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    Flunitrazolam Powder for sale

    Rated 5.00 out of 5 based on 2 customer ratings
    (2 customer reviews)

    $400.00 – $22,000.00

    Flunitrazolam is a benzodiazepine derivative that has been sold online as a designer drug, and is a potent hypnotic and sedative drug similar to related compounds such as flunitrazepam, clonazolam and flubromazolam.

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    Description

    Flunitrazolam Powder for sale

    What is Flunitrazepam Powder?

    Firstly, Flunitrazepam Powder. Wholesaler and supplier of Pure Flunitrazolam Powder and various >99% purity pharmaceutical raw materials, research chemicals, and generic medicine. Secure and discreet packaging with tracked shipping.Flunitrazolam Powder for sale

    Secondly, Supplier of Flunitrazolam Powder at the lowest price.http://: https://www.pureresearchchemical.com/product/Flunitrazolam Powder for sale/

    Flunitrazolam is a benzodiazepine derivative. It is a potent hypnotic and sedative drug similar to related compounds such as flunitrazepam, clonazolam and flubromazolam.

    Quick Details

    Product Name: Flunitrazolam
    Synonyms: Flunitrazolam
    CAS No.:
    Molecular Formula: C17H12FN5O2
    IUPAC: 1-methyl-8-nitro-6-(2-fluorophenyl)-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine
    Molecular weight: 337.308 g/mol
    Purity: 99.6%
    Appearance: White crystalline powder / off-white powder

    Moreover, We take the safety of our valued customers very seriously, so we wanted to let you know that at every step of manufacturing, processing, and shipping of each of our products, our highly professional team members (except for Tim, he’s a douche) use appropriate safety measures (gloves, masks, hair nets, body condoms, etc) to ensure there is no potential for contaminating your product or the packaging it comes in.

    However, Flunitrazepam (Rohypnol) has been used in Europe, Asia, and Latin America for insomnia and preoperative sedation since 1975. Although it has never been manufactured or sold in the United States, flunitrazepam has been documented in many sexual assault or “date rape” incidents. Moreover, Flunitrazepam has been an active agent in the illicit drug market, where it is used to alter the effects of other drugs, including ethanol, heroin, and cocaine.10

    Finally, Flunitrazepam has 10 times more affinity than diazepam for certain benzodiazepine receptors. CNS depression occurs within 30 minutes. The drug is most frequently ingest with alcohol, producing additional disinhibition and amnesia. Moreover, Despite marked CNS depression, patients can usually be arous with noxious stimuli. The half-life of the drug is 16 to 35 hours, but coma can be prolong for up to 48 hours. Flunitrazepam is easily obtain outside the United States and on the Internet. Moreover, Flunitrazolam Powder for sale

    Additional information
    Quantity

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

    Reviews (2)

    2 reviews for Flunitrazolam Powder for sale

    1. Rated 5 out of 5

      John Williams – September 1, 2022

      Expedient delivery, all working as intended. my first stop at researching chemical analogues.

    2. Rated 5 out of 5

      Dhanesh Juta – September 22, 2022

      Very good seller, serious, fast shipping, and excellent product.

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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. 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