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

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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.
 

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Pharmaceutical Intermediate Powder Peptide Lanreotide For Acromegaly 108736-35-2

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Pharmaceutical Intermediate Powder Peptide Lanreotide For Acromegaly 108736-35-2 
 
Lanreotide Basic Info.:
 
Product Name: Lanreotide
Synonyms: Lanreotide;Autogel;Bim-23014;Angiopeptin;Ipstyl 
CAS: 108736-35-2
MF: C54H69N11O10S2
MW: 1096.32
Storage temp.: −20°C
Chemical Properties: White to off-white lyophilised powder
Product Categories: hormones
 
Lanreotide Description:
 
Lanreotide (INN) is a medication used in the management of acromegaly and symptoms caused by neuroendocrine tumors, most notably carcinoid syndrome. It is a long-acting analogue of somatostatin, like octreotide. Its sequence is H-D-2Nal-Cys(1)-Tyr-D-Trp-Lys-Val-Cys(1)-Thr-NH2.
 
Lanreotide is used in the treatment of acromegaly, due to both pituitary and non-pituitary growth hormone-secreting tumors, and the management of symptoms caused by neuroendocrine tumors, particularly carcinoid tumors and VIPomas. In the United States and Canada, lanreotide is only indicated for the treatment of acromegaly. In the United Kingdom, it is also indicated in the treatment of thyrotrophic adenoma,a rare tumor of the pituitary gland which secretes TSH.
 
Lanreotide also shows activity against non-endocrine tumors, and, along with other somatostatin analogues, is being studied as a possible general antitumor agent.
 
Lanreotide Indications:
 
Lanreotide is used in the treatment of acromegaly, due to both pituitary and non-pituitary growth hormone-secreting tumors, and the management of symptoms caused by neuroendocrine tumors, particularly carcinoid tumors and VIPomas.  In the United States and Canada, lanreotide is only indicated for the treatment of acromegaly. In the United Kingdom, it is also indicated in the treatment of thyrotrophic adenoma, a rare tumor of the pituitary gland which secretes.
 
Lanreotide also shows activity against non-endocrine tumors, and, along with other somatostatin analogues, is being studied as a possible general antitumor agent.
 
Lanreotide ,In Dec 2014 the US FDA approved lanreotide for the treatment of patients with unresectable, well or moderately differentiated, locally advanced or metastatic gastroenteropancreatic neuroendocrine tumors (GEP-NETs).
 
Lanreotide Side Effects:
 
Lanreotide ,The main side effects of lanreotide treatment are mild to moderate pain at the injection site and gastrointestinal disturbances, such as diarrhea, nausea and vomiting. Isolated cases of gallstone formation have been associated with use of lanreotide, particularly over long periods of time.
 

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Pharmaceutical Raw Materials Hydrocortisone For Anti-Inflammatory Allergy 50-23-7

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Pharmaceutical Raw Materials Hydrocortisone For Anti-Inflammatory Allergy 50-23-7
 
Hydrocortisone Basic Info.:
 
Product Name: Hydrocortisone
CAS: 50-23-7
MF: C21H30O5
MW: 362.46
EINECS: 200-020-1
Assay: 98%
Appearance: white powder
Package: 1kg/foil bag
Grade:Medicine grade
 
Description About Hydrocortisone:
 
Suitable for contact dermatitis, lichen planus, etc. It is currently the most important supplementary glucocorticoid drugs, extensive drug effects, versatile, indispensable clinical drugs. Adrenal crisis in the rescue, anaphylactic shock, status asthmaticus critically ill played an important role. In systemic lupus erythematosus, rheumatism, autoimmune vasculitis treatment of autoimmune diseases is an important and indispensable therapy.
The advantage of this drug is its ethanol and hydrocortisone sodium succinate intravenously directly and quickly to play a role for the rescue of critically ill patients and shock therapy for certain diseases, generally do not cause peptic ulcers, purpura and spirit symptoms, but the row of potassium and sodium retention is stronger. Short-term large doses of hydrocortisone (24h infusion 2000 ~ 4000mg, once every 2 to 3 days) for some critically ill with the rescue, to receive good results, such as the rescue of septic shock, status asthmaticus , adult respiratory distress syndrome, short-term application, generally no adverse reactions.
 
Hydrocortisone Application:
 
1. Biochemical studies, adrenal cortical hormone drugs.
2. Glucocorticoids have anti-inflammatory, anti allergic, anti toxin, anti shock four role.
3. Adrenal corticoids
 
Hydrocortisone Pharmacological Action:
 
Anti-inflammatory effects: anti-inflammatory effects of hydrocortisone cortisone 1.25 times, in the pharmacological doses of infectious and non-infectious inflammation are inhibited. Hydrocortisone increases vascular tone, alleviate congestion, reducing capillary permeability, and therefore reduce the exudation, edema; by inhibition of inflammatory cells (including macrophages and leukocytes) aggregation at sites of inflammation, and inhibit phagocytosis cell function, lysosomal membrane stability, prevent complement chemical involved in inflammation and inflammatory mediators (such as prostaglandins, thromboxane, leukotriene) synthesis and release to relieve redness, swelling, heat, pain and other symptoms.
 

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Steroid Hormone Powder DHT Stanolone For Muscle Building Androstanolone 521-18-6

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Steroid Hormone Powder DHT Stanolone For Muscle Building Androstanolone 521-18-6 
 
Stanolone Basic Info.:
 
Product Name: Stanolone
Synonyms: Androstanolone;Stanolone;DHT
CAS: 521-18-6
MF: C19H30O2
MW: 290.44
EINECS: 208-307-3
Melting point: 178-183 °C
Assay: 99% min.
Storage temp.: Controlled Substance, -20°C Freezer
Chemical Properties: White Crystalline Solid
Usage: Anabolic steroid. Controlled substance
Product Categories: Steroids;Intermediates & Fine Chemicals;Pharmaceuticals;Steroid and Hormone;API
 
Stanolone Description:
 
Androstanolone binds to and activates specific nuclear receptors. This agent may be used for testosterone replacement therapy in hypogonadal men, in HIV-wasting syndrome, and in other conditions in order to increase nitrogen retention and fat-free muscle mass.
 
The main androgen which is secreted by the testes is of course testosterone. However, in most of the body, the androgenic sign is not carried through by testosterone. In these tissues inluding brain (CNS), skin, genitals - practically everything but muscle - the active androgen is actually dihydrotestosterone (DHT). 
 
Stanolone Applications:
 
Use for chronic wasting disease, osteoporosis, severe infection and trauma, burn, etc caused by the negative nitrogen balance, promote the growth of premature infants and immature, etc. The fracture is not easy to heal, hypercholesterolemia and postpartum depression can also be used.
 

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alpha-2-macroglobulin receptor-associated protein precursor (252-260) LAB GRADE 97%

Creative peptides is specialized in the process development and the manufacturing of bioactive peptides. We offer custom peptide synthesis, process development, GMP manufacturing as well as catalog products. We supply alpha-2-macroglobulin receptor-associated protein precursor (252-260).http://www.creative-peptides.com/product/alpha-macroglobulin-receptor-associated-protein-precursor-item-ta-126-6885.html

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99% Anti-Inflammatory Analgesic Naphazoline Hydrochloride Naphazoline HCl 550-99-2

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99% Anti-Inflammatory Analgesic Naphazoline Hydrochloride Naphazoline HCl 550-99-2
 
Naphazoline HCL Basic Info.:
 
Product Name: Naphazoline hydrochloride
Synonyms: 2-(1-Naphthylmethyl)-2-imidazoline hydrochloride; Naphazoline HCl; Naphthasoliumchloride; Privinehydrochloride;
CAS: 550-99-2
Molecular Formula: C14H15ClN2
Molecular Weight: 246.74
EINECS No.: 208-989-2
Assay: 99%
Melting point: 254-260 ° C
Boiling point: 440.5° C at 760 mmHg
Flashing point: 220.2° C
Solubillity in water: 170 g/L (20º C)
Sensibility: Hygroscopic
Appearance: White to off-white crystaline powder
Packing: 1kg/foil bag
Application: Sympathomimetic agent, vasoconstrictor
 
Naphazoline HCL Description:
 
Naphazoline hydrochloride is the common name for 2-(1-naphthylmethyl)-2-imidazoline hydrochloride. It is a sympathomimetic agent with marked alpha adrenergic activity. It is a vasoconstrictor with a rapid action in reducing swelling when applied to mucous membrane. It acts on alpha-receptors in the arterioles of the conjunctiva to produce constriction, resulting in decreased congestion. It is an active ingredient in several over-the-counter formulations including Clear Eyes and Naphcon eye drops.
 
Naphazoline HCL Application:
 
Naphazoline is a decongestant used to relieve redness, puffiness, and itchy/watering eyes due to colds, allergies, or eye irritations (smog, swimming, or wearing contact lenses). It is known as a sympathomimetic (alpha receptor agonist) that works in the eye to decrease congestion.
Some brands of naphazoline eye drops also contain other ingredients. Lubricants (such as glycerin, hypromellose, or polyethylene glycol 300) help protect the eyes from more irritation. Zinc sulfate, an astringent, helps reduce redness and irritation.
 

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99% Purity Hot Sale Ananbolic Steroid Hormone Powder Trenbolone Acetate 10161-34-9

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99% Purity Hot Sale Ananbolic Steroid Hormone Powder Trenbolone Acetate 10161-34-9
 
Trenbolone Acetate Basic Info.:
 
Product Name: Trenbolone Acetate
Synonym: Trenbolone Acetate; 
CAS No: 10161-34-9
Molecular formula: C20H24O
Molecular weight: 312.41
Assay: 99% min
Appearance: yellow or almost yellow crystalline powder
Place of origin: China
Quality standard: USP32
Effective Dose (Men): 200-600mgs/week
Effective Dose (Women):50-100mgs/week
Active life: 15 days
Detection Time: Up to 5 months
 
Product Description Of Trenbolone Acetate:
 
Trenbolone Acetate is an extremely powerful anabolic steroid and is considered the single greatest anabolic steroid by many performance enhancing athletes, it is much easier to maintain peaked and stable blood levels with this version.By carrying the Acetate ester, this gives Trenbolone an active half-life of approximately two days.
 
Trenbolone, whether as the acetate (Finaplix, Finajet), enanthate, or cyclohexylmethylcarbonate (Parabolan), should not be used as the sole anabolic in a steroid cycle. Mass gains are greatly limited when this is done. Instead, trenbolone should be stacked with Dianabol, Anadrol, or testosterone as the most common and highly suitable choices.
 
Application Of Trenbolone Acetate:
 
For bulking up, there may be no better steroid than Trenbolone Acetate also called Finaplix. Its anabolic effect is five times that of testosterone and it doesn't convert to estrogen, which makes it free from side effects like gynocomastia, water-retention, etc. Finaplix is not without its fair share of side effects, however. Testicular atrophy, hair loss, enlarged prostate and acne have been reported from using this drug. Finaplix will also shut down the body's natural testosterone production, which can lead to sexual dysfunction. Finaplix has a short-lived ester which means that it must be inject almost daily to maintain steady results. The good news for this is that the drug can be immediately stopped and the body can heal if adverse side effects appear.
 

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99.5% Purity USP Female Steroidal Progestin Hormone Megestrol Acetate CAS 595-33-5

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99.5% Purity USP Female Steroidal Progestin Hormone Megestrol Acetate CAS 595-33-5
 
Megestrol Acetate Basic Info.:
 
Product Name: Megestrol acetate
CAS: 595-33-5
MF: C24H32O4
MW: 384.51
EINECS: 209-864-5
mp: 214°C
refractive index: 11°(C=2, CHCl3)
Chemical Properties: Crystalline Solid
Usage:Progestogen;Progesterone receptor agonist,Orally active progestogen; formerly used in combinations as oral contraceptive,treatment of endometrial hyperplasia.
 
Megestrol Acetate Description:
 
Megestrol acetate is used mainly as an appetite stimulant in a variety of conditions and as an antineoplastic agent in the treatment of breast, endometrial, and prostate cancers.
 
When given in relatively high doses, it can substantially increase appetite in most individuals, even those with advanced cancer, and is often used to boost appetite and induce weight gain in patients with cancer or HIV/AIDS-associated cachexia. It is also used as a contraceptive in combination with an estrogen at relatively low doses.
 
Megestrol Acetate Application:
 
Megestrol acetate is used mainly as an appetite stimulant in a variety of conditions and as an antineoplastic agent in the treatment of breast, endometrial, and prostate cancers. When given in relatively high doses, it can substantially increase appetite in most individuals, even those with advanced cancer, and is often used to boost appetite and induce weight gain in patients with cancer or HIV/AIDS-associated cachexia. It is also used as a contraceptive in combination with an estrogen at relatively low doses.
In addition to its use in humans, megestrol acetate has been used extensively in veterinary medicine in the treatment of medical conditions in cats and dogs.
 
Megestrol Acetate Usage:
 
Megestrol acetate is available as 5 mg, 20 mg and 40 mg tablets and in oral suspensions of 125 mg/ml and 40 mg/ml. It is used at a dose of 5 mg in combination with an estrogen for contraception. Appetite stimulation is achieved with doses ranging from 400 mg to 800 mg a day. Doses used to treat cancer usually range from 40 mg to 320 mg.
 

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High Purity Pharmaceutical Raw Materials UDCA Powder Ursodeoxycholic Acid 128-13-2

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High Purity Pharmaceutical Raw Materials UDCA Powder Ursodeoxycholic Acid 128-13-2
 
Ursodeoxycholic Acid Basic Info.:
 
Product Name: Ursodeoxycholic Acid
EINECS: 204-879-3
CAS Registry Number: 128-13-2
Molecular Formula: C24H40O4
Molecular Weight: 392.58
Appearance: White crystalline powder
Application: For the prevention treatment of choles.
PackAge: Foil bag or drum
Production Capacity: 5000 Kilogram/Month
Purity: 99%
Storage: Sealed, light and oxygen resistant
 
Ursodeoxycholic Acid Description:
 
Ursodeoxycholic Acid is white powder,almost insoluble in water,freely soluble in alcohol.
Ursodeoxycholic acid (UDCA), also known as ursodiol, is a compound produced from bile by the action of intestinal bacteria. Since this bile acid is not produced directly by the body, it is known as a secondary bile acid.One of the functions of bile acids is to act in the intestine to help digest fats and fatsoluble vitamins from food.
Ursodeoxycholic acid has been used in pharmacology to dissolve gallstones made of cholesterol, and to treat liver disorders. It has been used for a long time in both human and veterinary medicine.
 
Ursodeoxycholic Acid Application:
 
UDCA Powder Ursodeoxycholic Acid Can increase the secretion of bile acid.
UDCA Powder Ursodeoxycholic Acid Reduce cholesterol in bile and cholesterol ester.
UDCA Powder Ursodeoxycholic Acid Is conducive to the cholesterol gradually dissolve gallstones.
UDCA Powder Ursodeoxycholic Acid Should not be used for surgical treatment of cholesterol stone, but cannot dissolve the bile pigment stone, mixing and opaque X line of stones.
 

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Muscle Building Customized Injectable Steroids Tri Tren 150mg/Ml 180mg/Ml 200mg/Ml

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Muscle Building Customized Injectable Steroids Tri Tren 150mg/Ml 180mg/Ml 200mg/Ml
 
Tri Tren Basic Info.:
 
Product Name: Tri Tren
Tritren 150mg/ml  180mg/ml  200mg/ml
Tri Tren blend 180 is a very powerful trenbolone blend , Good muscle bulk along with a hard solid vascular look will be acheived with this product.
Each ml CONTAINS:180mg
Trenbolone Acetate 60mg
Trenbolone Enanthate 60mg
Trenbolone Hexa Benzhydra Caproate 60mg
This is a potent product with extreme anabolic & andorgenic ratio. Serious quality muscle can be gained from this blend.
Trit ren 200 by IMD Pharmaceuticals is an injectable steroid which contains the hormone trenbolone in a blend of three different esters. This preparation contains 50mg/ml trenbolone acetate, 50mg/ml trenbolone hexahydrobenzylcarbonate, and 100mg/ml trenbolone enanthate. This combination of esters makes it possible to see results very early on in cycle, due to the acetate ester.
 
Tri Tren Description:
 
Created by UGL's to appease the ever-growing demands of the AAS using community, Tri-Trenabol is to Trenbolone what Sustanon is to Testosteronea combination of 3 different Tren esters combined in a single product.  New to the market, this version of Trenbolone has only been available for a few years, although each individual ester has received plenty of real-world use.        
 
Method administration: Tri-Trenabol is administered in injectable form. 
 
Drug Class: Tri-Trenabol belongs to the 19-nor family of steroids.  
 
Tri Tren Aplication: 
 
is one of the most well known, respected, and popular AAS used in BB'ing today.  This is not without good reason, as Trenbolone occupies a very unique place in the steroid world.  While most potent mass-building AAS tend to result in significant water retention, Trenbolone breaks the mold by providing the user with the best of both worlds; a steroid which not only causes substantial muscle growth, but also increases hardness, density, vascularity, and dryness at the same time. 
 
It is well known as one of the best strength enhancers available, with many strength athletes considering it an indispensable part of their program. As a recomping drug, it doesn't get any better, as Trenbolone's proven nutrient repartitioning capabilities have catapulted it to the top of the multi-billion dollar meat industry. In terms of fat loss, again, Trenbolone has no equal, ranking at the very top of the list.  As effective as Trenbolone is from a physical standpoint, its effect on the user's psyche are just as pronounced. 
 
One of the main steroids responsible for coining the term "roid rage", its ability to increase aggression/assertiveness and the alpha-male mind-set are almost unparalleled, being equaled only by Halotestin.  This steroid pairs well with nearly all AAS and can be put to good use in both the off-season and pre-contest. While many claim the drug to be unsuitable for beginners, such a broad statement is not always applicable. Still, those individuals contemplating its use should educate themselves beforehand.
 

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