Hormone drugs used in treating deficient hormone levels in body, thyroid problems, ovulation

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White Crystal Pharmaceutical Intermediates Hydrochloride Procaine HCL For Pain Relief 51-05-8

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White Crystal Pharmaceutical Intermediates Hydrochloride Procaine HCL For Pain Relief 51-05-8
 
Procaine HCL Basic Info.:
 
Product Name: Procaine Hydrochloride (Procaine HCL)
Synonyms: Aminocaine;Anadolor;Anesthesol;Anestil;Atoxicocaine;Bernocaine
CAS: 51-05-8
MF: C13H21ClN2O2
MW: 272.77
EINECS: 200-077-2
Melting point: 155-156 °C(lit.)
Boiling point: 195-196°C 17mm
Fp: 195-196°C/17mm
storage temp.: room temp
Water Solubility: soluble
Sensitive: Air Sensitive
Merck: 14,7757
Stability: Stable. Incompatible with strong oxidizing agents.
Chemical Properties: White crystalline powder
Product Categories: Pharmaceutical;Sodium channel;APIS;Anesthetics;Pharmaceutical intermediate
Usage: Local anesthesic;Na+ channel blocker;Procaine is a local anesthetic of the amino ester group that is primarily used as a topical anesthetic. Procaine is also used to control the pain of intramuscular injection of penicillin as well as in dentistry;Non Caine local anesthetic.
 
Procaine HCL Product description: 
 
Procaine HCl is a local anesthetic drug of the amino ester group. It is used primarily to reduce the pain of intramuscular injection of penicillin, and it is also used in dentistry. It acts mainly by being a sodium channel blocker. Today it is used therapeutically in some countries due to its sympatholytic, anti-inflammatory, perfusion enhancing, and mood enhancing effects.
 
Procaine HCl is indicated for the production of local or regional analgesia and anesthesia by local infiltration and peripheral nerve block techniques.
 
The routes of administration and concentrations are: For local infiltration use 0.25% to 0.5% (via dilution) and for peripheral nerve blocks use 0.5% (via dilution), 1%, and 2%. (See DOSAGE AND ADMINISTRATION for additional information. )
 
Procaine HCL Application:
 
Procaine HCl is a local anesthetic drug of the amino ester group. It is used primarily to reduce the pain of intramuscular injection of penicillin, and it is also used in dentistry. Owing to the ubiquity of the trade name Novocain, in some regions procaine is referred to generically . It acts mainly by being a sodium channel blocker. Today it is used therapeutically in some countries due to its sympatholytic, anti-inflammatory, perfusion enhancing, and mood enhancing effects.
 
Procaine HCl is indicated for the production of local or regional analgesia and anesthesia by local infiltration and peripheral nerve block techniques.
 
Application of procaine leads to the depression of neuronal activity. The depression causes the nervous system to become hypersensitive producing restlessness and shaking, leading to minor to severe convulsions. Studies on animals have shown the use of procaine LED to the increase of dopamine and serotonin levels in the brain. Other issues may occur because of varying individual tolerance to procaine dosage. Nervousness and dizziness can arise from the excitation of the central nervous system, which may lead to respiratory failure if overdosed. Procaine may also induce weakening of the myocardium leading to cardiac arrest.
 
Procaine can also cause allergic reactions causing the individuals to have problems with breathing, rashes, and swelling. Allergic reactions to procaine are usually not in response to procaine itself, but to its metabolite PABA. About one in 3000 people have an atypical form of pseudocholinesterase, [citation needed] which does not hydrolyze ester anesthetics such as procaine, resulting in a prolonged period of high levels of the anesthetic in the blood and increased toxicity.
 

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Anabolic Steroid Powder Androstenolone DHEA Dehydroepiandrosterone For Muscle Strength 53-43-0

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Anabolic Steroid Powder Androstenolone DHEA Dehydroepiandrosterone For Muscle Strength 53-43-0
 
DHEA Basic Info.:
 
Product name: Dehydroepiandrosterone
Other name: DHEA; Prasterone; Androstenolone
CAS No: 53-43-0
Molecular Formula: C19H28O2
Molecular Weight: 288.43
EINECS NO.: 200-175-5
Purity: 99%
Melting point: 149-151°C
Appearance: white or yellow crystalline powder.
Specification: USP30/BP2005
Packing: as your requires
Storage: Stored and protected from light
 
DHEA Description:
 
pharmaceutical material and intermediates, Steroid hormone.
 
Anabolic effects include growth of muscle mass and strength, increased bone density and strength, and stimulation of linear growth and bone maturation.
 
Androgenic effects include maturation of the sex organs, particularly the penis and the formation of the scrotum in the fetus, and after birth (usually at puberty) a deepening of the voice, growth of the beard and axillary hair. Many of these fall into the category of male secondary sex characteristics.
 
DHEA Applications:
 
Use: for the manufacture of steriod drug intermediates, with anti-aging and protein assimilation. Main function: 1. The delay senescence, retain green vigor; 2. Enhance physical ability, improve mood and sleep, improve memory; 3. Improve sexual function, enhance sexual desire; 4. Adjust the immune system function, improve immunity, 5. Weight loss; 6. Auxiliary cure disease
 

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Bodybuilding Prohormone Healthy Anabolic Muscle Building Steroids Trendione Trenavar 4642-95-9

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Bodybuilding Prohormone Healthy Anabolic Muscle Building Steroids Trendione Trenavar 4642-95-9
 
Trenavar Basic Info.:
 
Product Name: Trenavar 
Synonyms: Trendione;Trenavar;Trendione Trenavar
CAS: 4642-95-9
Molecular Formula: C18H20O2
Molecular Weight: 365.3046
Assay: 98%min
Melting Point: 140 centigrade
Density: 1.19 g/cm3
Package: Foil bag or tin, or as you require
Appearance: Light yellow powder
Usage: Pharmaceutical Intermediates 
 
Trenavar Description :
 
This is a prohormone/designer steroid first sold by PHF/IBE. There are no known "clones" at the time of writing.
This is a prohormone to the veterinary drug and black-market bodybuilding steroid trenbolone. Unlike previous "tren" prohormones, this one actually converts in the body to trenbolone. Previous "tren" PHs converted to the structurally similar - but markedly weaker - steroid dienolone.
 
Trenavar Application:
 
This prohormone has the same three conjugated double bonds as trenbolone, and differs from it only in that this hormone has a 17-ketone, where trenbolone has a 17b-hydroxy function. In the body this ketone will be readily hydrolysed by 17b-hydroxysteroid dehydrogenase type 5 (17b-HSD5) into the active form, trenbolone.
 

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DHEA Acetate Dehydroepiandrosterone Acetate Steroid Hormone Epiandrosterone Acetate 1239-31-2

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DHEA Acetate Dehydroepiandrosterone Acetate Steroid Hormone Epiandrosterone Acetate 1239-31-2 
 
Epiandrosterone Acetate Basic Info.:
 
Product Name: Epiandrosterone Acetate
Synonyms: Isoandrosterone Acetate;Epiandrosterone Acetate;
CAS: 1239-31-2
MF: C21H32O3
MW: 332.48
Purity: 99%  
Melting point: 169-173°C
Description: White to almost white crystalline powder
Storage: shading, confined preservation.
Product Categories: Pharmaceutical Intermediates;Steroids
 
Epiandrosterone Acetate Description:
 
Dehydroepiandrosterone acetate is an important intermediate for the synthesis of various hormones, family planning supplies of steroid hormones, synthesis of methyl estradiol, estriol and so on. As for pharmaceutical intermediates, For the synthesis of steroid hormone drugs. Preparation Products Epiandrosterone acetate
 
Dehydroepiandrosterone acetate is an important intermediate for the synthesis of various hormones, family planning supplies of steroid hormones,  synthesis estradiol, estriol and so on.
 
It applies in the field of pharmaceutical raw materials and pharmaceutical intermediates for the synthesis of steroid hormone drugs. Preparation Products Epiandrosterone acetate
 
Epiandrosterone Acetate Application:
 
It applies in the field of pharmaceutical raw materials and pharmaceutical intermediates for the synthesis of steroid hormone drugs. Preparation Products Epiandrosterone Acetate.
 
Dehydroepiandrosterone acetate is an important intermediate for the synthesis of various hormones, family planning supplies of steroid hormones, testosterone, synthesis of methyl testosterone, estradiol, estriol and so on.
 

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DSIP Bodybuilding Peptides 99% USP White Powder Delta Sleep Inducing Peptide (DSIP) 62568-57-4

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DSIP Bodybuilding Peptides 99% USP White Powder Delta Sleep Inducing Peptide (DSIP) 62568-57-4
 
DISP Basic Info.:
 
Product Name: DISP
Alias: Delta Sleep Inducing Peptide
CAS: 62568-57-4
Sequence: TRP-ALA-GLY-GLY-ASP-ALA-SER-GLY-GLU
MF: C35H48N10O15
MW: 848.813620
Purity: 99%
Specification: 2mg/vial
Appearance: White Lyophilized Powder
Place of Origin: China
Standard: USP
Certification: SGS
Method of Analysis: HPLC
Storage: Lyophilized peptides although stable at room temperature for 3 months, should be stored desiccated below -18°C. Upon reconstitution of the peptide it should be stored at 4° C between 2-21 days and for future use below -18°C.
 
Description Of DISP:
 
Delta sleep-inducing peptide, abbreviated DSIP, is a neuropeptide that when infused into the mesodiencephalic ventricle of recipient rabbits induces spindle and delta EEG activity and reduced motor activities.
 
Delta sleep-inducing peptide was first discovered in 1974 by the Swiss Schoenenberger-Monnier group who isolated it from the cerebral venous blood of rabbits in an induced state of sleep. It was primarily believed to be involved in sleep regulation due to its apparent ability to induce slow-wave sleep in rabbits, but studies on the subject have been contradictory.
 
DSIP is an amphiphilic peptide of molecular weight 850 daltons with the amino acid motif: N-Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu-C
It has been found in both free and bound forms in the hypothalamus, limbic system and pituitary as well as various peripheral organs, tissues and body fluids. In the pituitary it co-localises with many peptide and non-peptide mediators such as corticotropin-like intermediate peptide (CLIP), adrenocorticotrophic hormone (ACTH), melanocyte-stimulating hormone (MSH), thyroid-stimulating hormone (TSH) and melanin concentrating hormone (MCH). It is abundant in the gut secretory cells and in the pancreas where it co-localises with glucagon.
 
In the brain its action may be mediated by NMDA receptors. In another study Delta sleep-inducing peptide stimulated Acetyltransferase activity through α1 receptors in rats.It is unknown where DSIP is synthesized.
 
Applications Of DISP:
 
Delta sleep-inducing peptide, abbreviated DSIP, is a neuropeptide that when infused into the mesodiencephalic ventricle of recipient rabbits induces spindle and delta EEG activity and reduced motor activities.
Many roles for DSIP have been suggested following research carried out using peptide analogues with a greater molecular stability and through measuring DSIP-like immunological (DSIP-LI) response by injecting DSIP antiserum and antibodies.
 

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Female Steroids Exemestane Aromasin 107868-30-4 Aromatase Inhibitor Anabolic Steroids For Women

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Female Steroids Exemestane Aromasin 107868-30-4 Aromatase Inhibitor Anabolic Steroids For Women
 
Exemestane Basic Info.:
 
Product Name: Exemestane
Chemical Name: 6-Methylenandrosta-1,4-diene-3,17-dione
CAS NO.: 107868-30-4
Molecular Formula: C20H24O2 
Molecular weight: 296.40 
Assay: 99% 
Appearance: white to almost white powder 
Standard: Enterprise Standard
Packing: 1kg/aluminum foil bag
Min. order quantity: 10g 
Payment: Western Union, Moneygram
Shipment: EMS, DHL, FeDex
Delivery: safe & timely, around 12 hours after payment.
 
Exemestane Descriptions:
 
Exemestane is an aromatase inhibitor. This means it blocks the enzyme aromatase (found in the body's muscle, skin, breast and fat), which is used to convert androgens (hormones produced by the adrenal glands) into estrogen. In the absence of estrogen, tumors dependent on this hormone for growth will shrink.
 
Note: We strongly encourage you to talk with your health care professional about your specific medical condition and treatments. The information contained in this website is meant to be helpful and educational, but is not a substitute for medical advice.
 
Applications:
 
Many breast cancers are stimulated to grow by the female sex hormones oestrogen and progesterone. These breast cancers are called hormone sensitive or hormone receptor positive and can be treated with drugs that block the effects of these hormones.
 
In women who have had their menopause, oestrogen is mainly produced by changing androgens (sex hormones produced by the adrenal glands) into oestrogens. This process is called aromatisation and happens mainly in the fatty tissues, muscle and the skin. It needs a particular enzyme called aromatase.
 

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Male Sex Hormone Androsta-3, 5-Diene-7, 17-Dione / Arimistane Powder Cortisol Inhibitor 1420-49-1

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Male Sex Hormone Androsta-3, 5-Diene-7, 17-Dione / Arimistane Powder Cortisol Inhibitor 1420-49-1
 
Androsta-3,5-Diene-7,17-Dione Basic Info.:
 
Product Name: Androsta-3,5-diene-7,17-dione
Synonyms: 3,5-Androstadiene-7,17-dione;Androsta-3,5-diene-7,17-dione;Androst-3,5-diene-7,17-dione;NSC 134910;Androst-3,5-dien-7,17-dione;Arimistane
CAS: 1420-49-1
MF: C19H24O2
MW: 0
Melting point: 167-168℃
Appearance: Pale yellow crystalline powder
 
Androsta-3, 5-Diene-7, 17-Dione Arimistane Profile:
 
Arimistane (Androsta-3,5-diene-7,17-dione) is a metabolite of 7-Keto DHEA, which does not convert into testosterone or estrogen. In fact, just like the drug Aromasin, arimistane is actually a suicide aromatase inhibitor (AI), so it will permanently bind to the aromatase enzyme and prevent any estrogen rebound. Furthermore, it has also been shown to reduce cortisol, raise LH (luteinizing hormone), and increase testosterone levels.
 
How Do You Use Androsta-3, 5-diene-7, 17-dione?
 
Before taking Androsta-3, 5-diene-7, 17-dione, make it a point to check with your doctor and discuss your medical condition and the possible side effects. People who are suffering from diabetes, psychiatric disease, heart disease, and liver and kidney problems must follow the prescribed dosage and medical guidelines to make sure that the supplement would not set off any adverse effects sooner or later.
 
The Recommended Dosage to Use:
 
The right amount of Androsta-3, 5-diene-7, 17-dione to be taken for first time users is 30 mg daily. Taking this AI in larger quantities may cause discomfort and other side effects such as muscle pain, vaginal dryness, and hot flashes. If you experience some side effects, call your doctor immediately.
 

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Pharmaceutical Intermediate Anti-Estrogen Clomiphene Citrate Steroid Hormone Powder Clomid 50-41-9

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Pharmaceutical Intermediate Anti-Estrogen Clomiphene Citrate Steroid Hormone Powder Clomid 50-41-9
Male Anti Estrogenic Clomid for Steroid Cycle Clomiphene
 
Clomid Basic Info.:
 
Product Name: Clomid (Clomiphene Citrate)
Alias: Clomid;Clomifen;Clomiphene;Clomiphene Citrate;Serophene;Pergotime;Clomphid;Clomiphene Citrate Salt.
CAS No: 50-41-9
MF: C32H36ClNO8
MW: 598.09
Einecs No: 200-035-3
Purity: 99%
Melting point: 116.5-118°C
Storage temp.: 2-8°C
Appearance: Crystalline Solid; Odourless.
Product Categories: API;Intermediates & Fine Chemicals;Pharmaceuticals;Amines;Aromatics;Peptides;CLOMID
Usage:
(1)An unducer of ovulation. A gonad-stimulating principle
(2)Synthetic estrogen agonist-antagonist. Gonad-stimulating principle.
(3)A selective estrogen receptor modulator
 
Clomid Description:
 
Clomid is a mixed estrogen agonist/antagonist (activator/blocker) which, when bound to the estrogen receptor, puts it in a somewhat different conformation (shape) than does estradiol. The estrogen receptor requires binding of an estrogen or drug at its binding site and also the binding of any of several cofactors at different sites. Without the binding of the cofactor, the estrogen receptor is inactive. Different tissues use different cofactors. Some of these cofactors are able to bind to the estrogen receptor/Clomid complex, but others are blocked due to the change in shape. The result is that in some tissues Clomid acts as an antagonist - the cofactor used in that tissue cannot bind and so the receptor remains inactive - and in others Clomid acts as an agonist (activator), because the cofactors used in that tissue are able to bind. 
 
Clomid Applications:
 
Steroids Hormone Clomiphene Citrate/Clomid powders/CAS No: 50-41-9
Clomid is the anti-estrogen of choice for improving recovery of natural testosterone production after a cycle, improving testosterone production of endurance athletes, and is also effective in reducing risk of gynecomastia during a cycle employing aromatizable steroids. 
 

 

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GMP Standard Active Pharmaceutical Ingredient Bupivacaine HCl /Bupivacaine Hydrochloride 14252-80-3

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GMP Standard Active Pharmaceutical Ingredient Bupivacaine HCl /Bupivacaine Hydrochloride 14252-80-3
 
Bupivacaine HCL Basic Info.
 
Product Name: Bupivacaine Hydrochloride
Synonyms: Bupivacaine hydrochloride; Bupivocoine HCl; Sensorcaine;
CAS No.: 14252-80-3
EINECS No.: Bupivacaine Hydrochloride 
Molecular formula: C18H28N2O.ClH
Hydrochloride Molecular weight: 324.89
Hydrochloride Appearance: White crystalline powder
Hydrochloride Content: 99%Bupivacaine Hydrochloride Packing: 1KGS/Bag; 25KGS/DrumBupivacaine Hydrochloride Grade: Pharmaceutical gradeBupivacaine Hydrochloride Category: Pharmaceutical raw material
 
Bupivacaine HCL Description:
 
Anesthesia, local- Proparacaine and tetracaine are indicated to produce local anesthesia of short duration for ophthalmic procedures including measurement of intraocular pressure, removal of foreign bodies and sutures, and conjunctival and corneal scraping in diagnosis and gonioscopy.
 
Bupivacaine HCL Applications:
 
Proparacaine hydrochloride and tetracaine are also indicated to produce local anesthesia prior to surgical procedures such as cataract extraction and pterygium excision, usually as an adjunct to locally injected anesthetics.
Ophthalmic solutions used for intraocular procedures should be preservative-free. Preservatives may cause damage to the corneal epithelium if a significant quantity of solutionenters the eye through the incision.
 

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Hormone Raw Powders Anabolic Pharmaceutical Intermediates Epiandrosterone For Bodybuilding 481-29-8

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Hormone Raw Powders Anabolic Pharmaceutical Intermediates Epiandrosterone For Bodybuilding 481-29-8
 
Epiandrosterone Basic Info.:
 
Product Name: Epiandrosterone
Synonyms: Trans-Androsterone;3beta-Androsterone;3-Epiandrosterone;3-Hydroxyandrostan-17-one;
CAS No.: 481-29-8
MF: C19H30O2
MW: 290.44
EINECS: 207-563-3
Purity: ≥ 99%
Melting point: 172-174 °C
Loss on drying: 0.23%
Alpha: 91°(c=1, CH3OH)
Storage temp.: Refrigerator
Water Solubility: practically insoluble
Appearance: White to off-white crystalline powder
Packaged by: 25kg/drum
Product Categories: Pharmaceutical Intermediates;Steroids;17-Ketosteroids;Biochemistry;Hydroxyketosteroids;Intermediates & Fine Chemicals;Pharmaceuticals;API;Inhibitors
Usage: For the steroid hormone drugs.
 
Epiandrosterone Description:
 
Epiandrosterone, or 3β-androsterone, also known as 3β-hydroxy-5α-androstan-17-one or 5α-androstan-3β-ol-17-one, is a steroid hormone with weak androgenic activity. It is a natural metabolite of dehydroepiandrosterone (DHEA) via the 5α-reductase enzyme. It was first isolated in 1931, by Adolf Friedrich Johann Butenandt and Kurt Tscherning.
 
They distilled over 17,000 litres of male urine, from which they got 50 milligrams of crystalline androsterone (most likely mixed isomers), which was sufficient to find that the chemical formula was very similar to estrone.
 
Epiandrosterone Applications:
 
Typical dosage is in the range of 300-400 mg/day, though some users may dose higher than this. This is best used in 4-6 week cycles. Although Epiandrosterone does not cause severe shut down of testosterone production like many other prohormones, it is still a good idea too use a mild over the counter post-cycle therapy. An over the counter anti-estrogen/test booster will do just fine for recovery from an epiandrosterone cycle.
 
As mentioned earlier, epiandrosterone and its 3-alpha isomer androsterone are completely legal and available over the counter. LG Sciences MMv3 uses the 3-alpha isomer of this compound because it is better for the special sublingual delivery system that this product utilizes. By placing a tablet under the tongue, the compound is absorbed directly through the tissues in that area and into the blood stream.
 

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