol
FL/FR
farnesol
FL/FR
floral butanal
FR
floral pyranol
FR
floral specialty
FR
freesia acetate
FR
gardenia oxide
FR
geraniol
FL/FR
geranyl acetate
FL/FR
ginger lily fragrance
FR
hawthorn ethanol
FR
heliotropin
FL/FR
heliotropyl acetone
FL/FR
heliotropyl diethyl acetal
FR
(Z)-4-
hepten-2-yl salicylate
FR
(Z)-3-
hexen-1-yl salicylate
FL/FR
alpha-
hexyl cinnamaldehyde
FL/FR
hyacinth ether
FR
hydrangea fragrance
FR
3-(4-
hydroxy-4-methyl cyclohexyl) butanal
FR
hydroxycitronellal
FL/FR
hydroxycitronellal / methyl anthranilate schiff's base
FR
hydroxycitronellal diethyl acetal
FL/FR
hydroxycitronellal dimethyl acetal
FL/FR
hydroxycitronellal distillation residue distillates
FR
hydroxycitronellal nitrile
FR
hydroxycitronellal propylene glycol acetal
FL/FR
hydroxycitronellal residue
FR
hydroxycitronellol
FL/FR
jasimia
FR
leerall
FR
leerall / methyl anthranilate schiff's base
FR
lily flower absolute
FR
lily fragrance
FR
calla
lily fragrance
FR
water
lily fragrance
FR
lily of the valley fragrance
FR
lily of the valley specialty
FR
lilyall / methyl anthranilate schiff's base
FR
lilyall substitute
FR
linalool
FL/FR
linalool oxide
FL/FR
linalyl benzoate
FL/FR
lotus fragrance
FR
magnolia cyclohexanol
FR
magnolia decadienal
FR
methoxycitronellal
FR
4-
methyl cyclohexane propanal
FR
methyl dihydrojasmonate
FL/FR
2-
methyl octanal
FL/FR
1-
methyl-3-(2-methyl propyl) cyclohexanol
FR
4-(4-
methyl-4-hydroxyamyl)-delta3-cyclohexenecarboxaldehyde
FR
3-
methyl-6-ethyl-5-octen-1-ol
FR
mimosa absolute france
FL/FR
muguet butanal
FR
muguet butanol
FR
muguet carbaldehyde
FR
muguet carbinol
FL/FR
muguet carboxaldehyde
FR
muguet ethanol
FR
muguet nitrile
FR
muguet octadienol
FR
muguet propanol
FR
muguet shiseol
FL/FR
cis-
muguet shiseol
FL/FR
muguet specialty
FR
nerol
FL/FR
nerolidol
FL/FR
neryl acetate
FL/FR
ocean propanal
FL/FR
octahydro-4,7-methano-1H-indene-5-acetaldehyde
FR
octahydro-4,7-methano-1H-indene-5-acetaldehyde + 6-methyl-octahydro-4,7-methano-indene-5-carbaldehyd
FR
orchid specialty
FR
orris pyridine 25% IPM
FR
2-
pentyl-2-cyclohexen-1-one
FR
peony alcohol
FR
phenethyl alcohol
FL/FR
phenethyl phenyl acetate
FL/FR
phenethyl salicylate
FL/FR
phenyl acetaldehyde digeranyl acetal
FR
phenyl glycol diacetate
FR
4-
propyl cyclohexane propanal
FR
rhodinol
FL/FR
rose absolute pentanol
FR
rose butanoate
FL/FR
alpha-
terpinyl anthranilate
FL/FR
tetrahydrolinalool
FL/FR
(S,E)-3,7,11-
trimethyldodeca-6,10-dienal
FR
verdyl acetate
FR
violet methyl carbonate
FR
ylang ylang flower oil
FL/FR
ylang ylang flower oil CO2 extract
FL/FR
ylang ylang flower oil fractions
FR
ylang ylang flower oil I
FL/FR
ylang ylang flower oil II
FL/FR
ylang ylang oil III fractions
FR
ylang ylang oil replacer
FR
fruity
allyl amyl glycolate
FR
dimethyl benzyl carbinyl isobutyrate
FR
ethyl bicyclo(2.2.1)-5-heptene-2-carboxylate
FL/FR
peach pivalate
FR
green
acetaldehyde ethyl phenethyl acetal
FL/FR
(Z)-3-
hexen-1-ol
FL/FR
(Z)-3-
hexen-1-yl benzoate
FL/FR
2,4-
ivy carbaldehyde
FL/FR
(Z)-
leaf acetal
FL/FR
melon nonenoate
FL/FR
phenyl acetaldehyde diethyl acetal
FL/FR
phenyl acetaldehyde dimethyl acetal
FL/FR
phenyl acetaldehyde ethylene glycol acetal
FR
violet decenol
FR
violet leaf absolute
FL/FR
hay
hay absolute
FR
herbal
clary sage oil france
FL/FR
daucus carota fruit oil
FL/FR
dimethyl benzyl carbinyl formate
FL/FR
linalyl acetate
FL/FR
pine hexanol
FR
marine
marine pyridine
FR
ozone propanal
FR
melon
watermelon ketone
FR
mossy
veramoss (IFF)
FR
muguet
4-iso
butyl 1-(3-methoxy-2-propen-1-yl) benzene
FR
4-
ethyl 1-(3-methoxy-2-propen-1-yl) benzene
FR
4-
methyl 1-(3-methoxy-2-propen-1-yl) benzene
FR
4-
propyl 1-(3-methoxy-2-propen-1-yl) benzene
FR
naphthyl
beta-
naphthyl ethyl ether
FL/FR
powdery
para-
anisyl alcohol
FL/FR
spicy
iso
eugenyl acetate
FL/FR
terpenic
alpha-
terpineol
FL/FR
tonka
tonka bean absolute
FR
vanilla
ethyl vanillin
FL/FR
vanilla bean absolute (vanilla planifolia)
FL/FR
vanillyl acetate
FL/FR
waxy
decyl acetate
FL/FR
1-
dodecanol
FL/FR
ethyl laurate
FL/FR
1-
undecanol
FL/FR
woody
amber dioxane
FR
cedryl methyl ether
FR
guaiacwood oil
FL/FR
hydroxycitronellal diisotridecyl acetal
FR
patchouli ethanone
FR
santall
FR
tobacarol (IFF)
FR
woody acetate
FR
(Z)-
woody amylene
FR
For Flavor
No flavor group found for these
alpha-
amyl cinnamaldehyde dimethyl acetal
FL/FR
(E)-
cinnamyl alcohol
FL/FR
9-
decenal
FL/FR
dimethyl benzyl carbinyl formate
FL/FR
ethyl bicyclo(2.2.1)-5-heptene-2-carboxylate
FL/FR
(E,E)-
farnesol
FL/FR
hydroxycitronellal propylene glycol acetal
FL/FR
2-
methyl octanal
FL/FR
phenyl acetaldehyde diethyl acetal
FL/FR
alpha-
terpinyl anthranilate
FL/FR
alpha-
butyl cinnamaldehyde
FL/FR
aldehydic
aldehydic
nonanal (aldehyde C-9)
FL/FR
1-
undecanol
FL/FR
aromatic
para-
cresyl isobutyrate
FL/FR
balsamic
siam
benzoin resinoid
FL/FR
benzyl salicylate
FL/FR
iso
butyl cinnamate
FL/FR
ethyl cinnamate
FL/FR
berry
heliotropyl acetone
FL/FR
raspberry ketone
FL/FR
raspberry ketone acetate
FL/FR
raspberry ketone methyl ether
FL/FR
cherry
heliotropin
FL/FR
citrus
citronellyl oxyacetaldehyde
FL/FR
lime oil distilled mexico
FL/FR
linalool
FL/FR
nerol
FL/FR
alpha-
terpineol
FL/FR
cooling
iso
butyl salicylate
FL/FR
creamy
para-
anisaldehyde
FL/FR
fatty
(Z)-3-
hexen-1-yl benzoate
FL/FR
10-
undecenal (aldehyde C-11 undecylenic)
FL/FR
floral
bois de rose oil brazil
FL/FR
citronellol
FL/FR
citronellyl acetate
FL/FR
dihydrojasmone
FL/FR
dimethyl benzyl carbinyl acetate
FL/FR
farnesol
FL/FR
geraniol
FL/FR
linalyl acetate
FL/FR
linalyl benzoate
FL/FR
methyl dihydrojasmonate
FL/FR
muguet carbinol
FL/FR
muguet shiseol
FL/FR
cis-
muguet shiseol
FL/FR
neryl acetate
FL/FR
ocean propanal
FL/FR
phenethyl alcohol
FL/FR
rhodinol
FL/FR
tetrahydrolinalool
FL/FR
ylang ylang flower oil
FL/FR
ylang ylang flower oil CO2 extract
FL/FR
ylang ylang flower oil I
FL/FR
ylang ylang flower oil II
FL/FR
fruity
para-
anisyl alcohol
FL/FR
dimethyl anthranilate
FL/FR
linalyl cinnamate
FL/FR
rose butanoate
FL/FR
green
acetaldehyde ethyl phenethyl acetal
FL/FR
iso
amyl salicylate
FL/FR
cinnamyl alcohol
FL/FR
cuminyl acetaldehyde
FL/FR
cyclamen aldehyde
FL/FR
cyclohexyl ethyl alcohol
FL/FR
geranyl acetate
FL/FR
(Z)-3-
hexen-1-ol
FL/FR
(Z)-3-
hexen-1-yl salicylate
FL/FR
2,4-
ivy carbaldehyde
FL/FR
(Z)-
leaf acetal
FL/FR
linalool oxide
FL/FR
melon nonenoate
FL/FR
nerolidol
FL/FR
phenyl acetaldehyde dimethyl acetal
FL/FR
violet leaf absolute
FL/FR
herbal
clary sage oil france
FL/FR
coriander seed oil
FL/FR
daucus carota fruit oil
FL/FR
honey
phenethyl phenyl acetate
FL/FR
medicinal
dimethyl benzyl carbinol
FL/FR
phenethyl salicylate
FL/FR
melon
hydroxycitronellal diethyl acetal
FL/FR
powdery
hydroxycitronellol
FL/FR
beta-
naphthyl ethyl ether
FL/FR
soapy
dodecanal (aldehyde C-12 lauric)
FL/FR
1-
dodecanol
FL/FR
spicy
iso
eugenyl acetate
FL/FR
3-
phenyl propyl alcohol
FL/FR
tropical
alpha-
amyl cinnamaldehyde
FL/FR
vanilla
ethyl vanillin
FL/FR
vanilla bean absolute (vanilla planifolia)
FL/FR
vanillyl acetate
FL/FR
waxy
adoxal (Givaudan)
FL/FR
decanal (aldehyde C-10)
FL/FR
decanol
FL/FR
decyl acetate
FL/FR
ethyl laurate
FL/FR
alpha-
hexyl cinnamaldehyde
FL/FR
hydroxycitronellal
FL/FR
hydroxycitronellal dimethyl acetal
FL/FR
mimosa absolute france
FL/FR
woody
amyris wood oil
FL/FR
guaiacwood oil
FL/FR
 
Potential Uses:
 alliage
 anais anais
 azzaro
 blue mist
FRbouquet
FRbubble gum
 calyx
FRcedar
 charlie
FRcherry blossom
FRcitrus
 clean
 cloth clean cloths
FRcoconut tropical coconut
FRcountry meadow
FRcyclamen
 devin
 estee
 eternity
FRfern
FRfloral
FRgardenia
FRgrapefruit
FRgreen
 halston
FRherbal
FRhoneysuckle
 j' ai ose
FRlilac
FRlily
FRlily of the valley
FRlinden flower
FRlotus
 marbert man
FRmint
FRmusk
 new car
 paco rabanne
FRpine
FRpotpourri
 pour homme
FRrain
FRrose
FRsandalwood
FRsea breeze
FRspring rain
 tide
 turbulences
FRwoody
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
 aldehyde MBDC
 aldehyde MBDC pure
2-(4-tert-butyl benzyl) propionaldehyde
 butyl phenyl methyl propional
p-tert-butyl-a-methyldihydrocinnamic aldehyde
p-tert-butyl-a-methylhydrocinnamaldehyde
p-tert-butyl-a-methylhydrocinnamic aldehyde
p-tert-butyl-alpha-methyl dihydrocinnamaldehyde
para-tert-butyl-alpha-methyl dihydrocinnamaldehyde
meta-tert-butyl-alpha-methyl dihydrocinnamic aldehyde
p-tert-butyl-alpha-methyl dihydrocinnamic aldehyde
para-tert-butyl-alpha-methyl dihydrocinnamic aldehyde
p-tert-butyl-alpha-methyl hydrocinnamaldehyde
para-tert-butyl-alpha-methyl hydrocinnamaldehyde
p-tert-butyl-alpha-methyl hydrocinnamic aldehyde
para-tert-butyl-alpha-methyl hydrocinnamic aldehyde
m-tert-butyl-alpha-methyldihydrocinnamic aldehyde
2-(4-tert-butylbenzyl)propionaldehyde
3-(4-tert-butylphenyl)butanal
 butylphenylmethylpropional
4-(1,1-dimethyl ethyl)-alpha-methyl benzene propanal
4-(1,1-dimethylethyl)-alpha-methylbenzenepropanal
 hydrocinnamaldehyde, p-tert-butyl-a-methyl-
 lilestralis
 lilestralis pure
 lilial
 lilialdehyde
 liligul N 743 CLP
 lilyall
 lysmeral
 lysmeral extra
 mefloral
3-[4-(2-methyl-2-propanyl)phenyl]butanal
alpha-methyl-beta-(p-tert-butylphenyl)propionaldehyde
alpha-methyl-beta-(para-tert-butyl phenyl) propionaldehyde
a-methyl-p-(tert-butyl)hydrocinnamaldehyde
alpha-methyl-p-(tert-butyl)hydrocinnamaldehyde
alpha-methyl-para-(tert-butyl) hydrocinnamaldehyde
 

Articles:

US Patents:4,778,934 - Process for the manufacture of p-tert-butyl-.alpha.-methylhydrocinnamaldehyde
PubMed:Genotoxicity assessment of some cosmetic and food additives.
US Patents:4,568,772 - Process for the preparation of p-t-butyl-.alpha.-methyldihydrocinnamaldehyde
PubMed:Vocational interests of intellectually gifted and highly achieving young adults.
US Patents:4,568,772 - Process for the preparation of p-t-butyl-.alpha.-methyldihydrocinnamaldehyde
PubMed:Two fragrance chemicals may act as toxicants via TRPA1 stimulation rather than via direct mitochondrial action.
PubMed:Occurrences and potential risks of 16 fragrances in five German sewage treatment plants and their receiving waters.
PubMed:Fragrance chemicals lyral and lilial decrease viability of HaCat cells' by increasing free radical production and lowering intracellular ATP level: protection by antioxidants.
PubMed:Phosphoinositide 3-kinase-dependent antagonism in mammalian olfactory receptor neurons.
PubMed:Olfactory sensitivity for sperm-attractant aromatic aldehydes: a comparative study in human subjects and spider monkeys.
PubMed:Sorbent trapping solid-phase microextraction of fragrance allergens in indoor air.
PubMed:Determination of suspected allergens in cosmetic products by headspace-programmed temperature vaporization-fast gas chromatography-quadrupole mass spectrometry.
PubMed:Bioreduction of alpha-methylcinnamaldehyde derivatives: chemo-enzymatic asymmetric synthesis of Lilial and Helional.
PubMed:Quantitative determination of some volatile suspected allergens in cosmetic creams spread on skin by direct contact sorptive tape extraction-gas chromatography-mass spectrometry.
PubMed:Large-scale production and study of a synthetic G protein-coupled receptor: human olfactory receptor 17-4.
PubMed:Oestrogenic activity of benzyl salicylate, benzyl benzoate and butylphenylmethylpropional (Lilial) in MCF7 human breast cancer cells in vitro.
PubMed:Polyvalent type IV sensitizations to multiple fragrances and a skin protection cream in a metal worker.
PubMed:HMOX1 and NQO1 genes are upregulated in response to contact sensitizers in dendritic cells and THP-1 cell line: role of the Keap1/Nrf2 pathway.
PubMed:Odorant design based on the carbon/silicon switch strategy.
PubMed:Sensitization to 26 fragrances to be labelled according to current European regulation. Results of the IVDK and review of the literature.
PubMed:Fragrance ingredient labelling in products on sale in the U.K.
PubMed:High-performance liquid chromatographic method for the simultaneous determination of 24 fragrance allergens to study scented products.
PubMed:Prediction of perception: probing the hOR17-4 olfactory receptor model with silicon analogues of bourgeonal and lilial.
PubMed:Cross-adaptation between olfactory responses induced by two subgroups of odorant molecules.
PubMed:A psychophysical study of the relationship between temporal processing in odor mixtures and transduction pathways.
PubMed:Identification of Lilial as a fragrance sensitizer in a perfume by bioassay-guided chemical fractionation and structure-activity relationships.
PubMed:Blocking adenylyl cyclase inhibits olfactory generator currents induced by "IP(3)-odors".
PubMed:Regulation of cutaneous allergic reaction by odorant inhalation.
PubMed:Responses to putative second messengers and odorants in water nose olfactory neurons of Xenopus laevis.
PubMed:Subtypes of odorant-binding proteins--heterologous expression and ligand binding.
PubMed:Odorants selectively activate distinct G protein subtypes in olfactory cilia.
PubMed:Ca2+ and Cl(-)-dependence of the turtle olfactory response to odorants and forskolin.
PubMed:Chemosensitivity of the osphradium of the pond snail Lymnaea stagnalis
PubMed:Odor-induced phosphorylation of olfactory cilia proteins.
PubMed:Allergic contact dermatitis to the fragrance material lilial.
 
Notes:
fresh accord - lilyall and benzyl isoeugenol. autumn leaves accord - phenethyl phenyl acetate and lilyall and raspberry ketone. clean fresh accord - aldehyde C-12 10% and lilyall. cloth accord - musk gx, alcohol C-12, lilyall and santall.
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