2019年9月24日星期二

Steroid hormones powder 7-Keto DHEA for Weight Loss


7-keto-DHEA is formed from dehydroepiandrosterone (DHEA) in the body. DHEA is a "parent hormone" produced by glands near the kidneys. But unlike DHEA, 7-keto-DHEA is not converted to steroid hormones such as androgen and estrogen. Taking 7-keto-DHEA by mouth or applying it to the skin does not increase the level of steroid hormones in the blood.

People take 7-keto-DHEA to speed up metabolism and heat production, which can promote weight loss. 7-keto-DHEA is also used to improve lean body mass and build muscle, increase the activity of the thyroid gland, boost the immune system, enhance memory, and slow aging. It is also used to treat depression, anxiety, and post-traumatic stress disorder (PTSD).
7-keto-DHEA might promote weight loss by speeding up the body’s metabolism and converting more energy to heat instead of storing it as fat.

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Prohormones powder 4-Dehydroepiandrosterone (4-DHEA)


DHEA Supplements for Anti-Aging
Since DHEA levels decline with age, some researchers speculate that supplementing your body's falling levels of the hormone might help fight aging. And some small studies have reported positive anti-aging effects from the use of DHEA supplements. But a similar number of studies have reported no effect.

  • Building up the adrenal gland
  • Strengthening the immune system
  • Slowing natural changes in the body that come with age
  • Providing more energy
  • Improving mood and memory
  • Building up bone and muscle strength

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Prohormones powder Dehydroepiandrosterone (DHEA)


Dehydroepiandrosterone (DHEA), also known as androstenolone, is an endogenous steroid hormone. It is one of the most abundant circulating steroids in humans, in whom it is produced in the adrenal glands, the gonads, and the brain.

DHEA is also said to slow up the aging process, improve sports performance, enhance libido, promote weight loss, and bolster the immune system. In addition,DHEA supplements are frequently marketed as testosterone-boosting agents and used for such purposes as increasing muscle mass and reducing fat mass.
Dehydroepiandrosterone is a precursor hormone, which means it has little biological effect on its own, but has powerful effects when converted into other hormones such as testosterone. Dehydroepiandrosterone is produced from cholesterol mainly by the outer layer of the adrenal glands, known as the adrenal cortex, although it is also made by the testes and ovaries in small amounts. It circulates in the blood, mainly attached to sulphur as dehydroepiandrosterone sulphate, which prevents the hormone being broken down. In women, dehydroepiandrosterone is an important source of oestrogens in the body – it provides about 75% of oestrogens before the menopause, and 100% of oestrogens in the body after menopause. 
Dehydroepiandrosterone production increases from around nine or ten years of age, peaks during the 20s and gradually decreases into old age. Dehydroepiandrosterone is also produced in small amounts by the brain, although its precise role there is not clear.


Epiandrosterone Supplements for Fat Burner

Epiandrosterone is a prohormone that is completely legal and available over the counter. It may also appear under the name 3b-hydroxy-etioallocholan-17-one. Epiandrosterone is a precursor to Stanolone, a powerful steroid hormone. Epiandrosterone can be found naturally occuring in most mammals and is excreted in urine as a normal part of human metabolism. One of the reasons that this prohormone is legal because it has been found to be naturally occurring in pine pollen. Epiandrosterone and Androsterone are very closely related. Androsterone is the 3-alpha isomer and epiandrosterone is the 3-beta isomer of this compound. The actions of the two isomers in the body are different, but still very similar. Most epiandrosterone supplements are actually a mix of the two isomers, meaning that they contain some androsterone as well as the main ingredient epiandrosterone.

Epiandrosterone is a dehydroepiandrosterone metabolite and a precursor of testosterone and estradiol with hypolipidemic and anabolic property,also commonly known as Epi-Andro or 3β-androsterone.It is naturally produced by the enzyme 5α-reductase from the adrenal hormone DHEA,and can also be converted from the natural steroids androstanediol via 17β-hydroxysteroid dehydrogenase or from androstanedione via 3β-hydroxysteroid dehydrogenase.It was first isolated in 1931 and has been shown to naturally occur in most mammals including pigs. Epi-Andro is non-methylated and as a result will put little to no stress on the user's liver. DHT is 5 times more Androgenic than testosterone. As a dry compound, users will experience lean muscle gains while also increasing lipolysis.

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Trenavar / Trendione CAS 4642-95-9


Average Dose:
60-120mg/day standalone
30-60mg/day when stacked
Average Cycle Length:4-6 weeks

Estra-4,9,11-triene-3,17-dione (Trenavar, Trendione) was released in late 2011 by PHF/IBE and is represented as a true prohormone to Trenbolone, differing only by a ketone at the 17 position. Similar to other 17-one prohormones, this ketone is the target of 17b-HSD1, hydrogenating the compound to yield active Trenbolone.

What this means is that although Trenavar is a prohormone to trenbolone, it doesn't appear to be a significant metabolite in humans. The equilibrium of the reaction between 17-one and 17b-ol appears to be weighted heavily - in fact pretty much exclusively - in favour of the 17b-ol, so Trenavar should convert readily to the active form trenbolone. Once converted to trenbolone, it will be open to the same metabolism mechanisms as injectable tren - conversion via sulfatase to epitrenbolone and excretion as glucoronides.

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Prohormone powder Methylstenbolone


WHAT IS METHYLSTENBOLONE? 
 

Methylstenbolone or M-Sten is a mass-building prohormone that helps users gain size and strength without sacrificing definition.  M-Sten is derived from DHT, so it doesn’t convert to estrogen, resulting in little to no water retention. 
Methylstenbolone is methylated, so liver toxicity is associated with this compound. Taking a Cycle Support product can help minimize or eliminate the potential for side effects while on cycle.
Following a healthy diet, training intensely, and proper use of M-Sten can result in gains of 5-20 lbs of lean muscle mass during a cycle.

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Methylhydroxynandrolone (MHON)

Manufacturer: RAWSGEAR
Effective Dose (Men): 10-30 mg/day
Half-Life: Approx. 12 Hours
MOHN comes in tablet form for oral administration, and is generally found in 5 mg tablets. Neither MOHN, nor any of its generic versions are still being commercially manufactured as prescription medications.

Dose

Due to a high milligram for milligram potency, the typical effective daily dosage is comparatively lower than most orals. For example, recommended dosages for Anavar, Winstrol and Turinabol are all within the 50-100 mg/day range. Even the legendary mass building Dianabols average dosage of 20-40 mg, is considered high with regard to MOHNs recommended 10-30 mg per day for 6-8 weeks.

 Information

MOHN is a very adaptable compound that can be easily incorporated into all types of cycles, during both bulking and cutting phases of training. When used within mass building cycles its usually stacked with testosterone enanthate, Dianabol, Anadrol, and Equipoise. In cutting cycles its often combined with short-ester injectable anabolic steroids such as testosterone propionate, Stanozolol, Anavar, and Boldenone Acetate but there is virtually no limit to its applications.

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Local Anesthetic Chloroprocaine HCl CAS 3858-89-7


Chloroprocaine hydrochloride is a local anesthetic given by injection during surgical procedures and labor and delivery. Chloroprocaine, like other local anesthetics, blocks the generation and the conduction of nerve impulses, presumably by increasing the threshold for electrical excitation in the nerve, by slowing the propagation of the nerve impulse and by reducing the rate of rise of the action potential.

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Local Anesthetic Mepivacaine HCl CAS 1722-62-9

Mepivacaine is a local anesthetic of the amide type. Mepivacaine has a reasonably rapid onset (more rapid than that of procaine) and medium duration of action (shorter than that of procaine) and is marketed under various trade names including Carbocaine and Polocaine.
A local anesthetic that is chemically related to bupivacaine but pharmacologically related to lidocaine. It is indicated for infiltration, nerve block, and epidural anesthesia. Mepivacaine is effective topically only in large doses and therefore should not be used by this route. 
Local anesthetics block the generation and the conduction of nerve impulses, presumably by increasing the threshold for electrical excitation in the nerve, by slowing the propagation of the nerve impulse, and by reducing the rate of rise of the action potential. In general, the progression of anesthesia is related to the diameter, myelination, and conduction velocity of affected nerve fibers. Clinically, the order of loss of nerve function is as follows: pain, temperature, touch, proprioception, and skeletal muscle tone.

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Local Anesthetic Dyclonine Hydrochloride CAS 536-43-6


Dyclonine, the English name dyclonlne, this product can block or stimulate various nerve impulse conduction, inhibition of touch and pain, the skin pain, itching and sterilization. This product is a new and efficient analgesic antipruritic, and a very strong bactericidal anti-inflammatory effect. Rapid onset, long duration, safe and reliable without stimulation.

Dyclonine is an oral anaesthetic that is the active ingredient of Sucrets, an over the counter throat lozenge. It is also found in some varieties of the Cepacol sore throat spray. It is a local anesthetic, used topically as the hydrochloride salt. Dyclonine hydrochloride has been found to possess, in addition to its topical anesthetic properties, significant bactericidal and fungicidal activity. Selfsterilizing action manifested by preparations containing the drug was considerably enhanced upon the addition of chlorobutanol. Results of in vitro tests employing microorganisms commonly involved in local infections indicated that the two agents in combination act synergistically


Dyclonine Application
Topical anesthetics are used to relieve pain and itching caused by conditions such as sunburn or other minor burns, insect bites or stings, poison ivy, poison oak, poison sumac, and minor cuts and scratches. Pramocaine and dibucaine are also common ingredients in over the counter hemorrhoid preparations.

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Local Anesthetic Ropivacaine Mesylate 99%

Product description:

Ropivacaine because amide local anesthetic, is mainly used for surgical
anesthesia: epidural anesthesia (including cesarean section with epidural
anesthesia); local anesthesia. Acute pain management: for postoperative or
analgesia, continuous epidural infusion can also be intermittent medication;
local anesthesia.

Applications:
Beclomethasone is used to prevent and control symptoms (wheezing and shortness of breath) caused by asthma. This medication belongs to a class of drugs known as corticosteroids. It works directly in the lungs to make breathing easier by reducing the irritation and swelling of the airways.

This medication must be used regularly to prevent breathing problems (attacks of wheezing/shortness of breath). It does not work immediately and should not be used to relieve an asthma attack. If an attack occurs, use your quick-relief inhaler as prescribed.

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Local Anesthetics Ropivacaine Hydrochloride Powder


Ropivacaine Hydrochloride is the hydrochloride salt of ropivacaine, a local anesthetic of the amide type with analgesic activity. Ropivacaine binds to voltage-gated sodium ion channels in the neuronal membrane, thereby preventing the permeability of sodium ions and resulting in a stabilization of the neuronal membrane and inhibition of depolarization; nerve impulse generation and propagation are blocked, resulting in a reversible loss of sensation.

Ropivacaine Hydrochloride Application
1.Ropivacaine Hydrochloride is a local anaesthetic drug belonging to the amino amide group. The name ropivacaine refers to both the racemate and the marketed S-enantiomer.
2.Ropivacaine Hydrochloride is an anesthetic (numbing medicine) that blocks the nerve impulses that send pain signals to your brain. 
3.Ropivacaine Hydrochloride is used as a local (in only one area) anesthesia for a spinal block, also called an epidural. The medication is used to provide anesthesia during a surgery or C-section, or to ease labor pains. 
4.Ropivacaine Hydrochloride may also be used for purposes not listed in this medication guide. 

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Local Anesthetic Levobupivacaine HCL CAS 27262-48-2


Levobupivacaine is a local anaesthetic drug belonging to the amino amide group. It is the S-enantiomer of bupivacaine,it is a reversible neuronal sodium channel inhibitor, used as a long-acting local anesthetic.

Levobupivacaine hydrochloride is commonly marketed by Abbott under the trade name Chirocaine.

Compared to bupivacaine, levobupivacaine is associated with less vasodilation and has a longer duration of action. It is approximately 13 percent less potent (by molarity) than racemic bupivacaine and has a longer motor block onset time.

Levobupivacaine has similar nerve blocking potency with bupivacaine. Levobupivacaine at a dose of 0.125%, inhibits motor and nocifensive pinch responses with maximum %MPE of 99 and 68 respectively, and inhibits the duration of deficits of motor and nocifensive pinch responses (60 and 30 , respectively) after sciatic nerve block.

The hydrochloride salt of levobupivacaine, an amide derivative with anesthetic property. Levobupivacaine reversibly binds voltage-gated sodium channels to modulate ionic flux and prevent the initiation and transmission of nerve impulses (stabilizing neuronal membrane), thereby resulting in analgesia and anesthesia. In comparison with racemic bupivacaine, levobupivacaine is associated with less vasodilation and has a longer duration of action.

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Local Anesthetics Aarticaine HCL CAS 23964-57-0


Articaine HCL (23964-57-0) benefits:
 
1. Articaine is hypoallergenic; rapid onset of anesthesia; strong infiltration;low toxicity; appropriate duration of anesthesia.
2. Articaine has little impact on blood pressure and heart rate, and its' anesthetic effect is stable.
3. Articaine applies not only to the patient's alveolar surgery, but also safely to the  general cardiovascular disease
4. Articaine is a most effective analgesic drug, and has long duration of anesthesia, fewer complications, thus it is worthy of clinical application.

Articaine HCL (23964-57-0) Functions & traits:
 
Articaine is used for pain control. Like other local anesthetic drugs, articaine causes a transient and completely reversible state of anesthesia (loss of sensation) during (dental) procedures.
In dentistry, articaine is used both for infiltration and block injections, with the block technique yielding the greatest duration of anesthesia.In people with hypokalemic sensory overstimulation, lidocaine is not very effective, but articaine works well.

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99% Local Anesthetic Tetracaine HCL CAS 136-47-0


Tetracaine hydrochloride (TCH) is one of the potent local anaesthetics. A kinetic study of oxidation of tetracaine hydrochloride by sodium N-chlorobenzenesulfonamide (chloramine-B or CAB) has been carried in HClO4 medium at 303 K. The rate shows first-order dependence on , shows fractional-order dependence on , and is self-governing on acid concentration. Decrease of dielectric constant of the medium, by adding methanol, increased the rate. Variation of ionic strength and addition of benzenesulfonamide or NaCl have no significant effect on the rate. The reaction was studied at different temperatures and the activation parameters have been evaluated. The stoichiometry of the reaction was found to be 1 : 5 and the oxidation products were identified by spectral analysis. The conjugate free acid C6H5SO2NHCl of CAB is postulated as the reactive oxidizing species. The observed results have been explained by plausible mechanism and the related rate law has been deduced.

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Local Anesthetic Procaine HCL CAS 51-05-8 100% clearance from customs


Procaine hydrochloride is a drug. Procaine hydrochloride acts on the peripheral nerve to block the nerve. It diffuses into the nerve cell membrane by concentration gradient, blocks the sodium ion channel on the inner side, and makes the nerve cell excitation threshold rise. High, loss of excitability and conductivity, information transmission is blocked, with good local anesthesia.
Product NameProcaine Hydrochloride
Other Name4-Aminobenzoic acid 2-(diethylamino)ethyl ester hydrochloride
Assay (%)≥99.00OdorCharacteristic
ColorWhite crystalline powderCas No.51-05-8
Molecular FormulaC13H20N2O2.HClMolecular Weight272.77
StandardUSP34/BP2005
 
Function
Main functions are as follows:
1.Local anesthetic.
ApplicationsMain applications are as follows:
Applied in pharmaceuticalfields. 
Packing1kgor 5kg/bag,  25kg/drum
Shelf Life24 months
StorageStore in sealed containers at cool & dry place. Protect from light, moisture and pest infestation.
Gurantee 100% safe shipping . We will ship by special line that shipping company do custom clearance and deliver to door.100% pass customs,free of customs clearance !

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Local Anesthetic Benzocaine HCL CAS 23239-88-5


Product Name
benzocaine hcl
CAS.16595-80-5
MF : MF C11H12N2S. HCl
MW:240.75
EINECS Number:240-654-6
Purity:99.50%
Apprarance:White powder.
GradePharmaceutical Grade

Benzocaine is used to relieve pain and itching caused by conditions such as sunburn or other minor burns, insect bites or stings, poison ivy, poison oak, poison sumac, minor cuts, or scratches. 

Benzocaine belongs to a group of medicines known as topical local anesthetics. It deadens the nerve endings in the skin. This medicine does not cause unconsciousness like general anesthetics do when used for surgery. 

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Local Anesthetic Prilocaine CAS 721-50-6



Product Name: Prilocaine
Synonyms: 2-(propylamino)-o-propionotoluidid;
CAS: 721-50-6
MF: C13H20N2O
MW: 220.31
EINECS: 211-957-0
Product Categories: Active Pharmaceutical Ingredients
Packing:Foil bag or as requirments

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99% Benzocaine powder with 100% Safe Customs Clearance in EU

Benzocaine details:
  • Purity: 99.85%,USP36
  • Boiling point:172 °C (12.7517 mmHg)
  • Melting point : 88-90 °C
  • Role:local anesthesia
  • Appearance: White powder
  • Export Markets:Global
  • Storage conditions : Refrigerator(0-6°C) or Cool and dry at room temperature, avoiding sun exposure
Characteristics of benzocaine, tetracaine, lidocaine, procaine.
And which anesthesia effect is good?

 
  • Local anesthetic. Local anesthetic intensity: tetracaine>tetracaine hcl>lidocaine>lidcaine hcl> benzocaine > procaine>procaine hcl 
     
  • Tetracaine hcl local anesthetic intensity is 10 times that of procaine, the effect can be maintained for 2 to 3 hours, with strong penetrating power
     
  • The local anesthetic effect of benzocaine is weaker than procaine, and it cannot be infiltrated, and the local absorption is slow and long-lasting.
     
  • Lidocaine is a local anesthetic, also known as liddocaina, which has replaced procaine in recent years and is widely used in cosmetic plastic surgery for local infiltration anesthesia.
     
  • Procaine hydrochloride is a local anesthetic that temporarily blocks the conduction of nerve fibers and has an anesthetic effect. It has a strong effect and low toxicity.

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Local Anesthetic Lidocaine Hydrochloride CAS 73-78-9


Lidocaine hydrochloride is a local anesthetic because of amides. After blood absorption or intravenous administration, there is obvious excitatory and inhibitory biphasic effect on the central nervous system, and there is no pioneering excitement. When the blood concentration is low, analgesia and lethargy and pain threshold increase; as the dose increases The effect or toxicity is enhanced, and the sub-poisoning blood concentration has an anticonvulsant effect.

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Phenacetin cas 62-44-2


Phenacetin is mainly used as an antipyretic analgesic, with slow and lasting effects, treating headaches, neuralgia, joint pain, and fever, and weakly resisting rheumatism and inflammation. Because of toxic side effects and the rapid development of similar drugs, however, it is no longer used alone, only as a raw material in combination with other drugs. Commonly combined with aspirin and caffeine to form a less toxic compound aspirin used to treat the common cold. Can make chlorpheniramine cold tablets by adding a small amount of chlorpheniramine to the above compound, used to treat colds with headache, neuralgia, rheumatism, etc. Can be used as a material for organic synthesis or a pharmaceutical intermediate.

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Vardenafil hydrochloride (Levitra) CAS 224785-91-5


Vardenafil, known under the brand name Levitra is a prescription medication for male erectile dysfunctiontreatment. It belongs to a class of drugs called PDE5 inhibitors. Levitra increases blood flow to the penis, which helps gain and sustain an erection during sex. Levitra’s active ingredient works on the chain of reactions within the penis during arousal, when the corpus cavernosa (two large chambers) in the male’s penis fills with blood, resulting in an erection.A penile erection happens when the penis fills with blood. This occurs when the blood vessels that supply the penis with blood expand (dilate), and the vessels that take blood away from the penis contract, resulting in an accumulation of blood in the penis.

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