Buy API Intermediate from best API Intermediate Manufacturers, Suppliers

chemical-categories

Local Anesthetic Raw Materials Procaine White Crystalline Powder 59-46-1

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Local Anesthetic Raw Materials Procaine White Crystalline Powder 59-46-1
 
Procaine Basic Info.:
 
Product name: Procaine
Alias: Procaine hydrochloride; Aminocaine; Anadolor; Atoxicocaine;
CAS register number: 59-46-1
Molecular formula: C13H21ClN2O2
Molecular weight: 236.31
Appearance: White crystalline powder
 
Procaine Description:
 
Procaine hydrochloride, also called Novocain, synthetic organic compound used in medicine as a local anesthetic. It became the first and best-known substitute for cocaine in local anesthesia. Generally used in a 1 to 10 percent saline solution, procaine hydrochloride is administered by injection for infiltration (area flooding as in dental anesthesia), nerve-block, spinal, and caudal anesthesia. Unlike cocaine, procaine is not toxic, addicting, or irritating. It has been displaced somewhat by the chemically related drugs lidocaine and mepivacaine, which produce prompter, more intense anesthesia.
 
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 Usage:
 
Procaine is a kind of local anesthetics. With low toxicity but quick and safe effects, procaine is suitable for local anesthesia, applied to the eye, ear, nose, teeth and other department operation, used for infiltration anesthesia, anesthesia and closed therapy supervisor. Procaine is also used in the production of procaine penicillin.
 

Properties Suppliers
Local Anesthetics Proparacaine Hydrochloride Proparacaine HCl 5875-06-9

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Local Anesthetics Proparacaine Hydrochloride Proparacaine HCl 5875-06-9 
 
Proparacaine HCL Basic Info.
 
Product Name: Proparacaine hydrochloride 
Synonyms: Proparacaine HCl; Proparacaine Hydrochloride
CAS: 5875-06-9 
Molecular formula: C16H27ClN2O3 
Molecular Weight: 330.85 
EINECS number: 227-541-7 
Related Categories: API 
Use:anesthetic (local),Pharmaceutical raw materials
Packing:Foil bag or as requirments
 
Product Description Of Proparacaine HCL:
 
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. 
 
Proparacaine 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.
 

Properties Suppliers
Lose Stubborn Belly Fat Peptide Anabolic Peptide Cjc-1295 Without Dac 863288-34-0

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Lose Stubborn Belly Fat Peptide Anabolic Peptide Cjc-1295 Without Dac 863288-34-0
 
Basic Information For CJC-1295 Without DAC:
 
Product Name: 
Synonyms: CJC1295; CJC-1295 Acetate; CJC-1295 without DAC; CJC 1295 w/o DAC; MOD GRF 1-29; Neorelin; Modified Sermorelin
CAS: 863288-34-0
MF: C159H258N46O45
MW: 0
Density: 1.45
Molar Mass: 3368.7
Peptide purity: >98.0%
Appearance: White lyophilized powder
Related substance: Total Impurities (%) ≤ 2.0%
Acetate content: ≤ 15.0%
Bacterial Endotoxins: ≤5 IU/mg
Sequence: Tyr-d-ALA-Asp-Ala-Ile-Phe-Thr-Gln-Ser-Tyr-Arg-Lys-Val-Leu-Ala-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Leu-Ser-Arg-NH2
Source: Chemical Synthesis
Reconstitution: To follow best practice guidelines for reconstituting CJC-1295 without DAC, reconstitute in sterile, bacteriostatic, distilled water, with light sonication if necessary.
Storage for MOD GRF 1-29: Lyophilized MOD GRF 1-29 is stable at room temperature for 90 days, however it should be stored in a freezer below -8°C for any extended period of time. After reconstitution, may be stored for a maximum of 14 days in a refrigerator at 2°C - 8°C. Store vials in an upright position. Store MOD GRF-129 refrigerated between temperatures 2°C - 8°C. Keep in the outer carton in order to protect from light. For one month can be stored at room temperature.
Shelf life: One year from dispatch.
 
What is CJC-1295 without DAC and used for?
 
Modified GRF 1-29 is also known as Mod GRF 1-29, but even more commonly known as CJC-1295 without DAC. It is a protein that is 29 amino acids long and it is a GHRH analogue. CJC-1295 without DAC acts on receptors at the pituitary gland to stimulate the release of Human Growth Hormone.
 
CJC-1295 without DAC could be referred to more properly as a second generation derivative of GHRH. GHRH is modified to create what is known as Releasing Factor (GRF) 1-29, also known as Sermorelin. GRF 1-29 is then further modified to create Mod GRF 1-29 which is CJC-1295 without DAC.
 
Application & More information for CJC-1295 without DAC:
 
Releasing Hormone (GHRH), which is the endogenously secreted GHRH by the arcuate nucleus of the hypothalamus of the human body, is 44 amino acids long. It was discovered, however, that only the first 29 amino acids of the protein were equally as effective in binding to receptors on the pituitary gland as the full 44 amino acid structure. The first 29 amino acids in its protein structure were then isolated, which was then called GRF 1-29, but the problem with this derivative of GHRH was the fact that it was rapidly metabolized and cleared from the body by enzymes. Studies have reported that GRF 1-29's half-life is less than 10 minutes and as little as 5 minutes. This was obviously not enough time to ensure a maximized and sustained release of HGH from the pituitary gland, as studies have demonstrated that the full potential of an HGH pulse from the pituitary requires at least 30 minutes as evidenced by the fact that much higher HGH levels (50 times greater) were observed 15 - 30 minutes into subcutaneous administration of GHRH analogues.
 
Therefore, the solution to this was to modify GRF 1-29 by replacing various amino acids in its structure with other amino acids that would provide a greater resistance to breakdown and cleavage by enzymes. There were many modified analogues developed, and Mod GRF 1-29 (CJC-1295 without DAC) was eventually selected for use, which demonstrated the most promising effects. Mod GRF 1-29 is a modification of GRF 1-29, specifically at amino acids #2, #8, #15, and #27. The result is an extended half-life to that of at least 30 minutes.
 
Mod GRF 1-29 acts upon receptors located in the anterior pituitary gland, and signals the pituitary gland to increase Human  production and cause a release of massive quantities of Human Hormone in a pulsatile manner. The effects of Mod GRF 1-29 are very similar from what would be expected from synthetic HGH administration over the long term, although the amount of time that the released human growth hormone will remain in circulation is of a far less amount of time than synthetic Human Growth Hormone does. Therefore, multiple applications of Mod GRF 1-29 is recommended throughout the day in order to simulate Human Growth Hormone levels that remain high on a constant basis. Mod GRF 1-29 (CJC-1295 without DAC) is commonly combined with a Ghrelin mimetic (also known as a GHRP - Releasing Hexapeptide), such as GHRP-6, GHRP-2, Hexarelin, or Ipamorelin in order to initiate and amplify a greater pulse from the pituitary compared to Mod GRF 1-29 used solitarily on its own.
 

Properties Suppliers
Lose Weight Fast Fat Burning Steroids Synephrine No Side Effect 94-07-5

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Lose Weight Fast Fat Burning Steroids Synephrine No Side Effect 94-07-5
 
Synephrine Basic Info.
 
Product Name: Synephrine
Synonyms: Oxedrine;Synephrine;AKOS NCG1-0008;AURORA KA-6561
CAS: 94-07-5
MF: C9H13NO2
MW: 167.21
EINECS: 202-300-9
Assay: 99.2%
Appearance: White powder
Package: 25kg/drum
Storage:Keep away from fire and heat source, hermetically deposit, keep in shady, cool and dry condition, protect against the tide.
 
Synephrine Description:
 
Citrus aurantium extract synephrine as standard has been recommended. 4-20mg daily dose of synephrine is as bitter orange extract containing 200-600mg standard products (3-6% synephrine) typical dose.
 
Synephrine Use:
 
Synephrine is lime fruits of the main active ingredient, which can effectively prevent excess energy (heat accumulation), by the wind qi, warm the stomach stimulates the appetite and speeds up metabolism. It is also a mild fragrance expectorant agent, a neurological tranquilizers and laxative treatment of constipation. Users can expect variable effects include consumption of excess calories, reduce appetite and increase satiety, these are likely to lead to weight loss.
 

Properties Suppliers
Male Enhancement 4-Androstenedione 63-05-8 For Muscle Building

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Male Enhancement 4-Androstenedione 63-05-8 For Muscle Building
 
Androstenedione Basic Info.
 
Product Name: Androstenedione
Synonyms: 4-Androstenedione;4AD;3,17-Dioxoandrost-4-Ene;delta-(sup4)-Androsten-3,17-dione;delta(Sup4)-Androstene-3,17-dione;delta4-androsten-3,17-dione;delta-4-androstenedione;SKF 2170;skf2170;4-AD
CAS: 63-05-8
MF: C19H26O2
MW: 286.41
EINECS: 200-554-5
Purity: 98.88%
Manufacturer: Kafen
Characters: Near white crystalline powder, soluble in ethanol, insoluble in water
 
Androstenedione Applications:
 
Testo-ster-one precursor and metabolite with androgenic activity. Controlled substance (anabolic steroid); Simplified hormone drugs, from the testis or urine extracted with the role of a male hormone steroids, norethisterone, testosterone propionate in the middle body, is widely used in small rheumatoid arthritis, diuretic, and a variety of contraceptive to control infectious inflammation.
 
Androstenedione Description:
 
4-Androstenedione can be synthesized in one of two ways. The primary pathway involves conversion of 17-hydroxypregnenolone to dehydroepiandrosterone by way of 17,20-lyase, with subsequent conversion of dehydroepiandrosterone to 4-Androstenedione via the enzyme 3-β-hydroxysteroid dehydrogenase. The secondary pathway involves conversion of 17-hydroxyprogesterone, most often a precursor to cortisol, to 4-androstenedione directly by way of 17,20-lyase. Thus, 17,20-lyase is required for the synthesis of 4-androstenedione, whether immediately or one step removed.  
 
The production of adrenal 4-Androstenedione is governed by ACTH, whereas production of gonadal 4-Androstenedione is under control by gonadotropins. In premenopausal women, the adrenal glands and ovaries each produce about half of the total 4-androstenedione(about 3 mg/day). After menopause, 4-androstenedione production is about halved, due primarily to the reduction of the steroid secreted by the ovary. Nevertheless, 4-androstenedione is the principal steroid produced by the postmenopausal.
 

Properties Suppliers
Male Enhancement Raw Winstrol Powder Anabolic Steroid Hormone Stanozolol 10418-03-8

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

Male Enhancement Raw Winstrol Powder Anabolic Steroid Hormone Stanozolol 10418-03-8

Stanozolol Basic Info.

Product Name: Stanozolol (Stanazol)

Alias: Winstrol;Stromba;Stanozolol;Winny Depot;Stanazol.

CAS No: 10418-03-8

MF: C21H32N2O

MW: 328.49

Einecs No: 233-894-8

Purity: 99%

MOQ(minimum order quantity):10gram

Standard: Enterprise Standard

Appearance: White crystalline powder.

Usage: Stanazol Winstrol is the trade name for the anabolic steroid Stanazol. This is the third most popular and widely used anabolic steroid in all history and in the whole world;And is a very commonly used anabolic steroid for cutting cycles.

Stanozolol Description:

Winstrol - Stanazol  is a very commonly used anabolic steroid for cutting cycles. While many people will attempt to use Dianabol or even Anadrol for cutting cycles, Ive really never heard of anyone using Stanazol  for anything except a cutting cycle. Its a bit of a one-trick-pony in this respect. Let me repeat that: Stanazol  is a cutting drug. Not many people will argue for its use in a bulking cycle. Its certainly not a very effective compound for treating anemia (1) and thus, one could rightly assume that its role in bulking cycles is very limited. One novel use for Winstrol in any cycle (perhaps even bulking) would be to use it at a very limited dose, in order to lower SHBG. (2) One of the properties of Winstrol is its profound ability to lower SHBG much more than other steroids. A dose of .2mg/kg lowered SHBG significantly, which would in turn, raise the amount of free testosterone circulating in the body. As with 99% of steroids, however, its important to note that suppression of your natural hormonal levels will occur (though perhaps not to the extent that it will with many other steroids).(10) As with running virtually any compound, testosterone supplementation (i.e. running test in a cycle containing Winstrol) is warranted to avoid possible sexual dysfunction.

Stanozolol Applications:

Winstrol is the trade name for the anabolic steroid Stanazol . This is the third most popular and widely used anabolic steroid in all history and in the whole world. The first most popular anabolic steroid is Dianabol (Methandrostenolone), second most popular is Nandrolone Decanoate (Deca Durabolin), and the third most popular is Stanazol  In particular, Winstrol is the anabolic steroid best known for its supposed use by Canadian Olympic sprinter Ben Johnson when he was tested positive for this compound in the 1988 Seoul Summer Olympic Games. Winstrol's information was first documented, published, and released in 1959. Shortly thereafter, Winthrop Laboratories located in the United Kingdom manufactured it into a prescription drug for use, and in 1961 Sterling in the United States purchased the patent for the drug. Shortly thereafter, it was then released onto the North American market and given the brand name label of Winstrol.

 

Properties Suppliers
Male Hormone Fitness Anabolic Steroids Powder Nandrolone Undecylate / Dynabolon 862-89-5

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Male Hormone Fitness Anabolic Steroids Powder Nandrolone Undecylate / Dynabolon 862-89-5
 
Nandrolone Undecylate Basic Info.:
 
Product Name: Nandrolone Undecylate
Synonyms: Nandrolone Undecanoate; Nandrolone 17β-Undecanoate;Dynabolon
CAS: 862-89-5
MF: C29H46O3
MW: 442.68
EIENCS: 212-729-3
Assay: 99% min.
Packing: foil bag or tin.
Delivery: Express courier.
Usage: pharmaceutical material, Tibolone intermediate.
Standard: Enterprise standard
 
Nandrolone Undecylate Description: 
 
Nandrolone undecylate is an effective compound that produces quality, long-lasting muscle gains. This is because of the relatively long half-life of the drug (around 8 days). Users report mild side effects, with the biggest side effect being water retention. 
 
Nandrolone Undecylate Applications:
 
Nandrolone is most commonly found with a cypionate, laurate, decanoate or plenylpropionate ester. Briefly explained, the ester determines how much of the given hormone is released over a period of time. Longer esters such as decanoate peak slowly and can keep stable blood plasma levels up to ten days, shorter esters such as the phenylpropionate peak more rapidly but the half-live is shorter. Shorter esters usually release much more active hormone per mg than longer esters, and of course, allow the drugs effects to leave your system more quickly.
 

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

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
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.
 

Properties Suppliers
Manufacturer Terlipressin Acetate With High Quality 14636-12-5

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Manufacturer Terlipressin Acetate With High Quality 14636-12-5
 
Terlipressin Acetate Basic Info.:
 
Product Name: Terlipressin Acetate
Synonyms: Terlipressin;Terlipressin Acetate;Terilipressin;
CAS: 14636-12-5
MF: C52H74N16O15S2
MW: 1227.37
EINECS: 238-680-8
Product Categories: Amino Acid Derivatives;Peptide;hormones
Usage: Terlipressin is an analogue of vasopressin used as a vasoactive drug in the management of hypotension. Terlipressin is used norepinephrine-resistant septic shock and hepatorenal syndrome. Terlipressin is also used in the treatment of acute variceal bleeding.
 
Terlipressin Acetate Pharmacological Effects:
 
Terlipressin is a novel long-acting synthetic vasopressin reagent,its chemical name is three glycyl lysine vasopressin, it is a prodrug, itself has no activity ,in vivo  , it removes three glycyl residues in its N-terminus by aminopeptidase, and slowly "releases" the active lysine vasopressin. It is this "slow release" mechanism that makes it maintain the smooth muscle contraction up to 10 hours after a single administration, whereas the same dose of vasopressin, it can maintain its activity for 20-40 minutes. On the other hand,because of the slow digestion,  lysine vasopressin in the circulation cannot reach toxic levels, and usage of  terlipressin is safer.
Pharmacological effect of terlipressin is splanchnic vascular smooth muscle contraction, and reduction of visceral blood flow (such as reducing blood flow in the mesentery, spleen, uterus, etc.), thereby reducing portal vein blood flow,and reducing portal pressure, on the other hand it may also reduce plasma renin concentration, thereby increasing the renal blood flow in patients with hepatorenal syndrome, to improve kidney function, and increase urine output. Terlipressin is currently the only drug which is able to increase mortality in patients with esophageal varices bleeding , it is previously mainly used in clinical for the treatment of variceal bleeding, in addition,terlipressin now has also been successfully used for liver and kidney integrated syndrome and refractory shock, it is also likely to play a useful role in the cardiopulmonary resuscitation . Compared with vasopressin, it has a lasting effect, and it does not cause dangerous complications, including promoting  fibrinolysis and severe complications in the cardiovascular systems, and the use of it is simple (available intravenous injection), it is more suitable for rescue and treatment of emergent and critical  patients.
 
Terlipressin Acetate Mechanism of Action:
 
Terlipressin, a synthetic triglycyl-lysine derivative of vasopressin, is a inactive prodrug. It has pressor and antidiuretic effects. Following IV injection, lysine vasopressin are released following the enzymatic cleavage of 3 glycyl moieties.
Duration: 4-6 hr.
 

Properties Suppliers
Masteron Raw Steroid Powder Drostanolone Propionate For Muscle Building 521-12-0

Welcome to inquiry!

Email: tony@kafenbio.com

WhatsApp: +8618002259573

Skype: tony_14616

www.pharmhormone.com

 
Masteron Raw Steroid Powder Drostanolone Propionate For Muscle Building 521-12-0
 
Drostanolone Propionate Basic Info.
 
Product Name: Drostanolone Propionate 
Synonyms: Masteron; Dromostanolone Propionate 
CAS: 521-12-0 
Molecular formula: C23H36O3 
Molecular weight: 360.53 
EINECS: 208-303-1 
Assay: 99%
Packing: Foil bag or tin. 
Delivery: Express courier. 
Character: White crystalline powder. 
Min. order quantity: 100g
Payment: T/T, Western Union, Moneygram
Express: EMS, DHL, FeDex, etc(door-to-door)
Delivery : safe & timely, within 12 hours after payment
 
Drostanolone Propionate Description:
 
Masteron can be used somewhat effectively as bulking agent, providing a consistent gain of high quality muscle mass. It can also be successfully combined with other steroids for an enhanced effect. Mixing drostanolone with an injectable anabolic such as Deca-Durabolin or Equipoise can prove quite useful for example, the two providing notably enhanced muscle gain without excessive water retention. For greater mass gains, a stronger androgen such as Dianabol or an injectable testosterone would do the trick. The result here can be an extreme muscle gain, with a lower level of water retention & other estrogenic side effects than if these steroids were used alone (usually in higher doses). Masteron could of course be used during cutting phases of training as well. A cycle of this drug combined with Winstrol, Primobolan or Oxandrolone should provide great muscle retention and fat loss, during a period which can be very catabolic without steroids. It is an added benefit that none of these steroids aromatize, and therefore there is no additional worry of unwanted water and fat retention.
 
Drostanolone Propionate Applications:
 
Bodybuilders have a strong like for non-aromatizing androgens, and find Masteron very useful in a cutting phase. It is generally used for a number of weeks prior to a competition, in an effort to bring out an improved look of density and hardness to the muscles. As long as body fat percentage is low enough, considerably intensifies its anabolic effect. It can therefore be used somewhat effectively as bulking agent, providing a consistent gain of high quality muscle mass.
 
Masteron is often an ideal choice for inclusion in a steroid stack, or in some cases for use as the sole injectable for a steroid cycle.Androgens and assimilation hormonal.
 
An enanthate ester version having a half-life of probably 5 days has become available. This version of Masteron may be injected as infrequently as twice per week.
 

Properties Suppliers