3-Methylglutamic acid

Reagent Code: #213272
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CAS Number 63088-04-0

science Other reagents with same CAS 63088-04-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.16 g/mol
Formula C₆H₁₁NO₄
badge Registry Numbers
MDL Number MFCD09836097
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of neuroactive compounds and enzyme inhibitors. Its structural similarity to glutamic acid allows it to interact with glutamate receptors, such as NMDA and AMPA, and metabolic pathways, making it valuable in neuroscience research. Also employed in the preparation of specialty peptides and as a precursor in asymmetric synthesis for creating complex organic molecules with high stereochemical purity. Additionally, it serves as an internal standard in analytical techniques like chromatography and spectroscopy to identify and quantify biomolecules in biological samples.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿21,120.00

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3-Methylglutamic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of neuroactive compounds and enzyme inhibitors. Its structural similarity to glutamic acid allows it to interact with glutamate receptors, such as NMDA and AMPA, and metabolic pathways, making it valuable in neuroscience research. Also employed in the preparation of specialty peptides and as a precursor in asymmetric synthesis for creating complex organic molecules with high stereochemical purity. Additio

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of neuroactive compounds and enzyme inhibitors. Its structural similarity to glutamic acid allows it to interact with glutamate receptors, such as NMDA and AMPA, and metabolic pathways, making it valuable in neuroscience research. Also employed in the preparation of specialty peptides and as a precursor in asymmetric synthesis for creating complex organic molecules with high stereochemical purity. Additionally, it serves as an internal standard in analytical techniques like chromatography and spectroscopy to identify and quantify biomolecules in biological samples.

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