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High Quality Animal Extracts Powder CAS 474-25-9 Chenodeoxycholic Acid Cdca

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High Quality Animal Extracts Powder CAS 474-25-9 Chenodeoxycholic Acid Cdca
 
Chenodeoxycholic Acid Basic Info.:
 
Product Name: Chenodeoxycholic acid
Synonyms: Ursodeoxycholoc Acid
CAS: 474-25-9
MF: C24H40O4
MW: 392.57
EINECS: 207-481-8
Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Steroids;Intracellular receptor;Inhibitors
Melting point: 165-167 °C(lit.)
Alpha: 12 °(c=1, CHCl3)
Storage temp.: Refrigerator
Solubility: PRACTICALLY INSOLUBLE
Water Solubility: PRACTICALLY INSOLUBLE
Chemical Properties: Off-White Solid
Usage: vitamin D3, anticholithogenic, antilipemic agent, A major bile acid in many vertebrates, occurring as the N-glycine and/or N-taurine conjugate. With other bile acids, forms mixed micelles with lecithin in bile which solubilize cholesterol and thus fa cilitates its excretion. Fcilitates fat absorption in the small intestine by micellar solubilization of fatty acids and monoglycerides. Anticholelithogenic. Epimeric with Ursodiol.
 
Chenodeoxycholic Acid Description:
 
Cholic acid is a kind of sterols, is four major human one of the most abundant content of bile acid, derived from it and gca taurocholic acid is the main human bile acid. Liver secretion to bile in the bile salt (sodium salt of bile acid) is a powerful emulsifier.
After bile flow through the upper small intestine, bile salt emulsifying fat, help the digestion and absorption. In the emulsifying fat globules fatty acid glyceride and absorbed by the lower part of the small intestine, bile salt is absorbed by weight. They returned to the liver and be reused, so total bile salt circulation between liver and small intestine.Cholic acid is synthesized from liver, bile into the duodenum, as one part of the digestive juice, can promote digestion and absorption of lipid.
 
Chenodeoxycholic Acid Application:
 
(1) It can treat cholecystitis, the lack of bile, intestinal indigestion and gallstones etc.
(2) It can prevent and treat liver diseases.
(3) It is a kind of organic acid and can be used to produce vitamin D2 and D3.
 
Chenodeoxycholic Acid Function:
 
(1) It can emulsify fat and improve its function of digestion as a kind of organic acid.
(2) It can be applied in emulgator.
(3) It can be applied in the research of biochemistry as a kind of medical intermediate.
(4) It can be applied in non ion-modified detergent to extract membrane protein.
(5) It is mainly used as medicine raw materials.
(6) The cholesterol is still the raw material of cosmetics, and a good surfactant of medicine products. It can also be used for additive of animal feed.
 

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High Quality Anti-Estrogen Steroids Raloxifene HCl 82640-04-8

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High Quality Anti-Estrogen Steroids Raloxifene HCl 82640-04-8 
 
Raloxifene HCL Basic Info.:
 
Product Name: Raloxifene Hydrochloride
Synonyms: Raloxifene HCL;Raloxifene Hydrochloride;Ly156758;Piperidin;Keoxifene;Keoxifene Hydrochloride;Ly 139481;AKOS 92138
CAS: 82640-04-8
MF: C28H28ClNO4S
MW: 510.04
Melting Point: 250-253°C
Storage Temp.: -20°C Freezer
Solubility DMSO: 28 mg/mL, soluble
Chemical Properties: Light-Yellow Solid
Assay: 99%
Grade: Pharmaceutical Grade
Product Categories: Active Pharmaceutical Ingredients;Raloxifene;Intracellular receptor;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;Sulfur & Selenium Compounds;Pharmaceutical intermediate;API;Inhibitors;antifungal
Usage: amino acid, nutrient, Labeled Raloxifene, intended for use as an internal standard for the quantification of Raloxifene by GC- or LC-mass spectrometry.A nonsteroidal, selective estrogen receptor modulator (SERM). Antiosteoporotic.
 
Product Description:
 
Raloxifene HCL(marketed as Evista) is an oral selective estrogen receptor modulator (SERM) that has estrogenic actions on bone and anti-estrogenic actions on the uterus and breast. It is used in the prevention of osteoporosis in postmenopausal women and to reduce the risk of invasive breast cancer in postmenopausal women with osteoporosis and in postmenopausal women at high risk for invasive breast cancer.
 
This drug is different from hormones (including estrogens and progestins). It works by acting like estrogen (as a selective estrogen receptor modulator or SERM) in some parts of the body. Raloxifene HCL helps to preserve bone mass, but it does not affect the breast and uterus like estrogen or relieve symptoms of menopause such as hot flashes.
 
Raloxifene HCL is indicated for the treatment and prevention of osteoporosis in postmenopausal women. It is also used for reduction of risk and treatment of invasive breast cancer, and it also reduces breast density.For either osteoporosis treatment or prevention, supplemental calcium and/or vitamin D should be added to the diet if daily intake is inadequate.
 
Raloxifene HCL is used to prevent and treat bone loss (osteoporosis) in women after menopause. Maintaining strong bones by slowing bone loss helps to reduce the risk of fractures.
 
Raloxifene HCL may also lower the chance of getting a certain type of breast cancer (invasive) in women after menopause.
 

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High Quality Factory CAS 98319-26-7 Finasteride USP

Finasteride
 
Product Description:
CAS NO.: 98319-26-7                                                                  Assay: 99%
Molecular Formula:C23H36N2O2                                                  Molecular Weight:372.54 
Packing:foil bag
Appearance: White or white crystalline solid. Soluble in chloroform, dimethyl sulfoxide, ethanol, methanol or propanol, insoluble in propylene glycol or polyethylene glycol 400
 
Usage: The drug can be very effective in reducing blood and dihydro testosterone within the prostate. Finasteride no affinity to the androgen receptor
 
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!
 
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High Quality Factory Direct Supply Estrogen Hormone Estradiol Enanthate 4956-37-0

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High Quality Factory Direct Supply Estrogen Hormone Estradiol Enanthate 4956-37-0
 
Estradiol Enanthate Basic Info.
 
Product Name: Estradiol Enanthate
CAS Number: 4956-37-0
Purity: 99%
Molecular Weight: 384.556
Molecular Formula: C25H36O3
Appearance: Crystalline powder
Physical State: Solid
Solubility: Soluble in water (slightly).
Storage: Store at room temperature
Melting Point: 94-96 ° C
Boiling Point: ~509.5 ° C at 760 mmHg (Predicted)
Density: ~1.1 g/cm3 (Predicted)
 
Estradiol Enanthate Description:
 
Estradiol enanthate (INN, USAN), or estradiol enantate, is a synthetic ester, specifically the 17-heptanoyl ester, of the natural estrogen, estradiol. It is marketed under the brand names Anafertin, Deladroxate, Perlutan, and Topasel, which are combination formulations of estradiol enanthate and dihydroxyprogesterone acetophenide, as a once-monthly injectable hormonal contraceptive in Spain and Latin America, and has been used as such since at least the mid-1960s.
 
Estradiol, or more precisely, 17β-estradiol, is a human sex hormone and steroid, and the primary female sex hormone. It is named for and is important in the regulation of the estrous and menstrual female reproductive cycles. Estradiol is essential for the development and maintenance of female reproductive tissues but it also has important effects in many other tissues including bone. While estrogen levels in men are lower compared to women, estrogens have essential functions in men as well. Estradiol is found in most vertebrates as well as many crustaceans, insects, fish, and other animal species.
 
Estradiol or oestradiol (American or British English usages), derives from estra-, Gk. οστρο? (oistros, literally meaning "verve or inspiration") and -diol, a chemical name and suffix indicating that this form of steroid and sex hormone is a type of alcohol bearing two hydroxyl groups.
 
Estradiol is produced especially within the follicles of female ovaries, but also in other endocrine (i.e., hormone-producing) and non-endocrine tissues (e.g., including fat, liver, adrenal, breast, and neural tissues). Estradiol is biosynthesized from progesterone (arrived at in two steps from cholesterol, via intermediate pregnenolone). One principle pathway then converts progesterone to its 17-hydroxy-derivative, and then to androstenedione via sequential cytochrome P450-catalyzed oxidations.Action of aromatase on this dione generates estrone, and action of a dehydrogenase on this gives the title compound, 17β-estradiol.
 
Estradiol Enanthate Function:
 
Hormones and Regulation of Endocrine Function of Drug, Nutritional Therapeutics, Antibiotic and Antimicrobial Agents, Antiparasitic, Original Drug Resistant Microbes, Immune System Drugs, Specialist Drugs, Drug Detoxification, Diagnostic Agents, Blood System Agents, Visceral System Medication, Central Nervous System Agents, Cardiovascular Agents, Urinary System Agents, Respiratory System Agents.
 
A chemical derivative of estradiol, ethinyl estradiol with maximum dosage 200 µg, is a major component of hormonal contraceptive devices. Combined forms of hormonal contraception contain ethinyl estradiol and a progestin, which both contribute to the inhibition of GnRH, LH, and FSH, which accounts for the ability of these birth control methods to prevent ovulation and thus prevent pregnancy. Other types of hormonal birth control contain only progestins and no ethinyl estradiol.
 

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High Quality Glucocorticoid Hydrocortisone For Anti-Inflammatory 50-23-7

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High Quality Glucocorticoid Hydrocortisone For Anti-Inflammatory 50-23-7
 
Hydrocortisone Basic Info.:
 
Product Name: Hydrocortisone
Synonyms: 11beta-Hydrocortisone
CAS: 50-23-7
MF: C21H30O5
MW: 362.46
EINECS: 200-020-1
Melting point: 211-214 °C(lit.)
alpha: 166°(c=1, C2H5OH 25 ºC)
Fp: 220°C
storage temp.: −20°C
solubility: H2O: 100 mg/mL
Stability: Stable, but may be light sensitive. Incompatible with strong oxidizing agents.
Chemical Properties: crystalline white powder
Usage: Principle glucocorticoid hormone produced by adrenal cortex; An anti-inflammatory hormone; glucocorticoid, antiinflammatory.
Product Categories: TPI;Steroids;Veterinaries;Intermediates & Fine Chemicals;Pharmaceuticals;Steroid and Hormone;HYDROCORTONE;Isolabel;Hormone Drugs;adrenocortical hormones'drug;API;Inhibitors
 
Hydrocortisone Description:
 
Suitable for contact dermatitis, lichen planus, etc. It is currently the most important supplementary glucocorticoid drugs, extensive drug effects, versatile, indispensable clinical drugs. Adrenal crisis in the rescue, anaphylactic shock, status asthmaticus critically ill played an important role. In systemic lupus erythematosus, rheumatism, autoimmune vasculitis treatment of autoimmune diseases is an important and indispensable therapy.
 
The advantage of this drug is its ethanol and hydrocortisone sodium succinate intravenously directly and quickly to play a role for the rescue of critically ill patients and shock therapy for certain diseases, generally do not cause peptic ulcers, purpura and spirit symptoms, but the row of potassium and sodium retention is stronger. Short-term large doses of hydrocortisone (24h infusion 2000 ~ 4000mg, once every 2 to 3 days) for some critically ill with the rescue, to receive good results, such as the rescue of septic shock, status asthmaticus , adult respiratory distress syndrome, short-term application, generally no adverse reactions.
 
Hydrocortisone Application:
 
1. Biochemical studies, adrenal cortical hormone drugs.
2. Glucocorticoids have anti-inflammatory, anti allergic, anti toxin, anti shock four role.
3. Adrenal corticoids.
 

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High Quality L-Thyroxine CAS 51-48-9 for Bodybuilding 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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High Quality Legal Anabolic Steroids Trestolone For Muscle Growth 3764-87-2

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High Quality Legal Anabolic Steroids Trestolone For Muscle Growth 3764-87-2
 
Trestolone Basic Info.
 
Product Name: Trestolone
Synonyms: 19-Nor-7A-Methyltestosterone;7-Alpha-Methyl-19-Nortestosterone;
CAS: 3764-87-2
Molecular formula: C19H28O2
Molecular weight: 288.42
Appearance: white crystalline powder
Product Categories: Steroid and Hormone.
Usage: Trestolone is a synthetic androgen used as a potential hormonal male contraceptive method that induces a state of termporary infertility.
 
Trestolone Description:
 
Trestolone is a synthetic androgen taken to build muscle rapidly, and is a theoretical candidate drug for use in hormonal male contraceptive methods. In males, regular administration of sufficient quantities of trestolone induces a state of temporary infertility
 
Trestolone is an experimental contraceptive treatment and is not yet available commercially. It is currently being evaluated for safety and effectiveness in scientific studies, supported by the Population Council.
 
As a derivative of the anabolic steroid hormone nandrolone, trestolone's viability as a male contraceptive is twofold.
 
Trestolone Usage:
 
Trestolone is a synthetic androgen used as a potential hormonal male contraceptive method that induces a state of termporary infertility.
 

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High Quality Local Anesthetic Prilocaine Hydrochloride Prilocaine HCl 1786-81-8

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High Quality Local Anesthetic Prilocaine Hydrochloride Prilocaine HCl 1786-81-8
 
Prilocaine HCL Basic Info.:
 
Product Name: Prilocaine HCL
CAS: 1786-81-8
English name: Propitocaine hydrochloride
Other name: Prilocaine hydrochloride; 2 - propylamine base - o C amide toluene hydrochloride; Prilocaine hydrochloride; Prilocaine hydrochloride
Molecular formula: C13H21ClN2O
EINECS: 217-244-0
Molecular Weight: 256.7716
 
Prilocaine HCL Description:
 
Propitocaine hydrochloride is a local anesthetic of the amino amide type first prepared by Claes Tegner and Nils Lö Fgren. In its injectable form, it is often used in dentistry. It is also often combined with lidocaine as a preparation for dermal anesthesia (lidocaine/prilocaine or EMLA), for treatment of conditions like paresthesia. As it has low cardiac toxicity, it is commonly used forintravenous regional anaesthesia.
 
In some patients, a metabolite of prilocaine may cause the unusual side effect of methemoglobinemia, which may be treated with methylene blue.
 
Local anesthetic is a substance that causes loss of sensation only to the area to which it is applied without affecting consciousness. Most local anesthetics structures have amino-ester or an amino-amide group which are linked to hydrophilic (secondary or tertiary amine) and to hydrophobic group (aromatics) on the other side.
 
Local anesthetics, long duration, lower toxicity, chemicals that are also small Suitable for epidural anesthesia, block anesthesia and infiltration anesthesia, etc.
 

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High Quality Pharmaceutical Chemicals Melatonin Melatonine For Nutritional Supplement MLT 73-31-4

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High Quality Pharmaceutical Chemicals Melatonin Melatonine For Nutritional Supplement MLT 73-31-4
 
Melatonine Basic Info.:
 
Product Name: Melatonin (MLT)
Synonyms: MLT;Melatonin;
CAS: 73-31-4
Molecular Formula: C13H16N2O2
Molecular Weight: 232.28
EINECS: 200-797-7
Assay: 99%
Standard: USP
Packing: foil bag or tin.
Appearance: White or almost white crystalline powder.
Payment: T/T, Western Union and Money Gram
Delivery: Within 24hours After Your Payment
Express: EMS, DHL, FedEx, etc(door-to-door)
 
Melatonin (MLT) Info:
 
Mainly by the pineal gland in mammals and humans have a amine hormones. Human pineal gland is attached to the, the posterior wall of the third ventricle, beans granular size organization. Also reported mammalian retina and lacrimal gland can associate a small amount of melatonin produced; some of the cold-blooded animal's eyes, brain and skin (such as frogs) and some algae are able to synthesize melatonin.
 
Melatonin (MLT) Avail:
 
People use melatonin to adjust the body's internal clock. It is used for jet lag, for adjusting sleep-wake cycles in people whose daily work schedule changes (shift-work disorder), and for helping blind people establish a day and night cycle. Melatonin is also used for the inability to fall asleep (insomnia); delayed sleep phase syndrome (DSPS); insomnia associated with attention deficit-hyperactivity disorder (ADHD); insomnia due to certain high blood pressure medications called beta-blockers; and sleep problems in children with developmental disorders including autism, cerebral palsy, and intellectual disabilities. It is also used as a sleep aid after discontinuing the use of benzodiazepine drugs and to reduce the side effects of stopping smoking.
 

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High Quality Pharmaceutical Raw Material Conform USP Diethylstilbestrol 56-53-1 / 6898-97-1

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High Quality Pharmaceutical Raw Material Conform USP Diethylstilbestrol 56-53-1 / 6898-97-1
 
Diethylstilbestrol Basic Info.:
 
Product Name: Diethylstilbestrol
Synonyms: Stilbestrol;Diethylstilbesterol;Domestrol;Grafestrol;Estrosyn;Fonatol;LABOTEST-BB LT00233101;
CAS: 56-53-1 / 6898-97-1
MF: C18H20O2
MW: 268.35
EINECS: 200-278-5
Assay: 99%
Melting point: 170-172 °C(lit.)
Storage temp.: 0-6°C
Solubility methanol: 0.1 g/mL, clear, faintly yellow
Stability: Isomerizes rapidly in Benzene, Chloroform, and Ether. Keep Shielded from light.
Water Solubility: Practically insoluble
Chemical Properties: White Solid
Product Categories: Miscellaneous Biochemicals;Intermediates & Fine Chemicals;Pharmaceuticals;STILBESTROL;Other APIs
Usage: Mainly used for low disease and estrogen hormone imbalance caused by functional bleeding, amenorrhea, can also be used before induction of labor stillbirth to increase myometrial oxytocin sensitivity.
 
Diethylstilbestrol Description:
 
Diethylstilbestrol (DES, former BAN stilboestrol) is a synthetic nonsteroidal estrogen that was first synthesized in 1938. It is also classified as an endocrine disruptor. Human exposure to DES occurred through diverse sources, such as dietary ingestion from supplemented cattle feed and medical treatment for certain conditions, including breast and prostate cancers.:)
 
From about 1940 to 1971, DES was given to pregnant women in the mistaken belief it would reduce the risk of pregnancy complications and losses.:)
 
In 1971, DES was shown to cause a rare vaginal tumor in girls and women who had been exposed to this drug in utero. The United States Food and Drug Administration subsequently withdrew DES from use in pregnant women. Follow-up studies have indicated that DES also has the potential to cause a variety of significant adverse medical complications during the lifetimes of those exposed.:)
 
The United States National Cancer Institute recommends women born to mothers who took DES undergo special medical exams on a regular basis to screen for complications as a result of the drug. Individuals who were exposed to DES during their mothers' pregnancies are commonly referred to as "DES daughters" and "DES sons".
 
Diethylstilbestrol Application:
 
A synthetic, nonsteroidal estrogen. Recomended solvents are DMSO, DMF and ethanol, even in these solvents do not store in solution for any prolonged period of time.
 

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