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N1895

Sigma-Aldrich

4-Nitrophenyl α-D-xylopyranoside

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

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About This Item

Empirical Formula (Hill Notation):
C11H13NO7
CAS Number:
Molecular Weight:
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

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

Related Categories

Substrates

Chromogenic substrate for α-xylosidase

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

N1895-10MG:
N1895-VAR:
N1895-250MG:
N1895-BULK:
N1895-50MG:


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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M Gómez et al.
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The variation of kinetic parameters of beta-xylosidase from Trichoderma reesei QM 9414 with pH was used to elucidate the chemical mechanism of the p-nitrophenyl beta-D-xylopyranoside hydrolysis. The pH-dependence of V and V/K(m) showed that a group on the enzyme with
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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
Peter Biely et al.
Biochimica et biophysica acta, 1770(4), 565-570 (2007-01-31)
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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