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Merck

S9256

Sigma-Aldrich

Sulfanilic acid azochromotrop

≥80% purity, powder

Sinónimos:

1,8-Dihydroxy-2-(4-sulfophenylazo)naphthalene-3,6-disulfonic acid trisodium salt, 2-(4-Sulfophenylazo)-1,8-dihydroxy-3,6-naphthalene disulfonic acid trisodium salt, 2-(4-Sulfophenylazo)chromotropic acid trisodium salt, SPADNS

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About This Item

Fórmula empírica (notación de Hill):
C16H9N2Na3O11S3
Número de CAS:
Peso molecular:
570.41
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

product name

Sulfanilic acid azochromotrop, ≥80%

Quality Level

assay

≥80%

form

powder

composition

Carbon: 26.0-35.0%

Nitrogen: 3.6-5.9%

technique(s)

titration: suitable

color

dark red

solubility

water: 10 mg/mL

λmax

505-510 nm

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

[Na+].[Na+].[Na+].Oc1cc(cc2cc(c(\N=N\c3ccc(cc3)S([O-])(=O)=O)c(O)c12)S([O-])(=O)=O)S([O-])(=O)=O

InChI

1S/C16H12N2O11S3.3Na/c19-12-7-11(31(24,25)26)5-8-6-13(32(27,28)29)15(16(20)14(8)12)18-17-9-1-3-10(4-2-9)30(21,22)23;;;/h1-7,19-20H,(H,21,22,23)(H,24,25,26)(H,27,28,29);;;/q;3*+1/p-3/b18-17+;;;

InChI key

AEHGQXKBQBMQEK-GLCFPVLVSA-K

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General description

Sulfanilic acid azochromotrop is commonly known as SPADNS.

Application

Sulfanilic acid azochromotrop, commonly known as SPADNS, is used mostly as an indicator for complexometric determinations of transition metals like zirconium. It is used as a reagent for drinking and wastewater analysis.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificados de análisis (COA)

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Visite la Librería de documentos

Mechanism of azo dye degradation in Advanced Oxidation Processes: Degradation of Sulfanilic Acid Azochromotrop and its parent compounds in aqueous solution by ionizing radiation
Tamas Palfi
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Oliver Drews
Molecular and Cellular Proteomics (2007)
Sanjit Saha et al.
Physical chemistry chemical physics : PCCP, 19(42), 28588-28595 (2017-10-19)
The surface electronic properties of graphene oxide (GO) were modified through reduction and functionalization. Non-covalent functionalization was found to be superior compared to covalent functionalization due to the formation of few-layer graphene with a low defect content and average crystalline

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