N-Methyl-L-proline monohydrate

96%

Reagent Code: #66164
label
Alias N-methyl-L-proline, monohydrate
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CAS Number 199917-42-5

science Other reagents with same CAS 199917-42-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.17 g/mol
Formula C₆H₁₁NO₂H₂O
badge Registry Numbers
MDL Number MFCD00149962
thermostat Physical Properties
Melting Point 114-116 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily in pharmaceutical research, it serves as a chiral building block for the synthesis of complex molecules, particularly in the development of drugs targeting neurological disorders. Its structure is beneficial in creating peptidomimetics, which mimic peptides to enhance drug stability and bioavailability. Additionally, it is employed in asymmetric synthesis to produce enantiomerically pure compounds, crucial for the efficacy and safety of therapeutic agents.

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Test Parameter Specification
Melting point 114-116
Purity (HPLC) 95.5-100%
Specific Rotation (A20D) 82-84

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,980.00
inventory 250mg
10-20 days ฿460.00
inventory 1g
10-20 days ฿880.00

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N-Methyl-L-proline monohydrate
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Used primarily in pharmaceutical research, it serves as a chiral building block for the synthesis of complex molecules, particularly in the development of drugs targeting neurological disorders. Its structure is beneficial in creating peptidomimetics, which mimic peptides to enhance drug stability and bioavailability. Additionally, it is employed in asymmetric synthesis to produce enantiomerically pure compounds, crucial for the efficacy and safety of therapeutic agents.

Used primarily in pharmaceutical research, it serves as a chiral building block for the synthesis of complex molecules, particularly in the development of drugs targeting neurological disorders. Its structure is beneficial in creating peptidomimetics, which mimic peptides to enhance drug stability and bioavailability. Additionally, it is employed in asymmetric synthesis to produce enantiomerically pure compounds, crucial for the efficacy and safety of therapeutic agents.

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