N-tert-Butyl-N-ethylnitrosamine

98%

Reagent Code: #217813
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CAS Number 3398-69-4

science Other reagents with same CAS 3398-69-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 130.19 g/mol
Formula C₆H₁₄N₂O
badge Registry Numbers
MDL Number MFCD00059594
thermostat Physical Properties
Melting Point 21°C
Boiling Point 84°C/17mmHg(lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the preparation of functionalized amines and heterocyclic compounds. It serves as a nitrosating agent in specialized reactions where controlled introduction of the nitroso group is required. Due to the presence of the tert-butyl and ethyl groups, it can act as a sterically hindered reagent, influencing reaction selectivity in certain pathways. Its application is mostly confined to research laboratories for the development of pharmaceuticals and agrochemicals, where it participates in the formation of nitrogen-containing scaffolds. Handling requires caution due to the potential instability and toxicity associated with nitrosamine derivatives.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1ml
10-20 days ฿3,660.00
N-tert-Butyl-N-ethylnitrosamine
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Used primarily as an intermediate in organic synthesis, particularly in the preparation of functionalized amines and heterocyclic compounds. It serves as a nitrosating agent in specialized reactions where controlled introduction of the nitroso group is required. Due to the presence of the tert-butyl and ethyl groups, it can act as a sterically hindered reagent, influencing reaction selectivity in certain pathways. Its application is mostly confined to research laboratories for the development of pharmaceuti
Used primarily as an intermediate in organic synthesis, particularly in the preparation of functionalized amines and heterocyclic compounds. It serves as a nitrosating agent in specialized reactions where controlled introduction of the nitroso group is required. Due to the presence of the tert-butyl and ethyl groups, it can act as a sterically hindered reagent, influencing reaction selectivity in certain pathways. Its application is mostly confined to research laboratories for the development of pharmaceuticals and agrochemicals, where it participates in the formation of nitrogen-containing scaffolds. Handling requires caution due to the potential instability and toxicity associated with nitrosamine derivatives.
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