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Clonazolam Powder for sale

Rated 5.00 out of 5 based on 4 customer ratings
(4 customer reviews)

$400.00 – $25,000.00

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Buy Clonazolam Powder Online

What is Clonazolam Powder?

Clonazolam (also known as Clonitrazolam) is a novel depressant substance of the benzodiazepine chemical class which produces anxiolytic, sedative, muscle relaxant, and amnesic effects when administered. Clonazolam Powder for sale

This compound is a novel research chemical derivative of the FDA-approved drugs clonazepam (Klonopin, Rivitrol) and alprazolam (Xanax). Clonazolam is report to be roughly 2.5x as potent as alprazolam.

Clonazolam Powder for sale

Very little is known about this substance, but it has recently become easily accessible through online research chemical vendors where it is being purchase as a designer drug. Due to its extremely high potency, it is often  on blotter paper or in volumetrically dosed solutions. Ingestion of raw clonazolam powder is unsafe due to its microgram-range potency and the ease in which it can lead to multi-day blackouts.Clonazolam Powder for sale

How to buy Clonazolam Powder?

Clonazolam has sufficient cross-reactivity to trigger a positive result on urine screening using common commercial benzodiazepine immunoassays. However, these immunoassays cannot distinguish between prescribed benzodiazepines and clonazolam (Pettersson Bergstrand et al., 2017).
Clonazolam has been detect in blood samples using liquid chromatography with tandem mass spectrometry (LC-MS-MS) (Høiseth et al., 2016; Mei et al., 2019) and in urine and serum using liquid chromatography–high-resolution mass spectrometry (LC-HRMS) (Pettersson Bergstrand et al., 2018; van Wijk et al., 2019; Židková et al., 2019).

The metabolite 7-aminoclonazolam is in urine using nano-liquid chromatography-high-resolution mass spectrometry (nanoLC-HRMS/MS) (Meyer et al.,
2016). Clonazolam is typically  in low concentrations as the parent compound in urine (e.g. 7–23 ng/mL) (Pettersson Bergstrand et al., 2016). For this reason, screening for the metabolite is recommend (Meyer et al., 2016; Mc Namara et al., 2019). A lower cutoff of 10 ng/mL has been recommended for clonazolam (Pettersson Bergstrand et al.,2018).Clonazolam Powder for salehttps://www.pureresearchchemical.com/product/clonazolam-powder-for-sale/

A case report described testing of a drug sample (unconsumed tablets). Clonazolam is identify in the tablets using ultra-high-performance liquid chromatography quadrupole time-of-flight mass spectrometry (UHPLC-QTof) (Pope et al., 2018). Neither clonazolam or its metabolites were identifiable in the patient’s urine. However, it is unclear if this was due to limitations of the testing procedure, or because the contents of the unconsumed tablet were different to the consumed tablet.

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10 Grams, 50 Grams, 100 Grams, 250 Grams, 500 Grams, 1 Kilogram

Reviews (4)

4 reviews for Clonazolam Powder for sale

  1. Rated 5 out of 5

    Chris Griffin – June 23, 2022

    Genuine product. Third transaction with this seller. Highly reliable and fast shipment.

  2. Rated 5 out of 5

    Cetin Senol – June 28, 2022

    Excellent product Excellent customer service Very fast Delivery I will reorder from here again.Thank you

  3. Rated 5 out of 5

    Andrew Taylor – December 16, 2022

    Fast delivery and very attentive and efficient customer service. Very advisable website.

  4. Rated 5 out of 5

    Eric Johnson – February 2, 2023

    I have received my order and thanks for keeping in your words. I recommend’

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PHP is commonly referred to as alpha-pyrrolidinyl-hexaphenone, PHP, and alpha-PHP. The IUPAC name for a-PHP is (±)-1-Phenyl-2-(1-pyrrolidinyl)-1-hexanone. We can look at the research conducted on this research chemical.
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The family of phenylpiperidines (characterized by a phenyl moiety directly linked to a piperidine) includes also the NSO fentanyl (synthesized by P. Janssen in the 1960s) and its analogs, up to 1000 times more potent as analgesic than meperidine and differing in structure from the latter for a phenethyl group on the piperidine nitrogen in place of a methyl group (Elbaridi et al., 2017; Raffa et al., 2018).While extensive literature has been published in regards to pharmacology and toxicology of fentanyl and its illicit analogs (Bäckberg et al., 2015; Mounteney et al., 2015; Dwyer et al., 2017; Giorgetti et al., 2017; Guerrieri et al., 2017; Helander et al., 2017a; Pichini et al., 2017a,b; Shoff et al., 2017; Suzuki and El-Haddad, 2017), the pharmacological and toxicological properties of non-fentanyl derived NSOs have not yet been reviewed in detail.Compounds such as U-47700, U-51754, U-49900, U-448800, AH-7921 from the chemical family of benzamide, U-50488 and U-51754 from the acetamide family and MT-45 from the piperazine family are the NSOs most recently reported as health threats for opioids consumers (Mohr et al., 2016; Amin et al., 2017; Baumann et al., 2017; Domanski et al., 2017; Fabregat-Safont et al., 2017; Prekupec et al., 2017; Marchei et al., 2018). Indeed, this new generation of derivatives has been involved in a number of recent overdose deaths worldwide (Drug Enforcement Administration [DEA], 2016; Baumann et al., 2017; Domanski et al., 2017; Fabregat-Safont et al., 2017).Clandestine manufacturing of NSOs has been pirated from scientific literature or patent filings published by pharmaceutical companies attempting to search for new therapeutic drugs without addiction-related adverse effects (Logan et al., 2017).In a similar manner to fentanyl derivatives, these NSOs are being partly used as heroin adulterants or as constituents of counterfeit pain pills and they can be bought directly by users from online vendors via conventional web or cryptomarket (European Monitoring Centre for Drugs, and Drug Addiction [EMCDDA], 2016; Armenian et al., 2017b; Baumann et al., 2017; Van Hout and Hearne, 2017).Similarly to morphine and heroin (opiates) or to semi-synthetic opioids (like hydro- and oxycodone, hydro- and oxymorphone), these compounds produce CNS depressants effects such as respiratory depression, analgesia, hypothermia, sedation, euphoria, anxiety, sweating, disorientation, drowsiness, nausea, and miosis (Carroll et al., 2012; Guerrini et al., 2013; Hill and Thomas, 2016; Armenian et al., 2017b), and although the effects of tolerance and dependence may rapidly reach high levels, elevated risks of overdose and death are frequent for these compounds (United Nations Office on Drugs and Crime [UNODC], 2017b). Furthermore, the typical rewarding characteristics and the easy availability induce users to abuse of these opioids (Carroll et al., 2012).The main NSOs AH-7921, MT-45, and U-47700 have been identified in Europe between 2013 and 2016, and over 40 deaths were reported to the European Monitoring Centre for Drugs and Drug Addiction in a short time after that AH-7921 and MT-45 were found out on the European drug market (EMCDDA) (European Monitoring Centre for Drugs, and Drug Addiction [EMCDDA], 2017). Moreover, in 2016 U-47700 has been the cause of at least 46 confirmed fatalities as well as the subject of 88 reports from forensic laboratories submissions in the United States (Fabregat-Safont et al., 2017).Since the popularity of these substances is rapidly increasing and evolving over time, there is a great need to update all possible information, particularly with respect to their subjective and side effects and to tackle unsolved issues, including limited analytical methods to disclose and monitor different compounds (Katselou et al., 2015; Lucyk and Nelson, 2017).To fill this gap, we here sought to report the latest information available on non-fentanyl derived NSOs U-47700, U-50488, U-51754, U-49900, U-48800, AH-7921, and MT-45 with particular regard to their pharmacotoxicology and adverse effects on users (see Figure 1).We report a method for the detection and quantitation of 12 drugs and 2 metabolites in the same structural class as the illicit mu-opioid agonist U-47700 in human whole blood. These substances are either known or suspected to be present as potential novel opioids in illicit drug markets. The general class of these drugs was developed in pharmaceutical research programs in the 1970s, but these drugs have recently become of concern for overdoses and death in opioid users in the USA and internationally. The scope of analysis included the following compounds: methylenedioxy U-47700, ethylenedioxy U-47700, ethylenedioxy U-51754, U-69593, U-47931E (bromadoline), U-47700, U-48800, U-49900, U-51754, U-50488, propyl U-47700 and isopropyl U-47700. Additionally, two metabolites N,N-didesmethyl U-47700 and desmethyl U-47700 were also included in the scope. Drugs were extracted from human whole blood using solid-phase extraction, and the extracts were analyzed by liquid chromatography--tandem mass spectrometry. The assay was validated with respect to bias, carryover, interference, within-run and between-run precision, and accuracy. Eight medicolegal death investigation cases that had screened positive for U-48800 by liquid chromatography--time-of-flight mass spectrometry were successfully confirmed and quantified using this method. The mean and median concentrations of U-48800 in these cases were 2.5 (±2.1) and 1.8 ng/mL, respectively, with a range of concentrations of 0.27–6.2 ng/mL. Case history information including the presence of other drugs in combination are described and discussed.
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Ethylone(3,4-methylenedioxy-N-ethylcathinone)is also called MDEC or bk-MDEA.It belongs entactogen, stimulant, amphetamine, and psychedelic of the phenethylamine, and cathinone chemical classes. Ethylone began to be found from 2011, so less human use report.Usually,ethylone counts to be less potent than its relative methylone.
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Product Name: 4-Fluoroamphetamine Cas No: 459-02-9 Formula: C9H12FN Appearance: White crystals Purity: above 98.5%
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Before you take Valium, tell your doctor if you have glaucoma, asthma or other breathing problems, kidney or liver disease, seizures, or a history of drug or alcohol addiction, mental illness, depression, or suicidal thoughts.
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