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N2132

Sigma-Aldrich

4-Nitrophenyl β-D-xylopyranoside

greener alternative

≥98%

Sinonimo/i:

PNPX

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About This Item

Formula empirica (notazione di Hill):
C11H13NO7
Numero CAS:
2001-96-9
Peso molecolare:
271.22
Beilstein:
90066
Numero CE:
217-897-1
Numero MDL:
MFCD00047519
Codice UNSPSC:
12352204
ID PubChem:
24897350
NACRES:
NA.32

Livello qualitativo

300

Saggio

≥98%

Forma fisica

powder

Punteggio alternativa più verde

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

Caratteristiche più verdi

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

sustainability

Greener Alternative Product

Solubilità

methanol: 49.00-51.00 mg/mL

Categoria alternativa più verde

, Re-engineered

Temperatura di conservazione

−20°C

Stringa SMILE

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
MLJYKRYCCUGBBV-YTWAJWBKSA-N

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Descrizione generale

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.

Applicazioni

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.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

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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
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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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