(S)-()-2-Nonyl isothiocyanate

≥95%

Reagent Code: #238012
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CAS Number 737000-86-1

science Other reagents with same CAS 737000-86-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.33 g/mol
Formula C₁₀H₁₉NS
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MDL Number MFCD04039335
inventory_2 Storage & Handling
Storage 2-8°C, Sealed

description Product Description

Used primarily as a chiral derivatizing agent in analytical chemistry, particularly for the separation and determination of enantiomeric purity of amines and amino acids. Its isothiocyanate group reacts selectively with primary amines to form thiourea derivatives, which are more stable and easier to analyze by chromatographic or electrophoretic methods. Due to its chiral center, it enables stereoselective interactions, making it valuable in resolving racemic mixtures. Also employed in studies involving asymmetric synthesis and chiral recognition mechanisms.

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inventory 250mg
10-20 days ฿29,330.00

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(S)-()-2-Nonyl isothiocyanate
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Used primarily as a chiral derivatizing agent in analytical chemistry, particularly for the separation and determination of enantiomeric purity of amines and amino acids. Its isothiocyanate group reacts selectively with primary amines to form thiourea derivatives, which are more stable and easier to analyze by chromatographic or electrophoretic methods. Due to its chiral center, it enables stereoselective interactions, making it valuable in resolving racemic mixtures. Also employed in studies involving a

Used primarily as a chiral derivatizing agent in analytical chemistry, particularly for the separation and determination of enantiomeric purity of amines and amino acids. Its isothiocyanate group reacts selectively with primary amines to form thiourea derivatives, which are more stable and easier to analyze by chromatographic or electrophoretic methods. Due to its chiral center, it enables stereoselective interactions, making it valuable in resolving racemic mixtures. Also employed in studies involving asymmetric synthesis and chiral recognition mechanisms.

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