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Oral or Injection Trenbolones Steroids 6-Bronmandrostenedione For Gain Muscle 38632-00-7

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Oral or Injection Trenbolones Steroids 6-Bronmandrostenedione For Gain Muscle 38632-00-7
 
6-Bronmandrostenedione Basic Info.:
 
Product Name: 6-Bronmandrostenedione
Synonyms: (6b)-6-Bromoandrost-4-ene-3,17-dione; (6beta)-6-bromoandrost-4-ene-3,17-dione; 6-Bromoandrost-4-ene-3,17-dione
CAS RN.: 38632-00-7
Molecular Weight: 365.3046
Molecular Formula: C19H25BrO2
Density: 1.35g/cm3
Boiling Point(ºC): 467°C at 760 mmHg
Flash Point(ºC): 100.3°C
refractive_index: 1.577
Chemical Properties: Pale Yellow Solid
Usage: 6-Bronmandrostenedione analog, an aromatase inhibitor.
 
6-Bronmandrostenedione Description:
 
6-Bromodione is a fast acting competitive inhibitor of the aromatase enzyme. It works by binding to the aromatase enzyme to prevent it from aromatizing androgens. This is not a permanent binding and later acts to normalize aromatase (and thus estrogen levels) as hormone production returns to normal. It specifically targets aromatase and does not act as a central anti-androgen like some other post cycle products can. This means that your libido and mood will not be negatively affected.
 
6-Bronmandrostenedione Application:
 
6-beta-Bromodione works in a similar way but has an irreversible and permanent effect. This works well to mediate the excess aromatase that was produced while on cycle, while the alpha isomer works to normalize the natural levels. The goal is again to transition into normal production levels for all hormones affected by the anabolic cycle.
 

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Pharma Antiviral Agents Tenofovir Disoproxil Fumarate 202138-50-9 For Medicine Ingredients

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Pharma Antiviral Agents Tenofovir Disoproxil Fumarate 202138-50-9 For Medicine Ingredients

 

Tenofovir Basic Info.:

 

Product Name: Tenofovir

CAS:147127-20-6

MF: C9H14N5O4P

MW:287.21

mp:276-280°C

storage temp. Store at -20°C

Water Solubility :13.4 mg/mL (25 ºC)

Chemical Properties:White Crystalline Solid

Usage:Acyclic phosphonate nucleotide analogue. Used as an anti-HIV agent

Usage:Acyclic phosphonate nucleotide analogue; reverse transcriptase inhibitor. Used as an anti-HIV agent. Antiviral.

Usage:Tenofovir blocks reverse transcriptase and hepatitis B virus infections.

Biological Activity Selectively inhibits HIV reverse transcriptase (RNA-dependent DNA polymerase). Prevents cytotoxicity in SIV-infected C-8166 cells in vitro (IC 50 = 1.5 μ M). Antiviral agent.

 

Tenofovir Usage And Synthesis:

 

1. Antiviral drugs, Tenofovir is an acyclic nucleoside antiviral reverse transcriptase inhibitor. The active substance is Tenofovir disoproxil, while tenofovir is a prodrug that is used because of its better absorption in the gut.

2. Tenofovir can inhibit viral polymerase through direct competitively combine with natural deoxyribose or by insertion to terminate chain of human DNA. It is the first nucleotide analogs to treat HIV-1 infection that approved by the US Food and Drug Administration (FDA).

3. Tenofovir is a main medicine in AIDS cocktail therapy, researches has shown that it can effectively improve the monkeys` ability on prevention of immunodeficiency virus (similar to the human AIDS virus).

 

Tenofovir Pharmacokinetics:

 

Tenofovir is hardly absorbed through the gastrointestinal tract, for this reason, prodrug of Tenofovir has been developed by esterification, and then to make tenofovir fumarate ester. Tenofovir ester is water-soluble, can be rapidly absorbed and degraded into the active tenofovir, and then was metabolized to the active Tenofovir disoproxil. Tenofovir will reach the peak of plasma Concentration within 1-2 h after administration. When combined with food service, the bioavailability of Tenofovir can be increased by 40%. Intracellular half-life of Tenofovir disoproxil is about 10 h, it needs dosing everyday. Because Tenofovir is not a CYP-450 substrate, this may decrease the possibility of interactions with other drugs caused by CYP450. Elimination of Tenofovir is by glomerular filtration and active tubular secretion. Approximately 70% to 80% is recovered in urine as unchanged drug. Elimination half-life is approximately 17 h.

 

Indications: Tenofovir is indicated for the treatment of HIV, HBV infection. This product also can cooperated with other reverse transcriptase inhibitors for HIV-1 infection and hepatitis B treatment.

 

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Pharmaceutical Raw Materials Female Steroids Raw Hormone Powders Mifepristone 84371-65-3

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Pharmaceutical Raw Materials Female Steroids Raw Hormone Powders Mifepristone 84371-65-3
 
Mifepristone Basic Info.:
 
Product Name: Mifepristone (R38486)
Synonyms: 11-(4-(dimethylamino)phenyl)-17-hydroxy-17-(1-propynyl)-estra-9-dien-3-one;11beta-[4-(n,n-dimethylamino)phenyl]-17alpha-(prop-1-ynyl)-delta4,9-estradiene;r38486
CAS Number: 84371-65-3
Molecular Formula: C29H35NO2
Molecular Weight: 429.65
Assay: 99%
Melting Point: 195-198 °C
Storage temp.: 2-8°C
Appearance: Light yellowish powder
Product Categories: Steroids;Hormone;Acetylenes;Biochemistry;Functionalized Acetylenes;Hydroxyketosteroids;Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals;Intracellular receptor;Nuclear Receptors;Steroid and Hormone;API;Hormone Drugs.
Uses: It is a novel anti-progestin and has anti-glucocorticoid activity without the activity of progesterone, estrogen, androgen and anti-estrogen. It has a progesterone receptor affinity five times as high as progesterone. It is used for anti-pregnancy, inducing menstruation and terminating pregnancy, intrauterine inducer labor for dead fetal.
 
Mifepristone Description:
 
Mifepristone is a synthetic steroid compound with both antiprogesterone and antiglucocorticoid properties. The compound is a 19-nor steroid with substitutions at positions C11 and C17 (17 beta-hydroxy-11 beta-[4-dimethylamino phenyl] 17 alpha-[1-propynyl]estra-4, 9-dien-3-one), which antagonizes cortisol action competitively at the receptor level.
 
Mifepristone is a progesterone receptor antagonist used as an abortifacient in the first months of pregnancy, and in smaller doses as an emergency contraceptive. It is also a powerful glucocorticoid receptor antagonist.
 
Mifepristone Applications:
 
Mifepristone is used alone or in combination with misoprostol (Cytotec) to end an early pregnancy. Early pregnancy means it has been 49 days or less since your last menstrual period began. Mifepristone is in a class of medications called antiprogestational steroids. It works by blocking the activity of progesterone, a substance your body makes to help continue pregnancy.
 
Mifepristone is also available as another product (Korlym), which is used to control hyperglycemia (high blood sugar) in people with a certain type of Cushing's Syndrome in which the body makes too much of the hormone cortisol. This monograph only gives information about mifepristone (Mifeprex), which is used alone or in combination with another medication to end an early pregnancy. If you are using mifepristone to control hyperglycemia caused by Cushing's syndrome, read the monograph entitled mifepristone (Korlym) that has been written about this product.
 
Mifepristone (or RU-486) is a synthetic steroid compound with both antiprogesterone and antiglucocorticoid properties. The compound is a 19-nor steroid with substitutions at positions C11 and C17 (17 beta-hydroxy-11 beta-[4-dimethylamino phenyl] 17 alpha-[1-propynyl]estra-4, 9-dien-3-one), which antagonizes cortisol action competitively at the receptor level.
 
Mifepristone is a progesterone receptor antagonist used as an abortifacient in the first months of pregnancy, and in smaller doses as an emergency contraceptive. It is also a powerful glucocorticoid receptor antagonist, and has occasionally been used in refractory Cushing's syndrome (due to ectopic/neoplastic ACTH/cortisol secretion).
Mifepristone was the first antiprogestin to be developed and it has been evaluated extensively for its use as an abortifacient.
 

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Pharmaceutical Safe Organic Solvents Grape Seed Oil For Cooking Cosmetics CAS 85594-37-2

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Pharmaceutical Safe Organic Solvents Grape Seed Oil For Cooking Cosmetics CAS 85594-37-2
 
Grape Seed Oil Basic Info.:
 
Product Name: Grape seed oil
Synonyms: Grapeseed Oil; Oils, grape; Grape stem extract; VITIS VINIFERA (GRAPE) SEED OIL; Traubenkernoel; Grape seed oil;
CAS No.: 85594-37-2
Purity: 99%
Appearance: Pale yellow liquid
Standard: Enterprise Standard
Packing: 200KG/Drum or as per your requirements
Application: Natural Plant Extract; Flavors & Fragrances
 
Grape Seed Oil Description:
 
Appearance: pale green to pale yellow oily liquid
Relative Density: (20 °C) 0.915 ~ 0.925
Refractive index: (20 °C) 1.4700 ~ 1.4750
Linoleic acid: (%) 70 ~ 76
 
Grape Seed Oil Application:
 
1. Grape seed through the most advanced cold pressing method and refined, is one of the very popular in the base oil and the effect is outstanding varieties. Grape seed oil is a natural non-toxic properties, so children, pregnant women, the elderly and athletes are applicable.
2. Atioxidant, dilute the stain.
3. Endocrine disorders caused by dry skin, reduce melanin, whitening skin, removing chloasma.
4. To stimulate cell division and tissue regeneration, activation of the surface cells, reduce wrinkles, delay aging.
5. Inhibit and remove the body of free radicals, anti-cancer anti allergic effect.
6. Anti prostate cancer, the role of anti liver tumor, but also against damage to the nervous system.
 

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Safe Human Growth Hormone Peptide PT 141 Bremelanotide For Peptide Drum PT141 32780-32-8

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Safe Human Growth Hormone Peptide PT 141 Bremelanotide For Peptide Drum PT141 32780-32-8
 
PT 141 Basic Info.
 
Product Name: PT-141; PT141
CAS: 32780-32-8
MF: C50H69N15O10
MW: 1040.17736
Appearance: White powder
Water Content(Karl Fischer): ≤ 5.0%
Acetate Content(by HPLC): ≤ 15.0%
Amino Acid Composition: ± 10% of theoretical
Purity(by HPLC): ≥ 97.0%
Single Impurity(by HPLC): ≤ 1.0%
Peptide Content(by %N): ≥ 80%
Assay(By Anhydrous, Acetic Acid-free): 95.0~105.0%
Bacterial Endotoxins: ≤ 5EU/mg
Grade: Pharmceutical Grade
Storage: Shading, confined preservation
 
PT 141 Description:
 
PT-141 is a synthetic amino acid protein discovered during clinical trials using the Melanotan 2 for sunless tanning, photo-protection results from melanotans. Participants were documented as having experienced aphrodisiac reactions, leading to the further development PT-141. The melanocortin system targets receptors associated with desire through the melanocyte stimulating hormone paths that cross the blood-brain-barrier. Potentially the powerful sex-drug results feeling an aphrodisiac experience amplifying arousal pt141 reviews have shown the ability to increase libido effects of both men and women.
 
PT 141 Application:
 
PT-141 functions by activating the melanocortin receptor and MC4R namely. Bremelanotide originally was tested for nasal spray delivery but was discontinued after concerns about side effects. Bremelanotide PT141, as Melanotan II, may cause spontaneous arousal enhancing effect. Unlike other supplements, PT-141 results do not act on the vascular body, but directly increases desires through the nervous system.
 

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Sell Pharmaceutical Grade Plant Extract Glabridin Powder In Cosmetic Industry 59870-68-7

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Sell Pharmaceutical Grade Plant Extract Glabridin Powder In Cosmetic Industry 59870-68-7
 
Glabridin Basic Info.:
 
Product name: Glabridin
CAS No.: 59870-68-7
Molecular Formula: C20H20O4
Molecular Weight: 324.37
Appearance: Light-yellow powder
Package: 5kg/drum, or at customer's requirements
Storage: Store in a cool, dry place and keep away from direct strong light.
Shelf Life: 2 years
 
Product Functions Of Glabridin:
 
Glabridin is a chemical compound that is found in the root extract of licorice (Glycyrrhiza glabra). It is used as an ingredient in cosmetics and is listed in International Nomenclature of Cosmetic Ingredients (INCI). Glabridin is a flavonoid molecule, this product is a larger family of plant-derived phenols.
 
Glabridin (glycyrrhiza glabra extract) in its main function as a potent, natural skin-whitening agent It is known for its beneficial effects on the skin due to its anti-inflammatory and antioxidant properties. In addition, glabridin inhibits melanogenesis. Some researchers have established that this effect may be due to the inhibition of tyrosinase activity. Glabridin whitens skin without being cytotoxic (destruction of pigment cells).
 

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Weight Loss Steroid Hormone Powder Cytomel Liothyronine Sodium /T3 L-Triiodothyronine USP

Sodium L-Triiodothyronine(T3)
 
Basic Info.
Model NO.:CAS: 55-06-1                                                     Assay:99%
Molecular formula:C15H12I3NO4                                   Molecular Weight:650.97
Appearance:White or Light Yellow Powder                     Boiling Point:205 Centigrade
Export Markets:Global
 
Additional Info.
Trademark:nanjian                                                              Packing:Tin
Standard:CE                                                                         Origin:China
HS Code:2937290090                                                       water-solubility:4 M NH4OH in methanol: 125 g/5mL, clear, yellow-brown                                 
 
Description:
Triiodothyronine, also known as T3, is a thyroid hormone. It affects almost every physiological process in the body, including growth and development, metabolism, body temperature, and heart rate.
 
Production of T3 and its prohormone thyroxine (T4) is activated by thyroid-stimulating hormone (TSH), which is released from the pituitary gland. This pathway is regulated via a closed-loop feedback process: Elevated concentrations of T3, and T4 in the blood plasma inhibit the production of TSH in the pituitary gland. As concentrations of these hormones decrease, the pituitary gland increases production of TSH, and by these processes, a feedback control system is set up to regulate the amount of thyroid hormones that are in the bloodstream.
 
As the true hormone, the effects of T3 on target tissues are roughly four times more potent than those of T4. Of the thyroid hormone that is produced, just about 20% is T3, whereas 80% is produced as T4. Roughly 85% of the circulating T3 is later formed in the thyroid by removal of the iodine atom from the carbon atom number five of the outer ring of T4. In any case, the concentration of T3 in the human blood plasma is about one-fortieth that of T4. This is observed in fact because of the short half-life of T3, which is only 2.5 days. This compares with the half-life of T4, which is about 6.5 days.
 
Application:
It affects almost every physiological process in the body, including growth and development, metabolism, body temperature, and heart rate. T3 increases the basal metabolic rate and, thus, increases the body's oxygen and energy consumption. The basal metabolic rate is the minimal caloric requirement needed to sustain life in a resting individual.
 
T3 acts on the majority of tissues within the body, with a few exceptions including the spleen and testis. It increases the production of the Na+/K+ -ATPase and, in general, increases the turnover of different endogenous macromolecules by increasing their synthesis and degradation.
 
OUR ADWANTAGE: 
1, High quality with competitive price: 
1)Standard: Enterprise Standard
2)We are manufacturer and can provide high quality products with factory price.
 
2, Fast and safe delivery
1)Parcel can be sent out in 24 hours after payment. Tracking number available
2)Secure and discreet shipment. Various transportation methods for your choice.
3)Customs pass rate ≥99%
4) We have our own agent/remailer/distributor who can help us ship our products very fast and safe, and we have stock in there for transferring.
 
3, We have clients throughout the world. 
1)Professional service and rich experience make customers feel at ease, adequate stock and fast delivery meet their desire.
2)Market feedback and goods feedback will be appreciated, meeting customers's requirement is our responsibility.
3) High quality, competitive price, fast delivery, first-class service gain the trust and praise from the customers
 
If you need this or you are interest in this kind of products, you are free to send me email or call me directly, we can talk more about the details of the products.
No matter you become a customer to me or not at last, you are welcome to inquire from me!
 
Tel: +86-731-22290218
Fax: +86-731-22290218
Cell: +8618188938027
E-mail: YCWlb031@yccreate.com
Skype:andyjake@outlook.com(Andy Xu)
 

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Anabolic Androgenic Steroids Methyldrostanolone (Superdrol, Methasteron) CAS 3381-88-2 USP

Methasterone (Steroids)   
 
Basic Info
Synonyms: 2,17-Dimethyldihydrotestosterone; 17-hydroxy-2,17-dimethylandrostan-3-one
Model NO.:CAS: 3381-88-2                                           Function:Hormones and Regulation of Endocrine Function of Drug
MF: C19H30O2                                                            MW: 290.44 
Assay: 98.9% min.                                                       Export Markets:Global
 
Additional Info.
Trademark:great-steroids                                              Packing:foil bag or tin.
Density:1.04g/cm3                                                       Boiling Point:  423.8°C at 760 mmHg  
Flash Point:180.8°C                                                   Delivery: Express courier.
Origin:China                                                                Character: White crystalline powder.
HS Code:3004320036
Usage: pharmaceutical material, Steroid hormone, Anabolin. As a male hormone and anabolic hormones.
 
OUR ADWANTAGE: 
1, High quality with competitive price: 
1)Standard: Enterprise Standard
2)We are manufacturer and can provide high quality products with factory price.
 
2, Fast and safe delivery
1)Parcel can be sent out in 24 hours after payment. Tracking number available
2)Secure and discreet shipment. Various transportation methods for your choice.
3)Customs pass rate ≥99%
4) We have our own agent/remailer/distributor who can help us ship our products very fast and safe, and we have stock in there for transferring.
 
3, We have clients throughout the world. 
1)Professional service and rich experience make customers feel at ease, adequate stock and fast delivery meet their desire.
2)Market feedback and goods feedback will be appreciated, meeting customers's requirement is our responsibility.
3) High quality, competitive price, fast delivery, first-class service gain the trust and praise from the customers
 
If you need this or you are interest in this kind of products, you are free to send me email or call me directly, we can talk more about the details of the products.
No matter you become a customer to me or not at last, you are welcome to inquire from me!
 
Tel: +86-731-22290218
Fax: +86-731-22290218
Cell: +8618188938018
E-mail: YCWlb031@yccreate.com
Skype:andyjake@outlook.com(Andy xu)
 

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Factory Supply Muscle Building Steroids ATD / 1,4,6-Andorstatriene-3,17-Dione 144413-58-1

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Factory Supply Muscle Building Steroids ATD / 1,4,6-Andorstatriene-3,17-Dione 144413-58-1
 
ATD Basic information
 
Product Name: ATD
Synonyms: ADT;Androstatrienedione;ATD;Anthra[2,3-b:6,7-b']dithiophene;ADT AldrichCPR, sublimed;1,4,6-Androstatrien-3,17-Dione
CAS: 144413-58-1
MF: C19H22O2
MW: 282.38
EINECS: N/A
Product Categories: Materials Science;New Products for Materials Research and Engineering;Organic and Printed Electronics;Organic Field Effect Transistor (OFET) Materials;p-Type Organic Semiconductors;p-Type Small Molecules
Usage: A potential metabolitie of STS 557 (Dienogest). A steroid with antiglucocorticoid activity
 
Product ATD Description:
 
1,4,6-Androstatrien-3,17-dione (ATD) is considered to be a potent irreversible aromatase inhibitor that is useful for inhibiting estrogen biosynthesis by binding and inactivating aromatase in peripheral and adipose tissues in a permanent manner.
 
It is used to control estrogen synthesis and present in some of the over-the-counter muscle-enhancing and bodybuilding supplements. It increases testosterone levels in the body in an indirect manner and is therefore considered to be one of the favorite supplement among professional athletes and bodybuilders.
 
Application Of ATD:
 
1,4,6-Androstatrien-3,17-dione (ATD) offers benefits such as improvements in male fertility, mood levels, shortened recovery in case of burns or severe trauma and stimulation in developing mammals. It is considered to be a more effective anti-aromatase substance than many others and is potent enough to increase testosterone levels in the body without a concomitant reduction of the estrogen levels in men. It may be used for hormone or androgen replacement therapy in men without resulting in a concomitant reduction in endogenous estrogen levels when administered in an oral or transdermal way in dosages ranging from 25-150 mg/day.
 

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Pharmaceutical Raw Materials Dexamethasone Sodium Phosphate For Acute Disorders 2392-39-4

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Pharmaceutical Raw Materials Dexamethasone Sodium Phosphate For Acute Disorders 2392-39-4
 
Dexamethasone Sodium Phosphate Quick Detail:
 
Product name: Dexamethasone Phosphate Sodium
Synonyms: Dexamethasone sodium phosphate; Dexamethasone Phosphate Sodium; dexamethasone 21-(disodium phosphate); Dexamethasone Sodium Phosphate; Dexamethasone Phosphate Disodium
CAS: 2392-39-4
M.F.: C22H28FNa2O8P 
M.W.: 516.4
Usage : pharmaceutical raw materials, the hormone
Assay: 99%
Packaging Details: Foil bag or as requirement 
Payment Terms: T/T, Western Union, MoneyGram
Shipping way: EMS, HKEMS, DHL, Fedex, UPS (you can choose the fastest and your favourite)
 
Description of Dexamethasone Sodium Phosphate:
 
Dexamethasone sodium phosphate, a corticosteroid, is similar to a natural hormone produced by your adrenal glands. It often is used to replace this chemical when your body does not make enough of it. It relieves inflammation (swelling, heat, redness, and pain) and is used to treat certain forms of arthritis; skin, blood, kidney, eye, thyroid, and intestinal disorders (e.g., colitis); severe allergies; and asthma. Dexamethasone sodium phosphate is also used to treat certain types of cancer.
 
Dexamethasone sodium phosphate comes as a tablet and a solution to take by mouth. Your doctor will prescribe a dosing schedule that is best for you. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take Dexamethasone sodium phosphate exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.
 
Applications of Dexamethasone Sodium Phosphate:
 
Do not stop taking Dexamethasone sodium phosphate without talking to your doctor. Stopping the drug abruptly can cause loss of appetite, upset stomach, vomiting, drowsiness, confusion, headache, fever, joint and muscle pain, peeling skin, and weight loss. If you take large doses for a long time, your doctor probably will decrease your dose gradually to allow your body to adjust before stopping the drug completely. Watch for these side effects if you are gradually decreasing your dose and after you stop taking the tablets or oral liquid, even if you switch to an inhalation corticosteroid medication. If these problems occur, call your doctor immediately. You may need to increase your dose of tablets or liquid temporarily or start taking them again.
 

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