2-Iminothiolane hydrochloride

98%

Reagent Code: #111544
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Alias 2-Iminothiolane Hydrochloride
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CAS Number 4781-83-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.63 g/mol
Formula C₄H₇NSHCl
badge Registry Numbers
MDL Number MFCD00039013
thermostat Physical Properties
Melting Point 198-201 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

2-Iminothiolane hydrochloride is widely used in biochemical research for modifying proteins and peptides. Its primary application is in the introduction of thiol groups into molecules, facilitating the formation of disulfide bonds or conjugation with other thiol-reactive compounds. This property makes it valuable in the study of protein structure and function, as well as in the development of bioconjugates for therapeutic and diagnostic purposes. Additionally, it is employed in the preparation of affinity chromatography resins, where thiol groups are essential for coupling ligands to solid supports. Its ability to enhance the reactivity of biomolecules under mild conditions makes it a versatile tool in various biotechnological applications.

format_list_bulleted Product Specification

Test Parameter Specification
Free Sulfhydryl Groups 0-5
Melting Point 198-201
Purity (HPLC) 97.5-100
Appearance White To Off-White Powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days $74.17
inventory 500mg
10-20 days $263.99
inventory 2g
10-20 days $832.65
2-Iminothiolane hydrochloride
2-Iminothiolane hydrochloride is widely used in biochemical research for modifying proteins and peptides. Its primary application is in the introduction of thiol groups into molecules, facilitating the formation of disulfide bonds or conjugation with other thiol-reactive compounds. This property makes it valuable in the study of protein structure and function, as well as in the development of bioconjugates for therapeutic and diagnostic purposes. Additionally, it is employed in the preparation of affinity chromatography resins, where thiol groups are essential for coupling ligands to solid supports. Its ability to enhance the reactivity of biomolecules under mild conditions makes it a versatile tool in various biotechnological applications.
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