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Acetylfentanyl powder is a synthetic opioid that has gained attention in the research chemical and illicit drug markets due to its potency and chemical similarity to fentanyl. Structurally, acetylfentanyl is a derivative of fentanyl, making it a powerful analgesic with effects comparable to its parent compound. It is primarily encountered as a fine, white powder, often sold for research purposes or, illegally, as a street opioid.

Chemical Properties and Potency

Acetylfentanyl is chemically known as N-(1-phenethylpiperidin-4-yl)-N-phenylacetamide. While it is less potent than fentanyl itself, acetylfentanyl remains extremely potent compared to traditional opioids like morphine or heroin. This potency makes dosing particularly critical—small amounts can produce significant effects, and the risk of overdose is high. Users or researchers handling acetylfentanyl powder should exercise extreme caution, using precise scales and safety equipment.

Uses and Research Applications

Legally, acetylfentanyl powder is intended for chemical and pharmacological research. Researchers study its interaction with opioid receptors to better understand analgesic mechanisms and opioid receptor activity. In controlled laboratory environments, it is used for receptor binding studies, toxicology analysis, and forensic research. Outside regulated research, its misuse can be dangerous due to the narrow margin between a recreational dose and a lethal dose.

Risks and Safety Considerations

Acetylfentanyl is classified as a potent opioid and carries high overdose potential. Exposure, even in minute quantities, can be hazardous. Handling should always involve protective gloves, masks, and safety goggles. Ingestion, inhalation, or skin absorption can lead to respiratory depression, unconsciousness, or death. Authorities have reported acetylfentanyl-related fatalities, emphasizing the critical need for caution. Additionally, it is illegal in many jurisdictions, so possessing or distributing it outside authorized research contexts can result in severe legal consequences.

Market Trends and Availability

On the research chemical market, acetylfentanyl powder is sometimes sold online through specialized suppliers, typically for laboratory or forensic use. Prices vary based on purity, quantity, and supplier credibility. Due to its potency, suppliers often provide detailed safety instructions and recommend using analytical scales to ensure accurate dosing. Researchers prioritize sourcing from reputable distributors to avoid contamination or mislabeling.

Conclusion

Acetylfentanyl powder is a highly potent synthetic opioid with specific applications in scientific research. While its chemical similarity to fentanyl makes it effective for opioid receptor studies, it also poses significant risks for overdose and toxicity. Proper safety protocols, responsible handling, and adherence to legal regulations are essential for anyone working with this compound. Awareness of its potency and dangers ensures that acetylfentanyl is used safely and ethically in laboratory settings.

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What Is Valerylfentanyl?

Valerylfentanyl (also called valeryl fentanyl) is a synthetic opioid belonging to the fentanyl analog family. It is a potent mu-opioid receptor agonist structurally related to fentanyl, which is a powerful prescription opioid widely used for pain management. Valerylfentanyl is one of many designer fentanyls synthesized to mimic fentanyl’s effects but is generally illicit and unregulated.

The substance typically appears as a fine white or off-white powder, often sold on the illicit drug market.

Chemical Properties

• Chemical Class: Synthetic opioid (fentanyl analog)

• Molecular Formula: C23H30N2O

• IUPAC Name: N-phenyl-N-[1-(2-phenylethyl)piperidin-4-yl]valeramide

• Appearance: White or off-white powder

• Potency: Estimated to be somewhat less potent than fentanyl but significantly more potent than morphine

Mechanism of Action

Valerylfentanyl acts primarily as a mu-opioid receptor agonist, binding to opioid receptors in the central nervous system. Activation of these receptors leads to:

• Analgesia (pain relief)

• Euphoria

• Respiratory depression (dangerous slowing or stopping of breathing)

• Sedation

• Cough suppression

Its action is similar to fentanyl but varies slightly in potency and duration.

Effects

Typical opioid effects include:

• Intense pain relief

• Euphoria and feelings of well-being

• Relaxation and sedation

• Drowsiness or heavy sedation

• Respiratory depression, which can be life-threatening

• Constipation

• Miosis (pinpoint pupils)

• Nausea and vomiting

Due to its potency, valerylfentanyl can cause severe effects at very low doses.

Routes of Administration

• Oral ingestion (swallowed powder or tablets)

• Snorting (insufflation)

• Injection (intravenous or intramuscular)

• Transdermal (less common)

• Other routes are possible, depending on formulation

Risks and Dangers

Valerylfentanyl carries serious risks, especially because:

• It is highly potent, with overdose possible at very low amounts.

• Causes respiratory depression, the main cause of death in opioid overdoses.

• Can be accidentally ingested or absorbed by handlers due to its potency.

• Naloxone (Narcan) can reverse overdose but multiple doses may be necessary.

• Because it is a fentanyl analog, it may be mixed or sold as heroin or other opioids, increasing unintentional overdose risk.

Overdose Symptoms

• Severe respiratory depression (slow or stopped breathing)

• Loss of consciousness or coma

• Blue or pale skin, especially lips and fingertips

• Pinpoint pupils

• Weak pulse or low blood pressure

Overdose is a medical emergency. Immediate administration of naloxone and calling emergency services is critical.

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What Is Trefentanyl?

Trefentanil is a synthetic opioid analgesic belonging to the fentanyl analog class. Like other fentanyl derivatives, it is a powerful mu-opioid receptor agonist, meaning it produces strong opioid effects including pain relief and euphoria. Trefentanyl is much more potent than morphine and is considered a designer opioid, often encountered as a research chemical or illicit substance.

Trefentanyl generally appears as a white or off-white powder used recreationally or sold on the black market, sometimes unknowingly mixed with other opioids.

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Trefentanil has terribly similar effects to alfentanil, very like those of fentanyl itself but more potent and shorter lasting. aspect effects of Sublimaze analogs are almost like those of fentanyl itself, that embody itching, nausea and doubtless serious metastasis depression, which may be life-threatening. Fentanyl analogs have killed many folks throughout Europe and therefore the former Soviet republics since the foremost recent improvement in use began in Baltic State within the early 2000s, and novel derivatives still appear. the chance of respiratory depression is very high with potent fentanyl analogues cherish alfentanil and trefentanil, and these medication cause a big risk of death if used outside of a hospital setting with applicable artificial respiratory apparatus available.

Chemical and Pharmacological Properties

• Chemical Class: Synthetic opioid, fentanyl analog

• Potency: Estimated to be several times stronger than morphine, similar to other fentanyl analogs

• Mechanism of Action: Acts as a mu-opioid receptor agonist, binding to receptors in the brain and spinal cord to produce analgesia, sedation, and euphoria.

• Chemical Appearance: Fine white or off-white powder, often crystalline

Effects of Trefentanyl

Users report typical opioid effects such as:

• Intense analgesia (pain relief)

• Euphoria and relaxation

• Sedation and drowsiness

• Respiratory depression (dangerously slowed breathing)

• Constricted pupils (pinpoint pupils)

• Nausea and vomiting

• Reduced cough reflex

• Possible dizziness or confusion

Because of its high potency, the margin between a recreational dose and a fatal dose is very narrow, making trefentanyl extremely risky.

Routes of Administration

• Oral ingestion: swallowing powder or tablets (less common)

• Insufflation: snorting the powder

• Injection: intravenous, intramuscular, or subcutaneous

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Risks and Dangers

Trefentanyl carries significant risks typical of potent synthetic opioids:

• High overdose risk: respiratory depression is the main cause of death

• Accidental exposure risk: even small amounts can be dangerous to users or handlers due to potency

• Risk of dependence and addiction: psychological and physical dependence can develop quickly

• Risk of contamination: often sold mixed with heroin or other drugs without user knowledge

• Naloxone resistance: some fentanyl analogs may require higher or repeated naloxone doses for overdose reversal

Overdose Signs and Treatment

Symptoms of overdose include:

• Severe respiratory depression (slow or stopped breathing)

• Loss of consciousness or coma

• Pinpoint pupils

• Cyanosis (bluish skin coloration from lack of oxygen)

• Weak or absent pulse

Treatment:

• Immediate administration of naloxone (Narcan) can reverse overdose effects.

• Multiple doses may be necessary due to trefentanyl’s potency.

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Legal Status

• Trefentanyl is controlled or illegal in many countries due to its high abuse potential and overdose risk.

• In the United States, fentanyl analogs including trefentanyl are generally listed as Schedule I controlled substances, making unauthorized manufacture, possession, or distribution illegal.

• Other countries have similar laws regulating synthetic opioids.

Harm Reduction Advice

• Avoid using unknown powders or substances that may contain fentanyl analogs.

• If use occurs, do so with trusted individuals who can call for help.

• Keep naloxone readily available and learn how to use it.

• Avoid mixing opioids with other depressants such as alcohol or benzodiazepines.

• Use testing kits where possible to identify substances.

• Seek professional addiction treatment if struggling with opioid use.

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What Is Thiafentanil?

Thiafentanil is a highly potent synthetic opioid analgesic and a fentanyl analog, structurally related to the widely known opioid fentanyl. It was originally developed for veterinary use—notably as a tranquilizer for large animals such as elephants, rhinos, and deer—rather than for human medicine.

Due to its extreme potency, tiny doses can be effective—and potentially lethal—in humans. In powdered form, thiafentanil appears as a white to off-white fine powder.

🧬 Chemical and Pharmacological Information

• Chemical Name: Thiafentanil oxalate

• IUPAC Name: N-phenyl-N-[1-(2-thienyl)ethyl-4-piperidyl]-propanamide

• Molecular Formula: C20H26N2O2S

• Drug Class: Synthetic opioid, fentanyl analog

• Potency: More potent than carfentanil, which itself is 10,000 times stronger than morphine

  Mechanism of Action

  Thiafentanil is a mu-opioid receptor agonist, meaning it binds to the same receptors in the brain and nervous system that natural opioids (like endorphins) and other opioids (like morphine) target.

  By activating these receptors, it causes:

  • Powerful analgesia (pain relief)

  • Profound sedation

  • Severe respiratory depression

  • Euphoria (in recreational contexts)

  • Potential loss of consciousness

    Intended Uses

    • Veterinary medicine only

    • Used as an immobilizing agent in large or wild animals, especially in wildlife conservation and research settings.

    • Not approved for human medical use under any regulatory framework.

    ---

    ❌ Illicit Use and Concerns

    • Illicit manufacturing or misuse of thiafentanil is rare but extremely dangerous.

    • Some analogs may be sold online as “research chemicals” or mixed into street opioids without the user’s knowledge.

    • Given the incredibly small effective dose, unintentional overdoses are highly likely in such cases.

    • Thiafentanil is an ultra-potent synthetic opioid used only in veterinary medicine for sedating large animals. Due to its high potency, human exposure is extremely hazardous, even in minuscule amounts. Any handling or proximity to this substance outside of professional settings should be avoided. It serves as a stark example of the dangers posed by fentanyl analogs in the ongoing opioid crisis.

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What Is Thenylfentanyl?

Thenylfentanyl is a synthetic opioid and a structural analog of fentanyl, the powerful prescription painkiller. It belongs to the broader family of fentanyl analogs, which are man-made substances designed to act on mu-opioid receptors in the brain and spinal cord, producing effects like pain relief, euphoria, and sedation.

Thenylfentanyl was originally synthesized as part of pharmaceutical research in the 1970s and 1980s but was never approved for medical use. It reemerged more recently in the illicit drug market, often sold as a research chemical or mislabeled as other opioids.

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Chemical & Structural Information

• IUPAC Name: N-[1-(2-phenylethyl)piperidin-4-yl]-N-(2-thienylmethyl)propanamide

• Molecular Formula: C22H28N2OS

• Chemical Class: Synthetic opioid (fentanyl analog)

• Structure: Similar to fentanyl, but contains a thiophene (sulfur-containing aromatic) group instead of a phenyl ring.

Thenylfentanyl’s modified structure slightly alters its binding affinity and pharmacological activity, though it is generally less potent than fentanyl. However, its risks remain serious due to its opioid action and potential to depress respiration.

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aspect effects of fentanyl analogues are similar to those of painkiller itself, that embody itching, nausea and doubtless serious metabolic process depression, which might be life-threatening. Potent pure opioid antagonists reminiscent of narcotic antagonist or nalmefene are suggested within the event of accidental human exposure to thiafentanil. Fentanyl analogues have killed many individuals throughout Europe and also the former Soviet republics since the foremost recent revitalisation in use began in Estonia in the early 2000s, and novel derivatives still appear. a replacement wave of fentanyl analogues and associated deaths began in around 2014 in the US, and have continuing to grow in prevalence; particularly since 2016 these medicine have been to blame for many o.d. deaths each week.

status
Thiafentanil may be a Schedule II controlled drug within the USA since August 2016.

Chemical and physical information
Formula: C22H28N2O4S

Molar mass: 416.54 g·mol?1

see
Sufentanil
List of painkiller analogues

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What Is Sufentanil?

Sufentanil is a synthetic opioid analgesic in the fentanyl analog family. It is 1000 times more potent than morphine and about 5–10 times more potent than fentanyl, making it one of the most powerful opioids used in clinical medicine. It is typically used in hospitals, especially during major surgery or for intensive care patients, and is not intended for general or unsupervised use.

When in powdered form, sufentanil appears as a white to off-white fine powder—but in medical settings, it is most often administered as an injectable solution or sublingual tablet.

Sufentanil Powder is associate Opioid Agonist. The mechanism of action of sufentanil is as a Full Opioid Agonist. Sufentanil is an opioid analgesic that’s used as an adjunct in anesthesia, in balanced anesthesia, and as a primary anesthetic agent. it’s administered by the intravenous, epidural and articulator routes. additionally referred to as Dsuvia, the sublingual type is employed for the management of acute pain in adults that is severe to warrant the utilization of an opioid analgesic in certified medically supervised attention settings, as well as hospitals, surgical centers, and emergency departments. thought is also created in the future for the utilization of the articulator type within the U.S. military in cases wherever physiological state is needed immediately.

IUPAC Name
N-[4-(methoxymethyl)-1-(2-thiophen-2-ylethyl)piperidin-4-yl]-N-phenylpropanamide

InChI
InChI=1S/C22H30N2O2S/c1-3-21(25)24(19-8-5-4-6-9-19)22(18-26-2)12-15-23(16-13-22)14-11-20-10-7-17-27-20/h4-10,17H,3,11-16,18H2,1-2H3

InChI Key
GGCSSNBKKAUURC-UHFFFAOYSA-N

Canonical SMILES
CCC(=O)N(C1=CC=CC=C1)C2(CCN(CC2)CCC3=CC=CS3)COC

Mechanism of Action

Sufentanil, like other opioids, works by binding to mu-opioid receptors in the central nervous system. This leads to:

• Inhibition of pain signals

• Profound sedation

• Euphoria (in some contexts)

• Respiratory depression (potentially fatal)

Its high potency allows for very small doses to achieve clinical effects, which also dramatically increases the risk of accidental overdose in non-medical contexts.

💊 Medical Uses

Sufentanil is used in carefully controlled settings for:

• Surgical anesthesia (as part of balanced anesthesia regimens)

• Postoperative pain management (especially in critical care)

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chemical formula
C22H30N2O2S

Drug and medicine data
Drug Indication to Buy Sufentanil Powder Online
The indications for this drug are as follows: 1. As an analgesic adjunct in the maintenance of balanced general anaesthesia in patients who are intubated and ventilated. 2. As a primary anaesthetic agent for the induction associated maintenance of anaesthesia with one hundred pc chemical element in patients undergoing major surgical procedures, in patients who are intubated and ventilated, admire vessel surgery or neurosurgical procedures within the sitting position, to produce favorable cardiac muscle and cerebral oxygen balance or once extended operative ventilation is anticipated. 3. For epidural administration as an analgesic combined with low dose (usually 12.5 mg per administration) bupivacaine sometimes throughout labor and duct delivery 4. The articulator type is indicated for the management of acute pain in adults that’s severe to warrant the utilization of an opioid analgesic in certified medically supervised attention settings, as well as hospitals, surgical centers, and emergency departments.Buy Sufentanil Powder Europe , Purchase Sufentanil EU ,Sufentanil for sale Europe ,Order Sufentanil online Europe , Sufentanil research chemical Europe

Mechanism of Action
Sufentanil could be a synthetic, potent opioid with extremely selective binding to ?-opioid receptors [F2009]. These receptors are cosmopolitan within the human brain, spinal cord, and alternative tissues [A39636], [A39637]. In general, opioids decrease cAMP (affecting neural communication pathways), decrease neurochemical release, and cause membrane hyperpolarization, all of that contribute to the relief of painful symptoms [A39637]. narcotic receptors are including G-protein receptors and performance as each positive and negative regulators of conjugation neural transmission via G-proteins that activate effector proteins. Binding of the opiate receptor leads to the exchange of GTP for gross domestic product on the G-protein complex. because the effector system is adenylate cyclase and cAMP, placed at the inner surface of the plasma membrane, opioids decrease animate thing cAMP by inhibiting adenylate cyclase. the discharge of sensitive neurotransmitters admire substance P, GABA, dopamine, acetylcholine, and norepinephrine is then strangled [A39637]. Opioids shut N-type voltage-operated metal channels (OP2-receptor agonist), additionally preventing neurotransmitter release [A39637]. Sufentanil and alternative opioids open calcium-dependent inside rectifying metal channels, leading to hyperpolarization and reduced neural excitability [A39636], [A39637].

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Furanylfentanyl, often abbreviated as Fu-F, is a synthetic opioid analgesic chemically related to fentanyl, a powerful prescription painkiller. Furanylfentanyl belongs to the class of designer opioids—compounds structurally similar to known opioids but often made to circumvent drug laws.

It is classified as a fentanyl analog, meaning it has a chemical structure similar to fentanyl but with modifications that affect potency and duration. It was never approved for medical use but has appeared on illicit drug markets as a powder or in pressed tablets, frequently mixed with or sold as heroin or other opioids.

Buy Furanylfentanyl Fu-F Powder, it is an opioid analgesic that is an analog of fentanyl and has been sold as a designer drug. It demonstrates an ED50 value of 0.02 mg/kg in a mouse hot plate analgesia test.

This product is intended for forensic and research applications.

Side effects

Side effects of fentanyl analogs are similar to those of fentanyl itself, which include itching, nausea and potentially serious respiratory depression, which can be life-threatening.

Life-threatening adverse reactions caused by furanylfentanyl use have been observed in Sweden and Canada. At least seven deaths in Cook County, Illinois, have been linked to furanylfentanyl in 2016, with additional deaths in suburban Chicago in 2017.Buy Furanylfentanyl powder Europe , Purchase Fu-F powder online EU , Furanylfentanyl Fu-F for sale , Order Fu-F powder ,Fu-F synthetic opioid powder buy

Detection in biological fluids

Furanylfentanyl may be measured in blood or urine to monitor for abuse, confirm a diagnosis of poisoning, or assist in a medicolegal death investigation. Commercially available immunoassays are often used as initial screening tests, but chromatographic techniques are generally used for confirmation and quantitation. Blood furanylfentanyl concentrations are expected to be in a range of 1-45 ?g/L in victims of fatal overdosage.

Synonyms
Fu-F
2-Furanyl fentanyl
Technical Information
Formal Name: N-phenyl-N-[1-(2-phenylethyl)-4-piperidinyl]-2-furancarboxamide, monohydrochloride
CAS Number: 101365-56-4
Molecular Formula: C24H26N2O2 • HCl
Formula Weight: 410.9
Purity: ?98%

Formulation: A neat solid
SMILES: O=C(C1=CC=CO1)N(C2CCN(CCC3=CC=CC=C3)CC2)C4=CC=CC=C4.Cl
InChi CodeInChI=1S/C24H26N2O2.ClH/c27-24(23-12-7-19-28-23)26(21-10-5-2-6-11-21)22-14-17-25(18-15-22)16-13-20-8-3-1-4-9-20;/h1-12,19,22H,13-18H2;1H
InChi Key: MKKAYRKIIKMNAP-UHFFFAOYSA-N
DEA Schedule: I
Shipping & Storage Information
Storage: -20°C
Shipping: Room Temperature in continental US; may vary elsewhere
Stability: See Certificate of Analysis

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Buy Carfentanil Powder or carfentanyl is a structural analog of the synthetic opioid analgesic fentanyl. Short acting and with fast onset, it has, weight for weight, around one hundred times stronger effects than fentanyl and thousands of times stronger than heroin. It is more effective at reducing pain response in rats than any other opioid.

Carfentanil was first synthesized in 1974 by a team of chemists at Janssen Pharmaceutica which included Paul Janssen.

The effects of carfentanil, including overdose, can be reversed by naloxone.

Carfentanil is legally controlled in most jurisdictions, but has veterinary uses for anaesthetising large animals.

Typical use
Carfentanil was sold starting in 1986 under the brand name “Wildnil” for use in tranquilizer darts in combination with an ?2-adrenoreceptor agonist for large mammals including elk and elephants. It was chosen for its high therapeutic index. Commercial production of Wildnil ceased in 2003, and the drug is available only as a compounded dosage form.

Radiolabelled [11C]carfentanil is widely used as a selective radiotracer in animal and human positron emission tomography (PET) imaging studies of the ?-opioid system due to its high affinity for receptors.

Importation from China
According to an Associated Press article from 2016, “Chemical weapon for sale: China’s unregulated narcotic”, fentanyl, carfentanil and other highly potent derivatives of fentanyl are actively marketed by several Chinese chemical companies. Carfentanil was not a controlled substance in China until 1 March 2017, and until then was manufactured legally and sold openly over the Internet.

Authorities in Latvia and Lithuania reported seizing carfentanil as an illicit drug in the early 2000s. Around 2016, the US and Canada started reporting a dramatic increase in shipment of carfentanil and other strong opioid drugs to customers in North America from Chinese chemical supply firms. In June 2016 the Royal Canadian Mounted Police seized one kilogram of carfentanil shipped from China in a box labeled “printer accessories”. According to the Canada Border Services Agency, the shipment contained 50 million lethal doses of the drug, more than enough to wipe out the entire population of the country, in containers labeled as toner cartridges for Hewlett-Packard LaserJet printers. Allan Lai, an officer-in-charge at the Royal Canadian Mounted Police in Calgary who helped oversee the criminal investigation said, “With respect to carfentanil, we don’t know why a substance of that potency is coming into our country.

Pharmacology
Carfentanil is a lipophilic chemical, and hence can much more easily cross the blood-brain barrier. :pg 9 It thus has very rapid onset of effects, but is also shorter acting.

For pain relief, a unit of carfentanil is 100 times as potent as the same amount of fentanyl, 5,000 times as potent as a unit of heroin and 10,000 times as potent as a unit of morphine. This is despite only having 14-135 times higher affinity for the ? receptor.

Legal status
China
Carfentanil has been controlled in China since 1 March 2017. The trade war between China and the US has included controversy over the effectiveness of this control.

United States
Carfentanil is classified as Schedule II under the Controlled Substances Act in the United States with a DEA ACSCN of 9743 and a 2016 annual aggregate manufacturing quota of 19 grams (less than 0.7 oz.).

United Kingdom
Carfentanil has been specifically controlled as a Class A drug since 1986

Chemical and physical data
Formula: C24H30N2O3

Molar mass: 394.515 g·mol?1

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4-Phenylfentanyl is a synthetic opioid and a chemical analogue of fentanyl, a potent pharmaceutical used in pain management. While fentanyl itself has legitimate medical uses, analogues like 4-Phenylfentanyl are often synthesized and distributed illicitly. Due to their extreme potency and the unpredictable nature of their effects, such substances pose significant health and legal risks. This article provides an educational overview of 4-Phenylfentanyl powder, including its chemistry, pharmacology, potential uses, legal considerations, and public health concerns.

Buy 4-Phenylfentanyl Powder (4-Phenylfentanyl) is an opioid analgesic that is a derivative of fentanyl. It was developed during the course of research that ultimately resulted in super-potent opioid derivatives such as carfentanil, though it is a substantially less potent analogue. 4-Phenylfentanyl is around eight times the potency of fentanyl in analgesic tests on animals, but more complex 4-heteroaryl derivatives such as substituted thiophenes and thiazoles are more potent still, as they are closer bioisosteres to the 4-carbomethoxy group of carfentanil.

Side effects of fentanyl analogs are similar to those of fentanyl itself, which include itching, nausea and potentially serious respiratory depression, which can be life-threatening. Fentanyl analogs have killed hundreds of people throughout Europe and the former Soviet republics since the most recent resurgence in use began in Estonia in the early 2000s, and novel derivatives continue to appear.

Pharmacology and Effects

As an opioid receptor agonist, 4-Phenylfentanyl primarily binds to mu-opioid receptors in the central nervous system. This interaction results in:

• Analgesia (pain relief)

• Sedation

• Euphoria

• Respiratory depression

• Physical dependence

While the exact potency of 4-Phenylfentanyl compared to fentanyl is not fully documented, anecdotal reports and limited scientific literature suggest it is highly potent and capable of producing significant physiological effects even in small doses. Like other fentanyl analogues, it carries a high risk of overdose, especially when mixed with other central nervous system depressants like alcohol or benzodiazepines.

Chemical and physical data
Formula: C28H32N2O

Molar mass: 412.577 g·mol?1

CAS
120448-97-7

InChI
InChI=1S/C28H32N2O/c1-2-27(31)30(26-16-10-5-11-17-26)28(25-14-8-4-9-15-25)19-22-29(23-20-28)21-18-24-12-6-3-7-13-24/h3-17H,2,18-23H2,1H3

InChI Key
BXCJXJLHYMWMQU-UHFFFAOYSA-N

Canonical SMILES
CCC(=O)N(C1=CC=CC=C1)C2(CCN(CC2)CCC3=CC=CC=C3)C4=CC=CC=C4

Registry Number
Linked Records

Compounds: 313,587
Substances: 390,235
Classification (Parent Nodes)

ChemIDplus Chemical Information Classification
Shipping & Storage Information
Storage: -20°C
Shipping: Room Temperature in continental US; may vary elsewhere
Stability: ? 2 years

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