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35 Responses

  1. EFFECTS says:

    Physiological effects of LSD can be highly variable; however pupil dilation, reduced appetite, and wakefulness are the three main physical effects.

    Other physical effects include:

    Hypothermia or Hyperthermia
    Elevated Blood Sugar
    Goose Bumps
    Heart rate increase
    Jaw clenching
    Saliva Production
    Mucus Production
    Many of these effects depend on dose size and Set and Setting. Many of these effects are secondary to the overwhelming psychological aspects of an LSD trip.

    A common neurological effect is an exaggerated patellar reflex — the reflex that’s tested when a doctor taps below your kneecap and your leg kicks up involuntarily. Instability while walking, altered gait, and tremors are somewhat common as well.

  2. An Introduction into the world of RCs says:

    Research chemicals. Whether you’ve heard about them on your local news channel, national newspaper, here on DDW or by a friend who favours them; research chemicals are all over.
    But what are they? And why are they so readily available? Let’s find out together.

    Before we learn about NBOMes its advisable to backtrack slightly to learn about what a NBOMe actually refers to in terms to the group of drugs of which they belong to, This article has been crafted for those with little to no knowledge of research chemicals who want to learn the basics of research chemicals.

    What is a research chemical? A research chemical is a substance which has not yet been scientifically and/or medically researched. The word research in the combination ‘research’ and ‘chemical’ is used to suggest it’s use for research purposes; a drug with no proven benefits in medicine, a drug with no recorded interaction with humans and a drug that has not been approved by any means for human consumption.

    The word research in this scenario, is a catch-all term for a drug which science knows very little about. And what science doesn’t know, we shouldn’t know. Or at least that’s how drug laws work today anyway. However, selling drugs as research chemicals is one clever way of evading the law as research chemicals are up until being prohibited, perfectly legal to buy and sell for ‘research purposes’ which by the way, doesn’t include human consumption.

    The truth is, little research is ever done on these new chemicals and the only research ever done is often by the general public.

    Contrary to the knowledge of the people, trip reports and experiences are hardly scientific or medically sound in academic reference and nature and because of this, research chemicals are often mislabeled and discredited. Many drugs we know today have extensive scientific research behind their prevalence both in illegal drug use and in medicine. Drugs are tested to learn about their properties and their pharmacological actions on the human body. Much of the results come from lab testing and animal trials before they the drugs are administered to humans.
    However, research chemicals are rarely tested on humans in a scientific or medical setting before their subsequent release into the public domain and this is where the crossroads between empirical science, medical enquiry and the pursuit of getting high begin to veer off into their own long winding roads and off into the sunset.

    Research chemicals are not always considered drugs which are often created with the intention to sell to black markets and on the street, this is a common misconception. Many RCs are synthesised for the sole purpose of medical and scientific research. Many research chemicals are in fact developed by very well known and respected members of the scientific community who in their day to day life are credible chemists, pharmacologists and professors and hold prestigious positions at some of the worlds most favoured education establishments.

    This research is then gathered by people and companies looking to profit from the properties of the drug (if psychoactive in this case) and so begins the process of manufacturing research chemicals and selling them as alternatives to the drugs they seem to imitate or even worse to be fraudulently sold as a well known drug on black markets and out on the street to save money and to make massive profits.

    Did you Know? Part One

    In 2015 according to Global Drug Survey, Poland has the highest rate of use for research chemicals with 31% of respondents to the survey reporting using research chemicals. Switzerland has the lowest rate of research chemical use with only 1.1% of respondents taking research chemicals (100,000> people participated/responded in the survey from Nov-Dec 2014)

    Where do they come from?

    The birthplace of research chemicals are usually in academic or scientific settings, purely for the purpose of science and research. In this particular article as we are discussing NBOMEs specifically, NBOMEs were effectively released into the wild when the chemist who synthesised them released his Ph.D. thesis.

    Another scientist then re-evaluated the drugs in another scientific setting where he then released research paperwork which was then picked up by those seeking to make an investment from the psychoactive properties of the research chemicals and the rest is history.

    Today, research chemicals are churned out in the kilos in mass production operations mainly by chemical companies and clandestine manufacturers to cater to the large research chemical market.

    Designer Drugs

    Designer drugs are created to find alternating yet similar characteristics from already existing drugs where the properties of one drug (ie. the psychoactive properties) can be amplified by modifying the chemical structure and creating an analogue (a derivative). This article focuses on NBOMEs but the same consideration and premise applies to all research chemicals.

  3. 2-FDCK says:

    2-FDCK or 2-Fluorodeschloroketamine (AKA 2-Fluroketamine, Fluoroketamine, and 2-FK) is a synthetic dissociative substance of the arylcyclohexylamine chemical class.

    2-Fluorodeschloroketamine may function in the same way as Ketamine, however scientists have been showing results ending with 2-Fluorodeschlorohydroxynorketamine (2-Fluoro-2′-Oxo-3′-HO-PCA) instead of Hydroxynorketamine (2-Chloro-2′-Oxo-3′-HO-PCA). You could expect it to have similar results, observing dissociative, anaesthetic, and hallucinogenic properties, though there is much that is still unknown about the potential of this chemical.

    2-FDCK can only be ordered if you are over 18 years of age.

    Please ensure that 2-FDCK is NOT controlled in the country/state to which you wish it to be delivered.

    2-FDCK is not for human consumption.

  4. 2-FEA says:

    ResearchChemical from with fast dispatch
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    2-FEA (2-Fluoro N-Ethyl Amphetamine) OR ( N-ethyl-1-(2-fluorophenyl)propan-2-amine)

    Initial reports and chemical structure suggest this product could be a promising replacement for the highly sought after 2-FMA that is no longer available due to the China Ban.

    2-FEA can only be ordered if you are over 18 years of age.

    Please ensure that 2-FEA is NOT controlled in the country/state to which you wish it to be delivered.

    2-FEA is not for human consumption.

  5. 3-CMC says:

    3-CMC from with same day dispatch on all research chemical orders mon to friday

    shipping acrosss europe including France Germany spain,netherlands.3-CMC can only be ordered if you are over 18 years of age.

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  6. 3-FEA says:

    3-FEA is the common name for 3-Fluoroethamphetamine which is a synthetic ring-substituted fluorinated amphetamine compound. It can give a mixture of entactogenic and stimulant effects if consumed. 3-FEA is structurally related to a series of fluorinated, substituted amphetamines, that originally included other compounds such as 2-FA, 2-FMA, 3-FA, 4-FMA, 4-FA.

    3-FEA has a parent compound called 3-FA. The pharmacological, toxicological, and subjective effects of 3-FEA are similar to 3-FA. Early research reports suggest that 3-FEA as a moderately potent serotonin and norepinephrine-dominant triple monoamine releaser. It produces a medium-duration mixture of entactogenic and stimulating effects that skew more to the euphoric-recreational side, similar to one of its popular predecessors, 4-FA, than towards what some consider to be more functional or productivity-enhancing e.g. isopropylphenidate, 2-FA, or 2-FMA.

    3-FEA can only be ordered if you are over 18 years of age.

    Please ensure that 3-FEA is NOT controlled in the country/state to which you wish it to be delivered.

    3-FEA is not for human consumption.

  7. 3-MEO-PCE says:

    3-MeO-PCE, or 3-Methoxyeticyclidine (also known as Methoxieticyclidine) is a very novel dissociative substance that sits in the arylcyclohexylamine class, which produces dissociative and hallucinogenic effects when administered. It is a structural analog of PCE.

    3-MeO-PCE became popular back in 2010, and is sold as a research chemical alternative to PCP.

    3-MeO-PCE can only be ordered if you are over 18 years of age.

    Please ensure that 3-MeO-PCE is NOT controlled in the country/state to which you wish it to be delivered.

    3-MeO-PCE is not for human consumption.

  8. 3-MEO-PCP says:

    3-MeO-PCP, or 3-Methoxyphencyclidine, is a synthetic dissociative of the arylcyclohexylamine class. 3-MeO-PCP contains cyclohexane, a six member saturated ring, bonded to two additional rings at R1. One of these rings is a piperidine ring, a nitrogenous six member ring, bonded at its nitrogen group. The other ring is an aromatic phenyl ring, substituted at R3 with a methoxy group.

    Buy 3-MeO-PCP Research Chemical from shipping across Europe including France Germany Spain Netherlands, Wholesale bulk orders of Research Chems welcome.3-MeO-PCP is a PCP derivative and structurally analogous to 4-MeO-PCP.

    Although 3-MeO-PCP was once famously described as possessing opioid or dopaminergic activity (based on early phenomenological analysis), this supposition is contradicted by data showing 3-MeO-PCP to be a potent and selective ligand for the NMDA receptor without appreciable affinity for the µ-opioid receptor or dopamine transporter. 3-MeO-PCP was preceded by the less potent dissociative 4-MeO-PCP and first became available as a research chemical in 2011.

    This product is sold only for research uses in laboratory settings. Those who work with it are advised to wear the appropriate safety equipment and follow standard safety protocols while handling it.

    Strictly not for human consumption – if consumed seek immediate medical assistance.

    3-MeO-PCP can only be ordered if you are over 18 years of age.

    Please ensure that 3-MeO-PCP is NOT controlled in the country/state to which you wish it to be delivered.

    3-MeO-PCP is not for human consumption.

  9. 4-ACO-MET says:

    4-AcO-MET or as it’s full name is 4-Acetoxy-N-ethyl-N-methyltryptamine, is also known in some areas as Metacetin and Azomet. It’s a synthetic psychedelic substance of the tryptamine chemical class, and produces psilocybin mushroom-like psychedelic effects, our research shows. 4-AcO-MET possesses a molecular structure and pharmacological effect profile that resemble 4-HO-MET (Metocin).

    Very little is known about the pharmacological properties, metabolism, and toxicity of 4-AcO-MET, so please leave reviews from your researching. 4-AcO-MET is also occasionally found in pressed pills such as blue diamonds, which are sold on the streets in northern Switzerland under the name “Acomet” or “Azomet”. This is because we believe that 4-AcO-MET is one of a few research chemicals that are legal there, and easily bought. Please check the legality though…don’t just take our word!

    4-AcO-MET can only be ordered if you are over 18 years of age.

    Please ensure that 4-AcO-MET is NOT controlled in the country/state to which you wish it to be delivered.

    4-AcO-MET is not for human consumption.

  10. 4-CEC CRYSTAL says:

    4-CEC Crystal Research Chemical from,fast dispatch of all research chems monday to friday.Shipping wholesale research chemicals across europe including Netherlands Germany France .

    4-CEC is officially known as 1-(4-Chloro-phenyl)-2-ethylamino-propan-1-one.

    The chemical formula for 4-CEC Crystals is C11H14ClND.

    4-CEC is listed as a Cathinone. Cathinone is also known as benzoylethanamine, which is found in the plant Catha Edulis which makes it very similar to methcathinone, cathine, and other amphetamines that are known to create a stimulant effect. Cathinones help in releasing dopamine while slowing the re-uptake of serotonin, epinephrine, and norepinephrine into the central nervous system.

    4-CEC can only be ordered if you are over 18 years of age.

    Please ensure that 4-CEC is NOT controlled in the country/state to which you wish it to be delivered.

    4-CEC is not for human consumption.

  11. 4-EMC says:

    4-EMC delivers both stimulant and entactogen effects, which makes it a popular choice amongst chemical researchers. 4-EMC is officially known as 4-ethylmethcathinone, and it’s been available only for a short while. The compound represents an isomer of 4-MEC, another recently discovered research agent from the substituted cathinones class, as well as to now restricted 4-MMC (mephedrone). Pharmacological profile of this substance is likely to be based on interaction with monoamine transmitters, similar to its relatives from the same chemical group.

    Full IUPAC name of 4-EMC is 1-(4-ethylphenyl)-2-(methylamino)propan-1-one, with a simple chemical formula that can be summarized as C12H17NO

    4-EMC can only be ordered if you are over 18 years of age.

    Please ensure that 4-EMC is NOT controlled in the country/state to which you wish it to be delivered.

    4-EMC is not for human consumption.

  12. 4-HO-DET says:

    4-HO-DET or as it is formally known, 4-Hydroxy-N,N-diethyltryptamine is not so well-known the synthetic, psychedelic tryptamine chemical class. It produces psilocin-like psychedelic effects when administered. 4-HO-DETis a close structural and functional analog of psilocin (4-HO-DMT), the principal psychoactive component in magic mushrooms. It is notable for sharing many of its core features while retaining subtle variations in its duration, visual, cognitive and bodily effects.

    This compound was first discovered in the late 1950s, during investigations into various psychedelic compounds that were structurally and chemically related to the principle active components from magic mushrooms, psilocybin (4-PO-DMT) and psilocin (4-HO-DMT). The substance was used together with its phosphoryloxy-analog 4-PO-DET in human clinical trials in the 1960s, so research away!

    4-HO-DET can only be ordered if you are over 18 years of age.

    Please ensure that 4-HO-DET is NOT controlled in the country/state to which you wish it to be delivered.

    4-HO-DET is not for human consumption.

  13. 4-HO-MET says:

    4-HO-MET (4-hydroxy-N-methyl-N-ethyltryptamine, metocin or methylcybin) is a lesser known psychedelic tryptamine. It is a structural and functional analog of psilocin, as well as the 4-hydroxy analog of MET.

    Tryptamines share a core structure comprising a bicylic indole heterocycle attached at R3, to an amino group, via an ethyl side chain. 4-HO-MET is substituted at R4 of its indole heterocycle with a hydroxyl functional group OH−. It also contains a methyl group and an ethyl chain bound to the terminal amine RN of its tryptamine backbone (MET). 4-HO-MET is a 4-hydroxy analogue of 4-AcO-MET and the N-substituted ethyl homologue of 4-HO-DMT.

    Warning… This stuff is strong!

    4-HO-MET can only be ordered if you are over 18 years of age.

    Please ensure that 4-HO-MET is NOT controlled in the country/state to which you wish it to be delivered.

    4-HO-MET is not for human consumption.

  14. 4-HO-MIPT POWDER says:

    4-HO-MiPT (also known as Miprocin, 4-hydroxy-N-methyl-N-isopropyltryptamine) is a synthetically produced psychedelic substance of the tryptamine class. Tryptamines share a core structure that comprises a bicylic indole heterocycle attached at R3, to an amino group via an ethyl side chain. 4-HO-MiPT is substituted at R4 of its indole heterocycle with a hydroxyl (HO) functional group OH-. It also contains a methyl group and an isopropyl chain, bound to the terminal amine RN of its tryptamine backbone (MiPT). 4-HO-MiPT is the N-substituted isopropyl homologue of 4-HO-DMT

    WARNING…. This stuff is very strong!

    4-HO-MIPT can only be ordered if you are over 18 years of age.

    Please ensure that 4-HO-MIPT is NOT controlled in the country/state to which you wish it to be delivered.

    4-HO-MIPT is not for human consumption.

  15. 4-MPD CRYSTAL says:

    4-MPD wholesale at unbeatable prices from Europes Leading Research Chemical Supplier

    4-Methylpentedrone (also known as 4-MPD and 4-Methyl-α-methylamino-valerophenone), is a stimulant belonging to the Cathinone group.

    It is a higher homologue of 4-Methylmethcathinone (Mephedrone) and 4-Methylbuphedrone (4-MeMABP), and the p-Methyl analogue of Pentedrone.

  16. 4F-PHP CRYSTAL says:

    4F-PHP – 4′-Methyl-α-pyrrolidinohexiophenone or MPHP is a stimulant compound. It is closely related to pyrovalerone, being simply its chain-lengthened homologue. In the pyrrolidinophenone series, stimulant activity is maintained so long as the positions of the aryl, ketone and pyrrolidinyl groups are held constant, while the alkyl backbone can be varied anywhere between three and as many as seven carbons, with highest potency usually seen with the pentyl or isohexyl backbone, and a variety of substituents are tolerated on the aromatic ring.

    IUPAC: 1-(4-fluorophenyl)-2-(pyrrolidin-1-yl)hexan-1-one

    CAS: 117232-21-2

    Molecular Formula: C16H22FNO

    Molecular Weight: 263.350

  17. 4F-PHP POWDER says:

    IUPAC: 1-(4-fluorophenyl)-2-(pyrrolidin-1-yl)hexan-1-one

    CAS: 117232-21-2

    Molecular Formula: C16H22FNO

    Molecular Weight: 263.350

    4F-PHP Powder can only be ordered if you are over 18 years of age.

    Please ensure that 4F-PHP Powder is NOT controlled in the country/state to which you wish it to be delivered.

    4F-PHP Powder is not for human consumption.

  18. 6-APB says:

    6-APB is similar in structure to MDA, and is part of the phenethylamine and amphetamine classes. Its pharmacological action is an agonist to the three main serotonin receptors (5-HTP2A/B/C), with effects said to range from euphoria through to increased energy and empathy towards others.

    6-APB can only be ordered if you are over 18 years of age.

    Please ensure that 6-APB is NOT controlled in the country/state to which you wish it to be delivered.

    6-APB is not for human consumption.


    The abbreviation of Ethyl-Hexedrone is HEX-EN. The systematic name of this chemical is 2-(ehtylamino)-1-phenylhexan-1-one. Low doses of the chemical are advised at the start and according to the individual tolerance, metabolism and personal sensitivity of consumer. The duration of its stimulation is observed to last 1-4 hours with an onset of 15-30 minutes.

    · A Substituted Cathinone

    Before you buy Ethyl-Hexedrone, you should know it’s a substituted cathinone and features a phenethylamine core with Alkyl Group attached to its alpha carbon. There is also an oxygen group attached to its beta carbon. The Cathinones are better known as beta-ketone amephetamine analogues.

    The Ethyl-Hexedrone gives its better counterpart, pentedrone a tough competition. The Hexedrone itself is an extended chain of pentedrone. The extension makes the carbon less potent which is recovered with the addition of ethyl group. This concludes that Ethyl-Pentedrone would be more potent.

    · Pharmacology

    You should know that everything mentation here is based on the similarity of structure and affects Ethyl-Hexedrone shares with other cathinones. The Ethyl-Hexedrone works as both dopamine and prepinephrine which releases an agent or reuptake inhibitor. This lets the dopamine and norepinephrine to accumulate within the brain. This results in euphoric and stimulating effects.

    The following effects are based on subjective effects index, and data collected from different tests. Some of these effects can rarely occur, or may never at all. However, it depends on the dose and dependency on a stimulant.


    · Grinding of Teeth

    · Improved Focus

    · High Blood Pressure

    · Temporary Erectile Dysfunction

    · Stimulation

    · Bumps up heart beat

    · Kills Your Appetite

    · Tactile Improvement

    · Vasoconstriction


    · Improves Motivation

    · Inflates Ego

    · Euphoria

    · Time Distortion

    · Improves Analysis

    · Compulsive Redosing

    · Improves the appreciation for Music

    · Disinhibition

    After Effects

    · Anxiety

    · Wakefulness

    · Depression

    · Motivational Suppression

    · Irritability

    · Cognitive Fatigue

    Its safety and long term effects are not properly studied. The toxic dosage of Ethyl-Hexedrone is also unknown. The only reason for this lack of information is Ethyl-Hexedrone hasn’t been used much. The Anecdotal evident from groups that tried this stimulant says there are negative effects from low to moderate dose. However, it is strictly advised that one should use Harm reduction practices when using Ethyl-Hexedrone.

    Tolerance and Addiction

    Just like other stimulants, the chronic use of Ethyl-Hexedrone is believed to be moderately addictive which is likely to cause some psychological dependence among users. When the addiction is developed, withdrawal and cravings effects can be observed when the user stops taking this stimulation.

    The tolerance effects take some time to develop. It will result in the user needing a high dose to attain similar effects. Unfortunately, it takes 3-7 days to reduce the tolerance to half, with another two weeks to return to baseline. The problem is, Ethyl-Hexedrone shows cross tolerance with all dopaminergic stimulants which means that after consuming Ethyl-Hexedrone the stimulants will have a controlled effect.


    Abuse with a high dose for a long time can lead to stimulant psychosis. Delusions, Hallucinations and Paranoia, are some early symptoms. According to a review, the treatment of abuse-induced psychosis fails for 5-15% of users.

    Destructive Interactions

    While many drugs are safe, they can be harmful and may claim your life If taken with any other compounds. Following are a few dangerous combinations of Ethyl-Hexedrone. Some of these combinations may be safe in low doses but are still a potential threat.

    · Cocaine

    · Alcohol

    · Tramadol

    · Stimulants

    · MXE

    · MDMA


    While most designer drugs are not suggested for direct consumption, Ethyl-Hexedrone is safe in low dose. However, a regular or high dose of it can lead to a serious health condition. So, better stay safe from it.


    Methoxphenidine (MXP) aka 1-(1-(2-methoxyphenyl)-2-phenylethyl)piperidine aka 2-MeO-Diphenidine acts on the dopamine transport as a dopamine reuptake inhibitor and as a selective NMDA receptor antagonist, comparable to other NMDA antagonists, such as Methoxetamine and 4-Meo-PCP, although Methoxphenidine is completely legal to purchase in the UK for scientific research purposes. Our Methoxphenidine is certified at the highest grade purity available. This compound needs to be researched with caution.

    Since Methoxetamine, and 4-Meo-PCP were banned there has been a void in this area of research, although not a direct replacement of either Chemicals, Methoxphenidine should provide similar results within laboratory experiments.

    Methoxphenidine is likely to be popular with Scientists and researchers who have had previous research experience with Methoxetamine.

    Strictly not for human consumption and must be over 18 to purchase.

    Methoxphenidine Crystal can only be ordered if you are over 18 years of age.

    Please ensure that Methoxphenidine Crystal is NOT controlled in the country/state to which you wish it to be delivered.

    Methoxphenidine Crystal is not for human consumption.

  21. 1P-LSD MCG BLOTTERS says:

    1p-LSD, short for 1 Propionyl Lysergic Acid Diethylamide is the hallucinogenic, psychedelic drug that belongs to the family of lysergamide. This substance has almost no history of human use. This substance has never been reported in any formal scientific literature making it unknown to the public and the academics.
    Surprisingly it is structurally similar to LSD and ALD 52 which suggest it has an identical effect profile as well. With the lack of research related to this substance, every argument related to the pharmacology of this drug is completely according to its structure and the subjective effect that are not different from other such lysergamides.
    In the early months of 2015, 1p-LSD got its legal alternative LSZ and LSD, and it was marketed through online chemical vendors who were selling it. This compound as mainly sold in blotter sheet tabs. It was marketed as a research chemical that made it easy to sell it legal, although it was sold for human consumption
    According to its molecular structure, it belongs to lysergamide family. It is quite analogous to LSD, and it has been named for its propionyl group that is bound to the nitrogen of polycyclic indole group. The propionyl consists of carbonyl chain that is bound to an amino group. 1p-LSD contains a polycyclic group that features the bicyclic Hexahydro indole bound to its quinolone bicyclic group. At carbon 9 of quinoline, the n-diethyl carboxamide becomes bound.
    Right now it is in the grey market area that makes its purchase a bit unsafe.
    It acts as the partial agonist of 5 HT2A. Psychedelic effects come from efficacy at 5HT2A receptors. The role of such interactions and how these result in psychedelic experience always remain elusive.
    Moreover, it has been theorized that 1p-LSD is a prodrug to LS. It shows only 35% potency of LDS in mice. The LSD is detected with the help of LC-MS when the 1p-LSD is incubated in Human Serum. This means that 1p-LSD doesn’t only acts as a prodrug for LSD but also, it directly acts as serotonin receptor against its very own rights.
    Subjective Effects
    The subjective effects of 1p-LSD are similar to those structurally related to it. The differences are minuscule that are negligible and virtually indistinguishable from each other. As comparing to other psychedelics which includes LS and Psilocin, the 1p-LSD proves to be even more stimulating and fast paced when it comes to a specific type of its physical and cognitive effects. The effects are listed blow that are based on the subjective effects index and personal experience of some subjects. The listed effects rarely occur and only once. However if the dosage is heavy, it can lead to severe cases.
    Physical Effects
    • Tactile Sensations
    • Stimulation
    • Bodily controlled enhancement
    • Nausea
    • Tactile improved
    • Pupil Dilation
    • Increase heart rate
    Cognitive Effects
    • Current mind state enhancement
    • Thought acceleration
    • Novelty enhancement
    • Immersion enhancement
    • Time distortion
    • Ego death
    • Mindfulness
    • Thought loops
    • Delusions
    • Feeling interdepent opposites
    • Conceptual thinking
    • Self-design feeling
    • Wakefulness
    • Creativity enhancement
    • Though disorganization
    • Spiritual enhancement
    • Personal bias enhancement
    Auditory Effects
    • Distortions
    • Hallucination
    • Enhancement

    Trusted 1p-LSD Supplier

    1-propionyl-LSD also known as 1P-LSD or 1-propionyl-lysergic acid diethylamide is a new uncontrolled LSD analogue supplied in 100µg blotters for convenient research.

    This product is sold only for research uses in laboratory settings. Those who work with it are advised to wear the appropriate safety gear and follow standard safety protocols while handling it.

    Strictly not for human consumption if consumed seek immediate medical assistance

  22. ETH-LAD BLOTTERS says:

    ETH-LAD, or 6-ethyl-6-nor-lysergic acid diethylamide, is a semi-synthethic alkaloid of the lysergamide famiy. ETH-LAD is a structural analogue of lysergic acid with an N,N-diethylamide functional group bound to RN of the chemical structure. This core polycyclic structure is an indole derivative and has tryptamine and phenethylamine groups embedded within it. ETH-LAD’s structure contains a bicyclic hexahydroindole fused to a bicyclic quinoline group (nor-lysergic acid).

    ETH-LAD does not contain a methyl group substituted at R6 of its nor-lysgeric acid skeleton; this is represented by the nor- prefix. Instead, ETH-LAD is substituted at R6 with an ethyl group. At carbon 8 of the quinoline, a N,N-diethyl carboxamide is bound. ETH-LAD is a chiral compound with two stereocenters at R5 and R8. ETH-LAD, also called (+)-D-ETH-LAD, has an absolute configuration of (5R, 8R).

    This product is sold only for research uses in laboratory settings. Those who work with it are advised to wear the appropriate safety gear and follow standard safety protocols while handling it.

    Strictly not for human consumption…if consumed seek immediate medical assistance.


    Flualprazolam is a novel synthetic depressant substance of the benzodiazepine class which produces anxiolytic, disinhibiting, sedative, muscle relaxant, and memory suppressing effects when administered.

    Flualprazolam 1mg Pellets can only be ordered if you are over 18 years of age.

    Please ensure that Flualprazolam 1mg Pellets is NOT controlled in the country/state to which you wish it to be delivered.

    Flualprazolam 1mg Pellets is not for human consumption.


    Flubromazepam is another new benzodiazepine derivitive available now at High It is more formally known as 7-bromo-5-(2-fluorophenyl)-1,3-dihydro-1,4-benzodiazepin-2-one.

    Flubromazepam is structurally related to Bromazepam which itself contains anxiolytic, sedative and hypnotic properties.

    Early tests on Flubromazepam indicate that it might be a good replacement for Etizolam. So for those researchers who are now unable to purchase Etizolam due to it being prohibited in their region, such as Sweden, these could be a useful substitute.

    As with all the chemicals that we stock, Flubromazepam is not approved for any type of in-vivo research (i.e. not in humans or animals) or for clinical trials. And therefore if accidently ingested then seek immediate medical attention.

    Please ensure you adhere to standard laboratory safety practices including using suitable skin, eye and clothing protection.

    Flubromazepam is also available in 8mg research chemical pellets.

    Strictly not for human consumption.

    Must be over 18 to purchase.


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    Microdosing is the act of consuming sub-perceptual amounts of psychedelics, like LSD or Psilocybin Mushrooms.

    Sub-perceptual means the effects are subtle, but can have a noticeable influence on your life.

    Typically, individuals integrate sub-perceptual doses into their weekly routine. Microdosers often report higher levels of creativity, more energy, increased focus, and improved relational skills.

    Many people microdose in order to treat depression or anxiety, with often remarkable results.

    Some enthusiasts also report microdosing helps to heighten spiritual awareness and enhance all five senses.


    While the modern history of psychedelics reaches back to the 1950s, interest in microdosing saw a major revitalization with the publishing of Dr. James Fadiman’s The Psychedelic Explorer’s Guide: Safe, Therapeutic, and Sacred Journeys in 2011.

    Dr. Fadiman’s book explores microdosing as a subculture of psychedelic use. While a number of indigenous cultures, as well as modern professionals, have utilized microdosing as a way to unlock a host of benefits, Dr. Fadiman’s book formally introduced the term “microdosing” into the psychedelic mainstream.

    But Dr. Fadiman’s book didn’t just contribute a piece of terminology; it awakened the curiosity and imaginations of millions of people fascinated by the reports of experienced microdosers. It also provided a host of practical information for anyone that wanted to give it a try, much of which has been integrated into this course.

    Dr. Fadiman’s ongoing research into microdosing serves as one of the few modern studies into the effects of microdosing specifically (most other research deals with larger doses for specific therapeutic outcomes).

    Following the publication of The Psychedelic Explorer’s Guide, the next major boost in the public’s awareness of microdosing came from a podcast interview Dr. Fadiman gave with Tim Ferriss in March of 2015.

    Ferriss, who rose to fame after authoring the bestseller “The Four Hour Work Week,” has an enormous audience of individuals interested in entrepreneurship, “biohacking,” self-experimentation, psychology, spirituality, and an array of additional subject matters that would predispose them to an interest in the benefits of microdosing.

    His podcast interview with Dr. Fadiman blasted the core messages about microdosing contained in The Psychedelic Explorer’s Guide from a soapbox loud enough to significantly increase a basic awareness of the concept.

    Soon after its air date, listeners of Ferriss’ podcast were not only starting to experiment with microdosing on their own; they were discussing it and sharing their curiosity with their own personal networks. Consequently, journalists began writing articles about microdosing, leading to even greater awareness and interest.

    The most recent source of interest in microdosing came from Ayelet Waldman’s book “A Really Good Day: How Microdosing Made a Mega Difference in my Mood, My Marriage, and My Life,” published in February of 2016.

    Waldman’s book discusses her 30 day protocol of microdosing with LSD to address a variety of psychological symptoms primarily caused by hormonal changes related to menopause.

    Prior to microdosing, Waldman’s mood swings had become so severe as to put her marriage and relationship with her children at risk.

    Afterwards, in an interview with The Third Wave, she said, “This month changed my life, and I am sad every day that I can’t keep doing it legally.”

    Now, tens of thousands of people around the globe are being turned on to microdosing – whether it’s for treating mental health problems, boosting creativity, or giving entrepreneurs new directions.

  28. Lysergic acid diethylamide (LSD) says:

    Lysergic acid diethylamide (LSD), also known as acid, is a psychedelic drug known for its psychological effects, which may include altered awareness of one’s surroundings, perceptions, and feelings as well as sensations and images that seem real though they are not.[11] It is used mainly as a recreational drug and for spiritual reasons. LSD is typically either swallowed or held under the tongue.[11] It is often sold on blotter paper, a sugar cube, or gelatin. It can also be injected.

    LSD is not usually addictive.[11][12] However, adverse psychiatric reactions such as anxiety, paranoia, and delusions are possible.[7] LSD is in the ergoline family. LSD is sensitive to oxygen, ultraviolet light, and chlorine,[13] though it may last for years if it is stored away from light and moisture at low temperature. In pure form it is odorless, crystalline, and clear or white in color.[11] As little as 20–30 micrograms can produce an effect.[14]

    LSD was first made by Albert Hofmann in Switzerland in 1938 from ergotamine, a chemical from the fungus ergot. The laboratory name for the compound was the acronym for the German “Lyserg-säure-diäthylamid”, followed by a sequential number: LSD-25.[13][15] Hofmann discovered its psychedelic properties in 1943.[16] LSD was introduced as a commercial medication under the trade-name Delysid for various psychiatric uses in 1947.[17] In the 1950s, officials at the United States Central Intelligence Agency (CIA) thought the drug might be useful for mind control and chemical warfare and tested the drug on young servicemen and students, and others without their knowledge. The subsequent recreational use by youth culture in the Western world as part of 1960s counterculture resulted in its prohibition


    While psychedelic substances have been illegal and prohibited from study in the vast majority of countries up until the past few years, many of the world’s top experts have made incredible strides picking up on research started in the 1950s and 60s.

    Although almost no research has been done on microdosing specifically, we know something about what large doses of psychedelics do to the brain.

    Much of what we understand about how psychedelics work involves serotonin, a chemical that keeps our brains ticking. It is one of the most important neurotransmitters in the brain, and affects nearly everything we do, from how we feel to how we process information.

    Classic psychedelics such as LSD and Psilocybin share a similar structure to serotonin, and work along a similar pathway…

  30. Psychological says:

    The most common immediate psychological effects of LSD are visual hallucinations and illusions (colloquially known as “trips”), which can vary greatly depending on how much is used and how the brain responds. Trips usually start within 20–30 minutes of taking LSD by mouth (less if snorted or taken intravenously), peak three to four hours after ingestion, and last up to 12 hours. Negative experiences, referred to as “bad trips”, produce intense negative emotions, such as irrational fears and anxiety, panic attacks, paranoia, rapid mood swings, intrusive thoughts of hopelessness, wanting to harm others, and suicidal ideation. It is impossible to predict when a bad trip will occur.[27][28] Good trips are stimulating and pleasurable, and typically involve feeling as if one is floating, disconnected from reality, feelings of joy or euphoria (sometimes called a “rush”), decreased inhibitions, and the belief that one has extreme mental clarity or superpowers.


    Microdosing is the act of taking ‘sub-perceptual’ doses of psychedelics, meaning the dose level is not high enough to cause substantial deviations from reality.

    Ideally, a microdose will not cause a substantial change in mood, disposition, or mindset. Instead, its effect will be subtle but present.

    For LSD, a microdose is typically between 6 and 20 micrograms. This amount equates to between 1/16th and 1/5th of a single tab.

    When microdosing with LSD on blotter paper, there are two methods to prepare a microdose: cutting or volumetric.

    The cutting method is exactly what it sounds like: cutting the blotter paper with an Exacto knife or scissors.

    The drawback to this method is a lack of precision. Your microdoses may be quite variable if you cut up your tabs, since LSD blotter paper doses can be laid unevenly. When LSD is ‘laid’ it means a crystal of LSD is melted into a liquid form, then spread across a piece of blotter paper. Sometimes, the liquid can distribute unevenly on the blotter paper. An uneven lay causes variation in the amount of LSD you may consume in any given microdose.

    The volumetric method helps you get around any variation in how a tab is laid or cut. It involves submerging a full tab into distilled water and taking small, measured quantities of the water to microdose.

    This process requires a couple of small measurements, but will give you a more accurate, consistent dose.

    To describe it briefly, all you need to do is drop a 100ug tab into 10ml of distilled water or alcohol. Leave it for a day or so, in the dark. Then, 1ml of the liquid will contain 10ug of LSD, and will provide you with a consistent microdose. You can store your liquid in the fridge and it should last for months.


    While it’s certainly an oversimplification, people generally microdose for two different reasons: to decrease the frequency and intensity of undesirable mental states or to improve the frequency and intensity of desirable mental states.

    1: To reduce the frequency and intensity of undesirable states caused by various forms of “mental illness”, including:

    Anxiety (i.e. Generalized or Social)
    Mood disorders
    2: To increase the frequency and intensity of desirable states/outcomes:

    Flow states
    Improved relationships/increased empathy
    Athletic coordination
    Leadership development
    We’re not fond of the term “Mental Illness” because it pathologizes what is often a part of one’s natural progression towards a more coherent, actualized self.

    But for those struggling with depression, anxiety, PTSD, ADD/ADHD, mood disorders and/or addiction (to name a few), microdosing can create a number of positive changes.

    Clinical research has shown that larger doses of psychedelics are effective at treating depression, anxiety and addiction. Anecdotal evidence backs up the idea that a regular microdosing regimen can also have healing benefits for sufferers of various mental health conditions:

  33. Reactivity and degradation says:

    “LSD,” writes the chemist Alexander Shulgin, “is an unusually fragile molecule… As a salt, in water, cold, and free from air and light exposure, it is stable indefinitely.”[13]

    LSD has two labile protons at the tertiary stereogenic C5 and C8 positions, rendering these centres prone to epimerisation. The C8 proton is more labile due to the electron-withdrawing carboxamide attachment, but removal of the chiral proton at the C5 position (which was once also an alpha proton of the parent molecule tryptophan) is assisted by the inductively withdrawing nitrogen and pi electron delocalisation with the indole ring.[citation needed]

    LSD also has enamine-type reactivity because of the electron-donating effects of the indole ring. Because of this, chlorine destroys LSD molecules on contact; even though chlorinated tap water contains only a slight amount of chlorine, the small quantity of compound typical to an LSD solution will likely be eliminated when dissolved in tap water.[13] The double bond between the 8-position and the aromatic ring, being conjugated with the indole ring, is susceptible to nucleophilic attacks by water or alcohol, especially in the presence of light. LSD often converts to “lumi-LSD”, which is inactive in human beings.[13]

    A controlled study was undertaken to determine the stability of LSD in pooled urine samples.[88] The concentrations of LSD in urine samples were followed over time at various temperatures, in different types of storage containers, at various exposures to different wavelengths of light, and at varying pH values. These studies demonstrated no significant loss in LSD concentration at 25 °C for up to four weeks. After four weeks of incubation, a 30% loss in LSD concentration at 37 °C and up to a 40% at 45 °C were observed. Urine fortified with LSD and stored in amber glass or nontransparent polyethylene containers showed no change in concentration under any light conditions. Stability of LSD in transparent containers under light was dependent on the distance between the light source and the samples, the wavelength of light, exposure time, and the intensity of light. After prolonged exposure to heat in alkaline pH conditions, 10 to 15% of the parent LSD epimerized to iso-LSD. Under acidic conditions, less than 5% of the LSD was converted to iso-LSD. It was also demonstrated that trace amounts of metal ions in buffer or urine could catalyze the decomposition of LSD and that this process can be avoided by the addition of EDTA.

  34. Modern distribution says:

    LSD manufacturers and traffickers in the United States can be categorized into two groups: A few large-scale producers, and an equally limited number of small, clandestine chemists, consisting of independent producers who, operating on a comparatively limited scale, can be found throughout the country.[143] As a group, independent producers are of less concern to the Drug Enforcement Administration than the larger groups because their product reaches only local markets.[144]

    Many LSD dealers and chemists describe a religious or humanitarian purpose that motivates their illicit activity. Nicholas Schou’s book Orange Sunshine: The Brotherhood of Eternal Love and Its Quest to Spread Peace, Love, and Acid to the World describes one such group, the Brotherhood of Eternal Love. The group was a major American LSD trafficking group in the late 1960s and early 1970s.[145]

    In the second half of the 20th century, dealers and chemists loosely associated with the Grateful Dead like Owsley Stanley, Nicholas Sand, Karen Horning, Sarah Maltzer, “Dealer McDope,” and Leonard Pickard played an essential role in distributing

  35. Psychedelic therapy says:

    n the 1950s and 1960s LSD was used in psychiatry to enhance psychotherapy known as psychedelic therapy. Some psychiatrists[who?] believed LSD was especially useful at helping patients to “unblock” repressed subconscious material through other psychotherapeutic methods,[162] and also for treating alcoholism.[163][164] One study concluded, “The root of the therapeutic value of the LSD experience is its potential for producing self-acceptance and self-surrender,”[165] presumably by forcing the user to face issues and problems in that individual’s psyche.

    Two recent reviews concluded that conclusions drawn from most of these early trials are unreliable due to serious methodological flaws. These include the absence of adequate control groups, lack of followup, and vague criteria for therapeutic outcome. In many cases studies failed to convincingly demonstrate whether the drug or the therapeutic interaction was responsible for any beneficial effects.[166][167]

    In recent years organizations like the Multidisciplinary Association for Psychedelic Studies have renewed clinical research of LSD.

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