Merck
CN
所有图片(2)

文件

11074

Supelco

分散红 1

analytical standard

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别名:
N-乙基-N-(2-羟乙基)-4-(4-硝基苯基偶氮)苯胺
经验公式（希尔记法）:
C16H18N4O3
CAS号:
2872-52-8
分子量:
314.34
颜色索引号:
11110
Beilstein:
5353614
EC 号:
220-704-3
MDL编号:
MFCD00007312
PubChem化学物质编号:
329749138

等级

analytical standard

质量水平

100

检测方案

≥96.0% (HPLC)

保质期

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

160-162 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

格式

neat

SMILES string

CCN(CCO)c1ccc(cc1)\N=N\c2ccc(cc2)[N+]([O-])=O

InChI

1S/C16H18N4O3/c1-2-19(11-12-21)15-7-3-13(4-8-15)17-18-14-5-9-16(10-6-14)20(22)23/h3-10,21H,2,11-12H2,1H3/b18-17+

InChI key

FOQABOMYTOFLPZ-ISLYRVAYSA-N

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相关类别

一般描述

Disperse Red 1 is an azo dye. Its mutagenic activity depends on its chemical structure.

应用

It was used as a dye in lymphocyte assay performed to evalute the formation of micronucleus in human lymphocytes.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

特点和优势

将这一基准偶极发色团掺入芳香聚合物中，可得到模型电光学聚合物薄膜。

推荐产品

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H317

预防措施声明

P280

危险分类

Skin Sens. 1

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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T1503
货号
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包装规格/数量

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C W Ma et al.
Water research, 35(10), 2453-2459 (2001-06-08)
A typical insoluble chlorinated aromatic dye (CAD), disperse red (DR), was used to explore the reaction mechanism and kinetics of photodegradation in non-ionic surfactant solutions. The use of an additional hydrogen source and photosensitizer is also studied to improve the
Yuzhu Fu et al.
Bioresource technology, 82(2), 139-145 (2002-05-11)
Aspergillus niger is capable of removing dyes from an aqueous solution. In the study, the roles played by three major functional groups: carboxyl, amino and phosphate, and the lipid fraction in the biomass of A. niger in biosorption of four
E R A Ferraz et al.
Environmental toxicology, 26(5), 489-497 (2010-06-16)
Azo dyes are of environmental concern due to their degradation products, widespread use, and low-removal rate during conventional treatment. Their toxic properties are related to the nature and position of the substituents with respect to the aromatic rings and amino
Mirosława Poprawa-Smoluch et al.
The journal of physical chemistry. A, 110(43), 11926-11937 (2006-10-27)
The photoisomerization of the push-pull substituted azo dye Disperse Red 1 is studied using femtosecond time-resolved absorption spectroscopy and other spectroscopic and computational techniques. In comparison with azobenzene, the pipi* state is more stabilized by the effects of push-pull substitution
Yaoquan Tu et al.
The journal of physical chemistry. B, 111(14), 3591-3598 (2007-03-29)
We demonstrate a complete procedure for simulations of electric field poled polymeric nonlinear optical systems with the purpose to evaluate the macroscopic electro-optic coefficients. The simulations cover the electric field poling effects on the chromophore order at the liquid state
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