chemical-categories

 

Anti-Estrogens Nolvadex Steroids Powder Tamoxifen Citrate For Breast Cancer 54965-24-1

 

Tamoxifen Citrate Basic Info.:

 

Product Name: Tamoxifen Citrate

Product name: Tamoxifen Citrate

Synonym: Nolvadex

CAS Registry Number: 54965-24-1

Molecular Formula: C32H37NO8

Molecular Weight: 563.64

Assay: 99%

Packing: 1kg/bag

Appearance: White crystalline powder

 

Tamoxifen Citrate Description:

 

1.This product is most often referred to as "Nolvadex" by bodybuilders. Nolvadex is not a steroid, rather a selective estrogen blocker. While Nolvadex doesn't prevent the buildup of estrogen in the body, it does prevent it from acting on certain receptors, most notably, those located in the nipples. This has obvious benefits to bodybuilders, because this is the area in which "gyno" occurs during the use of aromatizing steroids such as testosterones.

 

2.Nolvadex (tamoxifen citrate) is very comparable to Clomid, behaves in the same manner in all tissues, and is a mixed estrogen agonist/antagonist of the same type as Clomid. The two molecules are also very similar in structure. It is not correct that Nolvadex reduces levels of estrogen: rather, it blocks estrogen from estrogen receptors and, in those tissues where it is an antagonist, causes the receptor to do nothing.

 

The belief that it reduces gains seems to stem from the fact that the scientific literature reports a slight reduction in IGF-1 (individuals using anabolic steroids were not studied though) from use of Nolvadex.

 

Thus, Dan Duchaine reported that it reduces IGF-1 and therefore reduces gains. However, if this effect exists at all,

it must be very minor, due to the excellent gains that many have made, and from the fact that no one has noticed any such thing from Clomid, which has the same activity profile.

 

The fact that Nolvadex will reduce water retention may result in the user agreeing that gains are less, since weight gain is less, thus reinforcing the bias.

 

Tamoxifen Citrate Applications:

 

Commonly known as Nolvadex or Nolva, Tamoxifen Citrate generally serves two purposes for the anabolic steroid user .Tamoxifen Citrate is one of the most commonly used medications among performance enhancers but more often than not it is used for remedy rather than solution.

 

For on cycle side-effect prevention and more commonly for post cycle therapy (PCT) needs. Regardless of the purpose at hand Nolva is generally very well-tolerated by those who use it and this includes both men and women. Women will use it at a much lower dose and many women who supplement with Nolvadex will do so for more of an actual solution rather than remedy.

 

Beyond on cycle use the most common time in-which Tamoxifen Citrate is used by performance enhancers is during the PCT period; after anabolic steroid use is complete. Nolva has been shown to greatly increase testosteronse stimulation in part by largely increasing Luteinizing release.

 

Tamoxifen Citrate is also used in medical practice to combat breast cancer.

 

 

High Purity Nootropic Powder Picamilon / Pikamilone For Cognition Enhancer 34562-97-5 

 

Pikamilone Basic Info.:

 

Product Name: Pikamilone

Synonyms: Pikamilone Hydrochloride;Nicotinoyl-Gaba;N-(3-Carboxypropyl) Nicotinamide;4-[(Pyridin-3-Ylcarbonyl)Amino]Butanoic Acid;4-(Nicotinamido)Butanoic Acid;Pikamiline;Pikamilone;

CAS: 34562-97-5

MF: C10H12N2O3

MW: 208.21

EINECS: N/A

Density: 1.245

Product Categories: Pharmaceutical Intermediates; Nootropic Drug; Heterocycles; Chemistry; API; Other APIs

Usage: anti-cancer agent; Used as a smart improve medicine

 

Picamilon Description:

What is the best way to use Picamilon powder and what Picamilon dosage should you be taking for optimal effects? This nootropic combination of GABA and Niacin offers a lot of cognitive benefits and mood enhancing effects. However, as an anxiolytic, it is often overlooked in favor of other nootropics like 

Sulbutiamine and Theanine. Picamilon is one of several Nootropic supplements that were originally developed in Russia (then called the Soviet Union) during the Cold War. This is probably why the supplement has been incredibly underused in the West for many years. Most of the studies and research were conducted and written in Russian, preventing its widespread dissemination even though Picamilon has been used since the early 1970′s. As such, it can be difficult to find usage and dosage information for this supplement online. In this article, we will tell you how to use Picamilon and what the recommended daily dose is. 

 

Picamilon Benefits:

The primary Nootropic benefits of this supplement center on mood boosting and overall brain function improvements. This includes helping to reduce feelings of stress and anxiety. In fact, many users feel that this supplement is so good at reducing these feelings that they use it on a regular basis to help relax. An improved positive outlook and attitude will also often follow. Once a person is relaxed, they will usually find themselves having improved sleep which is also more restful and deeper. As a brain booster, Picamilon benefits also include better mental energy and improved clarity and focus. It is easier to think and make decisions as well when using Picamilon supplements

 

Picamilon Function:

Picamilon is able to cross the blood-brain barrier and then is hydrolyzed into GABA and niacin. The released GABA in theory would activate GABA receptors potentially producing an anxiolytic response. The second released component, niacin acts as a strongvasodilator, which might be useful for the treatment of migraine headaches 

 

Picamilon Dosage:

The standard dosage range for Picamilon is between 50 and 300 mg per day.Of course, this may be split into several different administrations throughout the day, depending upon how it effects the user. Generally, a divided dose means one in the morning and one in the evening. Most supplements sell it in 150 mg tablets or capsules, but you can also buy it as a bulk powder to get more control over your dosages. Picamilon works best when taken on an empty stomach and the effects of this nootropic will last anywhere from two to four hours. You should always start out with the smallest effective Picamilon dose possible. Study the benefits obtained and then determine if increasing the dose is in order.

 

Stacking & Cycling Picamilon:

Many users have found that stacking and cycling their Picamilon dosages can be very effective. It is certainly very safe and it may even help to increase the effects of other Nootropic supplements like the Racetams including Aniracetam and Piracetam. There are a number of other Nootropics that have similar effects to Picamilon, but might lead to tolerance if used on a daily basis. This means that it might be helpful to include Picamilon as part of a cycle with something like, say, 

Start with the safer option (Picamilon) and use on a 3 or 4 day on and 2 day off cycle. For the days off of Picamilon, substitute with the 

 

 

Jin Yang Base Pharmaceutical Raw Materials For Treatment Sexual Disorder Jinyang Base 

 

Jin Yang Base Basic Info:

 

Product Name: Jin Yang Base

Synonyms: Jin Yang Base;Sildenafil Citrate Tablets;Jinyangjian;Jinyang Alkali;Jinyang Base

Assay: 99.5%

Packing: 1kg/foil bag

Appearance: Light yellow crystalline powder.

Solubility: slightly soluble in water and slightly soluble in ethanol, soluble in lipids, odorless.

Usage: Sexual function decline; Non-organic sexual disorder, ED patients

 

Jin Yang Base Description:

 

This ingredients belongs to phosphodiesterase type 5 of this kind of inhibitor. When sexuelle erregung, neurone of NANC and nitrogen oxide in endothelial cells synthase and catalyse L-arginine to synthetize nitrogen oxide, which activate guanosine to synthesis increase, then lead cavernous body of penis smooth muscle and artery of penis into relaxation, blood into penis sponge sinus, make penis erect.

 

Jin Yang Base Application:

 

For the treatment of erectile dysfunction (ED), the use of antidepressants, antipsychotics and anti-hypertensive drugs cause impotence, and after surgery or trauma caused by impotence are valid

 

 

Pharmaceutical Raw Materials Respiratory System Drugs Roflumilast For COPD 162401-32-3

 

Roflumilast Basic Info.:

 

Product Name: Roflumilast

Synonyms: ROFLUMILAST;3-(Cyclopropylmethoxy)-N-(3,5-dichloro-4-pyridinyl)-4-(difluoromethoxy)benzamide;B 9302-107;BY 217;BYK 20869;Daxas;Roflumilast / 3-(cyclopropylmethoxy)-N-(3,5-dichloropyridin-4-yl)-4-(difluoromethoxy)benzamide;3-(Cyclopropylmethoxy)-N-(3,5-dichloropyridin-4-yl)-4-(difluoromethoxy)benzamide 

CAS: 162401-32-3 

MF: C17H14Cl2F2N2O3 

MW: 403.21 

MP: 158°C 

Purity: 99%

Storage temp.: Refrigerator 

Chemical Properties: Crystallin Solid 

Usage: Selective phosphodiesterase 4(PDE4) inhibitor. Antiasthmatic; in treatment of chronic obstructive pulmonary disease 

Usage: API

Package: 1KG foil bag; 25Kg drum

 

Roflumilast Description:

 

Roflumilast is a phosphodiesterase-4 (PDE-4) inhibitor. Due to its selective inhibition of the PDE4 isoenzyme in lung cells, roflumilast is indicated for the management of chronic obstrtuctive pulmonary disease (COPD) exacerbations. Treatment with Roflumilast is associated with an increase in psychiatric adverse reactions, including suicide and suicidal attempts.

 

 

Anabolic Androgenic Steroid Hormone Trestolone Acetate For Male Contraception 6157-87-5

 

Trestolone Acetate Basic Info.

 

Product Name: Trestolone Acetate

Synonyms: 17β-Hydroxy-7α-methylestr-4-en-3-one acetate;3-Oxo-7α-methylestra-4-ene-17β-ol acetate;Acetic acid 3-oxo-7α-methylestra-4-ene-17β-yl ester;NSC-69948;U-15614

CAS No.: 6157-87-5

Molecular Formula: C21H30O3

Molecular Weight: 330.47

Melting Point: 447.571 °C at 760 mmHg

Flash Point: 194.228 °

Density: 1.117 g/cm3

Appearance: White powder

Usage: Pharmaceutical raw materials, bodybuilding and sex enhancement

 

Trestolone Acetate Description:

 

Chemically speaking, trestolone acetate(MENT) actually an alright looking drug. It doesn’t show much interaction with Sex Hormone Binding Globulin, which means that a good portion ought to stay unbound and active in the blood. Also, the drug is a potent binder to the androgen receptor, while showing minimal affinity for the progesterone and mineralocorticoid receptors respectively. Since it is not able to be 5a-reduced into a dihydro-version, it likely wouldn’t cause many of the side effects commonly associated with Dihydrotestosterone. This is also a likely reason that it is less apt to cause prostate enlargement, and may even be indicated for the treatment of specific prostate issues.

 

The ability of 7 alpha-methyl-19-nortestosterone acetate (MENT) to increase the weights of ventral prostate and seminal vesicles of castrated rats was four times higher than that of testosterone, while its effect on the weights of bulbocavernosus plus levator ani muscles (muscle), was 10 times that of testosterone.

 

Various forms of MENT in human pharmaceutical preparations and devices for contraception and hormone therapy, specifically MENT Ac implant and MENT transdermal gel and patch formulations, are currently under clinical investigation. MENT is absorbed transdermally up to three times the rate of testosterone - 17 methyl testosterone and 17-α methyl testosterone.

 

MENT will have application in a wide range of indications beyond androgen replacement therapy and contraception, including, without limitation, primary hypogonadism, testicular failure, ASIH, baldness, sarcopenia, loss of bone mass, muscle wasting and cachexia, BPH, prostate cancer and of course, bodybuilding and sports performance enhancement. Trestolone acetate is the chemical name of active ingredient in MENT. MENT is a registered trademark of Population Council, Inc. in the United States and/or other countries.

 

Trestolone Acetate Application:

 

MENT, as a transdermal and/or intramuscular preparation, will have application in a wide range of indications beyond androgen replacement therapy and contraception, including, without limitation, primary hypogonadism, testicular failure, ASIH, baldness, sarcopenia, loss of bone mass, muscle wasting and cachexia, BPH, prostate cancer and of course, bodybuilding and sports performance enhancement.

 

 

Anabolic Supplements Raw Steroid Powders Letrozole Femara For Breast Cancer 112809-51-5

 

Letrozole Basic Info.:

 

Product Name: Letrozole (Letrozol-e)

Alias: Letrazol-e; Letrozol-e Femara

CAS No: 112809-51-5

Molecular formula: C17H11N5

Molecular weight: 285.3

Appearance: White power

Assay: 99%

Delivery time: 5-7 days 

Minimum order: 10g

Supply ability: 500kg/month

Quality standard: USP32   

Payment:Western Union and Money Gram

Delivery:Within 24hours After Your Payment

 

Letrozole Descriptions:

 

This medication is used to treat certain types of breast cancer (such as hormone-receptor-positive breast cancer) in women after menopause. Letrozole is also used to help prevent the cancer from returning. Some breast cancers are made to grow faster by a natural hormone called estrogen. Letrozole decreases the amount of estrogen the body makes and helps to slow or reverse the growth of these breast cancers.

 

OTHER USES: This section contains uses of this drug that are not listed in the approved professional labeling for the drug but that may be prescribed by your health care professional. Use this drug for a condition that is listed in this section only if it has been so prescribed by your health care professional.

This medication may also be used to treat infertility in women.

 

Letrozole Application:

 

Femara is a non-steroidal aromatase inhibitor (lowers estrogen production) used to treat breast cancer in postmenopausal women. It is often given to women who have been taking tamoxifen (Nolvadex, Soltamox) for 5 years. Femara is available in generic form. Common side effects of Femara include hot flashes, hair loss, joint/bone/muscle pain, tiredness, unusual sweating or night sweats, nausea, diarrhea, dizziness, trouble sleeping, drowsiness, weight gain, weakness, flushing (warmth, redness, or tingly feeling), headache, constipation, numbness/tingling/weakness/stiffness in your hand or fingers, or pain in your hand that spreads to your arm, wrist, forearm, or shoulder.

 

 

Pharmaceutical Grade Treatment Of Prostate Cancer Peptide Deslorelin Acetate 57773-65-6

 

Deslorelin Basic Info.:

 

Product Name: Deslorelin

Specification: 50mg*50vials/kit

Synonyms: GLP-HIS-TRP-SER-TYR-D-TRP-LEU-ARG-PRO-NHET;Desorelin;Deslorelin; Deslorelin Acetate; Deslorelin (Human);

CAS: 57773-65-6

MF: C64H83N17O12

MW: 1282.45

Purity: 98%

Storage temp.: −20°C

Product Categories: Peptide;Hormones

Usage: Biochemical research;Clinical used in the treatment of prostate cancer.

 

Deslorelin Description:

 

Deslorelin acetate is an injectable gonadotropin releasing hormone super-agonist (GnRH agonist) also known as an LHRH agonist. It stops the production of sex hormones (and oestrogen). Deslorelin Acetate is marketed by Peptech with the brand name Ovuplant. It is currently approved for use in veterinary medicine and is used to induce ovulation in mares as part of the artificial insemination process. It is also used to stabilize high-risk pregnancies, mainly of livestock. Unlike other GnRH agonists, which are mainly used to inhibit uteinizing hormone and follicle-stimulating hormone by their ultimate downregulation of the pituitary gland, Deslorelin is primarily used for the initial flare effect upon the pituitary, and its associated surge of LH secretion.

 

Deslorelin Application:

 

Deslorelin was successfully trialed in the US and was approved for veterinary use under certain  circumstances. In Europe, it was approved for use in equine assisted reproduction. It is also being trialed in humans to study its efficacy in treatment of breast cancer in women,and in treating  precocious puberty and congenital adrenal hyperplasia in male and female children.

 

 

Pharmaceutical Raw Materials Natural Steroid Hormones Powder Methyldienedione 5173-46-6

 

Methyldienedione Basic Info.:

 

Product Name: Methyldienedione

Alias: Estra-4,9-diene-3,17-dione

CAS register number: 5173-46-6

Molecular Formula: C18H22O2

Molecular Weight: 270.37

Melting Point: 131-134°C

Assay: 98%min

Grade: Pharmaceutical Grade

Storage: Shading, confined preservation

Packing: 1kg/foil bag. 25kg/drum

Character: White crystalline powder.

Usage: A potential metabolitie of STS 557 (Dienogest). A steroid with antiglucocorticoid activity.

 

Methyldienedione Description:

 

Estra-4,9-diene-3,17-dione is a powerful pro-steroid chemically similar to the anabolic agent Trenbolone.

When in the body, estra-4,9-diene-3,17-dione completes the conversion to Trenbolone. Trenbolone is a potent anabolic steroid, which binds to specific receptors present in reproductive tissue, muscle and fat.

 

Estra Diene Dione (estra-4,9-diene-3,17-dione) is an anabolic steroid and a precursor to Estra Diene Dione. It became a controlled substance in the US on January 4, 2010, and is classified as a Schedule III anabolic steroid under the United States Controlled Substances Act. Previous to this, it was sold as a bodybuilding supplement within the United States, and often mistakenly marketed as a prohormone for trenbolone, a veterinary steroid. Prior to its scheduling, it was part of a number of supplements that were seized during FDA enforcement for selling unapproved new drugs. The actual target steroid, Estra Diene Dione has some structural similarity to trenbolone, but lacks the 11-carbon -ene bond.

 

Methyldienedione Applications:

 

1. Protection from gynomastia,

2. Increased sex drive/libido,

3. Enhanced intensity & focus,

4. Estrogen control,

5. Positive effects on strength & lean mass.

 

 

Pre-Mixed Injectable Steroids Trenbolone Enanthate, Drostanolone Enanthate TM Blend 500

 

TM Blend 500 Basic Info.:

 

Product Name: TM Blend 500

Testosterone Enanthate 125mg/ml

Trenbolone Enanthate 250mg/ml

Masteron Enanthate(Drostanolone Enanthate) 250mg/ml

 

Appearance: light yellow liquid

Delivery: 24 hours after payment; it takes about 5 or 7 working days to you

Package: foil bag or as requirement

Usage: they can be used directly. And have a much more good function.

 

TM Blend 500 Description:

 

1.Trenbolone Enanthate / Parabolan 

Chemical Name: 4,9,11-estratrien-17beta-ol-3-one Enanthate

Molecular Formula: C25H34O3

Molecular weight: 382.54

MP: 72~78°C

Standard: Enterprise Standard

Delivery: Express courier.

Appearance: pale yellow or yellow crystalline powder; 

Usage: pharmaceutical material, Steroid hormone, Anabolin. As a male hormone and anabolic hormones.

 

2.Drostanolone Enanthate 

Synonyms: Dromostanolone Enanthate

Assay: 99% min.

Molecular formula: C23H36O3 

Molecular Weight: 360

Delivery: Express courier.

Character: White crystalline powder.

Usage: pharmaceutical material, Steroid hormone, Anabolin. As a male hormone and anabolic hormones.

 

 

Weight Loss Pharma Grade Medicine 99% Purity Dxm Dextromethorphan Hydrobromide 125-69-9

 

Dextromethorphan Hydrobromide Basic Info.:

 

Product Name: Dextromethorphan Hydrobromide

Alias: Romilar

CAS No.: 125-69-9

EINECS No.: 204-750-1

MF: C18H26BrNO

MW: 352.31

Purity: 99.0%

Appearance: White or kind of white crystalline powder, soluble in water.

 

Product Description of Dextromethorphan Hydrobromide:

 

Dextromethorphan (DXM or DM) is an antitussive (cough suppressant) drug of the morphinan class with sedative and dissociative properties. It is one of the active ingredients in many over-the-counter cold and cough medicines, including generic labels and store brands, Benylin DM, Mucinex DM, Camydex-20 tablets, Robitussin, NyQuil, Dimetapp, Vicks, Coricidin, Delsym, TheraFlu, and others. Dextromethorphan has also found numerous other uses in medicine, ranging from pain relief (as either the primary analgesic, or an opioid potentiater) over psychological applications to the treatment of addiction. It is sold in syrup, tablet, spray, and lozenge forms. In its pure form, dextromethorphan occurs as a white powder.

 

Dextromethorphan Hydrobromide Applications:

 

DXM is also used recreationally. When exceeding label-specified maximum dosages, dextromethorphan acts as a dissociative hallucinogen. Its mechanism of action is via multiple effects, including actions as a nonselective serotonin reuptake inhibitor and a sigma-1 receptor agonist. The major metabolite of DXM, dextrorphan, also acts as an NMDA receptor antagonist. In high doses this produces effects similar to, yet distinct from, the dissociative states created by other dissociative anaesthetic such as ketamine and phencyclidine. As well, the metabolite 3-methoxymorphinan of dextrorphan (thus a second-level metabolite of DXM) produces local anesthetic effects in rats with potency above dextrorphan, but below that of DXM.