N-tert-Butylethylamine

98%

Reagent Code: #217812
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CAS Number 4432-77-3

science Other reagents with same CAS 4432-77-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 101.19 g/mol
Formula C₆H₁₅N
badge Registry Numbers
MDL Number MFCD00059367
thermostat Physical Properties
Boiling Point 89°C(lit.)
inventory_2 Storage & Handling
Density 0.73g/ml
Storage Room temperature, stored in inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure makes it suitable for use in the development of complex molecules where steric hindrance plays a role in reaction selectivity. Commonly employed in the synthesis of active ingredients in crop protection products due to its stability and reactivity profile. Also finds use as a building block in medicinal chemistry for designing bioactive compounds, especially in routes requiring selective amine protection or catalytic transformations.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1ml
10-20 days ฿2,240.00
N-tert-Butylethylamine
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Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure makes it suitable for use in the development of complex molecules where steric hindrance plays a role in reaction selectivity. Commonly employed in the synthesis of active ingredients in crop protection products due to its stability and reactivity profile. Also finds use as a building block in medicinal chemistry for designing bioactive compounds, especially in routes requiring

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure makes it suitable for use in the development of complex molecules where steric hindrance plays a role in reaction selectivity. Commonly employed in the synthesis of active ingredients in crop protection products due to its stability and reactivity profile. Also finds use as a building block in medicinal chemistry for designing bioactive compounds, especially in routes requiring selective amine protection or catalytic transformations.

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