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:
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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General description
Disperse Red 1 is an azo dye. Its mutagenic activity depends on its chemical structure.
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.
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。
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.
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
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
Farah Maria Drumond Chequer et al.
Toxicology in vitro : an international journal published in association with BIBRA, 25(8), 2054-2063 (2011-09-13)
Azo dyes constitute the largest class of synthetic dyes. Following oral exposure, these dyes can be reduced to aromatic amines by the intestinal microflora or liver enzymes. This work identified the products formed after oxidation and reduction of the dye
Roberto Bianchini et al.
Carbohydrate research, 356, 104-109 (2011-12-06)
Commercially available Disperse Orange 29 (1a) and Disperse Red 1 (2a) were elaborated to glycoconjugated species, following a new version of a previously-described 'naturalisation' procedure. Glutamic acid was chosen to achieve a double glycoconjugation, which is essential to give to
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