Pharmaceutical raw materials used in synthesizing new medications

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Male Enhancement Raw Winstrol Powder Anabolic Steroid Hormone Stanozolol 10418-03-8

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Male Enhancement Raw Winstrol Powder Anabolic Steroid Hormone Stanozolol 10418-03-8

Stanozolol Basic Info.

Product Name: Stanozolol (Stanazol)

Alias: Winstrol;Stromba;Stanozolol;Winny Depot;Stanazol.

CAS No: 10418-03-8

MF: C21H32N2O

MW: 328.49

Einecs No: 233-894-8

Purity: 99%

MOQ(minimum order quantity):10gram

Standard: Enterprise Standard

Appearance: White crystalline powder.

Usage: Stanazol Winstrol is the trade name for the anabolic steroid Stanazol. This is the third most popular and widely used anabolic steroid in all history and in the whole world;And is a very commonly used anabolic steroid for cutting cycles.

Stanozolol Description:

Winstrol - Stanazol  is a very commonly used anabolic steroid for cutting cycles. While many people will attempt to use Dianabol or even Anadrol for cutting cycles, Ive really never heard of anyone using Stanazol  for anything except a cutting cycle. Its a bit of a one-trick-pony in this respect. Let me repeat that: Stanazol  is a cutting drug. Not many people will argue for its use in a bulking cycle. Its certainly not a very effective compound for treating anemia (1) and thus, one could rightly assume that its role in bulking cycles is very limited. One novel use for Winstrol in any cycle (perhaps even bulking) would be to use it at a very limited dose, in order to lower SHBG. (2) One of the properties of Winstrol is its profound ability to lower SHBG much more than other steroids. A dose of .2mg/kg lowered SHBG significantly, which would in turn, raise the amount of free testosterone circulating in the body. As with 99% of steroids, however, its important to note that suppression of your natural hormonal levels will occur (though perhaps not to the extent that it will with many other steroids).(10) As with running virtually any compound, testosterone supplementation (i.e. running test in a cycle containing Winstrol) is warranted to avoid possible sexual dysfunction.

Stanozolol Applications:

Winstrol is the trade name for the anabolic steroid Stanazol . This is the third most popular and widely used anabolic steroid in all history and in the whole world. The first most popular anabolic steroid is Dianabol (Methandrostenolone), second most popular is Nandrolone Decanoate (Deca Durabolin), and the third most popular is Stanazol  In particular, Winstrol is the anabolic steroid best known for its supposed use by Canadian Olympic sprinter Ben Johnson when he was tested positive for this compound in the 1988 Seoul Summer Olympic Games. Winstrol's information was first documented, published, and released in 1959. Shortly thereafter, Winthrop Laboratories located in the United Kingdom manufactured it into a prescription drug for use, and in 1961 Sterling in the United States purchased the patent for the drug. Shortly thereafter, it was then released onto the North American market and given the brand name label of Winstrol.

 

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Pharmaceutical Powdered Female Sex Hormones Depofemin Fat Burning Steroids 313-06-4

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Pharmaceutical Powdered Female Sex Hormones Depofemin Fat Burning Steroids 313-06-4
 
Depofemin Basic Info.:
 
Product Name: Depofemin
CAS: 313-06-4
EINECS Number: 206-237-8
Formula: C26H36O3
MW: 396.5622
Density: 1.15g / cm3
Boiling point: 532.8 °C at 760 mmHg
Flash Point: 207.7 °C
Vapor Pressure: 5.73E-12mmHg at 25 °C
Assay:99%
Specification: USP/BP
Appearance: white crystalline powder.
 
Product Description Of Depofemin:
 
Depofemin is a sex hormone that is present in both males and females, and is the most important form of estrogen in humans. In women, it plays a key role in the development and functioning of the reproductive system, as well as in the growth of certain bones. It also governs the distribution of body fat in women and is the main hormone responsible for the fact that women are shorter than men, on average. Both the ovaries and the adrenal glands produce it.
 
The menstrual cycle in women involves predictable variations in the levels of several hormones, with estradiol being one of them. It is involved in the ovulation process and prepares the inner lining of the uterus for implantation, should the egg be fertilized. Certain tests done on baboons and other primates have indicated that his hormone also plays a continual role in maintaining a pregnancy, helping it to last for the full gestation period.
 
As a sex hormone, it also triggers many of the developments of the reproductive system that begin in puberty. It is present throughout the reproductive years, and declines during and after menopause. This decline is precisely what causes many of the symptoms of menopause, such as hot flashes and night sweats, vaginal dryness, and the loss of bone mass that may lead to osteoporosis.
 

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Pharmaceutical Raw Material Griseofulvin For Health Skin Tinea Inhibition 126-07-8

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Pharmaceutical Raw Material Griseofulvin For Health Skin Tinea Inhibition 126-07-8 
 
Griseofulvin Basic Info.:
 
Product Name: Griseofulvin
Synonyms: (+)-GRISEOFULVIN;GRISEOFULVIN;
CAS: 126-07-8 
MF: C17H17ClO6 
MW: 352.77 
EINECS: 204-767-4 
Chemical Properties: Crystalline Solid 
 
(+)-Griseofulvin Usage:
 
1.Adrenegic blocker, Ca channel blocker, coronary vasodilator, antiarrhythmic. 
2.Antifungal, inhibits mitosis in metaphase.
3.Griseofulvin is a spirobenzofuran produced by a number of Penicillium species, first isolated in the 1930s by Raistrick's group. Griseofulvin is a selective antifungal agent used to treat skin infections in animals and humans. Griseofulvin acts by binding to fungal tubulin and inhibiting the mitotic spindle. Griseofulvin's ability to bind to keratin is considered an important aspect of the metabolite's access to dermatophytic fungi. More recently, griseofulvin has become an important phenotypic marker in Penicillium taxonomy. 
4.It is an antifungal drug. It is used both in animal and in humans, to treat rigworm infections of the skin and nails. It is derived from the mold Penicillium griseofulvum.
 

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Raw Pharmaceutical Powder Capecitabine For Antineoplastic Function CAS 154361-50-9

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Raw Pharmaceutical Powder Capecitabine For Antineoplastic Function CAS 154361-50-9 
 
Capecitabine Basic Info.:
 
Product name: Capecitabine
Synonym: 5-Deoxy-5-fluoro-N-[(pentyloxy)carbonyl]cytidine
Assay:99%
Molecular formula:C15H22FN3O6 
Molecular weight: 359.358
CAS number: 154361-50-9
Appearance: White or almost white crystalline powder.
Pharmacology: Capecitabine combine with Docetaxel treatment includes failure of anthracycline chemotherapy in metastatic breast cancer and the The transfer of single-agent first-line treatment of colorectal cancer
 
Capecitabine Application:
 
Capecitabine is a chemotherapy drug| that usually given to treat cancer of the colon, rectum|, breast|, stomach|, pancreas|and gullet| (oesophagus).
Capecitabine is a prodrug, that is enzymatically converted to 5-fluorouracil in the tumor, where it inhibits DNA synthesis and slows growth of tumor tissue. The activation of capecitabine follows a pathway with three enzymatic steps and two intermediary metabolites, 5'-deoxy-5-fluorocytidine (5'-DFCR) and 5'-deoxy-5-fluorouridine (5'-DFUR), to form 5-fluorouracil.
 

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Ropivacaine Hydrochloride Ropivacaine Hcl 132112-35-7 Local Anesthetic Raw Material

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Ropivacaine Hydrochloride Ropivacaine Hcl 132112-35-7 Local Anesthetic Raw Material
 
Ropivacaine HCL Basic Info.:
 
Product Name: Ropivacaine hydrochloride
Synonyms: S-ROPIVACAINE HCL;
CAS: 132112-35-7
MF: C17H26N2O.ClH.H2O
MW: 328.88
EINECS: N/A
Product Categories: Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals
use:anesthetic (local),Pharmaceutical raw materials
Packing:Foil bag or as requirments
 
Ropivacaine HCL Description:
 
Ropivacaine is a local anaesthetic drug belonging to the amino amide group. The name ropivacaine refers to both the racemate and the marketed S-enantiomer. 
 
Ropivacaine is an anesthetic (numbing medicine) that blocks the nerve impulses that send pain signals to your brain. 
Ropivacaine is used as a local (in only one area) anesthesia for a spinal block, also called an epidural. The medication is used to provide anesthesia during a surgery or C-section, or to ease labor pains. 
Ropivacaine may also be used for purposes not listed in this medication guide.
 
Ropivacaine HCL Applications:
 
(1) Surgical anesthesia:Epidural anesthesia (including epidural anesthesia during cesarean section);Local infiltration anesthesia.
(2) Acute pain control:For postoperative or labor analgesia continuous epidural infusion can be used can also be intermittent medication;Local infiltration anesthesia.
 

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White Powder Male Sex Enhancement Yohimbine HCL For Sex Protein Supplements 65-19-0

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White Powder Male Sex Enhancement Yohimbine HCL For Sex Protein Supplements 65-19-0
 
Yohimbine HCL Basic Info:
 
Product Name: Yohimbine Hydrochloride
Other name: Corynine; Aphrodine
Synonyms: Corynine Hydrochloride;Aphrodine Hydrochloride;Aphrosol Hydrochloride;Yohimbe HCL;Yohimbine HCL;Yohimbine Hydrochloride
CAS: 65-19-0
MF: C21H27ClN2O3
MW: 390.9
EINECS: 200-600-4
Purity: 99%
Melting point: 288-290 °C (dec.)(lit.)
alpha: 99 º (c=1%, H2O, dry subst)
refractive index: 103 ° (C=1, H2O)
storage temp.: Refrigerator
solubility: H2O: 10 mg/mL
Chemical Properties: white to slightly yellow powder
Usage: 
(1)Indole alkaloid with α2-adrenergic blocking activity. Mydriatic. Used in the treatment of neurological disorders.
(2)alpha adrenergic blocker, mydriatic, antidepressant
(3)vasodilator, neuromodulator
(4)a2-adrenergic antagonist, used for erectile dysfunction
(5)Erectile dysfunction & Mydriatic agent
Product Categories: Alkaloids;Biochemistry;Indole Alkaloids;Natural Plant Extract;Adrenoceptor;Adrenoceptors;Chiral Reagents;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;API;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;ADENYL;Inhibitors.
 
Yohimbine HCL Description:
 
Yohimbine has been shown in human studies to be effective in the treatment of male impotence. Yohimbine has been shown to be effective in the treatment of orgasmic dysfunction in men. Yohimbine has also been used to treat hypoactive sexual desire disorder (reduced libido) in women. Increase muscular tension or urinary function no damage sex; Accelerate human body energy metabolism, increase energy supply.
 
Yohimbine has been used to facilitate recall of traumatic memories in the treatment of post traumatic stress disorder (PTSD). Use of yohimbine outside therapeutic settings may not be appropriate for persons suffering from PTSD. In pharmacology, yohimbine is used as a probe for α 2-adrenoceptor. In veterinary medicine, yohimbine is used to reverse anesthesia from the drug xylazine in small and large animals.
 
Yohimbine HCL Application:
 
Yohimbine readily penetrates the and produces a complex pattern of responses in lower doses than those required to produce peripheral alpha-adrenergic blockade. These include, anti-diuresis, a general picture of central excitation including elevation of blood pressure and heart rate, increased motor activity, nervousness, irritability and tremor. Sweating, nausea and vomiting are common after parenteral administration of the drug. Also, dizziness, headache skin flushing reported when used orally.
 
Generally, this drug is not proposed for use in females and certainly must not be used during pregnancy. Neither is this drug proposed for use in pediatric, geriatric or cardio-renal patients with gastric or duodenal ulcer history. Nor should it be used in conjunction with mood- modifying drugs such as antidepressants, or in psychiatric patients in general.
 
Renal diseases and patient's sensitive to the drug. In view of the limited and inadequate information at hand, no precise tabulation can be offered of additional contraindications. It is important that your doctor check your progress at regular visits to make sure that this medicine is working properly. Use yohimbine exactly as directed by your doctor. Do not use more of it and do not use it more often than ordered. If too much is used, the risk of side effects such as fast heartbeat and high blood pressure is increased.
 

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Anabolic Steroids Raw Stenbolone Powder Methylstenbolone For Muscle Growth 5197-58-0

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Anabolic Steroids Raw Stenbolone Powder Methylstenbolone For Muscle Growth 5197-58-0
 
Methylstenbolone Basic Info.
 
Product Name: Methylstenbolone (Methyl Stenbolone)
Alias: Methylstenbolone;Methyl Stenbolone;Stenbolone;NSC 34418;NSC 65890;Stenebolone
CAS: 5197-58-0
Molecular Formula: C20H30O2
Molecular Weight: 302.455
Assay: 99.5%
Melting Point: 154-156°C
Storage temp.: Refrigerator
Packing: 1kg/foil bags
Package: foil bag or tin, or as you require
Properties: white powder
Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Steroids
Usage: pharmaceutical intermediates.Nutritional Supplement.
 
Methylstenbolone Description:
 
MethylStenbolone is a very new and potent designer steroid recently brought to the market by Antaeus labs. Several products in the past have claimed to use this compound, however independent lab testing has revealed they only contained superdrol.
 
Methylstenbolone does not convert to an estrogenic metabolite or have any affinity for the progesterone receptor, so estrogen mediated side effects should be virtually non-existent. Methylstenbolone is also one of the most toxic substances available due to its ability to resist metabolization, although anecdotal reports lead us to believe it carries less side effects than superdrol.
 
ethylstenbolone is a DHT derived prohormone that provides lean mass gains with low water retention.
Methylstenbolone provides increases in mass, size, and strength. Unlike superdrol, Methylstenbolone retains little to no water retention meaning you can bulk up without losing definition. This will provide the lookof much fuller muscles. Many people after experiencing methylstenbolone prefer it over superdrol.MethylStenbolone is a powerful and extremely potent compound that has people in the steroid literally turned upside down.
 
Methylstenbolone is being called the "new superdrol." Compared to Superdrol,Methylstenbolone is more anabolic, rapidly increasing muscle size, density and strength. 
 
Methylstenbolone Applications:
 
Methylsten is a very strong compound therefore it's best to start with a lower dosage to asses tolerance and slowly increase it into the desired range. Methylsten cycles are typically 3-4 weeks in length with 4 weeks being the most common. Due to the extreme potency and toxicity of this compound use for longer than 4 weeks is not recommended. Below are two common dosing protocols:
Methylsten dosing for new users:  Week1:  4-8mg / per day | Week 2-3: 8mg / per day
Methylsten dosing for experienced users:  Week1: 8mg / per day | Week 2-3: 12mg / per day | Week 4: 16mg / per day
Methylsten works relatively quickly, therefore the majority of users typically begin to experience the effects within the first week. 
 

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Androgenic Steroid Intermediate Methoxydienone Max LMG Raw Hormone Powder 2322-77-2

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Androgenic Steroid Intermediate Methoxydienone Max LMG Raw Hormone Powder 2322-77-2 
 
Methoxydienone Basic Info.:
 
Product Name: Methoxydienone
CAS: 2322-77-2 
MF: C20H28O2 
MW: 300.44
EINECS: 219-034-4 
Assay: 90% min.
Packing: 1kg net/foil bag or 10kg net/tin.
Delivery: Express courier.
Character: White crystalline powder. 
Melting point: 150-160°C
Usage: 18-levonorgestrel,.Max LMG is a progestin derived steroid and not a 17-alpha alkylated steroid. Max LMG is structurally related to RU-486 and acts as an antiprogesterone, decreasing estrogen-like effects.
 
Methoxydienone Descriptions:
 
Methoxydienone particular to a process of synthesis of levonorgestrel, Levonorgestrel is a quick, short-term oral contraceptives, contraceptive mechanism is significantly inhibit ovulation and prevent embryo 
implantation, and to increase the consistency of the cervical mucus, sperm penetration resistance increases, and thus play a fast-acting contraception.
 
Max LMG is a progestin derived steroid and not a 17-alpha alkylated steroid. Max LMG is structurally related to RU-486 and acts as an antiprogesterone, decreasing estrogen-like effects.
 
Max LMG can cause rapid "wet" gains due to its progestogenic nature. Great for those needing fast weight gain and unconcerned about looking smooth or fat.
 
Methoxydienone Applications:
 
Methoxydienone is used for promoting the synthesis of protein and reduce the decomposition of amino acid, and for improving muscle hyperplasia, action and enhance male sexual characteristics.
 
Methoxydienone is often used in the medical practice activities chronic wasting disease.Max LMG is an excellent non methylated prohormone that provides muscle hardening and increased muscle mass.
 
Max LMG is progestin designed to give solid gains in muscle mass with low water retention. The progestational activity of methoxygonadiene (once it is converted to its active metabolites) is considered to be slightly stronger than nandrolone.
 

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Anti Aging Estrogen Steroids Tibolone Livial For Female Hormones Medicines 5630-53-5

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Anti Aging Estrogen Steroids Tibolone Livial For Female Hormones Medicines 5630-53-5
 
Tibolone Basic Info.
 
Product name: Tibolone
Alias: Liviella; Livial; Tibolone
CAS: 5630-53-5
MF: C21H28O2
MW: 312.45
EINECS: 227-069-1
Assay: 99% min.
Appearance: White or off-white crystal powder
Grade: Pharmaceutical Grade
Storage: Shading, confined preservation
Usage: It is a synthetic hormone-type drug which is used mainly for hormone replacement therapy in post-menopausal women.
 
Tibolone Description:
 
Tibolone (Livial/Liviella) is used mainly for treatment of endometriosis, as well as hormone replacement therapy in post-menopausal women. Tibolone is a synthetic steroid hormone drug, which is fairly non-selective in its binding profile, acting as an agonist mainly at estrogen receptors, with a preference for ER alpha. Tibolone has similar or greater efficacy compared to older hormone replacement drugs, but shares a similar side effect profile. It has also been investigated as a possible treatment for female sexual dysfunction.
 
Tibolone is a synthetic steroid hormone drug, which is fairly non-selective in its binding profile, acting as an agonist mainly at estrogen receptors, with a preference for ER alpha. It is used mainly for treatment of endometriosis,as well as hormone replacement therapy in post-menopausal women. Tibolone has similar or greater efficacy compared to older hormone replacement drugs, but shares a similar side effect profile.It has also been investigated as a possible treatment for female sexual dysfunction. 
 
Tibolone Applications:
 
Tibolone is an estrogen-like compound used for the treatment of the symptoms associated with menopausal transition (i.e., climacteric symptoms) and also for the treatment of osteoporosis.Three major metabolites of tibolone are responsible for its tissue selective mechanism of action. Conversion into 3α- and 3β-hydroxy-tibolone results in estrogenic effects in brain, vagina, and bone. The  isomer has progestrogenic and androgenic effects and does not cause estrogenic stimulation in the endometrium.A two-year longitudinal study indicates that low doses (1.25-2.5 mg) of tibolone effectively relieve climacteric symptoms and prevent loss of bone mass in early postmenopausal women.
 

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Anti-Aging Properties Thyrotropin TRH Peptide Thyroid Stimulating Hormone 24305-27-9

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Anti-Aging Properties Thyrotropin TRH Peptide Thyroid Stimulating Hormone 24305-27-9
 
Thyrotropin TRH Quick Details:
 
Product Name: Thyrotropin TRH
TRH (Thyrotropin Releasing Hormone) (Protirelin Acetate)
Synonyms:TRH;TRF;TRH,HUMAN;
Sequence: (pyro)Glu-His-Pro-NH2
CAS: 24305-27-9
MF: C16H22N6O4
MW: 362.38
EINECS: 246-143-4
Storage temp.: −20°C
Solubility: H2O: 10 mg/mL, clear, colorless
Appearance: Lyophilized Powder
PubChem: CID 439302
Product Categories: Peptide;Thypinone.
Usage: Prothyrotropin.
 
Product Description Of Thyrotropin TRH:
 
Anti-Aging Properties of Thyrotropin Releasing Hormone TRH By DR WALTER PIERPAOLI MD 2012 THE YEAR OF THE FOUNTAIN OF YOUTH MOLECULE - TRH - DR WALER PIERPAOLI MD - SWITZERLAND AND ITALIAN RESEARCH LABS AND CLINICS .. A4M AMERICAN ACADEMY OF ANTIAGING MEDICINE Aging-Reversing Properties of Thyrotropin Releasing Hormone (TRH) Walter Pierpaoli, MD, PhD Interbion Foundation for Basic Biomedical Research (TRH Absrtact)
 
Product Application Of Thyrotropin TRH:
 
Previous work from our laboratory prompted us to study the effects of short-term, acute administration of TRH or its chronic oral administration, on organs, tissues and aging-related metabolic and hormonal markers, in order to acquire more knowledge on effects, dosage and timing of administration according to its circadian cyclicity. In addition, we wanted to verify its anti-aging effects on two most fundamental functions, namely gonadal- reproductive and kidney-urinary. The results demonstrate that both a short-term, acute or a chronic, long-term oral administration of TRH to old, aging mice, results into positive changes and rapid correction to more juvenile levels of most typical aging-related hormonal and metabolic alterations.
 
Thyrotropin TRH Function:
 
Store the kit at 4°C upon receipt.The kit should be equilibrat4ed to room temperature before the assay. Remove any unneeded strips from Human MUSK Antibody-Coated plate, reseal them in zip-lock foil and keep at 4°C.
Precipitates may appear in concentrated washing buffer. Please heat the buffer to dissolve all the precipitates, which will not affect the results.
Accurate pipette should be used to avoid experimental error. Samples should be added to the Microplate in less than 5 minutes. If a large number of samples are included, multiple channel pipette is recommended.
Standard curve should be included in every assay. Replicate wells are recommended. If the OD value of the sample is greater than the first well of standards, please dilute the sample (n times) before test. When calculating the original MUSK? concentration, please multiply the total dilution factor (XnX5).
 

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