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Oral Cardarine Raw Gw501516 Powder On Sale
Keywords: Cardarine powder,Cardarine Powder,GSK-516 Powder,Raw Cardarine powder,Endurobol powder,
oral SARMs Cardarine powder,Endurobol raw powder,Cardarine cycles,Cardarine dosages,Cardarine effects,
Gw501516 oral liquid suspension 25mg/ml,Cardarine oral suspension 30mg/ml
The science behind how Cardarine GW-501516 is actually quite simple. Since it is a PPAR (Peroxisome proliferator-activated receptor beta) agonist it binds to the receptors. The gene activity is altered, which causes a change in energy output. This type of thing will cause a sharp boost in endurance in the body, allowing you to go harder and longer, without getting winded as easily.
From a 'bro' outlook your heart rate will not get as revved up while on this compound. Just imagine your heart was the RPM's on a car and you were pushing hard on the gas, well if you slam too hard the RPM's will go into the red zone causing your engine to burn up. If you added Cardarine (GW501516) to your car your RPM's would not go into the red, so you can 'rev up' your body the same way.
Keywords: Cardarine powder,Cardarine Powder,GSK-516 Powder,Raw Cardarine powder,Endurobol powder,
oral SARMs Cardarine powder,Endurobol raw powder,Cardarine cycles,Cardarine dosages,Cardarine effects,
Gw501516 oral liquid suspension 25mg/ml,Cardarine oral suspension 30mg/ml
The science behind how Cardarine GW-501516 is actually quite simple. Since it is a PPAR (Peroxisome proliferator-activated receptor beta) agonist it binds to the receptors. The gene activity is altered, which causes a change in energy output. This type of thing will cause a sharp boost in endurance in the body, allowing you to go harder and longer, without getting winded as easily.
From a 'bro' outlook your heart rate will not get as revved up while on this compound. Just imagine your heart was the RPM's on a car and you were pushing hard on the gas, well if you slam too hard the RPM's will go into the red zone causing your engine to burn up. If you added Cardarine (GW501516) to your car your RPM's would not go into the red, so you can 'rev up' your body the same way.
GW-501516 (Cardarine) is one of the most versatile performance enhancers
one will ever come across. Whether you are looking to drastically
increase endurance,melt fat,cut or recomp,GW will truly shine.In this
article,I am going to touch on the many ways and reason to incorporate
GW into every cycle that you run.There is a place for GW in every cycle,
regardless of the desired goal.It can only add extra benefits that will
further enhance the chances of accomplishing goals and maximizing
gains.Raw Cardarine powder
GW will only add positives to your cycle in every aspect as opposed to these other negative choices.GW can also work wonders when preparing for a competition. By incorporating GW into a prep cycle,you are allowing yourself to maximize the cleanliness of your gains by melting away fat with its usage.Another excellent benefit of GW is its ability to combat the negative impact that tren can have on a person's cardio performance.By adding GW into the equation, you will still be able to do cardio on atrenbolone cycle without all of the negative impacts. GW can be ran up to 12 weeks and should be ran between 10-20 mg a day.The optimal way to dose GW is to take one dose in the morning and another equivalent dose 12 hours later.It is a good option to take GW prior to your workout. GW can really work magic in so many ways and should be implemented on every cycle that you run.
GW-501516 Usage and Dosage :
It had been investigated as a potential treatment for obesity,diabetes,dyslipidemia and cardiovascular disease.GW501516 could be used by athletes as an ergogenic performance enhancing drug.The most common use of GW consists of the extreme amount of endurance and recovery increase.The other main use of GW-501516 is to aid in fat loss.GW-501516 has shown to melt away fat at a rapid pace.
There are two main uses with GW-501516. The first and most common use is that of increased endurance. GW has been banned for professional athletes due to the unfair advantage it provides to endurance athletes. Anyone want a drastic increase in endurance will find that GW truly shines in this aspect. It takes effect very quickly and the results can be staggering. A common dose of 10 mg day will provide a significant increase in endurance.
The second common usage with GW is that of fat loss. Many users turn to GW as it has shown to melt off fat while still being non-catabolic. You will find that you can still hold on to some muscle as you are losing fat. It helps when you are running it in conjunction with SARMS Ostarine and S4, to hold on to as much muscle as possible. A dosage of 10 mg a day will provide good amounts of fat loss, but an increase to 20 mg a day will provide much more in this area.
GW will only add positives to your cycle in every aspect as opposed to these other negative choices.GW can also work wonders when preparing for a competition. By incorporating GW into a prep cycle,you are allowing yourself to maximize the cleanliness of your gains by melting away fat with its usage.Another excellent benefit of GW is its ability to combat the negative impact that tren can have on a person's cardio performance.By adding GW into the equation, you will still be able to do cardio on atrenbolone cycle without all of the negative impacts. GW can be ran up to 12 weeks and should be ran between 10-20 mg a day.The optimal way to dose GW is to take one dose in the morning and another equivalent dose 12 hours later.It is a good option to take GW prior to your workout. GW can really work magic in so many ways and should be implemented on every cycle that you run.
GW-501516 Usage and Dosage :
It had been investigated as a potential treatment for obesity,diabetes,dyslipidemia and cardiovascular disease.GW501516 could be used by athletes as an ergogenic performance enhancing drug.The most common use of GW consists of the extreme amount of endurance and recovery increase.The other main use of GW-501516 is to aid in fat loss.GW-501516 has shown to melt away fat at a rapid pace.
There are two main uses with GW-501516. The first and most common use is that of increased endurance. GW has been banned for professional athletes due to the unfair advantage it provides to endurance athletes. Anyone want a drastic increase in endurance will find that GW truly shines in this aspect. It takes effect very quickly and the results can be staggering. A common dose of 10 mg day will provide a significant increase in endurance.
The second common usage with GW is that of fat loss. Many users turn to GW as it has shown to melt off fat while still being non-catabolic. You will find that you can still hold on to some muscle as you are losing fat. It helps when you are running it in conjunction with SARMS Ostarine and S4, to hold on to as much muscle as possible. A dosage of 10 mg a day will provide good amounts of fat loss, but an increase to 20 mg a day will provide much more in this area.
RAD140 is a highly effective, oral SARM currently being studied for both
anabolic and neuroprotective effects. RAD140 is in a class of androgen
receptor (AR) ligands that are tissue selective, developed to treat
muscle wasting associated with cancer, acute and chronic illness and
age-related muscle loss. Testolone powder
RAD140 (Testolone) is designed to replace testosterone in bodybuilding, getting your body to react in the same way as it would to a dose of the powerful hormone but without any of the nasty side effects. At the same time loss of fat tissue occurs, making it the ideal drug for bodybuilders and sports use.
Some of the future applications which have been penciled in for RAD140 include androgen deficiency, sarcopenia and muscle wasting diseases. So RAD140 could be of use to both the bodybuilding community and the general population. There are absolutely no androgenic side effects to RAD140 so if desired, women can use it within bodybuilding.
RAD–140(Testolone) Benefits:
1. RAD140 Faster buildup of muscular tissues that helps you achieve more gains in a shorter period of time
2. RAD140 Enhanced speed, stamina and endurance during high-intensity workouts
3. RAD140 SARM was also seen to help reduce the androgenic side effects that can be potentially caused by the same on the prostate.
4. RAD140 is a potent supplement that contains RAD 140, perfect for recomping and to help you build muscle and boost your strength to get that ripped physique you’ve always wanted.
5. RAD140 has anti-catabolic properties, so it will be a great help at preventing muscle wasting problems.
6. RAD140 is capable of increasing strength and muscle volume in a much shorter time, especially in those who are deficient in the male hormone testosterone
RAD140 (Testolone) is designed to replace testosterone in bodybuilding, getting your body to react in the same way as it would to a dose of the powerful hormone but without any of the nasty side effects. At the same time loss of fat tissue occurs, making it the ideal drug for bodybuilders and sports use.
Some of the future applications which have been penciled in for RAD140 include androgen deficiency, sarcopenia and muscle wasting diseases. So RAD140 could be of use to both the bodybuilding community and the general population. There are absolutely no androgenic side effects to RAD140 so if desired, women can use it within bodybuilding.
RAD–140(Testolone) Benefits:
1. RAD140 Faster buildup of muscular tissues that helps you achieve more gains in a shorter period of time
2. RAD140 Enhanced speed, stamina and endurance during high-intensity workouts
3. RAD140 SARM was also seen to help reduce the androgenic side effects that can be potentially caused by the same on the prostate.
4. RAD140 is a potent supplement that contains RAD 140, perfect for recomping and to help you build muscle and boost your strength to get that ripped physique you’ve always wanted.
5. RAD140 has anti-catabolic properties, so it will be a great help at preventing muscle wasting problems.
6. RAD140 is capable of increasing strength and muscle volume in a much shorter time, especially in those who are deficient in the male hormone testosterone
RAD-140 is a non-steroid selective androgen receptor modulator, or
SARM. RAD140 has demonstrated potent anabolic activity on muscle and
bone in preclinical studies and has completed 28-day preclinical
toxicology studies in both rats and monkeys.Testolone powder
Product Details:
Place of Origin: China
Product Name: Rad-140 (Testolone)
CAS No.: 1182367-47-0
Molecular Formula: C20H16ClN5O2
Molecular weight: 282.80892
Purity: 99.0%
Appearance: White crystalline fine powder
Certification: GMP, SFDA
Payment Terms:
Minimum Order Quantity: Ask
Payment Terms: Bitcoin, Money Gram, Bank Wire, Other
Delivery & Shipping Terms:
1. We will ship the goods within 1 days after payment.
2. We will ship the goods by UPS, EMS, DHL, TNT or FEDEX. We will choose the best courier depending on different countries, and find the safest way to deliver the goods for you.
3. Delivery time EMS: 5-14 days. DHL/UPS/FedEx: 4-7 days.
4. Customs in countries like Russia, Australia, Canada is very strict, but we can ensure 100% delivery.
5. As usual you can get the goods with in 4-7 days. If the goods were lost or not received for other reasons, we’ll resend.
Product Details:
Place of Origin: China
Product Name: Rad-140 (Testolone)
CAS No.: 1182367-47-0
Molecular Formula: C20H16ClN5O2
Molecular weight: 282.80892
Purity: 99.0%
Appearance: White crystalline fine powder
Certification: GMP, SFDA
Payment Terms:
Minimum Order Quantity: Ask
Payment Terms: Bitcoin, Money Gram, Bank Wire, Other
Delivery & Shipping Terms:
1. We will ship the goods within 1 days after payment.
2. We will ship the goods by UPS, EMS, DHL, TNT or FEDEX. We will choose the best courier depending on different countries, and find the safest way to deliver the goods for you.
3. Delivery time EMS: 5-14 days. DHL/UPS/FedEx: 4-7 days.
4. Customs in countries like Russia, Australia, Canada is very strict, but we can ensure 100% delivery.
5. As usual you can get the goods with in 4-7 days. If the goods were lost or not received for other reasons, we’ll resend.
As reported by Mamounas et al in The Lancet Oncology, the phase III NRG
Oncology/NSABP B-42 trial has shown no disease-free survival benefit
with 5 years of letrozole (Femara) vs placebo after 5 years of aromatase
inhibitor–based therapy in women with hormone receptor–positive
postmenopausal breast cancer.Raw Letrozole powder
Study Details
In the double-blind trial, conducted at 158 sites in the United States, Canada, and Ireland, 3,966 postmenopausal women with stage I–IIIA hormone receptor–positive breast cancer who were disease-free after approximately 5 years of treatment with an aromatase inhibitor or tamoxifen followed by an aromatase inhibitor were randomly assigned between September 2006 and January 2010 to receive 5 years of letrozole 2.5 mg per day (n = 1,983) or placebo (n = 1,983). The primary endpoint was disease-free survival, defined as time from randomization to breast cancer recurrence, second primary malignancy, or death. Follow-up information was available for 3,903 patients for the analysis of disease-free survival, including 1,950 in the letrozole group and 1,953 in the placebo group. The two-sided statistical significance level for disease-free survival was set at .0418 to adjust for previous interim analyses.
Disease-free survival events were observed in 292 patients in the letrozole group vs 339 patients in the placebo group (hazard ratio [HR] = 0.85, P = .048, which did not meet the prespecified significance level). Estimated disease-free survival at 7 years was 84.7% in the letrozole group vs 81.3% in the placebo group. In multivariate analysis adjusting for the significant prognostic factors of age, pathologic node status, previous tamoxifen use, and type of surgery, the HR for disease-free survival was 0.86 (P = .0501). A beneficial effect of letrozole was more pronounced in patients who underwent mastectomy, had received previous tamoxifen, and had a lowest bone mineral density score of –2.0 or less, although the differences in these groups were not statistically significant. The largest differences in disease-free survival events for the letrozole vs placebo groups were in distant recurrence (61 vs 87 events) and contralateral breast cancer (30 vs 59 events).
No significant difference in overall survival was observed for letrozole vs placebo (HR = 1.15, P = .22). Estimated 7-year overall survival was 91.8% vs 92.3%. A total of 93 patients died from breast cancer, including 46 in the letrozole group and 47 in the placebo group.
The most common grade 3 adverse events were arthralgia (3% vs 2
and back pain (2% vs 2.
The most common grade 4 adverse events were urinary tract infection,
hypokalemia, and left ventricular systolic dysfunction (four patients
each, < 1% each) in the letrozole group and thromboembolic events (8
patients, < 1in the placebo group.
The investigators concluded: “After 5 years of aromatase inhibitor–based therapy, 5 years of letrozole therapy did not significantly prolong disease-free survival compared with placebo. Careful assessment of potential risks and benefits is required before recommending extended letrozole therapy to patients with early-stage breast cancer.
Study Details
In the double-blind trial, conducted at 158 sites in the United States, Canada, and Ireland, 3,966 postmenopausal women with stage I–IIIA hormone receptor–positive breast cancer who were disease-free after approximately 5 years of treatment with an aromatase inhibitor or tamoxifen followed by an aromatase inhibitor were randomly assigned between September 2006 and January 2010 to receive 5 years of letrozole 2.5 mg per day (n = 1,983) or placebo (n = 1,983). The primary endpoint was disease-free survival, defined as time from randomization to breast cancer recurrence, second primary malignancy, or death. Follow-up information was available for 3,903 patients for the analysis of disease-free survival, including 1,950 in the letrozole group and 1,953 in the placebo group. The two-sided statistical significance level for disease-free survival was set at .0418 to adjust for previous interim analyses.
Disease-free survival events were observed in 292 patients in the letrozole group vs 339 patients in the placebo group (hazard ratio [HR] = 0.85, P = .048, which did not meet the prespecified significance level). Estimated disease-free survival at 7 years was 84.7% in the letrozole group vs 81.3% in the placebo group. In multivariate analysis adjusting for the significant prognostic factors of age, pathologic node status, previous tamoxifen use, and type of surgery, the HR for disease-free survival was 0.86 (P = .0501). A beneficial effect of letrozole was more pronounced in patients who underwent mastectomy, had received previous tamoxifen, and had a lowest bone mineral density score of –2.0 or less, although the differences in these groups were not statistically significant. The largest differences in disease-free survival events for the letrozole vs placebo groups were in distant recurrence (61 vs 87 events) and contralateral breast cancer (30 vs 59 events).
No significant difference in overall survival was observed for letrozole vs placebo (HR = 1.15, P = .22). Estimated 7-year overall survival was 91.8% vs 92.3%. A total of 93 patients died from breast cancer, including 46 in the letrozole group and 47 in the placebo group.
The most common grade 3 adverse events were arthralgia (3% vs 2
and back pain (2% vs 2.
The most common grade 4 adverse events were urinary tract infection,
hypokalemia, and left ventricular systolic dysfunction (four patients
each, < 1% each) in the letrozole group and thromboembolic events (8
patients, < 1in the placebo group.The investigators concluded: “After 5 years of aromatase inhibitor–based therapy, 5 years of letrozole therapy did not significantly prolong disease-free survival compared with placebo. Careful assessment of potential risks and benefits is required before recommending extended letrozole therapy to patients with early-stage breast cancer.
Tamoxifen has been shown to protect bone from estrogen-deficiency bone
loss and lower plasma cholesterol in the rat. A 10 µM solution has
exhibited fungicidal activity (optimal pH 7,5) against yeast cells of C.
albicans. It has been implemented in liver carcinogenesis in rats.
Other actions of tamoxifen are: Reduction of plasma levels of insulin-like growth factor; Induction of cells surrounding cancer cells to secrete transforming growth factor b; Inhibition of membrane lipid peroxidation probably by decreasing membrane fluidity.
Protein kinase C inhibitor. Induces apoptosis in human malignant glioma cell lines. Tamoxifen and its metabolite 4-hydroxytamoxifen are selective estrogen response modifiers (SERMs) that act as estrogen antagonists in mammary gland. Blocks estradiol-stimulated VEGF production in breast tumor cells.
Soluble in methanol (50 mg/mL with heat) or ethanol (10 mg/mL with sonication); very slightly soluble in water (0.3 mg/L at 20 °C; the pH is approximately 3.0-3.5), 0.02 N HCl (0.2 mg/mL at 37 °C), acetone or chloroform.www.aasraw.com/products/tamoxifen-citrate-nolvadex-powder /a>
Other actions of tamoxifen are: Reduction of plasma levels of insulin-like growth factor; Induction of cells surrounding cancer cells to secrete transforming growth factor b; Inhibition of membrane lipid peroxidation probably by decreasing membrane fluidity.
Protein kinase C inhibitor. Induces apoptosis in human malignant glioma cell lines. Tamoxifen and its metabolite 4-hydroxytamoxifen are selective estrogen response modifiers (SERMs) that act as estrogen antagonists in mammary gland. Blocks estradiol-stimulated VEGF production in breast tumor cells.
Soluble in methanol (50 mg/mL with heat) or ethanol (10 mg/mL with sonication); very slightly soluble in water (0.3 mg/L at 20 °C; the pH is approximately 3.0-3.5), 0.02 N HCl (0.2 mg/mL at 37 °C), acetone or chloroform.www.aasraw.com/products/tamoxifen-citrate-nolvadex-powder /a>
Raloxifene hydrochloride is the second generation of selective estrogen
receptor modulators (SERM) for the benzothiophene series. The drug is
similar to tamoxifen and exhibits estrogen receptor antagonist
(blocking) properties in some tissues as an estrogen receptor agonist
(activator) in other tissues.Raloxifene powder
The major change between these two agents is their tissue selectivity. Although raloxifene hydrochloride is a strong antiestrogen in the mammary gland and uterine tissue, it appears to be estrogen in the bones. This allows it to protect bone density and mimic the beneficial effects of endogenous estradiol. This is quite different from tamoxifen, tamoxifen in the breast and bone are anti-estrogen effect.
In the fight against estrogen, raloxifene hydrochloride has been approved by the FDA for the prevention and treatment of postmenopausal women with osteoporosis. Other potential uses are being studied, including treatment and prevention of cardiovascular disease, breast cancer, men's breast development, prostate cancer, acromegaly and uterine cancer.
Usually products are send in discreet way,based on our rich in shipping products to every countries,we usually use disguised way.
The photo of food disguised package for your reference,which has passed through every countries smoothly,products are packed well in food box,which mixed with real visible chinese food,and in the express bill we will declare food and sample,customs just think it chinese food and release it.
Professional Manufacture: GUANGZHOU Quanao CHEMICAL CO,LTD is a legit and professional pharmaceutical manufacturer specialized in steroid hormone powders, steroid injectable liquids, peptides,pharmaceutical raw materials & its intermediate.Our factory is in Nanhu Shouyi Industrial District, just by the side of the beautiful South Lake in Wuhan. Our company integrates R&D,producing, operating and marketing into an organic whole.
The major change between these two agents is their tissue selectivity. Although raloxifene hydrochloride is a strong antiestrogen in the mammary gland and uterine tissue, it appears to be estrogen in the bones. This allows it to protect bone density and mimic the beneficial effects of endogenous estradiol. This is quite different from tamoxifen, tamoxifen in the breast and bone are anti-estrogen effect.
In the fight against estrogen, raloxifene hydrochloride has been approved by the FDA for the prevention and treatment of postmenopausal women with osteoporosis. Other potential uses are being studied, including treatment and prevention of cardiovascular disease, breast cancer, men's breast development, prostate cancer, acromegaly and uterine cancer.
Usually products are send in discreet way,based on our rich in shipping products to every countries,we usually use disguised way.
The photo of food disguised package for your reference,which has passed through every countries smoothly,products are packed well in food box,which mixed with real visible chinese food,and in the express bill we will declare food and sample,customs just think it chinese food and release it.
Professional Manufacture: GUANGZHOU Quanao CHEMICAL CO,LTD is a legit and professional pharmaceutical manufacturer specialized in steroid hormone powders, steroid injectable liquids, peptides,pharmaceutical raw materials & its intermediate.Our factory is in Nanhu Shouyi Industrial District, just by the side of the beautiful South Lake in Wuhan. Our company integrates R&D,producing, operating and marketing into an organic whole.
Raloxifene hydrochloride is an estrogen agonist/antagonist, referred to
as a selective estrogen receptor modulator (SERM) and belongs to the
benzothiophene class of compounds. The biological actions of raloxifene
Hcl are largely mediated through binding to estrogen receptors.Raloxifene powder
This binding results in activation of estrogenic pathways in some tissues (agonism) and and the blockade of estrogenic pathways in other tissues (antagonism). The agonistic or antagonistic activity of raloxiffene depends on the extent of recruitment of coactivators and corepressors to estrogen receptor (ER) target gene promotors.
Raloxifene Hcl appears to act as an estrogen agonist in bone. It decreases bone resorption and bone turnover, increases bone mineral density and decreases fracture incidence.
Raloxifene Hydrochloride Application:
1) Raloxifene Hcl used to prevent & treat osteoporosis in women who have undergone menopause.
2) Raloxifene Hcl used to decrease the risk of developing invasive breast cancer in women who are at high risk of developing this type of cancer or who have osteoporosis. Raloxifene Hcl cannot be used to treat invasive breast cancer or to prevent invasive breast cancer from coming back in women who have already had the condition.
3) Raloxifene Hcl prevents and treats osteoporosis by mimicking the effects of estrogen to increase the density (thickness) of bone.
4) Raloxifene Hcl decreases the risk of developing invasive breast cancer by blocking the effects of estrogen on breast tissue, which may stop the development of tumors that need estrogen to grow.
This binding results in activation of estrogenic pathways in some tissues (agonism) and and the blockade of estrogenic pathways in other tissues (antagonism). The agonistic or antagonistic activity of raloxiffene depends on the extent of recruitment of coactivators and corepressors to estrogen receptor (ER) target gene promotors.
Raloxifene Hcl appears to act as an estrogen agonist in bone. It decreases bone resorption and bone turnover, increases bone mineral density and decreases fracture incidence.
Raloxifene Hydrochloride Application:
1) Raloxifene Hcl used to prevent & treat osteoporosis in women who have undergone menopause.
2) Raloxifene Hcl used to decrease the risk of developing invasive breast cancer in women who are at high risk of developing this type of cancer or who have osteoporosis. Raloxifene Hcl cannot be used to treat invasive breast cancer or to prevent invasive breast cancer from coming back in women who have already had the condition.
3) Raloxifene Hcl prevents and treats osteoporosis by mimicking the effects of estrogen to increase the density (thickness) of bone.
4) Raloxifene Hcl decreases the risk of developing invasive breast cancer by blocking the effects of estrogen on breast tissue, which may stop the development of tumors that need estrogen to grow.
Nandrolone Decanoate Powder / Injectable liquid Durabol 99.5% Deca
Deca Quick Detail:
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.
Durabolin Standard: USP28; BP2003
Deca Storage: Shading, Confined Preservation
Package: Discreet Packing ways for your choice.Fluoxymesterone powder
Delivery: Deliver out within 24 hours after payment (Week day), by DHL, TNT, FedEx, HKEMS, UPS, etc.
Payment: West Union, T/T, Money Gram.
We own several sets of analyzing instruments with high efficiency and high sensitivity, all products are guaranteed to be of the highest quality, and we have many safety ways to ship the parcels to different countries(such as Germany, Australia, Sweden, France, Brazil, Mexico ans so on), delivery is guaranteed.
Recipe for DECA 160mg/ml @250ml
40 grams Nandrolone Decanoate
162.5 ml sesame oil
12.5ml BA 5%
37.5ml BB 15%
Recipe for DECA 50 ml @ 200 mg/ml
10 grams Nandrolone Decanoate
32.50 ml sesame oil
2.5ml BA 5%
7.50ml BB 15%
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.
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
Deca Quick Detail:
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.
Durabolin Standard: USP28; BP2003
Deca Storage: Shading, Confined Preservation
Package: Discreet Packing ways for your choice.Fluoxymesterone powder
Delivery: Deliver out within 24 hours after payment (Week day), by DHL, TNT, FedEx, HKEMS, UPS, etc.
Payment: West Union, T/T, Money Gram.
We own several sets of analyzing instruments with high efficiency and high sensitivity, all products are guaranteed to be of the highest quality, and we have many safety ways to ship the parcels to different countries(such as Germany, Australia, Sweden, France, Brazil, Mexico ans so on), delivery is guaranteed.
Recipe for DECA 160mg/ml @250ml
40 grams Nandrolone Decanoate
162.5 ml sesame oil
12.5ml BA 5%
37.5ml BB 15%
Recipe for DECA 50 ml @ 200 mg/ml
10 grams Nandrolone Decanoate
32.50 ml sesame oil
2.5ml BA 5%
7.50ml BB 15%
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.
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
Appearance: White crystalline powder.
Usage: Can be used as pharmaceutical material, As a male hormone and anabolic hormones. It is an anabolic steroid with strong androgenic properties that has been used in the treatment of male hypogonadism, delayed puberty in males, and in the treatment of breast neoplasms in women,
Description:
Fluoxymesterone powder-e Halotestin is used to treat low testosterone levels in males and breast cancer in females. Though the half-life of fluoxymesterone is about 9.2 hours.
Halotestin also exerts its effects on strength and fat loss by both regulation of fatty acid oxidation in the liver and fast-twitch muscle mitochondria.
Halotestin is used in men who do not make enough of a natural substance called testosterone.
Abnormal drug-seeking behavior is possible with Halotestin, and it is frequently misused for its muscle-enhancing effects.
Fluoxymesteron also exerts its effects on strength and fat loss by both regulation of fatty acid oxidation in the liver and fast-twitch muscle mitochondria. Oddly, for a drug which exerts such a nice anabolic effect, and promotes such good strength gains, Halotestin has a pretty low Androgen Receptor Binding affinity. I suppose, in this respect it can be compared to Winstrol (Stanozolol).
As far as strength and agression goes, Halo is a great drug. Halotestin is especially useful on a cutting or strength cycle. Its use for mass and weight gains have been pretty disappointing for most users, however.
Our Advantages:
1. Rich experienced in delivering, package will be reshipped if sent failed.
2. Enough Fluoxymesteron-e Halotestin stock ensure the prompt delivery time.
3. Good after-sales service, any of your question would be solved for the first as soon as possible.
Usage: Can be used as pharmaceutical material, As a male hormone and anabolic hormones. It is an anabolic steroid with strong androgenic properties that has been used in the treatment of male hypogonadism, delayed puberty in males, and in the treatment of breast neoplasms in women,
Description:
Fluoxymesterone powder-e Halotestin is used to treat low testosterone levels in males and breast cancer in females. Though the half-life of fluoxymesterone is about 9.2 hours.
Halotestin also exerts its effects on strength and fat loss by both regulation of fatty acid oxidation in the liver and fast-twitch muscle mitochondria.
Halotestin is used in men who do not make enough of a natural substance called testosterone.
Abnormal drug-seeking behavior is possible with Halotestin, and it is frequently misused for its muscle-enhancing effects.
Fluoxymesteron also exerts its effects on strength and fat loss by both regulation of fatty acid oxidation in the liver and fast-twitch muscle mitochondria. Oddly, for a drug which exerts such a nice anabolic effect, and promotes such good strength gains, Halotestin has a pretty low Androgen Receptor Binding affinity. I suppose, in this respect it can be compared to Winstrol (Stanozolol).
As far as strength and agression goes, Halo is a great drug. Halotestin is especially useful on a cutting or strength cycle. Its use for mass and weight gains have been pretty disappointing for most users, however.
Our Advantages:
1. Rich experienced in delivering, package will be reshipped if sent failed.
2. Enough Fluoxymesteron-e Halotestin stock ensure the prompt delivery time.
3. Good after-sales service, any of your question would be solved for the first as soon as possible.