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215740

Sigma-Aldrich

Disperse Red 1

Dye content 50 %

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:
12352103
PubChem Substance ID:
329752173

composition

Dye content, 50%

mp

160-162 °C (lit.)

λmax

503 nm

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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Features and Benefits

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

replaced by

Product No.
Description
Pricing

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H317

pcodes

P280

Hazard Classifications

Skin Sens. 1

Storage Class

11 - 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

Certificates of Analysis (COA)

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Shigekatsu Fujii et al.
Journal of peptide science : an official publication of the European Peptide Society, 14(12), 1295-1302 (2008-10-28)
Cyclic octapeptide carrying one or two nonlinear optical chromophores, disperse red 1 (DR-1), was synthesized and immobilized on a substrate to attain an active surface for second-harmonic generation (SHG). Each cyclic octapeptide was transferred on a fused quartz substrate by
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
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
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
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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