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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:
90066
Número CE:
Número MDL:
Código UNSPSC:
12352204
ID de la sustancia en PubChem:
NACRES:
NA.32

Nivel de calidad

Ensayo

≥98%

Formulario

powder

puntuación de productos alternativos más sostenibles

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

características de los productos alternativos más sostenibles

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

sustainability

Greener Alternative Product

solubilidad

methanol: 49.00-51.00 mg/mL

categoría alternativa más sostenible

temp. de almacenamiento

−20°C

cadena SMILES

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

Clave InChI

MLJYKRYCCUGBBV-YTWAJWBKSA-N

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Descripción general

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.

Aplicación

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.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Gloves


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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
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
T Bravman et al.
FEBS letters, 495(1-2), 115-119 (2001-04-27)
A beta-xylosidase from Bacillus stearothermophilus T-6 was cloned, overexpressed in Escherichia coli and purified to homogeneity. Based on sequence alignment, the enzyme belongs to family 39 glycoside hydrolases, which itself forms part of the wider GH-A clan. The conserved Glu160
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
Mária Mastihubová et al.
Carbohydrate research, 339(7), 1353-1360 (2004-04-29)
Di-O-acetates and mono-O-acetates of 4-nitrophenyl beta-D-xylopyranoside were prepared by use of lipase PS-30. Polarity of organic solvents and reaction time affected the regioselectivity of the di-O-acetylation as well as the yields of monoacetates. The kinetics of acetyl groups migration in

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