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Merck

W288608

Sigma-Aldrich

2-Phenylpropionaldehyde

≥95%, FCC, FG

Sinónimos:

2-Phenylpropanal, Hydratropaldehyde

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About This Item

Fórmula lineal:
CH3CH(C6H5)CHO
Número de CAS:
Peso molecular:
134.18
FEMA Number:
2886
Beilstein/REAXYS Number:
1905601
EC Number:
Council of Europe no.:
126
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
5.038
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

assay

≥95%

refractive index

n20/D 1.517 (lit.)

bp

92-94 °C/12 mmHg (lit.)

density

1.002 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

fresh; green; floral

storage temp.

2-8°C

SMILES string

[H]C(=O)C(C)c1ccccc1

InChI

1S/C9H10O/c1-8(7-10)9-5-3-2-4-6-9/h2-8H,1H3

InChI key

IQVAERDLDAZARL-UHFFFAOYSA-N

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General description

2-Phenylpropionaldehyde is used in perfumes for its green hyacinth odor.

Application


  • Cytotoxicity, early safety screening, and antimicrobial potential of minor oxime constituents of essential oils and aromatic extracts.: Explores the safety and effectiveness of 2-Phenylpropionaldehyde among other compounds in essential oils, highlighting its potential antimicrobial properties and implications for food safety and preservation (Strub DJ et al., 2022).

  • Spectroscopic Evidence for a Cobalt-Bound Peroxyhemiacetal Intermediate.: This study provides spectroscopic evidence of a cobalt-bound intermediate in reactions involving 2-Phenylpropionaldehyde, advancing our knowledge of chemical reaction mechanisms and catalysis (Cho J et al., 2021).

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

174.2 °F

flash_point_c

79 °C

ppe

Eyeshields, 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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tert-Butyldimethylsilylated cyclodextrins: versatile chiral stationary phases in capillary gas chromatography.
Maas B, et al.
Journal of Chromatographic Science, 33(5), 223-228 (1995)
M Popović et al.
Chemical research in toxicology, 17(12), 1568-1576 (2004-12-21)
Felbamate (2-phenyl-1,3-propanediol dicarbamate, FBM) can cause aplastic anemia and hepatotoxicity. The mechanism of FBM-induced toxicities is unknown; however, it has been proposed that 2-phenylpropenal, a reactive metabolite of FBM, is responsible. The pathway leading to this metabolite involves hydrolysis of
C M Dieckhaus et al.
Chemical research in toxicology, 14(5), 511-516 (2001-05-23)
Felbamate has proven to be an effective therapy for treating refractory epilepsy. However, felbamate therapy has been limited due to the associated reports of hepatotoxicity and aplastic anemia. Previous research from our laboratory has proposed 2-phenylpropenal as the reactive metabolite
Shane G Roller et al.
Chemical research in toxicology, 15(6), 815-824 (2002-06-18)
Felbamate is an anti-epileptic drug associated with hepatotoxicity and aplastic anemia. These toxicities are believed to be mediated by the formation of the reactive species 2-phenylpropenal. 4-Hydroxy-5-phenyl-[1,3]oxazinan-2-one is a metabolic precursor for 2-phenylpropenal. 4-Hydroxy-5-phenyl-[1,3]oxazinan-2-one exists in equilibrium with 3-oxo-2-phenylpropyl carbamate
Robert J Parker et al.
Chemical research in toxicology, 18(12), 1842-1848 (2005-12-20)
Evidence has been presented suggesting that a reactive metabolite, 2-phenylpropenal (ATPAL), may be responsible for the toxicities observed during therapy with the antiepileptic drug felbamate (FBM). Formation of ATPAL from its unstable immediate precursor, 3-carbamoyl-2-phenylpropionaldedhyde (CBMA) requires the loss of

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