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Documenti fondamentali

N3877

Sigma-Aldrich

Potassium 4-nitrophenyl sulfate

sulfatase substrate, chromogenic, ≥98% (TLC), powder

Sinonimo/i:

4-Nitrophenyl sulfate potassium salt

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About This Item

Formula condensata:
NO2C6H4OSO2OK
Numero CAS:
Peso molecolare:
257.26
Beilstein:
3786392
Numero CE:
Numero MDL:
Codice UNSPSC:
12352204
ID PubChem:
NACRES:
NA.32

product name

Potassium 4-nitrophenyl sulfate, sulfatase substrate

Livello qualitativo

Saggio

≥98% (TLC)

Forma fisica

powder

Punto di fusione

246-250 °C (lit.)

Solubilità

water: 50 mg/mL, clear, colorless to very faintly greenish-yellow (to Very Light Yellow)

Condizioni di spedizione

wet ice

Temperatura di conservazione

−20°C

Stringa SMILE

[K+].[O-][N+](=O)c1ccc(OS([O-])(=O)=O)cc1

InChI

1S/C6H5NO6S.K/c8-7(9)5-1-3-6(4-2-5)13-14(10,11)12;/h1-4H,(H,10,11,12);/q;+1/p-1
BITVAZYUWRLLCN-UHFFFAOYSA-M

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Applicazioni

Potassium 4-nitrophenyl sulfate has been used:
  • as a substrate to measure arylsulfatase activity in cell-free coelomic fluid
  • as a substrate for p-nitrophenyl glycoside-based enzyme assay
  • to inhibit arylsulfatase
  • as an inorganic analog of organic aryl ester sulphate

Substrati

Chromogenic sulfatase substrate.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)


Certificati d'analisi (COA)

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Maternal and neonatal urinary excretion of sulfate and glucuronide ritodrine conjugates
Brashear WT, et al.
Clinical Pharmacology and Therapeutics, 44(6), 634-641 (1988)
Elif Akin Kazancioğlu et al.
Journal of enzyme inhibition and medicinal chemistry, 27(6), 880-885 (2011-12-08)
The possible sulfatase activity of several carbonic anhydrase (CA, EC 4.2.1.1) isoforms have been investigated with a series of synthesized methanesulfonate derivatives of phenols. Four α-CA isozymes, i.e. hCA I, hCA II, hCA IV and hCA VI (h = human
Shina Caroline Lynn Kamerlin
The Journal of organic chemistry, 76(22), 9228-9238 (2011-10-11)
Both phosphoryl and sulfuryl transfers are ubiquitous in biology, being involved in a wide range of processes, ranging from cell division to apoptosis. Additionally, it is becoming increasingly clear that enzymes that can catalyze phosphoryl transfer can often cross-catalyze sulfuryl
M D Burkart et al.
Analytical biochemistry, 274(1), 131-137 (1999-10-21)
We have developed a continuous spectrophotometric coupled-enzyme assay for sulfotransferase activity. This assay is based on the regeneration of 3'-phosphoadenosine-5'-phosphosulfate (PAPS) from the desulfated 3'-phosphoadenosine-5'-phosphate (PAP) by a recombinant aryl sulfotransferase using p-nitrophenyl sulfate as the sulfate donor and visible
E S Lin et al.
Biochemical and biophysical research communications, 271(3), 818-822 (2000-05-18)
The sulfation of a nucleotide is an indispensable step for the sulfuryl group transfer in a biological system. The product and cosubstrate of sulfotransferase in physiological condition are adenosine 3',5'-bisphosphate (PAP) and 3'-phospho adenosine 5'-phosphosulfate (PAPS), respectively. We find that

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