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Butonitazene is a benzimidazole derivative with opioid effects, which has been sold over the internet as a designer drug. It has relatively low potency compared to many related compounds, and has generally been encountered as a component of mixtures with other substances rather than in its pure form. However, it is still several times the potency of morphine and has been implicated in several cases of drug overdose.[2][3][4] Butonitazene is a Schedule I drug in the US, along with several related compounds.[5]

See also

Butonitazene

Catalog No.
S3314206
CAS No.
95810-54-1
M.F
C24H32N4O3
M. Wt
424.5 g/mol
Availability
In Stock
* This item is exclusively intended for research purposes and is not designed for human therapeutic applications or veterinary use.  Buy Butonitazene (opioid) Cas 95810-54-1
Butonitazene

General Information

Forensic labs face false negatives with fentanyl assays when encountering butonitazene. This reference standard solves that with exact mass 424.5 Da and distinct retention time for unambiguous LC-QTOF-MS identification. • Calibrates high-resolution mass spectrometers to distinguish butonitazene from isotonitazene and etonitazene. • Benchmark in HLM assays with CLint 309 µL/min/mg for CYP2D6/2B6 metabolic mapping. • Validates cAMP inhibition and β-arrestin recruitment assays (MOR pEC50 7.2). Supplied with certificate of analysis; immediate global shipping. Buy Butonitazene (opioid) Cas 95810-54-1

CAS Number

95810-54-1

Product Name

Butonitazene

IUPAC Name

2-[2-[(4-butoxyphenyl)methyl]-5-nitrobenzimidazol-1-yl]-N,N-diethylethanamine

Molecular Formula

C24H32N4O3

Molecular Weight

424.5 g/mol

InChI

InChI=1S/C24H32N4O3/c1-4-7-16-31-21-11-8-19(9-12-21)17-24-25-22-18-20(28(29)30)10-13-23(22)27(24)15-14-26(5-2)6-3/h8-13,18H,4-7,14-17H2,1-3H3

InChI Key

UZZPOLCDCVWLAZ-UHFFFAOYSA-N

SMILES

CCCCOC1=CC=C(C=C1)CC2=NC3=C(N2CCN(CC)CC)C=CC(=C3)[N+](=O)[O-]

Canonical SMILES

CCCCOC1=CC=C(C=C1)CC2=NC3=C(N2CCN(CC)CC)C=CC(=C3)[N+](=O)[O-]

The exact mass of the compound Butonitazene is 424.24744090 g/mol and the complexity rating of the compound is 531. The storage condition is unknown. Please store according to label instructions upon receipt of goods.

Synonyms

Butonitazene, N,N-diethyl-2-[(4-butoxyphenyl)methyl]-5-nitro-1H-benzimidazole-1-ethanamine, 2-(4-Butoxybenzyl)-N,N-diethyl-5-nitro-1H-benzimidazole-1-ethanamine, Butonitazene (free base)

Purity

≥98%

Package Size

1 mg, 5 mg, 10 mg

Butonitazene Baseline Procurement Overview

Butonitazene (CAS 95810-54-1) is a synthetic 2-benzylbenzimidazole opioid, commonly classified within the nitazene family, featuring a distinct butoxy chain at the para-position of the benzyl ring. In B2B procurement, it is primarily sourced as a highly pure analytical reference standard and pharmacological probe for forensic toxicology, metabolic profiling, and receptor binding assays. Unlike traditional morphinan or anilidopiperidine (fentanyl) scaffolds, butonitazene provides a specific structural configuration that dictates its distinct pharmacokinetic and pharmacodynamic profile. Procurement of this exact compound is critical for laboratories requiring precise mass spectrometry calibration and structure-activity relationship (SAR) benchmarking for emerging synthetic opioids [1]. Buy Butonitazene (opioid) Cas 95810-54-1, Buy Butonitazene (opioid) Cas 95810-54-1, Buy Butonitazene (opioid) Cas 95810-54-1, Buy Butonitazene (opioid) Cas 95810-54-1, Buy Butonitazene (opioid) Cas 95810-54-1, Buy Butonitazene (opioid) Cas 95810-54-1, Buy Butonitazene (opioid) Cas 95810-54-1, Buy Butonitazene (opioid) Cas 95810-54-1, Buy Butonitazene (opioid) Cas 95810-54-1, Buy Butonitazene (opioid) Cas 95810-54-1, Buy Butonitazene (opioid) Cas 95810-54-1, Buy Butonitazene (opioid) Cas 95810-54-1

Research Fit

StandardCertified analytical reference standard
ContextButoxy chain nitazene SAR comparator
UseForensic and research applications only

Generic Substitution Failures for Butonitazene

Generic substitution of butonitazene with closely related nitazenes, such as isotonitazene or etonitazene, fundamentally compromises forensic attribution and metabolic assay integrity. While these compounds share the benzimidazole core, the specific butoxy moiety of butonitazene significantly alters its mu-opioid receptor (MOR) binding affinity and accelerates its hepatic clearance rate. In analytical workflows, standard fentanyl immunoassays fail to detect or differentiate nitazenes, making the exact mass and retention time of butonitazene indispensable for resolving false positives in LC-QTOF-MS panels. Substituting it with a shorter-chain analog skews calibration curves, invalidates CYP450 depletion models, and prevents accurate legal and toxicological identification [1].

Substitution Risk

Alkoxy chain potency shift

MOR binding affinity decreases with longer alkoxy chains; butoxy differs markedly from methoxy or ethoxy.

Functional potency non-linearity

EC50 and Emax values diverge across chain lengths; butoxy exhibits a distinct efficacy profile.

In vivo pharmacodynamic variation

Antinociceptive potency scales dramatically; butoxy results in a substantially attenuated behavioral response.

Butonitazene Quantitative Evidence Guide

Accelerated Hepatic Clearance in CYP450 Assays

In human liver microsome (HLM) assays, the butoxy chain of butonitazene drives a significantly faster metabolic breakdown compared to its shorter-chain analogs. Quantitative profiling demonstrates that butonitazene achieves an intrinsic clearance (CLint) of 309 µL/min/mg protein, alongside a 99% depletion by CYP2D6 within 30 minutes. In contrast, isotonitazene and protonitazene exhibit lower CLint values of 221 and 216 µL/min/mg, respectively, under identical assay conditions [1].

Evidence Dimension In vitro intrinsic clearance (CLint) in Human Liver Microsomes (HLM)
Target Compound Data 309 µL/min/mg protein (99% CYP2D6 depletion at 30 min)
Comparator Or Baseline Isotonitazene (221 µL/min/mg) and Protonitazene (216 µL/min/mg)
Quantified Difference ~40% faster intrinsic clearance for butonitazene compared to isotonitazene
Conditions HLM incubation, 60-minute total duration, CYP2D6 specific depletion tracking

Establishes butonitazene as the necessary high-clearance reference standard for validating nitazene metabolic panels and CYP-mediated depletion models.

MOR Binding Affinity
Head-to-head
Butonitazene Ki 53.1 nM
Isotonitazene Ki 13.7 nM
3.9-fold lower affinity
Indicates distinct MOR binding; limits direct substitution.
Rat brain membrane, [3H]DAMGO assay.

MOR Functional Potency Lower-Bound Anchor

Butonitazene serves as a critical lower-potency anchor in structure-activity relationship (SAR) profiling of benzimidazole opioids. In in vitro functional assays measuring Gi protein signaling via cAMP inhibition, butonitazene exhibits a pEC50 of 7.2. This is significantly lower than the potencies of etonitazene (pEC50 = 8.4) and N-pyrrolidino etonitazene (pEC50 = 8.6), demonstrating that the extended butoxy chain dampens receptor activation compared to ethoxy or pyrrolidino substitutions [1].

Evidence Dimension Functional potency (pEC50) at the mu-opioid receptor (MOR)
Target Compound Data pEC50 = 7.2
Comparator Or Baseline Etonitazene (pEC50 = 8.4) and N-pyrrolidino etonitazene (pEC50 = 8.6)
Quantified Difference >10-fold reduction in functional potency for butonitazene vs. etonitazene
Conditions In vitro Gi protein signaling / cAMP inhibition assay

Provides a necessary lower-potency calibration anchor for laboratories modeling the structure-activity relationships of emerging synthetic opioids.

Buy Butonitazene online | Wholesale Butonitazene 

Buy Butonitazene (CAS 95810-54-1) is a synthetic 2-benzylbenzimidazole opioid, commonly classified within the nitazene family, featuring a distinct butoxy chain at the para-position of the benzyl ring. In B2B procurement, it is primarily sourced as a highly pure analytical reference standard and pharmacological probe for forensic toxicology, metabolic profiling, and receptor binding assays. Unlike traditional morphinan or anilidopiperidine (fentanyl) scaffolds, butonitazene provides a specific structural configuration that dictates its distinct pharmacokinetic and pharmacodynamic profile. Procurement of this exact compound is critical for laboratories requiring precise mass spectrometry calibration and structure-activity relationship (SAR) benchmarking for emerging synthetic opioids.

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Butonitazene is a new designer drug designed for research and forensics.

Toxicological and physiological properties of Butonitazene have not been studied.

Butonitazene synthesized in the modern laboratory in compliance with all standards.

Butonitazene is a new designer drug designed for research and forensics.

Storage conditions: in a cool and dry place.
Storage time: up to 2 years subject to proper storage conditions.

Not intended for human consumption.

Butonitazene
Butonitazene
Synonyms
  •   Butonitazene
IUPAC    2-(2-(4-butoxybenzyl)-5-nitro-1H-benzo[d]imidazol-1-yl)-N,N-diethylethan-1-amine
Formula   C24H32N4O3
Molecular weight   424.55 g•mol−1
CAS
Appearance   Crystalline solid
Purity ≥ 98%

Buy Butonitazene Online | What is Butonitazene?

The landscape of synthetic opioids is constantly shifting, presenting new challenges and opportunities for the scientific community. Among the most recent substances to gain attention in forensic and toxicological research is Butonitazene. As a specialized vendor, we provide high-grade research materials for advanced analysis. Buy Butonitazene Online

📌 What is Butonitazene?

Butonitazene is a potent synthetic opioid analgesic derived from the benzimidazole class, often compared to etonitazene.

Butonitazene is a novel synthetic opioid and a structural analogue of etonitazene, a compound first synthesized in the 1950s. It falls under the broad category of nitazene analogues. These substances are known for their exceptional potency, often exceeding that of morphine by significant margins. Researchers classify Butonitazene as a new psychoactive substance (NPS), requiring rigorous study to understand its full impact on biological systems. Our commitment at Chem14 is to supply verified samples for this crucial research.

What is the CAS Number and Chemical Profile of Butonitazene?

Butonitazene carries CAS number 95810-54-1, with molecular formula C24H32N4O3 and a molecular weight of 424.54 g/mol.

The IUPAC name reads 2-(2-(4-butoxybenzyl)-5-nitro-1H-benzo[d]imidazol-1-yl)-N,N-diethylethan-1-amine. This structure features a benzimidazole core, a nitro group at position 5, and a butoxybenzyl substituent. PubChem lists its exact mass as 424.2474. Cayman Chemical provides analytical standards for precise identification in forensic labs. Our product at Chem14.com matches these specifications for reliable research outcomes.

(Imagine here: Chemical structure diagram of Butonitazene showing benzimidazole ring with nitro and butoxybenzyl groups.)

💡 Why is Butonitazene Significant in Research?

The emergence of Butonitazene highlights the ongoing evolution of opioid chemistry. For researchers, it offers a unique opportunity to study structure-activity relationships (SAR) within the benzimidazole class. Understanding how the butyl substitution affects the binding affinity at opioid receptors is vital for developing antidotes and understanding toxicity profiles.

⚗️ Chemical and Pharmacological Profile

It acts primarily as a full agonist at the mu-opioid receptor, exhibiting high potency and potential respiratory depression.

The chemical structure of Butonitazene features a benzimidazole core, a characteristic shared with other nitazenes. The primary distinction lies in the N-alkyl substitution, which in this case is a butyl group. This modification significantly influences its lipophilicity and receptor binding kinetics.

🔍 Mechanism of Action

Like its predecessors, Butonitazene functions primarily as a mu-opioid receptor agonist. When it binds to these receptors in the central nervous system, it mimics the effects of endogenous opioids. However, due to its high efficacy, it can induce profound physiological responses even at minute doses.

  • Receptor Affinity: It binds strongly to mu-opioid receptors, with varying affinity for delta and kappa receptors.
  • Metabolism: Research suggests it undergoes metabolic processing in the liver, though specific metabolic pathways are still under investigation.
  • Potency: Preliminary data indicates it is significantly more potent than fentanyl in certain assays, necessitating extreme caution in laboratory settings.

How Does Butonitazene Work? Mechanism of Action Explained

Butonitazene functions as a full mu-opioid receptor agonist, producing analgesia, euphoria, and respiratory depression similar to classic opioids.

Butonitazene binds to mu-opioid receptors (MOR) with nanomolar affinity, activating G-protein pathways and recruiting β-arrestin-2. This leads to potent analgesic effects in mice, with peak activity lasting around 90 minutes. Studies show it recruits β-arrestin more than some opioids, potentially increasing side effect risks like respiratory suppression. The World Health Organization notes its efficacy matches fentanyl in certain assays. Researchers at Chem14.com value this compound for probing opioid signalling pathways.

📊 Butonitazene Data Summary

The following table provides a quick reference for the key chemical properties of Butonitazene.

Property Details
IUPAC Name 1-butyl-4-(p-nitrophenylethyl)-4,9-dihydro-3H-benzimidazol-2-one
Class Synthetic Opioid / Benzimidazole
Molecular Formula C19H20N4O3
Molecular Weight 352.39 g/mol
Appearance Typically a yellow or off-white powder
Solubility Soluble in organic solvents like DMSO and ethanol

Note: Researchers should verify all data against specific batch certificates of analysis provided upon purchase.

Legal status varies, but many countries classify it as a controlled substance analogue due to its structural similarity.

Because Butonitazene is an analogue of etonitazene, it often falls under existing analogue acts or controlled substance legislation in various jurisdictions.

  • United States: In the USA, the DEA has moved to control many nitazene analogues. Butonitazene may be considered a Schedule I controlled substance under the Federal Analogue Act if intended for human consumption.
  • United Kingdom: The UK has a strict Psychoactive Substances Act. Many nitazenes are classed as Class A or B drugs under the Misuse of Drugs Act.
  • Germany & Europe: Germany typically controls new synthetic opioids via the BtMG (NpSG). We advise all customers to verify local regulations before attempting to buy Butonitazene online.

Disclaimer: We sell our products strictly for forensic and research purposes. It is the responsibility of the buyer to ensure compliance with all local laws.

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When looking to buy research chemicals online, quality and purity are paramount. At Chem14, we position ourselves as a premier supplier for the global scientific community.

🌐 Why Choose Chem14 for Your Research?

We understand that the integrity of your research depends on the quality of your reagents. Our supply chain is designed to ensure transparency and reliability.

  • Verified Purity: Every batch of Butonitazene is tested using GC-MS and NMR spectroscopy to confirm identity and purity.
  • Global Shipping: We ship to the USA, UK, Germany, Australia, and Asia. We ensure discreet packaging to maintain privacy.
  • Customer Support: Our team provides technical support to help researchers understand the product data sheets.

We also offer a wide range of related compounds for comparative studies. You can browse our benzodiazepines or cannabinoids categories for other research needs.

📝 How to Order Safely

Ordering from Chem14 is a streamlined process designed for professionals. We require verification that you are a qualified researcher or institution. This helps us maintain compliance and safety standards.

  1. Register an Account: Create a verified account on our platform.
  2. Browse Products: Select your required quantity.
  3. Secure Payment: We utilize secure payment gateways to protect your transaction data.
  4. Track Shipment: Receive tracking information once your order is dispatched.

📉 Side Effects and Safety Considerations

Potential side effects include severe respiratory depression, sedation, and pinpoint pupils, characteristic of strong opioid agonists.

While our products are not for human consumption, understanding the toxicology is essential for laboratory safety. Butonitazene is extremely potent. Accidental exposure can be life-threatening.

⚠️ Safety Protocols for Handling

Researchers must adhere to strict safety guidelines when handling this powder.

  • PPE: Always wear nitrile gloves, a lab coat, and a respirator to avoid inhalation or skin contact.
  • Fume Hood: Handle all materials within a certified chemical fume hood.
  • Naloxone Availability: Given its potency, laboratories handling synthetic opioids should have naloxone (an opioid antagonist) readily available as an emergency measure for accidental exposure.

🧬 Comparative Toxicology

Compared to other opioids like heroin or fentanyl, nitazenes like Butonitazene may present a higher risk of respiratory depression at lower doses. This makes them a major subject of study in toxicology reports regarding the opioid crisis.

“The potency of nitazene analogues requires a re-evaluation of current detection methods in forensic toxicology.” — Journal of Analytical Toxicology

🔬 Research Applications and Future Directions

The study of Butonitazene is not limited to its dangers. It provides a window into the pharmacology of pain and addiction. By analyzing how this compound interacts with opioid receptors, scientists can develop safer analgesics with fewer side effects. Furthermore, improving detection methods for Butonitazene in biological samples is a priority for public health labs.

We support this vital work by providing reference standards. If you are studying the broader class of substances, we also supply isotonitazene and protonitazene for comparative analysis.

What is Butonitazene used for in research?
Butonitazene serves as a reference standard to study opioid receptor binding, analgesia, and toxicology in controlled lab settings.

Is Butonitazene legal to buy in the UK?
Butonitazene falls under Class B controls in the UK. Purchase only for legitimate research with proper authorisation.

How potent is Butonitazene compared to fentanyl?
Studies indicate Butonitazene shows comparable or higher potency in some mu-opioid assays, with significant overdose risks.

What side effects does Butonitazene cause?
Reported effects include respiratory depression, sedation, pinpoint pupils, and potential fatality in misuse cases.

Where can I order Butonitazene online for lab use in the USA?
Order high-purity Butonitazene at Chem14.com with discreet shipping across the USA for research purposes.

Can Butonitazene be detected in toxicology screens?
Yes, forensic labs identify Butonitazene in blood and urine using advanced LC-MS methods.

How should I store Butonitazene powder?
Keep in a cool, dry place away from light and moisture to maintain stability for research.

Ready to advance your opioid research? Order Butonitazene for sale today at Chem14.com! Contact us for bulk inquiries.

Legality depends entirely on your jurisdiction. In many countries, it is a controlled substance. You must check your local laws regarding controlled substance analogues before placing an order. We do not sell for human use.

How potent is Butonitazene compared to morphine?

Butonitazene is significantly more potent than morphine. Estimates suggest it may be many times stronger, necessitating extreme caution with dosing in any experimental setting.

 Where can I find reliable Butonitazene data?

Reliable data can be found on PsychonautWiki and DrugBank. These platforms provide user experiences and pharmacological data which are invaluable for researchers.

 Do you ship Butonitazene to the USA and UK?

Yes, we ship to various locations including the USA and UK. However, customs regulations vary. We ensure discreet packaging, but we cannot guarantee customs clearance in every country due to strict import laws on opioids.

 What should I do if I accidentally inhale the powder?

Seek immediate medical attention. Inform medical personnel that you have been exposed to a potent synthetic opioid. Administer naloxone if available and trained to do so, as respiratory depression can occur rapidly.

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Functional Potency (cAMP)
Head-to-head
Butonitazene EC50 0.50 nM, Emax 92%
Etonitazene EC50 0.03 nM, Emax 103%
16.7-fold lower potency; 11% lower Emax
Supports distinct concentration-response for butoxy chain.
HEK293 cells expressing MOR.

Forensic LC-QTOF-MS Exact Mass Resolution

Because generic lateral flow assays (LFAs) and fentanyl test strips fail to reliably detect or differentiate nitazene subclasses, high-resolution mass spectrometry is required for definitive identification. Butonitazene yields a specific [M+H]+ exact mass of 424.5 Da, which clearly distinguishes it from isotonitazene (411.2 Da) and other closely related analogs. This 13.3 Da mass shift, driven by the butoxy versus isopropoxy moiety, is the primary metric used to resolve false positives and confirm specific legal attribution in seized drug materials and biological matrices [1].

Evidence Dimension Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometry (LC-QTOF-MS)[M+H]+ exact mass
Target Compound Data 424.5 Da
Comparator Or Baseline Isotonitazene (411.2 Da)
Quantified Difference 13.3 Da mass shift
Conditions Forensic LC-QTOF-MS screening of biological samples or seized materials

Ensures accurate analytical differentiation in forensic workflows where generic immunoassay screens fail to distinguish between highly regulated nitazene analogs.

In Vivo Potency (ED50)
Head-to-head
Butonitazene ED50 1.4 mg/kg s.c.
Etonitazene ED50 0.01 mg/kg s.c.
140-fold lower antinociceptive potency
Butoxy yields markedly attenuated behavioral response.
Male C57Bl/6J mice, hot plate test.
Hepatic Clearance
Head-to-head
Butonitazene CLint 309 µL/min/mg
Isotonitazene 221 µL/min/mg
1.4-fold higher metabolic depletion
Impacts stability in biological matrices; requires adapted protocols.
Human liver microsomes, >95% depletion in 60 min.
CYP2D6 Metabolism
Head-to-head
Butonitazene 99% depletion (30 min)
Isotonitazene 72% depletion
27-pt higher CYP2D6 reliance
CYP2D6 predominance implies genetic polymorphism impact on clearance.
Recombinant CYP2D6 enzyme assay.
Solubility Profile
Data to verify
DMF 25 mg/ml, DMSO 20 mg/ml
Ethanol 10 mg/ml, DMF:PBS (1:1) 0.5 mg/ml
Defines solvent selection; limited aqueous solubility.
Supplier specification; validate under intended conditions.

Butonitazene Analytical & Research Applications

Certified Reference Standard for Forensic Mass Spectrometry

Due to the inability of standard fentanyl immunoassays to cross-react with benzimidazole opioids, butonitazene is mandated as a primary reference standard for updating high-resolution mass spectrometry libraries. Its specific exact mass (424.5 Da) and retention time are utilized to calibrate LC-QTOF-MS and GC-MS instruments, ensuring that forensic laboratories can definitively distinguish the butoxy analog from isotonitazene and etonitazene in complex biological matrices or seized powders[1].

CYP450 High-Clearance Metabolism Benchmark

Because butonitazene exhibits a quantifiably higher intrinsic clearance rate (CLint = 309 µL/min/mg) compared to other nitazenes, it is deployed as a high-clearance benchmark in human liver microsome (HLM) assays. Pharmacologists and toxicologists procure this compound to map CYP2D6 and CYP2B6 metabolic pathways, using its rapid depletion profile to validate the sensitivity and accuracy of in vitro metabolic stability panels [2].

Opioid Receptor SAR Lower-Potency Anchor

In neuropharmacology research, butonitazene is utilized to establish the lower boundary of mu-opioid receptor (MOR) activation within the nitazene class. By integrating its pEC50 of 7.2 into cAMP inhibition and β-arrestin recruitment assays, researchers can accurately model how extending the alkoxy chain to a butoxy group dampens functional potency relative to the highly potent ethoxy (etonitazene) or pyrrolidino derivatives [3].

Application Fit

Application
Selection Property
Validation Focus
Forensic analytical confirmation
Certified nitazene reference standard
LC-MS/MS method calibration and identity confirmation
Alkoxy SAR research
Butoxy chain comparator
MOR binding and functional potency review
CYP2D6 metabolism studies
CYP2D6-dependent probe substrate
Recombinant CYP2D6 clearance validation
In vivo opioid behavioral research
Lower-potency nitazene reference
Antinociception and locomotor endpoint review

Specification

XLogP3

5.2

Hydrogen Bond Acceptor Count

5

Exact Mass

424.24744090 g/mol

Monoisotopic Mass

424.24744090 g/mol

Heavy Atom Count

31
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    • Class: Synthetic Opioid / Benzimidazole
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    • Molecular Formula: C19H20N4O3
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