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High Purity Dapoxetine / Dapoxetine Hydrochloride (119356-77-3 /129938-20-1) USP

Dapoxetine hydrochloride
 
Product Description:
CAS NO.:  119356-77-3                                                         Assay: 99% 
Molecular Formula: C21H23NO HCL                                       Molecular Weight: 341.88
Packing: 1kg/ Foil Bag
 
Appearance: This product is light yellow powder, odorless, sweet, soluble in water, alcohol. Can be made into tablets, beverages, wine, capsules and other dosage forms
 
Usage: Dapoxetine (dapoxetine) as a new fast SSRI, a short half life, a selective 5 - HT reuptake inhibitor (SSRI), for the treatment of premature ejaculation and erectile dysfunction. Dapoxetine is a selective 5 - HT reuptake inhibitor (SSRI), such drugs widely used to treat depression and related affective disorders
 
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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
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Skype:andyjake@outlook.com(Andy Xu)
 

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High Purity Dutasteride Avodart For Bodybuilding 164656-23-9

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High Purity Epinephrine Hydrogen Tartrate CAS 51-42-3 USP

Epinephrine hydrogen tartrate
 
Basic Info.
Model NO.:CAS: 51-42-3                                           Name:Epinephrine Hydrogen Tartrate
Molecular Formula:C9H13NO3.C4H6N6              MW:333.29
Assay: 98.0% min                                                      Export Markets:Global
 
Additional Info.
Packing: 20g-1kg /vacuum aluminum foil bag     Origin:China
Standard:USP                                                             HS Code:3101009010
Appearance: White or almost white crystals 
 
Application: 
Liothyronine is used to treat hypothyroidism, a condition where the thyroid gland does not produce enough thyroid hormone. It is also used to help decrease the size of enlarged thyroid glands (known as goiter). Liothyronine is also used in some medical tests to help diagnose problems with the thyroid gland. 
 
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 Purity Estrogen Raw Female Steroid Powders Ethynyl Estradiol 57-63-6

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High Purity Estrogen Raw Female Steroid Powders Ethynyl Estradiol 57-63-6
 
Ethynyl Estradiol Basic Info.:
 
Ethynyl estradiol Basic information
Product Name: Ethynyl estradiol
CAS: 57-63-6
MF: C20H24O2
MW: 296.4
EINECS: 200-342-2
Chemical Properties: Off-White to Light-Yellow Crystalline Powder
Usage: A metabolite of 17A-Ethynylestradiol
Usage: A synthetic steroid with high oral estrogenic potency
Usage estrogen, plus progestogen as oral contraceptive
Standard: USP28
 
Ethynyl Estradiol Description:
 
Ethinylestradiol is a man-made form of the naturally occurring female hormone called oestrogen.
It is prescribed to treat period (menstrual) problems, and also to help ease menopausal symptoms. It is usually prescribed alongside another female hormone called a progestogen.
 
Ethinyl estradiol also sometimes written as ethinylestradiol, ethynyl estradiol, or ethinyl? Stradiol, is a derivative of 17β -estradiol (E2), the major endogenous estrogen in humans. EE is an orally bioactive estrogen used in many formulations of combined oral contraceptive pills. It is one of the most commonly used medications for this purpose.
 
Estinyl was a preparation of EE alone that was used for the management of menopausal symptoms and female hypogonadism.
EE is released into the environment as a xenoestrogen from the urine and feces of people who take it as a medication.
 
Ethynyl Estradiol Application:
 
When estrogen is prescribed for a woman with a uterus, progestin should also be initiated to reduce the risk of endometrial cancer. A woman without a uterus does not need progestin. Use of estrogen, alone or in combination with a progestin, should be with the lowest effective dose and for the shortest duration consistent with treatment goals and risks for the individual woman. Patients should be reevaluated periodically as clinically appropriate (e.g., 3-month to 6-month intervals) to determine if treatment is still necessary. For women who have a uterus, adequate diagnostic measures, such as endometrial sampling, when indicated, should be undertaken to rule out malignancy in cases of undiagnosed persistent or recurring abnormal vaginal bleeding.
Short-term cyclic use for treatment of moderate to severe vasomotor symptoms, vulval and vaginal atrophy associated with the menopause, the lowest dose and regimen that will control symptoms should be chosen and medication should be discontinued as promptly as possible.
Attempts to discontinue or taper medication should be made at 3- to 6-month intervals. The usual dosage range is 1 to 5 mg injected every 3 to 4 weeks.
For treatment of female hypoestrogenism due to hypogonadism 1.5 to 2 mg injected at monthly intervals.
 

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High Purity Gw-501516 GW501516 For Weight Loss 317318-70-0

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High Purity Gw-501516 GW501516 For Weight Loss 317318-70-0
 
GW 501516 Basic Info:
 
Product Name: GW501516
Alias: Cardarine
CAS No.: 317318-70-0
Molecular Formula: C21H18F3NO3S2
Molecular Weight: 453.50
Purity: 99%
Grade: Pharmaceutical Grade
Appearance: White Powder
Usage: Fat loss
Dose: The recommended dosage for GW is 10-20 mg and for 8 weeks length
 
GW 501516 Description:
 
GW501516 is the name of a Glaxo Wellcome drug (the GW stands for the company and the number
is that of the product). It is also known as GW-501,516, GW1516, GSK-516).
 
GW-501516 is a selective agonist with high affinity and it is very potent. Various studies on this
PPAR receptor in lab rats indicates that it regulates the various proteins that the body uses for
energy. Rats with high fat and low metabolism were given the product and they were able to
lose weight and to increase overall energy levels.
 
GW 501516 Application:
 
GW501516 (also known as GW-501,516, GW1516, GSK-516 and on the black market as Endurobol) is a PPARδ receptor agonist that was invented in a collaboration between Ligand Pharmaceuticals and GlaxoSmithKline in the 1990s, was entered into clinical development as a drug candidate for metabolic diseases and cardiovascular diseases, and was abandoned in 2007 because animal testing showed that the drug caused cancer to develop rapidly in several organs.
 
In 2007 research was published showing that high doses of GW501516 given to mice dramatically improved their physical performance; the work was widely discussed in popular media, and led to a black market for the drug candidate and to its abuse by athletes as a doping agent. The World Anti-Doping Agency (WADA) developed a test for GW501516 and other related chemicals and added them to the prohibited list in 2009; it has issued additional warnings to athletes that GW501516 is not safe.
 
History Of GW 501516:
 
Concerns were raised prior to the 2008 Beijing Olympics that GW501516 could be used by athletes as an ergogenic performance-enhancing drug that was not currently controlled by regulations or detected by standard tests. One of the main researchers from the study on enhanced endurance consequently developed a urine test to detect the drug, and made it available to the International Olympic Committee. The World Anti-Doping Agency (WADA) developed a test for GW501516 and other related PPARδ modulators,and added such drugs to the prohibited list in 2009.
 
GW501516 has been promoted on bodybuilding and athletics websites and by 2011 had already been available for some time on the black market. In 2011 it was reported to cost $1000 for 10 g.In 2012, WADA recategorised GW501516 from a gene doping compound to a "hormone and metabolic modulator".
 

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High Purity Health Care Product Avanafil CAS 330784-47-9 USP

Avanafil
 
Product Description:
Assay: 99% min.                                                  CAS: 330784-47-9
Molecular Formula:C23H26ClN7O3             Molecular Weight:483.9506
Character: White to Off-White Cyrstalline Solid.
HS Code:3001200020
 
Usage: Used for the treatment of erectile dysfunction. A phosphodiesterase 5 inhibitor. 
 
Categories: Active Pharmaceutical Ingredients; Cnbio; Erectile Dysfunction; Inhibitors; Intermediates & Fine Chemicals; Pharmaceuticals; API's. 
  
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 Purity Male Hormone Raw Anabolic Trenbolone Steroids Mibolerone 3704-09-4

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High Purity Male Hormone Raw Anabolic Trenbolone Steroids Mibolerone 3704-09-4
 
Mibolerone Basic Info.:
 
Product Name: Mibolerone
CAS: 3704-09-4
MF: C20H30O2
MW: 302.45
EINECS: 223-046-5
Chemical Properties: White Crystalline Solid
Usage: Synthetic anabolic steroid related to testosterone. Controlled substance (anabolic steroid)
 
Mibolerone Description:
 
Mibolerone was initially as a veterinary product used to keep female dogs under control while they are in heat by shutting down the cycling of their ovaries. With proper timing, breeders are able to regulate the heat cycles of their bitches. Eventually, athletes began to utilize the product in order to boost aggression before events. It was even rumored that Mike Tyson was on Cheque Drops during the infamous ear biting incident during his bout with Holyfield. 
 
However, the late great guru Dan Duchaine discovered the application of Cheque Drops in modern bodybuilding far before that. The drops went in and out of production several times, before making a recent insurgence due to the piqued interest in the product thanks to the growing popularity of ultimate fighting circles.
 
Mibolerone Applications:
 
It is most commonly used by athletes about 30-40 minutes before their sporting event. Cheque drops are placed under the athletes tongue, and effects including aggression, strength and adrenaline rush are felt rapidly.  The drug leaves the body with in approximately four hours.
 
As well as being one of the most androgenic compounds, mibolerone is also one of the most toxic.   The most common side effect is progesterone related gynecomastia because it is a 19 nor-androgen.  
 

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High Purity Male Sex Hormones Sildenafil Mesylate For Male 131543-23-2

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High Purity Male Sex Hormones Sildenafil Mesylate For Male 131543-23-2
 
Sildenafil Mesylate Basic Info.:
 
Product Name: Sildenafil Mesylate
English name: Win 55,212-2 Mesylate
English Synonyms: Sildenafil Mesylate
CAS: 131543-23-2
MF: C28H30N2O6S
MW: 522.6126
Boiling point: 627.7 °C at 760 mmHg
Flash Point: 333.4 °C
Vapor Pressure: 1.14E-15mmHg at 25 °C
Properties:Solubility: 0.1 M HCl: 0.25 mg / mL
Appearance: White or white crystalline powder, odorless, bitter astringent taste, soluble in water and ethanol
Usage: Pharmaceutical raw materials, aphrodisiac It is medicine treatment raw material, indicated for the treatment of erectile dysfunction.
 
Sildenafil Mesylate Description:
 
Sildenafil Mesylate, same as Sildenafil is an inhibitor of type 5 -cGMP phosphodiesterase relaxing and smoothing muscle cells of the corpus cavernosum which leads to penile erection. This relaxation may be
mediated by nitric oxide via cyclic guanosine monophosphate.
 
pharmaceutical material, hormone. As a cyclic guanosine monophosphate (cGMP) specific phosphodiesterase type 5 (PDE5) selective inhibitor, penile smooth muscle relaxation allows rapid erection. Sildenafil is cheap, is the development and production of low-cost classes available kidney yang-like the perfect material for medicine and health products.
 
Sildenafil Mesylate Applications:
 
In 16 separate 4-24 week trials of men (over 18 years old) who suffered from impotence for longer than 6 months, dosages between 10-200 mgs were administered. Significant improvements in erectile function, including frequency of penetration as well as erection duration post penetration, were reported with Sildenfi* treatment compared to the placebo group.
Erections were improved in 72% of group verses 18% of the placebo group. In all cases effects were dependant upon dosage and improvement was the greatest when dosage exceeded 100 mgs. Responses were decreased by 40-60% in patients suffering from diabetes and prostatectomy, respectively. Withdrawal rates were less than 5% related to negative side effects and limited response rates
 

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High Purity Male Sex Hormones Vardenafil HCL / Levitra For Sex Enhancer Powder 224785-91-5

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High Purity Male Sex Hormones Vardenafil HCL / Levitra For Sex Enhancer Powder 224785-91-5
 
Vardenafil HCL Basic Info:
 
Product Name: 
Synonym: Fardenafil; Vardenafil hydrochloride
CAS No: 224785-91-5
MF: C23H33ClN6O4S
MW: 525.06
Purity: 99%
Melting point: 214-216°C
Half life: 4-5 hours
Appearance: White to Off-White Cyrstalline Solid, odorless, taste bitter and astringent soluble in water and alcohol.
Storage: in a cool and dry well-closed container and in ventilated area.
Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Vardenafil
Usage: A selective phsphodiesterase type 5 (PDE5) inhibitor.
 
Vardenafil HCL Description:
 
Vardenafil (INN) is a PDE5 inhibitor used for treating erectile dysfunction. Vardenafil's indications and contra-indications are the same as with other PDE5 inhibitors; it is closely related in function to sildenafil citrate (Viagra) and tadalafil (Cialis). The difference between the vardenafil molecule and sildenafil citrate is a nitrogen atom's position and the change of sildenafil's piperazine ring methyl group to an ethyl group. Tadalafil is structurally different from both sildenafil and vardenafil. Vardenafil's relatively short effective time is comparable to but somewhat longer than sildenafil's.
 
Vardenafil HCL Application:
 
Beyond its indications for erectile dysfunction, vardenafil may be effective in the treatment of premature ejaculation, where it may significantly increase the time from vaginal penetration to ejaculation.Vardenafil, as with all PDE5 inhibitors, should not be used by men taking nitrate medications, because combining them with vardenafil might provoke potentially life-threatening hypotension (low blood pressure).
 
Further, Vardenafil causing lengthening of the QT interval. Therefore it should not be taken by men taking other medications that affect the QT interval (such as amiodarone).
 

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High Purity Nootropic Powder Fasoracetam 110958-19-5

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High Purity Nootropic Powder Fasoracetam 110958-19-5
 
Fasoracetam Basic Info.:
 
Product Name: Fasoracetam
Synonyms: Fasoracetam; Aka NS-105; LAM-105
CAS: 110958-19-5
MF: C10H16N2O2
MW: 196.248
EINECS: N/A
Product Categories: Pharmaceutical Intermediates; Nootropic Drug
 
Fasoracetam description:
 
Fasoracetam is a research compound and member of the racetam family of nootropics,primarily known for their cognitive enhancing abilities. Fasoracetam is also an anxiolytic and may be able to improve mood as well. This racetam works by affecting three receptors within the brain: acetylcholine,GABA and glutamate, all of three of which are involved in the creation and retention of memories.
 
it is now a nootropic smart drug which portrays itself in one of the most powerful racetams in the nootropic universe. Made from a class of compounds called the racetams, and acting on not only acetylcholine but also GABA receptors in the brain, this has the ability of activating both cholinergic and glutamate receptors of the cerebral cortex, and is a revolutionary racetam drug due to its extremely unique mechanism of action. Fasoracetam currently also shows benefits as an anti-depressant, ADHD stimulant, and an anxiolytic, it also, as proven in laboratories across the nation, helps with the formation and retention of new memories.
 
Fasoracetam has also been observed to block the amnestic effects of scopolamine in a rat model of cholinergic dysfunction, which was noted as an increase of both ACh release in the cerebral cortex, as well as HACU enhancement in both the cerebral cortex and hippocampus. ChAT activity remained unaffected. In the same study, Fasoracetam was able to reverse baclofen-induced memory disruption, thus suggesting a blocking role at the GABAB receptor.
 

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