(S)-2-Amino-4-azidobutanoic acid hydrochloride

98%

Reagent Code: #113739
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CAS Number 942518-29-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.59 g/mol
Formula C₄H₉ClN₄O₂
badge Registry Numbers
MDL Number MFCD13184931
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This compound is primarily utilized in biochemical research and pharmaceutical development. It serves as a key intermediate in the synthesis of modified peptides and proteins, enabling the study of protein structure and function. The azide group allows for click chemistry reactions, facilitating the attachment of fluorescent tags or other functional groups for imaging and diagnostic purposes. Additionally, it is employed in the development of targeted drug delivery systems, where its unique structure aids in creating precise and efficient therapeutic agents. Its applications also extend to the field of bioconjugation, where it helps in linking biomolecules for various experimental and clinical purposes.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to Off-White Solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days $228.90
inventory 500mg
10-20 days $1,005.72
inventory 1g
10-20 days $1,772.18
inventory 5g
10-20 days $6,181.09
(S)-2-Amino-4-azidobutanoic acid hydrochloride
This compound is primarily utilized in biochemical research and pharmaceutical development. It serves as a key intermediate in the synthesis of modified peptides and proteins, enabling the study of protein structure and function. The azide group allows for click chemistry reactions, facilitating the attachment of fluorescent tags or other functional groups for imaging and diagnostic purposes. Additionally, it is employed in the development of targeted drug delivery systems, where its unique structure aids in creating precise and efficient therapeutic agents. Its applications also extend to the field of bioconjugation, where it helps in linking biomolecules for various experimental and clinical purposes.
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