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Merck
CN

N7251

4-硝基邻苯二酚硫酸盐 二钾盐

chromogenic sulphatase substrate, crystalline

别名:

2-羟基-5-硝基苯硫酸盐, 2-羟基-5-硝基苯硫酸盐 二钾盐 一水合物, 对硝基儿茶酚硫酸盐 二钾盐

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关于此项目

线性分子式:
C6H3NO7SK2
化学文摘社编号:
14528-64-4
分子量:
311.35
NACRES:
NA.77
PubChem Substance ID:
24897816
UNSPSC Code:
12352200
EC Number:
238-550-0
MDL number:
MFCD00007465
Beilstein/REAXYS Number:
3805018

主要文件

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产品名称

4-硝基邻苯二酚硫酸盐 二钾盐, crystalline

SMILES string

[K+].[K+].[O-]c1ccc(cc1OS([O-])(=O)=O)[N+]([O-])=O

InChI key

CKWWBDCAYRJAJB-UHFFFAOYSA-L

InChI

1S/C6H5NO7S.2K/c8-5-2-1-4(7(9)10)3-6(5)14-15(11,12)13;;/h1-3,8H,(H,11,12,13);;/q;2*+1/p-2

form

crystalline

color

yellow

storage temp.

−20°C

Quality Level

100

相关类别

General description

4-硝基儿茶酚硫酸盐是一种芳香族硫酸盐。
显色硫酸酯酶底物。

Application

4-硝基儿茶酚硫酸二钾盐被用作粘多糖 VI（MPS VI）分析的底物。它也被用来测量糖胺聚糖（GAG）降解酶-芳基磺化酶B和外糖苷酶的活性。

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SHBT0871
SHBS1165
SHBR0969
MKCN3971
SHBM6097

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Zunnan Huang et al.
Biophysical journal, 93(12), 4141-4150 (2007-09-04)
Using the docking of p-nitrocatechol sulfate to Yersinia protein tyrosine phosphatase YopH as an example, we showed that an approach based on mining minima followed by cluster and similarity analysis could generate useful insights into docking pathways. Our simulation treated
The potassium salt of p-nitrocatechol sulfate.
R von Bülow et al.
Acta crystallographica. Section C, Crystal structure communications, 56 ( Pt 2), 152-153 (2000-04-25)
A continuous spectrophotometric assay for arylsulfatase activity, dependent on the formation of complexes between cupric ions and nitrocatechols.
A G Clark et al.
Analytical biochemistry, 118(2), 231-239 (1981-12-01)
A Km mutant of arylsulfatase A.
A M Harben et al.
Clinica chimica acta; international journal of clinical chemistry, 125(3), 351-354 (1982-11-10)
S Partanen
The Histochemical journal, 16(5), 501-506 (1984-05-01)
A new, direct-colouring, metal precipitation method for the light microscopical demonstration of arylsulphatases A and B is described. It is based on the reducing capacity of nitrocatechol liberated by arylsulphatases from p-nitrocatechol sulphate. The reaction is carried out in Karnovsky-Roots'
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商品

Drug Conjugate Analysis using β-Glucuronidases

Drug conjugate analysis and the enzymatic hydrolysis of glucuronides

实验方案

Enzymatic Assay of Sulfatase (EC 3.1.6.1.)

Enzymatic Assay of Sulfatase (EC 3.1.6.1.)

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