N-Carbobenzoxy-1,4-diaminobutane Hydrochloride

≥97%

Reagent Code: #121562
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CAS Number 18807-73-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.75 g/mol
Formula C₁₂H₁₈N₂O₂HCl
badge Registry Numbers
MDL Number MFCD00270149
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

N-Carbobenzoxy-1,4-diaminobutane Hydrochloride is primarily used in organic synthesis as a protecting group for amines. It is particularly valuable in peptide synthesis, where it helps prevent unwanted reactions at the amine group during the formation of peptide bonds. This compound is also employed in the preparation of polyamines and other complex organic molecules, where selective protection and deprotection of functional groups are required. Additionally, it serves as an intermediate in the development of pharmaceuticals and bioactive compounds, aiding in the creation of structurally diverse and functional molecules. Its stability and ease of removal under specific conditions make it a versatile tool in synthetic chemistry.

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Test Parameter Specification
Appearance White to almost white powder to crystal
Purity (%) 96.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days $68.45
inventory 1g
10-20 days $132.13
N-Carbobenzoxy-1,4-diaminobutane Hydrochloride
N-Carbobenzoxy-1,4-diaminobutane Hydrochloride is primarily used in organic synthesis as a protecting group for amines. It is particularly valuable in peptide synthesis, where it helps prevent unwanted reactions at the amine group during the formation of peptide bonds. This compound is also employed in the preparation of polyamines and other complex organic molecules, where selective protection and deprotection of functional groups are required. Additionally, it serves as an intermediate in the development of pharmaceuticals and bioactive compounds, aiding in the creation of structurally diverse and functional molecules. Its stability and ease of removal under specific conditions make it a versatile tool in synthetic chemistry.
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