1-benzylhydrazine hydrochloride

≥95%

Reagent Code: #143852
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CAS Number 1073-62-7

science Other reagents with same CAS 1073-62-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.63 g/mol
Formula C₇H₁₀N₂·HCl
badge Registry Numbers
MDL Number MFCD01722685
thermostat Physical Properties
Melting Point 113 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of hydrazine-based drugs. It serves in the development of antitubercular agents and antidepressants due to its ability to form bioactive heterocyclic compounds. Also employed in the production of agrochemicals and specialty polymers where hydrazide or hydrazone linkages are required. Its benzyl-protected hydrazine structure makes it valuable in peptide coupling and protection strategies in organic synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿810.00
inventory 10g
10-20 days ฿1,440.00
inventory 25g
10-20 days ฿3,320.00
inventory 100g
10-20 days ฿12,850.00
1-benzylhydrazine hydrochloride
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Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of hydrazine-based drugs. It serves in the development of antitubercular agents and antidepressants due to its ability to form bioactive heterocyclic compounds. Also employed in the production of agrochemicals and specialty polymers where hydrazide or hydrazone linkages are required. Its benzyl-protected hydrazine structure makes it valuable in peptide coupling and protection strategies in organic sy

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of hydrazine-based drugs. It serves in the development of antitubercular agents and antidepressants due to its ability to form bioactive heterocyclic compounds. Also employed in the production of agrochemicals and specialty polymers where hydrazide or hydrazone linkages are required. Its benzyl-protected hydrazine structure makes it valuable in peptide coupling and protection strategies in organic synthesis.

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