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N3877

Sigma-Aldrich

4-Nitrophenyl-sulfat Kaliumsalz

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

Synonym(e):

Kalium-4-Nitrophenylsulfat

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About This Item

Lineare Formel:
NO2C6H4OSO2OK
CAS-Nummer:
6217-68-1
Molekulargewicht:
257.26
Beilstein:
3786392
EG-Nummer:
228-288-5
MDL-Nummer:
MFCD00007466
UNSPSC-Code:
12352204
PubChem Substanz-ID:
24897664
NACRES:
NA.32

product name

4-Nitrophenyl-sulfat Kaliumsalz, sulfatase substrate

Assay

≥98% (TLC)

Form

powder

mp (Schmelzpunkt)

246-250 °C (lit.)

Löslichkeit

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

Versandbedingung

wet ice

Lagertemp.

−20°C

SMILES String

[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

InChIKey

BITVAZYUWRLLCN-UHFFFAOYSA-M

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Anwendung

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

Substrate

Chromogenic sulfatase substrate.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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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
A dietary fiber-deprived gut microbiota degrades the colonic mucus barrier and enhances pathogen susceptibility
Desai MS, et al.
Cell, 167(5), 1339-1353 (2016)
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
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
J O Falkinham
International journal of systematic bacteriology, 40(1), 66-70 (1990-01-01)
A rapid (3-h) arylsulfatase assay for cell suspensions of mycobacteria, in which p-nitrophenyl sulfate is used as the substrate, was developed. Arylsulfatase activity was found in cell suspensions of representative strains of Mycobacterium avium, Mycobacterium intracellulare, and Mycobacterium scrofulaceum grown
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