Since Restandol (Andriol) is quickly eliminated by

the body it should also be considered for use before competitions requiring doping tests. Women should avoid Restandol (Andriol) since the androgenic component common with testosterone is also strongly developed in this compound. Restandol (Andriol) intake can occasionally lead to high blood pressure, retention of fluids, acne, sexual over stimulation, and, in women, the well known virilization symptoms.

Wrinkle removal

Withdrawal of treatment leads to gradual reversal of effect within 12 months.

Ara-Test 25 mg/ml, 10 ml; Aranda Laboratories Mexico

DO NOT TAKE CIALIS:

Reductil precautions

Tadalafil is currently undergoing clinical trials for the treatment of pulmonary hypertension. The clinical trials are based on tadalafil's inhibitiong of PDE5. It is hoped that by inhibiting this enzyme, tadalafil will prove effective in opening up blood vessels in the lungs, lowering pulmonary arterial resistance and pressure, and thus reducing the workload of the right ventricle of the heart.

Testosterone is still number one steroid for building mass and can help anyone to within a short time increase his strength and weight. It aromatises in high dosages therefore, it is wise to use it with antiestrogens

such as Proviron, Nolvadex or Arimidex. Most people will experience water retention which can be also minimized with antiestrogen products. Gynocomastia and water retention are the most common side effects and should be watched for. Being an injectable testosterone, liver values are generally not elevated much by this product. The typical side effects can include nausea, acne, excitation or increased aggressiveness, chills, hypertension, increase in libido. Users often report less gyno trouble, lower water retention and commonly claim to be harder on it than with the others.

Warning! If your erection lasts

longer than 4 hours (priapism), consult a doctor immediately. Treatment of this condition should not be delayed more than 6 hours, as this can cause damage to the erectile tissue in the penis and irreversible erectile dysfunction. Regular check-ups with your doctor are recommended to detect any signs of fibrous tissue formation in the penis. Do not use this medicine more than once a day and no more than three times a week. Re-constituted solutions of alprostadil are for single use only. Any remaining solution should be discarded carefully, as instructed by your doctor, and not be kept for a second injection. This medicine

will not prevent pregnancy and a reliable form of contraception should be used by couples who do not wish to conceive. Follow the printed instructions you have been given with this medicine. This medicine will not protect you or your partner from sexually transmitted diseases. Using a condom can provide this protection. This is particularly important since the injection can cause bleeding, which increases the risk of disease transmission. Use with caution if you have a history of Blood clotting disorders. Coronary artery disease. Heart failure. Drug dependence or abuse. Psychiatric illness. Small temporary strokes (transient
ischaemic attacks). Lung disease. Not to be used in Children. Conditions in which sexual activity is not advisable, for example severe heart disorders. Conditions such as sickle cell disease, bone cancer or leukaemia in which there is an increased risk of prolonged erections (priapism). Men who have an implant in their penis. Physical abnormality of the penis, such as severe curvature, scarring or Peyronie's disease. Women. This medicine should not be used if you are allergic to one or any of its ingredients. Please inform your doctor or pharmacist if you have previously experienced such an allergy. If you feel you have experienced
an allergic reaction, stop using this medicine and inform your doctor or pharmacist immediately. Side effects Medicines and their possible side effects can affect individual people in different ways. The following are some of the side effects that are known to be associated with this medicine. Because a side effect is stated here, it does not mean that all people using this medicine will experience that or any side effect. Pain in the penis. Blood clots which form a solid swelling at the injection site (haematoma). Formation of fibrous tissue within the penis. Persistent painful erection of the penis (priapism). Redness,
swelling or itching at the injection site. Tightening of the foreskin. Pain in the testicles. Inflammation of the end of the penis (balanitis). Yeast infection. Urethral bleeding. Urgent need to pass urine. Abnormal ejaculation. Low blood pressure (hypotension). Abnormal heart beats (arrhythmias). The side effects listed above may not include all of the side effects reported by the drug's manufacturer. For more information about any other possible risks associated with this medicine, please read the information provided with the medicine or consult your doctor or pharmacist. How can this medicine affect other medicines?

This medicine should not be used with any other treatment for erectile dysfunction. People taking medicines to prevent the blood clotting (anticoagulants), such as warfarin and heparin, may have an increased risk of bleeding after the injection.

Indications

Take this medicine by mouth as needed between four hours and one-half hour before sexual activity (about 1 hour before is most effective); or take as directed by your doctor. Do not take this medicine more often than once daily as needed. A high fat meal may delay the time of onset of this medicine.

Clenbuterol should therefore be used primarily

for fat loss and cutting purposes.

Andriol testocaps are the oral form of Testosterone Undecanoato. While not considered to be as good as the injectable form of the compound, as they do more damage to your liver than the injectable form (as do all steroids), Andriol Testocaps do removew the need for regular (or any) injections.

Anavar should be taken two to three times daily after meals thus assuring an optimal absorption of the oxandrolone. Common dosage is 8-12 tablets in men and 5-6 tablets in women. The rule of thumb to take 0.125 mg./pound of body weight daily has proven successful in clinical tests.

Effective Dose: 1IU per 10-20 lbs. of body weight.

So why else may you keep such a high proportion of what you gained on ´var? Well, I think it may be due to it´s relatively light impact on the HPTA, which brings me to my final point; Bonavar will not totally shut down your HPTA, especially at lower doses (unlike testosterone, which will eventually do this even at a 100mg dose, or deca which will do it with a single 100mg dose). This could be due, at least partly, to the fact that Bonavar doesn´t aromatize (convert to estrogen).

Both Deca and Dianabol rely on quality protein intake.

Steak has a particular affinity with this combination and further contributes to raw power and growth.Dianabol will convert your protien intake to raw size so be sure to consume a protein drink and eat chicken and steak and eat well!!

by Damian Bachs

Tablet Core: lactose monohydrate, croscarmellose sodium, hydroxyproplycellulose, microcrystalline cellulose, sodium laurilsulfate, magnesium stearate.

American athletes have a long a fond relationship with Testosterone cypionate. While Testosterone enanthate is manufactured widely throughout the world, cypionate seems to be almost exclusively

an American item. It is therefore not surprising that American athletes particularly favor this testosterone ester. But many claim this is not just a matter of simple pride, often swearing cypionate to be a superior product, providing a bit more of a "kick" than enanthate. At the same time it is said to produce a slightly higher level of water retention, but not enough for it to be easily discerned. Of course when we look at the situation objectively, we see these two steroids are really interchangeable, and cypionate is not at all superior. Both are long acting oil-based injectables, which will keep testosterone
levels sufficiently elevated for approximately two weeks. Enanthate may be slightly better in terms of testosterone release, as this ester is one carbon atom lighter than cypionate (remember the ester is calculated in the steroids total milligram weight). The difference is so insignificant however that no one can rightly claim it to be noticeable (we are maybe talking a few milligrams per shot). Regardless, cypionate came to be the most popular testosterone ester on the U.S. black market for a very long time

The propionate ester used with this compound will extend its activity for only a few days. With such a short

duration of effect, injections need to be repeated at least every 3 or 4 days in order to maintain a consistent level of hormone in the blood. Factoring this in with its low strength (50 mg/ml), men will generally inject a full 2 ml ampule of Masteron (100 mg) every two or three days. The weekly dosage therefore lands in the range of 200-350 mg, a level more than sufficient to receive good results. We also should mention that while some women do profess to using this item before a show, it is much too androgenic in nature to recommend. Virilization symptoms can result quickly with its use, making Masteron a very risky item
to experiment with. If attempted, the dosage should be limited to no more than 25 to 50 mg each week. The female athlete would be further served by increasing the number of days between injections to prevent buildup of steroid in the body. In this case, Masteron can perhaps be administered once every 7 days.

Effective Dose: 25-100 mcg / day orally

The information on this site is not intended to substitute for professional medical advice. Be sure to contact your physician, pharmacist or other health care provider for more information about this medication.

Winstrol depot is very popular anabolic

steroid and is a derivative of DHT. It is a relatively low androgenic steroid which does not seem to aromatize. It can be toxic to the liver in excessive dosages. Winstrol Depot is manufactured by Winthrop in USA and by Zambon in Europe.

Brand Names: Broncodil, Broncoterol, Cesbron, Clenasma, Clenbuter, Pharmachim, Contrasmina, Contraspasmina, Monores, Novegam, Oxyflux, Prontovent, Spiropent, Ventolase, Ventapulmin... Is available in 10-20 mcg tablets. Clenbuterol is known as a sympathomimetic. These hormones are taken to mimic adrenaline and noradrenaline in the human body. Clenbuterol is a selective beta-2 agonist that

is used to stimulate the beta-receptors in fat and muscle tissue in the body.

Trenbolones chemical structure makes it resistant to the aromatize enzyme (conversion to estrogen) thus absolutely no percentage of trenbolone will convert to estrogen. Trenbolone administration would not promote estrogenic side effects such as breast tissue growth in men (gynecomastia, bitch tits) accelerated fat gain, decline in fat break down and water retention trenbolone. Trenbolone is also resistant to the 5- alpha-reductase enzyme, this enzyme reduces some steroid hormones into a more androgenic form, in trenbolones case however this

does not matter, trenbolone boasts an androgenic ratio of 500, it can easily cause adverse androgenic side effects in any steroid.com members who are prone cases of hair loss, prostate enlargement, oily skin and acne have been reported. Unfortunately trenbolones potential negative side effects do not end there. Trenbolone is also a noted progestin: it binds to the receptor of the female sex hormone progesterone (with about 60% of the actual strength progesterone). In sensitive steroid.com members this can lead to bloat and breast growth worse still, trenbolones active metabolite17beta-trenbolone has a binding affinity to the
progesterone receptor (PgR) that is actually greater than progesterone itself. No need to panic though, the anti-estrogens letrzole or fulvestrant can lower progesterone levels, and combat any progestenic sides. The use of a 19-nor compound like trenbolone also increases prolactin&. bromocriptine or cabergoline are often recommended to lower prolatin levels. Testicular atrophy (shrunken balls) may also occur; HCG used intermittently throughout a cycle can prevent this. It is also wise for Tren users to closely monitor their cholesterol levels, as well as kidney function and liver enzymes, as Tren has the potential to negatively

affect all of those functions. Trenbolone, being a powerful progestin, will also shut down natural testosterone production which even a relatively small dose and keep the testosterone level suppressed for an extended period of time, this can lower libido and cause erectile dysfunction (fina dick). It is essential that you always stack trenbolone with testosterone.

Clomiphene Citrate (Clomid®): Description

Special precautions

HCG is a glycoprotein that is secreted in the urine by pregnant women. It is legally used as a fertility drug for women to help induce ovulation. This drug is used by male athletes

to elevate natural levels of testosterone production, mostly after a steroid cycle. This drug is used to kick start your testosterone after a cycle. While on steroids for long periods of time (more than 3 - 4 weeks) your natural testosterone shuts down. A shot of this each week for 2 weeks straight will get things going again. It should be used for no more than 2 weeks at a time because it also raises a male's natural production of estrogen. For that reason take some Nolvadex with it also. HCG is always packaged in 2 different vials, one with a powder and the other with a sterile solvent. These vials need to be mixed before

injecting.

Drug Class: Leutenizing Hormone (LH) - Gonadotropin

It tells us that we should use IGF-1 to make more muscle cells. It's the only thing that can give it to us and more cells is more growth, which is our goal.

Proviron has four distinct uses in the world of bodybuilding. The first being the result of its structure. It is 5-alpha reduced and not capable of forming estrogen, yet it nonetheless has a much higher affinity for the aromatase enzyme (which converts testosterone to estrogen) than testosterone does. That means in administering it with testosterone or another aromatizable compound,

it prevents estrogen build-up because it binds to the aromatase enzyme very strongly, thereby preventing these steroids from interacting with it and forming estrogen. So Mesterolone use has the extreme benefit of reducing estrogenic side-effects and water retention noted with other steroids, and as such still help to provide mostly lean gains. Its also been suggested that it may actually downgrade the actual estrogen receptor making it doubly effective at reducing circulating estrogen levels.

Tiratricol is available from Genesis Meds, 50tbs/bottle, 1mg/tb.

In May 2005, the U.S. Food and Drug Administration

found that tadalafil (along with other PDE5 inhibitors) could lead to vision impairment in certain patient groups, including diabetics. An investigation is currently ongoing.

For most men, the recommended dose is 50 mg. taken, as needed, approximately 1 hour before sexual activity. However, sildenafil citrate may be taken anywhere from 4 hours to 0.5 hour before sexual activity. Based on effectiveness and toleration, the dose may be increased to a maximum recommended dose of 100 mg or decreased to 25 mg. The maximum recommended dosing frequency is once per day.

StanolV 10 mg tab; Ttokkyo Labs

Trenbolone

also has a very strong binding affinity to the androgen receptor (A.R), binding much more strongly than testosterone. This is important, because the stronger a steroid binds to the androgen receptor the better that steroid works at activating A.R dependant mechanisms of muscle growth. There is also strong supporting evidence that compounds which bind very tightly to the androgen receptor also aid in fat loss. Think as the receptors as locks and androgens as different keys, with some keys (androgens) opening (binding) the locks (receptors) much better than others. This is not to say that AR-binding is the final word on a
steroid´s effectiveness. Anadrol doesn´t have any measurable binding to the AR& and we all know how potent Anadrol is for mass-building.

Boldenone is very common in the precontest arena for two main reasons. First off, there is a low amount of aromitization and secondly there is very little water retention while taking Boldenone (Equipoise). This makes Boldenone (Equipoise) a good precontest steroid. Boldenone is well known to give a good increase in the pumps you get while working out. This is caused from the increase in red blood cells that you will experience while taking Boldenone. It is also well known

to help cause a dramatic increase in appetite. When taken with a good mass building steroid like Dianabol, this is a sure formula for successful gains in muscle mass.

Phentermine Side Effects

Danabol / Dianabol is an orally applicable steroid with a great effect on the protein metabolism. Danabol / Dianabol has a very strong anabolic and androgenic effect giving a great buildup of strength and muscle mass in its users. The additional body weight consists of a true increase in tissue and, in particular, in a noticeable retention of fluids.

Sexual activity may put extra strain on your heart, especially

if you have heart problems, if you have heart problems and experience any serious side effects while having sex, stop having sex and tell your doctor immediately. These side effects include severe dizziness, fainting, chest pain, or nausea. In the unlikely event that you have a painful or prolonged erection (lasting more than 4 hours), stop using this medicine and seek immediate medical attention or permanent problems could occur.

Loeffler: Cypiotest L/A (MX) - 250 mg/ml

Winstrol comes in 50 mg/cc, 2 mg/tab or 5mg/tab. Winstrol Depot is manufactured by Winthrop in USA and by Zambon in Europe. Winstrol depot

is very popular anabolic steroid and is a derivative of DHT. It is a relatively low androgenic steroid which does not seem to aromatize. It can be toxic to the liver in excessive dosages. Very few user report water retention or any other side effects. It is a popular all purpose steroid; many stack with Primobolan depot for cutting, others stack it with testosterone for size and strength gains. Women often use winstrol depot but occasionally it can cause virilization, even at low dosages. Users report that the muscle gains they make are solid, they are well retained after the drug use is discontinued. Athletes also find that
the injectable version is far superior to the oral. Dosages range from 3-5 ccs per week for men, 1-2 ccs in women. Oral dosages are usually in the area of 16-30 mg per day for men, 4-8 mg for women.

How often can I take KAMAGRA?

It is important to stress that a cycle should last no longer than 6 weeks and it should never be halted abruptly. As slowly as the dosage was built up it should also be lowered, one tablet every 3-4 days. Taking CytomelŽ for too long and/or at too high a dosage can result in a permanent thyroid deficiency. After doing such, one might need to be treated with a drug like CytomelŽ for

life. It is also a good idea to first consult your physician and have your thyroid function tested. An undiagnosed hyperfunction would not mix well with the added hormone. An athlete should also be sure never to purchase an injectable form of the drug. It is generally an emergency room product, much too powerful for athletic use. Since T-3 is the most powerful thyroid hormone athletes are using, this is generally not the starting point for a beginner. Before using such a powerful item, it is a good idea to become familiar with a weaker substance. The highly popular Triacana is very mild, allowing the user much more latitude

(from severe side effects) than CytomelŽ. An in-between point is Synthroid (synthetic T-4), still weaker in action than CytomelŽ. Once the user is ready however, the fat burning effect of this hormone can be extremely dramatic.

Insulin is a hormone which is manufactured in the pancreas and which has a number of important physiological actions in the body. It is an essential hormone in maintaining the body's blood glucose level so that the brain, muscles, heart and other tissues are adequately supplied with the fuel they require for normal cellular metabolism and normal function. Insulin also plays an essential role in

fat and protein metabolism. For example, it promotes transport of amino acids from the bloodstream into muscle and other cells. Within these cells, insulin increases the rate of incorporation of amino acids into protein (amino acids are the building blocks of protein) and reduces protein break down in the body ("catabolism"). These physiological actions probably form the basis of speculation regarding the additional anabolic gains which might be made through the use of exogenously administered insulin.

Longer intake of anadrol and/or higher doses can cause a yellow discoloration of fingernails, eyes, or skin.

The liver enzyme gamma-GT also reacts sensitively to the oxymetholone, causing it to elevate. If high dosages of anadrol are taken over a long period, there is an increased risk that the described liver changes could end up damaging the liver. During the intake of Androlic / Anadrol 50, the liver values as well as the LDH/HBDH quotient, should always be checked by a competent physician. Oxymetholone is the only anabolic/androgenic steroids which has been linked with liver cancer.

It appears to cause less inhibition than Deca or testosterone for any given degree of anabolic effect, perhaps because of low CNS activity,

lack of conversion to DHT, and lack of aromatization to estrogen. Unlike Deca, it is not metabolically deactivated by 5a-reductase and therefore is not as kind to the skin and hair as that drug. However, when used by itself at modest doses, by suppressing natural testosterone and DHT production, it can improve skin relative to using no anabolic steroids at all.

Sexual function

Primobolan, I believe, should be considered a superior compound, offering the same activity at (usually) a lower price and without the alkylated-toxicity issue.

Third, and often overlooked, is the fact that STH strengthens the

connective tissue, tendons, and cartilages which could be one of the main reasons for the significant increase in strength experienced by many athletes. Several bodybuilders and powerlifters report that through the simultaneous intake with steroids STH protects the athlete from injuries while inereasing his strength.

DNP accomplishes the astounding boost in metabolic rate via inhibition of the F0F1 ATP synthase molecule, located in the inner wall of each mitochondrion. While the electron transport chain still functions to pump hydrogen ions into the intermembrane space, the coupling of the proton gradient to ATP production

is rendered impossible by DNP. As a result, ATP production is dramatically reduced, and the energy is instead thrown off as heat. This results in an astounding production of heat; when using dinitrophenol, the athlete will radiate so much heat that it is uncomfortable to be within any proximity of them. Luckily, this heat does not fully contribute to body temperature increases, and is instead thrown off from the entire body surface, particularly the head. As a result, adequate doses of DNP will usually only elevate body temperature by about 1-1.5?C. This is a good thing for your central nervous system and other delicate

tissues; if the heat produced by ATP contributed in a more direct matter to body temperature, effective doses for fat loss would cause supraphysiological body temperature increases on a level unwitnessed at this time. Nonetheless, overheating is a very real danger; this and other side effects shall now be addressed.

It is also important to remember that endogenous Testosterone production is likely to be suppressed after a cycle of Testosterone enanthate. When this occurs, one runs the risk of losing muscle mass once the steroid is discontinued. HCG and/or Clomid are in most cases considered to be a necessity, used effectively

to restore natural Testosterone production and avoid a post-cycle "crash".

Yes, but taking KAMAGRA after a high-fat meal (such as a cheeseburger and french fries) may cause the medication to take a little longer to start working.

• It increase muscle strength ( 88%) and muscle size ( 81%)

Andriol, is a unique version of testosterone undecanoate developed by Organon. This version of testosterone is based in oil and is sealed in a capsule to be taken orally. According to the manufacturer, this method bypasses the liver and enters the body as a fat through the lymphatic system. In theory

this seems quite interesting, however, athletes find Organon's claims don't hold up well. In doses of less than 240mg per day effects are generally non-existent. With higher doses, effects are small at best. This leads one to think most of the steroid is not making it to circulation. Generally, steroid users experienced with any strong anabolics will be disappointed with Andriol's results. Combined with other anabolics it may lend some effectiveness but should be questioned.

To combat the aromatization of testosterone, you can simply take an aromatase inhibitor such as Arimidex. This and other Anti-estrogenic compounds

are generally considered a must with testosterone doses over ½ a gram per week (500mgs). Also among side effects (as if acne and going bald aren´t enough) is increased aggression. This is a hotly debated issue in steroid-culture. Generally the consensus is that if you are prone to being a jerk, you´ll be a bigger jerk ...if you aren´t, then your temper will not get much worse (this is supported by research as well Also, high levels of test are generally only associated with aggression and anti-social behavior in males with lower intelligence (1)(2).

Although this particular ester is active

for a much longer duration, most athletes prefer to inject Testosterone Enanthate on a weekly basis in order to keep blood levels more uniform. The usual dosage for Testosterone Enanthate would be in the range of 250 mg-750 mg (200 mg-800 mg U.S. strength). This level is quite sufficient, and should provide the user a rapid gain of strength and body weight. Above this level estrogenic side effects will no doubt become much more pronounced, outweighing any new muscle that is possibly gained. Those looking for greater bulk would be better served by adding an oral like Anadrol 50?or Dianabol, combinations which prove to be nothing
less than dramatic. If the athlete wishes to use a testosterone yet retain a level of quality and definition to the physique, an injectable anabolic like Deca-Durabolin or Equipoise may prove to be a better choice. Here we can use a lower dosage of enanthate, so as to gain an acceptable amount of muscle but keep the buildup of estrogen to a minimum. Of course the excess estrogen that is associated with testosterone makes it a bulking only drug, producing too much water (and fat) retention for use near contest time.

Agovirin inj. 25 mg/ml; Leciva CZ

Serum testosterone, SHBG (Sex Hormone Binding Globulin),

and LH (Leutinizing Hormone) will be slightly suppressed with low doses of Bonavar, but less than with other compounds. FSH (Follicle Stimulating Hormone) , IGF1 (Insulin Like Growth Factor 1) and GH (Growth Hormone) will not be suppressed with a low dose of Bonavar, but will actually be raised significantly as you may have guessed, and LH will even experience a "rebound" effect when you stop using Bonavar. If your endocrine system and HPTA are funtioning normally, you should be able to use Bonavar with minimal insult to it, and can even keep most of your values within the normal range.

HCG's form of administration

is also unusual. The substance choriongonadotropin is a white powdery freeze dried substance which is usually used as a compress. For each HCG ampule, includes another ampule with an injection solution containing isotonic sodium chloride. This liquid, after both ampules have been opened in a sterile manner, is injected into the HCG ampule and mixed with the dried substance. The solution is then ready for use and should be injected intramuscularly. If only part of the substance is injected the residual solution should be stored in the refrigerator. It is not necessary to store the unmixed HCG in the refrigerator; however,
it should be kept out of light and below a temperature of 25C. HCG is an expensive compound, it costs approx. $30 - $40 for 1 ampule of 5000IU.

If taken for 4 weeks, then run each dose for 4 days, 5 weeks then each dose for 5 days and so on. It is extremely important that the doses are tapered on and off and that a cycle never exceeds 6 weeks at the most.

DHT Conversion: No, converts to NOR-DHT with low activity

2. Before starting Roaccutane Treatment

Testosterone Cypionate is a single-ester, long-acting form of testosterone. Due to the length of its ester (8 carbons) it is stored mostly in

the adipose tissue upon intra-muscular injection, and then slowly but very steadily released over a certain period of time. A peak is noted after 24-48 hours of injection and then a slow decline, reaching a steady point after 12 days and staying there over 3 weeks time. A long-acting testosterone ester may be the best for all your mass-building needs, but it's not an easy product to use. Nolvadex and Proviron will come in very handy in such cases and post-cycle. HCG and Clomid or Nolvadex will be required as well to help restore natural testosterone.Frequency of side effects is probably highest with this type of product.

The substance; 2, 4-Dinitrophenol has many other brand names such as, 1 Hydroxy-2,4-dinitrophenol, Solfo Black, Nitrophen, Aldifen, and Chemox are just a few and is among many things, a metabolic stimulant. That is it's popularity here in our world, it burns fat like no other. Let us just tell you of it's other uses before we continue. First, it is a toxic dye, chemically related to Trinitrophenol (Picric Acid), second, it is found in insecticides, wood preservatives, herbicides, explosives, and is also a hazardous material. Third, it is used in science to couple or attach to DNA molecules.

All of this should tell you that it is not a run-of-the-mill metabolic stimulant, like Clenbuterol or Triacana or Ephedrine or any other for that matter. Here is DNP's tox faq's from the international chemical safety cards to you give an idea of what it is considered to be; Combustible. Gives off irritating or toxic fumes (or gases) in a fire. Risk of fire and explosion. DO NOT expose to friction or shock. MAY BE ABSORBED! Redness. Roughness. Yellow staining on the skin. PHYSICAL STATE; APPEARANCE: YELLOW CRYSTALS ROUTES OF EXPOSURE: The substance can be absorbed into the body by inhalation, through the skin and by ingestion. PHYSICAL DANGERS: Dust explosion possible if in powder or granular form, mixed with air.

INHALATION RISK: Evaporation at 20C is negligible; a harmful concentration of airborne particles can, however, be reached quickly. CHEMICAL DANGERS: May explosively decompose on shock, friction, or concussion. May explode on heating. Shock-sensitive compounds are formed with alkalis, ammoniaand most metals. The substance decomposes on heating producing toxic gases including nitrogen oxides. EFFECT OF SHORT-TERM EXPOSURE: The substance may cause effects on metabolism, resulting in very high body temperature. Exposure may result in death.

EFFECTS OF LONG TERM OR REPEATED EXPOSURE: Repeated or prolonged contact with skin may cause dermatitis. The substance may have effects on the peripheral nervous system. The substance may have effects on the eyes, resulting in cataracts. Boiling point: sublimes C, Melting point: 112C, Relative density (water=1): 1.68. Solubility in water, g/100 ml at 54.5C: 0.14. Relative vapor density (air=1): 6.36. This product is handled and shipped in a 15% solution of water, making it a paste, so that it will not explode due to shock or friction.

DNP is an uncoupling agent that inhibits the flow of electrons and the pumping of H+ ions for ATP synthesis. Fifty years ago it was used for weight loss, however, in 1938 the FDA removed it from the counter, as it caused cataracts and even sometimes death. If electron transport does not produce ATP, then much more sugar must be metabolized for energy needs. Very low production of ATP would be lethal. In oxidative phosphorylation, the flow of electrons from NADH (the reduced form of NAD+, oxidized from NAD. This enzyme is important in accepting electrons in the course of metabolic reactions. When NAD+ gives up it's electron, it is converted to it's reduced form NADH) and FADH2 (the reduced form of FAD) to oxygen results in the pumping of H+ from the matrix to the inner membrane space of the mitochondria. This gradient of H+ can produce ATP by flowing through ATP synthetase in the mitochondrial inner membrane. Dinitrophenol disrupts the H+ gradient reducing ATP synthesis. Under these conditions, much of the food that we eat could not be used for ATP synthesis and we lose weight. However, too much inhibitor and we could make too little ATP for life. The difference between weight loss and death is only a small concentration change in dinitrophenol, making the drug dangerous. Simply put, this means that while eating your normal diet, you will have somewhere between 20% and 40% reduction of calories.

You may now be wondering just what kind of dose would be effective, but not harmful. A dose of 2mg/kg/day (or two mgs per kg of body weight per day) would be an effective dose, causing the loss of about 5 to 10 pounds in a 10 to 14 day period, maybe less. So, a person weighing 200 lbs would weigh about 91 kgs, so 2mgs per kg of body weight would be the equivalent of 182 mgs of DNP per day, but since it typically comes in 200 mg capsules, you would take one cap per day. Since DNP has this inhibiting effect, glycolosis is inhibited as well, causing a diabetic effect due to the conversion of glucose without insulin, so you may have heard that people take insulin with DNP, which is a great way to DIE, so DO NOT EVER MIX INSULIN AND DNP!

NOTE: WE HIGHLY SUGGEST AGAINST THE USE OF DNP! DNP IS DEADLY AND YOU CAN DIE FROM USING IT!