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Merck

N2132

Sigma-Aldrich

4-Nitrophenyl β-D-xylopyranoside

greener alternative

≥98%

Sinónimos:

PNPX

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About This Item

Fórmula empírica (notación de Hill):
C11H13NO7
Número de CAS:
Peso molecular:
271.22
Beilstein/REAXYS Number:
90066
EC Number:
MDL number:
UNSPSC Code:
12352204
PubChem Substance ID:
NACRES:
NA.32

Quality Level

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

storage temp.

−20°C

SMILES string

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

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

InChI key

MLJYKRYCCUGBBV-YTWAJWBKSA-N

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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.

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.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificados de análisis (COA)

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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
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
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)
Peter Biely et al.
Analytical biochemistry, 332(1), 109-115 (2004-08-11)
Three different monoacetates of 4-nitrophenyl beta-D-xylopyranoside were tested as substrates for beta-xylosidase and for microbial carbohydrate esterases and a series of non-hemicellulolytic esterases. The acetyl group in 2-O-acetyl, 3-O-acetyl, and 4-O-acetyl 4-nitrophenyl beta-D-xylopyranoside makes the glycoside resistant to the action

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