ETHYL ACETIMIDATE HYDROCHLORIDE

90%

Reagent Code: #73479
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CAS Number 2208-07-3

science Other reagents with same CAS 2208-07-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 123.58 g/mol
Formula C₄H₉NOHCl
badge Registry Numbers
MDL Number MFCD00012572
thermostat Physical Properties
Melting Point 112-114°C (Lit.)
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used primarily in biochemical research, this compound serves as a reagent for modifying proteins and peptides. It is particularly effective in amidination reactions, where it introduces amidine groups into molecules, enhancing their stability and altering their biochemical properties. This modification is crucial in studies involving protein structure and function, aiding in the identification of active sites and interaction points. Additionally, it finds application in the synthesis of various pharmaceuticals, where it helps in the development of drugs with improved efficacy and specificity. Its role in the preparation of modified biomolecules also supports advancements in diagnostic assays and therapeutic agents.

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Test Parameter Specification
Purity 89.5-100%
Melting point 112-114
Appearance White crystalline powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50g
10-20 days ฿2,100.00
inventory 1kg
10-20 days ฿25,500.00
inventory 10g
10-20 days ฿660.00
inventory 250g
10-20 days ฿8,890.00

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ETHYL ACETIMIDATE HYDROCHLORIDE
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Used primarily in biochemical research, this compound serves as a reagent for modifying proteins and peptides. It is particularly effective in amidination reactions, where it introduces amidine groups into molecules, enhancing their stability and altering their biochemical properties. This modification is crucial in studies involving protein structure and function, aiding in the identification of active sites and interaction points. Additionally, it finds application in the synthesis of various pharmaceu

Used primarily in biochemical research, this compound serves as a reagent for modifying proteins and peptides. It is particularly effective in amidination reactions, where it introduces amidine groups into molecules, enhancing their stability and altering their biochemical properties. This modification is crucial in studies involving protein structure and function, aiding in the identification of active sites and interaction points. Additionally, it finds application in the synthesis of various pharmaceuticals, where it helps in the development of drugs with improved efficacy and specificity. Its role in the preparation of modified biomolecules also supports advancements in diagnostic assays and therapeutic agents.

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