Ethylhydrazine oxalate

95%

Reagent Code: #121996
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CAS Number 6629-60-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.13 g/mol
Formula C₄H₁₀N₂O₄
badge Registry Numbers
MDL Number MFCD00043287
thermostat Physical Properties
Melting Point 170-173°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Ethylhydrazine oxalate is primarily utilized in organic synthesis as a versatile reagent. It is commonly employed in the preparation of various heterocyclic compounds, which are essential in the development of pharmaceuticals and agrochemicals. The compound is particularly useful in the synthesis of hydrazine derivatives, which serve as intermediates in the production of drugs targeting conditions like cancer, tuberculosis, and hypertension. Additionally, it is used in the formulation of certain herbicides and pesticides, contributing to crop protection and agricultural efficiency. Its role in chemical research also extends to the study of reaction mechanisms and the development of novel synthetic pathways.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Solid
Purity (%) 95-100%

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿500.00
inventory 25g
10-20 days ฿5,850.00
inventory 250mg
10-20 days ฿290.00
inventory 5g
10-20 days ฿1,200.00
Ethylhydrazine oxalate
Ethylhydrazine oxalate is primarily utilized in organic synthesis as a versatile reagent. It is commonly employed in the preparation of various heterocyclic compounds, which are essential in the development of pharmaceuticals and agrochemicals. The compound is particularly useful in the synthesis of hydrazine derivatives, which serve as intermediates in the production of drugs targeting conditions like cancer, tuberculosis, and hypertension. Additionally, it is used in the formulation of certain herbicides and pesticides, contributing to crop protection and agricultural efficiency. Its role in chemical research also extends to the study of reaction mechanisms and the development of novel synthetic pathways.
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