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201987

Sigma-Aldrich

Acid Yellow 17

Dye content 60 %

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About This Item

Empirical Formula (Hill Notation):
C16H10Cl2N4Na2O7S2
CAS Number:
Molecular Weight:
551.29
Colour Index Number:
18965
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

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

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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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
Xue Jiang et al.
Journal of hazardous materials, 173(1-3), 298-304 (2009-09-12)
To react with the cationic monomer, N-trimethylaminoethylmethacrylate chloride (TMAEMC), a beta-CD derivative carrying vinyl carboxylic acid groups (beta-CD-MAH) was designed and synthesized via esterfying reaction between beta-CD and maleic anhydride (MAH). Whereafter, a water-soluble amphoteric flocculant, the copolymer of TMAEMC
Raman Srinivasan et al.
Bioresource technology, 102(3), 2242-2247 (2010-11-06)
Degradation of Tectilon Yellow 2G (TY2G), an azo dye has been studied by hybrid technique involving pretreatment by sonochemical method and further biological treatment by Pseudomonas putida mutant. Pretreatment experiments were carried out by sonolysis of the dye solution at

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