N-(6-Aminohexyl)-2-nitrobenzenesulfonamide Hydrochloride

≥95%

Reagent Code: #121401
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CAS Number 95915-82-5

science Other reagents with same CAS 95915-82-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 337.82 g/mol
Formula C₁₂H₁₉N₃O₄SHCl
badge Registry Numbers
MDL Number MFCD06797045
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily used in organic synthesis as a protecting group for amines during complex chemical reactions. Its structure allows it to temporarily shield amine functionalities, preventing unwanted side reactions while other parts of the molecule are modified. This is particularly useful in peptide synthesis, where selective protection and deprotection of amino groups are critical. Additionally, it can serve as a reagent in biochemical research, aiding in the study of enzyme interactions or protein modifications. Its water solubility, due to the hydrochloride form, makes it convenient for use in aqueous solutions, expanding its applicability in various laboratory settings.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,591.00
inventory 200mg
10-20 days ฿1,314.00

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N-(6-Aminohexyl)-2-nitrobenzenesulfonamide Hydrochloride
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This compound is primarily used in organic synthesis as a protecting group for amines during complex chemical reactions. Its structure allows it to temporarily shield amine functionalities, preventing unwanted side reactions while other parts of the molecule are modified. This is particularly useful in peptide synthesis, where selective protection and deprotection of amino groups are critical. Additionally, it can serve as a reagent in biochemical research, aiding in the study of enzyme interactions or p

This compound is primarily used in organic synthesis as a protecting group for amines during complex chemical reactions. Its structure allows it to temporarily shield amine functionalities, preventing unwanted side reactions while other parts of the molecule are modified. This is particularly useful in peptide synthesis, where selective protection and deprotection of amino groups are critical. Additionally, it can serve as a reagent in biochemical research, aiding in the study of enzyme interactions or protein modifications. Its water solubility, due to the hydrochloride form, makes it convenient for use in aqueous solutions, expanding its applicability in various laboratory settings.

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