N3641

Sigma-Aldrich

4-Nitrophenyl α-L-arabinofuranoside

≥98% (TLC)

Empirical Formula (Hill Notation):
C11H13NO7
CAS Number:
Molecular Weight:
271.22
Beilstein/REAXYS Number:
1688357
MDL number:
PubChem Substance ID:
NACRES:
NA.32

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

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Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

NONH for all modes of transport

WGK Germany

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis
Certificate of Origin
Andrew Diener
Molecular plant-microbe interactions : MPMI, 25(12), 1531-1541 (2012-08-17)
Host-specific forms of Fusarium oxysporum infect the roots of numerous plant species. I present a novel application of familiar methodology to visualize and quantify F. oxysporum in roots. Infection in the roots of Arabidopsis thaliana, tomato, and cotton was detected...
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...
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...
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...

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