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About This Item
Empirical Formula (Hill Notation):
C16H10Cl2N4Na2O7S2
CAS Number:
Molecular Weight:
551.29
NACRES:
NA.47
PubChem Substance ID:
UNSPSC Code:
12171500
EC Number:
228-819-0
MDL number:
form
powder
Quality Level
composition
Dye content, 60%
λmax
400 nm
ε (extinction coefficient)
≥8000 at 252-258 nm in water at 0.02 g/L
application(s)
diagnostic assay manufacturing
hematology
histology
storage temp.
room temp
SMILES string
[Na+].[Na+].CC1=NN(C(=O)C1\N=N\c2ccc(cc2)S([O-])(=O)=O)c3cc(Cl)c(cc3Cl)S([O-])(=O)=O
InChI
1S/C16H12Cl2N4O7S2.2Na/c1-8-15(20-19-9-2-4-10(5-3-9)30(24,25)26)16(23)22(21-8)13-6-12(18)14(7-11(13)17)31(27,28)29;;/h2-7,15H,1H3,(H,24,25,26)(H,27,28,29);;/q;2*+1/p-2/b20-19+;;
InChI key
FTZLWXQKVFFWLY-LLIZZRELSA-L
General description
Acid yellow-17 (C.I. 18965), also known as Disodium 2, 5-dichloro-4-(5-hydroxy-3-methyl-4-(sulphophenylazo)pyrazol-1-yl) benzenesulphonate, and Yellow 2G is an anionic, reactive textile dye. This synthetic azo dye possesses a stable aromatic structure with SO3H and OH groups.
Application
The applications of Acid yellow-17 are seen in detergent, soap, textile, printing, and cosmetic industries.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Cong Lyu et al.
Environmental science and pollution research international, 23(20), 20893-20903 (2016-08-05)
Traditionally, a few processes have to be employed in sequence for multi-dye removal, due to the different physical and chemical characteristics of the dyes. In this study, we innovatively developed an integrated adsorption and Fenton oxidation fluidized bed reactor (FBR)
Jing-Feng Gao et al.
Bioresource technology, 101(15), 5793-5801 (2010-03-23)
This study focused on the competitive biosorption of Yellow 2G (Y2G) and Reactive Brilliant Red K-2G (RBR) by inactive aerobic granules in binary solutions. A first-order derivative spectrophotometric method for the simultaneous determination of Y2G and RBR in binary solutions
Roohan Rakhshaee
Journal of hazardous materials, 197, 144-152 (2011-10-25)
In this study, cyclohexane 1,3,5-tericarboxylic acid (CHA) and β-isopropylglutaric acid (IPA) were used to obtain the cross-linked forms of the extracted pectin from orange skin (PO), viz. PO-CHA and PO-IPA. These agents were used to stabilize the synthesized Fe(0) nano-particles
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 201987-100G | 04061832338910 |