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Merck

N3877

Potassium 4-nitrophenyl sulfate

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

Sinónimos:

4-Nitrophenyl sulfate potassium salt

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500 MG

MXP 1,842.00

1 G

MXP 2,001.00

5 G

MXP 8,818.00

MXP 1,842.00


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Fórmula lineal:
NO2C6H4OSO2OK
Número CAS:
Peso molecular:
257.26
NACRES:
NA.32
PubChem Substance ID:
UNSPSC Code:
12352204
EC Number:
228-288-5
MDL number:
Beilstein/REAXYS Number:
3786392

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Nombre del producto

Potassium 4-nitrophenyl sulfate, sulfatase substrate

InChI key

BITVAZYUWRLLCN-UHFFFAOYSA-M

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

SMILES string

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

assay

≥98% (TLC)

form

powder

mp

246-250 °C (lit.)

solubility

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

shipped in

wet ice

storage temp.

−20°C

Quality Level

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1 of 4

Este artículo
B1379N3002N0252
assay

≥98% (TLC)

assay

≥98% (TLC)

assay

≥99% (TLC)

assay

≥98% (TLC)

solubility

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

solubility

water: 50 mg/mL, clear to slightly hazy

solubility

water: 20 mg/mL, clear to very slightly hazy

solubility

chloroform: soluble 100 mg/mL, colorless to faintly yellow

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

form

powder

form

powder

form

powder

form

powder

shipped in

wet ice

shipped in

-

shipped in

-

shipped in

-

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

Application

Potassium 4-nitrophenyl sulfate has been used:
  • as a substrate to measure arylsulfatase activity in cell-free coelomic fluid[1]
  • as a substrate for p-nitrophenyl glycoside-based enzyme assay[2]
  • to inhibit arylsulfatase[3]
  • as an inorganic analog of organic aryl ester sulphate[4]

General description

Chromogenic sulfatase substrate.

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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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
Maternal and neonatal urinary excretion of sulfate and glucuronide ritodrine conjugates
Brashear WT, et al.
Clinical Pharmacology and Therapeutics, 44(6), 634-641 (1988)
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
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
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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