(S)-2-Aminopentan-1-ol hydrochloride

95%

Reagent Code: #87180
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CAS Number 2025376-01-4

science Other reagents with same CAS 2025376-01-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 139.62 g/mol
Formula C₅H₁₄ClNO
badge Registry Numbers
MDL Number MFCD26407337
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

The chemical is primarily used in pharmaceutical research and development as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its chiral nature makes it valuable in creating enantiomerically pure compounds, which are crucial for developing drugs with specific biological activity and reduced side effects. It is also employed in organic synthesis for the preparation of complex molecules, particularly in the field of medicinal chemistry. Additionally, it finds application in the study of biochemical pathways and enzyme interactions due to its structural similarity to natural amino alcohols. Its hydrochloride form enhances solubility, making it suitable for use in aqueous-based reactions and formulations.

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Test Parameter Specification
APPEARANCE White Powder
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,118.00
inventory 1g
10-20 days ฿16,677.00

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(S)-2-Aminopentan-1-ol hydrochloride
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The chemical is primarily used in pharmaceutical research and development as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its chiral nature makes it valuable in creating enantiomerically pure compounds, which are crucial for developing drugs with specific biological activity and reduced side effects. It is also employed in organic synthesis for the preparation of complex molecules, particularly in the field of medicinal chemistry. Additionally, it finds a

The chemical is primarily used in pharmaceutical research and development as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its chiral nature makes it valuable in creating enantiomerically pure compounds, which are crucial for developing drugs with specific biological activity and reduced side effects. It is also employed in organic synthesis for the preparation of complex molecules, particularly in the field of medicinal chemistry. Additionally, it finds application in the study of biochemical pathways and enzyme interactions due to its structural similarity to natural amino alcohols. Its hydrochloride form enhances solubility, making it suitable for use in aqueous-based reactions and formulations.

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