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
EC Number:
220-704-3
PubChem Substance ID:
UNSPSC Code:
85151701
Beilstein/REAXYS Number:
5353614
Colour Index Number:
11110
MDL number:
产品名称
分散红 1, analytical standard
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
SMILES string
CCN(CCO)c1ccc(cc1)\N=N\c2ccc(cc2)[N+]([O-])=O
grade
analytical standard
assay
≥96.0% (HPLC)
shelf life
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
format
neat
Quality Level
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Features and Benefits
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。
Application
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.
General description
Disperse Red 1 is an azo dye. Its mutagenic activity depends on its chemical structure.
Other Notes
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.
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
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
An outbreak of occupational textile dye dermatitis from Disperse Blue 106.
F Mota et al.
Contact dermatitis, 43(4), 235-237 (2000-09-30)
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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