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

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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.
 

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

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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.
 

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

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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.
 

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

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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.
 

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

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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.
 

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

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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!
 

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

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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.
 

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High Quality Factory Direct Supply Estrogen Hormone Estradiol Enanthate 4956-37-0

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High Quality Factory Direct Supply Estrogen Hormone Estradiol Enanthate 4956-37-0
 
Estradiol Enanthate Basic Info.
 
Product Name: Estradiol Enanthate
CAS Number: 4956-37-0
Purity: 99%
Molecular Weight: 384.556
Molecular Formula: C25H36O3
Appearance: Crystalline powder
Physical State: Solid
Solubility: Soluble in water (slightly).
Storage: Store at room temperature
Melting Point: 94-96 ° C
Boiling Point: ~509.5 ° C at 760 mmHg (Predicted)
Density: ~1.1 g/cm3 (Predicted)
 
Estradiol Enanthate Description:
 
Estradiol enanthate (INN, USAN), or estradiol enantate, is a synthetic ester, specifically the 17-heptanoyl ester, of the natural estrogen, estradiol. It is marketed under the brand names Anafertin, Deladroxate, Perlutan, and Topasel, which are combination formulations of estradiol enanthate and dihydroxyprogesterone acetophenide, as a once-monthly injectable hormonal contraceptive in Spain and Latin America, and has been used as such since at least the mid-1960s.
 
Estradiol, or more precisely, 17β-estradiol, is a human sex hormone and steroid, and the primary female sex hormone. It is named for and is important in the regulation of the estrous and menstrual female reproductive cycles. Estradiol is essential for the development and maintenance of female reproductive tissues but it also has important effects in many other tissues including bone. While estrogen levels in men are lower compared to women, estrogens have essential functions in men as well. Estradiol is found in most vertebrates as well as many crustaceans, insects, fish, and other animal species.
 
Estradiol or oestradiol (American or British English usages), derives from estra-, Gk. οστρο? (oistros, literally meaning "verve or inspiration") and -diol, a chemical name and suffix indicating that this form of steroid and sex hormone is a type of alcohol bearing two hydroxyl groups.
 
Estradiol is produced especially within the follicles of female ovaries, but also in other endocrine (i.e., hormone-producing) and non-endocrine tissues (e.g., including fat, liver, adrenal, breast, and neural tissues). Estradiol is biosynthesized from progesterone (arrived at in two steps from cholesterol, via intermediate pregnenolone). One principle pathway then converts progesterone to its 17-hydroxy-derivative, and then to androstenedione via sequential cytochrome P450-catalyzed oxidations.Action of aromatase on this dione generates estrone, and action of a dehydrogenase on this gives the title compound, 17β-estradiol.
 
Estradiol Enanthate Function:
 
Hormones and Regulation of Endocrine Function of Drug, Nutritional Therapeutics, Antibiotic and Antimicrobial Agents, Antiparasitic, Original Drug Resistant Microbes, Immune System Drugs, Specialist Drugs, Drug Detoxification, Diagnostic Agents, Blood System Agents, Visceral System Medication, Central Nervous System Agents, Cardiovascular Agents, Urinary System Agents, Respiratory System Agents.
 
A chemical derivative of estradiol, ethinyl estradiol with maximum dosage 200 µg, is a major component of hormonal contraceptive devices. Combined forms of hormonal contraception contain ethinyl estradiol and a progestin, which both contribute to the inhibition of GnRH, LH, and FSH, which accounts for the ability of these birth control methods to prevent ovulation and thus prevent pregnancy. Other types of hormonal birth control contain only progestins and no ethinyl estradiol.
 

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Hot Item Legit Gear Boldenone Undecylenate/Equipoise/EQ 13103-34-9 99.5% Steroids

Boldenone undecylenate (Steroids) 
 
Basic Info.
Model NO.:CAS NO.: 13103-34-9                                  Assay: 97.0~103.0%
MF:C30H44O3                                                            MW:452.67
Export Markets:Global                                                
 
Additional Info.
Trademark:Holybiological                                             Packing:1kg/tin
Standard: Enterprise Standard                                      Origin:China
EINECS: 236-024-5                                                      Appearance:Yellowish oily liquid.
HS Code:2937290018
Usage: pharmaceutical material, Steroid hormone, Anabolin. As a male hormone and anabolic hormones.
 
Description: 
It is a derivative, which exhibits strong anabolic and moderately androgenic properties. The undecylenate ester greatly extends the activity of the drug (the undecylenate ester is only one carbon atom longer than decanoate), so that clinically injections would need to be repeated every three or four weeks. 
In the veterinary feild Equipoise is most commonly used on horses, exhibiting a pronounced effect on lean bodyweight, appetite and general disposition of the animal. As with all steroids, this compound shows a marked ability for increasing red blood cell production. In recent years this compound has become a favorite among athletes. Many consider it an ideal replacement to Deca-Durabolin. 
The side effects of Equipoise are generally mild. The structure of boldenone does allow it to convert into estrogen, but it does not have an extremely high affinity to do so. If we look at aromatization studies, they suggest that its rate of estrogen conversion should be about half that. 
Water retention with this drug would therefore be slightly higher than that with Deca-Durabolin (with an estimated 20% conversion), but much less than we would find with a stronger compound. While there is still a chance of encountering an estrogen related side effect as such when using Equipoise, problems are usually not encountered at a moderate dosage level. 
 
Applications: 
Equipoise (boldenone undecylenate) is historically a veterinary steroid but for some time has been available as an UGL human preparation as well. 
For bodybuilders, it should be used as Equipoise can cause sexual dysfunction. 
In order to maintain stable blood levels, Equipoise should be injected at least once per week. It is most commonly used at a dosage of 400-600mg per week for men, 50-150 mg per week for women. 
Equipoise is not a rapid mass builder, but will provide a slow but steady gain of strength and quality muscle mass. The most positive effects of this drug are seen when it is used for longer cycles, usually lasting at least 10 weeks in length. 
 
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2)We are manufacturer and can provide high quality products with factory price.
 
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4) We have our own agent/remailer/distributor who can help us ship our products very fast and safe, and we have stock in there for transferring.
 
3, We have clients throughout the world. 
1)Professional service and rich experience make customers feel at ease, adequate stock and fast delivery meet their desire.
2)Market feedback and goods feedback will be appreciated, meeting customers's requirement is our responsibility.
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If you need this or you are interest in this kind of products, you are free to send me email or call me directly, we can talk more about the details of the products.
No matter you become a customer to me or not at last, you are welcome to inquire from me!
 
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Injectable Premade Steroids Oil TMT 425 Mg/Ml Semi Finished Blend for Bodybuiling

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Injectable Premade Steroids Oil TMT 425 Mg/Ml Semi Finished Blend for Bodybuiling
 
What is TMT 425 Blend ?
 
TMT 425 (long acting rip blend) is a blend of Mast E, Tren E and Test E aimed at individuals looking to obtain a lean physique. Boasting a potent combination of long acting hormones, this product is perfect for a cutting cycle where lower injection frequency is preferred. Typically taken biweekly.
Each 1 ml of product contains:
Testosterone Enanthate: 225mg;
Trenbolone Enanthate: 100mg;
Drostanolone Enanthate: 100mg.
 
Testosterone Enanthate:
Testosterone enanthate is a long lasting single ester steroid. It is 7 carbons in length. What this means, is that more of the weight of the steroid is testosterone as opposed to ester weight. When taking a quantity of an esterified steroid, the total weight is a combination of both the ester weight and the steroid. That said, longer esters such as cypionate have more ester weight (due to it's 8 carbon length), and less overall steroid weight. For this reason, enanthate would be preferred over cypionate. Sustanon has even more steroid weight.
 
Trenbolone Enanthate:
trenbolone Enanthate used as pharmaceutical raw materials. In the eyes of many, the Trenbolone hormone is considered the ultimate in cutting cycles; thats not surprising with its strong metabolic increasing and fat burning properties. While those are tremendous benefits, where Trenbolone Enanthate truly shines is in its ability to greatly preserve lean muscle tissue; perhaps better than any anabolic steroid on earth.
Trenbolone enanthate is a steroid used by veterinarians on livestock to increase muscle growth and appetite. Trenbolone compounds have a binding affinity for the androgen receptor five times as high as that of testosterone.
 
Masteron Enanthate:
The benefits of Masteron-Enanthate should be summed up in three words, lean and hard. For the performance enhancers and outside of a breast cancer patient largely it will only be performance enhancers of a bodybuilding nature who supplement with Masteron in the first place as it is an excellent physique transforming steroid but it is not a miracle in a bottle. Even though it has a rather mildly low androgenic rating the story it tells is rather different as it will harden one up quite decently. Further, as is by its nature Masteron-Enanthate effects overall metabolic activity by directly stimulating lipolysis; no, it is not the only steroid that presents such benefits nor is it the strongest one but these are largely the traits.
 

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