2-Iodoethanamine Hydroiodide

≥98%

Reagent Code: #198897
label
Alias 2-Iodide-1-amine hydroiodide
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CAS Number 19874-84-1

science Other reagents with same CAS 19874-84-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.89 g/mol
Formula C₂H₇I₂N
badge Registry Numbers
MDL Number MFCD26936188
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in organic synthesis as an alkylating agent, particularly in the preparation of heterocyclic compounds and pharmaceutical intermediates. Serves as a building block in the development of bioactive molecules due to its amine and iodide functionalities. Commonly employed in the synthesis of aminoethyl derivatives and in medicinal chemistry for constructing nitrogen-containing rings. Also utilized in the modification of peptides and in the preparation of labeled compounds for biochemical research.

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Test Parameter Specification
Purity (%) 98-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure
Appearance White solid

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿18,520.00
inventory 25g
10-20 days ฿62,200.00
inventory 250g
10-20 days ฿216,000.00
inventory 1g
10-20 days ฿5,340.00
inventory 50g
10-20 days ฿106,280.00

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2-Iodoethanamine Hydroiodide
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Used in organic synthesis as an alkylating agent, particularly in the preparation of heterocyclic compounds and pharmaceutical intermediates. Serves as a building block in the development of bioactive molecules due to its amine and iodide functionalities. Commonly employed in the synthesis of aminoethyl derivatives and in medicinal chemistry for constructing nitrogen-containing rings. Also utilized in the modification of peptides and in the preparation of labeled compounds for biochemical research.

Used in organic synthesis as an alkylating agent, particularly in the preparation of heterocyclic compounds and pharmaceutical intermediates. Serves as a building block in the development of bioactive molecules due to its amine and iodide functionalities. Commonly employed in the synthesis of aminoethyl derivatives and in medicinal chemistry for constructing nitrogen-containing rings. Also utilized in the modification of peptides and in the preparation of labeled compounds for biochemical research.

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