N3641
4-Nitrophenyl α-L-arabinofuranoside
chromogenic, ≥98% (TLC), powder
Synonym(s):
4-nitrophenyl-ARA
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Empirical Formula (Hill Notation):
C11H13NO7
CAS Number:
Molecular Weight:
271.22
Beilstein:
1688357
MDL number:
UNSPSC Code:
12352204
PubChem Substance ID:
NACRES:
NA.32
Recommended Products
Product Name
4-Nitrophenyl α-L-arabinofuranoside, ≥98% (TLC)
Quality Level
Assay
≥98% (TLC)
form
powder
solubility
methanol: 50 mg/mL
storage temp.
−20°C
SMILES string
OC[C@@H]1O[C@@H](Oc2ccc(cc2)[N+]([O-])=O)[C@H](O)[C@H]1O
InChI
1S/C11H13NO7/c13-5-8-9(14)10(15)11(19-8)18-7-3-1-6(2-4-7)12(16)17/h1-4,8-11,13-15H,5H2/t8-,9-,10+,11+/m0/s1
InChI key
DUYYBTBDYZXISX-UKKRHICBSA-N
Looking for similar products? Visit Product Comparison Guide
Application
4-Nitrophenyl α-L-arabinofuranoside has been used:
- as a substrate for α-arabinofuranosidase in an enzymatic assay to determine glycosidase activities in Oenococcus oeni strains
- to determine the enzymatic activity of α-arabinofuranosidase
- as a p-nitrophenol linked substrate to determine its activity in Aspergillus niger NW249 culture filtrate
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
B C Saha et al.
Applied and environmental microbiology, 64(1), 216-220 (1998-01-22)
A color-variant strain of Aureobasidium pullulans (NRRL Y-12974) produced alpha-L-arabinofuranosidase (alpha-L-AFase) when grown in liquid culture on oat spelt xylan. An extracellular alpha-L-AFase was purified 215-fold to homogeneity from the culture supernatant by ammonium sulfate treatment, DEAE Bio-Gel A agarose
Mária Mastihubová et al.
Bioorganic & medicinal chemistry, 14(6), 1805-1810 (2005-11-18)
All possible di-O-acetates and mono-O-acetates of p-nitrophenyl alpha-L-arabinofuranoside were prepared by chemoenzymatic way using lipases. The 2,3-di-O-acetate was obtained in 90% yield by deacetylation of the primary acetyl group of per-O-acetylated p-nitrophenyl alpha-L-arabinofuranoside by Candida cylindracea lipase (CCL) or Candida
M J Renner et al.
Applied and environmental microbiology, 64(1), 43-52 (1998-01-22)
An alpha-L-arabinofuranosidase (alpha-L-arabinofuranoside arabinofuranohydrolase [EC 3.2.1.55]; referred to below as ArfI) from Cytophaga xylanolytica XM3 was purified 85-fold by anion-exchange and hydrophobic interaction column chromatography. The native enzyme had a pI of 6.1 and an apparent molecular mass of 160
Liudmila V Kozlova et al.
Planta, 241(5), 1159-1172 (2015-01-23)
Specific α- l -arabinofuranosidases are involved in the realisation of elongation growth process in cells with type II cell walls. Elongation growth in a plant cell is largely based on modification of the cell wall. In type II cell walls
José Manuel Inácio et al.
Journal of bacteriology, 190(12), 4272-4280 (2008-04-15)
The extracellular depolymerization of arabinopolysaccharides by microorganisms is accomplished by arabinanases, xylanases, and galactanases. Here, we characterize a novel endo-alpha-1,5-l-arabinanase (EC 3.2.1.99) from Bacillus subtilis, encoded by the yxiA gene (herein renamed abn2) that contributes to arabinan degradation. Functional studies
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service