Cat. No JK1810804_1_G
J&K Chemical

Product Information

Product Name
4,6-Ethylidene-4-nitrophenyl-α-D-maltoheptaoside, 90%
Brand Name
J&K
Product Number
1810804
CAS
96597-16-9
Molecular Formula
C50H77NO38
Molecular Weight
1300.1
SDS Document
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
E-4-NP-G7
PubChem CID
13455716
IUPAC Name
(4aR,6R,7R,8R,8aS)-6-(2R,3S,4R,5R,6R)-6-(2R,3S,4R,5R,6R)-6-(2R,3S,4R,5R,6R)-6-(2R,3S,4R,5R,6R)-6-(2R,3S,4R,5R,6R)-6-(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-(4-nitrophenoxy)oxan-3-yloxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yloxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yloxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yloxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yloxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yloxy-2-methyl-4,4a,6,7,8,8a-hexahydropyrano3,2-d1,3dioxine-7,8-diol
InChI Key
QOGJBGFYMYQFNE-SECAJZLMSA-N
SMILES
CC1OCC@@H2C@@H(O1)C@@H(C@H(C@H(O2)OC@@H3C@H(OC@@H(C@@H(C@H3O)O)OC@@H4C@H(OC@@H(C@@H(C@H4O)O)OC@@H5C@H(OC@@H(C@@H(C@H5O)O)OC@@H6C@H(OC@@H(C@@H(C@H6O)O)OC@@H7C@H(OC@@H(C@@H(C@H7O)O)OC@@H8C@H(OC@@H(C@@H(C@H8O)O)OC9=CC=C(C=C9)N+(=O)O-)CO)CO)CO)CO)CO)CO)O)O

Safety Information

GHS Symbols
Hazard Symbol
Precautionary Statement
P262
Storage Condition
Store at 2-8℃

Description

Product Introduction

4,6-Ethylidene-4-nitrophenyl-α-D-maltoheptaoside (EPS-G7) is a chromogenic substrate widely used for the determination of α-amylase activity in biochemical and clinical assays. The compound contains a maltoheptaoside oligosaccharide chain linked to a p-nitrophenyl chromogenic group, enabling colorimetric detection after enzymatic hydrolysis.

In the presence of α-amylase and auxiliary enzymes such as α-glucosidase, the substrate is cleaved to ultimately release p-nitrophenol (pNP). Under alkaline conditions, p-nitrophenol produces a yellow chromogenic product, which can be quantitatively measured by spectrophotometry.

Because of its specificity and reliability, EPS-G7 is widely used in clinical chemistry assays, enzymology research, and diagnostic reagent development for measuring α-amylase activity.

Mechanism of Reaction

4,6-Ethylidene-4-nitrophenyl-α-D-maltoheptaoside functions as a chromogenic substrate for α-amylase detection.During the enzymatic reaction:

  • α-Amylase cleaves the α-1,4-glycosidic bonds of the maltoheptaoside chain
  • Auxiliary enzymes further process the hydrolysis products
  • p-Nitrophenol (pNP) is released
  • Under alkaline conditions, pNP forms a yellow phenolate ion
  • The reaction is typically monitored by absorbance at 405 nm

The increase in absorbance is proportional to α-amylase activity in the sample.

Key Research Applications

1.α-Amylase Activity Assays

This compound is commonly used for quantitative determination of α-amylase activity in biological and biochemical samples.Typical applications include:

  • Serum α-amylase assays
  • Pancreatic enzyme activity determination
  • Digestive enzyme studies

2.Clinical Diagnostic Research

EPS-G7 is widely used in clinical chemistry assays designed to measure α-amylase activity in biological fluids.Applications include:

  • Clinical enzyme diagnostics
  • Pancreatic function assessment research
  • Diagnostic reagent development

3.Enzyme Kinetics Studies

The compound can be applied in enzyme kinetics experiments investigating catalytic properties of amylases.Typical uses include:

  • Determination of kinetic parameters (Km, Vmax)
  • Enzyme activity comparison
  • Substrate specificity analysis

4.Pharmaceutical and Biochemical Research

EPS-G7 is also used in biochemical and pharmaceutical studies involving carbohydrate-degrading enzymes.Applications include:

  • Amylase inhibitor screening
  • Carbohydrate metabolism research
  • Drug discovery targeting digestive enzymes

Recommended Experimental Conditions

Parameter Recommended Conditions
Detection Method Colorimetric spectrophotometric detection
Detection Wavelength 405 nm
Buffer Systems Phosphate buffer or Tris buffer
Temperature 25–37 °C
Assay Format Spectrophotometric assays, microplate reader assays

Optimization may be required depending on enzyme source and assay design.

Advantages in Enzyme Assays

  • Highly specific chromogenic substrate for α-amylase
  • Reliable and sensitive colorimetric detection
  • Suitable for automated clinical analyzers
  • Compatible with microplate-based assays

Storage & Handling

Recommended storage temperature 2 - 8 °C, Moisture sensitive
Store in a cool place. Keep container tightly closed in a dry and wellventilated place. Containers which are opened must be carefully resealed and kept upright to prevent leakage.

FAQ

What is 4,6-Ethylidene-4-nitrophenyl-α-D-maltoheptaoside used for?
It is primarily used as a chromogenic substrate for α-amylase activity assays in biochemical and clinical diagnostic research.

 

What wavelength is used to detect the reaction product?
The released p-nitrophenol is typically measured at 405 nm under alkaline conditions.

 

Why is EPS-G7 commonly used in clinical amylase assays?
Because it provides specific, reliable, and sensitive colorimetric detection of α-amylase activity, making it suitable for clinical laboratory analysis.

 

4,6-Ethylidene-4-nitrophenyl-α-D-maltoheptaoside, 90%

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