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

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Oral Anabolic Steroids Anadrol Oxymetholone For Anemia Treatment And Anti-cancer 434-07-1

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Oral Anabolic Steroids Anadrol Oxymetholone For Anemia Treatment And Anti-cancer 434-07-1
 
Oxymetholone Basic Info.:
 
Product Name: Oxymetholone 
Alias: Anadrol
CAS No: 434-07-1
MF: C21H32O3
MW: 332.482
Purity: 99%
Melting point: 172-180°C
Alpha: 34 º
Refractive index: 38 ° (C=1, CHCl3)
Storage temp.: 2-8°C
Water Solubility: <0.1 g/100 mL at 23 ºC
Stability: Stability May be light sensitive. Combustible. Incompatible with strong oxidizing agents.
Quality standard: USP28/BP2005          
Apperance: Off-White to Pale Yellow Solid
Packing: as your require pack powder
Usage: Anabolic steroid. Controlled substance
 
Anadrol is the strongset effective oral steroid and oxymetholone(anadrol) has an extremely androgenic which hand in hand with an extremely intense anabolic component, by taking the oxymetho-lone(anadrol) the athletes experiences an enormous"pump effect"during the workout in the exercised muscles.
 
Oxymetholone Description:
 
Anadrol (Anadrol, Anadrol 50, Androyd) is one of the most popular anabolic steroids of all time in both performance and medical circles. It also represents one of the oldest steroids on the market. Provided by both Syntex and Park Davis & Co. in the 1960's, Anadrol hit the market in an effort to treat muscle wasting diseases, osteoporosis and any such related conditions. While still used for such purposes today, Anadrol is also used to treat the low red blood cell condition anemia, and in the U.S. is one of the only reasons the steroid is prescribed; most commonly to HIV patients.
 
While carrying numerous therapeutic benefits, many of which have been ignored by the FDA despite medical evidence, most who are interested in Anadrol are so for the purpose of performance enhancement. If it's good for treating a muscle wasting disease it's going to be good for building muscle mass, and this is the primary reason this steroid is a favorite of many performance enhancing athletes.
 
Anadrol is an extremely estrogenic steroid. A dihydrotestosterone (DHT) derivative, like all DHT compounds it does not aromatize but Anadrol still carries strong estrogenic traits. Due to this estrogenic nature as well as its tremendous anabolic nature, users of this steroid often report gains of 20-30lbs in only a few weeks, and that's not an exaggeration. This makes Anadrol one of the premier off-season steroids for many athletes, and overall that will be its only performance purpose in a general sense. Of course, as we'll see later on, competitive bodybuilders often use this steroid for contest prep at the very end, but in the grand scheme of things this is a bulking steroid.Due to its strong estrogenic nature coupled with its DHT composition, the side effects of Anadrol can be quite extensive. This steroid will carry nearly every last primary possible side effect of anabolic steroid use. Not only does this include things like gynecomastia, water retention, hair loss and acne, but it also includes liver toxicity. Anadrol is an oral steroid belonging to the C17-alpha alkylated (C17-aa) class of medications, and of all C17-aa steroids it is one of the most liver toxic.
 
While carrying only a moderate androgenic rating, Anadrol tends to display androgenic traits that are far beyond what its rating would imply. For this reason, Anadrol is not recommended to women as it will produce strong virilization symptoms. Women who are looking for anabolic assistance will find other DHT compounds such as (Anavar) or Methenalone (Primobolan) to be far more valuable as well as safer.
 
Like many anabolic steroids, Anadrol is plagued by myths and half-truths; however, in this case it may be a little more so. As we dive into this powerful anabolic steroid, we'll do our best to separate fact from fiction; we'll do our best to separate misconceptions about this steroid in comparison to Methandrostenolone (Dianabol), which are the most common misconceptions of all. We'll look at the primary Anadrol traits, how they translate into benefits, the side effects of the steroid, and of course, what you can do to avoid them and remain safe. We'll cover every last aspect of the Anadrol hormone, and enable your supplementation experience to be successful should you choose to undertake it.  
 
Oxymetholone Applications: 
 
Anadrol can be use in treating HIV wasting syndrome. Presented most commonly as a 50 mg tablet, oxymetholone is one of the strongest androgenic steroids available. Similarly, there is a risk of side effects. Despite very low binding affinity with the androgen receptor, oxymetholone is highly effective in promoting extensive gains in body mass, citation needed mostly by greatly improving protein synthesis.
 
For this reason, it is often used by bodybuilders and athletes. Many athletes also use anadrol as a method of protection for the joints under heavy loads. That's why anadrol is widely considered by bodybuilders to have the strongest anabolic effect out of all oral steroids available.    
 

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Pharmaceutical Raw Materials Indometacin Powder 53-86-1 For Pain Killer Anti Inflammatory

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Pharmaceutical Raw Materials Indometacin Powder 53-86-1 For Pain Killer Anti Inflammatory
 
Indometacin Basic Info.:
 
Product Name: Indometacin
Synonyms: Amuno; Chrono-Indocid 75; Confortid; Dolovin; Elmetacin; Flam; Indo-Rectolmin; Indo-Tablinen; IndoRich; Indocid
CAS: 53-86-1
MF: C19H16ClNO4
MW: 357.79
Appearance: White crystalline powder
EINECS: 200-186-5
Density: 1.327 g/cm3
Melting Point: 155-162°C
Boiling Point: 499.363°C at 760 mmHg
Storage: Store in cool and dry places, keep away from light
Indometacin or indomethacin is a non-steroidal anti-inflammatory drug (NSAID), to reduce fever, pain, stiffness, and swelling.
 
Product Description Of Indometacin: 
 
Indometacin (INN) or indomethacin (USAN and former BAN) is a non-steroidal anti-inflammatory drug (NSAID) commonly used as a prescription medication to reduce fever, pain, stiffness, and swelling. It works by inhibiting the production of prostaglandins, molecules known to cause these symptoms. It is marketed under more than seventy different trade names. 
 
Indomethacin is a nonsteroidal anti-inflammatory drug (NSAID) that reduces fever, pain and inflammation. It is similar to ibuprofen (Motrin) and naproxen (Naprosyn, Aleve). Indomethacin works by reducing the production of prostaglandins. Prostaglandins are chemicals that the body produces and which cause the fever and pain that are associated with inflammation. Indomethacin blocks the enzymes that make prostaglandins (cyclooxygenase 1 and 2) and thereby reduces the levels of prostaglandins. As a result, fever, pain and inflammation are reduced. Indomethacin is available in an extended release form. 
 
Indomethacin is in a group of drugs called nonsteroidal anti-inflammatory drugs (NSAIDs). Indomethacin works by reducing hormones that cause inflammation and pain in the body. 
Indomethacin is used to treat pain or inflammation caused by many conditions such as arthritis, gout, ankylosing spondylitis, bursitis, or tendinitis. 
 
Indomethacin may also be used for other purposes not listed in this medication guide. 
Ndomethacin is a medication that is often used to relieve pain caused by various types of arthritis and other painful conditions. Sold under the brand name Indocin, the medication is also available in generic form. Indomethacin belongs to a class of drugs known as NSAIDs and is commonly used to treat symptoms of conditions such as osteoarthritis, rheumatoid arthritis, and gout. The medicine is available in capsule, oral suspension, and suppository form. 
 
Indomethacin is in a group of drugs called nonsteroidal anti-inflammatory drugs (NSAIDs). Indomethacin works by reducing hormones that cause inflammation and pain in the body. 
Indomethacin is used to treat pain or inflammation caused by many conditions such as arthritis, gout, ankylosing spondylitis, bursitis, or tendinitis. 
Indomethacin may also be used for other purposes not listed in this medication guide.
 
Indometacin Application: 
 
This product has obvious effect on anti-inflammation and antipyretic, can be easily absorbed and excreted. It can be fully absorbed after taken orally in the gastrointestinal tract, and in 1-4 hours the plasma concentration will reach a peak; It will be excreted by liver metabolism, with the urine. Analgesic effects on inflammatory pain there, and its mechanism of inhibiting prostaglandin synthesis. Salicylic acid is mainly used on the efficacy of drugs difficult to tolerate, or not significant rheumatoid arthritis, ankylosing spondylitis, osteoarthritis and so on. Can also be used for acute gout and cancer, fever, or other difficult to control fever.
 

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99.9% Local Anesthetic Levobupivacaine HCl Powder Levobupivacaine Hydrochloride 5875-06-9

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99.9% Local Anesthetic Levobupivacaine HCl Powder Levobupivacaine Hydrochloride 5875-06-9 
 
Levobupivacaine 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
 
Levobupivacaine HCL Description:
 
Levobupivacaine (rINN) is a local anaesthetic drug belonging to the amino amide group. It is the S-enantiomer of bupivacaine.
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.
 
Levobupivacaine HCL Applications:
 
Levobupivacaine is the S-enantiomer of bupivacaine hydrochloride and is chemically described as (S)-1-butyl-2-piperidylformo-2', 6'-xylidide hydrochloride.
Levobupivacaine is a member of the amino amide class of local anaesthetics. It is indicated for surgical anesthesia and postoperative pain management.
 

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High Purity Male Sex Hormones Vardenafil HCL / Levitra For Sex Enhancer Powder 224785-91-5

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High Purity Male Sex Hormones Vardenafil HCL / Levitra For Sex Enhancer Powder 224785-91-5
 
Vardenafil HCL Basic Info:
 
Product Name: 
Synonym: Fardenafil; Vardenafil hydrochloride
CAS No: 224785-91-5
MF: C23H33ClN6O4S
MW: 525.06
Purity: 99%
Melting point: 214-216°C
Half life: 4-5 hours
Appearance: White to Off-White Cyrstalline Solid, odorless, taste bitter and astringent soluble in water and alcohol.
Storage: in a cool and dry well-closed container and in ventilated area.
Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Vardenafil
Usage: A selective phsphodiesterase type 5 (PDE5) inhibitor.
 
Vardenafil HCL Description:
 
Vardenafil (INN) is a PDE5 inhibitor used for treating erectile dysfunction. Vardenafil's indications and contra-indications are the same as with other PDE5 inhibitors; it is closely related in function to sildenafil citrate (Viagra) and tadalafil (Cialis). The difference between the vardenafil molecule and sildenafil citrate is a nitrogen atom's position and the change of sildenafil's piperazine ring methyl group to an ethyl group. Tadalafil is structurally different from both sildenafil and vardenafil. Vardenafil's relatively short effective time is comparable to but somewhat longer than sildenafil's.
 
Vardenafil HCL Application:
 
Beyond its indications for erectile dysfunction, vardenafil may be effective in the treatment of premature ejaculation, where it may significantly increase the time from vaginal penetration to ejaculation.Vardenafil, as with all PDE5 inhibitors, should not be used by men taking nitrate medications, because combining them with vardenafil might provoke potentially life-threatening hypotension (low blood pressure).
 
Further, Vardenafil causing lengthening of the QT interval. Therefore it should not be taken by men taking other medications that affect the QT interval (such as amiodarone).
 

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Natural Herbal Viagra Maca Extract Pharmaceutical Raw Materials For Men Sexual Enhancement

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Natural Herbal Viagra Maca Extract Pharmaceutical Raw Materials For Men Sexual Enhancement
 
Maca Extract Basic Info:
 
Product Name: Maca Extract
Maca Root Extract; Maca Extract
Model: 4:1 10:1 20:1 TLC
English name: Peruvian Maca Root Extract Powder
Latin name: Lepidium meyenii
Active ingredients: Beta Ecdysone
Appearance: Brownish Yellow Powder
Origin: Root
Specification: Ratio Extract: 4:1 10:1 20:1
Test Method: TLC
 
Maca Extract Description:
 
Maca extract is taken from the root of the maca plant. It is consumed as a root vegetable and it grows naturally in Peru. This extract is thought to have many health benefits and healing properties. There are many ways to prepare maca extract, including drying the roots and grinding them into a fine powder or boiling the roots to extract the natural oils. The extract typically is sold in a liquid or a gel-like capsule.
 
Maca is a cruciferous plant Lepidium in the shape of radish-like hypertrophy of the roots, originating in Peru and Central's (Jinin) and Pasco (Pasco) near the Andes above 4,000 meters, the area cold, strong winds, eco- harsh conditions unsuitable for other crops, and thus Mame a source of food for Inca.. Maca can increase with physical, energetic, eliminate anxiety and improve sexual function. Its fresh roots can eat with meat and vegetables , also be dried food cooked with water or milk.
 
Body builders or people who are trying to lose weight can sometimes benefit by taking maca extract. It contains many vitamins and minerals as well as amino acids, which help to boost themetabolism and this makes the body run more efficiently. Amino acids can also help to improve muscle structure. Maca extract is sometimes used as an alternative to dangerous anabolic steroids used by body builders to improve muscle mass.
 
Maca Extract Application:
 
The nutritional value of dried maca root is high, similar to cereal grains such as rice and wheat. The average composition is 60-75% carbohydrates, 10-14% protein, 8.5% dietary fiber, and 2.2% fats. Maca is rich in the dietary minerals calcium and potassium (with low content of sodium), and contains the essential trace elementsiron, iodine, copper, manganese, and zinc as well as fatty acids including linolenic acid, palmitic acid, andoleic acids, and 19 amino acids.
 
Maca is consumed as food for humans and livestock, suggesting any risk from consumption is rather minimal. It is considered as safe to eat as any other vegetable food. However, maca does contain glucosinolates, which can causegoiters when high consumption is combined with a diet low in iodine. This being said, darker colored maca roots (red, purple, black) contain significant amounts of natural iodine, a 10-gram serving of dried maca generally containing 52 µg of iodine. Though this is common in other foods with high levels of glucosinolate, it is uncertain if maca consumption can cause or worsen a goiter.
 
Small-scale clinical trials performed in men have suggested that maca extracts can improve semen quality, and boost libido. A small double-blind, randomized, parallel group dose-finding pilot study has shown that Maca root may alleviate SSRI-induced sexual dysfunction.A 12-week randomized, double-blind, placebo-controlled study in 56 subjects found that Maca has no effect on sex hormone levels in men, including LH, FSH,prolactin, 17-OH progesterone, testosterone or estradiol.
 
A recent review states "Randomized clinical trials have shown that maca has favorable effects on energy and mood, may decrease anxiety and improve sexual desire. Maca has also been shown to improve sperm production, sperm motility, and semen volume." In total over 160 studies into the health effect of Maca have been indexed by the United States National Library of Medicine,National Institutes of Health.However, a 2010 review of the extant evidence for the effect of Maca on libido found only tentative support for its aphrodisiac claims.
 
Maca Extract Function:
 
Adaptogenic Properties
Maca root considered an adaptogenic herb. Adaptogenic herbs help increase the bodies resistance to stress whether the stress is a physical or emotional ailment it doesn’t matter. Adaptogens helps normalize body functions one in particular is to restore proper adrenal gland and endocrine functions.
 
Balance Hormones
One of the best benefits to using maca is its ability to balance hormones naturally. It makes Maca great for a variety of hormonal disorders such as PMS( Pre-menstrual syndrome), menopause, andropause and various other conditions which involve unbalanced hormones. Maca does not stimulate production or directly work any particular hormone, its hormone balancing effects come from its adaptogenic properties which aid the adrenal glands and support the endocrine system.
 
Increase Energy
Much like other adaptogenic herbs, maca provides a non central nervous stimulating and adrenal gland friendly way to naturally increase energy. Adaptogenic herbs support the adrenal glands and don’t cause burn out like various other CNS stimulants such as caffeine. Maca has also been shown to increase stamina and endurance.
 
Increase Libido/Sex Drive
Another of maca most prized benefits is its ability to increase libido and boost sex drove. Studies have shown maca can heighten libido and sexual desire and may alleviate SSRI induced erectile dysfunction. If that wasn’t enough maca has shown in studies to boost fertility by increasing sperm quality, volume, motility and production.
 
Rich Source of Nutrients
Maca is a source of nutrients such as amino acids, fatty acids, sterols, vitamins, minerals such as selenium, calcium, magnesium, and iron. Maca is also rich in over 60 health boosting phyto-chemicals/compounds which are where a lot of its benefits stem from also.
 

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Pentadecapeptide Bpc 157 Human Growth Hormone Supplements Peptide Peptide Drum 137525-51-0

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Pentadecapeptide Bpc 157 Human Growth Hormone Supplements Peptide Peptide Drum 137525-51-0
 
Pentadecapeptide Bpc 157 Basic Info.
 
Product Name: Pentadecapeptide Bpc 157
Alias: Booly Protection Compound 15, Pentadecapeptide, BPC 157;
Sequence: Gly-Glu-Pro-Pro-Pro-Gly- Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val 
CAS: 137525-51-0 
MF: C62H98N16O22 
MW: 1419.53552 
Purity: 99% 
Specification: 2mg/vial 
Appearance: White Lyophilized Powder 
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. 
 
Pentadecapeptide Bpc 157 Description:
 
Pentadecapeptide BPC 157, composed of 15 amino acids, is a partial sequence of body protection
compound (BPC) Pentadecapeptide BPC 157, composed of 15 amino acids, is a partial sequence 
of body protection compound (BPC) that is discovered in and isolated from human gastric juice.
The promoting effect of pentadecapeptide BPC 157 on tendon healing involves tendon outgrowth, 
cell survival, and cell migration
 
Stable gastric pentadecapeptide BPC 157 (GEPPPGKPADDAGLV, M.W. 1419) may be the new drug stable in human gastric juice, effective both in the upper and lower GI tract, and free of side effects.
 
BPC 157, in addition to an antiulcer effect efficient in therapy of inflammatory bowel disease (IBD)(PL 14736) so far only tested in clinical phase II, has a very safe profile, and exhibited a particular wound healing effect. It also has shown to interact with the NO-saystem, providing endothelium protection and angiogenic effect, even in severely impaired conditions (i.e., it stimulated expression of early growth response 1 gene responsible for cytokine and factor generation and early extracellular matrix (collagen) formation (but also its repressor nerve factor 1- A binding protein-2)), important to counteract severe complications of advanced and poorly controlled IBD. Hopefully, the lessons from animal studies, particularly advanced intestinal anastomosis healing, reversed short bowel syndrome and fistula healing indicate BPC 157s high significance in further IBD therapy. Also, this supportive evidence (i.e., no toxic effect, limit test negative, LD1 not achieved, no side effect in trials) may counteract the problems commonly exercised in the use of peptidergic agents, particularly those used on a long-term basis
 
Pentadecapeptide Bpc 157 Application:
 
1. BPC 157 has a strong anti-inflammatory activity in both acute and chronic inflammation models. In fact, preliminary results in clinical trials suggest that BPC 157 may become an important therapeutic tool for the treatment of inflammatory bowel disease.
 
2. BPC 157 was shown to accelerate wound healing and to have a marked angiogenic effect. In addition, it significantly facilitates the healing of bone fracture in rats. This peptide also exhibits an osteogenic effect significantly improving the healing of segmental bone defect. BPC 157 accelerates the healing of transected rat Achilles tendon and transected rat quadriceps muscle.
 
3. FITC-phalloidin staining was able to demonstrate that BPC 157 induces F-actin formation in fibroblasts. Likewise, Western blot analysis was able to detect the production and activation of paxillin and FAK proteins. The western blot analysis also showed that BPC 157 increases the extent of phosphorylation of paxillin and FAK proteins without affecting the amounts produced.
 

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S4 Most Effective Sarm Supplement Andarine Muscle Building Raw Steroids Powder 401900-40-1

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S4 Most Effective Sarm Supplement Andarine Muscle Building Raw Steroids Powder 401900-40-1
 
Andarine Basic Info:
 
Product name: Andarine
Synonyms: Andarine;S4;S-4;GTX-007
CAS No.: 401900-40-1
MF: C19H18F3N3O6
MW: 441.36
Purity: 99.92%
Product categories APIs; Amines; Aromatics; Chiral Reagents; Intermediates & Fine Chemicals; Pharmaceuticals; SARMS
Appearance: White crystalline powder
Natural Bodybuilding SARM Powder Andarine S4 GTX-007 High Purity CAS 401900-40-1
 
Andarine Description:
 
Selective androgen receptor modulators or SARMs are a novel class of androgen receptor ligands. They are intended to have the same kind of effects as androgenic drugs like anabolic steroids but be much more selective in their action, allowing them to be used for many more clinical indications than the relatively limited legitimate uses that anabolic steroids are currently approved for.
 
S-4 is an experimental or investigation-stage proprietary SARM research chemical developed by GTx Inc for treatment of benign prostatic hypertrophy, muscle wasting, and osteoporosis. S-4 is considered a partial agonist of the androgen receptors in target tissue. S-4 has less pronounced anabolic and androgenic compared to other SARMs. In trials treating BPH induced in animal models, S-4 reduced prostate weight as effectively as finasteride and without producing any reduction in muscle mass or other side effects common with androgen receptor binding compounds. Gao et al suggest that by binding to androgen receptors, S-4 prevents DHT from binding and activating, but bypasses the expected anti-androgenic effects that would occur from occupying androgen receptors due to the fact that S-4 itself is a partial agonist of androgen receptors. S-4 has also been shown to prevent bone loss, reduce body fat, and improve muscle strength and body composition in orchidectomized and ovariectomized rats.
 
Andarine Application:
 
S4 Andarine is an orally active partial agonist for androgen receptors. It is less potent in both anabolic and androgenic effects than other SARMs. In an animal model of benign prostatic hypertrophy, andarine was shown to reduce prostate weight with similar efficacy to finasteride, but without producing any reduction in muscle mass or anti-androgenic side effects.
 
Andarine Function:
 
1. 1/3 as androgenic as testosterone in muscle tissue.
2. Anabolic at doses above 50mg.
3. Great for strength.
4. Great for muscle hardness.
5. Great for enhanced vascularity.
6. Great for endurance (aerobic or anaerobic).
7. Accelerated fat loss above 50mg.
8. Joint healing effects.
 

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98% Pharmaceutical Anabolic Weight Loss Steroids Raw Powder Halodrol-50 Turinadiol 2446-23-3

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98% Pharmaceutical Anabolic Weight Loss Steroids Raw Powder Halodrol-50 Turinadiol 2446-23-3
 
Halodrol Basic Info.:
 
Product Name: Halodrol (Turinadiol)
Chemical Name: Halodrol-50; Turinadiol; Turinabol-oral; 4-Chlorodehydromethyltestosterone; 4-Chlorodehydrone Thyltestosterone;Oral turinabol;4-ChlordehydroMethyl Testosterone
CAS Number: 2446-23-3
Molecular Formula: C20H31CLO2
Molecular Weight: 336.8960
Assay: 99.5%
Appearance: White powder
 
Halodrol Description:
 
Halodrol also known as 4-chloro-17a-methyl-androst-1,4-diene-3b,17b-diol, or HD is an excellent compound for adding lean hard muscles as well as strength gains. Halodrol is good for improved vascularity, dry gains with only a small to no amount of water retention.
 
Halodrol exhibits an extremely high anabolic to androgenic ratio translating into hard and consistent muscle gains with No aromatization. These gains are notably extremely lean and dry in nature, making this a favorite for the pre-contest athlete, or as an anabolic addition to many stacks. Mainly used to increase muscle mass most particularly in the abdomen region and will increase muscle endurance and decrease your recovery time after workouts.
 
Halodrol Application:
 
1. It is common for Halodrol users to see strength and size gains within the first 1-2 weeks.
2. Halodrol provides exactly that, lean, hard, dry gains as well as strength gains.
 

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Pharmaceutical Trenbolone Steroids Parabolan Trenbolone Enanthate For Weight Loss 10161-33-8

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Pharmaceutical Trenbolone Steroids Parabolan Trenbolone Enanthate For Weight Loss 10161-33-8
 
Trenbolone Enanthate Basic Info.
 
Product Name: Trenbolone Enanthate
Alias: Trenbolone Enanthate;Parabolan;Tren E;10161-33-8;Primobolan-depot;Primobolan-depot
CAS No.: 10161-33-8
Molecular Formula: C25H34O3
Molecular weight: 382.54
Assay: 99.02%
Appearance: pale yellow or yellow crystalline powder
Usage: Trenbolone Enanthate is only available from underground labs and was not designed for human consumption, although it is considered to be an ideal drug for bodybuilders who want to burn fat and gain muscle, although its long ester makes unwise for professional athletes who undergo testing to use.
 
Trenbolone Enanthate Description:
    
Trenbolone Enanthate also shines is in its ability to greatly preserve lean muscle tissue.When we diet, in-order to lose body fat, not weight but body fat we must be in a caloric deficit; we must burn more calories than we consume. As a result, as the body fights change with a desire to hang onto stored body fat due to its survival nature lean muscle tissue is often sacrificed in-order to meet its energy needs. As we lose more lean muscle tissue, this slows down the metabolic rate, and of course, it makes the physique look worse; Trenbolone Enanthate will prevent this. Of course, it gets even better; through its traits, Trenbolone Enanthate will provide the ultimate in visual conditioning effects.
 
Trenbolone Enanthate is a steroid that will greatly increase muscular endurance, more work can be done and you will not tire out as fast and it will also play an important role in recovery and healing.
 
Trenbolone Enanthate Applications:
 
Trenbolone is notably more potent than testosterone, and has an effect that is as much as three times as strong on a milligram for milligram basis. Likewise we can expect to see some level of androgenic side effects with use of this compound. Oily skin, aggressive behavior, acne and hair loss are therefore not uncommon during a cycle with this steroid. The androgenic nature of this drug of course makes it a very risky item for women to use, the chance for virilization symptoms extremely high with such a potent androgen.
 
Trenbolone is also much more potent than testosterone at suppressing endogenous androgen production. This makes clear the fact that estrogen is not the only culprit with negative feedback inhibition, as here there is no buildup of this hormone to report here. There is however some activity as a progestin inherent in this compound, as trenbolone is a 19-nortestosterone (nandrolone) derivative (a trait characteristic of these compounds).
 

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White Crystal Pharmaceutical Intermediates Hydrochloride Procaine HCL For Pain Relief 51-05-8

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White Crystal Pharmaceutical Intermediates Hydrochloride Procaine HCL For Pain Relief 51-05-8
 
Procaine HCL Basic Info.:
 
Product Name: Procaine Hydrochloride (Procaine HCL)
Synonyms: Aminocaine;Anadolor;Anesthesol;Anestil;Atoxicocaine;Bernocaine
CAS: 51-05-8
MF: C13H21ClN2O2
MW: 272.77
EINECS: 200-077-2
Melting point: 155-156 °C(lit.)
Boiling point: 195-196°C 17mm
Fp: 195-196°C/17mm
storage temp.: room temp
Water Solubility: soluble
Sensitive: Air Sensitive
Merck: 14,7757
Stability: Stable. Incompatible with strong oxidizing agents.
Chemical Properties: White crystalline powder
Product Categories: Pharmaceutical;Sodium channel;APIS;Anesthetics;Pharmaceutical intermediate
Usage: Local anesthesic;Na+ channel blocker;Procaine is a local anesthetic of the amino ester group that is primarily used as a topical anesthetic. Procaine is also used to control the pain of intramuscular injection of penicillin as well as in dentistry;Non Caine local anesthetic.
 
Procaine HCL Product description: 
 
Procaine HCl is a local anesthetic drug of the amino ester group. It is used primarily to reduce the pain of intramuscular injection of penicillin, and it is also used in dentistry. It acts mainly by being a sodium channel blocker. Today it is used therapeutically in some countries due to its sympatholytic, anti-inflammatory, perfusion enhancing, and mood enhancing effects.
 
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 HCL Application:
 
Procaine HCl is a local anesthetic drug of the amino ester group. It is used primarily to reduce the pain of intramuscular injection of penicillin, and it is also used in dentistry. Owing to the ubiquity of the trade name Novocain, in some regions procaine is referred to generically . It acts mainly by being a sodium channel blocker. Today it is used therapeutically in some countries due to its sympatholytic, anti-inflammatory, perfusion enhancing, and mood enhancing effects.
 
Procaine HCl is indicated for the production of local or regional analgesia and anesthesia by local infiltration and peripheral nerve block techniques.
 
Application of procaine leads to the depression of neuronal activity. The depression causes the nervous system to become hypersensitive producing restlessness and shaking, leading to minor to severe convulsions. Studies on animals have shown the use of procaine LED to the increase of dopamine and serotonin levels in the brain. Other issues may occur because of varying individual tolerance to procaine dosage. Nervousness and dizziness can arise from the excitation of the central nervous system, which may lead to respiratory failure if overdosed. Procaine may also induce weakening of the myocardium leading to cardiac arrest.
 
Procaine can also cause allergic reactions causing the individuals to have problems with breathing, rashes, and swelling. Allergic reactions to procaine are usually not in response to procaine itself, but to its metabolite PABA. About one in 3000 people have an atypical form of pseudocholinesterase, [citation needed] which does not hydrolyze ester anesthetics such as procaine, resulting in a prolonged period of high levels of the anesthetic in the blood and increased toxicity.
 

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