Sodium amide

95%

Reagent Code: #71512
label
Alias Sodium Amide
fingerprint
CAS Number 7782-92-5

science Other reagents with same CAS 7782-92-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 39.01 g/mol
Formula NaNH₂
badge Registry Numbers
EC Number 231-971-0
MDL Number MFCD00011117
thermostat Physical Properties
Melting Point 210 °C(lit.)
Boiling Point 400 °C(lit.)
inventory_2 Storage & Handling
Storage -20°C, combustible area, dry, sealed

description Product Description

Used primarily as a strong base in organic synthesis, it facilitates the deprotonation of weak acids, enabling the formation of carbanions. It is particularly valuable in the production of indigo dyes and pharmaceuticals, where it assists in condensation reactions. In the synthesis of sodium cyanide, it acts as a key intermediate. Additionally, it is employed in the Birch reduction process to generate radical anions from aromatic compounds. Its reactivity with water requires careful handling, often in anhydrous conditions, to prevent hazardous reactions.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 94-106
Appearance Off-white to tan to grey powder or pellets
X-ray Diffraction Conforms to structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500g
10-20 days ฿1,560.00
inventory 2.5kg
10-20 days ฿5,380.00
inventory 100g
10-20 days ฿440.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Sodium amide
No image available

Used primarily as a strong base in organic synthesis, it facilitates the deprotonation of weak acids, enabling the formation of carbanions. It is particularly valuable in the production of indigo dyes and pharmaceuticals, where it assists in condensation reactions. In the synthesis of sodium cyanide, it acts as a key intermediate. Additionally, it is employed in the Birch reduction process to generate radical anions from aromatic compounds. Its reactivity with water requires careful handling, often in an

Used primarily as a strong base in organic synthesis, it facilitates the deprotonation of weak acids, enabling the formation of carbanions. It is particularly valuable in the production of indigo dyes and pharmaceuticals, where it assists in condensation reactions. In the synthesis of sodium cyanide, it acts as a key intermediate. Additionally, it is employed in the Birch reduction process to generate radical anions from aromatic compounds. Its reactivity with water requires careful handling, often in anhydrous conditions, to prevent hazardous reactions.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...