chemical-categories

 

Masteron Raw Steroid Powder Drostanolone Propionate For Muscle Building 521-12-0

 

Drostanolone Propionate Basic Info.

 

Product Name: Drostanolone Propionate 

Synonyms: Masteron; Dromostanolone Propionate 

CAS: 521-12-0 

Molecular formula: C23H36O3 

Molecular weight: 360.53 

EINECS: 208-303-1 

Assay: 99%

Packing: Foil bag or tin. 

Delivery: Express courier. 

Character: White crystalline powder. 

Min. order quantity: 100g

Payment: T/T, Western Union, Moneygram

Express: EMS, DHL, FeDex, etc(door-to-door)

Delivery : safe & timely, within 12 hours after payment

 

Drostanolone Propionate Description:

 

Masteron can be used somewhat effectively as bulking agent, providing a consistent gain of high quality muscle mass. It can also be successfully combined with other steroids for an enhanced effect. Mixing drostanolone with an injectable anabolic such as Deca-Durabolin or Equipoise can prove quite useful for example, the two providing notably enhanced muscle gain without excessive water retention. For greater mass gains, a stronger androgen such as Dianabol or an injectable testosterone would do the trick. The result here can be an extreme muscle gain, with a lower level of water retention & other estrogenic side effects than if these steroids were used alone (usually in higher doses). Masteron could of course be used during cutting phases of training as well. A cycle of this drug combined with Winstrol, Primobolan or Oxandrolone should provide great muscle retention and fat loss, during a period which can be very catabolic without steroids. It is an added benefit that none of these steroids aromatize, and therefore there is no additional worry of unwanted water and fat retention.

 

Drostanolone Propionate Applications:

 

Bodybuilders have a strong like for non-aromatizing androgens, and find Masteron very useful in a cutting phase. It is generally used for a number of weeks prior to a competition, in an effort to bring out an improved look of density and hardness to the muscles. As long as body fat percentage is low enough, considerably intensifies its anabolic effect. It can therefore be used somewhat effectively as bulking agent, providing a consistent gain of high quality muscle mass.

 

Masteron is often an ideal choice for inclusion in a steroid stack, or in some cases for use as the sole injectable for a steroid cycle.Androgens and assimilation hormonal.

 

An enanthate ester version having a half-life of probably 5 days has become available. This version of Masteron may be injected as infrequently as twice per week.

 

 

Oral Anabolic Steroid Hormone Dianabol Methandienone Gain in Muscle Size 72-63-9

 

Methandienone Basic Info.:

 

Product Name: Metandienone

Alias: Dianabole, Dianabole,  Encephan, Geabol, Metanabol, Metandienon, Metandienonum, Metandrostenolon, Metandrostenolone, Metastenol, Methandrolone, Naposim, Nerobol, Nerobolettes, NSC-42722, Protobolin, Stenolon, Stenolone, Sterolon.

CAS: 72-63-9

MF: C20H28O2

MW: 300.43512

EINECS: 200-787-2

Purity: 99%

Melting point: 165-166 °C

Storage temp.: 2-8°C

Appearance: White powder.

Product Categories: Biochemistry;Hydroxyketosteroids;Steroids;Intermediates & Fine Chemicals;Pharmaceuticals;Steroid and Hormone;Finished Steroid and Hormone;API

Usage: 

(1)It can be should as medicines of androgens and anabolic hormones. 

(2)It can be used for treating expendable chronic disease, children mal-development, osteoporosis and hyperlipidemia.

(3)Anabolic steroid. Androgen. Controlled substance. 

 

Methandienone Description:

 

One of the most important anabolic steroids in bodybuilding ever since its introduction in 1958. Also commonly known as "Dbol", this oral compound is best used for steroid cycles in combination with injectable steroids, but can be of value used alone as well. Methandrostenolone is a derivative , and exhibits a strong anabolic effect along with a moderate androgenic effect. Methandrostenolone is also commonly known as 'dianabol' which is the old Ciba brand name. Methandrostenolone is an oral steroid, which is potent. 

 

Methandienone Applications:

 

One of the most important anabolic steroids in bodybuilding ever since its introduction in 1958. Also commonly known as "Dbol", this oral compound is best used for steroid cycles in combination with injectable steroids, but can be of value used alone as well.

 

(Dianabol) is the most well known Steroid in existance today and was considered by Arnold schwarzenegger to be the 'breakfast of champions'. Dianabol is a very strong compound and takes very litle time to take effect, by two weeks you will be noticing huge effects from this drug.

 

One of the great benefits of Dianabol is its ability to make one feel good inside, confident and powerful. All three are vastly important in performing well in the gym and Dianabol will certainly make you perform well in the gym! In the gym you will notice huge gains in strength and you will find that your muscle fill very full and large, this is mostly due to the fact that it dramatically increases protein synthesis and nitrogen retention within the muscle cells. - training on Dianabol is a great experience.

 

With regards to weight gains Dianabol is a champion at making the scales go up and almost nothing can do that faster than this compound. Because of this it is an ideal Steroid to take at the start of a Steroid cycle, what is known as a 'kick-start' and for this reason it is best used, and almost always used, in conjunction with injectable Steroids.

 

A typical dose would be 40-60mg/day and many serious Bodybuilders will go up to 100mg/day, however, it is important to note that Dianabol can impact your blood pressure levels at higher doses.

 

 

Pharmaceutical Intermediates Pregabalin For Anti-Epileptic Treatment 148553-50-8

 

Pregabalin Basic Info.:

 

Product Name: Pregabalin 

Synonym: Pregablin;3-(Aminomethyl)-5-methyl-hexanoic acid

CAS: 148553-50-8

MF: C8H17NO2

MW: 159.23

Assay: 99.5%

Appearance: White Crystal Powder

Payment: T/T, Western Union and Money Gram

Delivery: Within 12hours After Your Payment

Express: EMS, DHL, FedEx, etc(door-to-door)

Usage: New antiepileptic drugs. Used in the treatment of peripheral neuropathy, or partial seizures adjuvant treatment.

 

Product Introduction Of Pregabalin:

 

Pregabalin works by reducing the abnormal electrical activity in the brain. It is taken alongside other medicines for epilepsy. Pregabalin can also be helpful in treating the symptoms of generalised anxiety disorder (GAD), particularly if other medicines which are more often prescribed for people with this condition are not suitable. GAD is a long-term condition where anxiety is a major symptom.

 

Pregabalin, also known as β-isobutyl-γ-Aminobutyric acid (β-isobutyl-GABA) and sold under the trade name Lyrica among others, is a medication used to in the treatment of epilepsy, neuropathic pain, fibromyalgia and generalized anxiety disorder. Its use for epilepsy is as an add-on therapy for partial seizures with or without secondary generalization in adults.

 

Pregabalin is a structural analogue of the neurotransmitter GABA, consequently it belongs to the γ-Aminobutyric acid analogue class of antiepileptic drugs. Its a ion channel modulator that has analgesic, anticonvulsant, sedative, and anxiolytic properties. Pregabalin is a potent gabapentinoid and close analogue of GABOB (β-hydroxy-GABA), baclofen (β-(4-chlorophenyl)-GABA), and phenibut (β-phenyl-GABA).

 

Pregabalin Usage:

 

Pregabalin belongs to a group of medicines known as anti-epileptic medicines, although it is prescribed for the treatment of several different conditions. You may have been prescribed it for the treatment of partial seizures, which is a type of epilepsy. A seizure is a short episode of symptoms which is caused by a burst of abnormal electrical activity in the brain. With a partial seizure, the burst of electrical activity stays in one part of the brain. Therefore, you tend to have localised or 'focal' symptoms. Pregabalin is also prescribed to treat certain types of long-lasting pain caused by damage to nerves. This type of pain, called neuropathic pain, can be caused by a number of different conditions, including diabetes (where it is called diabetic neuropathy) and shingles(where it is called postherpetic neuralgia).

 

 

Pharmaceutical Raw Material Hydroxypropyl Beta Cyclodextrin 128446-35-5 For Food

 

Hydroxypropyl Beta Cyclodextrin Basic Info.:

 

Product Name: Hydroxypropyl-Beta-Cyclodextrin

Name: (2-HYDROXYPROPYL)-BETA-CYCLODEXTRIN

CAS NO: 128446-35-5

MF: C63H112O42

MW: 1541.54

EINECS: 420-920-1

Assay: 99%

Packing: 10kg/drum

Appearance: White powder

Characteristics and Uses: The introduction of hydroxypropyl β - cyclodextrin breaking intramolecular hydrogen bond ring, while maintaining the cyclodextrin cavity while overcoming the poorly water-soluble β - cyclodextrin major drawback. Is currently the most in-depth study, the most widely used one cyclodextrin derivatives. Mainly used in food, pharmaceutical, cosmetics industries.

 

Product Description Of Hydroxypropyl Beta Cyclodextrin:

 

1, In the food, spices fields, can improve the stability and long-term nutritional molecules, can mask or correct nutritional elements of food smells and tastes bad, you can improve the production process and product quality. The product is very good solubility in water, the degree of substitution can be 4 or more miscible in any proportion with water, 50 % ethanol and methanol can also be dissolved.

2, In cosmetic raw materials used as a stabilizer, emulsifier, to taste and the like, organic molecules can be reduced in cosmetics mucosal tissue irritation on the skin, enhance the stability of active ingredients, to prevent volatilization of nutrients, oxidation. It has a certain relative hygroscopicity.

3, In the pharmaceutical industry, due to the relative surface activity and hemolytic activity is relatively low and is not irritating to muscle, so it is an ideal injection solubilizer and pharmaceutical excipients. Insoluble drugs can increase the water solubility, increased drug stability, improved bioavailability, efficacy of the pharmaceutical dosage increase or decrease, can be adjusted or controlled drug release rate, reduce drug side effects.

4. For oral drugs, injections, drug delivery systems (including nasal, rectal, cornea, etc.), transdermal drug delivery systems for targeted drug lipophilic carrier protein can be used as protective agents and stabilizers.

 

 

Pharmaceutical Raw Materials Lipoic Acid For Fat-Metabolism Stimulator 1077-28-7

 

Lipoic Acid Basic Info.:

 

Product Name: Lipoic Acid

Purity: 99.5%

CAS: 1077-28-7

MF: C8H14O2S2

MW: 206.33

Appearance: Yellow crystalline powder,no obvious odor.

Melting point: 60.0-62.0 degree centigrade 

Drying loss: Not more than 0.2%  

Usage: Lipoic acid is a vitamin drugs, limited physical activity in its dextral, basically no physical activity in its Lipoic acid, and no side effects. It is always used for acute and chronic hepatitis, liver cirrhosis, hepatic coma, fatty liver, diabetes, Alzheimer's disease, and applies as an antioxidant health products

 

Lipoic Acid Function:

 

Lipoic acid is a vitamin drugs, limited physical activity in its dextral, basically no physical activity in its Lipoic acid, and no side effects. It is always used for acute and chronic hepatitis, liver cirrhosis, hepatic coma, fatty liver, diabetes, Alzheimer's disease, and applies as an antioxidant health products

 

Lipoic Acid Applications:

 

1.Lipoic Acid is a good antioxidant. Taken internally, it is a water  and fat soluble antioxidant that is capable of regenerating other antioxidants, such as vitamins C and E; it also can help prevent cellular damage via its antioxidant properties. 

2.Usually it  is used for diabetes, peripheral neuropathy, cardiac autonomic neuropathy, retinopathy, cataracts, and glaucoma. Alpha-lipoic acid is also used orally for dementia, chronic fatigue syndrome, HIV/AIDS, cancer, liver disease, cardiovascular disease, peripheral arterial disease, intermittent claudication, Lyme disease, and lactic acidosis caused by inborn errors of metabolism.

3.It also has anti-inflammatory effects.

4.Topically, alpha-lipoic acid is used to reduce facial wrinkles, lines, and sun damage.

but it is extremely vulnerable to degradation by sunlight, and 5% or higher alpha lipoic acid are capable of causing burning or stinging sensations or a mild rash on skin.

 

 

Prohormones Steroids White Powder Misoprostol For Terminate Pregnancy 59122-46-2

 

Misoprostol Basic Info.

 

Product Name: Misoprostol

Synonyms: Misoprostol;Cytotec;SC-29333

CAS: 59122-46-2

Molecular Formula: C22H38O5

Molecular Weight: 382.60

Assay: 99%

Chemical Properties: White Solid

Solubility: Soluble to 100 mM in Ethanol

Safety: Poison by ingestion, intramuscular, and intraperitoneal routes. When heated to decomposition it emits acrid smoke and irritating fumes.

Package: Aluminium foil bag packing 

Storage: Keep in cool and dry place, away from light

 

Misoprostol Description:

 

Misoprostol is a medication used to start labor, induce abortions, prevent and treat stomach ulcers, and treat postpartum bleeding due to insufficient contraction of the uterus. For abortions it is used with mifepristone or methotrexate. It is a synthetic prostaglandin E1 (PGE1).

 

Common side effects include diarrhea and abdominal pain. It is pregnancy category X meaning that it is known to result in negative fetal outcomes if taken during pregnancy. Uterine rupture may occur.

 

It is on the World Health Organization's List of Essential Medicines, the most important medications needed in a basic health system. Misoprostol was invented and marketed by G.D. Searle & Company under the trade name Cytotec, but other trade names and generic formulations are available.

 

Misoprostol Usage

 

Misoprostol is approved for use in the prevention of NSAID-induced gastric ulcers. It acts upon gastric parietal cells, inhibiting the secretion of gastric acid by G-protein coupled receptor-mediated inhibition of adenylate cyclase, which leads to decreased intracellular cyclic AMP levels and decreased proton pump activity at the apical surface of the parietal cell. Because other classes of drugs, especially H2-receptor antagonists and proton pump inhibitors, are more effective for the treatment of acute peptic ulcers, misoprostol is only indicated for use by people who are both taking NSAIDs and are at high risk for NSAID-induced ulcers, including the elderly and people with ulcer complications. Misoprostol is sometimes coprescribed with NSAIDs to prevent their common adverse effect of gastric ulceration (e.g. with diclofenac in Arthrotec).

 

Misoprostol has other protective actions, but is only clinically effective at doses high enough to reduce gastric acid secretion. For instance, at lower doses, misoprostol may stimulate increased secretion of the protective mucus that lines the gastrointestinal tract and increase mucosal blood flow, thereby increasing mucosal integrity. However, these effects are not pronounced enough to warrant prescription of misoprostol at doses lower than those needed to achieve gastric acid suppression.

However, even in the treatment of NSAID-induced ulcers, omeprazole proved to be at least as effective as misoprostol,but was significantly better tolerated, so misoprostol should not be considered a first-line treatment. Misoprostol-induced diarrhea and the need for multiple daily doses (typically four) are the main issues impairing compliance with therapy.

 

The most commonly reported adverse effect of taking a misoprostol orally for the prevention of stomach ulcers is diarrhea. In clinical trials, an average 13% of patients reported diarrhea, which was dose-related and usually developed early in the course of therapy (after 13 days) and was usually self-limiting (often resolving within 8 days), but sometimes (in 2% of patients) required discontinuation of misoprostol.

 

The next most commonly reported adverse effects of taking misoprostol orally for the prevention of gastric ulcers are: abdominal pain, nausea, flatulence, headache, dyspepsia, vomiting, and constipation, but none of these adverse effects occurred significantly more often than when taking placebos. In practice, fever is almost universal when multiple doses are given every 4 to 6 hours.

 

Misoprostol should not be taken by pregnant women to reduce the risk of NSAID-induced gastric ulcers because it increases uterine tone and contractions in pregnancy, which may cause partial or complete abortions, and because its use in pregnancy has been associated with birth defects.

 

 

Tetramisole Hydrochloride Pharmaceutical Raw Materials Tetramisole HCL 5086-74-8

 

Tetramisole HCL Basic Info.:

 

Product Name: Tetramisole Hydrochloride

Other names: (+-)-2,3,5,6-tetrahydro-6-phenylimidazo(2,1-b)thiazolemonohydrochloride; (+-)-anthelvet;1-b)thiazole,2,3,5,6-tetrahydro-6-phenyl-,monohydrochloride,(+-)-imidazo(;anthelvet;bayer9051;citarin;dl-6-phenyl-2,3,5,6-tetrahydroimidazole(2,1-b)thiazole-hydrochloride;dl-tetramisolehydrochloride

CAS NO.: 5086-74-8

EINECS: 225-799-5

M.F.: C11H12N2S.HCl

M.W.: 240.7523

Assay:98%

Packing: 25kg/drum

Appearance: White to white crystalline powder or needle crystal

Usage: A muscarinic receptor antagonist. Used in the treatment of urinary incontinence.

 

Product Description of Tetramisole HCL:

 

Tetramisole was originally used as an anthelminthic to treat worm infestations in both humans and animals. Most current commercial preparations are intended for veterinary use as a dewormer in cattle, pigs, and sheep.

However, tetramisole has also recently gained prominence among aquarists as an effective treatment for Camallanus roundworm infestations in freshwater tropical fish. It is a broad-spectrum anthelminthics, used to control roundworm and hoodworm.

 

Tetramisole HCL Application:

 

Tetramisole hydrochloride is used as an anthelmintic in the treatment of many nematodes particularly in veterinary applications. Tetramisole is a racemic mixture.

It is used as Hydrochloric acid levorotatory sulfonated intermediates.

It is flooding bowel insect poisons, anti-worm medicine.

Used for fishing and pinworms roundworm, insect infection.

 

 

99% High Purity Local Anesthetic Tetracaine Hydrochloride/Tetracaine HCL 136-47-0

 

Tetracaine HCL Basic Info.:

 

Product Name: Tetracaine hydrochloride

Synonyms: Tetracaine HCL

CAS: 136-47-0

MF: C15H25ClN2O2

MW: 300.82

EINECS: 205-248-5

mp: 149°C

storage temp: Refrigerator

Appearance: White Solid

Usage: Local anesthetic; Mainly used in mucosa anesthetic.The function is stronger than Procaine and Lidocaine.

 

Tetracaine HCL Description:

 

Tetracaine HCl is synthesized from 4-butylaminobenzoic acid. The ethyl ester is formed through an acid-catalyzed esterification reaction. Base-catalyzed transesterification is achieved by boiling the ethyl ester of 4-butylaminobenzoic acid with excess 2-dimethylaminoethanol in the presence of a small amount of sodium ethoxide.

 

Tetracaine HCL Applications:

 

Tetracaine (INN, also known as amethocaine; trade name Pontocaine. Ametop and Dicaine) is a potent local anesthetic of the ester group. It is mainly used topically in ophthalmology and as an antipruritic, and it has been used in spinal anesthesia.

 

In biomedical research, tetracaine is used to alter the function of calcium release channels (ryanodine receptors) that control the release of calcium from intracellular stores. Tetracaine is an allosteric blocker of channel function. At low concentrations, tetracaine causes an initial inhibition of spontaneous calcium release events, while at high concentrations, tetracaine blocks release completely.

 

 

99% Muscle Bodybuilding Supplement Anabolic Steroid Methenolone Acetate 434-05-9 

 

Methenolone Acetate Basic Info.

 

Product Name: Methenolone Acetate

Alias: Primobolan-depot;Primobolandepot;Methenolone Acetate

CAS No.: 434-05-9

MF: C22H32O3

MW: 344.49

Einecs No: 207-097-0

Purity: 99%

MOQ(minimum order quantity): 10gram

Standard: Enterprise Standard

Appearance: White powder. 

Usage: It is very strong, the synthesis of the metabolism and male characteristics is very low, making it the best choice for the game. 

 

Methenolone Acetate Description:

 

Primobolan (methenolone acetate), all things being equal, is an excellent oral steroid drug. Unlike most other oral steroids, Primobolan is not 17-alkylated and does not have liver toxicity problems. Methenolone is perhaps only half as potent by the oral route as by injection, so dosages need to be high, at least 100 and preferably 200-300 mg per day, but if that can be afforded it is an excellent drug. It is unusual among oral steroids as being Class I, binding well to the androgen receptor. 

 

Methenolone Acetate Applications: 

 

Primobolan (methenolone acetate), all things being equal, is an excellent oral steroid drug. Unlike most other oral steroids, Primobolan is not 17-alkylated and does not have liver toxicity problems. 

Primobolan is toxic to the liver, especially the oral versions, although the toxicity is gradual and slight. Acne and hair loss can occur with long-term use. 

Primobolan is a good base compound in a stack and can produce results just slightly below that of nandrolone and is best used in a cutting stack. Because Primobolan doesn't aromatize, there is no use for Clomid or Nolvadex.

Primobolan Acetate is very strong, the synthesis of the metabolism and male characteristics is very low, making it the best choice for the game. The drug for women is very good!

 

 

99% Purity High Quality Steroid Hormone Powder Methandriol Dipropionate 3593-85-9

 

Methandriol Dipropionate Details:

 

Product Name: Methandriol Dipropionate

Synonyms: 5-Androsten-17Alpha-Methyl-3Beta;17Alpha-Methylandrostendiol Dipropionate;Methandriol Dipropionate;

CAS: 3593-85-9

MF: C26H40O4

MW: 416.6

EINECS: 222-735-8

Standard: Enterprise Standard

Packing: 1kg/Aluminum foil bag

Min. Order Quantity: 10g

Payment: Western Union, Moneygram

Shipment: EMS, DHL, FedEx, etc.

Delivery: Safe & Timely, Around 1 Day After Payment.

Product Categories: Steroids

 

Methandriol Dipropionate Descriptions:

 

Methandriol Dipropionate (M.D.) is a form of the water-dissolved Methandriol but Methandriol Dipropionate remains effective for a longer period of time. On the one hand, Methandriol Dipropionate can be dissolved in oil for injection purposes and, on the other hand, Methandriol Dipropionate is produced in tablet form since it is also effective when taken orally M.D. has a strong anabolic and androgenic component so that it is suitable for the buildup of strength and muscle mass. The effect can be compared to a cross between Deca-Durabolin and Testosterone enanthate. Like testosterone it con- tributes to a gain in both strength and muscle but does not retain more water than Deca-Durabolin.

 

The best results can be obtained, however, if Methandriol Dipropionate is not taken alone but in combination with an- other steroid. This is because Methandriol Dipropionate is able to magnify the effects of other steroid compounds. It does this by increasingly sensitizing the androgenic receptors of the muscle cell, allowing a higher amount of the steroid molecules of the additionally taken steroids to be absorbed by the receptors. This also explains why injectable Methandriol Dipropionate is only available today as a combination compound with an additional steroid substance. Injectable Methandriol Dipropionate is only available in the Australian veterinary steroids Drive, Spectriol, Geldabol, and Filibol Forte so that procurement of the compound is difficult. The few athletes using this drug report good strength gains, a solid muscle gain, and low water retention. The combination steroids aromatize only slightly so, when taking only Methandriol Dipropionate, the use of antiestrogens is perhaps appropriate. The injectable form is only slightly toxic.

 

Methandriol Dipropionate Dosage:

 

The usual dosage for athletes is 100 mg every 2-3 days. In Europe only the oral form of M.D. is available. Also in this case it is beneficial to combine M.D. with another steroid, preferably an injectable one. The normal daily dose is 40-60 mg and is usually taken in 2-3 individual doses spread over & day The tablets are usually taken for only 4-6 weeks since the effect decreases quickly, thus requiring higher dosages.