Medicines Tonics And Drugs #6351476

product name methenolone enanthate

alias primobolan-depot

cas no 303-42-4

einecs no 206-141-6

mf c27h42o3

mw 414.62

purity 99%

description:

methenolone enanthate is the injectable version of methenolone with a long ester attached to slow absorption of a the active methenolone compound and provide steady blood concentrations. The oral version of this compound is practically identical with the difference being the attached ether (the oral version has a shorter acetate ester attached). Both versions of methenolone are good choices for cutting cycles for men and/or women and have shown to maintain muscle while on a low-calorie diet. Methenolone enanthate provides a less frequent administration mode for methenolone and anecdotally appears to require a lower overall dose in order to be as effective as the oral acetate version.

methenolone has a reputation as being a very safe steroid and in doses of up to 200 mgs/week very little side effects are reported. Unfortunately, many users also report minor gains at best using such a low dose and more pronounced gains seem to occur at 350 mgs/week (100 mg eod) and up. While methenolone is mild without much hpta suppression, higher doses will result in negative feedback in this regard. Also, some users report hair loss while using primo so a product like finasteride may be necessary while cycling methenolone. On the plus side, because of the few side effects exhibited by primo use, an anti-estrogen is likely not necessary.

applications:

methenolone enanthate is a dihydrotestosterone based anabolic steroid, methenolone enanthate is an ester derivative of methenolone sold commonly under the brand name primobolan, methenolone enanthate is used by people who are very susceptible to estrogenic aide effect, having lower estrogenic properities than nandrolone, methenolone, in form of enanthate and acetate, methenolone has no estrogenic side effects and its effects on cholesterol, methenolone is also not overly suppressive of the hpta axis, for this reason, mang bodybuilder use methenolone in between steroid cycles.

cook recipe of methenolone enanthate

50 ml for 200mg/ml

10 grams primobolan e powder (7.5ml)

1ml ba (2%)

7.5ml bb (15%)

17ml grapeseed oil

17ml ethyl oleate

40ml for 100mg/ml

4 grams methenolone enanthate

29 ml grapeseed oil

2ml benzyl alcohol = 5%

6ml benzyl benzoate = 15%

The testosterone suspension is an injectable testosterone hormone developed and used in water for decades and is actually the first synthetical androgenic steroid. In order to build the purpose of the public, testosterone suspensions have never been exceeded because it was the first development in the 1930s. Many underground laboratories also suspend this product in propylene glycol or oil (which makes very painful injections). It has no ester attached; therefore no weight of the ester is calculated.

100 USP injections provide testosterone propionate, a major endogenous androgenic testosterone derivative, for intramuscular administration. The esterification of 17-beta-hydroxy increases the duration of testosterone action. Testosterone propionate has been prepared in an oily solution and is slowly absorbed from the liquid phase when intramuscularly injected. This allows testosterone 100 to be administered at intervals of 3-4 days. 100 contains testosterone propionate in 10 ml of solution (100 mg of testosterone propionate / ml) for injection only.

100 is a transparent, pale yellow oily solution for intramuscular injection.

Testosterone Propionate is for the treatment of primary gonadal dysfunction (congenital or acquired), testicular failure in men due to cryptorchidism, bilateral torsion, orchitis, testicular syndrome or testicular resection.

Product Applications

Testosterone propionate has been used to study its effects on pregnant ewes.

Testosterone propionate is the shortest ester attached to the testosterone hormone. This means that your body needs the least time to get rid of the ester and release the parent hormone into the body. Because of its short active life, testosterone propionate usually needs to be injected at least once every other day. Incredible, testosterone propionate leads to minimal side effects and minimal bloating; these side effects usually fade quickly when used to stop.

Androgen guides the development of male phenotypes during the embryogenesis and the male sterility secreted by testes. The hormone is converted to dihydrotestosterone in the target tissue, where it regulates several biological functions. Testosterone pyruvate has been obtained from plant synthesis. The product has an extended and faster effect when compared to the product.

Testosterone propionate is the shortest ester attached to testosterone. This means that your body needs the least time to get rid of the ester and release the parent hormone into the body. Due to its short active life, testosterone propionate usually needs to be injected at least every other day. Interestingly, testosterone propionate leads to minimal side effects and minimal bloating; these side effects usually fade rapidly when used to stop.

testosterone cypionate; good quality testosterone cypionate; test cypionate;

testosterone cypionate cas no: 58-20-8

testosterone cypionate molecular formula: c27h40o3

testosterone cypionate molecular weight: 412.61

testosterone cypionate assay: 99% min

testosterone cypionate appearance: white crystalline powder

testosterone cypionate quality standard: usp32

testosterone cypionate effective dose (men): 300-2000mg+ week

testosterone cypionate packing: aluminum foil bag testosterone cypionate

testosterone cypionate min. order quantity: 10g testosterone cypionate

testosterone cypionate payment: western union ;;t/t. testosterone cypionate

Product Name: testosterone decanoate

MolecularFormula: C29H46O3

MolecularWeight: 442.68

EINECS: 227-226-4

Specification: 200mg/ml

Packing: foilbagortin

Appearance: white powder

Usage: Pharmaceutical material

CAS: 5721-91-5

Testosterone decanoate is a steroid hormone derived from androgen, found in mammals and other vertebrates, testosterone decanoate is mainly secreted in test mail and female ovaries, although a small amount is also secreted by the adrenal gland, but testosterone decanoate is the principle of male sex hormones and Anabolic steroids.

Testosterone decanoate plays a key role in the development of male reproductive tissues such as testes and prostate glands. In addition, testosterone decanoate is a necessary condition for the health and well-being and prevention of osteoporosis, and testosterone decanoate is retained through most vertebrates, although the fish makes a little difference.

Nandrolone Decanoate Deca Durabolin Durabol

Nandrolone Decanoate CAS No: 360-70-3

Deca Einecs No: 206-639-3

Durabolin MF: C28H44O3

Durabol MW: 428.65

Deca Purity: Nandrolone Decanoate purity is 99.5%

Durabolin Appearance: Nandrolone Decanoate white or oyster white to pale yellow crystalline powder

Durabol Usage: Pharmaceutical material, Steroid hormone, Anabolin. Is a male hormone, anabolic hormones drugs.

Nandrolone Decanoate / Deca Description:

Nandrolone decanoate is an injectable sort of the anabolic steroid. Nandrolone decanoate displays relatively powerful anabolic attributes. Dissimilar testosterone, however, Nandrolone decanoate tissue-building action is attended by weak androgenic facilities. The modest attributes of nandrolone decanoate have made it among the most pop injectable steroids in global, highly preferred by athletes for its power to promote important strength and lean muscle mass increases without strong androgenic or estrogenic side effects.

Nandrolone Decanoate / Deca Applications:

Nandrolone decanoate is wide disposable in human andveterinary drug marketplaces. Structural. Nandrolone decanoate is a modified sort of nandrolone. Esterified steroids are proposed to prolong the window of therapeutical effect following administration, allowable for a lower periodic injection docket compared to injections of free (unesterified) steroid. Nandrolone decanoate offers a keen top in nandrolone release 24-48 hours accompanying deep intramuscular injection, which constantly goes down to near baseline points about 2 weeks later. The average depot-release half life of nandrolone decanoate is eight days.

Finasteride is a popular anti-androgen medication manufactured by Merck most commonly known as either Proscar or Propecia. Based on the progesterone skeleton, Finasteride belongs to a class of medications known as 5alpha-reductase inhibitors and as such is used for the treatment revolving

around type 2 5-AR based occurrences.This is important for performance enhancers as DHT based anabolic steroids have specific side-effects that may occur that can largely be remedied with the use of a 5-AR inhibitor such as Finasteride.

2. As a type 2 5-AR inhibitor Finasteride was designed for the purpose of treating hair-loss, prostate enlargement, as well as prostate cancer.Finasteride is very common among those who supplement with anabolic steroids yet fear hair-lossbut there are important things you need to understand before you consider Finasteride use. As an androgen suppressor Finasteride can seriously inhibit the gains made while on cycle, severely and on that basis it is not highly recommended for on-cycle hair preservation.

The 2005 Prostate Cancer Prevention Trial (PCPT) showed at a dosage of 5 mg per day, as is commonly prescribed for BPH, participants taking finasteride were 25% less likely to have developed prostate cancer at the end of the trial compared to those taking a placebo. It appeared (incorrectly) that finasteride increased the specificity and selectivity of prostate cancer detection, thus creating an apparently increased rate of high Gleason grade tumor.

3. A 2008 update of this study found that finasteride reduces the incidence of prostate cancer by 30%. In the original study, the smaller prostate caused by finasteride facilitated detection of cancer nests and aggressive-looking cells. Most of the men in the study who had both low and high-grade prostate cancer chose to be treated, and many had their prostates removed. A pathologist then carefully examined each of those 500 prostates and compared the kinds of cancers found at surgery to those initially diagnosed at biopsy. This study concluded that finasteride did not increase the risk of high-grade prostate cancer.

Finasteride Applications

1. Benign prostatic hyperplasia

Physicians use finasteride for the treatment of benign prostatic hyperplasia (BPH), informally known as an enlarged prostate.The FDAapproved dose is 5 mg once a day. Six months or more of treatment with finasteride may be required to determine the therapeutic results of treatment. If the drug is discontinued, any therapeutic benefits reverse within about 6 to 8 months. Finasteride may improve the symptoms associated with BPH such as difficulty urinating, getting up during the night to urinate, hesitation at the start of urination, and decreased urinary flow.

2. Male pattern baldness

Finasteride is used to treat male pattern hair loss (androgenetic alopecia) in men only. Treatment provides about 30% improvement in hair loss after six months of treatment, and effectiveness only persists as long as the drug is taken.

GHRP-6 is most commonly provided in small vials of 5 mg, which should be stored under refrigeration. (It is acceptable however for them to be mailed unrefrigerated.) The vial is diluted with a convenient volume of sterile or bacteriostatic water. For example, the vial might be diluted with 2.5 mL of water, yielding a solution of 2 mg/mL (2000 mcg/mL.) After the water addition, the vial again will be stored under refrigeration.

When dosing, an appropriate volume will be drawn from the vial with (typically) an insulin syringe, according to the desired dose and the concentration of the preparation. In the above example, a 100 mcg dose would require only 0.05 mL, or 5 IU as marked on an insulin syringe. A 300 mcg would require 0.15 mL, or 15 IU as marked on an insulin syringe.

Injection may be subcutaneous, intramuscular, or intravenous according to personal preference.

Dosing will ordinarily be at least twice per day and preferably 3x/day for best effect, taken at least 30-60 minutes before a meal and at a time of non-elevated blood sugar (in other words, after blood sugar has had time to fall since the most recent meal.) The amount taken generally will be from 50-300 mcg at a time. When using a GHRH along with GHRP-6, dosing should be reduced to 50-100 mcg at a time.

For increase in GH levels, higher doses within the suggested range definitely increase effect. With regard to healing benefit, for example for tendonitis, the low end of the range is often entirely sufficient and noticeably greater effect is not necessarily seen with increased dose.

While there is no sharp cut-off between a solution of GHRP-6 still being good and having lost potency with time, as a general guideline, a vial should be used within a month of having been reconstituted. Past this, I would discard the vial and start a new one.

Myostatin (GDF-8) is a member of the transforming growth factor-beta (TGF-beta) superfamily that is highly expressed in skeletal muscle, and myostatin loss-of-function leads to doubling of skeletal muscle mass. Myostatin-deficient mice have been used as a model for studying muscle-bone interactions, and here we review the skeletal phenotype associated with altered myostatin signaling. It is now known that myostatin is a key regulator of mesenchymal stem cell proliferation and differentiation, and mice lacking the myostatin gene show decreased body fat and a generalized increase in bone density and strength.

The increase in bone density is observed in most anatomical regions, including the limbs, spine, and jaw, and myostatin inhibitors have been observed to significantly increase bone formation. Myostatin is also expressed in the early phases of fracture healing, and myostatin deficiency leads to increased fracture callus size and strength. Together, these data suggest that myostatin has direct effects on the proliferation and differentiation of osteoprogenitor cells, and that myostatin antagonists and inhibitors are likely to enhance both muscle mass and bone strength.

GDF-8 Application

The gene encoding myostatin was discovered in 1997 by geneticists Se-Jin Lee and Alexandra McPherron who produced a strain of mutant mice that lack the gene. These myostatin "knockout" mice have approximately twice as much muscle as normal mice. These mice were subsequently named "mighty mice".

Product name: Benzocaine HCL

Other name: Benzocaine hydrochloride

CAS: 23239-88-5

Appearance: white powder

Purity: 99%

Product description

Benzocaine hydrochloride is a local anesthetic in the form of hydrochloride salt benzocaine, pharmacological effects with benzocaine, procaine than anesthetic effect is weak. Part of the absorption is slow and lasting effect. Because they are insoluble in water, can not be used for anesthesia, relieve pain, anti-itching, drugs are usually made of powder or oil paste for the treatment of wound clinical, ulcers, burns, skin abrasions and hemorrhoids.

Benzocaine is also known as aminobenzoate, cenuxacin.

Benzocaine HCL acts by creating a chemical barrier that prevents the accumulation of sodium, and when the nerve endings are stimulated by pain, sodium accumulates. When the sodium accumulates, the electrical signal will also increase the nerve endings. These are eventually passed to the brain, which interprets the signal as pain.

Benzocaine Hcl is also known as ethyl aminobenzoate, colorless or white diagonal needle-like crystals or crystalline powders. Benzocaine hydrochloride is the hydrochloride form of local anesthesia benzocaine, and benzocaine has the same pharmacological effect and weaker anesthesia compared to procaine. Local absorption is slow, sustained effect. Because it is insoluble in water, can not be used for anesthesia. Can be used for pain and itching.

Benzazacaine hydrochloride is usually made into powder or ointment for the treatment of wounds, ulcers, burns, skin abrasions and hemorrhoids.

Product application

Benzocaine hydrochloride is an narcotic drug that is used primarily for direct application to the skin. Benzocaine HCl is salt modification of benzocaine when benzocaine is complexed with hydrochloric acid. In general, the drug salts have enhanced properties compared to the parent compound. For example, benzocaine carbazate is more soluble than benzocaine, making it more suitable for oral administration.

Benzocaine hydrochloride has many different uses, including

(1) as a component of cough syrup

(2) treatment of cold sores

(3) treatment of toothache

(4) treatment of dentures stimulation

(5) treatment of earache

(6) as anesthesia for surgery

(7) condoms for delayed ejaculation

(8) tranquil fish

Razivacaine Mesylate, is a new long-acting amide type local anesthetic, pure isoleine, with anesthesia and analgesic dual role, high concentrations of ropivacaine mesylate (molecular formula C17H26N2O CH4O3S, English name Ropivacaine Mesylate Injection) Resulting in surgical anesthetic effects, lower concentrations can effectively block the sensory nerve transmission and the impact of motor nerve is very small. Its pharmacological properties for the lower cardiac toxicity, sensory block separation is more obvious, there is vasoconstriction, so no need to add adrenaline. Clinical mainly for surgical anesthesia, local anesthesia and acute pain control.

Pharmacological effects

With anesthesia and analgesic dual role, high concentration can produce surgical anesthesia, lower concentrations can effectively block the sensory nerve transmission and the impact of motor nerve is very small. Its pharmacological properties for the lower cardiac toxicity, sensory block separation is more obvious, there is vasoconstriction, so no need to add adrenaline.

Clinical application

1. Local anesthesia

2. Epidural block.

3. Peripheral nerve block.

4. Subretinal subcavity.

5. Local intravenous anesthesia.

6. Postoperative analgesia.

7. Obstetric anesthesia.

8. Labor analgesia.