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Merck

N1895

Sigma-Aldrich

4-Nitrophenyl α-D-xylopyranoside

α-xylosidase substrate, ≥99% (HPLC), powder

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About This Item

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

product name

4-Nitrophenyl α-D-xylopyranoside, α-xylosidase substrate

Quality Level

assay

≥99% (HPLC)

form

powder

solubility

methanol: soluble 20 mg/mL, clear, colorless to faintly yellow

storage temp.

−20°C

SMILES string

OC1COC(Oc2ccc(cc2)N(=O)=O)C(O)C1O

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

InChI key

MLJYKRYCCUGBBV-UHFFFAOYSA-N

Substrates

Chromogenic substrate for α-xylosidase

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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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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Positional specificity of NodB-like domain of a multidomain xylanase U from Clostridium thermocellum (CtAxe) was investigated. Of three monoacetates of 4-nitrophenyl beta-d-xylopyranoside the acetylxylan esterase domain showed a clear preference for the 2-acetate. Moreover, the enzyme was significantly activated by

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