api raw powder

Generic Name : Trestolone Trestolone (7α-methyl-19-nortestosterone) is a synthetic androgen developed by the Population Council as a potential 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 acetate (also called 7α-methyl-19-nortestosterone, MENT acetate) is a synthetic anabolic–androgenic steroid (AAS). Male contraception Investigational use as a potent androgen that suppresses spermatogenesis while maintaining secondary sex characteristics. Hypogonadism in men (experimental) Explored as a long-acting androgen therapy for low testosterone. Key properties Highly androgenic and anabolic Does not aromatize to estrogen Potent at low doses due to strong receptor affinity Long-lasting effects in injectable form Rapid muscle mass gain: It has a highly favorable anabolic-to-androgenic ratio, making it effective for building muscle. Increased strength: It is considered extremely powerful, surpassing the strength of natural testosterone, leading to significant strength enhancement.

Tamoxifen API (Active Pharmaceutical Ingredient) is the pure, bulk powder form of the drug Tamoxifen Citrate, a key selective estrogen receptor modulator (SERM) used mainly to treat and prevent hormone-receptor-positive breast cancers, working as an anti-estrogen by blocking estrogen's effects on cancer cells. INN / Common name: Tamoxifen citrate CAS No.: 54965-24-1 Molecular formula: C₂₈H₃₂N₂O·C₆H₈O₇ (citrate salt) Molecular weight: ~563.64 g/mol Breast cancer treatment For estrogen receptor–positive (ER+) breast cancer in pre- and postmenopausal women. Used in adjuvant therapy (after surgery) or treatment of metastatic disease. Breast cancer prevention In high-risk women, tamoxifen reduces the risk of developing breast cancer. Other estrogen-related conditions (off-label, limited) Certain gynecomastia cases in men Fertility treatments (rare off-label use in women to induce ovulation) Mechanism of action (brief) Tamoxifen blocks estrogen receptors in breast tissue, preventing estrogen from promoting tumor growth. In other tissues (bone, uterus), it may act as a partial agonist, producing estrogen-like effects. Identification IR spectroscopy: Conforms to reference spectrum UV / HPLC: Retention time matches certified reference standard Melting point: Within reference range (~140–144 °C for citrate salt) Assay (Potency) Typically 98.0–102.0% (on anhydrous basis)

Clomifene Citrate Raw API (Active Pharmaceutical Ingredient) is the pure, bulk powder form of the drug used in manufacturing fertility medicines, primarily to induce ovulation in women with ovulation issues like PCOS, working as a SERM (Selective Estrogen Receptor Modulator) by stimulating hormone release for egg growth. Usage: An essential ingredient in making ovulation-inducing medications INN / Common name: Clomifene citrate CAS No.: 50-41-9 Molecular formula: C₂₆H₂₈ClNO·C₆H₈O₇ (citrate salt) Molecular weight: ~598.08 g/mol Identification IR spectroscopy: Conforms to reference spectrum UV / HPLC: Retention time matches certified reference standard Melting point: Within reference range (~109–110 °C for citrate salt) Assay (Potency) Typically 98.0–102.0% (on anhydrous basis)

INN / Common name: Stanolone / Dihydrotestosterone (DHT) CAS No.: 521-18-6 Molecular formula: C₁₉H₃₀O₂ Molecular weight: ~290.45 g/mol Identification IR spectroscopy: Conforms to reference spectrum HPLC / UV: Retention time matches certified reference standard Melting point: Within reference range (~180–184 °C) Assay (Potency) Typically 98.0–102.0% (on anhydrous basis) Androgen Deficiency and Male Hypogonadism: Stanolone is primarily used as a hormone replacement therapy for men with low testosterone levels or other forms of androgen deficiency. Treatment of Specific Conditions in Males: It can be used to treat certain conditions related to androgen development, such as microphallus (small penis) in infancy or males, and male breast development. Muscle Wasting Diseases and Osteoporosis: Due to its potent anabolic properties, it has been explored for treating muscle wasting diseases and osteoporosis, promoting muscle growth and maintaining bone density. Aplastic Anemia: It may be used in the treatment of rare forms of aplastic anemia that are responsive to anabolic androgens.

The Exemestane Raw Active Pharmaceutical Ingredient (API) is primarily used for manufacturing medications to treat hormone-receptor-positive breast cancer in postmenopausal women. INN: Exemestane CAS No.: 107868-30-4 Molecular formula: C₂₀H₂₄O₂ Molecular weight: ~296.41 g/mol White to off-white crystalline powder Practically insoluble in water; soluble in organic solvents Assay (Potency) Typically 98.0–102.0% (on anhydrous basis)

Muscle Growth: Promotes protein synthesis, leading to significant increases in muscle size and mass. Strength Enhancement: Known for producing rapid and substantial strength gains. Athletic Performance: Used to enhance overall performance in strength sports and weight training. Fat Loss: Some users report concurrent fat reduction, possibly due to an increased metabolic rate from added muscle mass. Specifications : INN / Common name: Methasterone Other name: Superdrol CAS No.: 3381-88-2 Molecular formula: C₂₁H₃₄O₂ Molecular weight: ~318.49 g/mol Assay (Potency) Commonly 98.0% – 102.0% (on anhydrous basis), per internal specification

Generic Name : Mesterolone Mesterolone is a synthetic anabolic-androgenic steroid (AAS) and derivative of dihydrotestosterone (DHT). It is inactivated by 3α-hydroxysteroid dehydrogenase in skeleta muscules so it is considered a weak androgen. It is not a substrate for aromatase so it is not converted into estrogen. Mesterolone demonstrated to have minimal effect on sperm counts and levels of FSH or LH 1,2. Experiments of mesterolone serving as a potential treatment of depression are still undergoing. Male Hypogonadism/Androgen Deficiency: The primary medical use is to treat low testosterone levels in men due to hypogonadism (a condition where the testes produce little or no hormones). This helps restore normal sexual function, mood, and energy levels. Male Infertility: It is used to manage male infertility that stems from low androgen levels, as it can improve sperm count and quality in affected men. INN: Mesterolone CAS No.: 1424-00-6 Molecular formula: C₂₀H₃₂O₂ Molecular weight: ~304.47 g/mol Assay (Potency) Typically 98.0% – 102.0% (on anhydrous basis), depending on pharmacopeial or internal standard

Oxymetholone raw active pharmaceutical ingredient (API) is used to produce medications for various medical conditions, primarily anemias and muscle-wasting syndromes, as well as for illicit performance enhancement in sports. INN: Oxymetholone CAS No.: 434-07-1 Molecular formula: C₂₁H₃₂O₃ Molecular weight: ~332.48 g/mol White to off-white crystalline powder Practically insoluble in water; soluble in certain organic solvents USES : Bodybuilding, muscle enhancement, or performance enhancement Cosmetic or recreational use Oxymetholone binds to androgen receptors inside target cells (e.g., bone marrow, muscle). The drug–receptor complex moves into the cell nucleus. There, it binds to specific DNA sequences (androgen response elements), changing gene expression.

Stanozolol is used to treat hereditary angioedema. Stanozolol is one of the AAS commonly used as performance-enhancing drugs and is banned from use in sports competition. It is an anabolic steroid that is known to have a diuretic effect. Stanozolol has been used with some success to treat venous insufficiency. It stimulates blood fibrinolysis and has been evaluated for the treatment of the more advanced skin changes in venous disease such as lipodermatosclerosis. Several randomized trials noted improvement in the area of lipodermatosclerosis, reduced skin thickness, and possibly faster ulcer healing rates with stanozolol. It is also being studied to treat hereditary angioedema, osteoporosis, and skeletal muscle injury. Stanozolol is used for physique- and performance-enhancing purposes by competitive athletes, bodybuilders, and powerlifters. Name: Stanozolol CAS Number: 10418-03-8 Molecular Formula: C₂₁H₃₂N₂O Molecular Weight: ~328.5 g/mol Description: 17-alpha-alkylated DHT-derived anabolic steroid API Assay / Purity Assay (potency): 97.0% – 103.0% Related substances / impurities: Within specified limits Residual solvents: Compliant with ICH Q3C Heavy metals: Within pharmacopeial limits

Metandienone (also known as Methandrostenolone or Dianabol) is a synthetic anabolic–androgenic steroid (AAS) derived from testosterone. Metandienone (Dianabol) — API Specification Name: Metandienone Synonyms: Methandrostenolone, Dianabol Chemical class: Anabolic–androgenic steroid (AAS) CAS Number: 72-63-9 Molecular Formula: C₂₀H₂₈O₂ Molecular Weight: ~300.44 g/mol Description: 17-alpha-alkylated anabolic steroid API Assay / Purity Typical pharmaceutical API quality expectations: Assay (potency): 97.0% – 103.0% Related substances / impurities: Within specified limits Residual solvents: Compliant with ICH Q3C guidelines Heavy metals: Within pharmacopeial limits Metandienone enters androgen-responsive cells (e.g., skeletal muscle) It binds to the androgen receptor (AR) in the cytoplasm The hormone–receptor complex translocates into the cell nucleus It binds to androgen response elements (AREs) on DNA USES : Muscle wasting conditions Severe weight loss Osteoporosis Recovery from major illness or surgery

Name: Fluoxymesterone Chemical class: Anabolic–androgenic steroid (AAS), fluorinated testosterone derivative CAS Number: 76-43-7 Molecular Formula: C₂₀H₂₉FO₃ Molecular Weight: ~336.44 g/mol Description: 17-alpha-alkylated oral androgenic steroid API Appearance White to off-white crystalline powder Odorless or nearly odorless Practically insoluble in water Assay / Purity Typical pharmaceutical API quality expectations: Assay (potency): 97.0% – 103.0% Related substances / impurities: Within specified limits Fluoxymesterone is a synthetic anabolic–androgenic steroid (AAS) derived from testosterone, with strong androgenic activity Male hypogonadism (testosterone deficiency) Delayed puberty in males Certain androgen-responsive breast cancers in women (historical use) Palliative treatment in advanced cancers (limited, historical)

Oxandrolone is a synthetic anabolic–androgenic steroid (AAS) derived from dihydrotestosterone (DHT). The RAW API form is a pharmaceutical active ingredient Name: Oxandrolone Chemical class: Anabolic–androgenic steroid (AAS), DHT derivative CAS Number: 53-39-4 Molecular Formula: C₁₉H₃₀O₃ Molecular Weight: ~306.44 g/mol Description: 17-alpha-alkylated oral anabolic steroid API Appearance White to off-white crystalline powder Odorless or nearly odorless Practically insoluble in water Where approved by regulators, oxandrolone API has been used to manufacture prescription medicines for: Weight gain after severe weight loss due to: Surgery Chronic infection Severe trauma Catabolic states (muscle wasting) Burn injury recovery (to help preserve lean body mass) Certain genetic growth disorders Oxandrolone is prohibited in competitive sports, so the API is used as: Reference standards Calibration materials Analytical validation compounds Oxandrolone enters target cells such as skeletal muscle and bone It binds to the androgen receptor (AR) in the cytoplasm The oxandrolone–AR complex translocates into the cell nucleus .