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Merck
CN

107395

苯乙醛

≥90%

别名:

2-苯基乙醛

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线性分子式:
C6H5CH2CHO
化学文摘社编号:
分子量:
120.15
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39023706
UNSPSC Code:
12352100
EC Number:
204-574-5
MDL number:
Beilstein/REAXYS Number:
385791
Assay:
≥90%
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InChI key

DTUQWGWMVIHBKE-UHFFFAOYSA-N

InChI

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

SMILES string

O=CCc1ccccc1

assay

≥90%

refractive index

n20/D 1.535 (lit.)

bp

195 °C

mp

−10 °C (lit.)

solubility

H2O: slightly soluble, alcohol: soluble, diethyl ether: soluble

density

1.027 g/mL at 25 °C

functional group

aldehyde, phenyl

storage temp.

2-8°C

Quality Level

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Application

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棉铃虫的觅食的作用

Biochem/physiol Actions

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

Other Notes

含有不定量的聚氧化苯乙烯

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

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

存储类别

8A - Combustible corrosive hazardous materials

wgk

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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)
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

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