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Carfentanil | CAS:59708-52-0

  • Name：Carfentanil
  • CAS：59708-52-0
  • Synonyms：Carfentanyl; R 31833; 4-[(1-Oxopropyl)phenylamino]-1-(2-phenylethyl)-4-piperidinecarboxylic acid methyl ester
  • Molecular Formula：C24H30N2O3
  • Molecular Weight：394.51
  • EINESC：
Properties
Density 1.142

Products protected by valid patents are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer’s risk.

Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1).

Carfentanil is a potent synthetic opioid analgesic and is an analogue of Fentanyl. It is a controlled substance and acts as an opioid receptor agonist. Carfentanil is a monocarboxylic acid amide resulting from the formal condensation of the aryl amino group of methyl 4-anilino-1-(2-phenylethyl)piperidine-4-carboxylate with propanoic acid. It is a pale yellow oil in its chemical form.

59708-52-0

  • 59708-52-0 Structure

  • Basic information

    1. Product Name: Carfentanil
    2. Synonyms: 4-[(1-Oxopropyl)phenylamino]-1-(2-phenylethyl)-4-piperidinecarboxylic Acid Methyl Ester;Carfentanil;Carfentanyl;R 3183;4-Piperidinecarboxylic acid, 4-[(1-oxopropyl) phenylamino]-1-(2-phenylethyl), methyl ester ethanedioate;R 31833;1-[2-(Phenyl)ethyl]-4-(N-phenylpropanoylamino)piperidine-4β-carboxylic acid methyl ester;1-Phenethyl-4-[phenyl(propanoyl)amino]piperidine-4-carboxylic acid methyl ester
    3. CAS NO:59708-52-0
    4. Molecular Formula: C24H30N2O3
    5. Molecular Weight: 394.512
    6. EINECS: N/A
    7. Product Categories: Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;PHARMACEUTICAL
    8. Mol File: 59708-52-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 508.1°C at 760 mmHg
    3. Flash Point: 261.1°C
    4. Appearance: /
    5. Density: 1.142
    6. Vapor Pressure: 1.91E-10mmHg at 25°C
    7. Refractive Index: 1.577
    8. Storage Temp.: Controlled Substance, -20°C Freezer
    9. Solubility: N/A
    10. PKA: 7.76±0.20(Predicted)
    11. CAS DataBase Reference: Carfentanil(CAS DataBase Reference)
    12. NIST Chemistry Reference: Carfentanil(59708-52-0)
    13. EPA Substance Registry System: Carfentanil(59708-52-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 59708-52-0(Hazardous Substances Data)

59708-52-0 Suppliers

This product is a nationally controlled contraband or patented product, and the Lookchem platform doesn’t provide relevant sales information.

59708-52-0 Usage

Uses

Used in Pharmaceutical Industry:
Carfentanil is used as an opioid receptor agonist for its potent analgesic effects. It is primarily utilized in veterinary medicine for its rapid onset and short duration of action, making it suitable for use in large animals that require anesthesia or pain management.
Used in Research and Development:
In the field of research, Carfentanil is used to study the effects of opioid receptor agonists on the central nervous system. Its high potency and selectivity for the mu-opioid receptor make it a valuable tool for understanding the mechanisms of opioid action and developing new therapeutic strategies for pain management.
Used in Controlled Substance Regulation:
As a controlled substance, Carfentanil is subject to strict regulations and monitoring to prevent its misuse and diversion for illicit purposes. Its high potency and potential for abuse make it a significant concern for law enforcement and public health officials, who work to ensure that it is used only for its intended medical and veterinary applications.

Check Digit Verification of cas no

The CAS Registry Mumber 59708-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,0 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59708-52:
(7*5)+(6*9)+(5*7)+(4*0)+(3*8)+(2*5)+(1*2)=160
160 % 10 = 0
So 59708-52-0 is a valid CAS Registry Number.

InChI:InChI=1/C24H30N2O3/c1-3-22(27)26(21-12-8-5-9-13-21)24(23(28)29-2)15-18-25(19-16-24)17-14-20-10-6-4-7-11-20/h4-13H,3,14-19H2,1-2H3

59708-52-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) – Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name carfentanyl

1.2 Other means of identification

Product number –
Other names Wildnil

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier’s details

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1.5 Emergency phone number

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More Details:59708-52-0 SDS

59708-52-0Upstream product

For researchers and forensic laboratories requiring precision and reliability, Carfentanil Analytical Reference Standard – CAS 59708-52-0 provides a dependable calibration solution. If you’re looking to buy Carfentanil analytical reference standard online California, Pure Lab Chem offers laboratory-grade material manufactured under strict quality controls, ensuring reproducible results for forensic and analytical applications.

Carfentanil is a synthetic opioid analogue primarily used in research and toxicology studies. Our reference standard is intended strictly for laboratory use, including chemical analysis, forensic investigations, and method validation. It is not intended for human or veterinary consumption.

Product Overview

Each batch of Carfentanil reference standard undergoes rigorous quality assurance.

  • CAS Number: 59708-52-0

  • IUPAC Name: N-(1-(2-Phenylethyl)-4-piperidinyl)-N-phenylpropanamide

  • Form: High-purity analytical solid / pellet

  • Purity: ≥ 98 % (HPLC)

  • Intended Use: Laboratory, forensic, and analytical research only

The product is supplied with a Certificate of Analysis (COA) and spectral data for reproducibility and compliance in research environments.

Chemical Composition and Mechanism

Carfentanil is a potent synthetic opioid analogue with a complex chemical structure designed for high receptor binding in opioid studies. In analytical laboratories, it is used to:

  • Develop and validate LC-MS/MS and GC-MS detection protocols

  • Calibrate reference curves for forensic toxicology

  • Investigate metabolic pathways and opioid analog identification

Its stability, purity, and solubility make it an ideal reference material for method development and analytical training.

Quality & Safety

At Pure Lab Chem, every analytical standard is:

  1. Tested via HPLC and GC-MS to confirm purity

  2. Documented with batch-specific COA and analytical spectra

  3. Packaged securely to prevent contamination or degradation

Safety Note: Carfentanil is an extremely potent opioid and must only be handled by trained laboratory personnel. Use gloves, lab coats, and eye protection. Avoid inhalation or ingestion. This material is for research use only, not for human or veterinary application.

Storage & Stability

Store in a cool, dry environment away from light, ideally 2–8°C, in tightly sealed containers.
Under proper laboratory conditions, Carfentanil reference material retains analytical stability for up to 24 months.

Applications

Carfentanil reference standards are used in:

  • Forensic laboratories for toxicological casework

  • Analytical method development for opioid detection

  • Academic research for chemical characterization

  • Instrument calibration in LC-MS/MS and GC-MS systems

Reliable reference materials are essential for accurate, reproducible results in all analytical and forensic settings.

Packaging & Delivery

Carfentanil is supplied in tamper-evident vials with desiccant and secondary containment. Every order comes with:

  • Batch-specific COA and analytical data

  • Secure, temperature-controlled shipping

  • Discreet packaging with tracking information

International shipping is available where permitted by law and in compliance with regulations

59708-52-0Downstream Products

59708-52-0Relevant academic research and scientific papers

Synthetic method of anesthetic analgesic drug

–

, (2019/12/29)

The invention discloses a synthetic method of an anesthetic analgesic drug. According to the synthetic method, 4-piperidinecarboxylic acid is used as a raw material and subjected to alkylation, bromination, methylation, acylation and the like to prepare the anesthetic analgesic drug. The method avoids the usage of highly toxic cyanide, so the safety and controllability of operation are improved; the method avoids an elimination reaction in reaction process, thereby accelerating reaction speed and shortening reaction time; and the method reduces reaction temperature, shortens the reaction time,and is more suitable for industrial production.

New method for synthesizing carfentanil

–

, (2019/06/08)

The invention belongs to the field of synthesis of organic matters and specifically relates to a method for synthesizing carfentanil. The synthesis method comprises the following steps of taking N-Bocprotective group piperidone as a raw material, and carrying out five steps of performing a Bargellini reaction, N-acylation, methylation, deprotection and N-alkylation to obtain a target product, namely the carfentanil. According to the invention, by adopting the new method for synthesizing the carfentanil, the use of a extremely-toxic substance, namely potassium cyanide, is avoided, so that theenvironment-friendly effect is achieved; the yield is high; a synthesis route is relatively simple; and the requirements of a modern high-efficiency and low-cost synthesis idea can be met.

Ugi reaction for the synthesis of 4-aminopiperidine-4-carboxylic acid derivatives. Application to the synthesis of carfentanil and remifentanil

Malaquin, Sandra,Jida, Mouhamad,Gesquiere, Jean-Claude,Deprez-Poulain, Rebecca,Deprez, Benoit,Laconde, Guillaume

experimental part, p. 2983 – 2985 (2010/07/06)

A two-step sequence involving an Ugi four-component reaction was developed for the preparation of 4-aminopiperidine-4-carboxylic acid derivatives. This strategy has led to the successful preparation of two drugs carfentanil and remifentanil in shorter times and better yields than previously described methods.

Carfentanil
CAS:
59708-52-0
EINECS:
Molecular Formula:
C24H30 N2 O3
MDL:
Synonym:
r 3183 ; r 31833 ; carfentanyl ; carfentanil ; 1-phenethyl-4-[phenyl(propanoyl)amino]piperidine-4-carboxylic acid methyl ester ; 4-[(1-oxopropyl)phenylamino]-1-(2-phenylethyl)-4-piperidinecarboxylic acid methyl ester ; 1-[2-(phenyl)ethyl]-4-(n-phenylpropanoylamino)piperidine-4?-carboxylic acid methyl ester ; 4-piperidinecarboxylic acid, 4-[(1-oxopropyl) phenylamino]-1-(2-phenylethyl), methyl ester ethanedioate

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