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N3641

Sigma-Aldrich

4-Nitrophenyl α-L-arabinofuranoside

chromogenic, ≥98% (TLC), powder

Synonym(s):

4-nitrophenyl-ARA

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About This Item

Empirical Formula (Hill Notation):
C11H13NO7
CAS Number:
6892-58-6
Molecular Weight:
271.22
Beilstein/REAXYS Number:
1688357
MDL number:
MFCD00057269
UNSPSC Code:
12352204
PubChem Substance ID:
329818639
NACRES:
NA.32

product name

4-Nitrophenyl α-L-arabinofuranoside, ≥98% (TLC)

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

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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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

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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
Joost van den Brink et al.
Biotechnology journal, 9(10), 1329-1338 (2014-08-15)
Plant-degrading enzymes can be produced by fungi on abundantly available low-cost plant biomass. However, enzymes sets after growth on complex substrates need to be better understood, especially with emphasis on differences between fungal species and the influence of inhibitory compounds
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
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
Preparation of arabinoxylobiose from rye xylan using family 10 Aspergillus aculeatus endo-1, 4-beta-D-xylanase
Rantanen H, et al.
Carbohydrate Polymers null
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