(S)-2-Amino-4,4-dimethylpentanoic acid

≥95%

Reagent Code: #50138
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CAS Number 57224-50-7

science Other reagents with same CAS 57224-50-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 145.20 g/mol
Formula C₇H₁₅NO₂
badge Registry Numbers
MDL Number MFCD00066079
thermostat Physical Properties
Boiling Point 236°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in an inert gas

description Product Description

This chemical is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting neurological and metabolic disorders. Its unique structure allows it to act as a building block for peptides and small molecules that modulate specific enzymes or receptors in the body. Additionally, it is employed in the study of amino acid metabolism and as a chiral precursor in asymmetric synthesis, contributing to the production of enantiomerically pure drugs. Its applications also extend to the development of novel therapeutic agents for conditions such as epilepsy, chronic pain, and neurodegenerative diseases.

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Test Parameter Specification
Appearance White to Yellow Solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿31,662.00
inventory 250mg
10-20 days ฿3,735.00
inventory 1g
10-20 days ฿10,287.00

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(S)-2-Amino-4,4-dimethylpentanoic acid
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This chemical is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting neurological and metabolic disorders. Its unique structure allows it to act as a building block for peptides and small molecules that modulate specific enzymes or receptors in the body. Additionally, it is employed in the study of amino acid metabolism and as a chiral precursor in asymmetric synthesis, contributing to the production of enantiomerically pure drugs. Its applications also extend to the development of novel therapeutic agents for conditions such as epilepsy, chronic pain, and neurodegenerative diseases.
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