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    Ethylphenidate (EPH) is a psychostimulant and a close analog of methylphenidate.

    Ethylphenidate acts as both a dopamine reuptake inhibitor and norepinephrine reuptake inhibitor, meaning it effectively boosts the levels of the norepinephrine and dopamine neurotransmitters in the brain, by binding to, and partially blocking the transporter proteins that normally remove those monoamines from the synaptic cleft.

    There have been anecdotal reports of a perforated septum resulting from even just a few uses of ethylphenidate by insufflation (snorting)

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    CAS No.: 57413-43-1

    Formula: C15H21NO2

    Molecular Weight: 247.33274

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    MDAI – is also known as 5,6-Methylenedioxy-2-aminoindane, and is a compound developed in the 1990s by a team led by David E. Nichols at Purdue University. It acts as a non-neurotoxic and highly selective serotonin releasing agent (SSRA) in vitro and produces entactogen effects in humans.

    The chemical structure of MDAI is indirectly derived from that of the illicit drug MDA, but the alpha-methyl group of the alkylamino amphetamine side chain has been bound back to the benzene nucleus, to form an indane ring system, which changes its pharmacological properties substantially.

    MDAI, can be produced from 3-(3,4-Methylenedioxyphenyl)propionic acid which is converted to the acid chloride and then heated to produce 5,6-Methylenedioxy-1-indanone. Treatment of the indanone with amyl nitrite in methanol with HC1 afforded the hydroxyimino ketone. This is reduced to the 2-aminoindan following a modification of Nichols’ earlier method from a paper discussing DOM analogues, using a Pd/C catalyst in glacial acetic acid with catalytic H2SO4.

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    Mild euphoria and increased levels of awareness are said to be some of the effects that Methiopropamine can have, making it an ideal substitute for researchers studying the receptor actions brought about by methamphetamine (Crystal Meth).

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    β-Keto-Methylbenzodioxolylpentanamine is a stimulant compound developed in the 1960s, which has been reported as a novel designer drug and identified in some samples of powders sold as “NRG-1”

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    Ching is a research chemical powder containing Ethylphenidate, also known as ethyl 2-phenyl-2-piperidin-2-ylacetate, and other chemicals to give it that unique experience in the lab.

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    Tadalafil relaxes muscles and increases blood flow to particular areas of the body.

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    CJC-1295 DAC has shown some amazing results as a growth hormone releasing hormone (GHRH) analog. Not only has CJC-1295 shown the ability to increase growth hormone and IGF-I secretion and its benefits, but it has been able to do so in very large amounts. Recent research studies have shown that CJC – 1295 stimulates GH and IGF-1 Secretion, and will keep a steady increase of HGH and IGF-1 with no increase in prolactin, leading to intense fat loss, and increases protein synthesis.

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    CJC-1295 DAC has shown some amazing results as a growth hormone releasing hormone (GHRH) analog. Not only has CJC-1295 shown the ability to increase growth hormone and IGF-I secretion and its benefits, but it has been able to do so in very large amounts. Recent research studies have shown that CJC – 1295 stimulates GH and IGF-1 Secretion, and will keep a steady increase of HGH and IGF-1 with no increase in prolactin, leading to intense fat loss, and increases protein synthesis.

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    CAS No.:  186028-79-5

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    Synonyms:  ice, crystal meth;

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    formula: C17H15ClN4S
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    Appearance: white crystalline powder/ yellow powder

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    Dimethocaine is a stimulant blend containing Phenzacaine and Caffeine Anhydrous

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    Drostanolone (INN; also known as dromostanolone or Drolban), marketed as Masteron, is an anabolic steroid. Drostanolone is a part of thedihydrotestosterone (DHT) family. Its main medical uses include lowering cholesterol levels and as an antineoplastic agent in the treatment of some cancers. It is most commonly marketed as the ester drostanolone propionate (trade name Masteron).

    Drostanolone binds to a receptor and activates a cascade of genetic changes, which increases the protein synthesis (anabolism) and decreases the amino acids degradation (catabolism). Other effects of Drostanolone are reduction or inhibition of prolactin or estrogen receptors, which are linked to its anti tumor properties.

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