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Naphthol Yellow S

analytical standard

Synonyme(s) :

2,4-Dinitro-1-naphthol-7-sulfonic acid sodium salt, 5,7-Dinitro-8-hydroxy-2-naphthalenesulfonic acid sodium salt, Acid Yellow 1, Flavianic acid sodium salt

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About This Item

Formule empirique (notation de Hill):
C10H4N2Na2O8S
Numéro CAS:
Poids moléculaire :
358.19
Numéro C.I. (Colour Index):
10316
Beilstein:
3839220
Numéro CE :
Numéro MDL:
Code UNSPSC :
85151701
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Essai

≥99.0% (HPLC)

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

cleaning products
cosmetics
food and beverages
personal care

Format

neat

Chaîne SMILES 

[Na+].[Na+].[O-]c1c(cc([N+]([O-])=O)c2ccc(cc12)S([O-])(=O)=O)[N+]([O-])=O

InChI

1S/C10H6N2O8S.2Na/c13-10-7-3-5(21(18,19)20)1-2-6(7)8(11(14)15)4-9(10)12(16)17;;/h1-4,13H,(H,18,19,20);;/q;2*+1/p-2

Clé InChI

CTIQLGJVGNGFEW-UHFFFAOYSA-L

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Description générale

Naphthol Yellow S is a dye that is known for its hazardous nature.

Application

Naphthol Yellow S may be used as an analytical reference standard for the determination of Naphthol Yellow S in:
  • Foodstuffs by solid phase extraction (SPE) and high performance liquid chromatography (HPLC)-diode array detection (DAD)-ion trap time-of-flight tandem mass spectrometry (IT-TOF-MS3) equipped with multiple reaction monitoring (MRM) detection.
  • Drinks and candies by SPE followed by analysis using HPLC coupled to photodiode array (PDA) detector.
  • Wastewater samples by adsorption column chromatography.
  • Embroideries designed by the famous 19th century French painter Emile Bernard.

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Conditionnement

Bottomless glass bottle. Contents are inside inserted fused cone.

Produits recommandés

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictogrammes

Health hazardExclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Skin Sens. 1 - STOT RE 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


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Certificats d'analyse (COA)

Lot/Batch Number

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Identification and determination of 34 water-soluble synthetic dyes in foodstuff by high performance liquid chromatography-diode array detection-ion trap time-of-flight tandem mass spectrometry.
Li XQ, et al.
Food Chemistry, 182(9), 316-326 (2015)
Photodegradation of hazardous dye naphthol yellow s over titanium dioxide.
Jain R and Sikarwar S
Journal of Dispersion Science and Technology, 32(9), 1345-1352 (2011)
High-performance liquid chromatography and non-destructive three-dimensional fluorescence analysis of early synthetic dyes.
van Bommel MR, et al.
Journal of Chromatography A, 1157(1-2), 260-272 (2007)
W M Frederiks et al.
Histochemistry, 68(1), 49-53 (1980-01-01)
The purpose of this study is to compare the protein content of parenchymal and non-parenchymal nuclei, as isolated from rat liver. The nuclei have been separated by means of a 1 g-sedimentation technique. The protein content of the separated nuclei
J Tas et al.
Acta histochemica. Supplementband, 20, 69-73 (1979-01-01)
After staining with Naphthol Yellow S (NYS) at optimal conditions of pH (2.8), the protein content of rat liver cells isolated by means of a collagenase perfusion technique was found to be cytophotometrically immeasurable, because of too high local dye

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