3-((4-Formylphenyl)(methyl)amino)propanoic acid

95%

Reagent Code: #129985
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CAS Number 27425-56-5

science Other reagents with same CAS 27425-56-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.23 g/mol
Formula C₁₁H₁₃NO₃
badge Registry Numbers
MDL Number MFCD06208354
thermostat Physical Properties
Boiling Point 418.6±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.242±0.06 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and bioactive molecules, particularly in the development of targeted drug delivery systems. Its aldehyde functional group allows for easy conjugation with amines or hydrazides, making it valuable in bioconjugation chemistry. Commonly employed in the preparation of prodrugs and antibody-drug linkers due to its stability and reactive handle for coupling. Also utilized in the fabrication of functionalized polymers and sensors where controlled binding or release is required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,080.00
inventory 100mg
10-20 days ฿8,280.00

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3-((4-Formylphenyl)(methyl)amino)propanoic acid
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Used as an intermediate in the synthesis of pharmaceuticals and bioactive molecules, particularly in the development of targeted drug delivery systems. Its aldehyde functional group allows for easy conjugation with amines or hydrazides, making it valuable in bioconjugation chemistry. Commonly employed in the preparation of prodrugs and antibody-drug linkers due to its stability and reactive handle for coupling. Also utilized in the fabrication of functionalized polymers and sensors where controlled bindi

Used as an intermediate in the synthesis of pharmaceuticals and bioactive molecules, particularly in the development of targeted drug delivery systems. Its aldehyde functional group allows for easy conjugation with amines or hydrazides, making it valuable in bioconjugation chemistry. Commonly employed in the preparation of prodrugs and antibody-drug linkers due to its stability and reactive handle for coupling. Also utilized in the fabrication of functionalized polymers and sensors where controlled binding or release is required.

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