1,6,2',3',6'-O-Pentaacetyl-3-O-trans-p-coumaroylsucrose

98%

Reagent Code: #222146
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CAS Number 138213-63-5

science Other reagents with same CAS 138213-63-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 698.62 g/mol
Formula C₃₁H₃₈O₁₈
thermostat Physical Properties
Boiling Point 799.1±60.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as an intermediate in the synthesis of high-intensity sweeteners derived from natural sucrose compounds. It plays a role in modifying sugar molecules to enhance sweetness and stability while maintaining low caloric content. Commonly applied in research and development of novel sweetening agents for food and beverage industries, especially in creating non-cariogenic and diabetic-friendly sugar alternatives. Its acetylated and coumaroyl-protected structure allows selective deprotection and further chemical modifications, making it valuable in organic synthesis pathways targeting sucrose analogs with improved sensory and functional properties.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿61,750.00
1,6,2',3',6'-O-Pentaacetyl-3-O-trans-p-coumaroylsucrose
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Used as an intermediate in the synthesis of high-intensity sweeteners derived from natural sucrose compounds. It plays a role in modifying sugar molecules to enhance sweetness and stability while maintaining low caloric content. Commonly applied in research and development of novel sweetening agents for food and beverage industries, especially in creating non-cariogenic and diabetic-friendly sugar alternatives. Its acetylated and coumaroyl-protected structure allows selective deprotection and further chemic
Used as an intermediate in the synthesis of high-intensity sweeteners derived from natural sucrose compounds. It plays a role in modifying sugar molecules to enhance sweetness and stability while maintaining low caloric content. Commonly applied in research and development of novel sweetening agents for food and beverage industries, especially in creating non-cariogenic and diabetic-friendly sugar alternatives. Its acetylated and coumaroyl-protected structure allows selective deprotection and further chemical modifications, making it valuable in organic synthesis pathways targeting sucrose analogs with improved sensory and functional properties.
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