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Merck
CN

11074

分散红 1

analytical standard

别名:

N-乙基-N-(2-羟乙基)-4-(4-硝基苯基偶氮)苯胺

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关于此项目

经验公式(希尔记法):
C16H18N4O3
化学文摘社编号:
分子量:
314.34
颜色索引号:
11110
Beilstein:
5353614
EC 号:
MDL编号:
UNSPSC代码:
85151701
PubChem化学物质编号:
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等级

analytical standard

质量水平

方案

≥96.0% (HPLC)

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

mp

160-162 °C (lit.)

应用

cleaning products
cosmetics
environmental
food and beverages
personal care

包装形式

neat

SMILES字符串

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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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。

其他说明

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

警示用语:

Warning

危险声明

预防措施声明

危险分类

Skin Sens. 1

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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An outbreak of occupational textile dye dermatitis from Disperse Blue 106.
F Mota et al.
Contact dermatitis, 43(4), 235-237 (2000-09-30)
Francine Inforçato Vacchi et al.
The Science of the total environment, 442, 302-309 (2012-11-28)
Azo dyes, the most widely used family of synthetic dyes, are often employed as colorants in areas such as textiles, plastics, foods/drugs/cosmetics, and electronics. Following their use in industrial applications, azo dyes have been found in effluents and various receiving
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
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
Farah Maria Drumond Chequer et al.
Mutation research, 676(1-2), 83-86 (2009-05-16)
The use of azo dyes by different industries can cause direct and/or indirect effects on human and environmental health due to the discharge of industrial effluents that contain these toxic compounds. Several studies have demonstrated the genotoxic effects of various

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