2-Nitrophenyl a-D-galactopyranoside

95%

Reagent Code: #104025
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CAS Number 19887-85-5

science Other reagents with same CAS 19887-85-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.25 g/mol
Formula C₁₂H₁₆NO₈
badge Registry Numbers
MDL Number MFCD00069785
thermostat Physical Properties
Boiling Point 572.4 °C at 760 mmHg (lit.)
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a substrate in enzymatic assays to study the activity of α-galactosidase enzymes, which are crucial in breaking down complex carbohydrates. It is particularly valuable in biochemical research for understanding metabolic disorders like Fabry disease, where α-galactosidase activity is deficient. The compound’s nitrophenyl group releases a yellow-colored product upon enzymatic cleavage, allowing for easy spectrophotometric detection and quantification of enzyme activity. This makes it a useful tool in both diagnostic laboratories and research settings for monitoring enzyme kinetics and screening potential enzyme inhibitors or activators.

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Test Parameter Specification
Appearance Off-white or light yellow powder
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿19,800.00
inventory 1g
10-20 days ฿66,800.00

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2-Nitrophenyl a-D-galactopyranoside
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Used as a substrate in enzymatic assays to study the activity of α-galactosidase enzymes, which are crucial in breaking down complex carbohydrates. It is particularly valuable in biochemical research for understanding metabolic disorders like Fabry disease, where α-galactosidase activity is deficient. The compound’s nitrophenyl group releases a yellow-colored product upon enzymatic cleavage, allowing for easy spectrophotometric detection and quantification of enzyme activity. This makes it a useful tool

Used as a substrate in enzymatic assays to study the activity of α-galactosidase enzymes, which are crucial in breaking down complex carbohydrates. It is particularly valuable in biochemical research for understanding metabolic disorders like Fabry disease, where α-galactosidase activity is deficient. The compound’s nitrophenyl group releases a yellow-colored product upon enzymatic cleavage, allowing for easy spectrophotometric detection and quantification of enzyme activity. This makes it a useful tool in both diagnostic laboratories and research settings for monitoring enzyme kinetics and screening potential enzyme inhibitors or activators.

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