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N1884

Sigma-Aldrich

4-Nitrophenyl β-D-maltoside

β-maltosidase substrate

Synonym(s):

4-Nitrophenyl-beta-D-maltopyranoside

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About This Item

Empirical Formula (Hill Notation):
C18H25NO13
CAS Number:
56846-39-0
Molecular Weight:
463.39
MDL number:
MFCD00069844
UNSPSC Code:
12352204
PubChem Substance ID:
24897533
NACRES:
NA.28

Quality Level

200

Assay

≥98% (TLC)

form

powder

solubility

water: 19.60-20.40 mg/mL, clear, colorless to light yellow

storage temp.

−20°C

SMILES string

OCC1OC(OC2C(O)C(O)C(OC2CO)Oc3ccc(cc3)N(=O)=O)C(O)C(O)C1O

InChI

1S/C18H25NO13/c20-5-9-11(22)12(23)14(25)18(30-9)32-16-10(6-21)31-17(15(26)13(16)24)29-8-3-1-7(2-4-8)19(27)28/h1-4,9-18,20-26H,5-6H2

InChI key

IAYJZWFYUSNIPN-UHFFFAOYSA-N

General description

4-Nitrophenyl β-D-maltoside is a substrate for amyloglucosidase enzyme and releases chromogenic end product p-nitrophenol, which is measured colorimetrically at 410 nm.

Application

4-Nitrophenyl β-D-maltoside has been used as a substrate for amyloglucosidase enzyme activity.

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

Certificates of Analysis (COA)

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G Telford et al.
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The wound-healing maggot, Lucilia sericata Meigen (Diptera: Calliphoridae), degrades extracellular matrix components by releasing enzymes. The purpose of this study was to investigate the glycosylation profiles of wound slough/eschar from chronic venous leg ulcers and the complementary presence of glycosidase
Enzymatic preparation of mushroom dietary fibre: A comparison between analytical and industrial enzymes
Wong, K.H, et al
Food Chemistry, 115(3), 795-800 (2009)

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