Hormone drugs used in treating deficient hormone levels in body, thyroid problems, ovulation

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Melanotan II Polypeptide Hormones Melanotan 2 Human Growth Hormone MT-2

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Melanotan II Polypeptide Hormones Melanotan 2 Human Growth Hormone MT-2
 
Basic Info.
 
Product Name: 
Melanotan 2; MT2; Melanotan-II; Melanotan2
CAS: 121062-08-6
Molecular Formula: C50H69N15O9
Molecular weight: 1024.2
Purity (by HPLC): 99.00%
Appearance: White Powder
Sequence: Ac-Nle-Asp-His-D-Phe-Arg-Trp-Lys-NH2
Storage Condition: away from light, cold storage (2-8 degree)
Usage: prevention sunlight-induce skin cancer; Sexual Dysfunction & Fat Decomposition
 
What is Melanotan 2 ?
Melanotan 2  Tanning Injections (otherwise known as MT2) was first synthesized at the University of Arizona.  Researches there knew that onc of the best defenses against skin cancer was melanin activated in the skin, a tan.  They hypothesized that an effective way to reduce skin cancer rates in people would be to induce the body's natural pigmentary system to produce a protective tan prior to UV exposure.  The body's naturally occuring hormone MSH causes melanogenesis, a process by which the skin's pigment cells (melanocytes) produce the skin's pigment (melanin).  They tested to see if administering this endogenous hormone to the body directly could be an effective method to cause sunless tanning.  What they found was that while it appeared to work, natural MSH had too short a half life in the body to be practical as a therapeutic drug.  So they decided to find a more potent and stable alternative, one that would be more practical.
 
After synthesizing and screening hundreds of molecules, the researchers headed by Victor J. Hruby and Mac E. Hadley, found a peptide, [Nle4, D-Phe7] MSH, that was approimately 1,000 times more potent than the natural MSH.  They dubbed this new peptide molecule, "Melanotan" (later Melanotan-1, now know as afamelanotide).  They subsequently developed another analog, Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH2), which they called "Melanotan" Tanning Injections.  The scientists hoped to use these peptides to combat melanoma by stimulating the body's natural pigmentary mechanism to create a tan without first needing exposure to harmful levels of UV radiation.  This in turn, they hypothesized, could reduce the potential for skin damage that can eventually lead to skin cancer.
 
A pilot phase I clinical trial conducted on three males by the College of Medacine, Pharmacology Department, University of Arizona in Tuscon, Arizona pulished in 1996 reported that, "Melanotan" Tanning Injections has tanning activity in humans given only 5 low doses every other day by subcutaneous injection."  The side effects reported were mild nausea and a "stretching and yawning complex" that correlated with spontaneous penile erections.
 
The Department of Pharmacology, University of Arizona College of Medacin published in 1998 that involved 10 men who suffered from psychogenic erectile dysfunction.  Their trial concluded that, "Melanotan" Tanning Injections is a potent initiator of erections in men with pyschogenic erectile dydfunction and has manageable side effects at a dose of 0.025mg/kg.
 
A clinical study published in 2000 of 20 men with psychogenic and organic erectile dysfunction conducted at the Section of Urology of The University of Arizona College of Medacin concluded, "that Melanotan II Tanning Injections is a potent initiator of penile erection in men with ecrectile dysfunction.
 
How to use Melanotan 2 Mixing the solutionv:
 
Flip off the cap from the Melanotan 2 Tanning Injection vial.
Wipe the surface of the top of the vial with the enclosed alcohol wipe and discard the wipe.
Wipe the surface of the injectable water tube (or glass water vial depending on the pack ordered) with the enclosed alcohol wipe and discard the wipe.
Remove the enclosed syringe from the packaging. Making sure the injectable water tube is upright, insert the needle of the syringe into the sidewall of the water.
Now pull back the plunger of the syringe so you withdraw 1ml of water and slowly pull the syringe out.
Insert the syringe into the Melanotan 2 Tanning Injection vial and depress the plunger so you completely empty the syringe of the water and slowly remove the syringe from the vial.  Do not shake the solution.
Place the Melanotan 2 solution in the fridge for storage until ready for use.
Make sure you put the syringe caps on and carefully dispose of it.
You have now mixed your Melanotan 2 Tanning Injection solution. Please store the solution in the fridge.
 
How to use Melanotan II for tanning?
 
Melanotan II is typically provided in vials containing 10 mg of lyophilized (freeze-dried) powder. The vials are reconstituted with a convenient amount of bacteriostatic or sterile water, added to the vial by syringe. An example convenient amount of water is 2.5 mL. When this amount of water is used, the resulting solution contains 4 mg of MT-II per mL. If for example wishing to take a dose of 1 mg, a volume of 0.25 mL, or "25 IU" as marked on an insulin syringe, would be taken by injection. Injection may be subcutaneous, intramuscular, or intravenous, according to personal preference.
 
Injection typically is only once per day, but where a person is first trying the drug and judging tolerance, injection may be divided into two smaller amounts per day.
Typical dosage range is 0.5 to 2.0 mg/day, with a preferred range of 0.5 to 1.0 mg/day. However, it's best to first assess tolerance with lower dosing of 0.25 mg at a time.
After reconstitution, a Melanotan II vial should preferably be consumed entirely within 30 days. Prior to reconstitution, MT-II should be stored in the refrigerator or freezer, but it's acceptable for it to be shipped without refrigeration.
 
Use generally should be discontinued if MT-II, in the individual case, causes problems with increased growth, number, or darkness of moles.
 
Melanotan II's effect is fairly long-lasting. It can even be the case that it takes a year or more for a cycle's effect to largely disappear. Use of maintenance cycles can maintain effect indefinitely. As a rule of thumb, maintenance typically requires about 2 to 3 times as much MT-II per year as was needed for the first cycle. This can be taken either as a total of 2 to 3 cycles per year done in the same way as the initial cycle, or any more frequent dosing pattern providing this total amount of MT-II per year.
 

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Mesterolone USP 99%

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Androviron 99% Purity Raw Steroid Powders Mesterolone For Bodybuilding Steroids 1424-00-6
 
Mesterolone Basic Info.
 
Product Name: Mesterolone
Synonyms: 17-beta-hydroxy-1-alpha-methyl-5-alpha-androstan-3-on; 1-alpha-methyl-17-beta-hydroxy-5-alpha-androstan-3-one; Androviron; Mesteranum; Mesterolon
CAS: 1424-00-6
MF: C20H32O2
MW: 304.47
Assay: 99% min.
Packing: 1kg foil bag
Characteristic: White crystalline powder.
Categories: Biochemistry; Hydroxyketosteroids; Steroids
Usage: Pharmaceutical material, Steroid hormone, Anabolin. For the treatment of male hypogonadism and reduced sperm infertility. 
 
Mesterolone Description:
 
Mesterolone is an oral anabolic steroid, a synthetic product of the male hormone testosterone. The drug has shown value in treating men with mental health issues, such as depression, anxiety and bipolar disorders. The drug also is commonly used to treat sexual dysfunction, including low sperm count. Additionally, mesterolone may enhance the effectiveness of other steroids. Interestingly, unlike other steroids, the drug shows little value for bodybuilding, but has the same health risks involved in steroid use for that purpose.
 
Mesterolone Applications:
 
Mesterolone is often used as an antiestrogenic treatment and may be used by those who have had a poor reaction to testosterone treatments. The drug has shown to be beneficial in treating sexual dysfunction, impotency and low libido. Mesterolone binds to estrogen receptors, reducing their activity, which not only reduces estrogen production, but also encourages natural testosterone production in the body.
During the late 1970s, doctors who performed studies on mesterolone concluded that the drug could be used to treat depression in some men. Patients with symptoms of anxiety and low sex drive reported improvement with low doses of the steroid. During the study, higher doses proved helpful to patients with dysthymia and bipolar depression as well. Since this time, newer studies have shown that patients taking a placebo improved at the same rate as patients taking mesterolone, leading medical professionals to believe that better drug options exit.
 

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Mk-677 Oral Grow Hormone Sarm Ibutamoren Mesylate 159752-10-0

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Mk-677 Oral Grow Hormone Sarm Ibutamoren Mesylate 159752-10-0
 
MK-677 Basic Info.:
 
Product Name: Ibutamoren Mesylate ( MK-677 )
Synonyms: MK-677; Crescendo; IbutaMoren Mesylate; MK-667; IBUTAMORIN; Nutrobal
CAS: 159752-10-0
MF: C27H36N4O5S.CH4O3S
MW: 624.776
Purity: 99%
Boiling Point: 868.9°C at 760 mmHg
Appearance: white powder
Storage temp.: 2-8°C
Product Categories: SARMs(Selective androgen receptor modulator)
Application: active growth secretagpgie, mk-677 Effective for age -related fraity Active.
 
MK-677 Description:
 
Nutrobal (Mk-677) is an orally administrated growth hor secretagogue originally developed by Reverse Pharmacology. A secretagogue is the term for a substance that chemically signals for the pituitary gland to secrete growth hor . In other words, Nutrobal could be compared to peptides like GHRP-6 or Ipamorelin, only it doesn't require any injections nor does it have any side effects like GHRP-6. This GHS (Growth Hormone Secretagogue) was developed in an aim to combat such conditions as muscle wasting, obesity and osteoporosis. It was also targeted towards treatment of elderly hip fracture patients, so there are a myriad of studies done on safety.
 
Ibutamoren (MK-677, L-163,191) is a drug which acts as a potent, orally active secretagogue,mimicking the GH stimulating action of the endogenous hormone ghrelin.It has been demonstrated to increase the release of, and producessustained increases in plasma levels of several hormones including , but without affecting cortisol levels.
 
It is currently under development as a potential treatment for reduced levels of these hormones, such as
in deficient children or elderly adults, and human studies have shown it to increase both muscle mass
and bone mineral density, making it a promising therapy for the treatment of frailty in the elderly.It also
alters metabolism of body fat and so may have application in the treatment of obesity.Some mk-677 study shows the suggested mk-677 dosage is 25mgs-50mgs when it is the oral.
 
MK-677 Application:
 
Produced by Reverse Pharmacology, MK 677 (Nutrobal) is an orally administered growth hormone secretagogue that is designed to stimulate the pituitary gland to release growth hormones. In case you're
wondering, "secretagogue" is basically a natural substance that causes another substance to be
secreted, such as gastrin.
 
MK 677 (Nutrobal) was originally formulated to keep health problems like osteoporosis, obesity and
muscle wasting, but has been seen to promote an increase in lean body mass as well as a boost in
IGF-1 serum concentration during clinical runs.
 
Moreover, here are the positive effects of MK 677 (Nutrobal) in terms of improving growth hormone
pulse intensity:Inhibits the signaling of somatostatin receptors.Slows down the activity of somastostatin in the system.Improves somatotroph signaling in growth hormone releasing hormones (GHRH).Amplifies and increases the overall production and release of GHRH.
 

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Mstn Muscle Hypertrophy Peptide Gdf 8 / Myostatin Hmp For Bodybuilding

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Mstn Muscle Hypertrophy Peptide Gdf 8 / Myostatin Hmp For Bodybuilding 
 
Gdf 8 Basic Info
 
Product Name: GDF-8 Human 
Alias: GDF-8 Human;MSTN;Myostatin HMP;Myostatin;Myostatin Human;Human Myostatin;Human Gdf-8;Gdf-8 Human;Growth Differentiation Factor-8
Purity: >98%
Appearance: Lyophilized Powder
Specification: 1mg/vial
Storage: −20°C
Customized: Accepted.
 
Gdf 8 Description:   
 
Myostatin (also known as growth differentiation factor 8, abbreviated GDF-8) is a myokine, a protein produced and released by myocytes that acts on muscle cells' autocrine function to inhibit myogenesis: muscle cell growth and differentiation. In humans it is encoded by the MSTN gene. Myostatin is a secreted growth differentiation factor that is a member of the TGF beta protein family.
Animals either lacking myostatin or treated with substances that block the activity of myostatin have significantly more muscle mass. Furthermore, individuals who have mutations in both copies of the myostatin gene have significantly more muscle mass and are stronger than normal. Blocking the activity of myostatin may have therapeutic application in treating muscle wasting diseases such as muscular dystrophy.
 

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Muscle Building Oral Sarms Powder Rad 140 1182367-47-0

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Muscle Building Oral Sarms Powder Rad 140 1182367-47-0
 
RAD 140 Basic Info:
 
Product Name: RAD 140
CAS: 118237-47-0
MF: C20H16ClN5O2
MW: 393.826
Purity: 99.5%(HPLC)
Apprarance: White crystalline powder
 
Product Description Of RAD 140:
 
RAD140 is a highly effective, oral SARM (Selective Androgen Receptor Modulator) currently being studied for both anabolic and neuroprotective effects. It 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. Recent research of RAD140 shows superior lean tissue selectivity, and reduced androgenic side effects when compared to competing SARM compounds. This compound provides is being studied for neuroprotection as well; an important neural action of endogenous androgens that is relevant to neural health and resilience to neurodegenerative diseases, and to be as effective as testosterone in reducing cell death induced by apoptotic insults. Easy to dose oral SARM that increases lean mass while remaining tissue selective in current research Added value for research with pronounced neuroprotective properties Myotrophic and neuroregeneration research compound.
 
Application Of RAD 140:
 
According to the Cambridge-based pharmaceuticals company Radius, the potent, orally bioavailable and nonsteroidal RAD 140 SARM is designed to make the hormonal receptors in the tissues of the body act the same way as if they're getting a good dose of testosterone, setting off the same effects as if you're cycling with prohormones and anabolic steroids minus unwanted side effects.
 
Moreover, clinical studies also show that RAD 140 SARM also has a few other benefits, which we will discuss more thoroughly in a moment.
 
Enhanced speed, stamina and endurance during high-intensity workoutsFaster buildup of muscular tissues that helps you achieve more gains in a shorter period of timeBased on medical tests, RAD 140 SARM also displayed a greater anabolic effect than testosterone when used. Researchers pointed out that besides having a more "reinforced" effect than testosterone, RAD 140 SARM was also seen to help reduce the androgenic side effects that can be potentially caused by the same on the prostate.
 

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Muscle Building Steroids Powder Epistane Methyl E 4267-80-5

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Muscle Building Steroids Powder Epistane Methyl E 4267-80-5
 
Epistane Basic Info.
 
Product name: Epistane
Alias: Methyl Epitiostanol
Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Steroids;Sulfur & Selenium Compounds
CAS: 4267-80-5
M.F.: C20H32OS
Assay: 98%
M.P.: 168-169°C
Appearance: White powder
Package: foil bag
Usage: Epistane is a methylated derivative of the steroid epitiostanol (E588800). Epistane is a readily orally active compound that lacks the 3-ketone common to most anabolic steroids. Epistane greatly incr eases protein synthesis and build up in lean muscle mass
 
Epistane Description:
 
Epistane, exhibits a strong, long lasting anti-estrogen effect that is organ tissue specific. This means it works only where you want it to work. Broad range estrogen blockers and aromatase inhibitors can result in system shut down, aching joints, and decreased IGF-I expression. Epistane binds specifically to the 17-estradiol receptor protein in the target tissues. Because of its long lasting and strong effects on specific tissue,
 
Epistane can significantly reduce and reverse the effects of gynocomastia because not only does Epistane specifically block estrogen in breast tissue but it induces an estrogen-depleted condition which leads to apoptosis or the death of the breast tissue cells. Studies show that small doses of the parent compound, Epitiostanol, at just 10-20mg/week showed a complete disappearance of the mass and pain in 25% of the male patients in the clinical trail, while the other 75% of the patients showed at least a 50% reduction in the mass and complete loss of pain in just 4-8 weeks. Thats results in 100% of the male users with no side effects.
 
Epistane is more than an anti-estrogen, though, as it also binds to androgen receptors in skeletal muscle. As a PRO-Anabolic compound Epistane promotes increases in strength and lean body mass with an anabolic/androgenic value (Q ratio) of 12. With most powerful androgens there is a high risk of the natural suppression of the gonads. Epistane, unlike other PRO-Anabolic compounds that have recently been released, is relatively mild on the gonads and, due to the anti-estrogenic effects and the fact that Epistane keeps LH levels elevated, post cycle therapy becomes a breeze.
 
Application Of Epistane:
 
Epistane is a DHT derived prohormone that was brought to market by RPN with their product "Havoc. " Epistane is an anti-estrogenic dry compound that will aid users in adding lean muscle mass as well as cutting fat. In addition to this, Epistane does not aromatize and is non-progestagenic. This basically means that while on Epistane, estrogen related side effects like gyno and progesterone related side effects like sensitive breast tissue are virtually non-existent. Users will experience little to no side effects while on Epistane, making it an ideal beginner prohormone.
 
Epistane Function:
 
Epistane also binds to androgen receptors in skeletal muscle cells and muscle stem cells. This leads to changes in muscle cell function and protein synthesis. In the case of muscle stem cells, which will actually change and fuse with your active adult skeletal muscles increasing the muscles potential for growth and repair. On the opposite side, the presence of androgens actually decreases the ability of stem cells to form new fat cells. So now have increased stem cell conversion to muscle cells and decrease the conversion of stem cells to fat cells, giving you more positive effects of nutrition and training.
 

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Muscle Growth Steriods Polypeptide Hormone Oxytocin 50-56-6 For Hasten Parturition

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Muscle Growth Steriods Polypeptide Hormone Oxytocin 50-56-6 For Hasten Parturition
 
Oxytocin Basic Info.:
 
Product Name: Oxytocin
Synonyms: Oxytocin Acetate Salt Hydrate;Ocytocinum;Alpha-Hypophamine 
Unit Size: 2 mg/vial 
Unit Quantity: 1 Vial 
CAS NO.: 50-56-6 
Molecular Formula: C43H66N12O12S2 
Molecular Mass: 1,007.19    
Appearance: White Powder 
Purity: 98.2%  
Source: Chemical Synthesis 
Storage: Lyophilized Oxytocin is stable at room temperature for 90 days,however it should be stored in a freezer below -8C for any extended period of time. After reconstituting Oxytocin should be refrigerated at temperatures not to exceed 36 F.
 
Oxytocin Description:
 
Oxytocin is a hormone that is made in the brain, in the hypothalamus, and it is transported to, and secreted by, the pituitary gland, which is located at the base of the brain.
 
Chemically it is known as a nonapeptide (a peptide containing nine amino acids), and biologically, as a neuropeptide. It acts both as a hormone and as a brain neurotransmitter.
In both men and women, sexual intercourse stimulates the release of oxytocin, which has a role in erection and orgasm. The reason for this is not fully understood, although in women, it has been proposed that the increased uterine motility may help sperm to reach their destination.
 
The research to uncover oxytocin's "anxiolytic and pro-social influences, beneficial to relief, reproduction, and love" is what has led scientists to describe it as a one of the "most promising neuromodulator/neurotransmitter systems of the brain for psychotherapeutic intervention and treatment of numerous psychiatric illnesses, for example social phobia, autism, and postpartum depression.
 
Oxytocin (Oxt) is a mammalian neurohypophysial hormone. Produced by the hypothalamus and stored and secreted by the posterior pituitary gland, oxytocin acts primarily as a neuromodulator in the brain.
Oxytocin plays an important role in the neuroanatomy of intimacy, specifically in sexual reproduction of both sexes, in particular during and after childbirth; its name, meaning "swift childbirth", comes from Greek, oksys "swift" and , tokos "birth." It is released in large amounts after distension of the cervix and uterus during labor, facilitating birth, maternal bonding, and, after stimulation of the nipples, lactation. Both childbirth and milk ejection result from positive feedback mechanisms.
 
Oxytocin Application:
 
Injected oxytocin analogues are used for labor induction and to support labor in case of difficult parturition. It has largely replaced ergometrine as the principal agent to increase uterine tone in acute postpartum hemorrhage. Oxytocin is also used in veterinary medicine to facilitate birth and to stimulate milk release. The tocolyticagent atosiban (Tractocile) acts as an antagonist of oxytocin receptors; this drug is registered in many countries to suppress premature labor between 24 and 33 weeks of gestation. It has fewer side effects than drugs previously used for this purpose (ritodrine).
 

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Muscle Growth Supplement White Powder PEG Mechano Growth Factor PEG MGF 2mg

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Muscle Growth Supplement White Powder PEG Mechano Growth Factor PEG MGF 2mg
 
PEG MGF Basic Info.
 
Product Name: PEG MGF
2mg*10vial/kit
CAS No.: N/A
Molecular Formula: C121H200N42O39
Molecular Weight: 2867.2
Sequence: Tyr-Gln-Pro-Pro-Ser-Thr-Asn-Lys-Asn-Thr-Lys-Ser-Gln- Arg-Arg-Lys-Gly-Ser-Thr-Phe-Glu-Glu-Arg-Lys-NH2
 
PEG MGF Description:
 
PEGylation is the act of attaching a Polyethylene glycol (PEG) structure to another larger molecule (in this case, MGF). The PEG acts as a protective coating and the theory here is that this will allow the MGF to be carried through the blood stream without being broken down. Neurological research has shown that utilizing PEGylated MGF resulted in a longer more stable acting version of the MGF peptide in serum/blood.
 
PEG MGF Application:
 
Using PEG MGF on cycle or off cycle, you are going to experience recovery that is far superior to any generic peptide available. Just like normal peptides, remember that PEG MGF comes in the form of a white delicate powder that needs to be reconstituted with bacteriostatic water and kept in the refrigerator.
 
PEG MGF Dosage:
 
Typical dosage of PEG-MGF is between 200mcg. - 400mcg. per week but many bodybuilders have said to "research" this peptide at dosages exceeding 1,500 mcg weekly with no adverse effects.
Because PEG MGF can cause site specific muscle growth, it is recommended to inject PEG MGF bi-laterally to ensure symmetrical gains. The most effective test results were experienced in users injecting the PEG MGF post exercise.
 

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Muscle Supplements Norandrostenolone Nandrolone For Bodybuilding 434-22-0

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Muscle Supplements Norandrostenolone Nandrolone For Bodybuilding 434-22-0
 
Nandrolone Basic Info.
 
Product Name: Nandrolone
Other name: Nandrolon; Norandrostenolone; Nortestosterone
CAS No: 434-22-0
Molecular Formula: C18H26O2
Molecular Weight: 274.4
Einecs No: 207-101-0
Purity: 99%
Appearance: White powder.
Usage:can be used as pharmaceutical material
 
Nandrolone Description:
 
Nandrolone base is usually synthesized from the male reproduction hormone testosterone. It can help rebuild body tissue, increase body and bone mass and encourage the formation of red blood cells. It also can make muscle growth, appetite stimulation and increase red blood cell production and bone density. Clinical studies have shown it to be effective in treating anaemia, osteoporosis and some forms of neoplasia including breast cancer, and also acts as a progestin-based contraceptive. Nandrolone is most commonly sold commercially as its decanoate ester (Deca-Durabolin) and less commonly as a phenylpropionate ester (Durabolin).
 
Nandrolone Applications:
 
Nandrolone is an anabolic steroid which are a group of drugs that are usually synthesized from the male reproduction hormone testosterone , and it can helps to rebuild body tissue, increase body and bone mass and encourage the formation of red blood cells.
 
The positive effects of the drug include muscle growth, appetite stimulation and increased red blood cell production and bone density. Clinical studies have shown it to be effective in treating anaemia, osteoporosis and some forms of neoplasia including breast cancer, and also acts as a progestin-based contraceptive.
 
Nandrolone is most commonly sold commercially as its decanoate ester (Deca-Durabolin) and less commonly as a phenylpropionate ester (Durabolin).
 

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Natual Fat Burners T4 Raw Steroids Powder Levothyroxine Sodium L-thyroxine 25416-65-3

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Natual Fat Burners T4 Raw Steroids Powder Levothyroxine Sodium L-thyroxine 25416-65-3
 
Levothyroxine Sodium Basic info:
 
Product Name: Sodium Levothyroxine
Synonyms: Sodium Levothyroxine;T4;Sodium levothyroxine Hydrate;L-Thyroxine Sodium Salt;
CAS: 25416-65-3
MF: C15H10I4NNaO4
MW: 798.85
EINECS: 200-221-4
Assay: 99%
Melting point: 207 °C
Alpha: 16 º (c=2,1M HCl/alcohol 1/4)
Storage temp.: Store at 0-5°C
Water Solubility: 0.15 g/L (25 ºC)
Specific Rotation: -0.10 o --- +0.10 o
Residue on ignition: 0.10% max
Water-insoluble substance: 0.1% max
Fumaric Acid: 1.0% max
Maleic Acid: 0.05% max
Heavy metals(as Pb): 10 ppm max
Arsenic(As) : 4 ppm max
Appearance: almost white to beige powder
Product Categories: Hormone Drugs
 
Levothyroxine Sodium Description:
 
Levothyroxine (INN, USAN) or L-thyroxine is a synthetic thyroid hormone that is chemically identical to thyroxine (T4), which is naturally secreted by the follicular cells of the thyroid gland. It is used to treat thyroid hormone deficiency, and occasionally to prevent the recurrence of thyroid cancer. Like its naturally secreted counterpart, levothyroxine is a chiral compound in the L-form. The related drug dextrothyroxine (D-thyroxine) was used in the past as a treatment for hypercholesterolemia (elevated
cholesterol levels) but was withdrawn due to cardiac side effects. It is on the World Health Organization's List of Essential Medicines, a list of the most important medication needed in a basic health system.
 
Levothyroxine (INN, USAN) or L-thyroxine is a synthetic thyroid hormone that is chemically identical to thyroxine (T4), which is naturally secreted by the follicular cells of the thyroid gland. It is used to treat thyroid hormone deficiency, and occasionally to prevent the recurrence of thyroid cancer. Like its naturally secreted counterpart, levothyroxine is a chiral compound in the L-form. The related drug dextrothyroxine (D-thyroxine) was used in the past as a treatment for hypercholesterolemia (elevated
cholesterol levels) but was withdrawn due to cardiac side effects.
 
Levothyroxine is typically used to treat hypothyroidism, and is the treatment of choice for patients with hypothyroidism, who often require lifelong thyroid hormone therapy. It may also be used to treat goiter via its ability to lower thyroid-stimulating hormone (TSH), a hormone that is considered goiter-inducing. Levothyroxine is also used as interventional therapy in patients with nodular thyroid disease or thyroid cancer to suppress thyroid-stimulating hormone (TSH) secretion.
 
Levothyroxine Sodium Applications:
 
Levothyroxine is typically used to treat hypothyroidism,and is the treatment of choice for patients with hypothyroidism, who often require lifelong thyroid hormone therapy.It may also be used to treat goiter via its ability to lower thyroid-stimulating hormone (TSH), a hormone that is considered goiter-inducing.Levothyroxine is also used as interventional therapy in patients with nodular thyroid disease or thyroid cancer to suppress thyroid-stimulating hormone (TSH) secretion.
 

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