W288608
2-Phenylpropionaldehyde
≥95%, FCC, FG
Synonym(s):
2-Phenylpropanal, Hydratropaldehyde
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Linear Formula:
CH3CH(C6H5)CHO
CAS Number:
Molecular Weight:
134.18
FEMA Number:
2886
Beilstein:
1905601
EC Number:
Council of Europe no.:
126
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
5.038
NACRES:
NA.21
grade:
FG
Halal
Kosher
Halal
Kosher
biological source:
synthetic
food allergen:
no known allergens
Recommended Products
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
Looking for similar products? Visit Product Comparison Guide
Related Categories
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 Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
174.2 °F
Flash Point(C)
79 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| W288608-SAMPLE-K | 4061837517570 |
| W288608-1KG-K | 4061837835261 |
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service