BUY TENOCYCLIDINE (TCP) ONLINE

TCP was patented in the early 1960s by Parke-Davis — the same company to patent and eventually brought PCP and ketamine to market. TCP (TENOCYCLIDINE).

This compound is essentially a PCP molecule with a thiophene ring rather than a benzene ring. The rest of the chemical structure is identical between the two molecules. This alteration doesn’t make a massive amount of difference — in fact, Parke Davis considered it to be interchangeable with PCP aside from having a slightly higher potency than PCP by weight and a slightly longer duration of effects. Buy tenocyclidine online

Parke-Davis focused on developing PCP as a medicine and shelved their research on TCP. After the compound ended up on the street, the US government eventually placed it on the Schedule I restricted drug list — marking it as the very first arylcyclohexylamine to earn the distinction. Regulators viewed it as a drug with a high potential for abuse, but since it wasn’t approved by the FDA, like PCP, it was without medical value. Tenocyclidine street name.

The receptor binding (Ki) values for tenocyclidine have not been reported but are believed to share a similar profile to that of PCP. Where to buy tenocyclidine online.

TENOCYCLIDINE SPECS

Chemical Name	Tenocyclidine
Status	Research Chemical 🧪
Duration of Effects	Unknown
Estimated Threshold Dose	1 mg
Common Dose	Unknown
PubChem ID	62751
CAS#	21500-98-1

IUPAC Name: 1-[1-(Thiophen-2-yl)cyclohexyl]piperidine (TCP)

WAYS TO ADMINISTER ARYLCYCLOHEXYLAMINE

Arylcyclohexylamines can be used in virtually all forms of administration. They can be taken orally in the form of a pill or capsule, snorted, injected into the muscles, or directly into the veins, smoked, or vaporized. TCP (TENOCYCLIDINE).

Each method comes with its own set of pros and cons. Oral tablets are the easiest and safest to consume, but they take longer to kick in and aren’t as bioavailable as injections. Likewise, injections kick in quickly but can be dangerous to administer without sterile medical equipment and an understanding of the dose and how to inject the drug safely. TCP (TENOCYCLIDINE).

Bioavailability of various arylcyclohexylamine dosage forms: 

Route	Bioavailability (%)
Oral	17–24%
Sublingual	24–30%
Intranasal	25–50%
Intramuscular (IM)	93%
Intravenous (IV)	100%

1. ORAL

Taking ketamine orally means swallowing a pill or capsule. Some users will wrap the powder in a rolling paper if they don’t have a capsule — this practice is referred to as parachuting. Others mix the powder into a drink. Buy TCP powder online.

The downside of oral use is that this form offers the lowest bioavailability (refers to the amount of a drug that’s absorbed into the body after it’s consumed). This means the dosages for oral consumption are going to be the highest overall — usually around 10–20% higher than the dose for insufflation (snorting). Order tenocyclidine online.

For ketamine and other lipid-soluble arylcyclohexylamines, the onset time for oral consumption is around 20 or 30 minutes. 

2. SUBLINGUAL – TCP (TENOCYCLIDINE)

Sublingual administration involves the absorption of drugs through the microcapillaries lining the underside of the tongue and mouth. Here, tiny blood vessels located near the surface allow the passage of various drugs directly into the bloodstream. Tenocyclidine near me.

This is how drugs like LSD are normally administered. By holding the LSD tab under the tongue for several minutes, the active ingredients transfer into the blood vessels — offering a relatively fast onset of effects and bypassing first-pass metabolism. Drugs taken orally are sent to the liver, which attempts to neutralize as much of the active ingredients as possible before entering circulation. By avoiding first-pass metabolism via the liver, the potency of a given drug is preserved. Pennsylvania mushroom shop

Sublingual ketamine is common for low-dose at-home treatments in the form of a lozenge containing between 25 and 75 mg of ketamine each — taken every couple of days in between integration sessions.

For ketamine (and likely other arylcyclohexylamines), the onset time for sublingual administration is around 10–15 minutes. TCP (TENOCYCLIDINE).

3. SNORTING

Most recreational users snort arylcyclohexylamines because it offers the best blend of relative safety (no injections) and dose efficiency (the effects kick in stronger and hit harder than oral consumption). Tenocyclidine powder.

The problem with insufflation is that the crystals can cause serious damage to the nasal cavity, especially with repeated use. Some compounds are worse than others, and it depends on how finely ground the powder was before ingestion.

Drugs that require larger doses, such as 3-MeO-PCMo or 2-BrDCK, pose the biggest risk to the nasal cavity and tend to cause a lot of pain. Drugs with a much lower dose require less powder to reach the desired effects and are generally preferred for intranasal use.

Johnson & Johnson created a nasal ketamine spray called Spravato® (esktamine) that has been well-received by the medical community as a means of administering ketamine to children and adults alike. The spray doesn’t burn the nose and is rapidly absorbed within a couple of minutes.

Most arylcyclohexylamines kick in within 5 or 10 minutes after snorting them. 

4. INTRAMUSCULAR INJECTION (IM) – TCP (TENOCYCLIDINE)

People who take these compounds intending to reach a K-hole state most often turn to intramuscular or intravenous injections. These modes of administration offer the fastest onset of effects and ensure very high bioavailability.

IM injections carry a substantially higher level of risk than snorting or taking orally. Contaminated needles can lead to infections and mistakes with dosages can lead to experiences that are significantly more intense than expected. Source material contaminated with other drugs, such as fentanyl, benzodiazepines, amphetamines, or other compounds, can lead to serious side effects in a very short period of time.

Most arylcyclohexylamines kick in within 2 or 3 minutes when used intramuscularly. 

5. INTRAVENOUS INJECTION – Magic mushrooms online store

therefore, IV injection is the most common method used to administer ketamine in hospitals. The dose can be precisely measured and titrated to ensure consistent anesthesia for as long as necessary.

This form of administration carries the highest risk of introducing blood-borne pathogens like HIV or hepatitis. IV injections also carry the highest risk of resulting in overdoses if the dosage isn’t measured with precise accuracy.

Drugs administered via IV usually kick in within 1 minute or less. 

6. VAPED OR SMOKED – TCP (TENOCYCLIDINE)

Firstly, many members of the arylcyclohexylamine family can be vaped or smoked as well. In fact, one of the most common ways PCP is used today is by dipping a cigarette in a liquid solution of PCP.

Some of the PCP will be destroyed by combustion. A lot still ends up in the lungs and subsequently transferred into the bloodstream. Despite being one of the least efficient means of administration, smoking arylcyclohexylamines. It is still very affordable and provides powerful effects with just a few puffs. It costs an average of $5 to dip a cigarette in PCP. It can contain anywhere from 2–30 mg each.

Vaporizing arylcyclohexylamines is another popular means of administration. This is because users can control the temperature to prevent degradation. Even of the active ingredients due to extreme heat. Mesh-style vaporizers work best for this because you can apply the powder directly to the mesh heat screen. This also allows users to carefully and accurately measure out the desired dose.  Rather than leaving this up to guesswork with dipped cigarettes.

Lastly, the effects of vaping or smoking arylcyclohexylamines usually kick in within about 3 to 5 minutes.