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11074

Supelco

Disperse Red 1

analytical standard

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C16H18N4O3
CAS Number:
2872-52-8
Molecular Weight:
314.34
Colour Index Number:
11110
Beilstein/REAXYS Number:
5353614
EC Number:
220-704-3
MDL number:
MFCD00007312
UNSPSC Code:
85151701
PubChem Substance ID:
329749138

grade

analytical standard

Quality Level

100

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

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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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

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

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pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H317

pcodes

P280

Hazard Classifications

Skin Sens. 1

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCD6265
BCBW7311
BCBR4959V
1258722V
1258722

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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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