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Merck

N2132

4-Nitrophenyl β-D-xylopyranoside

greener alternative

≥98%

Synonym(s):

PNPX

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About This Item

Empirical Formula (Hill Notation):
C11H13NO7
CAS Number:
2001-96-9
Molecular Weight:
271.22
UNSPSC Code:
12352204
NACRES:
NA.32
PubChem Substance ID:
24897350
EC Number:
217-897-1
Beilstein/REAXYS Number:
90066
MDL number:
MFCD00047519

Product Name

4-Nitrophenyl β-D-xylopyranoside, ≥98%

InChI key

MLJYKRYCCUGBBV-YTWAJWBKSA-N

InChI

1S/C11H13NO7/c13-8-5-18-11(10(15)9(8)14)19-7-3-1-6(2-4-7)12(16)17/h1-4,8-11,13-15H,5H2/t8-,9+,10-,11+/m1/s1

SMILES string

O[C@@H]1CO[C@@H](Oc2ccc(cc2)[N+]([O-])=O)[C@H](O)[C@H]1O

assay

≥98%

form

powder

greener alternative product score

old score: 100
new score: 51
Find out more about DOZN™ Scoring

greener alternative product characteristics

Waste Prevention
Safer Solvents and Auxiliaries
Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

solubility

methanol: 49.00-51.00 mg/mL

greener alternative category

, Re-engineered

storage temp.

−20°C

Quality Level

300

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Application

4-Nitrophenyl β-D-xylopyranoside has been used as a substrate to assay the activity of β-xylosidase. It has also been used in the pharmaceutical inhibition of heparan sulfate proteoglycan (HSPG) biosynthesis.

General description

We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product belongs to category of Re-engineered products, showing key improvements in Green Chemistry Principles “Waste Prevention”, “Safer Solvents and Auxiliaries” and “Enhanced Energy Efficiency”. Click here to view its DOZN scorecard.

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000488207
0000488207
0000438979
0000438979
0000431714

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Junhua Zhang et al.
Biotechnology for biofuels, 4, 12-12 (2011-05-20)
In the hydrolysis of lignocellulosic materials, thermostable enzymes decrease the amount of enzyme needed due to higher specific activity and elongate the hydrolysis time due to improved stability. For cost-efficient use of enzymes in large-scale industrial applications, high-level expression of
Junjarus Sermsathanaswadi et al.
Enzyme and microbial technology, 96, 75-84 (2016-11-23)
A newly isolated endo-β-1,4-xylanase (Xyn10E) from Paenibacillus curdlanolyticus B-6 has a modular structure consisting of a family 22 carbohydrate-binding module (CBM), a glycoside hydrolase (GH) family 10 catalytic domain, two fibronectin type III (Fn3) domains, and a family 3 CBM
Hetti Palonen et al.
Applied biochemistry and biotechnology, 117(1), 1-17 (2004-05-06)
The wet oxidation pretreatment (water, oxygen, elevated temperature, and pressure) of softwood (Picea abies) was investigated for enhancing enzymatic hydrolysis. The pretreatment was preliminarily optimized. Six different combinations of reaction time, temperature, and pH were applied, and the compositions of
Beatriz Vieira Dos Santos et al.
Applied biochemistry and biotechnology, 189(1), 37-48 (2019-03-14)
This study evaluated the production of lignocellulose-degrading enzymes by solid-state fermentation (SSF) using a microbial consortium of Aspergillus fumigatus SCBM6 and A. niger SCBM1 (AFN extract). The fungal strains were cultivated in sugarcane bagasse (SCB) and wheat bran (WB) as
Preparation of arabinoxylobiose from rye xylan using family 10 Aspergillus aculeatus endo-1, 4-beta-D-xylanase
Rantanen H, et al.
Carbohydrate Polymers, 68(2), 350-359 (2007)
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