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Merck

D4645

Sigma-Aldrich

Natrium-3,5-dichlor-2-Hydroxybenzolsulfonat Natriumsalz

≥98% purity (TLC), powder

Synonym(e):

3,5-Dichlor-2-hydroxy-benzolsulfonsäure

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About This Item

Empirische Formel (Hill-System):
C6H3Cl2NaO4S
CAS-Nummer:
Molekulargewicht:
265.05
Beilstein:
3640643
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12171500
PubChem Substanz-ID:
NACRES:
NA.47

product name

Natrium-3,5-dichlor-2-Hydroxybenzolsulfonat Natriumsalz, used for peroxide measurement

Assay

≥98% (TLC)

Form

powder

Farbe

white to off-white

pH-Wert

7 (20 °C, 53 g/L)

mp (Schmelzpunkt)

>300 °C

Löslichkeit

H2O: 50 mg/mL

Anwendung(en)

diagnostic assay manufacturing
hematology
histology

Lagertemp.

room temp

SMILES String

[Na+].Oc1c(Cl)cc(Cl)cc1S([O-])(=O)=O

InChI

1S/C6H4Cl2O4S.Na/c7-3-1-4(8)6(9)5(2-3)13(10,11)12;/h1-2,9H,(H,10,11,12);/q;+1/p-1

InChIKey

NMWCVZCSJHJYFW-UHFFFAOYSA-M

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Allgemeine Beschreibung

Sodium 3,5-dichloro-2-hydroxybenzenesulfonate is used in conjunction with 4-aminoantipyrine (4-AAP) and hydrogen peroxide (H2O2) for chromogenic quantitation of uric acid in serum and urine samples.

Anwendung

Used in conjunction with 4-aminoantipyrine (4-AAP) and hydrogen peroxide (H2O2) for chromogenic quantitation of peroxidase in coupled enzymatic reactions. Component of Trinder reagent for use with peroxidase to measure generation of hydrogen peroxide in automated systems.

Piktogramme

Exclamation mark

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Die Dokumentenbibliothek aufrufen

Use of 3,5-dichloro-2-hydroxybenzenesulfonic acid/4-aminophenazone chromogenic system in direct enzymatic assay of uric acid in serum and urine.
Fossati P, et al.
Clinical Chemistry, 26(2), 227-231 (1980)
Lucas F de Castro et al.
Analytical and bioanalytical chemistry, 411(19), 4919-4928 (2019-04-04)
Microfluidic paper-based devices (μPADs) and wearable devices have been highly studied to be used as diagnostic tools due to their advantages such as simplicity and ability to provide instrument-free fast results. Diseases such as periodontitis and diabetes mellitus can potentially
Teresa Ramon-Marquez et al.
Talanta, 187, 83-90 (2018-06-02)
In this study, we have optimised the sterically directed attachment of biomolecules on the surface of coaxial membranes prepared by co-electrospinning which have been proved to be a material with very high performance for the development of biosensors with optical
J D Artiss et al.
Clinical biochemistry, 16(6), 334-337 (1983-12-01)
A study into the substitution of sodium 2-hydroxy-3,5-dichlorobenzenesulfonate for phenol in the indicator reaction for an automated glucose procedure is presented. Apart from having physical properties that are more conducive to easy handling than phenol, the former material affords considerably
Ana C Fernandes et al.
New biotechnology, 47, 39-49 (2018-04-24)
The need for fast and comprehensive characterization of biocatalysts has pushed the development of new screening platforms based on microfluidics, capable of monitoring several parameters simultaneously, with new configurations of liquid handling, sample treatment and sensing. Modular microfluidics allows the

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