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98% Pharmaceutical Anabolic Weight Loss Steroids Raw Powder Halodrol-50 Turinadiol 2446-23-3

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98% Pharmaceutical Anabolic Weight Loss Steroids Raw Powder Halodrol-50 Turinadiol 2446-23-3
 
Halodrol Basic Info.:
 
Product Name: Halodrol (Turinadiol)
Chemical Name: Halodrol-50; Turinadiol; Turinabol-oral; 4-Chlorodehydromethyltestosterone; 4-Chlorodehydrone Thyltestosterone;Oral turinabol;4-ChlordehydroMethyl Testosterone
CAS Number: 2446-23-3
Molecular Formula: C20H31CLO2
Molecular Weight: 336.8960
Assay: 99.5%
Appearance: White powder
 
Halodrol Description:
 
Halodrol also known as 4-chloro-17a-methyl-androst-1,4-diene-3b,17b-diol, or HD is an excellent compound for adding lean hard muscles as well as strength gains. Halodrol is good for improved vascularity, dry gains with only a small to no amount of water retention.
 
Halodrol exhibits an extremely high anabolic to androgenic ratio translating into hard and consistent muscle gains with No aromatization. These gains are notably extremely lean and dry in nature, making this a favorite for the pre-contest athlete, or as an anabolic addition to many stacks. Mainly used to increase muscle mass most particularly in the abdomen region and will increase muscle endurance and decrease your recovery time after workouts.
 
Halodrol Application:
 
1. It is common for Halodrol users to see strength and size gains within the first 1-2 weeks.
2. Halodrol provides exactly that, lean, hard, dry gains as well as strength gains.
 

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Pharmaceutical Trenbolone Steroids Parabolan Trenbolone Enanthate For Weight Loss 10161-33-8

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Pharmaceutical Trenbolone Steroids Parabolan Trenbolone Enanthate For Weight Loss 10161-33-8
 
Trenbolone Enanthate Basic Info.
 
Product Name: Trenbolone Enanthate
Alias: Trenbolone Enanthate;Parabolan;Tren E;10161-33-8;Primobolan-depot;Primobolan-depot
CAS No.: 10161-33-8
Molecular Formula: C25H34O3
Molecular weight: 382.54
Assay: 99.02%
Appearance: pale yellow or yellow crystalline powder
Usage: Trenbolone Enanthate is only available from underground labs and was not designed for human consumption, although it is considered to be an ideal drug for bodybuilders who want to burn fat and gain muscle, although its long ester makes unwise for professional athletes who undergo testing to use.
 
Trenbolone Enanthate Description:
    
Trenbolone Enanthate also shines is in its ability to greatly preserve lean muscle tissue.When we diet, in-order to lose body fat, not weight but body fat we must be in a caloric deficit; we must burn more calories than we consume. As a result, as the body fights change with a desire to hang onto stored body fat due to its survival nature lean muscle tissue is often sacrificed in-order to meet its energy needs. As we lose more lean muscle tissue, this slows down the metabolic rate, and of course, it makes the physique look worse; Trenbolone Enanthate will prevent this. Of course, it gets even better; through its traits, Trenbolone Enanthate will provide the ultimate in visual conditioning effects.
 
Trenbolone Enanthate is a steroid that will greatly increase muscular endurance, more work can be done and you will not tire out as fast and it will also play an important role in recovery and healing.
 
Trenbolone Enanthate Applications:
 
Trenbolone is notably more potent than testosterone, and has an effect that is as much as three times as strong on a milligram for milligram basis. Likewise we can expect to see some level of androgenic side effects with use of this compound. Oily skin, aggressive behavior, acne and hair loss are therefore not uncommon during a cycle with this steroid. The androgenic nature of this drug of course makes it a very risky item for women to use, the chance for virilization symptoms extremely high with such a potent androgen.
 
Trenbolone is also much more potent than testosterone at suppressing endogenous androgen production. This makes clear the fact that estrogen is not the only culprit with negative feedback inhibition, as here there is no buildup of this hormone to report here. There is however some activity as a progestin inherent in this compound, as trenbolone is a 19-nortestosterone (nandrolone) derivative (a trait characteristic of these compounds).
 

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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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Raloxifene Hydrochloride Anti Estrogen Supplements 82640-04-8 Raloxifene HCL Anti Cancer Steroid

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Raloxifene Hydrochloride Anti Estrogen Supplements 82640-04-8 Raloxifene HCL Anti Cancer Steroid
 
Raloxifene HCL Basic Info.:
 
Product Name: Raloxifene HCL (Raloxifene Hydrochloride)
Synonyms: Raloxifene HCL;Raloxifene hydrochloride;Ly156758;Keoxifene;Keoxifene hydrochloride;Ly 139481;Akos 92138;
CAS: 82640-04-8 
MF: C28H28ClNO4S 
MW: 510.04 
Assay:99%
Standard:USP32
Chemical Properties: Light-Yellow Solid 
Usage: amino acid, nutrient. A nonsteroidal, selective estrogen receptor modulator (SERM). Antiosteoporotic. 
Packing: 1kg/foil bag or as required.
 
Raloxifene HCL Description:
 
Raloxifene hydrochloride (HCl) has the empirical formula C28H27NO4SHCl, which corresponds to a molecular weight of 510.05 g/mol. Raloxifene HCl is an off-white to pale-yellow solid that is slightly soluble in water.SERMs mimic estrogen in some tissues and have anti-estrogen activity in others. Other SERMs, such as Pfizer's lasofoxifene and Wyeth's bazedoxifene are in the later development phases.
 
Evista (Raloxifene Hydrochloride) is an estrogen agonist/antagonist, referred to as a selective estrogen receptor modulator (SERM) and belongs to the benzothiophene class of compounds. The biological actions of Raloxifene are largely mediated through binding to estrogen receptors. This binding results in activation of estrogenic pathways in some tissues (Agonism) and and the blockade of estrogenic pathways in other tissues (Antagonism).
 
Raloxifene HCL Usage:
 
Evista is specifically approved for the treatment and prevention of osteoporosis in postmenopausal women, the reduction in risk of invasive breast cancer in postmenopausal women with osteoporosis and the reduction in risk of invasive breast cancer in postmenopausal women at high risk of invasive breast cancer. Evista is supplied as a 60 mg tablet designed for oral administration. The recommended initial dose of the drug is one 60 mg tablet daily, which may be administered any time of day without regard to meals.
 

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High Quality Pharmaceutical Chemicals Melatonin Melatonine For Nutritional Supplement MLT 73-31-4

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High Quality Pharmaceutical Chemicals Melatonin Melatonine For Nutritional Supplement MLT 73-31-4
 
Melatonine Basic Info.:
 
Product Name: Melatonin (MLT)
Synonyms: MLT;Melatonin;
CAS: 73-31-4
Molecular Formula: C13H16N2O2
Molecular Weight: 232.28
EINECS: 200-797-7
Assay: 99%
Standard: USP
Packing: foil bag or tin.
Appearance: White or almost white crystalline powder.
Payment: T/T, Western Union and Money Gram
Delivery: Within 24hours After Your Payment
Express: EMS, DHL, FedEx, etc(door-to-door)
 
Melatonin (MLT) Info:
 
Mainly by the pineal gland in mammals and humans have a amine hormones. Human pineal gland is attached to the, the posterior wall of the third ventricle, beans granular size organization. Also reported mammalian retina and lacrimal gland can associate a small amount of melatonin produced; some of the cold-blooded animal's eyes, brain and skin (such as frogs) and some algae are able to synthesize melatonin.
 
Melatonin (MLT) Avail:
 
People use melatonin to adjust the body's internal clock. It is used for jet lag, for adjusting sleep-wake cycles in people whose daily work schedule changes (shift-work disorder), and for helping blind people establish a day and night cycle. Melatonin is also used for the inability to fall asleep (insomnia); delayed sleep phase syndrome (DSPS); insomnia associated with attention deficit-hyperactivity disorder (ADHD); insomnia due to certain high blood pressure medications called beta-blockers; and sleep problems in children with developmental disorders including autism, cerebral palsy, and intellectual disabilities. It is also used as a sleep aid after discontinuing the use of benzodiazepine drugs and to reduce the side effects of stopping smoking.
 

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