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Merck
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Documentos

95338

Supelco

2-(4-tert-Butylbenzyl)propionaldehyde

analytical standard

Sinónimos:

4-tert-Butyl-α-methyl-benzenepropanal, 4-tert-Butyl-α-methyl-hydrocinnamaldehyde, Butylphenyl methylpropional, Lilial

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About This Item

Fórmula empírica (notación de Hill):
C14H20O
Número de CAS:
80-54-6
Peso molecular:
204.31
Beilstein:
880140
Número CE:
201-289-8
Número MDL:
MFCD00047655
Código UNSPSC:
85151701
ID de la sustancia en PubChem:
329770446

grado

analytical standard

Análisis

≥90.0% (GC)

caducidad

limited shelf life, expiry date on the label

Características

standard type calibration

técnicas

HPLC: suitable
gas chromatography (GC): suitable

índice de refracción

n20/D 1.505

densidad

0.946 g/mL at 20 °C (lit.)

aplicaciones

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

formato

neat

temp. de almacenamiento

2-8°C

cadena SMILES

[H]C(=O)C(C)Cc1ccc(cc1)C(C)(C)C

InChI

1S/C14H20O/c1-11(10-15)9-12-5-7-13(8-6-12)14(2,3)4/h5-8,10-11H,9H2,1-4H3

Clave InChI

SDQFDHOLCGWZPU-UHFFFAOYSA-N

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Aplicación

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Envase

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictogramas

Health hazardExclamation mark
GHS08,GHS07

Palabra de señalización

Danger

Clasificaciones de peligro

Acute Tox. 4 Oral - Aquatic Chronic 3 - Repr. 1B - Skin Irrit. 2 - Skin Sens. 1

Código de clase de almacenamiento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

174.2 °F - closed cup

Punto de inflamabilidad (°C)

79 °C - closed cup

Equipo de protección personal

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
BCBQ2253V
BCBD4618V
1307266V
1307266
450030/1

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A Jinks et al.
Brain research. Cognitive brain research, 12(2), 273-288 (2001-10-06)
Depending on the odorant, transduction during the olfactory reception process is reported to be mediated by the second messengers cyclic adenosine 3',5'-monophosphate (cAMP) or inositol 1,4,5-triphosphate (IP(3)). The present study with humans investigates the relationship between temporal processing in mixtures
Hiroko Takeuchi et al.
The Journal of general physiology, 122(3), 255-264 (2003-08-27)
It has long been believed that vertebrate olfactory signal transduction is mediated by independent multiple pathways (using cAMP and InsP3 as second messengers). However, the dual presence of parallel pathways in the olfactory receptor cell is still controversial, mainly because
E G Arnau et al.
Contact dermatitis, 43(6), 351-358 (2001-01-05)
Fragrance materials are among the most common causes of allergic contact dermatitis. The aim of this study was to identify in a perfume fragrance allergens not included in the fragrance mix, by use of bioassay-guided chemical fractionation and chemical analysis/structure-activity
Prediction of perception: probing the hOR17-4 olfactory receptor model with silicon analogues of bourgeonal and lilial.
Leszek Doszczak et al.
Angewandte Chemie (International ed. in English), 46(18), 3367-3371 (2007-04-03)
A Iida et al.
Chemical senses, 25(1), 55-59 (2000-02-11)
Using the whole-cell mode of the patch-clamp technique, we attempted to record inward currents in response to cAMP, inositol 1,4, 5-trisphosphate (IP(3)) and odorants from sensory neurons in the olfactory epithelium of the Xenopus laevis lateral diverticulum (water nose). Dialysis
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