Pharmaceutical raw materials used in synthesizing new medications

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Pharmaceutical Raw Material Hydroxypropyl Beta Cyclodextrin 128446-35-5 For Food

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Pharmaceutical Raw Material Hydroxypropyl Beta Cyclodextrin 128446-35-5 For Food
 
Hydroxypropyl Beta Cyclodextrin Basic Info.:
 
Product Name: Hydroxypropyl-Beta-Cyclodextrin
Name: (2-HYDROXYPROPYL)-BETA-CYCLODEXTRIN
CAS NO: 128446-35-5
MF: C63H112O42
MW: 1541.54
EINECS: 420-920-1
Assay: 99%
Packing: 10kg/drum
Appearance: White powder
Characteristics and Uses: The introduction of hydroxypropyl β - cyclodextrin breaking intramolecular hydrogen bond ring, while maintaining the cyclodextrin cavity while overcoming the poorly water-soluble β - cyclodextrin major drawback. Is currently the most in-depth study, the most widely used one cyclodextrin derivatives. Mainly used in food, pharmaceutical, cosmetics industries.
 
Product Description Of Hydroxypropyl Beta Cyclodextrin:
 
1, In the food, spices fields, can improve the stability and long-term nutritional molecules, can mask or correct nutritional elements of food smells and tastes bad, you can improve the production process and product quality. The product is very good solubility in water, the degree of substitution can be 4 or more miscible in any proportion with water, 50 % ethanol and methanol can also be dissolved.
2, In cosmetic raw materials used as a stabilizer, emulsifier, to taste and the like, organic molecules can be reduced in cosmetics mucosal tissue irritation on the skin, enhance the stability of active ingredients, to prevent volatilization of nutrients, oxidation. It has a certain relative hygroscopicity.
3, In the pharmaceutical industry, due to the relative surface activity and hemolytic activity is relatively low and is not irritating to muscle, so it is an ideal injection solubilizer and pharmaceutical excipients. Insoluble drugs can increase the water solubility, increased drug stability, improved bioavailability, efficacy of the pharmaceutical dosage increase or decrease, can be adjusted or controlled drug release rate, reduce drug side effects.
4. For oral drugs, injections, drug delivery systems (including nasal, rectal, cornea, etc.), transdermal drug delivery systems for targeted drug lipophilic carrier protein can be used as protective agents and stabilizers.
 

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Pharmaceutical Raw Materials Lipoic Acid For Fat-Metabolism Stimulator 1077-28-7

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Pharmaceutical Raw Materials Lipoic Acid For Fat-Metabolism Stimulator 1077-28-7
 
Lipoic Acid Basic Info.:
 
Product Name: Lipoic Acid
Purity: 99.5%
CAS: 1077-28-7
MF: C8H14O2S2
MW: 206.33
Appearance: Yellow crystalline powder,no obvious odor.
Melting point: 60.0-62.0 degree centigrade 
Drying loss: Not more than 0.2%  
Usage: Lipoic acid is a vitamin drugs, limited physical activity in its dextral, basically no physical activity in its Lipoic acid, and no side effects. It is always used for acute and chronic hepatitis, liver cirrhosis, hepatic coma, fatty liver, diabetes, Alzheimer's disease, and applies as an antioxidant health products
 
Lipoic Acid Function:
 
Lipoic acid is a vitamin drugs, limited physical activity in its dextral, basically no physical activity in its Lipoic acid, and no side effects. It is always used for acute and chronic hepatitis, liver cirrhosis, hepatic coma, fatty liver, diabetes, Alzheimer's disease, and applies as an antioxidant health products
 
Lipoic Acid Applications:
 
1.Lipoic Acid is a good antioxidant. Taken internally, it is a water  and fat soluble antioxidant that is capable of regenerating other antioxidants, such as vitamins C and E; it also can help prevent cellular damage via its antioxidant properties. 
2.Usually it  is used for diabetes, peripheral neuropathy, cardiac autonomic neuropathy, retinopathy, cataracts, and glaucoma. Alpha-lipoic acid is also used orally for dementia, chronic fatigue syndrome, HIV/AIDS, cancer, liver disease, cardiovascular disease, peripheral arterial disease, intermittent claudication, Lyme disease, and lactic acidosis caused by inborn errors of metabolism.
3.It also has anti-inflammatory effects.
4.Topically, alpha-lipoic acid is used to reduce facial wrinkles, lines, and sun damage.
but it is extremely vulnerable to degradation by sunlight, and 5% or higher alpha lipoic acid are capable of causing burning or stinging sensations or a mild rash on skin.
 

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Prohormones Steroids White Powder Misoprostol For Terminate Pregnancy 59122-46-2

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Prohormones Steroids White Powder Misoprostol For Terminate Pregnancy 59122-46-2
 
Misoprostol Basic Info.
 
Product Name: Misoprostol
Synonyms: Misoprostol;Cytotec;SC-29333
CAS: 59122-46-2
Molecular Formula: C22H38O5
Molecular Weight: 382.60
Assay: 99%
Chemical Properties: White Solid
Solubility: Soluble to 100 mM in Ethanol
Safety: Poison by ingestion, intramuscular, and intraperitoneal routes. When heated to decomposition it emits acrid smoke and irritating fumes.
Package: Aluminium foil bag packing 
Storage: Keep in cool and dry place, away from light
 
Misoprostol Description:
 
Misoprostol is a medication used to start labor, induce abortions, prevent and treat stomach ulcers, and treat postpartum bleeding due to insufficient contraction of the uterus. For abortions it is used with mifepristone or methotrexate. It is a synthetic prostaglandin E1 (PGE1).
 
Common side effects include diarrhea and abdominal pain. It is pregnancy category X meaning that it is known to result in negative fetal outcomes if taken during pregnancy. Uterine rupture may occur.
 
It is on the World Health Organization's List of Essential Medicines, the most important medications needed in a basic health system. Misoprostol was invented and marketed by G.D. Searle & Company under the trade name Cytotec, but other trade names and generic formulations are available.
 
Misoprostol Usage
 
Misoprostol is approved for use in the prevention of NSAID-induced gastric ulcers. It acts upon gastric parietal cells, inhibiting the secretion of gastric acid by G-protein coupled receptor-mediated inhibition of adenylate cyclase, which leads to decreased intracellular cyclic AMP levels and decreased proton pump activity at the apical surface of the parietal cell. Because other classes of drugs, especially H2-receptor antagonists and proton pump inhibitors, are more effective for the treatment of acute peptic ulcers, misoprostol is only indicated for use by people who are both taking NSAIDs and are at high risk for NSAID-induced ulcers, including the elderly and people with ulcer complications. Misoprostol is sometimes coprescribed with NSAIDs to prevent their common adverse effect of gastric ulceration (e.g. with diclofenac in Arthrotec).
 
Misoprostol has other protective actions, but is only clinically effective at doses high enough to reduce gastric acid secretion. For instance, at lower doses, misoprostol may stimulate increased secretion of the protective mucus that lines the gastrointestinal tract and increase mucosal blood flow, thereby increasing mucosal integrity. However, these effects are not pronounced enough to warrant prescription of misoprostol at doses lower than those needed to achieve gastric acid suppression.
However, even in the treatment of NSAID-induced ulcers, omeprazole proved to be at least as effective as misoprostol,but was significantly better tolerated, so misoprostol should not be considered a first-line treatment. Misoprostol-induced diarrhea and the need for multiple daily doses (typically four) are the main issues impairing compliance with therapy.
 
The most commonly reported adverse effect of taking a misoprostol orally for the prevention of stomach ulcers is diarrhea. In clinical trials, an average 13% of patients reported diarrhea, which was dose-related and usually developed early in the course of therapy (after 13 days) and was usually self-limiting (often resolving within 8 days), but sometimes (in 2% of patients) required discontinuation of misoprostol.
 
The next most commonly reported adverse effects of taking misoprostol orally for the prevention of gastric ulcers are: abdominal pain, nausea, flatulence, headache, dyspepsia, vomiting, and constipation, but none of these adverse effects occurred significantly more often than when taking placebos. In practice, fever is almost universal when multiple doses are given every 4 to 6 hours.
 
Misoprostol should not be taken by pregnant women to reduce the risk of NSAID-induced gastric ulcers because it increases uterine tone and contractions in pregnancy, which may cause partial or complete abortions, and because its use in pregnancy has been associated with birth defects.
 

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Tau Peptide (255-314) (Repeat 2 Domain) (human)Tau Peptide (268-282) LAB GRADE 98%

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Tetramisole Hydrochloride Pharmaceutical Raw Materials Tetramisole HCL 5086-74-8

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Tetramisole Hydrochloride Pharmaceutical Raw Materials Tetramisole HCL 5086-74-8
 
Tetramisole HCL Basic Info.:
 
Product Name: Tetramisole Hydrochloride
Other names: (+-)-2,3,5,6-tetrahydro-6-phenylimidazo(2,1-b)thiazolemonohydrochloride; (+-)-anthelvet;1-b)thiazole,2,3,5,6-tetrahydro-6-phenyl-,monohydrochloride,(+-)-imidazo(;anthelvet;bayer9051;citarin;dl-6-phenyl-2,3,5,6-tetrahydroimidazole(2,1-b)thiazole-hydrochloride;dl-tetramisolehydrochloride
CAS NO.: 5086-74-8
EINECS: 225-799-5
M.F.: C11H12N2S.HCl
M.W.: 240.7523
Assay:98%
Packing: 25kg/drum
Appearance: White to white crystalline powder or needle crystal
Usage: A muscarinic receptor antagonist. Used in the treatment of urinary incontinence.
 
Product Description of Tetramisole HCL:
 
Tetramisole was originally used as an anthelminthic to treat worm infestations in both humans and animals. Most current commercial preparations are intended for veterinary use as a dewormer in cattle, pigs, and sheep.
However, tetramisole has also recently gained prominence among aquarists as an effective treatment for Camallanus roundworm infestations in freshwater tropical fish. It is a broad-spectrum anthelminthics, used to control roundworm and hoodworm.
 
Tetramisole HCL Application:
 
Tetramisole hydrochloride is used as an anthelmintic in the treatment of many nematodes particularly in veterinary applications. Tetramisole is a racemic mixture.
It is used as Hydrochloric acid levorotatory sulfonated intermediates.
It is flooding bowel insect poisons, anti-worm medicine.
Used for fishing and pinworms roundworm, insect infection.
 

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V-erb-b2 avian erythroblastic leukemia viral oncoprotein 2 isoform C LAB GRADE 97%

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99% High Purity Local Anesthetic Tetracaine Hydrochloride/Tetracaine HCL 136-47-0

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99% High Purity Local Anesthetic Tetracaine Hydrochloride/Tetracaine HCL 136-47-0
 
Tetracaine HCL Basic Info.:
 
Product Name: Tetracaine hydrochloride
Synonyms: Tetracaine HCL
CAS: 136-47-0
MF: C15H25ClN2O2
MW: 300.82
EINECS: 205-248-5
mp: 149°C
storage temp: Refrigerator
Appearance: White Solid
Usage: Local anesthetic; Mainly used in mucosa anesthetic.The function is stronger than Procaine and Lidocaine.
 
Tetracaine HCL Description:
 
Tetracaine HCl is synthesized from 4-butylaminobenzoic acid. The ethyl ester is formed through an acid-catalyzed esterification reaction. Base-catalyzed transesterification is achieved by boiling the ethyl ester of 4-butylaminobenzoic acid with excess 2-dimethylaminoethanol in the presence of a small amount of sodium ethoxide.
 
Tetracaine HCL Applications:
 
Tetracaine (INN, also known as amethocaine; trade name Pontocaine. Ametop and Dicaine) is a potent local anesthetic of the ester group. It is mainly used topically in ophthalmology and as an antipruritic, and it has been used in spinal anesthesia.
 
In biomedical research, tetracaine is used to alter the function of calcium release channels (ryanodine receptors) that control the release of calcium from intracellular stores. Tetracaine is an allosteric blocker of channel function. At low concentrations, tetracaine causes an initial inhibition of spontaneous calcium release events, while at high concentrations, tetracaine blocks release completely.
 

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99% Muscle Bodybuilding Supplement Anabolic Steroid Methenolone Acetate 434-05-9

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99% Muscle Bodybuilding Supplement Anabolic Steroid Methenolone Acetate 434-05-9 
 
Methenolone Acetate Basic Info.
 
Product Name: Methenolone Acetate
Alias: Primobolan-depot;Primobolandepot;Methenolone Acetate
CAS No.: 434-05-9
MF: C22H32O3
MW: 344.49
Einecs No: 207-097-0
Purity: 99%
MOQ(minimum order quantity): 10gram
Standard: Enterprise Standard
Appearance: White powder. 
Usage: It is very strong, the synthesis of the metabolism and male characteristics is very low, making it the best choice for the game. 
 
Methenolone Acetate Description:
 
Primobolan (methenolone acetate), all things being equal, is an excellent oral steroid drug. Unlike most other oral steroids, Primobolan is not 17-alkylated and does not have liver toxicity problems. Methenolone is perhaps only half as potent by the oral route as by injection, so dosages need to be high, at least 100 and preferably 200-300 mg per day, but if that can be afforded it is an excellent drug. It is unusual among oral steroids as being Class I, binding well to the androgen receptor. 
 
Methenolone Acetate Applications: 
 
Primobolan (methenolone acetate), all things being equal, is an excellent oral steroid drug. Unlike most other oral steroids, Primobolan is not 17-alkylated and does not have liver toxicity problems. 
Primobolan is toxic to the liver, especially the oral versions, although the toxicity is gradual and slight. Acne and hair loss can occur with long-term use. 
Primobolan is a good base compound in a stack and can produce results just slightly below that of nandrolone and is best used in a cutting stack. Because Primobolan doesn't aromatize, there is no use for Clomid or Nolvadex.
Primobolan Acetate is very strong, the synthesis of the metabolism and male characteristics is very low, making it the best choice for the game. The drug for women is very good!
 

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99% Purity High Quality Steroid Hormone Powder Methandriol Dipropionate 3593-85-9

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99% Purity High Quality Steroid Hormone Powder Methandriol Dipropionate 3593-85-9
 
Methandriol Dipropionate Details:
 
Product Name: Methandriol Dipropionate
Synonyms: 5-Androsten-17Alpha-Methyl-3Beta;17Alpha-Methylandrostendiol Dipropionate;Methandriol Dipropionate;
CAS: 3593-85-9
MF: C26H40O4
MW: 416.6
EINECS: 222-735-8
Standard: Enterprise Standard
Packing: 1kg/Aluminum foil bag
Min. Order Quantity: 10g
Payment: Western Union, Moneygram
Shipment: EMS, DHL, FedEx, etc.
Delivery: Safe & Timely, Around 1 Day After Payment.
Product Categories: Steroids
 
Methandriol Dipropionate Descriptions:
 
Methandriol Dipropionate (M.D.) is a form of the water-dissolved Methandriol but Methandriol Dipropionate remains effective for a longer period of time. On the one hand, Methandriol Dipropionate can be dissolved in oil for injection purposes and, on the other hand, Methandriol Dipropionate is produced in tablet form since it is also effective when taken orally M.D. has a strong anabolic and androgenic component so that it is suitable for the buildup of strength and muscle mass. The effect can be compared to a cross between Deca-Durabolin and Testosterone enanthate. Like testosterone it con- tributes to a gain in both strength and muscle but does not retain more water than Deca-Durabolin.
 
The best results can be obtained, however, if Methandriol Dipropionate is not taken alone but in combination with an- other steroid. This is because Methandriol Dipropionate is able to magnify the effects of other steroid compounds. It does this by increasingly sensitizing the androgenic receptors of the muscle cell, allowing a higher amount of the steroid molecules of the additionally taken steroids to be absorbed by the receptors. This also explains why injectable Methandriol Dipropionate is only available today as a combination compound with an additional steroid substance. Injectable Methandriol Dipropionate is only available in the Australian veterinary steroids Drive, Spectriol, Geldabol, and Filibol Forte so that procurement of the compound is difficult. The few athletes using this drug report good strength gains, a solid muscle gain, and low water retention. The combination steroids aromatize only slightly so, when taking only Methandriol Dipropionate, the use of antiestrogens is perhaps appropriate. The injectable form is only slightly toxic.
 
Methandriol Dipropionate Dosage:
 
The usual dosage for athletes is 100 mg every 2-3 days. In Europe only the oral form of M.D. is available. Also in this case it is beneficial to combine M.D. with another steroid, preferably an injectable one. The normal daily dose is 40-60 mg and is usually taken in 2-3 individual doses spread over & day The tablets are usually taken for only 4-6 weeks since the effect decreases quickly, thus requiring higher dosages.
 

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Cleavage and polyadenylation specificity factor subunit 1 (1360-1369) LAB GRADE 97%

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