Isonicotinyl hydrazide

98%

Reagent Code: #80430
label
Alias Isoniazid; Isoniazid, Ramifen, γ-pyridinecarbohydrazide, 4-pyridineacetylhydrazide, 4-pyridinecarboxyhydrazine, pyridine-4-carboxylhydrazide
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CAS Number 54-85-3

science Other reagents with same CAS 54-85-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.14 g/mol
Formula C₆H₇N₃O
badge Registry Numbers
EC Number 200-214-6
MDL Number MFCD00006426
thermostat Physical Properties
Melting Point 171-173 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C, dry, sealed

description Product Description

Widely used as a primary treatment for tuberculosis by inhibiting the synthesis of mycolic acids, essential components of the cell wall in Mycobacterium tuberculosis, thereby preventing bacterial growth. It is often combined with other antitubercular drugs such as rifampicin, pyrazinamide, and ethambutol to enhance efficacy and prevent resistance. Additionally, it is employed in the synthesis of various hydrazone derivatives, which are explored for their potential antimicrobial and anticancer properties. In research, it serves as a reagent in organic synthesis and analytical chemistry for detecting and quantifying carbonyl compounds. Its role in preventing the spread of tuberculosis in high-risk populations has made it a critical component in global health programs. Use under medical supervision is recommended due to potential side effects such as hepatotoxicity or neurological symptoms.

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Test Parameter Specification
Loss on Drying <=0.5%
Melting Point 169-173
Purity (HPLC) 98-100%
Appearance White to off-white powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿390.00
inventory 100g
10-20 days ฿990.00
inventory 500g
10-20 days ฿3,740.00
inventory 2.5kg
10-20 days ฿15,330.00
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Isonicotinyl hydrazide
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Widely used as a primary treatment for tuberculosis by inhibiting the synthesis of mycolic acids, essential components of the cell wall in Mycobacterium tuberculosis, thereby preventing bacterial growth. It is often combined with other antitubercular drugs such as rifampicin, pyrazinamide, and ethambutol to enhance efficacy and prevent resistance. Additionally, it is employed in the synthesis of various hydrazone derivatives, which are explored for their potential antimicrobial and anticancer prop

Widely used as a primary treatment for tuberculosis by inhibiting the synthesis of mycolic acids, essential components of the cell wall in Mycobacterium tuberculosis, thereby preventing bacterial growth. It is often combined with other antitubercular drugs such as rifampicin, pyrazinamide, and ethambutol to enhance efficacy and prevent resistance. Additionally, it is employed in the synthesis of various hydrazone derivatives, which are explored for their potential antimicrobial and anticancer properties. In research, it serves as a reagent in organic synthesis and analytical chemistry for detecting and quantifying carbonyl compounds. Its role in preventing the spread of tuberculosis in high-risk populations has made it a critical component in global health programs. Use under medical supervision is recommended due to potential side effects such as hepatotoxicity or neurological symptoms.

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