(S)-()-2-Aminobutanamide hydrochloride

99.0%

Reagent Code: #113893
label
Alias L-2-aminobutanamide hydrochloride
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CAS Number 7682-20-4

science Other reagents with same CAS 7682-20-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 138.6 g/mol
Formula C₄H₁₀N₂OHCl
badge Registry Numbers
MDL Number MFCD00136565
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various chiral drugs. Its role is crucial in the development of medications targeting neurological disorders, where enantiomeric purity is essential for efficacy and safety. Additionally, it finds application in the production of active pharmaceutical ingredients (APIs) that require specific stereochemical configurations to interact effectively with biological targets. In medicinal chemistry, it is employed to create analogs and derivatives for screening potential therapeutic agents, particularly in the realm of central nervous system (CNS) diseases. Its utility extends to academic laboratories, where it aids in studying stereoselective reactions and chiral synthesis pathways.

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Test Parameter Specification
Purity (HPLC) 99-100
Purity (Titration By AgNO3) 99-100.5
Specific Rotation [α]20/D (C=1, H2O) 23-25
Appearance White To Tan Powder, Crystals And/Or Chunks
Infrared Spectrum Conforms To Structure
Proton NMR Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿5,000.00
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿850.00
inventory 500g
10-20 days ฿17,900.00
inventory 25g
10-20 days ฿1,990.00
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(S)-()-2-Aminobutanamide hydrochloride
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Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various chiral drugs. Its role is crucial in the development of medications targeting neurological disorders, where enantiomeric purity is essential for efficacy and safety. Additionally, it finds application in the production of active pharmaceutical ingredients (APIs) that require specific stereochemical configurations to interact effectively with biological targets. In medicinal chemistry, it is e

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various chiral drugs. Its role is crucial in the development of medications targeting neurological disorders, where enantiomeric purity is essential for efficacy and safety. Additionally, it finds application in the production of active pharmaceutical ingredients (APIs) that require specific stereochemical configurations to interact effectively with biological targets. In medicinal chemistry, it is employed to create analogs and derivatives for screening potential therapeutic agents, particularly in the realm of central nervous system (CNS) diseases. Its utility extends to academic laboratories, where it aids in studying stereoselective reactions and chiral synthesis pathways.

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