N1895
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
NACRES:
NA.32
PubChem Substance ID:
UNSPSC Code:
12352204
EC Number:
233-572-7
MDL number:
Product Name
4-Nitrophenyl α-D-xylopyranoside, α-xylosidase substrate
InChI key
MLJYKRYCCUGBBV-UHFFFAOYSA-N
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
SMILES string
OC1COC(Oc2ccc(cc2)N(=O)=O)C(O)C1O
assay
≥99% (HPLC)
form
powder
solubility
methanol: soluble 20 mg/mL, clear, colorless to faintly yellow
storage temp.
−20°C
Quality Level
General description
Chromogenic substrate for α-xylosidase
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Talia Weinstein et al.
Connective tissue research, 53(2), 169-179 (2011-12-14)
The familial disease of hereditary multiple exostoses is characterized by abnormal skeletal deformities requiring extensive surgical procedures. In hereditary multiple exostoses patients there is a shortage in the pericellular glycosaminoglycan (GAG) of heparan sulfate (HS), related to defective activity of
M Gómez et al.
Biochimie, 83(10), 961-967 (2001-12-01)
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
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
Siyuan Li et al.
Histochemistry and cell biology, 139(1), 59-74 (2012-08-23)
Chondroitin/dermatan sulphate (CS/DS) sulphation motifs on cell and extracellular matrix proteoglycans (PGs) within stem/progenitor cell niches are involved in modulating cell phenotype during the development of many musculoskeletal connective tissues. Here, we investigate the importance of CS/DS chains and their
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