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Troparil

Troparil Structure
CAS No.
74163-84-1
Chemical Name:
Troparil
Synonyms
Β-CPT;B-CPT;Tropari;Troparil;Topalate;Troparil Β-CPT;Troparil Whatsapp;Troparil Impurity;Troparil USP/EP/BP;high purity,Troparil
CBNumber:
CB51095921
Molecular Formula:
C16H21NO2
Molecular Weight:
259.34
MOL File:
74163-84-1.mol
MSDS File:
SDS
Modify Date:
2024/8/12 15:55:19

Troparil Properties

Boiling point 350.2±42.0 °C(Predicted)
Density 1.099±0.06 g/cm3(Predicted)
pka 9.95±0.60(Predicted)
InChI InChI=1/C16H21NO2/c1-17-12-8-9-14(17)15(16(18)19-2)13(10-12)11-6-4-3-5-7-11/h3-7,12-15H,8-10H2,1-2H3/t12-,13+,14+,15-/s3
InChIKey OMBOXYLBBHNWHL-YRABYYAXNA-N
SMILES [C@@]12([H])N(C)[C@@]([H])(CC1)C[C@H](C1=CC=CC=C1)[C@@H]2C(OC)=O |&1:0,4,9,16,r|

Troparil Chemical Properties,Uses,Production

Description

Troparil is a phenyltropane-based dopamine reuptake inhibitor that is derived from methylecgonidine. It is a stimulant drug used in scientific research. The most commonly used form of troparil is the tartrate salt, but the hydrochloride and naphthalenedisulfonate salts are also available, as well as the free base.

History

Troparil (another name: WIN 35,065-2) is a synthetic derivative of cocaine and was synthesized during the 1970s to separate the stimulant and depressant actions of cocaine from its toxicity and dependence liability. This compound was also used as a starting material or intermediate in synthesising several 3β-phenyltropane derivatives. With a phenyl group directly attached to the tropane ring, troparil is a 3-phenyltropane.

Uses

Troparil is used in scientific research into the dopamine reuptake transporter. 3H-radiolabelled forms of troparil have been used in humans and animals to map the distribution of dopamine transporters in the brain. It is also used for animal research into stimulant drugs as an alternative to cocaine which produces similar effects, but avoids the stringent licensing requirements for the use of cocaine itself.

Pharmacokinetics

Troparil is a few times more potent than cocaine as a dopamine reuptake inhibitor, but is less potent as a serotonin reuptake inhibitor, and has a duration spanning a few times longer, since the phenyl ring is directly connected to the tropane ring through a non-hydrolyzable carbon-carbon bond. The lack of an ester linkage removes the local anesthetic action from the drug, so troparil is a pure stimulant. This change in activity also makes troparil slightly less cardiotoxic than cocaine.

Troparil Preparation Products And Raw materials

Raw materials

Preparation Products

Troparil Suppliers

Global( 46)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6739 58 Inquiry
Akshar Homoeo Pharmacy 08048372804Ext 868 Gujarat, India 6 58 Inquiry
Pharma Affiliates 172-5066494 Haryana, India 6754 58 Inquiry
Xiamen Wonderful Bio Technology Co., Ltd. +8613043004613 China 283 58 Inquiry
RongNa Biotechnology Co.,Ltd +86-86-13583358881 +8618560316533 China 3084 58 Inquiry
Hebei Dangtong Import and export Co LTD +86-86-4001020630 +8619831957301 China 998 58 Inquiry
Hebei Kangcang new material Technology Co., LTD +8615713292910 China 341 58 Inquiry
Hebei Saisier Technology Co., LTD +86-18400010335 +86-18034520335 China 1015 58 Inquiry
Hebei Longbang Technology Co., LTD +86-18633929156 +86-18633929156 China 972 58 Inquiry
HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD +8615350851019 China 1001 58 Inquiry
(–)-2β-Carbomethoxy-3β-phenyltropane,WIN 35,065-2, orβ-CPT) 8-Azabicyclo[3.2.1]octane-2-carboxylicacid, 8-Methyl-3-phenyl-, Methyl ester, (1R,2S,3S,5S)-rel- 8-Azabicyclo(3.2.1)octane-2-carboxylic acid, 8-methyl-3-phenyl-, methyl ester, (exo,exo)- 2-beta-Methoxycarbonyl-3-beta-phenyltropane (Exo,exo)-8-methyl-3-phenyl-8-azabicyclo(3.2.1)octane-2-carboxylic acid methyl ester Troparil high purity,Troparil Troparil USP/EP/BP Troparil Β-CPT methyl 8-methyl-3-phenyl-8-azabicyclo[3.2.1]octane-4-carboxylate Troparil Whatsapp B-CPT 2β-Carbomethoxy-3β-phenyltropane Β-CPT 2-beta-Methoxycarbonyl Topalate (–)-2β-Carbomethoxy-3β-phenyltropane Tropari Troparil Impurity 74163-84-1