lilyall
 
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.
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas
3-(4-tert-butylphenyl)butanal (Click)
CAS Number: 80-54-6Picture of molecule
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
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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
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
Odor Type: floral
Odor Strength: medium
Odor Description:
at 100.00 %. 
floral muguet watery green powdery cumin
Substantivity: 236 Hour(s)
  
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Safety 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.
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
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: fragrance agents
IFRA Critical Effect: 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)
0.10 % (1)
Category 2:  0.20 %
Category 3:  0.60 %
Category 4:  1.90 %
Category 5:  1.00 %
Category 6:  3.00 % (1)
Category 7:  0.30 %
Category 8:  2.00 %
Category 9:  2.50 %
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.
Synonyms   Articles   Notes   Search   Top
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
Synonyms   Articles   Notes   Search   Top
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
Synonyms   Articles   Notes   Search   Top
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
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
aldehydic
 adoxal (Givaudan)FL/FR
 citronellyl oxyacetaldehydeFL/FR
 citrus carbaldehydeFR
 decanal (aldehyde C-10)FL/FR
9-decenalFL/FR
 dodecanal (aldehyde C-12 lauric)FL/FR
 lily pentanalFR
 nonanal (aldehyde C-9)FL/FR
10-undecenal (aldehyde C-11 undecylenic)FL/FR
animal
para-cresyl isobutyrateFL/FR
anisic
para-anisaldehydeFL/FR
balsamic
 amyris wood oilFL/FR
siam benzoin resinoidFL/FR
 benzyl salicylateFL/FR
isobutyl cinnamateFL/FR
 cinnamyl alcoholFL/FR
(E)-cinnamyl alcoholFL/FR
 clover nitrileFR
 ethyl cinnamateFL/FR
 fir balsam absoluteFR
 linalyl cinnamateFL/FR
3-phenyl propyl alcoholFL/FR
berry
 raspberry ketoneFL/FR
 raspberry ketone acetateFL/FR
 raspberry ketone methyl etherFL/FR
citrus
 benzyl anthranilateFR
 citrus ocimenolFR
isodecyl acetateFR
 lime oil distilled mexicoFL/FR
 methyl indole-1-carboxylateFR
 myrmac aldehydeFR
 tetrahydromyrcenolFR
fatty
 decanolFL/FR
floral
 aeolanthus graveolens oilFR
alpha-amyl cinnamaldehydeFL/FR
alpha-amyl cinnamaldehyde dimethyl acetalFL/FR
isoamyl salicylateFL/FR
 bois de rose oil brazilFL/FR
alpha-butyl cinnamaldehydeFL/FR
4-isobutyl cyclohexane propanalFR
isobutyl salicylateFL/FR
 citronellolFL/FR
 citronellyl (R)-lactateFR
 citronellyl acetateFL/FR
 citronellyl ethoxalateFR
 citrus propanolFR
 coriander seed oilFL/FR
 corps popinalFR
 cumin carbinolFR
 cuminyl acetaldehydeFL/FR
 cyclamen aldehydeFL/FR
 cyclamen homoaldehydeFR
 cyclohexyl ethyl alcoholFL/FR
 cyclohexyl propanolFR
2-decalinolFR
 dihydrojasmoneFL/FR
 dimethyl anthranilateFL/FR
 dimethyl benzyl carbinolFL/FR
 dimethyl benzyl carbinyl acetateFL/FR
2,5-dimethyl-2-indan methanolFR
4-ethyl cyclohexane propanalFR
 ethyl linalyl acetalFR
(E,E)-farnesolFL/FR
 farnesolFL/FR
 floral butanalFR
 floral pyranolFR
 floral specialtyFR
 freesia acetateFR
 gardenia oxideFR
 geraniolFL/FR
 geranyl acetateFL/FR
 ginger lily fragranceFR
 hawthorn ethanolFR
 heliotropinFL/FR
 heliotropyl acetoneFL/FR
 heliotropyl diethyl acetalFR
(Z)-4-hepten-2-yl salicylateFR
(Z)-3-hexen-1-yl salicylateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 hyacinth etherFR
 hydrangea fragranceFR
3-(4-hydroxy-4-methyl cyclohexyl) butanalFR
 hydroxycitronellalFL/FR
 hydroxycitronellal / methyl anthranilate schiff's baseFR
 hydroxycitronellal diethyl acetalFL/FR
 hydroxycitronellal dimethyl acetalFL/FR
 hydroxycitronellal distillation residue distillatesFR
 hydroxycitronellal nitrileFR
 hydroxycitronellal propylene glycol acetalFL/FR
 hydroxycitronellal residueFR
 hydroxycitronellolFL/FR
 jasimiaFR
 leerallFR
 leerall / methyl anthranilate schiff's baseFR
 lily flower absoluteFR
 lily fragranceFR
calla lily fragranceFR
water lily fragranceFR
 lily of the valley fragranceFR
 lily of the valley specialtyFR
 lilyall / methyl anthranilate schiff's baseFR
 lilyall substituteFR
 linaloolFL/FR
 linalool oxideFL/FR
 linalyl benzoateFL/FR
 lotus fragranceFR
 magnolia cyclohexanolFR
 magnolia decadienalFR
 methoxycitronellalFR
4-methyl cyclohexane propanalFR
 methyl dihydrojasmonateFL/FR
2-methyl octanalFL/FR
1-methyl-3-(2-methyl propyl) cyclohexanolFR
4-(4-methyl-4-hydroxyamyl)-delta3-cyclohexenecarboxaldehydeFR
3-methyl-6-ethyl-5-octen-1-olFR
 mimosa absolute franceFL/FR
 muguet butanalFR
 muguet butanolFR
 muguet carbaldehydeFR
 muguet carbinolFL/FR
 muguet carboxaldehydeFR
 muguet ethanolFR
 muguet nitrileFR
 muguet octadienolFR
 muguet propanolFR
 muguet shiseolFL/FR
cis-muguet shiseolFL/FR
 muguet specialtyFR
 nerolFL/FR
 nerolidolFL/FR
 neryl acetateFL/FR
 ocean propanalFL/FR
 octahydro-4,7-methano-1H-indene-5-acetaldehydeFR
 octahydro-4,7-methano-1H-indene-5-acetaldehyde + 6-methyl-octahydro-4,7-methano-indene-5-carbaldehydFR
 orchid specialtyFR
 orris pyridine 25% IPMFR
2-pentyl-2-cyclohexen-1-oneFR
 peony alcoholFR
 phenethyl alcoholFL/FR
 phenethyl phenyl acetateFL/FR
 phenethyl salicylateFL/FR
 phenyl acetaldehyde digeranyl acetalFR
 phenyl glycol diacetateFR
4-propyl cyclohexane propanalFR
 rhodinolFL/FR
 rose absolute pentanolFR
 rose butanoateFL/FR
alpha-terpinyl anthranilateFL/FR
 tetrahydrolinaloolFL/FR
(S,E)-3,7,11-trimethyldodeca-6,10-dienalFR
 verdyl acetateFR
 violet methyl carbonateFR
 ylang ylang flower oilFL/FR
 ylang ylang flower oil CO2 extractFL/FR
 ylang ylang flower oil fractionsFR
 ylang ylang flower oil IFL/FR
 ylang ylang flower oil IIFL/FR
 ylang ylang oil III fractionsFR
 ylang ylang oil replacerFR
fruity
 allyl amyl glycolateFR
 dimethyl benzyl carbinyl isobutyrateFR
 ethyl bicyclo(2.2.1)-5-heptene-2-carboxylateFL/FR
 peach pivalateFR
green
 acetaldehyde ethyl phenethyl acetalFL/FR
(Z)-3-hexen-1-olFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
2,4-ivy carbaldehydeFL/FR
(Z)-leaf acetalFL/FR
 melon nonenoateFL/FR
 phenyl acetaldehyde diethyl acetalFL/FR
 phenyl acetaldehyde dimethyl acetalFL/FR
 phenyl acetaldehyde ethylene glycol acetalFR
 violet decenolFR
 violet leaf absoluteFL/FR
hay
 hay absoluteFR
herbal
 clary sage oil franceFL/FR
 daucus carota fruit oilFL/FR
 dimethyl benzyl carbinyl formateFL/FR
 linalyl acetateFL/FR
 pine hexanolFR
marine
 marine pyridineFR
 ozone propanalFR
melon
 watermelon ketoneFR
mossy
 veramoss (IFF)FR
muguet
4-isobutyl 1-(3-methoxy-2-propen-1-yl) benzeneFR
4-ethyl 1-(3-methoxy-2-propen-1-yl) benzeneFR
4-methyl 1-(3-methoxy-2-propen-1-yl) benzeneFR
4-propyl 1-(3-methoxy-2-propen-1-yl) benzeneFR
naphthyl
beta-naphthyl ethyl etherFL/FR
powdery
para-anisyl alcoholFL/FR
spicy
isoeugenyl acetateFL/FR
terpenic
alpha-terpineolFL/FR
tonka
 tonka bean absoluteFR
vanilla
 ethyl vanillinFL/FR
 vanilla bean absolute (vanilla planifolia)FL/FR
 vanillyl acetateFL/FR
waxy
 decyl acetateFL/FR
1-dodecanolFL/FR
 ethyl laurateFL/FR
1-undecanolFL/FR
woody
 amber dioxaneFR
 cedryl methyl etherFR
 guaiacwood oilFL/FR
 hydroxycitronellal diisotridecyl acetalFR
 patchouli ethanoneFR
 santallFR
 tobacarol (IFF)FR
 woody acetateFR
(Z)-woody amyleneFR
 
For Flavor
 
No flavor group found for these
alpha-amyl cinnamaldehyde dimethyl acetalFL/FR
(E)-cinnamyl alcoholFL/FR
9-decenalFL/FR
 dimethyl benzyl carbinyl formateFL/FR
 ethyl bicyclo(2.2.1)-5-heptene-2-carboxylateFL/FR
(E,E)-farnesolFL/FR
 hydroxycitronellal propylene glycol acetalFL/FR
2-methyl octanalFL/FR
 phenyl acetaldehyde diethyl acetalFL/FR
alpha-terpinyl anthranilateFL/FR
alpha-butyl cinnamaldehydeFL/FR
aldehydic
 nonanal (aldehyde C-9)FL/FR
1-undecanolFL/FR
aromatic
para-cresyl isobutyrateFL/FR
balsamic
siam benzoin resinoidFL/FR
 benzyl salicylateFL/FR
isobutyl cinnamateFL/FR
 ethyl cinnamateFL/FR
berry
 heliotropyl acetoneFL/FR
 raspberry ketoneFL/FR
 raspberry ketone acetateFL/FR
 raspberry ketone methyl etherFL/FR
cherry
 heliotropinFL/FR
citrus
 citronellyl oxyacetaldehydeFL/FR
 lime oil distilled mexicoFL/FR
 linaloolFL/FR
 nerolFL/FR
alpha-terpineolFL/FR
cooling
isobutyl salicylateFL/FR
creamy
para-anisaldehydeFL/FR
fatty
(Z)-3-hexen-1-yl benzoateFL/FR
10-undecenal (aldehyde C-11 undecylenic)FL/FR
floral
 bois de rose oil brazilFL/FR
 citronellolFL/FR
 citronellyl acetateFL/FR
 dihydrojasmoneFL/FR
 dimethyl benzyl carbinyl acetateFL/FR
 farnesolFL/FR
 geraniolFL/FR
 linalyl acetateFL/FR
 linalyl benzoateFL/FR
 methyl dihydrojasmonateFL/FR
 muguet carbinolFL/FR
 muguet shiseolFL/FR
cis-muguet shiseolFL/FR
 neryl acetateFL/FR
 ocean propanalFL/FR
 phenethyl alcoholFL/FR
 rhodinolFL/FR
 tetrahydrolinaloolFL/FR
 ylang ylang flower oilFL/FR
 ylang ylang flower oil CO2 extractFL/FR
 ylang ylang flower oil IFL/FR
 ylang ylang flower oil IIFL/FR
fruity
para-anisyl alcoholFL/FR
 dimethyl anthranilateFL/FR
 linalyl cinnamateFL/FR
 rose butanoateFL/FR
green
 acetaldehyde ethyl phenethyl acetalFL/FR
isoamyl salicylateFL/FR
 cinnamyl alcoholFL/FR
 cuminyl acetaldehydeFL/FR
 cyclamen aldehydeFL/FR
 cyclohexyl ethyl alcoholFL/FR
 geranyl acetateFL/FR
(Z)-3-hexen-1-olFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
2,4-ivy carbaldehydeFL/FR
(Z)-leaf acetalFL/FR
 linalool oxideFL/FR
 melon nonenoateFL/FR
 nerolidolFL/FR
 phenyl acetaldehyde dimethyl acetalFL/FR
 violet leaf absoluteFL/FR
herbal
 clary sage oil franceFL/FR
 coriander seed oilFL/FR
 daucus carota fruit oilFL/FR
honey
 phenethyl phenyl acetateFL/FR
medicinal
 dimethyl benzyl carbinolFL/FR
 phenethyl salicylateFL/FR
melon
 hydroxycitronellal diethyl acetalFL/FR
powdery
 hydroxycitronellolFL/FR
beta-naphthyl ethyl etherFL/FR
soapy
 dodecanal (aldehyde C-12 lauric)FL/FR
1-dodecanolFL/FR
spicy
isoeugenyl acetateFL/FR
3-phenyl propyl alcoholFL/FR
tropical
alpha-amyl cinnamaldehydeFL/FR
vanilla
 ethyl vanillinFL/FR
 vanilla bean absolute (vanilla planifolia)FL/FR
 vanillyl acetateFL/FR
waxy
 adoxal (Givaudan)FL/FR
 decanal (aldehyde C-10)FL/FR
 decanolFL/FR
 decyl acetateFL/FR
 ethyl laurateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 hydroxycitronellalFL/FR
 hydroxycitronellal dimethyl acetalFL/FR
 mimosa absolute franceFL/FR
woody
 amyris wood oilFL/FR
 guaiacwood oilFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 alliage 
 anais anais 
 azzaro 
 blue mist 
 bouquetFR
 bubble gumFR
 calyx 
 cedarFR
 charlie 
 cherry blossomFR
 citrusFR
 clean 
 cloth clean cloths 
 coconut tropicalFR
 cyclamenFR
 devin 
 estee 
 eternity 
 fern fougereFR
 floralFR
 gardeniaFR
 grapefruitFR
 greenFR
 halston 
 herbalFR
 honeysuckle chevrefeuilleFR
 j' ai ose 
 lilac lilas syringaFR
 lilyFR
 linden blossom limeflower tilleulFR
 lotusFR
 marbert man 
 meadow countryFR
 mintFR
 muguet lily of the valleyFR
 muskFR
 new car 
 ocean sea breezeFR
 paco rabanne 
 pineFR
 potpourriFR
 pour homme 
 rainFR
 rain springFR
 roseFR
 sandalwoodFR
 tide 
 turbulences 
 woodyFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 not found in nature
Synonyms   Articles   Notes   Search   Top
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
Synonyms   Articles   Notes   Search   Top
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.
Synonyms   Articles   Notes   Search   Top
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