(S)-2-(Dimethylamino)propanoic acid

97%

Reagent Code: #38159
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CAS Number 2812-31-9

science Other reagents with same CAS 2812-31-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 117.15 g/mol
Formula C₅H₁₁NO₂
badge Registry Numbers
MDL Number MFCD00154416
thermostat Physical Properties
Boiling Point 179.9°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of enantiomerically pure drugs. It serves as an intermediate in the development of active pharmaceutical ingredients (APIs) for treatments targeting neurological and cardiovascular conditions. Additionally, it is employed in asymmetric synthesis to create compounds with high stereochemical purity. Its role in peptide modification and as a ligand in catalytic processes is also notable, enhancing the efficiency and selectivity of chemical reactions.

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Test Parameter Specification
Appearance White to Yellow Solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,570.00
inventory 250mg
10-20 days ฿13,150.00

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(S)-2-(Dimethylamino)propanoic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of enantiomerically pure drugs. It serves as an intermediate in the development of active pharmaceutical ingredients (APIs) for treatments targeting neurological and cardiovascular conditions. Additionally, it is employed in asymmetric synthesis to create compounds with high stereochemical purity. Its role in peptide modification and as a ligand in catalytic processes is also notable, enhancing the efficie

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of enantiomerically pure drugs. It serves as an intermediate in the development of active pharmaceutical ingredients (APIs) for treatments targeting neurological and cardiovascular conditions. Additionally, it is employed in asymmetric synthesis to create compounds with high stereochemical purity. Its role in peptide modification and as a ligand in catalytic processes is also notable, enhancing the efficiency and selectivity of chemical reactions.

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