U-48800 is an opioid analgesic drug analog of originally U-47700, simply introducing one methylene at the benzene ring,on an equal time, 2,4-dichlorophenyl replaced the 3,4-dichlorophenyl.

Buy u-48800 online is selective for the µ-opioid receptor, having around 7.5 x the potency of morph in animal fashions. research results show that U-48800 has the same potency level as at the beginning U-47700. Use for laboratory studies best, no longer for human consumption.

U-47700 studies chemicals

U-47700 is a legal dressmaker chemical or research chemical, we are official chemicals dealer and suppliers offering U-47700 studies chemical substances for 5 years. by purchasing at our online shop site you’ll get a safe and clean buying enjoy, and that is where to shop for satisfactory and reasonably-priced china research chemical, America Europe UK Nederland Canada studies chemical resources. please sense free to purchase U-47700 from us .U-47700 is derived from AH-7921. U-47700 is selective for the µ-opioid receptor, having around 7. five x the potency of morphine in animal fashions.

 Approximately U-47700 studies chemical

U-48800

U-47700 receives the systematic and formal IUPAC call 3,four-Dichloro-N-[(1R,2R)-2-(dimethylamino)cyclohexyl]-N-methylbenzamide. It offers a molar mass of 329.27 grams plus an empirical chemical formula of C16H22Cl2N2O. U47700 is part of the drug magnificence opioid analgesics. in particular, U47700 is a number of the benzamide sort of opioids. It isn’t used medically however within research.

In animal models, Buy u-48800 online become proven to possess a potency of 7.5 events extra than the classical medicinal opiate morphine. It had been initially created by means of several researchers within the pharmaceutical firm Upjohn 4 many years in the past. This compound isn’t fit for human or animal intake. U47700 can be a structural analog from the sooner opioid AH-7921.

Pharmacologically U47700 may be a selective agonist in the ì-opioid receptor getting a Kd of five. three nM instead of an appreciably weakened binding interaction inside the kappa opioid receptor wherein U47700 has a completely Kd fee of 910 nM. online reports even though subjective and unverifiable do suggest numerous characteristics of the chemical substance.

U47700 is reported to provide feelings of pleasure, pain comfort, and suppression of hysteria. a number of customers have reported effects just like the broadly mistreated pharmaceutical oxycodone.

pleasure is mentioned as a decrease whilst in comparison with morphine or heroin. the feeling produced is known as emotions of °warm temperature ± and °comfort ± which matches the use of your body. U47700 is pronounced as causing considerably extra sedation than comparable opiates like oxycodone or hydrocodone.

Different outcomes include domestic loan commercial enterprise libido, constriction inside the students, problem urinating, suppression of cough, and constipation. this will be in conjunction with the general unwanted effects of opiates. U47700 may want to motive boom the danger for skin sense completely itchy because of relieve histamine.
Respiratory gadget system despair may be a serious side-after impact of numerous opioids and makes up for the lethality of people compounds.

regardless of there being no formal research on the physiological motion of U47700 in humans, anecdotal reports indicate an inclination of U47700 to supply plenty more powerful respiratory system depression than heroin or morphine.

This makes U47700 a dangerous compound and customers need to technique with careful interest. At low doses, it’s pronounced that U47700 slows the breath fairly and won’t produce a very great impairment.

U47700 functions marked toxicity in compliance with dose because of its extreme potency while compared with traditional opioids and opiates. This makes it an ideal leisure compound with a large possibility of accidents for the purchaser. therefore warning needs to be worked out regarding the dose. Lethality inside the compound may also be exacerbated by way of concurrent utilization of different depressants for example alcohol, benzodiazepines, GHB/GBL, and dissociatives for example ketamine.

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What is thirtylone used for?

Thirtylone is listed as a research chemical and has found applications in forensic science and mass spectrometry.

THIRTYLONE is usually used for recreational purposes and is known to be a stimulant substance in nature. It can cause Color enhancement and increase the ability of the person to perceive colors. It can produce the feelings of Empathy and feelings for wellbeing of other people. It is also used for causing Entactogenic effects while it also gives the users Inner peace and Tranquility when administered.

The overall effect of the drug is the feeling of connectedness with others and the world. It is used in distress and depression for the people as it can be a potent stress –release drug.

The drug is also known to be used by people for recreational purposes.

Effects of Thirtylone

Thirtylone has wide range of effects ranging from physical and cognitive. While it can be used for relief from depression it’s one of the negative effects is depression itself. It can cause anxiety and hypertension on misuse. The drug is also known to cause high temperature and heart problems while Paranoia and Nausea are also among some of the side effects of the disease. In rare and extreme cases the drug is known to cause mild hallucinations on administration.

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4-CL-PVP is another research compound and is characterized in a group of energizers. The chemical formula for 4-CL-PVP is C15H20ClNO with an IUPAC name of 1-(4-chlorophenyl)- 2-(pyrrolidin-1-yl) pentan-1-one 265.12 and a sub-atomic mass of 265.12.

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Pseudoephedrine is in a class of medications called nasal decongestants, which cause smooth muscles around the airway and nasal cavity to relax, allowing more air to flow through. It also causes blood vessels to contract. Pseudoephedrine is also sometimes used “off-label” to treat urinary or stress incontinence and to prevent ear pain and blockage from pressure changes due to elevation or scuba diving.

cheap pseudoephedrine

Pseudoephedrine (PSE) is a safe and effective active ingredient found in leading cold, allergy, and sinus medicines to provide congestion relief. While over 18 million American families rely on these medicines every year, PSE can also be used in the illegal manufacture of methamphetamine. As a result, some policymakers and law enforcement officials in a number of states support requiring a doctor’s prescription to obtain PSE-containing medicines, even though the vast majority of these medicines are sold to law-abiding consumers.

Depending on the medication, pseudoephedrine may be paired with other drugs. For instance, the active components of the allergy medication Zyrtec-D are pseudoephedrine and the antihistamine cetirizine hydrochloride.

Advil Cold and Sinus contains pseudoephedrine and ibuprofen, a non-steroidal anti-inflammatory drug (NSAID) for pain and swelling. Pseudoephedrine can be used to make methamphetamine, or meth, a powerful and highly addictive stimulant. For many years, the drug was available over-the-counter (OTC) without prescription or restrictions.

Probenecid, also sold under the brand name Probalan, is a medication that increases uric acid excretion in the urine. It is primarily used in treating gout and hyperuricemia.

It was developed as an alternative to caronamide to competitively inhibit renal excretion of some drugs, thereby increasing their plasma concentration and prolonging their effects.

It is primarily used to treat gout and hyperuricemia.

It is sometimes used to increase the concentration of some antibiotics. Specifically, a small amount of evidence supports the use of intravenous cefazolin once rather than three times a day when it is combined with probenecid.

It has also found use as a masking agent, potentially helping athletes using performance-enhancing substances to avoid detection by drug tests.

Some of the important clinical interactions of probenecid include those with captopril, indomethacin, ketoprofen, ketorolac, naproxen, cephalosporins, quinolones, penicillins, methotrexate, zidovudine, ganciclovir, lorazepam, and acyclovir. In all these interactions, the excretion of these drugs is reduced due to probenecid.

This product is intended for forensic and research applications.
This product has been manufactured and tested to meet ISO17025:2005 and Guide 34:2009 guidelines
This product is intended to be used as an analytical reference standard
Bulk material is available for academic research at qualified institutions; please contact our sales department for pricing

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This product is a white amorphous lump or a crystalline mass with a faint odor of bitter almonds. Density 1.52 g / cm3 Toxic by skin absorption through open wounds, by ingestion. Heating to decomposition produces toxic fumes. Used for gold and silver extraction, in chemical analysis, to make other chemicals, and as an insecticide.

It is a cyanide salt-containing equal numbers of potassium cations and cyanide anions. It has a role as an EC 1.9.3.1 (cytochrome c oxidase) inhibitor, an EC 1.15.1.1 (superoxide dismutase) inhibitor, and a neurotoxin. It is a cyanide salt, a one-carbon compound, and a potassium salt.

This product is highly toxic. The moist solid emits small amounts of hydrogen cyanide due to hydrolysis, which smells like bitter almonds. Not everyone, however, can smell this; the ability to do so is a genetic trait.

The taste of potassium cyanide has been described as acrid with a burning sensation.

DOSAGE | OVERDOSE

The minimum lethal dose can be ingested in (50mg/kg) or (100mg/kg) for a guaranteed effect. When ingested, Potassium Cyanide releases hydrogen cyanide gas which is highly poisonous and reacts by completely capturing the whole body and its sensitive organs such as the brain, heart and central nervous system.

If cyanide is taken overly (overdose) consequently the victim will fall into a comma or go unconscious after a few seconds, thus might also witness symptoms such as dilated or red eyes and colored chicks or in extreme cases will witness convulsions while the patient is still alive, generally, at this stage, the hearth and other sensory organs will stop working.

Phenobarbital, also known as phenobarbitone or phenobarb, is a medication recommended for the treatment of certain types of epilepsy in developing countries In the developed world it is commonly used to treat seizures in young children, while other medications are generally used in older children and adults. It may be used intravenously, injected into a muscle, or taken by mouth. The injectable form may be used to treat status epilepticus. It is occasionally used to treat trouble sleeping, anxiety, and drug withdrawal and to help with surgery.

Medical uses
It is used in the treatment of all types of seizures except absence seizures. It is no less effective at seizure control than phenytoin, however phenobarbital is not as well tolerated. It may provide a clinical advantage over carbamazepine for treating partial onset seizures. Carbamazepine may provide a clinical advantage over phenobarbital for generalized onset tonic-clonic seizures.

It  is the first-line choice for the treatment of neonatal seizures.

It is sometimes used for alcohol detoxification and benzodiazepine detoxification for its sedative and anticonvulsant properties. The benzodiazepines chlordiazepoxide (Librium) and oxazepam (Serax) have largely replaced phenobarbital for detoxification.

It’s properties can effectively reduce tremors and seizures associated with abrupt withdrawal from benzodiazepines.

This product is intended for forensic and research applications.
This product has been manufactured and tested to meet ISO17025:2005 and Guide 34:2009 guidelines
This product is intended to be used as an analytical reference standard
Bulk material is available for academic research at qualified institutions; please contact our sales department for pricing