Sodium cyanoborohydride

1.0 M in THF

Reagent Code: #78919
label
Alias Sodium cyanoborohydride; Sodium cyanoborohydride, (cyano-C) sodium trihydroborate
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CAS Number 25895-60-7

science Other reagents with same CAS 25895-60-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 62.84 g/mol
Formula CH₃BNNa
badge Registry Numbers
MDL Number MFCD00003516
thermostat Physical Properties
Melting Point >242 °C (dec.)(lit.)
Boiling Point 307°C
inventory_2 Storage & Handling
Density 1.083 g/mL at 25 °C
Storage Room temperature, inert gas atmosphere

description Product Description

Sodium cyanoborohydride is widely used as a selective reducing agent in organic synthesis. It is particularly effective in reductive amination reactions, where it reduces imines or iminium ions to amines without affecting other functional groups. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and other complex organic molecules. It is also employed in the stabilization of sensitive intermediates during multi-step reactions. Additionally, it finds application in biochemical processes, such as the modification of proteins and nucleic acids, where its mild reducing properties are advantageous.

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Test Parameter Specification
Concentration (Titration by Na2S2O3) 0.95-1.1
Appearance Colorless liquid
X-ray Diffraction Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100ml
10-20 days ฿3,980.00

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Sodium cyanoborohydride
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Sodium cyanoborohydride is widely used as a selective reducing agent in organic synthesis. It is particularly effective in reductive amination reactions, where it reduces imines or iminium ions to amines without affecting other functional groups. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and other complex organic molecules. It is also employed in the stabilization of sensitive intermediates during multi-step reactions. Additionally, it finds application in biochemical pro

Sodium cyanoborohydride is widely used as a selective reducing agent in organic synthesis. It is particularly effective in reductive amination reactions, where it reduces imines or iminium ions to amines without affecting other functional groups. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and other complex organic molecules. It is also employed in the stabilization of sensitive intermediates during multi-step reactions. Additionally, it finds application in biochemical processes, such as the modification of proteins and nucleic acids, where its mild reducing properties are advantageous.

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