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Merck

00298

Supelco

Yellow 2G

analytical standard

Sinónimos:

Acid Yellow 17

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About This Item

Fórmula empírica (notación de Hill):
C16H10Cl2N4Na2O7S2
Número de CAS:
Peso molecular:
551.29
Colour Index Number:
18965
EC Number:
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
E Number:
E107
NACRES:
NA.24

grade

analytical standard

Quality Level

assay

≥98.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

cleaning products
cosmetics
food and beverages
personal care

format

neat

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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Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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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
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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Journal of hazardous materials, 138(2), 357-362 (2006-08-15)
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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

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