4-(N-nitrosomethylamino)-1-(3-pyridyl)-1-butanone

98%

Reagent Code: #218459
label
Alias NNK,N-nitrosonicotinicone
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CAS Number 64091-91-4

science Other reagents with same CAS 64091-91-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.23 g/mol
Formula C₁₀H₁₃N₃O₂
badge Registry Numbers
MDL Number MFCD00274580
thermostat Physical Properties
Melting Point 63 - 65 °C
Boiling Point 423.9 ºC at 760 mmHg
inventory_2 Storage & Handling
Density 1.15 g/cm3
Storage -20 °C

description Product Description

Used primarily in research settings as a potent tobacco-specific nitrosamine (TSNA) to study carcinogenesis, particularly in models of lung, oral, and esophageal cancers. It serves as a biomarker for tobacco exposure and helps evaluate the metabolic activation of procarcinogens in toxicology studies. Due to its high mutagenic and tumorigenic activity, it is also employed in assessing the efficacy of chemopreventive agents and understanding DNA adduct formation in cellular systems.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿580.00
inventory 25mg
10-20 days ฿1,450.00
inventory 100mg
10-20 days ฿3,100.00
inventory 250mg
10-20 days ฿5,250.00
inventory 1g
10-20 days ฿13,470.00
inventory 5g
10-20 days ฿47,230.00

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4-(N-nitrosomethylamino)-1-(3-pyridyl)-1-butanone
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Used primarily in research settings as a potent tobacco-specific nitrosamine (TSNA) to study carcinogenesis, particularly in models of lung, oral, and esophageal cancers. It serves as a biomarker for tobacco exposure and helps evaluate the metabolic activation of procarcinogens in toxicology studies. Due to its high mutagenic and tumorigenic activity, it is also employed in assessing the efficacy of chemopreventive agents and understanding DNA adduct formation in cellular systems.

Used primarily in research settings as a potent tobacco-specific nitrosamine (TSNA) to study carcinogenesis, particularly in models of lung, oral, and esophageal cancers. It serves as a biomarker for tobacco exposure and helps evaluate the metabolic activation of procarcinogens in toxicology studies. Due to its high mutagenic and tumorigenic activity, it is also employed in assessing the efficacy of chemopreventive agents and understanding DNA adduct formation in cellular systems.

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