Nootropics Pramiracetam cas 68497-62-1

Quick details

Name: Pramiracetam
Purity: 98% min
Appearance: White powder
CAS No.: 68497-62-1
Molecular Formula: C14H27N3O2·H2O 
Molecular Weight: 287.38
Usage: Smart enhancer
 
What Is Pramiracetam ?

Nootropics are a category of chemicals that are referred to as "Smart Drugs," which are proving to be advantageous as memory, neural, intelligences and cognitive enhancers, that are beneficial as supplements as well as therapeutic in the treating of certain diseases. Pramiracetam is one such Nootropic, defined as a lipid-soluble of the Racetams, which are identified by the sharing of a "pyrrolidone nucleus." Pramiracetam was patented in Belgium in 1978 and is remarked to be much stronger than its chemical "cousins," like Aniracetam or Piracetam. Pramiracetam has proven, over the last four decades, to be incredibly beneficial in restoring and maintaining overall health of the human brain.

99% Pharma Grade Piracetam for Improving Intelligence

Product name: Piracetam
Synonyms: IFLAB-BB F1918-0022;2-(2-OXOPYRROLIDIN-1-YL)ACETAMIDE;2-(2-OXOPYRROLIDINO)ACETAMIDE;2-OXO-1-PYRROLIDINEACETAMIDE;N-CARBAMOYLMETHYL-2-PYRROLIDINONE;PIRACETAM;1-Acetamido-2-pyrrolidinone;1-Pyrrolidineacetamide, 2-oxo- 
CAS: 7491-74-9 
MF: C6H10N2O2 
MW: 142.16 
EINECS: 231-312-7 
Chemical Properties White Solid 
Usage antinauseant 
Usage Nootropic. 
Usage: Nootropic. Biological Activity Nootropic that displays cognitive enhancing properties. Proposed to enhance neurotransmission via modulation of ion flux; Potentiates Na + influx through AMPA receptors. Facilitates efficiency of cholinergic neurotransmission at muscarinic receptors. 
Package: 25KG/cardboard drum
Biological Activity Nootropic that displays cognitive enhancing properties. Proposed to enhance neurotransmission via modulation of ion flux; potentiates Na + influx through AMPA receptors. Facilitates efficiency of cholinergic neurotransmission at muscarinic receptors. 

 Product introduction

Piracetam is a nootropic supplement that has the ability to enhance memory and has stood the test of time making it a popular choice for those that want to enhance their cognitive abilities. It is known to allow your creative and logical thoughts to run together into a stream of higher level thinking and can increase the amount of knowledge that your brain can retain for later access.


Benefits and Effects

Piracetam is most known for its ability to enhance cognitive function.

Piracetam won't make you more intelligent perse, but especially when combined with a choline supplement, it has the ability to improve your memory quite substantially. What piracetam does, in layman's terms, is increase the communication between the left and right part of your brain by increasing the blood flow between these two parts. Essentially, your logical thinking part of your mind will share more with the more imaginative part of your brain. This is why it increases memory in the brain. You can feel the fluidity of your thoughts increase, ideas seem to flow, if nootropics don't increase memory, I can certainly say they put your thoughts on a higher level.

Piracetam's effects are considered less strong compared to its more recent descendants but still remains a very popular choice for a well-rounded nootropic supplement. Many individuals use piracetam as a supplement to boost mental performance.

Dosage

Piracetam has a large range of effective doses. A low baseline dose of 400 mg is the bottom of most suggested servings, while 800 mg is the median which many people take in a single sitting. This amount can be repeated three times a day with zero toxicity effects.

Although not applicable to every individual, the standard dosage of piracetam is 1600 mg thrice a day in the starting. This dose may vary if the patient is a child. The recommended piracetam dosage varies based on the reason of use, usually ranging from 1.6-9.6 grams daily (2-12 pills daily). Some people report better results when taking 1-2 pills per hour for 4-6 hours or taking 4-8 pills at once for the first few days to notice an effect.

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Nootropic raw powder noopept for memory enhancement

Product Name: Noopept
CAS: 157115-85-0
Molecular formula C17H22N2O4
Molecular weight 318.37
Natural/Synthetic: Synthesis
Level: Pharmaceutical Grade
Content: 99.5%
Appearance: white powder
Packing: 5KG/Foil Bag
Ingredients: Ethyl N-(1-(phenylacetyl)-L-prolyl)glycine
Physicochemical properties: white crystalline powder
Category: Pharmaceutical Raw Materials
Field: Nootropic
Deferred Products: Puzzle Health Products
Use: Improve the memory and cognitive function

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99% Sunifiram (DM-235) Smart Drugs

Product Name: Sunifiram/ DM-235
Synonyms: 1-benzoyl-4-(1-oxopropyl)-; SunifiraM; 1-(4-Benzoyl-1-piperazinyl)-1-propanone; 1-Benzoyl-4-(1-oxopropyl)-piperazine; 1-(4-Benzoylpiperazin-1-yl)propan-1-one; 1-Benzoyl-4-propanoylpiperazine
CAS: 314728-85-3
MF: C14H18N2O2
MW: 246.30492
Appearance: White powder
Purity: 99.32%
Shelf life: 2 years
Standard: In-house Standard
Usage: For the treatment of Alzheimers Dementia, Cognition Disorder, Neurologic Drugs, Senile Dementia, Acetylcholine Release Enhancers.

Sunifiram (DM-235) is a piperazine derived research chemical which has anti-amnesiac effects in animal studies with significantly higher potency than piracetam. Sunifiram is a molecular simplification of unifiram. Based on in vitro and animal studies, it appears that sunifiram acts via AMPA-receptor activation.

Sunifiram operates by activating AMPA receptors; that is, the receptors that are responsible for the mediation of synaptic transmission in the central nervous system. Its mechanics also increases phosphorylation of AMPAR and NMDAR through protein kinase activation, which in turn enhances long-term potentiation - that is, an enhancement in signal transmission between two neurons resulting from simultaneous stimulation.
The kinase activation that is influenced by Sunifiram also improves cognitive defects. Additionally, Sunifiram works in the cerebral cortex of animal test subjects by assisting in the release of acetylcholine, the organic molecule that acts as a neurotransmitter in a host of various organisms. These operational mechanisms enable Sunifiram to exert anti-amnesiac properties.

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Nootropics Supplement 99% Coluracetam

Coluracetam is a choline uptake enhancer. It is also a derivative of piracetam-the first ever created nootropic drug. Numerous studies have shown its versatility in producing a range of benefits such as learning, learning and working improvement, neuroprotection, and treatment of Alzheimer's disease and schizophrenia. Dosing studies further revealed that daily repeated doses enhance its effects amongst its users.

Coluracetam funcction

1.Increases coordination.
2.Improves mood.
3.Helps fight fatigue.
4.Prevents oxidation within the brain.
5.Treats alcohol related brain damage.
6.Prevents caffeine withdrawal symptoms.

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Nutritional Supplement Creatine Monohydrate

Product name	Creatine monohydrate
Chemical name	Creatine monohydrate
CAS	6020-87-7
Molecular formula	C4H11N3O3
Molecular weight	149.15
Appearance	White powder
Package	1Kg/Foil Bag , 25Kg/Drum or As per your request
Storage	Store in cool and dry places ,keep away from strong light
Shelf life	2 years when properly stored
Safety	Non-toxic, non-stimulating, safe and reliable

What is Creatine monohydrate ?

Creatine monohydrate is a natural substance that turns into creatine phosphate in the body.
Creatine phosphate helps make a substance called adenosine triphosphate (ATP). ATP provides
the energy for muscle contractions;one of the most popular supplements used by people looking tobuild lean muscle mass, maximize performance and increase strength. 

98%+ Trestolone Acetate (MENT) powder

Trestolone acetate is a synthetic and injected anabolic–androgenic steroid (AAS) and a derivative of nandrolone (19-nortestosterone). It is an androgen ester – specifically, the C17 acetate ester of  Trestolone.

Trestolone Acetate Dosage

With a maximum dose of 50 mgs a day, users can anticipate considerable gains within three months of use. It is possible to increase strength levels and muscle mass with a weight gain of as much as 20 pounds in that time period.

About Trestolone Acetate Cycle Length, even a 2 week cycle will have significant results. 4-6 weeks is ideal if you want to maximize your progress without having to ramp up the dose. One of the main reasons guys don’t run longer than 6 weeks is because they can’t tolerate the sides. With Trestolone, those sides don’t exist. So longer runs should be feasible.

Trestolone should be between 25 mg and 50 / mg / day, or 50-100 mg / EOD.
Based on hypotheses, the ideal dose of Trestolone should be between 25 mg and 50/mg/day, or 50-100 mg/EOD. If this steroid were obtainable, it would be ideal to not only use an anti-aromatase, but Nolvadex as well. Trestolone stacked with testosterone (such as propionate) could be a very potent combination for real growth. However, there is not enough known about Trestolone yet to experiment with it for bodybuilding purposes.

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Epistane Methylepitiostanol

Epistane, exhibits a strong, long lasting anti-estrogen effect that is organ tissue specific. This means it works only where you want it to work. Broad range estrogen blockers and aromatase inhibitors can result in system shut down, aching joints, and decreased IGF-I expression. Epistane binds specifically to the 17-estradiol receptor protein in the target tissues. Because of its long lasting and strong effects on specific tissue,Epistane can significantly reduce and reverse the effects of gynocomastia because not only does Epistane specifically block estrogen in breast tissue but it induces an estrogen-depleted condition which leads to apoptosis or the death of the breast tissue cells. Studies show that small doses of the parent compound, Epitiostanol, at just 10-20mg/week showed a complete disappearance of the mass and pain in 25% of the male patients in the clinical trail, while the other 75% of the patients showed at least a 50% reduction in the mass and complete loss of pain in just 4-8 weeks. Thats results in 100% of the male users with no side effects.

Epistane is more than an anti-estrogen, though, as it also binds to androgen receptors in skeletal muscle. As a PRO-Anabolic compound Epistane promotes increases in strength and lean body mass with an anabolic/androgenic value (Q ratio) of 12. With most powerful androgens there is a high risk of the natural suppression of the gonads. Epistane, unlike other PRO-Anabolic compounds that have recently been released, is relatively mild on the gonads and, due to the anti-estrogenic effects and the fact that Epistane keeps LH levels elevated, post cycle therapy becomes a breeze.

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Prohormone powder Methyldienedione

Methyltrienolone is a steroid compound that is mostly unavailable on the market black or otherwise. The reason for its obscurity is because it is so highly toxic to the liver that even doses of as little as 2 mgs a week have caused jaundice of the liver. Besides its toxicity to the liver, it will also cause sexual dysfunction and can cause other compounds it is stacked with to exaggerate the effects of estrogen in the body. Although this compound is obviously dangerous and not recommended for use by anybody who values their health, it is worth noting that its muscle building and fat burning burning properties are on par with the highest-rated steroids available today.

Methyltrienolone application

1. Protection from gynomastia,
2. Increased drive/libido,
3. Enhanced intensity & focus,
4. Positive effects on strength

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Norandrostenedione Powder

Product Name:Norandrostenedione
CAS NO: 734-32-7
EINECS: 211-995-8
Molecular Formula: C18H24O2
Molecular Weight: 272.38
Density: 1.13 g/cm3
Boiling Point: 433.4 ° C at 760 mmHg
Melting Point: 169-172° C
Flash Point: 433.4 ° C at 760 mmHg
Standard: Enterprise standard
Color: white powder
Assay: 99.3%
Package: 1kg/AL bag

19-Norandrostenedione (4-estrene-3,17-dione, NOR) is a precursor of the anabolic steroids nandrolone. Until 2005 19-Norandrostenedione was available without prescription in United States, where it was marketed as a prohormone, but it is now classified as a Schedule III drug. It is also banned from use in many sports, including the Olympic Games, under the World Anti-Doping Code. 19-Norandrostenedione is readily metabolized to nandrolone after oral administration, but its potency to transactivate the androgen receptor dependent reporter gene expression is 10 times lower as compared to dihydrotestosterone (DHT).

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Methoxydienone Powder

Product name: Methoxydienone
CAS: 2322-77-2
EINECS Number: 219-034-4
Formula: C20H28O2
MW: 300.4351
Density: 1.09g / cm3
Boiling point: 448C at 760 mmHg
Flash Point: 188.8C
Vapor Pressure: 3.21E-08mmHg at 25C
Assay: 99%
Appearance:White powder
Usage: Methoxydienone particular to a process of synthesis of levonorgestrel,Levonorgestrel is a quick, short-term oral contraceptives, contraceptive mechanism is significantly inhibit ovulation and prevent embryo implantation, and to increase the consistency of the cervical mucus, sperm penetration resistance increases, and thus play a fast-acting contraception.

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Prohormone powder 1,4-Androstadienedione

1,4-Androstadienedione Description

Androstadienedione is obtained in high yield from both plant and animal sterols by biotransformation. The chemical is a common byproduct derived from other processes (e.g. vegetable oil deodorization and the production of lanolin fromwool processing). The product is produced in a single step via a simultaneous side-chain cleavage at the 17th positionand an alcohol oxidation in the 3rd position.

1,4-Androstadienedione Application

Chemical Properties White Crystalline Powder
Usage Boldenone related steroid; anabolic androgenic steroid

Androstadienedione ( Androsta-1,4-diene-3,17-dione ) is a next generation orally active prohormone. It is a direct precursor to the anabolic steroid boldenone. Boldenone is an anabolic steroid most often found in injectable form as a veterinary medication ( EQ ). It is chemically a derivative of testosterone. 1,4-androstadiene-3,17-dione converts to estrogen at roughly half the rate of androstenedione and testosterone. This significantly reduces the level of estrogen buildup during use compared to that achieved with testosterone precursors, and similarly also lowers the chance of noticing strong estrogen related side effects such as increased body fat, gynecomastia and definition hiding water retention. Androstadienedione is used as a pharmaceutical intermediate for further synthesis of female sex hormones, hormone replacement therapies and oral contraceptives.

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Prohormone powder 4-Androstenedione (4-Andro)

Another name: 4 - androstenedione; 4 - male (steroid)-ene -3,17 - dione;
CAS No: 63-05-8
Molecular Formula: C19H26O2
Molecular Weight: 286.41
Packing: 5kg (aluminum cans)
Specification: 99%  Heavy 10PPM Rotation +193 ° - +202 ° Loss on drying 0.5% impurity 1% steroid hormone
Characters: near white crystalline powder, soluble in ethanol, insoluble in water
Uses: Simplified hormone drugs, from the testis or urine extracted with the role of a male hormone steroids, norethisterone, testosterone propionate in the middle
Body, is widely used in small rheumatoid arthritis, diuretic, and a variety of contraceptive to control infectious inflammation.

Prohormone Steroids ndrostenedione is a steroid hormone . Also known as:  4-Androstene 3, 17-dione, Andro, Androstene, Androstenediona, Androsténédione. It is used to make medicine. Prohormone Steroids Androstenedione is used to increase the production of the hormone testosterone to enhance athletic performance , increase energy . keep red blood cells healthy , enhance recovery and growth from exercise , and increase sexual desire and performance.

Androstenedione is a steroid hormone produced by the adrenal glands, testes, and ovaries. It is a direct precursor of testosterone and estrogen in both men and women.

It is used as an alternative to anabolic steroids to:

• Increase testosterone levels
• Improve athletic performance
• Build muscle
• Increase energy
• Enhance recovery and growth from exercise
• Heighten sexual arousal and function

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Steroid hormones powder 7-Keto DHEA for Weight Loss

7-keto-DHEA is formed from dehydroepiandrosterone (DHEA) in the body. DHEA is a "parent hormone" produced by glands near the kidneys. But unlike DHEA, 7-keto-DHEA is not converted to steroid hormones such as androgen and estrogen. Taking 7-keto-DHEA by mouth or applying it to the skin does not increase the level of steroid hormones in the blood.

People take 7-keto-DHEA to speed up metabolism and heat production, which can promote weight loss. 7-keto-DHEA is also used to improve lean body mass and build muscle, increase the activity of the thyroid gland, boost the immune system, enhance memory, and slow aging. It is also used to treat depression, anxiety, and post-traumatic stress disorder (PTSD).

7-keto-DHEA might promote weight loss by speeding up the body’s metabolism and converting more energy to heat instead of storing it as fat.

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Prohormones powder 4-Dehydroepiandrosterone (4-DHEA)

DHEA Supplements for Anti-Aging

Since DHEA levels decline with age, some researchers speculate that supplementing your body's falling levels of the hormone might help fight aging. And some small studies have reported positive anti-aging effects from the use of DHEA supplements. But a similar number of studies have reported no effect.

• Building up the adrenal gland
• Strengthening the immune system
• Slowing natural changes in the body that come with age
• Providing more energy
• Improving mood and memory
• Building up bone and muscle strength

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Prohormones powder Dehydroepiandrosterone (DHEA)

Dehydroepiandrosterone (DHEA), also known as androstenolone, is an endogenous steroid hormone. It is one of the most abundant circulating steroids in humans, in whom it is produced in the adrenal glands, the gonads, and the brain.

DHEA is also said to slow up the aging process, improve sports performance, enhance libido, promote weight loss, and bolster the immune system. In addition,DHEA supplements are frequently marketed as testosterone-boosting agents and used for such purposes as increasing muscle mass and reducing fat mass.

Dehydroepiandrosterone is a precursor hormone, which means it has little biological effect on its own, but has powerful effects when converted into other hormones such as testosterone. Dehydroepiandrosterone is produced from cholesterol mainly by the outer layer of the adrenal glands, known as the adrenal cortex, although it is also made by the testes and ovaries in small amounts. It circulates in the blood, mainly attached to sulphur as dehydroepiandrosterone sulphate, which prevents the hormone being broken down. In women, dehydroepiandrosterone is an important source of oestrogens in the body – it provides about 75% of oestrogens before the menopause, and 100% of oestrogens in the body after menopause. 

Dehydroepiandrosterone production increases from around nine or ten years of age, peaks during the 20s and gradually decreases into old age. Dehydroepiandrosterone is also produced in small amounts by the brain, although its precise role there is not clear.

Epiandrosterone Supplements for Fat Burner

Epiandrosterone is a prohormone that is completely legal and available over the counter. It may also appear under the name 3b-hydroxy-etioallocholan-17-one. Epiandrosterone is a precursor to Stanolone, a powerful steroid hormone. Epiandrosterone can be found naturally occuring in most mammals and is excreted in urine as a normal part of human metabolism. One of the reasons that this prohormone is legal because it has been found to be naturally occurring in pine pollen. Epiandrosterone and Androsterone are very closely related. Androsterone is the 3-alpha isomer and epiandrosterone is the 3-beta isomer of this compound. The actions of the two isomers in the body are different, but still very similar. Most epiandrosterone supplements are actually a mix of the two isomers, meaning that they contain some androsterone as well as the main ingredient epiandrosterone.

Epiandrosterone is a dehydroepiandrosterone metabolite and a precursor of testosterone and estradiol with hypolipidemic and anabolic property,also commonly known as Epi-Andro or 3β-androsterone.It is naturally produced by the enzyme 5α-reductase from the adrenal hormone DHEA,and can also be converted from the natural steroids androstanediol via 17β-hydroxysteroid dehydrogenase or from androstanedione via 3β-hydroxysteroid dehydrogenase.It was first isolated in 1931 and has been shown to naturally occur in most mammals including pigs. Epi-Andro is non-methylated and as a result will put little to no stress on the user's liver. DHT is 5 times more Androgenic than testosterone. As a dry compound, users will experience lean muscle gains while also increasing lipolysis.

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Trenavar / Trendione CAS 4642-95-9

Average Dose:
60-120mg/day standalone
30-60mg/day when stacked
Average Cycle Length:4-6 weeks

Estra-4,9,11-triene-3,17-dione (Trenavar, Trendione) was released in late 2011 by PHF/IBE and is represented as a true prohormone to Trenbolone, differing only by a ketone at the 17 position. Similar to other 17-one prohormones, this ketone is the target of 17b-HSD1, hydrogenating the compound to yield active Trenbolone.

What this means is that although Trenavar is a prohormone to trenbolone, it doesn't appear to be a significant metabolite in humans. The equilibrium of the reaction between 17-one and 17b-ol appears to be weighted heavily - in fact pretty much exclusively - in favour of the 17b-ol, so Trenavar should convert readily to the active form trenbolone. Once converted to trenbolone, it will be open to the same metabolism mechanisms as injectable tren - conversion via sulfatase to epitrenbolone and excretion as glucoronides.

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Prohormone powder Methylstenbolone

WHAT IS METHYLSTENBOLONE? 
 

Methylstenbolone or M-Sten is a mass-building prohormone that helps users gain size and strength without sacrificing definition.  M-Sten is derived from DHT, so it doesn’t convert to estrogen, resulting in little to no water retention. 

Methylstenbolone is methylated, so liver toxicity is associated with this compound. Taking a Cycle Support product can help minimize or eliminate the potential for side effects while on cycle.

Following a healthy diet, training intensely, and proper use of M-Sten can result in gains of 5-20 lbs of lean muscle mass during a cycle.

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Methylhydroxynandrolone (MHON)

Manufacturer: RAWSGEAR
Effective Dose (Men): 10-30 mg/day
Half-Life: Approx. 12 Hours

MOHN comes in tablet form for oral administration, and is generally found in 5 mg tablets. Neither MOHN, nor any of its generic versions are still being commercially manufactured as prescription medications.

Dose

Due to a high milligram for milligram potency, the typical effective daily dosage is comparatively lower than most orals. For example, recommended dosages for Anavar, Winstrol and Turinabol are all within the 50-100 mg/day range. Even the legendary mass building Dianabols average dosage of 20-40 mg, is considered high with regard to MOHNs recommended 10-30 mg per day for 6-8 weeks.

 Information

MOHN is a very adaptable compound that can be easily incorporated into all types of cycles, during both bulking and cutting phases of training. When used within mass building cycles its usually stacked with testosterone enanthate, Dianabol, Anadrol, and Equipoise. In cutting cycles its often combined with short-ester injectable anabolic steroids such as testosterone propionate, Stanozolol, Anavar, and Boldenone Acetate but there is virtually no limit to its applications.

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Local Anesthetic Chloroprocaine HCl CAS 3858-89-7

Chloroprocaine hydrochloride is a local anesthetic given by injection during surgical procedures and labor and delivery. Chloroprocaine, like other local anesthetics, blocks the generation and the conduction of nerve impulses, presumably by increasing the threshold for electrical excitation in the nerve, by slowing the propagation of the nerve impulse and by reducing the rate of rise of the action potential.

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Local Anesthetic Mepivacaine HCl CAS 1722-62-9

Mepivacaine is a local anesthetic of the amide type. Mepivacaine has a reasonably rapid onset (more rapid than that of procaine) and medium duration of action (shorter than that of procaine) and is marketed under various trade names including Carbocaine and Polocaine.

A local anesthetic that is chemically related to bupivacaine but pharmacologically related to lidocaine. It is indicated for infiltration, nerve block, and epidural anesthesia. Mepivacaine is effective topically only in large doses and therefore should not be used by this route. 

Local anesthetics block the generation and the conduction of nerve impulses, presumably by increasing the threshold for electrical excitation in the nerve, by slowing the propagation of the nerve impulse, and by reducing the rate of rise of the action potential. In general, the progression of anesthesia is related to the diameter, myelination, and conduction velocity of affected nerve fibers. Clinically, the order of loss of nerve function is as follows: pain, temperature, touch, proprioception, and skeletal muscle tone.

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