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Documentos

11074

Supelco

Disperse Red 1

analytical standard

Sinónimos:

N-Ethyl-N-(2-hydroxyethyl)-4-(4-nitrophenylazo)aniline

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About This Item

Fórmula empírica (notación de Hill):
C16H18N4O3
Número de CAS:
2872-52-8
Peso molecular:
314.34
Número de índice de color:
11110
Beilstein:
5353614
Número CE:
220-704-3
Número MDL:
MFCD00007312
Código UNSPSC:
85151701
ID de la sustancia en PubChem:
329749138

grado

analytical standard

Nivel de calidad

100

Análisis

≥96.0% (HPLC)

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
gas chromatography (GC): suitable

mp

160-162 °C (lit.)

aplicaciones

cleaning products
cosmetics
environmental
food and beverages
personal care

formato

neat

cadena SMILES

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+

Clave InChI

FOQABOMYTOFLPZ-ISLYRVAYSA-N

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Descripción general

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

Aplicación

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.

Características y beneficios

This benchmark dipolar chromophore was incorporated into aromatic polymers to obtain model electrooptic polymer films.

Productos recomendados

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.

Pictogramas

Exclamation mark
GHS07

Palabra de señalización

Warning

Frases de peligro

H317

Consejos de prudencia

P280

Clasificaciones de peligro

Skin Sens. 1

Código de clase de almacenamiento

13 - Non Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

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

Choose from one of the most recent versions:

Certificados de análisis (COA)

Lot/Batch Number
BCCD6265
BCBW7311
BCBR4959V
1258722V
1258722

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Sigma-Aldrich

215767

Disperse Red 19

Solvent Yellow 124 analytical standard

Supelco

49639

Solvent Yellow 124

Disperse Red 13 Dye content 95 %

Sigma-Aldrich

364827

Disperse Red 13

Methyl Orange ACS reagent, Dye content 85 %

Sigma-Aldrich

114510

Methyl Orange

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
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
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
Mehmet Cinar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 83(1), 561-569 (2011-10-01)
This study reports the characterization of disperse red 1 acrylate compound by spectral techniques and quantum chemical calculations. The spectroscopic properties were analyzed by FT-IR, UV-vis, (1)H NMR and (13)C NMR techniques. FT-IR spectrum in solid state was recorded in
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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