4-Nitrohippuric Acid

≥98%

Reagent Code: #217549
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CAS Number 2645-07-0

science Other reagents with same CAS 2645-07-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.17 g/mol
Formula C₉H₈N₂O₅
badge Registry Numbers
MDL Number MFCD00007349
thermostat Physical Properties
Melting Point 131-133 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

4-Nitrohippuric acid is a derivative of hippuric acid utilized in organic synthesis and biochemical research. It serves as a key intermediate in the production of p-aminohippuric acid (PAH), which is used to measure effective renal plasma flow and assess kidney function. Due to its structural analogy to natural metabolites, it is employed in studies of glycine conjugation, xenobiotic metabolism, and detoxification processes in the liver and kidneys. Additionally, it acts as a model compound in pharmacokinetic research and the development of bioactive pharmaceutical agents.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿300.00
5g
10-20 days ฿680.00
25g
10-20 days ฿2,410.00
100g
10-20 days ฿9,620.00
4-Nitrohippuric Acid
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4-Nitrohippuric acid is a derivative of hippuric acid utilized in organic synthesis and biochemical research. It serves as a key intermediate in the production of p-aminohippuric acid (PAH), which is used to measure effective renal plasma flow and assess kidney function. Due to its structural analogy to natural metabolites, it is employed in studies of glycine conjugation, xenobiotic metabolism, and detoxification processes in the liver and kidneys. Additionally, it acts as a model compound in pharmacokinet
4-Nitrohippuric acid is a derivative of hippuric acid utilized in organic synthesis and biochemical research. It serves as a key intermediate in the production of p-aminohippuric acid (PAH), which is used to measure effective renal plasma flow and assess kidney function. Due to its structural analogy to natural metabolites, it is employed in studies of glycine conjugation, xenobiotic metabolism, and detoxification processes in the liver and kidneys. Additionally, it acts as a model compound in pharmacokinetic research and the development of bioactive pharmaceutical agents.
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