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Merck
CN

D4630

Sigma-Aldrich

2,5-二苯基噁唑

suitable for liquid scintillation spectrometry

别名:

DPO, PPO

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About This Item

经验公式(希尔记法):
C15H11NO
CAS号:
分子量:
221.25
Beilstein:
157021
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

表单

powder

质量水平

沸点

360 °C (lit.)

mp

72-74 °C (lit.)

适用性

suitable for liquid scintillation spectrometry

SMILES字符串

c1ccc(cc1)-c2cnc(o2)-c3ccccc3

InChI

1S/C15H11NO/c1-3-7-12(8-4-1)14-11-16-15(17-14)13-9-5-2-6-10-13/h1-11H

InChI key

CNRNYORZJGVOSY-UHFFFAOYSA-N

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一般描述

2,5-二苯基恶唑(也称为PPO或对苯基苯恶唑)是一种荧光有机化合物。由于光致发光量子产率高、发光性能独特,也可用作有机闪烁体。它在分析化学和生物化学领域广泛用作荧光探针或染料。

应用

2,5-二苯基恶唑(PPO)可用于:
  • 荧光法检测氚、氚化糖肽和35S标记的蛋白质。
  • 作为闪烁液的初级荧光体和次级荧光体。

相关产品

产品编号
说明
价格

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

386.6 - 393.8 °F - closed cup

闪点(°C)

197 - 201 °C - closed cup

个人防护装备

Eyeshields, Gloves, type N95 (US)


从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

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访问文档库

Study of new luminophores for use in modern scintillation cocktails
Janda J, et al.
Journal of Luminescence, 201, 390-396 (2018)
Two-component molecular materials of 2, 5-diphenyloxazole exhibiting tunable ultraviolet/blue polarized emission, pump-enhanced luminescence, and mechanochromic response
Yan, et al.
Advanced Functional Materials , 24, 587-594 (2014)
Wavelength dependant quenching of 2, 5-diphenyloxazole fluorescence by nucleotides
KrishnaMurthy NV, et al.
Journal of Fluorescence, 18, 29-34 (2008)
J T Ahokas et al.
Pharmacology & toxicology, 61(3), 184-190 (1987-09-01)
The oxidative metabolism of 2,5-diphenyloxazole (PPO) is associated with 3-methylcholanthrene inducible cytochrome P-450. The major metabolite formed has m/z of 237, corresponding to hydroxylated PPO. All the possible hydroxylated metabolites of PPO were synthesized and characterized, enabling the assignment of
F M Williams et al.
British journal of clinical pharmacology, 22(3), 263-268 (1986-09-01)
As a substrate for human liver microsomes, ethoxyresorufin appears to be metabolised by a group of cytochrome P450 isoenzymes which are inducible by cigarette smoking. Kinetic studies in microsomes from four human livers indicate that only one enzyme component is

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