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Anabolic Steroid Hormones Powder Metribolone Legal Oral Steroids Methyltrienolone 965-93-5

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Anabolic Steroid Hormones Powder Metribolone Legal Oral Steroids Methyltrienolone 965-93-5 
 
Methyltrienolone Basic Info.
 
Product Name: Methyltrienolone (Steroids)
Synonyms: Metribolone;Methyltrienolone 
CAS: 965-93-5
MF: C19H24O2
MW: 284.39
EINECS: N/A
Assay: 99%
Chemical Properties: Pale Yellow Solid.
Storage temp.: 2-8°C
Product Categories: Steroids;Intermediates & Fine Chemicals;Pharmaceuticals;trenbolone series
Usage: An anabolic steroid.
Quality standard: Enterprise standard
 
Methyltrienolone Description:
 
Methyltrienolone is a steroid compound that is mostly unavailable on the market black or otherwise. The reason for its obscurity is because it is so highly toxic to the liver that even doses of as little as 2 mgs a week have caused jaundice of the liver. Besides its toxicity to the liver, it will also cause sexual dysfunction and can cause other compounds it is stacked with to exaggerate the effects of estrogen in the body. Although this compound is obviously dangerous and not recommended for use by anybody who values their health, it is worth noting that its muscle-building and fat-burning properties are on par with the highest-rated steroids available today.
Character: White to light yellow crystalline powder.
Usage An anabolic steroid. pharmaceutical material, Steroid hormone, Anabolin.
 
Methyltrienolone Applications:
 
1. Metribolone (methyltrienolone aka R1881) is a potent, non-aromatizable androgen that is structurally similar to trenbolone and has been referred to as “oral tren.” Methyltrienolone binds strongly to the androgen receptor (AR) and is a more potent agonist (activator) of the androgen receptor than is DHT. 17a-methyltrienolone is listed at 30,000 times more anabolic than methyltestosterone according to Julius Vida in “Androgens and Anabolic Agents: Chemistry and Pharmacology.” Effective dosages begin at only 25mcg.
 
2. Studies have shown that taking an oral anabolic steroid with food may decrease its bioavailability.630 This is caused by the fat-soluble nature of steroid hormones, which can allow some of the drug to dissolve with undigested dietary fat, reducing its absorption from the gastrointestinal tract. For maximum utilization, methyltrienolone should be taken on an empty stomach.
 

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Corticosteroid Drug Fluocinolone Acetate Fluocinolone Acetonide For Anti-inflammatory 67-73-2

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Corticosteroid Drug Fluocinolone Acetate Fluocinolone Acetonide For Anti-inflammatory 67-73-2
 
Fluocinolone Acetate Basic Info.:
 
Product Name: Fluocinolone Acetonide
Synonyms: dermalar; fluocinolone16,17-acetonide; Fluocinoloneacetate; Fluocinolone acetonide; Fluocinoloneacetate
CAS: 67-73-2
MF: C24H30F2O6
MW: 452.49
EINECS: 200-668-5
Product Categories: Organics;Alkaloids;Biochemistry;Quinoline Alkaloids;Intermediates & Fine Chemicals;Pharmaceuticals;Steroids;RETISERT;Hormone Drugs
Melting point: 267-269 °C(lit.)
refractive index: 103°(C=1, MeOH)
storage temp.: Refrigerator
Chemical Properties: Crystalline Solid
Uses: It is suitable in the treatment of eczema, neurodermatitis, skin pruritus, contact dermatitis, psoriasis, dermatitis and other diseases, Glucocorticoid; anti-inflammatory.
 
Fluocinolone Acetate Description:
 
Fluocinolone acetonide is a corticosteroid primarily used in dermatology to reduce skin inflammation and relieve itching. It is a synthetic hydrocortisone derivative. The fluorine substitution at position 9 in the steroid nucleus greatly enhances its activity. It was first synthesized in 1959 in the Research Department of Syntex Laboratories S.A. Mexico City. Preparations containing it were first marketed under the name Synalar. A typical dosage strength used in dermatology is 0.01-0.025%. One such cream is sold under the brand name Flucort-N and includes the antibioticneomycin.
Fluocinolone acetonide was also found to strongly potentiate TGF-β-associated chondrogenesis of bone marrow mesenchymal stem/progenitor cells, by increasing the levels of collagen type II by more than 100 fold compared to the widely used dexamethasone.
 
Fluocinolone Acetate Application:
 
Fluocinolone acetonide is used to decrease inflammation in the skin. 
It is a corticosteroid, sometimes known as a steroid. 
In general this drug is used to treat inflammatory skin disorders such aseczema and psoriasis. 
Benefits of being on this drug can include reduction of inflammation and relief of itch. 
Listed below are the typical uses of fluocinolone acetonide. 
 

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Health Muscle Building Steroids Injectable Blend Nandro Test 225 Steroid Liquid Injection for Muscle Gain

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Health Muscle Building Steroids Injectable Blend Nandro Test 225 Steroid Liquid Injection for Muscle Gain
 
Nandro Test 225 Basic Info.:
 
Product Name: Nandro Test 225
Nandro Test 225 mg each ml contains:
Test phenylpropionate 150mg
Nandrolone Phenypropionate 75mg
we also sell vials, syringe and filter equipments etc.
 
Product Description Of Nandro Test 225:
 
Testosterone Phenylpropionate:
Testosterone Phenylpropionate plays a key role in the development of male reproductive tissue such as the testis and prostates. In addition, testosterone cypionate is essential for health and well-being as well as the prevention of osteoporosis, testosterone Phenylpropionate is conserved through most vertebrates, although fish make a slightly difference from called 11-ketotestosterone.
Testosterone Phenylpropionate is a steroids hormone from the androgen and is found in mammals and other vertebrates, testosterone Phenylpropionate is primarily secreted in the tests of mails and the ovaries of female, although small amount are also secreted by the adrenal glands, testosterone Phenylpropionate is the principle male sex hormone and an anabolic steroids.
 
Nandrolone Phenypropionate:
Use male gonad hypofunction and implied sperm sterility, hydrogen to methyl testosterone intermediate.
Mestanolone is the 17α-methylated version of dihydrotestosterone (DHT). The systematic name of mestanolone is: 17β-hydroxy-17α-methylandrost-3-one.It is an orally bioavailable androgenic steroid that is highly androgenic while only slightly anabolic. It is incapable of aromatization and is not an agonist of the progesterone receptor.
 
Nandro Test 225 Application:
 
1. We only use USP/BP standard steroid powders, oil and solvents to make steroid injections.
2. We only offer semi-finished steroid injections. You just need to buy some syringe filters.
3. To filter it before injection. Heating semi-finished steroid injections to 20º C will make Filtering smoother.
 

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High Purity 99.5% Lincomycin Hydrochloride Pharmaceutical Raw Materials Lincomycin HCl For Antibacterial

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High Purity 99.5% Lincomycin Hydrochloride Pharmaceutical Raw Materials Lincomycin HCl For Antibacterial 
 
Lincomycin HCL Basic Info.:
 
Product Name: Lincomycin Hcl
Synonyms: Lincomycin Hydrochloride
CAS: 859-18-7
MF: C18H35ClN2O6S
MW: 443
EINECS: 212-726-7
Assay: 99%
Standard: EP7.0/BP/USP
Packing: 20Bou/cardboard drum
Character: White crystalline powder. MP 156-158°C, PH3.5~5.5, Optical rotation +135~+150°. Solubility: H2O: 50 mg/mL, clear, colorless.
 
Lincomycin HCL Description:
 
Lincomycin kills bacteria by interfering with the ability of bacteria to produce important proteins necessary for them to survive. Lincomycin is effective against many types of bacteria including Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus pyogenes, Propionibacterium acnes, and others. Use of lincomycin is reserved for penicillin-allergic patients or when penicillin-based treatment is not appropriate. This antibiotic should only be used to treat serious infections because of rare but sometimes fatal intestinal problems have occurred. The specific infections for which LINCOCIN is used include: Ear, throat and lung infections; Skin infections; Bone and joint infections; And infections of the blood. LINCOCIN will not work against viral infections such as colds or flu.
 
Lincomycin HCL Usage:
 
An antibiotic produced by Streptomyces lincolnensis. Lincomycin is a lincosamide antibiotic .An antibiotic produced by Streptomyces lincolnensis. Lincomycin is a lincosamide antibiotic that forms cross-links within the peptidyl transferase loop region of the 23S rRNA. Inhibits bacterial protein synthesis. Antibacterial.
Lincomycin (hereinafter referred to as LCM) biosynthesis, in addition to produce LCM, but under certain conditions, also produced the LCM B, C, D, K, S and other analogues, thus refining process more difficult and costly.
LD50 acute toxicity test showed that mice injected 1000mg/kg, rat oral greater than 4000mg/kg, toxicity is low.
Indications: Effect as erythromycin, do not have to do skin test, the product of Gram-positive bacteria and gram-negative bacteria is stronger for osteomyelitis, sepsis, respiratory and soft tissue infections. This product is very strong penetration of bone, is the medicine of choice for osteomyelitis.
 

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4-Thiazolidinone, 5-[[3-chloro-4-[(2R)-2,3-dihydroxypropoxy]phenyl]methylene]-3-(2-methylphenyl)-2-(propylimino)-, (2Z,5Z)- LAB GRADE 97%

4-Thiazolidinone, 5-[[3-chloro-4-[(2R)-2,3-dihydroxypropoxy]phenyl]methylene]-3-(2-methylphenyl)-2-(propylimino)-, (2Z,5Z)-, also called Ponesimod, ACT-128800, is a potent, and orally active selective S1P(1) agonist with potential immunomodulating activity.
In vivio: upon oral administration, ponesimod selectively binds to S1PR1 on lymphocytes and causes transient receptor activation followed by S1PR1 internalization and degradation.  http://www.bocsci.com/4-thiazolidinone-5-3-chloro-4-2r-2-3-dihydroxypropoxy-phenyl-cas-854107-55-4-item-459885.html

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