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Boldenone Acetate


Synonym: Adrostadienolone acetate
Key words:Boldenone Acetate,Adrostadienolone acetate,Adrostadienolone acetate powder,steroid and hormones,anabolic,bodybuilding raw powder
.
Chemical name:Boldenone 17-acetate
CAS:   2363-59-9
Assay: 99%min
Molecular formula: C21H28O3
Molecular weight: 328.45
Packing: 1kg Aluminum foil bags
Shipping:Express Courier
Minimum order quantity:10grams
Payment term:Western Union;Moneygram;T/T;Bitcoin
Appearance: white or off-white crystalline powder
Melting Point: 125°C min
Loss On Drying: 1.0%max

Boldenone Acetate would be more intense to raises red blood cells, increase the appetite, and repaire connective tissue which are also a huge plus for bodybuilders during training. Boldenone Acetate is going to be a painful injection. This steroid is containing 25mg/ml of the hormone boldenone attatched to the acetate ester and 75mg/ml of the hormone boldenone attatched to the propiopate ester. Having Boldenone attatched to these esters allows for it to raise blood levels rather quickly and for the effects to be faster than those seen with the slower ester of traditional EQ. This will favor athletes looking to run shorter cycles and those who are worried about frequent drug testing and need to be able to clear hormones from their system in a timely manner.


Boldenone Acetate can be effectively incorporated in both "cutting" and "bulking" cycles due to the well balanced effects of this anabolic substance. This steroid aromatizes very little, and therefore produces almost no estrogenic side effects such as water retention or "gyno".

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Boldenone Cypionate


Product Name: BOLDENONE CYPIONATE
CAS: 106505-90-2
MF: C26H38O3
MW: 398.58
Purity: 98%

Boldenone Cypionate Usage:

Boldenone cypionateis is an ester of boldenone cypionateis and recommended as an aid for the treatment of debilitated horses when an improvement in weight, hair coat or general physical condition is desired. Debilitation often follows disease or may occur following overwork and overexertion.

Boldenone Cypionate improves the general state of debilitated horses, thus aiding in correcting weight losses and improving appetite. It is not a substitute for a well-balanced diet. Optimal results can be expected only when good management and feeding practices are utilized.

Boldenone Cypionate should be considered only as adjunctive therapy to other specific and supportive therapy for diseases, surgical cases and traumatic injuries.

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Boldenone (Steroids)
Synonym: dehydrotestosterone; 17beta-Hydroxyandrosta-1,4-dien-3-one; 1-Dehydrotestosterone
CAS: 846-48-0
EINECS: 212-686-0
Assay: 98% min
Molecular Formula:C19H26O2
Molecular Weight:286.41
Packing: 1kg net/ plastic bottle or tin.
Delivery: Express courier.
The min. order is 10 grams.
Character: White crystalline powder.

Description And Applications Of Bolden base:
Bolden  base was synthesized in an attempt to create a long-acting injectable methandrostenolone (Dianabol), but in reality bolden  base acts nothing like methandrostenolone. It has a very long half-life, and can show up on a steroid test for up to 1.5 years, due to the long undecylenate ester attached to the parent steroid. Trace amounts of the drug can easily be detected for months after discontinued use.

 Anabolic steroid. It is one of the most popular used in veterinary steroids, used in veterinary medicine.Male hormone level is very high, the synthetic effect is also very strong.Bao Dan ketone can be effective, stable and sustainable growth muscle and strength, better if with other drugs, is the most popular used in veterinary the easiest way to keep the muscle after the "cycle" one of the steroid (and other group of drug, stanozolol, HGH, pure testosterone, etc.). In addition, the natural conditions in the human body can produce trace amounts of Bolden base.

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Boldenone undecylenate (Steroids)


Synonym:Equipoise;Equipoise:EQ
CAS NO.: 13103-34-9
EINECS: 236-024-5
Assay: 97.0~103.0%
Molecular Formula:C30H44O3
Molecular Weight:452.67
Appearance:Yellowish oily liquid.
Standard: USP28

Boldenone Undeclynate has become a very popular steroid with athletes and bodybuilders due to the fact that it has very low side effects and has anabolic properties which promote a steady gain in quality muscle mass over time.  
This steroid is a favorite among bodybuilders who are looking to make solid gains without the extra bloat, or are nearing contest.
This steroid also dramatically increases protein synthesis and red blood cell count meaning that nutrients are transported throughout the body much more effectively. Because of this, Equipoise is able to make much more use of less food, enhancing its capabilities as an effective steroid to use when "cutting" and a bodybuilder is trying to reduce calories to get into contest shape.

How to Dose Boldenone Undecylenate ? 

 Equipoise is used by athletes and bodybuilders to increase endurance, muscle mass and the production of red blood cells in the body. It is best known for providing slow but steady gains during bulking cycles (usually called the EQgains). EQ can be used in dosages ranging from 200mg to 600mg per week for as long as 12 weeks.

In recent years, equipoise has become a favorite among powerlifters and is considered by coaches as an ideal replacement for deca durabolin. This is primarily because the quality of muscle mass and strength gains that are experienced while on equipoise happen without the nasty side effects of deca. Also, EQ has a positive effect on the circulation of blood in the body; allowing for maximum blood flood to muscles during intense training sessions.

In medical use, equipoise can promote erythropoietin (EPO) stimulating factor that, in turn, stimulates the bone marrow growth that leads to an increased production of red blood cells. More red blood cell means more hemoglobin, and a higher oxygen carrying capacity. EQ may also result in changes to electrolyte levels because of its potent mineralocorticoid properties.

For men, the average dose is 400-600mgs per week, but I've seen guys go up to 1000mgs per week as long as cycle aids were used.
For women, the average dose is 25-50mgs per week, but you have to be very careful. If you see heavy side effects, discontinue EQ or lower dosages.

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Fulvestrant (Steroids)
CAS:129453-61-8
Synonyms: FASLODEX
Purity: 99%
Molecular Fomular:C32H47F5O3S
Molecular Weight:606.77
Density:1.201 g/cm3
Melting Point:104-106℃
Boiling Point:674.8 °C at 760 mmHg
Appearance:white powder
Usage:Antineoplastic (hormonal)

Faslodex Description

FASLODEX(Faslodex, AstraZeneca) is a drug treatment of hormone receptor-positive metastatic breast cancer in postmenopausal women with disease progression following anti-estrogen therapy. It is an estrogen receptor antagonist with no agonist effects, which works by down-regulating the estrogen receptor.

Faslodex is a selective estrogen receptor antagonist or estrogen receptor down-regulator. It is able to eliminate the action of estrogen in the body by blocking the available estrogen receptors. So therefore unlike aromatase inhibitors, it does not prevent aromatization but rather limits the activity of the estrogen after it is created. As with most aromatase inhibitors and selective estrogen receptor modulators the primary use of Faslodex is in the treatment of estrogen-dependent breast cancer. This is still what it is predominantly used for medically now.

Faslodex Usage

Faslodex is administered using intramuscular injections. For the most part, the full effects of the drug can be achieved using 250 milligrams per injection. Due to the active life of the compound, these injections only have to be administered approximately once every four to five weeks. This is obviously a benefit when compared to the frequent dosing schedule that is required with aromatase inhibitors or selective estrogen receptor modulators.

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Letrozole (Steroids)
Alias: Femara
CAS No: 112809-51-5
Molecular formula: C17H11N5
Molecular weight: 285.3
Appearance: White power
Assay: 99%
Delivery time: 5-7 days
Minimum order: 10g
Supply ability: 5000kg/month
Quality standard: USP32  
Usage: Used as API in Treatment of breast disease.

Femara is used for the treatment of post-menopause breast cancer.
Femara is a powerful Aromatase Inhibitor that was developed to fight breast cancer. For athletes and bodybuilders, it is a drug used to combat the estrogenic side effects of anabolic steroids water-retention, acne and gynocomastia. It will also raise testosterone levels because of the lowered estrogen in the body. Side effects from include a lowered sex drive and continuous use can lead to lowered lipid function and an impaired immune system.

Femara Dosage

Femara comes in tablets of 2.5 milligrams (mg).

How much Femara your doctor tells you to take may vary, but for cancer, a usual dose is 2.5 mg a day.

If you're taking Femara for fertility treatment, your doctor may tell you to take either 2.5 mg or 5 mg of the drug, beginning on the third day of your period for five days.

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Anastrozole (arimidex) (Steroids)
arimidex
Molecular formula: C17H19N5
Molecular weight: 293.37
CAS NO: 120511-73-1
Appearance: an off-white color crystalline powder
Melting point:81.0~84.0°C
Assay: 99%
Delivery:EMS,DHL,FedEx
Delivery time:within 8 hours after payment confirmed
Payment:T/T, Western Union,Money Gram and Bitcoin

Description:
Most commonly called Arimidex, this substance is a true aromatase inhibitor which works by blocking the aromatase enzyme in the body, thus limiting the amount of estrogen buildup that takes place. This compound has obvious benefits to bodybuilders who use aromatizing steroids such as testosterone. These individuals might face estrogen related side effects such as water bloat and "gyno", but by taking GP Anastrozole while on cycle, the chance of any of these sides are greatly reduced.

 In studies that have been done, Arimidex has been shown to reduce estrogen in the body by roughly 50%. This is a good balance for bodybuilders , because some estrogen is needed in order for the full anabolic benefits of the steroids being taken to be achieved. These results are typically the same with a dosage of .5 mg a day as they are with a dosage of 1 mg a day, meaning that in most cases, a half tablet a day will be sufficient for estrogen control throughout cycle.

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Exemestane (Steroids)  

Other name: Aromasin
Product Category: Pharmaceutical raw materials and intermediates
Assay(by HPLC): 98.0-101.2%min
CAS Number: 107868-30-4
Molecular formula: C20H24O2
Molecular Weight:296.40
Packing specifications: 25kg / barrel
Molecular weight: 296.4
Appearance: White or Almost White Crystalline Powder
Density: 1.13g/cm3
Melting Point(°C): 155.13°C
Boiling Point(°C): 453.7°C at 760 mmHg
Flash Point(°C): 169°C
refractive_index: 1.572

Aromasin (Exemestanne acetate) is one of those weird compounds that nobody really knows what to do with. It's a third generation Aromatase Inhibitor (AI) just like Arimidex () and Femera ().


the third generation aromatase inhibitors, used in the treatment of metastatic breast cancer and used as aid in the treatment of early breast cancer.
1. Aromasin is one of the most powerful estrogen suppressing compounds.
2. Aromasin is one of the best compounds to lower the aromatizing effect of steroids.
3. Aromasin is available for body builders taking anabolic steroids.
4. Aromasin is also known as .
5. It acts by blocking the enzyme aromatase, subsequently blocking the production of estrogen.
6. Aromasin is also a kind of .antineoplastic (hormonal) raw materials.

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TOREMIFENE CITRATE (Steroids)
Synonyms: FC 1157a; Fareston; NK 622; NSC 613680
CAS: 89778-27-8
Molecular Formula:  C26H28ClNO.C6H8O7
Molecular Weight: 598.09
Melting Point:  158-164 ºC
Boiling Point:  535.1 ºC at 760 mmHg
Density: 1.045g/cm3
Refractive index: 1,416-1,418
Appearance: White or almost white powder
Use as anti-cancer drug. Suitable for the treatment of postmenopausal women with estrogen receptor positive and / or unknown in metastatic breast cancer

Description

Toremifene citrate is an oral selective estrogen receptor modulator (SERM) which helps oppose the actions of estrogen in the body. Licensed in the United States under the brand name Fareston, toremifene citrate is FDA-approved for use in advanced (metastatic) breast cancer. It is also being evaluated for prevention of prostate cancer under the brand name Acapodene.

 Application

Toremifene is used in postmenopausal women to treat breast cancer that has spread to other parts of the body (metastatic breast cancer). It is usually used to treat cancerthat needs estrogen, a female hormone, in order to grow (estrogen-receptor positive). Toremifene is a nonsteroidal antiestrogen that blocks the effects of estrogen in thebreast tissue, thereby slowing or stopping the growth of cancer.

Dosages

For bodybuilding purposes, a dose of 40-60mgs per day seems to be a good starting point. If the user is trying to fight existing gynecomastia (bitch tits), they may choose to double the dose and add an aromatase inhibitor like Aromasin with it. For PCT, some users will kick-start with 100-120mgs per day and then lower to 40-60mgs per day for 4-6 weeks.

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Clomifene citrate (Clomid) (Steroids)

Synonyms: Clomid; Clomiphene citrate
Key words:Clomifene citrate,Clomifene,
Clomifene,Clomid ,Anti-estrogen Raw Powder
CAS No: 50-41-9
Einecs No: 200-035-3
MF: C32H36ClNO8
MW: 598.09

Purity: 99%
Appearance: White power; Odourless.

Use: the goods to anti-estrogen fertility inducer, the objects in dysfunctional uterine bleeding, polycystic ovary, menstrual disorders and drug-induced amenorrhea and other gynecologic diseases

Clomid is a selective estrogen receptor modulator (SERM) that increases production of gonadotropins by inhibiting negative feedback on the hypothalamus.

It is used mainly in female infertility, in turn mainly as ovulation induction to reverse oligoovulation or anovulation such as in infertility in polycystic ovary syndrome, as well as being used for ovarian hyperstimulation, such as part of an in vitro fertilization procedure. Clomifene citrate is marketed under various trade names including Clomid, Serophene, and Milophene. Prohibited use in sports and use in bodybuilding

Clomifene is commonly used by male anabolic steroid users to bind the estrogen receptors in their bodies, thereby blocking the effects of estrogen, such as gynecomastia. It also restores the body's natural production of testosterone. It is commonly used as a "recovery drug" and taken toward the end of a steroid cycle. It is included on the World Anti-Doping Agency list of illegal doping agents in sport.