(S)-2-Hydroxyethyl 2-amino-3-methylbutanoate 4-methylbenzenesulfonate

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Reagent Code: #57159
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CAS Number 86150-61-0

science Other reagents with same CAS 86150-61-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 333.40 g/mol
Formula C₁₄H₂₃NO₆S
badge Registry Numbers
MDL Number MFCD22666220
inventory_2 Storage & Handling
Storage room temperature, inert gas storage

description Product Description

This compound is primarily utilized in the pharmaceutical and biochemical industries as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its structure, containing both hydroxyl and amino functional groups, makes it a valuable intermediate in the production of enantiomerically pure compounds, which are crucial for drugs requiring high stereochemical specificity. It is often employed in the development of peptide-based therapeutics and other biologically active molecules. Additionally, its sulfonate group enhances solubility, making it suitable for use in formulations where improved bioavailability is desired. The compound is also explored in research for its potential in creating novel drug delivery systems and as a precursor in organic synthesis for complex molecular architectures.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,927.00
inventory 100mg
10-20 days ฿6,624.00
inventory 1g
10-20 days ฿24,813.00

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(S)-2-Hydroxyethyl 2-amino-3-methylbutanoate 4-methylbenzenesulfonate
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This compound is primarily utilized in the pharmaceutical and biochemical industries as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its structure, containing both hydroxyl and amino functional groups, makes it a valuable intermediate in the production of enantiomerically pure compounds, which are crucial for drugs requiring high stereochemical specificity. It is often employed in the development of peptide-based therapeutics and other biologically active

This compound is primarily utilized in the pharmaceutical and biochemical industries as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its structure, containing both hydroxyl and amino functional groups, makes it a valuable intermediate in the production of enantiomerically pure compounds, which are crucial for drugs requiring high stereochemical specificity. It is often employed in the development of peptide-based therapeutics and other biologically active molecules. Additionally, its sulfonate group enhances solubility, making it suitable for use in formulations where improved bioavailability is desired. The compound is also explored in research for its potential in creating novel drug delivery systems and as a precursor in organic synthesis for complex molecular architectures.

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