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Safety Benzyl Benzoate Safe Organic Solvents Insoluble In Water Cas 120-51-4

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Safety Benzyl Benzoate Safe Organic Solvents Insoluble In Water Cas 120-51-4
 
Benzyl Benzoate Basic Info.:
 
Product name: Benzyl benzoate
CAS NO: 120-51-4
MF: C14H12O2
MW:  212.24
EINECS: 204-402-9
Purity: 99%
Package: 250kg/plastic bucket
Appearance: Colorless liquid
 
Benzyl Benzoate Description:
 
Benzyl benzoate is the organic compound with the formula C6H5CH2O2CC6H5. It is the ester of benzyl alcohol and benzoic acid. It forms either a viscous liquid or solid flakes and has a weak, sweet-balsamic odor. It occurs in a number of blossoms (e.g. Tuberose, hyacinth) and is a component of Balsam of Peru and Tolu balsam.
It is on the World Health Organization's List of Essential Medicines, a list of the most important medication needed in a basic health system.
 
Benzyl Benzoate Application:
 
Benzyl benzoate is used as an acaricide, scabicide, and pediculicide in veterinary hospitals. It is also a repellent for chiggers, ticks, and mosquitoes. It is an effective and inexpensive topical treatment for human scabies. It has vasodilating and spasmolytic effects and is present in many asthma and whooping cough drugs.
Other uses of benzyl benzoate are dye carrier, solvent for cellulose derivatives, plasticizer, and fixative in the perfume industry.
 

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Tacrolimus FK-506 Pharmaceutical Intermediates Organ Transplant 104987-11-3

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Tacrolimus FK-506 Pharmaceutical Intermediates Organ Transplant  104987-11-3
 
Tacrolimus Basic info: 
 
Product Name: Tacrolimus
Synonyms: Tacrolimus;Fr900506;Prograf;Tsukubaenolide;FK-506;
CAS: 104987-11-3
MF: C44H69NO12
MW: 804.02
Purity: 99%
Melting Point: 113-115°C
Boiling Point: 871.7 °C at 760 mmHg
Solubility: DMSO: >3 mg/mL
Appearance: White Crystalline Powder
Storage temp.: −20°C
Storage: Store in a cool, dry place. Do not store in direct sunlight. Store in a tightly closed container.
Product Categories: Active Pharmaceutical Ingredients;Immunosuppressant.;Intermediates & Fine Chemicals;Pharmaceuticals;API;Chiral Reagents;Fujimycin, Prograf;antibiotic;Inhibitors.
Usage: FK-506 (Tacrolimus) is a macrolide immunosuppressive drug that is mainly used after allogeneic organ transplant to reduce the activity of the patient's immune system.
 
Tacrolimus Application: 
 
L Immunosuppression following transplantation It has similar immunosuppressive properties to ciclosporin, but is much more potent. Immunosuppression with tacrolimus was associated with a significantly lower rate of acute rejection compared with ciclosporin-based immunosuppression (30.7% vs 46.4%) in one study. Clinical outcome is better with tacrolimus than with ciclosporin during the first year of liver transplantation. Long term outcome has not been improved to the same extent. Tacrolimus is normally prescribed as part of a post-transplant cocktail including steroids, mycophenolate and IL-2 receptor inhibitors. Dosages are titrated to target blood levels. Typical starting doses for once daily tacrolimus are 0.15-0.20 mg/kg body weight.
 
Tacrolimus Interactions:
 
Also like cyclosporin it has a wide range of interactions, including that with grapefruit which increases plasma-tacrolimus concentration. Several of the newer class of antifungals, especially of the azole class (fluconazole, posaconazole) also increase drug levels by competing for degradative enzymes.
 
Ulcerative colitis: 
In recent years, tacrolimus has been used to suppress the inflammation associated with ulcerative colitis, a form of inflammatory bowel disease. Although almost exclusively used in trial cases only, tacrolimus has shown to be significantly effective in the suppression of outbreaks of UC.
 
Tacrolimus Dermatological Use: 
 
As an ointment, tacrolimus is used in the treatment of eczema, in particular atopic dermatitis. It suppresses inflammation in a similar way to steroids, and is equally as effective as a mid-potency steroid. An important advantage of tacrolimus is that, unlike steroids, it does not cause skin thinning (atrophy), or other steroid related side-effects.
 
It is applied on the active lesions until they heal off, but may also be used continuously in low doses (twice a week), and applied to the thinner skin over the face and eyelids[citation needed]. Clinical trials of up to one year have been conducted. Recently it has also been used to treat segmental vitiligo in children, especially in areas on the face.
 

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99% High Quality Anesthetic CAS 61-12-1 Dibucaine Hydrochloride Dibucaine HCl

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99% High Quality Anesthetic CAS 61-12-1 Dibucaine Hydrochloride Dibucaine HCl
 
Dibucaine HCL Basic Info.:
 
Product Name: Dibucaine hydrochloride
Dibucaine hydrochloride Synonyms: 2-butoxy-n-(2-(diethylamino)ethyl)-4-quinolinecarboxamidmonohydrochlorid;butoxycinchoninicaciddiethylethylenediamidehydrochloride;c3225
CAS: 61-12-1
MF: C20H30ClN3O2
MW: 379.92
EINECS: 200-498-1
Product Categories: Heterocycles;Intermediates & Fine Chemicals;PharmaceuticalsDibucaine hydrochloride  Chemical Properties:whitepowder Dibucaine hydrochloride  Usage Anesthetic (local).
 
Dibucaine HCL Description:
 
Dibucaine hydrochloride is a local anesthetic of the amide type now generally used for surface anesthesia. It is one of the most potent and toxic of the long-acting local anesthetics and its parenteral use is restricted. The drug blocks both the initiation and conduction of nerve impulses by decreasing the neuronal membrane's permeability to sodium ions. This reversibly stabilizes the membrane and inhibits depolarization, resulting in the failure of a propagated action potential and subsequent conduction blockade.
 
In combination sodium dibucaine hydrochloride is administered to dogs to induce rapid, humane, painless euthanasia. The euthanasia solution is toxic to wildlife. Euthanized animals must be properly disposed of by deep burial, incineration or other method in compliance with state and local laws.
 
Dibucaine HCL Applications:
 
Spinal anesthesia (high, low, saddle block) and topically to produce surface anesthesia. Eye: To anesthetize conjunctiva and cornea prior to superficial procedures (including tonometry, gonioscopy, removal of foreign bodies or sutures, corneal scraping).
 
Nose and Throat: To abolish laryngeal and esophageal reflexes prior to bronchoscopy, esophagoscopy.
Skin: To relieve pruritus, pain, burning.
 

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Body Building Anabolic Sarms LGD-4033 Purity 99% Sarms Ligandrol 1165910-22-4

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Body Building Anabolic Sarms LGD-4033 Purity 99% Sarms Ligandrol 1165910-22-4
 
LGD-4033 Basic Info.:
 
Product Name: LGD-4033
Synonyms: LGD-4033;LGD4033;Ligandrol;
CAS: 118237-47-0
MF: C20H16ClN5O2
MW: 393.826
Purity: 99.5%(HPLC)
Apprarance: White crystalline powder.
 
LGD-4033 Product Description:
 
LGD-4033 is a selective androgen receptor modulator (SARMS), and a novel non-steroidal oral SARM that binds to AR with high affinity (Ki of ~1 nM) and selectivity. It’s in a class of androgen receptor (AR) ligands that is tissue selective, developed to treat muscle wasting associated with cancer, acute and chronic illness and age-related muscle loss. LGD-4033 is expected to produce the therapeutic benefits of testosterone with improved safety, tolerability and patient acceptance due to tissue-selective mechanism of action and an oral route of administration.
 
LGD-4033, a novel nonsteroidal, oral selective androgen receptor modulator, binds to the androgen receptor with high affinity and selectivity. It demonstrates anabolic activity in muscles, anti-resorptive and anabolic activity in bones and a robust selectivity for muscle and bone versus prostate and sebaceous glands. LGD-4033 has recently completed a Phase I Multiple Ascending Dose study in healthy volunteers. This randomized, double-blind, placebo-controlled Phase I study established the safety and tolerability up to doses of 22 mg per day.
 
LGD-4033 Application:
 
LGD is still fairly new (3-5 years), but the results have been very similar in studies and logs. LGD-4033 has undergone several recent studies and trials to find the best and safest way to use it. From these trials, the results have shown increases in lean body mass and decreases in body fat. There is also a significant increase in strength, well being, as well as healing possibilities.
 
LGD has shown the most ability of any SARM to put on size that could be considered a bulk. This will, of course, be dependent upon the diet used. Users that have experienced more than 10lb. increases, and have had a significant increase in calorie intake. The possibility of this type of size is present with LGD use. A recommend dosage for this type of goal would be 5-10 mg day for 8 weeks.
 
LGD seems to shine with this method. Many have seen an increase in lean body mass and a decrease in body fat. LGD seems to work the best with this method. Ran in conjunction with other SARMS, like cardarine (GW-501516), will only increase the likelihood of a stronger recomp. Recommended doses for recomping would be 5-8 mg a day for 8 weeks.
 
LGD can be used to cut as well. It will shine more-so if ran in conjunction with SARMS S-4 and Cardarine (GW-501516). This would be similar to a SARMS triple stack that is normally ran with Ostarine, except there is a possibility of more size being put on while cutting. A good dose for this method would be 3-5 mg a day for 8 weeks.
 

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High Purity Body Supplement Kola Nut Extract Cola Acuminata Powder 68916-19-8

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High Purity Body Supplement Kola Nut Extract Cola Acuminata Powder 68916-19-8
 
Kola Nut Extract Basic Info.:
 
Product Name: Kola Nut Extract
Cola Acuminata 
Latin Name: Cola acuminata
CAS No.: 68916-19-8
Active Ingredient: Caffeine theobromine
Specifications: 1-99%
Test Method: HPLC
 
Kola Nut Extract Description:
 
Kola Nut is also known as Cola Nut and Cola. Kola Nut is the seed kernel of a large African tree grown commercially around the world. It is extremely popular in the tropics as a caffeine-containing stimulant. The properties of Kola are the same as caffeine, modified only by the astringents present.
Kola nut extract is a natural supplement from the seeds of the tree Kola vera, also known as Cola nitida and Cola acuminate. The Kola vera tree is a member of the Sterculiaceae family of evergreens, which grow in Africa and South America and can reach 60 feet tall.
 
Kola Nut Extract Application:
 
You can find kola nut extract as an ingredient in energy drinks or sold separately as an energy supplement or weight-loss aid. According to the "Encyclopedia of Natural Medicine," kola nut contains high quantities of caffeine, which is why manufacturers.
market the extract for weight loss and as an energy supplement. Additionally, you can use kola nut extract as a diuretic. Further uses have been as a remedy for headaches, rheumatism, whooping cough and asthma.
 

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Injectable Anabolic Steroid Nandrolone Cypionate For Muscle Building 601-63-8

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Injectable Anabolic Steroid Nandrolone Cypionate For Muscle Building 601-63-8
 
Nandrolone Cypionate Basic Info.
 
Product Name: Nandrolone Cypionate
Synonyms: Nandrolone Cypionate; Nandrolone Cipionate; Nortestosterone Cypionate; Nandrolone Cypionate;Nandrolone Cyclopentanepropionate; Nandrolone Cypiontate
CAS: 601-63-8
MF: C26H38O3
MW: 398.57812
EINECS: 210-006-7
Assay: 99% 
Appearance: Pale yellow oily liquid
Product Categories: Steroid and Hormone
 
Nandrolone Cypionate Description: 
 
Nandrolone cypionate is recommended as an aid for the treatment of debilitated horses when an improvement in weight, hair coat or general physical condition is desired. Debilitation often follows disease or may occur following overwork and overexertion.
 
Nandrolone improves the general state of debilitated horses, thus aiding in correcting weight losses and improving appetite. It is not a substitute for a well-balanced diet. Optimal results can be expected only when good management and feeding practices are utilized.
 
Nandrolone should be considered only as adjunctive therapy to other specific and supportive therapy for diseases, surgical cases and traumatic injuries.
 
Testosterone Cypionate is the longest-estered testosterone available today. It has a half-life in the body of 15 to 16 days and is found as injectable oil. Because it reacts in the body for so long, it can cause more water retention than other steroids and is best used as bulking compound in a stack.
 
As with all testosterone injectables, one can expect a considerable gain in muscle mass and strength during a cycle. Since testosterone readliy converts to estrogen, the mass gained from this drug is likely to be accompanied by quite a bit of water retention. The resulting loss of definition of course makes cypionate a very poor choice for dieting or cutting phases. The excess level of estrogen brought about by this drug can also cause one to develop gynecomastia rather quickly. Should one notice an uncomfortable soreness, swelling or lump under the nipple, an ancillary drug like Nolvadex should be added immediately. This will minimize the effect of estrogen greatly, making the steroid much more tolerable to use. The powerful anti-aromatases Arimidex, Femara, or Aromasin are yet a better choice. Those who have a known sensitivity to estrogen may find it more beneficial to use ancillary drugs like Nolvadex and Proviron from the onset of the cycle, in order to prevent estrogen related side effects before they become apparent.
 
Nandrolone Cypionate Applications:
 
Nandrolone-Cypionate is one of the numerous Nandrolone compounds on the market,however, it's not as common as the immensely popular and highly available Nandrolone-Decanoate (Deca-Duraboli)). Deca-Durabolin is carried by every supplier on earth and any pharmacy the world over,and after that we have Nandrolone-Phenylpropionate (Durabolin or NPP),and then we have
 
It can help to rebuild body tissue, increase body and bone mass and encourage the formation of red blood cells. Nandrolone cypionate is an anabolic steroid which is a group of drugs that are usually synthesized from the male reproduction hormone testosterone. 
 
intermediate. It self as an anabolic hormone drugs, can promote protein synthesis and inhibiting protein dysplasia, and can lower blood cholesterol, reduce calcium phosphorus excretion and reduce bone marrow suppression, promoting development, promote tissue freshmen and granulation. Caused by long-term use of adrenal cortical hormone have prevention and protection against the adrenal cortex hypofunction.
Second only to Dianabol (methandrostenolone) as a bodybuilding anabolic steroid. Additionally, it has had considerable medical importance particularly for treatment of anemia, and more recently to help maintain lean body mass in HIV-compromised patients.
Alienation can promote protein synthesis and inhibiting protein, and can lower blood cholesterol, reduce calcium phosphorus excretion and reduce bone marrow suppression, promote development and so on.
 

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Injectable Steroid Yellow Oils Andropen 275 Mg/Ml Muscle Building Supplements

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Injectable Steroid Yellow Oils Andropen 275 Mg/Ml Muscle Building Supplements
 
Andropen 275 Basic Info.:
 
Product Name: Andropen 275
Andropen 275mg per ml
Andropen 275 is an androgenic/anabolic steroid mix. A perfect blend of slow and fast acting.
Each ml contains:
Testosterone acetate USP 20mg
Testosterone decanoate USP 90mg
Testosterone Propionate USP 45mg
Testosterone Phenylpropionate USP 45MG
Testosterone Cypionate USP 75 mg
 
Andropen 275 Description:
 
Andropen 275is a combination of five of testosterones. The presence of the acetate ester allows the testosterone to display a rapid initial physiological response. The other four esters, which release at slower rates, prolong the physiological response with a relatively flat absorption curve over the duration of the injection life - cycle. Testosterone is a male sexual hormone with pronounced, mainly androgenic action, possessing the biological and therapeutic properties of the natural hormone.
 
It is normally produced in women in small physiological quantities. In addition to the specific action that determines the sexual characteristics of the individual, testosterone also has a general anabolic action, manifested in enhancement of protein synthesis. Under the effect of testosterone, body weight increases and urea excretion is reduced. High doses suppress the production of hypophyseal gonadotropin, while low doses stimulate it. It has an antitumor effect on mammary gland metastases.
 

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Omeprazole Pharmaceutical Raw Materials 73590-58-6 For Treatment Peptic Ulcer

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Omeprazole Pharmaceutical Raw Materials 73590-58-6 For Treatment Peptic Ulcer
 
Omeprazole Basic Info.:
 
Product Name: Omeprazole
Alias: OMEPRAL; MOPRAL; MEPRAL; LOSEC
CAS Registry Number: 73590-58-6
Purity: 99%
Molecular Formula: C17H19N3O3S
Molecular Weight: 345.42
Appearance: white powder
Packaging Detail: 1kg/Aluminum foil bag, 25kgs/Fibre drum
Usage: Suitable for peptic ulcer, reflux esophagitis, have strong and persistent inhibition of basal gastric acid and food, five peptide secretin induced gastric acid secretion of gastric acid.
 
Product Description of Omeprazole:
 
Omeprazole is one of the most widely prescribed drugs internationally and is available over-the-counter in some countries.It is on the World Health Organization's List of Essential Medicines, a list of the most important medications needed in a basic health system. Omeprazole can be used in the treatment of gastroesophageal reflux disease, peptic ulcers, erosive esophagitis, and Zollinger-Ellison syndrome.
 
Gastroesophageal reflux disease: Gastroesophageal reflux disease (GERD) is a chronic condition in which acidic stomach content leaks back into the esophagus and irritates it. It may cause heartburn, which is a painful burning feeling in the chest or throat.
 
Peptic ulcers: Peptic ulcers are sores that develop in the lining of either the stomach or the duodenum due to damage from stomach acid. The most common cause of a peptic ulcer is infection by Helicobacter pylori. Another major cause of a peptic ulcer is long term usage of non-steroidal anti-inflammatory drugs (NSAIDs), such as aspirin or ibuprofen. Treatment of Helicobacter pylori infection can be completed by taking a triple therapy combination of omeprazole, amoxicillin, and clarithromycin for 7-14 days.
 
Erosive esophagitis:Erosive esophagitis is due to tissue damage to the lining of the esophagus, because of inflammation or irritation over time. It may be caused by acid reflux from GERD, infection by a virus or fungus, an autoimmune disorder, certain medications,or alcohol abuse.
 
Zollinger Ellison syndrome:Zollinger Ellison syndrome is a rare disorder that occurs when a tumor of the pancreas or duodenum releases a hormone that stimulates overproduction of stomach acid. This condition may form multiple peptic ulcers.
 

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