(S)-3-Aminobutanoic acid

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Reagent Code: #235036
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CAS Number 3775-72-2

science Other reagents with same CAS 3775-72-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 103.12 g/mol
Formula C₄H₉NO₂
thermostat Physical Properties
Melting Point 229-231°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of antiepileptic and neuroprotective agents. It serves as an intermediate in the production of beta-amino acids with biological activity. Also employed in the preparation of peptidomimetics and enzyme inhibitors due to its structural similarity to natural amino acids. Its stereochemistry makes it valuable in asymmetric synthesis and drug design where specific enantiomeric forms are required for optimal activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿300.00
inventory 1g
10-20 days ฿680.00
inventory 5g
10-20 days ฿1,860.00
inventory 25g
10-20 days ฿9,220.00

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(S)-3-Aminobutanoic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of antiepileptic and neuroprotective agents. It serves as an intermediate in the production of beta-amino acids with biological activity. Also employed in the preparation of peptidomimetics and enzyme inhibitors due to its structural similarity to natural amino acids. Its stereochemistry makes it valuable in asymmetric synthesis and drug design where specific enantiomeric forms are required for optimal ac

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of antiepileptic and neuroprotective agents. It serves as an intermediate in the production of beta-amino acids with biological activity. Also employed in the preparation of peptidomimetics and enzyme inhibitors due to its structural similarity to natural amino acids. Its stereochemistry makes it valuable in asymmetric synthesis and drug design where specific enantiomeric forms are required for optimal activity.

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