推荐产品
生物源
synthetic
品質等級
等級
FG
Halal
Kosher
agency
meets purity specifications of JECFA
法律遵循
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 172.515
化驗
≥95%
折射率
n20/D 1.517 (lit.)
bp
92-94 °C/12 mmHg (lit.)
密度
1.002 g/mL at 25 °C (lit.)
應用
flavors and fragrances
文件
see Safety & Documentation for available documents
食物過敏原
no known allergens
感官的
fresh; green; floral
儲存溫度
2-8°C
SMILES 字串
[H]C(=O)C(C)c1ccccc1
InChI
1S/C9H10O/c1-8(7-10)9-5-3-2-4-6-9/h2-8H,1H3
InChI 密鑰
IQVAERDLDAZARL-UHFFFAOYSA-N
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一般說明
2-Phenylpropionaldehyde is used in perfumes for its green hyacinth odor.
應用
- 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).
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 1
閃點（°F）
174.2 °F
閃點（°C）
79 °C
個人防護裝備
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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 D Thompson et al.
Chemical research in toxicology, 9(8), 1225-1229 (1996-12-01)
We propose that 3-carbamoyl-2-phenylpropionaldehyde is an intermediate in the metabolism of felbamate, an anti-epileptic drug with a unique profile of the therapeutic activity, and undergoes a cascade of chemical reactions responsible for the toxic properties of the parent drug. To
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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