Ethyl 2,3,4-Tri-O-acetyl-β-D-glucuronide Methyl Ester

≥98%

Reagent Code: #183453
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CAS Number 77392-66-6

science Other reagents with same CAS 77392-66-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 362.33 g/mol
Formula C₁₅H₂₂O₁₀
thermostat Physical Properties
Melting Point 102-103℃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of glucuronide conjugates for drug metabolism studies. Enables the preparation of labeled or modified glucuronides used in pharmaceutical research to understand detoxification pathways and excretion mechanisms. Also applied in the development of reference standards for bioanalytical assays, particularly in LC-MS/MS applications. Its protected functional groups allow selective deprotection and coupling reactions, making it valuable in the synthesis of complex glycoconjugates and prodrugs.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,350.00
inventory 25g
10-20 days ฿23,500.00
inventory 5g
10-20 days ฿5,200.00
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Ethyl 2,3,4-Tri-O-acetyl-β-D-glucuronide Methyl Ester
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Used as a key intermediate in the synthesis of glucuronide conjugates for drug metabolism studies. Enables the preparation of labeled or modified glucuronides used in pharmaceutical research to understand detoxification pathways and excretion mechanisms. Also applied in the development of reference standards for bioanalytical assays, particularly in LC-MS/MS applications. Its protected functional groups allow selective deprotection and coupling reactions, making it valuable in the synthesis of complex gl

Used as a key intermediate in the synthesis of glucuronide conjugates for drug metabolism studies. Enables the preparation of labeled or modified glucuronides used in pharmaceutical research to understand detoxification pathways and excretion mechanisms. Also applied in the development of reference standards for bioanalytical assays, particularly in LC-MS/MS applications. Its protected functional groups allow selective deprotection and coupling reactions, making it valuable in the synthesis of complex glycoconjugates and prodrugs.

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