Skip to Content
MilliporeSigma
All Photos(2)

Documents

N1884

Sigma-Aldrich

4-Nitrophenyl β-D-maltoside

β-maltosidase substrate

Synonym(s):

4-Nitrophenyl-beta-D-maltopyranoside

Sign Into View Organizational & Contract Pricing
All Photos(2)

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.

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 4

1 of 4

4-Nitrophenyl N-acetyl-β-D-glucosaminide ≥99% (TLC)

Sigma-Aldrich

N9376

4-Nitrophenyl N-acetyl-β-D-glucosaminide

4-Nitrophenyl α-D-glucopyranoside ≥99%

Sigma-Aldrich

N1377

4-Nitrophenyl α-D-glucopyranoside

D-(−)-Fructose ≥99% (HPLC)

Sigma-Aldrich

F0127

D-(−)-Fructose

Nα-Benzoyl-DL-arginine 4-nitroanilide hydrochloride ≥98%

Sigma-Aldrich

B4875

Nα-Benzoyl-DL-arginine 4-nitroanilide hydrochloride

G Telford et al.
Medical and veterinary entomology, 26(3), 291-299 (2012-05-25)
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)

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