1-Phenyl-2-Nitropropene (P2NP) is a chemical compound with the molecular formula C9H9NO2. It is commonly known as P2NP and is widely used in the field of chemistry for various purposes, including pharmaceuticals and illicit drug synthesis. Phenyl-2-nitropropene is employed in the pharmaceutical industry to produce Adderall, an Amphetamine blend used to address ADHD and narcolepsy. P2NP is a yellow crystalline powder that is soluble in organic solvents and has a distinct odor. Due to its versatile properties, P2NP has gained popularity among chemists and researchers for its diverse applications.
CAS Number: 705-60-2;
Chemical formula: C9H9NO2;
Molar mass: 163.173 g/mol;
Density: 1.141±0.06 g/cm3;
Melting Point: 64 – 66 °C (147 to 151 °F; 337 to 339 K);
Boiling point: 263.0 ± 9.0 °C (352.6 °F; 451.2 K);
Appearance: light-yellow crystalline solid;
Solubility in water: practically insoluble in water;
Soluble:
DMF 30 mg/ml
DMSO 30 mg/ml
Ethanol 10 mg/ml
Acetone
Chloroform
Dichloromethane
Methanol
IUPAC name: (2-Nitroprop-1-en-1-yl)benzene
Other names: P2NP; 1-Phenyl-2-nitropropene; β-methyl-β-nitropropene; trans-beta-Methyl-beta-Nitrostyrene; (2-Nitro-1-propenyl)benzene
Step-by-Step Synthesis of Phenyl-2-Nitropropene: Popular Methods and Tips
The Henry reaction can be used to make phenyl-2-nitropropene out of benzaldehyde and Nitroethane. It can be purified by recrystallization using hexane, methanol, ethanol, or isopropanol.
It is important to note that the synthesis of phenyl-2-nitropropene involves handling hazardous chemicals and should only be performed by trained professionals in a controlled environment. Additionally, proper safety precautions, including the use of personal protective equipment (PPE) and adequate ventilation, should be followed to minimize the risk of exposure to toxic chemicals.
P2NP has application in the pharmaceutical industry, phenyl-2-Nitropropene is used as an intermediate in the synthesis some medications like Adderall. It serves as a key building block in the production of this drug, contributing to their chemical structure and overall pharmacological properties.
However, phenyl-2-Nitropropene has also been associated with illicit drug synthesis, particularly in the production of amphetamine and methamphetamine, an illegal stimulant. Phenyl-2-Nitropropene is commonly used as a precursor in the “Reduction” method, which involves converting phenyl-2-Nitropropene into amphetamine using a one-pot reduction reaction. It is important to note that the production of amphetamine is illegal in most countries and is associated with severe legal consequences. Phenyl-2-nitropropene also is employed as an analytical reference or starting point for creating nitro-lacquers.
In many countries, phenyl-2-nitropropene is considered a controlled substance due to its potential for misuse in the illicit manufacture of drugs such as amphetamines and methamphetamines. As such, its production, distribution, and use may be subject to strict regulations and laws aimed at preventing its diversion for illegal purposes.
P2NP is legal uncontrolled substance in USA according lists [1] of Scheduling Actions, Controlled Substances and Regulated Chemicals of DEA. Also, P2NP is legal in European union according European Monitoring Centre for Drugs and Drug Addiction (EMCDDA) lists [2].
It’s crucial for individuals and businesses involved in the production, distribution, or use of P2NP to be aware of the legal status and regulations applicable in their respective jurisdictions. Failure to comply with these regulations can have serious legal consequences, including fines, penalties, and criminal charges.
It’s also important to note that regulations related to phenyl-2-nitropropene and its derivatives can change over time, and it’s essential to stay updated with the latest regulations and guidelines issued by relevant regulatory authorities. Consulting with legal professionals or regulatory experts can provide further guidance on compliance with applicable laws and regulations related to P2NP.
As with any chemical compound, Phenyl-2-Nitropropene poses potential hazards if not handled properly. It is crucial to follow appropriate safety precautions when working with Phenyl-2-Nitropropene to minimize the risks associated with its handling. Some of the key safety precautions for handling phenyl-2-nitropropene include:
On the skin: Can cause irritation to the skin and mucous membranes.
On the eye: Can be irritating.
LD/LC50 values that are pertinent for the classification:
An oral dose of 500 mg/kg or more is lethal to rats
An int*****ritoneal dose of 200 mg/kg is LD50 to rats.
No particular precautions are required if used appropriately. Refrain from inhaling dust/fumes/gases/mists/vapours/spray. Abstain from extended or recurrent exposure. Keep away from ignition sources. Ensure safety against static electricity. Make sure the container is sealed tight.
The optimal temperature for storage is 2-8°C. When kept at a temperature higher than this, phenyl-2-nitropropene is not very enduring, and decomposes over time.
In conclusion, 1-Phenyl-2-Nitropropene (P2NP) is a chemical compound with diverse applications in various industries, including pharmaceuticals and illicit drug synthesis. It is important to be aware of the proper synthesis methods, legal status, and safety precautions associated with phenyl-2-nitropropene to ensure responsible handling and use. Always follow local regulations, guidelines, and best practices when working with P2NP or any other chemical compound to protect human health and the environment.
[1] Green List – List of Psychotropic Substances Under International Control (International Narcotics Control Board (INCB)).
[2] DEA Drug Scheduling.
Verweij, Anthonie MA. “Impurities in illicit drug preparations: amphetamine and methamphetamine.” Forensic Sci. Rev 1.1 (1989): 1-11. https://erowid.org/archive/rhodium/chemistry/meth.impurities3.html
DeRuiter, Jack, C. Randall Clark, and F. Taylor Noggle. “Gas chromatographic and mass spectral analysis of amphetamine products synthesized from 1-phenyl-2-nitropropene.” Journal of chromatographic science 32.11 (1994): 511-519. https://academic.oup.com/chromsci/article-abstract/32/11/511/609027
Phenyl-2-nitropropene https://en.wikipedia.org/wiki/Phenyl-2-nitropropene
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