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Merck

W287407

Sigma-Aldrich

Phenylacetaldehyde

≥95%, FCC, FG

Sinónimos:

2-Phenylacetaldehyde, α-Tolyaldehyde

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About This Item

Fórmula lineal:
C6H5CH2CHO
Número de CAS:
Peso molecular:
120.15
FEMA Number:
2874
Beilstein/REAXYS Number:
385791
EC Number:
Council of Europe no.:
116
MDL number:
UNSPSC Code:
12164502
eCl@ss:
39023706
PubChem Substance ID:
Flavis number:
5.030
NACRES:
NA.21

biological source

synthetic

Quality Level

grade

FG
Halal
Kosher

agency

meets purity specifications of JECFA

reg. compliance

EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 172.515

description

may contain Citric acid

assay

≥95%

refractive index

n20/D 1.535 (lit.)

bp

195 °C

mp

−10 °C (lit.)

density

1.035 g/mL at 25 °C

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

chocolate; green; honey; hyacinth

storage temp.

2-8°C

SMILES string

O=CCc1ccccc1

InChI

1S/C8H8O/c9-7-6-8-4-2-1-3-5-8/h1-5,7H,6H2

InChI key

DTUQWGWMVIHBKE-UHFFFAOYSA-N

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General description

Phenylacetaldehyde is an important aroma volatile found in tomato and roses. It has also been identified in potato, roasted cocoa beans and honey. Phenylacetaldehyde is also a potent moth attractant.

Biochem/physiol Actions

Taste at 5.0 ppm

Other Notes

Natural occurrence: Apple, apricot, bilbery, cherry, grapefruit, guava, orange peel, peach, raisin, grape, asparagus, blackberry, papaya, melon, cabbage, sweet pepper and celery leaves.

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1A

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 1

flash_point_f

154.4 °F - (External MSDS)

flash_point_c

68 °C - (External MSDS)

ppe

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


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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A review of volatile analytical methods for determining the botanical origin of honey.
Cuevas-Glory LF, et al.
Food Chemistry, 103(3), 1032-1043 (2007)
Phenylacetaldehyde: a chemical attractant for common green lacewings (Chrysoperla carnea sl, Neuroptera: Chrysopidae).
Toth MIKLOS, et al
European Journal of Entomology, 103(1), 267-267 (2006)
Tomato phenylacetaldehyde reductases catalyze the last step in the synthesis of the aroma volatile 2-phenylethanol.
Tieman DM, et al.
Phytochemistry, 68(21), 2660-2669 (2007)
Characterization of some volatile potato components.
Buttery RG, et al.
Journal of Agricultural and Food Chemistry, 18(3), 538-539 (1970)
Rajib Saha et al.
PloS one, 6(7), e21784-e21784 (2011-07-15)
The scope and breadth of genome-scale metabolic reconstructions have continued to expand over the last decade. Herein, we introduce a genome-scale model for a plant with direct applications to food and bioenergy production (i.e., maize). Maize annotation is still underway

Protocolos

GC Analysis of Aldehydes (PFBOA Derivatives) in Beer on SLB®-5ms after SPME using a 65 µm PDMS/DVB Fiber

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