推荐产品
质量水平
方案
≥90%
折射率
n20/D 1.535 (lit.)
沸点
195 °C
mp
−10 °C (lit.)
溶解性
H2O: slightly soluble
alcohol: soluble
diethyl ether: soluble
密度
1.027 g/mL at 25 °C
官能团
aldehyde
phenyl
储存温度
2-8°C
SMILES字符串
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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应用
在一项研究中使用苯乙醛来分析植物来源的挥发性化学物质对一龄棉铃虫的觅食的作用。
生化/生理作用
苯乙醛是一种昆虫引诱剂，可用于害虫的黑光诱捕器 。它是花香的组成部分。是多种生化途径的中间体 。
其他说明
含有不定量的聚氧化苯乙烯
警示用语：
Danger
危险分类
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1A
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 1
闪点(°F)
154.4 °F - (External MSDS)
闪点(°C)
68 °C - (External MSDS)
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
The role of two plant-derived volatiles in the foraging movement of 1st instar Helicoverpa armigera (Hubner): time to stop and smell the flowers.
Perkins LE, et al.
Arthropod-Plant Interactions, 3(3), 173-179 (2009)
Yasuhisa Kaminaga et al.
The Journal of biological chemistry, 281(33), 23357-23366 (2006-06-13)
We have isolated and characterized Petunia hybrida cv. Mitchell phenylacetaldehyde synthase (PAAS), which catalyzes the formation of phenylacetaldehyde, a constituent of floral scent. PAAS is a cytosolic homotetrameric enzyme that belongs to group II pyridoxal 5'-phosphate-dependent amino-acid decarboxylases and shares
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
Fong Lam Chu et al.
Journal of agricultural and food chemistry, 56(22), 10697-10704 (2008-10-29)
Benzaldehyde, a potent aroma chemical of bitter almond, can also be formed thermally from phenylalanine and may contribute to the formation of off-aroma. To identify the precursors involved in its generation during Maillard reaction, various model systems containing phenylalanine, phenylpyruvic
Rosario Zamora et al.
Journal of agricultural and food chemistry, 60(21), 5491-5496 (2012-05-15)
The chemical conversion of phenylethylamine into phenylacetaldehyde in the presence of lipid oxidation products (LOPs) was studied to investigate the possibility that biogenic amines can be converted into Strecker aldehydes upon processing. Model systems of phenylethylamine and methyl 13-hydroperoxyoctadeca-9,11-dienoate (HP)
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