Ethoxyamine hydrochloride

99%

Reagent Code: #72905
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Alias Ethoxylated amine hydrochloride
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CAS Number 3332-29-4

science Other reagents with same CAS 3332-29-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 97.54 g/mol
Formula C₂H₇NOHCl
badge Registry Numbers
MDL Number MFCD00012956
inventory_2 Storage & Handling
Storage room temperature, sealed

description Product Description

Ethoxyamine hydrochloride is widely used in organic synthesis as a versatile reagent. It is particularly valuable in the preparation of oxime derivatives, which are essential intermediates in the synthesis of various pharmaceuticals and agrochemicals. The compound is also employed in the protection of carbonyl groups during complex chemical reactions, ensuring selective transformations. Additionally, it plays a role in the modification of nucleosides and nucleotides, aiding in the development of antiviral and anticancer drugs. Its application extends to the field of analytical chemistry, where it is used for the derivatization of aldehydes and ketones to enhance their detection in chromatographic analyses.

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Test Parameter Specification
Appearance White to off-white solid
Purity 98.5
Melting Point 125-140
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿640.00
inventory 100g
10-20 days ฿1,750.00

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Ethoxyamine hydrochloride
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Ethoxyamine hydrochloride is widely used in organic synthesis as a versatile reagent. It is particularly valuable in the preparation of oxime derivatives, which are essential intermediates in the synthesis of various pharmaceuticals and agrochemicals. The compound is also employed in the protection of carbonyl groups during complex chemical reactions, ensuring selective transformations. Additionally, it plays a role in the modification of nucleosides and nucleotides, aiding in the development of antivira

Ethoxyamine hydrochloride is widely used in organic synthesis as a versatile reagent. It is particularly valuable in the preparation of oxime derivatives, which are essential intermediates in the synthesis of various pharmaceuticals and agrochemicals. The compound is also employed in the protection of carbonyl groups during complex chemical reactions, ensuring selective transformations. Additionally, it plays a role in the modification of nucleosides and nucleotides, aiding in the development of antiviral and anticancer drugs. Its application extends to the field of analytical chemistry, where it is used for the derivatization of aldehydes and ketones to enhance their detection in chromatographic analyses.

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