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Lose Weight Fast Fat Burning Steroids Synephrine No Side Effect 94-07-5

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Lose Weight Fast Fat Burning Steroids Synephrine No Side Effect 94-07-5
 
Synephrine Basic Info.
 
Product Name: Synephrine
Synonyms: Oxedrine;Synephrine;AKOS NCG1-0008;AURORA KA-6561
CAS: 94-07-5
MF: C9H13NO2
MW: 167.21
EINECS: 202-300-9
Assay: 99.2%
Appearance: White powder
Package: 25kg/drum
Storage:Keep away from fire and heat source, hermetically deposit, keep in shady, cool and dry condition, protect against the tide.
 
Synephrine Description:
 
Citrus aurantium extract synephrine as standard has been recommended. 4-20mg daily dose of synephrine is as bitter orange extract containing 200-600mg standard products (3-6% synephrine) typical dose.
 
Synephrine Use:
 
Synephrine is lime fruits of the main active ingredient, which can effectively prevent excess energy (heat accumulation), by the wind qi, warm the stomach stimulates the appetite and speeds up metabolism. It is also a mild fragrance expectorant agent, a neurological tranquilizers and laxative treatment of constipation. Users can expect variable effects include consumption of excess calories, reduce appetite and increase satiety, these are likely to lead to weight loss.
 

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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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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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Purity 99% Medical Androsterone Androgenic Prohormone Steroids 53-41-8

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Purity 99% Medical Androsterone Androgenic Prohormone Steroids 53-41-8 
 
Androsterone Basic Info.:
 
Product Name: Androsterone
Synonyms: 3-alpha-hydroxy-17-androstanone;3alpha-Hydroxy-17-androstanone;3-alpha-hydroxy-5-alpha-androstan-17-on;3-Epihydroxyetioallocholan-17-one;3-hydroxy-,(3-alpha,5-alpha)-androstan-17-on;3-hydroxy-,(3alpha,5alpha)-androstan-17-on;5alpha-Androstan-17-one, 3alpha-hydroxy-;5alpha-Androstane-3alpha-ol-17-one
CAS: 53-41-8
MF: C19H30O2
MW: 290.44
EINECS: 200-173-4
Melting point: 181-184 °C(lit.)
Alpha: 96 º (c=1, C2H5OH)
Storage temp.: -20°C
Chemical Properties: white to light beige crystalline powder.
Usage: It was isolated from male urine after removed of the phenolic estrogen fraction. Antihypertensor.
Product Categories: Steroids;Steroids & Hormones - 13C & 2H;Intermediates & Fine Chemicals;Pharmaceuticals.
 
Androsterone Description:
 
Androsterone, or 3α-hydroxy-5α-androstan-17-one, is an endogenous steroid hormone, neurosteroid, and putative pheromone. It is a weak androgen with a potency that is approximately 1/7th that of testosterone. In addition, it can be converted to dihydrotestosterone (DHT) from 3α-hydroxysteroid dehydrogenase and 17β-hydroxysteroid dehydrogenase, bypassing conventional intermediates such as androstenedione and testosterone, and as such, can be considered to be a metabolic intermediate in its own right. 
Androsterone is also known to be an inhibitory androstane neurosteroid, acting as a positive allosteric modulator of the GABAA receptor, and possesses anticonvulsant effects. The unnatural enantiomer of androsterone is more potent as a positive allosteric modulator of GABAA receptors and as an anticonvulsant than the natural form. Androsterone's 3β-isomer is epiandrosterone, and its 5β-epimer is etiocholanolone.
 
Androsterone Applications:
 
Androsterone is one of the androgens, which are steroid hormones that affect the masculinization of the fetus and child and that maintain or create masculine traits in adults. Testosterone is the most active and abundant of the androgens. Androsterone was originally isolated from male urine in very small amounts. Many scientists believe it to be a metabolic byproduct of the breakdown of testosterone, and many scientists who study pheromones think it might be active in human relations.
 
A molecule of androsterone is very similar to testosterone. It consists of three six-member carbon rings and one five member ring joined along common sides. The molecular formula is C19 H30 O2. It has a beta-isomer called epiandrosterone, in which an hydroxyl group occupies a different geometric position. 
 
The ratio of androsterone to epiandrosterone is thought to be important in how masculine behavior is interpreted by others Pheromones are well known in insect behavior. Their role in insect mating, navigation and nest protection has been studied, and active compounds have been isolated. Pheromones are the basis of some insect baits. Their effect on mammal behavior patterns is less well understood.
 

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Skin Lightening Hormone Peptide Nonapeptide-1 For Whitening 158563-45-2

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Skin Lightening Hormone Peptide Nonapeptide-1 For Whitening 158563-45-2
 
Nonapeptide-1 Basic Infor:
 
Product Name: Nonapeptide-1
Synonyms: Melanostatine-5;Nonapeptide-1;Melanostatine
CAS: 158563-45-2
MF: C61H87N15O9S
MW: 0
Product Categories: birth-giving pharm;Beauty peptide
 
Nonapeptide-1 Description:
 
Nonapeptide-1, also called Melanostatine 5, is a propriety peptide that was originally developed for its antimicrobial activities. Animal research has revealed, however, that nonapeptide-1 can inhibit the synthesis of melanin, which makes it of interest for treating certain skin conditions. Animal models suggest that nonapeptide-1 can reduce synthesis of melanin and help decrease skin pigmentation to a substantial degree.
 
Nonapeptide-1 is a skin lightening peptide, derived from the melanocyte stimulating hormone (MSH). It prevents the activity of tyrosine in the melanocytes, melanin synthesis inhibition and helps to even out your skin tone by lessening hyper-pigmentation. This process reduces the formation of unwanted pigmentation, allowing for the control over skin tone and brown spots.
 
Nonapeptide-1 Application:
 
Nonapeptide-1 is of primary research interest for its ability to reduce hyperpigmentation by inhibiting the action of tyrosinase in melanin-producing cells. The ability to regulate melanin production has potential application in a number of conditions, including photodamage of the skin.
 
Research also suggests that nonapeptide-1 may play a role in the central nervous system where it may act on both dopaminergic receptors and opioid receptors to modify pain signaling as well as behavior. Studies in mice support the idea that nonapeptide-1 may have central actions that affect behavior and pain.
 

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Growth Hormone Peptides Raw Powder MT1 Melanotan 1 75921-69-6 Melanotan1

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Growth Hormone Peptides Raw Powder MT1 Melanotan 1 75921-69-6 Melanotan1
 
Melanotan 1 Basic View:
 
Product Name: Melanotan 1
Alias: Melanotan-1, MT1, Melanotan I, Afamelanotide, Melanotan, CUV1647, EPT1647, NDP-MSH, [Nle4, D-Phe7]α -MSH
Sequence: Ac-Ser-Tyr-Ser-Nle-Glu-His-D-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH2
CAS: 75921-69-6
MF: C78H111N21O19
MW: 1646.845
Purity: 99%
Specification: 10mg/vial
Appearance: White Lyophilized Powder
Place of Origin: China
Standard: USP
Certification: SGS
Method of Analysis: HPLC
Storage: Lyophilized peptides although stable at room temperature for 3 months, should be stored desiccated below -18° C. Upon reconstitution of the peptide it should be stored at 4° C between 2-21 days and for future use below -18° C.
Shipment:FedEx, EMS, Hkems, DHL, etc.
Payment:Western Union, Money Gram, Bank Transfer
Price: Competitive
Packaging Details: Very discreet. As required.
Delivery Time: Within 12 hours after payment
Supply Ability: 100000 vials/month
Minimum Order Quantity: 1 vials
 
Melanotan 1 Usage:
 
Melanotan 1 (also referred to as Afamelanotide) is a synthetic peptide variant of a peptide hormone, called alpha-Melanocyte stimulating hormone or MSH that is naturally produced in the body and is responsible for stimulating melanogenesis, a peptide process for pigmentation of the skin. Alpha-MSH activates certain melanocortin receptors in the process of exerting its effects. Indeed, MSH also exerts potent influence over lipid metabolism, appetite, and sexual libido via these melanocortin receptors. As a result, Melanotan-1 sunless skin tanning effects. While Melanotan 2 and PT-141 have been studied at length as a potential remedies for the treatment of sexual dysfunction, Melanotan-has been researched extensively for use in protecting against the harmful effects of ultraviolet radiation from sunlight due to its melanogenesis-stimulating properties.
 

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Hexarelin Human Growth Peptide Human Growth Hormone Peptides 140703-51-1

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Hexarelin Human Growth Peptide Human Growth Hormone Peptides 140703-51-1
 
Hexarelin Basic Info.
 
Product Name: Hexarelin
Synonyms: Hexarelin Acetate, HEX, Examorelin
Sequence: His-D-2-methyl-Trp-Ala-Trp-D-Phe-Lys-NH2
CAS number: 140703-51-1
Molecular formula: C47H58N12O6
Molar Mass: 887.04022
PubChem: CID 5464109
Peptide purity: > 98.0%
Appearance: White powder
Related substance: Total Impurities(%) ≤ 2.0%
Acetate content:≤15.0%
Bacterial Endotoxins: ≤5 IU/mg
Packing: 2mg/vial
 
What is Hexarelin?
 
Hexarelin (HEX) may be a amide GH secretagogue with a potent ability to stimulate GH secretion and recently reportable cardioprotective actions. as a result of Hexarelin’s aminoalkanoic acid sequence might facilitate in promoting the body to provide a lot of hormone, it’ll not finish off the body’s own production. Hexarelin may be a artificial amide composed of vi amino acids creating it a hexaptide with a structure that has been thought of to push the discharge of hormone. Effects from GH embody raised bone mineral density, raised cellular division and meiosis that ends up in a lot of muscle mass, acylglycerol chemical reaction that causes distinguished fat loss, animal tissue strengthening, and improved skin physical property. as a result of Hexarelin’s aminoalkanoic acid sequence might facilitate in promoting the body to provide a lot of hormone, it’ll not finish off the body’s own production. this is often a really necessary issue and makes Hexarelin a pretty chain compared to hormone alone. For analysis functions solely. 
 
Hexarelin may be a non-natural (synthetic) hormone (GH)-releasing hexapeptide that belongs to the GHS family. This specific supermolecule has been found to act on each ductless gland and also the neural structure, however, its mechanisms of action within the human physiological system has not nonetheless been totally elucidated (Arvat et al. 1995).
 
This artificial amide has similar GH-secreting properties with its predecessors like the GHRP-6, GHRP-2 and GHRP-1. Hexarelin is GHRP analog during which the Trp was substituted with with chemicals a lot of table 2-Methyl-Trp (Denghenghi et al. 1994). The chemical structure of that is shown within the following: several studies on mice are disbursed double-geared towards deeper understanding of its chemical activity.
 
Hexarelin (HEX) may be a amide GH secretagogue with a potent ability to stimulate GH secretion and recently reportable cardioprotective actions. However, hexarelin (HEX) effects within the brain area unit mostly unknown, and also the aim of the current study was to look at the potential protecting impact of hexarelin (HEX) on the central systema nervosum once injury, also as on caspase-3, Akt, and animate thing signal-regulated supermolecule enzyme (ERK) signal cascades in an exceedingly rat model of babe hypoxia-ischemia.
 
The Functionality of Hexarelin:
 
Hexarelin (Hexarelin Acetate) is chemically designed as L-Histidyl-2-methyl-D-tryptophyl-L-alanyl-L-tryptophyl-D-phenylalanyl-L-lysinamide. Hexarelin (Hexarelin Acetate) is a potent GHRP-6 analog,
whose structure (His-D-2-methyl-Trp-Ala-Trp-D-Phe-Lys-NH2) creates a greater stability than GHRP-6 due to a substituted (2 Me)Trp. Hexarelin has a half-life of about 70 min, longer than that of GHRP-6. Replacement of the naturally occurring L-amino acids for the D-configuration results in these longer
half-lives.
 
Hexarelin has shown that it is highly stimulated at 30 minutes after being induced by rapid and sustained GH secretion. The pituitary gland produces GH in the brain, in children this hormone helps them to grow and in adults it helps to maintain muscle and burn fat. In one sixteen-week study, it has been shown that GH levels return to normal after stopping use after four weeks.
 

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Local Anesthetic Raw Materials Procaine White Crystalline Powder 59-46-1

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Local Anesthetic Raw Materials Procaine White Crystalline Powder 59-46-1
 
Procaine Basic Info.:
 
Product name: Procaine
Alias: Procaine hydrochloride; Aminocaine; Anadolor; Atoxicocaine;
CAS register number: 59-46-1
Molecular formula: C13H21ClN2O2
Molecular weight: 236.31
Appearance: White crystalline powder
 
Procaine Description:
 
Procaine hydrochloride, also called Novocain, synthetic organic compound used in medicine as a local anesthetic. It became the first and best-known substitute for cocaine in local anesthesia. Generally used in a 1 to 10 percent saline solution, procaine hydrochloride is administered by injection for infiltration (area flooding as in dental anesthesia), nerve-block, spinal, and caudal anesthesia. Unlike cocaine, procaine is not toxic, addicting, or irritating. It has been displaced somewhat by the chemically related drugs lidocaine and mepivacaine, which produce prompter, more intense anesthesia.
 
Procaine HCl is indicated for the production of local or regional analgesia and anesthesia by local infiltration and peripheral nerve block techniques.
 
The routes of administration and concentrations are: for local infiltration use 0.25% to 0.5% (via dilution) and for peripheral nerve blocks use 0.5% (via dilution), 1%, and 2%. (See DOSAGE AND ADMINISTRATION for additional information.)
 
Procaine Usage:
 
Procaine is a kind of local anesthetics. With low toxicity but quick and safe effects, procaine is suitable for local anesthesia, applied to the eye, ear, nose, teeth and other department operation, used for infiltration anesthesia, anesthesia and closed therapy supervisor. Procaine is also used in the production of procaine penicillin.
 

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Local Anesthetics Proparacaine Hydrochloride Proparacaine HCl 5875-06-9

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Local Anesthetics Proparacaine Hydrochloride Proparacaine HCl 5875-06-9 
 
Proparacaine HCL Basic Info.
 
Product Name: Proparacaine hydrochloride 
Synonyms: Proparacaine HCl; Proparacaine Hydrochloride
CAS: 5875-06-9 
Molecular formula: C16H27ClN2O3 
Molecular Weight: 330.85 
EINECS number: 227-541-7 
Related Categories: API 
Use:anesthetic (local),Pharmaceutical raw materials
Packing:Foil bag or as requirments
 
Product Description Of Proparacaine HCL:
 
Anesthesia, local- Proparacaine and tetracaine are indicated to produce local anesthesia of short duration for ophthalmic procedures including measurement of intraocular pressure, removal of foreign bodies and sutures, and conjunctival and corneal scraping in diagnosis and gonioscopy. 
 
Proparacaine HCL Applications: 
 
Proparacaine hydrochloride and tetracaine are also indicated to produce local anesthesia prior to surgical procedures such as cataract extraction and pterygium excision, usually as an adjunct to locally injected anesthetics.Ophthalmic solutions used for intraocular procedures should be preservative-free. Preservatives may cause damage to the corneal epithelium if a significant quantity of solutionenters the eye through the incision.
 

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99% Pharmaceutical Raw Materials 1, 3-Dimethylpentylamine HCl 71776-70-0

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99% Pharmaceutical Raw Materials 1, 3-Dimethylpentylamine HCl 71776-70-0 
 
1,3-Dimethylpentylamine HCL Basic Info.:
 
Product Name: 1,3-Dimethylbutylamine hydrochloride
Alias: 4-Methyl-2-pentanamine hydrochloride, 1.3-Dimethylbutylamine HCl
CAS Registry Number: 71776-70-0
Assay: 99%
Molecular Weight:137.65
Molecular Formula: C6H16ClN
Related Substances: Pharmaceutical Grade
Appearance: Solid white powder
Storage: Shading, confined preservation
Usage: used in weight class where you can significantly reduce the appetite suppressing effects caused by heat.
 
1,3-Dimethylpentylamine HCL Description:
 
Dimethylpentylamine was first used in nasal decongestants and nutritional supplements. Since 1944, it has been used for nutritional supplements. Dimethylpentylamine has become a famous substance. It wasn't co-opted for being used in nasal decongestants for many years, when it was found that Dimethylpentylamine has smaller side effects on peoples' blood vessel construction.
 
Recently, Dimethylpentylamine has been widely used in energy supplement  for weight loss and bodybuilding. What's more, Dimethylpentylamine was used in AMP2 and AMP energy supplements,considered by their developping low side effects in comparison to .
 
In health care products, 1, 3-dimethylamylamine can increase energy, refreshing, and improve the body's energy, particularly effective to athletes caloric restriction or gather energy. At the same time, to reduce weight, 1, 3-dimethylamine hydrochloride (DMAA) can improve levels of a AMP, promote adipose decompose in the body.
 
1,3-dimethyleamine hydrochloride (DMAA) in the health products used in losing weight can be reduced significantly Low appetite, inhibit thermal effect. Reports show 1, 3-dimethyleamine hydrochloride (DMAA) can increase the physical fitness, improve concentration, significantly suppress appetite, curb hyperactive.
 
1,3-Dimethylpentylamine HCL Applications:
 
1. Improve Menopausal problem.
2. Has the characteristics of geranium diuresis, can help to liver, kidney discharges poison.
3. Stimulate lymph system to avoid infection, eliminate waste. Strengthen circulation system, make cycle more smooth.
4. A kind of sweet the insect repellent.
5. It is used in nasal decongestants and nutritional supplements.
6. It is widely used in energy supplement  for weight loss and bodybuilding.
7. It can be take as  health care products,increasing energy, refreshing, and improving the body's energy.
8. It  can increase the physical fitness, improve concentration, significantly suppress appetite, curb hyperactive.
 

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