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9-Bromo-3-(2-Bromo Acetyl)-10,11-Dihydro-5H-dibenzo(c,g) Chromen-8(9H)-one 99%

Shanghai Ansion Pharma Technology Co.,Ltd
www.ansionpharma.com
ann.xu@ansionpharma.com

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98% Androstene Safe Steroids 11-Oxo For Muscle Building 382-45-6

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98% Androstene Safe Steroids 11-Oxo For Muscle Building 382-45-6
 
11-Oxo Basic Info.:
 
Product Name: 11-Oxo
Synonyms: Androst-4-ene-3,11,17-trione 
CAS Number: 382-45-6
Molecular Formula: C19H24O3
Molecular Weight: 300.3921
Density: 1.18g/cm3
Appearance: white crystalline powder
Package: 1kg/ Aluminum foil bag
Payment: T/T, Western Union and Money Gram
Delivery: Within 12hours After Your Payment
Express: EMS, DHL, FedEx, etc(door-to-door) 
 
11-Oxo Description:
 
Adrenosterone is a steroid hormone with weak androgenic effect first isolated in 1936 from the adrenal cortex. Adrenosterone occurs in trace amounts in humans as well as most mammals and in larger amounts in fish, where it is a precursor to the primary androgen, 11-ketotestosterone. Adrenosterone has shown to be converted into 11-ketotestosterone in humans, which contributes to adrenosterone's androgenic effects.
 
11-Oxo Applications:
 
Adrenosterone's main action is it lowers cortisol levels. Cortisol is the main catabolic (muscle-eating) hormone and it also promotes fat gain. Cortisol and testosterone also work in an inverse relationship, so high cortisol levels lower testosterone. Adrenosterone acts as a competitive inhibitor, preventing cortisone from attaching to the 11b-hydroxysteroid dehydrogenase type I reductase. By competing at the receptor, it keeps cortisone from attaching and converting to cortisol through the enzyme. Adrenosterone is found naturally in the body and is released by the adrenal glands. The body uses it as a way to help regulate cortisol levels.
 

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98% Injectable Polypeptide Hormones Eptifibatide Raw Steroid Powders 148031-34-9

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98% Injectable Polypeptide Hormones Eptifibatide Raw Steroid Powders 148031-34-9
 
Eptifibatide Basic Info.
 
Product Name: Eptifibatide
Synonyms: Human Eptifibatide; Eptifitide
Sequence: Mpr-Har-Gly-Asp-Trp-Pro-Cys-NH2
Cas No.: 148031-34-9
Molecular Formula: C35H49N11O9S2
Molecular Weight: 831.96
Appearance: White slightly yellwish powder.
Specific Rotation[20/D]: -75.0~-95.0°(C=1,1%HAc)
Amino Acids composition: ± 10%
Peptide Purity (By HPLC): >98% by area integration.
Related Substance (By HPLC): Total Impurities (%)<2.0%;Largest Single Impurity (%)< 1.0%
Water Content (Karl Fischer): <8.0%
Peptide Content(N determination): >80%
Acetate Content: <15%
IR spectrum: in accordance
Grade : Pharmaceutical Grade
Storage: Closed, below 2 ~ 8ºC preservation
Usage : Platelet glycoprotein receptor antagonist model, the third generation of antiplatelet drugs. For acute coronary syndrome (including unstable angina or non Q wave myocardial infarction) or percutaneous coronary interventional therapy (including angioplasty or atheromatous plaque excision).
 
Description Of Eptifibatide:
 
Eptifibatide (Integrilin, Millennium Pharmaceuticals, also co-promoted by Schering-Plough/Essex), is an antiplatelet drug of the glycoprotein IIb/IIIa inhibitor class.[1] Eptifibatide is a cyclic heptapeptide derived from a protein found in the venom of the southeastern pygmy rattlesnake (Sistrurus miliarius barbouri). It belongs to the class of the so-called arginin-glycin-aspartat-mimetics and reversibly binds to platelets. Eptifibatide has a short half-life. The drug is the third inhibitor of GPIIb/IIIa that has found broad acceptance after the specific antibody abciximab and the non-peptide tirofiban entered the global market.
Integrilin is sold in two strengths, globally: vials containing 2 mg/ml (20 mg totally) and 0.75 mg/ml (75 mg totally).
 
Application Of Eptifibatide:
 
Eptifibatide is used to reduce the risk of acute cardiac ischemic events (death and/or myocardial infarction) in patients with unstable angina or non-ST-segment-elevation (e.g., non-Q-wave) myocardial infarction (i.e., non-ST-segment elevation acute coronary syndromes) both in patients who are to receive non surgery (conservative) medical treatment and those undergoing percutaneous coronary intervention (PCI).
 
The drug is usually applied together with aspirin or clopidogrel and (low molecular weight or unfractionated) heparin. Additionally, the usual supportive treatment consisting of applications of nitrates, beta-blockers, opioid analgesics and/or benzodiazepines should be employed as indicated. Angiographic evaluation and other intensive diagnostic procedures may be considered a first line task before initiating therapy with eptifibatide.
 

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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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98% Purity Aicar 2627-69-2 Sarms White Solid Raw Material

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98% Purity Aicar 2627-69-2 Sarms White Solid Raw Material
 
Aicar Basic Info:
 
Product Name: Aicar
CAS: 2627-69-2
MF: C9H14N4O5
MW: 258.23
EINECS: 220-097-5
Assay: 99%
Product Categories: Carbohydrates & Derivatives;Nucleotides;Protein Kinase;Cardiovascular;
Chemical Properties: White or off-white solid
 
Product Description Of Aicar:
 
Aicar is a peptide whose technical name is 5-Aminoimidazole-4-carboxamide ribonucleotide.
It can also be known as AICA ribonucleotide, ZMP, or Acadesine. It is an intermediate contained in the generation of inosine monophosphate. It primarily functions as an AMP-activated protein kinase agonist, meaning that it has the ability to promote the operation of nutrient stores for energy production. It has a molecular mass of 338.211, and it has a molecular formula of C9H15N4O8P.
 
Aicar is an adenosine analog that selectively activates AMP-activated protein kinase (AMPK). AMPK regulates lipid and glucose metabolism to maintain cellular energy homeostasis (Hardie and Carling).
 
Aicar can play a hand in boosting these processes because it contains the ability to penetrate cardiac
cells and block the production of enzymes tied to regulating glucose intake and energy expulsion. With these regulatory enzymes inhibited, the affected cells can in turn boost the amount of glucose that can be received, and it can also increase its level of energy conversion. Additionally, the peptide’s presence has been determined to aid in lowering programmed cell death, a process that is also known as apoptosis.
 
Aicar Application:
 
Glucose uptake stimulant; AMPK activator.AICAR is a nucleoside analogue that is able to enter
nucleoside pools and is able to significantly increase levels of adenosine during periods of ATP
breakdown. Adenosine-regulating agents (ARAs) hav e been recognized for therapeutic potential
in myocardial ischemia. Cardioprotective.
 
Aicar is a nucleoside analogue that is able to enter nucleoside pools and is able to significantly increase levels of adenosine during periods of ATP breakdown. Adenosine-regulating agents (ARAs) hav e been recognized for therapeutic potential in myocardial ischemia. Cardioprotective.
Biological Activity Cell-permeable, allosteric activator of AMP-activated protein kinase (AMPK). Augments proliferation, differentiation and mineralization of osteoblastic MC3T3-EI cells and attenuates psychosine-induced expression of proinflammatory cytokines and iNOS in astrocytes.
 
Aicar is a peptide whose technical name is 5-Aminoimidazole-4-carboxamide ribonucleotide. It can also be known as AICA ribonucleotide, ZMP, or Acadesine. It is an intermediate contained in the generation of inosine monophosphate. It primarily functions as an AMP-activated protein kinase agonist, meaning that it has the ability to promote the operation of nutrient stores for energy production. It has a molecular mass of 338.211, and it has a molecular formula of C9H15N4O8P.
 
Aicar Function:
 
Aicar is an adenosine analog that selectively activates AMP-activated protein kinase (AMPK). AMPK regulates lipid and glucose metabolism to maintain cellular energy homeostasis (Hardie and Carling).
 
Aicar can play a hand in boosting these processes because it contains the ability to penetrate cardiac cells and block the production of enzymes tied to regulating glucose intake and energy expulsion. With these regulatory enzymes inhibited, the affected cells can in turn boost the amount of glucose that can be received, and it can also increase its level of energy conversion. Additionally, the peptide's presence has been determined to aid in lowering programmed cell death, a process that is also known as apoptosis.
 

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99% Antiestrogen Steroid Hormones Toremifene Citrate For Cancer Patients 89778-27-8

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99% Antiestrogen Steroid Hormones Toremifene Citrate For Cancer Patients 89778-27-8

Toremifene Citrate Basic Info.

Product Name: Toremifene Citrate

Synonyms: FC 1157a; Fareston; NK 622; NSC 613680

CAS: 89778-27-8

Molecular Formula: C32H36ClNO8

Molecular Weight: 598.08

Melting point: 160-162°C

Boiling point: 146-148C

Density: 1,045g/cm

Refractive index: 1,416-1,418

Storage temp.: -20°C Freezer

Appearance: White or almost white powder

Toremifene Citrate Descriptions:

Fareston will display both estrogen antagonist / agonist properties in the body. This puts Fareston in the same category as Nolvadex and Clomid, the two most popular drugs in Farestons category. FARESTON is an estrogen agonist/antagonist indicated for the treatment of metastatic breast cancer in postmenopausal women with estrogen-receptor positive or unknown tumors.

Toremifene administration for a period of 3 months in men with idiopathic oligozoospermia is associated with significant improvements of sperm count, motility, and morphology, mediated by increased gonadotropin secretion and possibly a direct beneficial effect of toremifene on the testes. The above findings are also indicative of a better testicular exocrine (improved sperm parameters) response to treatment in men whose partners achieved pregnancy compared with those who did not. Further randomized, placebo-controlled trials should be conducted to determine whether this particular selective estrogen receptor modulator can be useful as an initial approach in men with oligozoospermia.

Toremifene Citrate Applications:

Toremifene Citrate improved lipid profiles, particularly as an enhancer of high density lipoprotein cholesterol. it improved low density lipoprotein cholesterol levels.Both fareston and tamoxifen selective estrogen receptor modulators and equivalent treatments for metastatic breast cancer.No significant differences were found between treatment with either tamoxifen or fareston Treatment of HR-positive patients with either tamoxifen or toremifene is appropriate.In treating idiopathic oligozoospermia, tamoxifen and fareston are roughly equally effective but raloxifene is not.The antiestrogenic effects of SERMs at the hypothalamic level result in a statistically significant increase of gonadotropin levels, which is more marked for tamoxifen and fareston compared with raloxifene.

 

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99% Benzocaine Hydrochloride Local Anesthetic Agents Benzocaine HCL 23239-88-5

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99% Benzocaine Hydrochloride Local Anesthetic Agents Benzocaine HCL 23239-88-5
 
Benzocaine HCL Basic Info.:
 
Product Name: Benzocaine HCL
Synonyms: Ethyl 4-Aminobenzoate Hydrochloride;Benzocaine Hcl;Benzocaine Hydrochloride;Benzocaine Hydrochl;
CAS: 23239-88-5
MF: C9H11NO2.ClH
MW: 201.65
Assays: 99%
Melting point: 92°C
Boiling point: 310°C, 183-184°C (1.87×103Pa)
Density: 1.17
Stability: Stable. Combustible.
Chemical Properties: White odourless crystals.
Uses: 
(1)The goods are used to relieve pain for the local anesthetic, wounds, ulcers and hemorrhoids facial, also are cough suppressants retreat intermediates.
(2)Used in cosmetic ultraviolet absorption, local anesthetics and used to relieve pain in the wound, ulcer surface and Hemorrhoids.
 
Benzocaine HCL Description:
 
Benzocaine is also called amino ethyl benzoate, a colorless or white orthorhombic needle-like crystals or crystalline powder. Benzocaine hydrochloride salt is the hydrochloride salt form of the local anesthetic benzocaine, with the same pharmacological effects of benzocaine and weaker effect of anesthesia than procaine. Local absorption is slow with lasting effect. It cannot be used for anesthesia as a result of not being dissolved in water. It can be used for pain relief and anti-itch. Benzocaine hydrochloride is usually made into powder or oil paste and used to heal wounds, ulcers, burns, skin abrasions and hemorrhoids.
 
Benzocaine is commonly found, particularly in Britain, as an impurity in street cocaine. Whilst giving a numbing effect similar to cocaine on users' gums it does not actually produce the effects of cocaine. But in terms of an orally based saliva drug test benzocaine can and has been mistaken for a false positive for cocaine.
 
Benzocaine HCL Applications:
 
Benzocaine HCL works by creating a chemical barrier that halts the build-up of sodium, which accumulates as the nerve endings are stimulated by pain. When sodium builds up, electrical signals also build in the nerve endings. These are eventually transmitted to the brain, which interprets the signals as pain.
 
Benzocaine is a local anesthetic commonly used as a topical pain reliever or in cough drops. It is the active ingredient in many over-the-counter anesthetic ointments such as products for oral ulcers. It is also combined with antipyrine to form A/B otic drops to relieve ear pain and remove earwax
 
Benzocaine is used as a key ingredient in numerous pharmaceuticals:
Over the counter throat lozenges such as Cepacol.
Some glycerol-based ear medications for use in removing excess wax as well as relieving ear conditions such as otitis media and swimmers ear.
Some previous diet products such as Ayds.
Some condoms designed to prevent premature ejaculation. Benzocaine largely inhibits sensitivity on the penis, and can allow for an erection to be maintained longer (in a continuous act) by delaying ejaculation. Conversely, an erection will also fade faster if stimulus is interrupted.
Benzocaine mucoadhesive patches have been used in reducing orthodontic pain.
In Poland it is included, together with menthol and zinc oxide, in the liquid powder (not to be confused with the liquid face powder) used mainly after mosquito stings. Today's ready made Pudroderm was once used there as pharmaceutical compound.
 

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99% Benzocione Local Anesthetic Benzocaine For Anti-Paining 94-09-7

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99% Benzocione Local Anesthetic Benzocaine For Anti-Paining 94-09-7
 
Benzocaine Basic Info.:
 
Product Name: Benzocaine
Synonyms: Aethoform;Anesthesin;Akos Bbs-00003658;4-Aminobenzoic Acid Ethyl Ester;Labotest-Bb Ltbb000527;H-4-Abz-Oet;Ethyl 4-Aminobenzoate;Ethyl P-Aminobenzoate
CAS: 94-09-7
Molecular Formula: C9H11NO2
Molecular Weight: 166.1965
EINECS number: 202-303-5
Purity: 99%
Size: 40 mesh and 200 mesh
Melting point: 88-90°C
Boiling point: 172°C (12.7517 mmHg)
Density: 1.17
Flash Point: 164.2°C
Vapor Pressure: 0.000589mmHg at 25 °C
Fp: 172°C/13mm
Storage temp.: 0-6°C
Stability: Stable. Combustible. Incompatible with strong oxidizing agents.
Chemical Properties: White odourless crystals.
Product Categories: Aromatic Esters;C8 to C9;Carbonyl Compounds;Esters;Amines;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;Research Chemical;Pharmaceutical intermediate;API;Pharma materials;Intermediate of Tetracaine hydrochloride.
Uses: 
(1)The goods are used to relieve pain for the local anesthetic, wounds, ulcers and hemorrhoids facial, also are cough suppressants retreat intermediates.
(2)Used in cosmetic ultraviolet absorption, local anesthetics and used to relieve pain in the wound, ulcer surface and Hemorrhoids.
 
Product Description Of Benzocaine:
 
Benzocaine is used to relieve pain and itching caused by conditions such as sunburn or other minor burns, insect bites or stings, poison ivy, poison oak, poison sumac, minor cuts, or scratches.
 
Benzocaine belongs to a group of medicines known as topical local anesthetics. It deadens the nerve endings in the skin. This medicine does not cause unconsciousness like general anesthetics do when used for surgery.
 
This medicine is available without a prescription; However, your doctor may have special instructions on the proper use and dose for your medical condition.
 
Fat soluble surface anaesthetic. It's for the local anesthetic for wound, pain, ulcer and hemorrhoids, as well as cough suppressants retreat Benzocaine intermediates. Also can be used for ultraviolet absorption in cosmetic. Related product: Lidocaine. 
 
Benzocaine Applications: 
 
Benzocaine is a topical analgesic (meaning it is to be used on the body surface or in the mouth but should not be swallowed) that has a number of different uses in over-the-counter (OTC) medicines. Depending on the dose and form, the active ingredient benzocaine can be used to relieve throat and mouth pain; To alleviate external vaginal itching and burning; To stop pain and itching due to hemorrhoids; Or to relieve minor skin irritations, pain, and itching. Because benzocaine is available in different doses and forms, it is very important to read the Drug Facts label carefully to determine whether the medicine is intended to be used for the symptoms you are experiencing. 
 
Benzocaine can be the only active ingredient in oral treatments that relieve sore throat or address mouth pain caused by cold sores, canker sores, teething, and other issues. It also can be combined with other active ingredients in oral treatments that not only relieve mouth and throat pain, but also protect irritated areas, provide a soothing coating, or relieve dryness. 
 
While oral discomfort treatments containing benzocaine are intended to be used in and around the mouth, there are other topical benzocaine medicines that should only be used externally, or on the outer surface of the body (not near or in the mouth). For example, benzocaine can be found in vaginal medicines that contain more than one external analgesic ingredient or in single active ingredient hemorrhoid treatments. Benzocaine also is available in topical pain relievers that not only relieve skin irritations, pain, and itching, but also contain other active ingredients that kill germs and help prevent infection. 
 
Benzocaine is approved by the U. S. Food and Drug Administration (FDA) and is safe and effective when used according to label directions. Some oral discomfort treatments can be used to temporarily relieve pain due to toothaches; However, these medicines are not intended for long-term treatment. If your toothache pain is severe or lasts for more than seven days, you should talk to your dentist.
 
Benzocaine may not be contained in all products sold under these brands. Please read the OTC Drug Facts label carefully for active ingredient information for specific products.
 

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99% Female Steroids Hormone Flibanserin For Gaining Women Sexy-Enhancement 167933-07-5

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99% Female Steroids Hormone Flibanserin For Gaining Women Sexy-Enhancement 167933-07-5
 
Flibanserin Basic Info:
 
Product Name: Flibanserin
Chemical Name: Centrophenoxine HCL
CAS Number: 167933-07-5
EINECS Number: 222-975-3
Molecular Formula: C20H21F3N4O
Molecular Weight: 294.17
Melting Point: 139-143°C
Assay: 99.5%
Appearance: White powder
 
Flibanserin Description:
 
Flibanserin is a novel, non-hormonal drug that has been studied in clinical trials for the treatment of HSDD in premenopausal and postmenopausal women. The application submitted to the FDA is for premenopausal women. Flibanserin is believed to work on key neurotransmitters, or chemicals, in the brain that affect sexual desire. More specifically, it is thought that flibanserin corrects an imbalance of levels of these neurotransmitters by increasing dopamine and norepinephrine (both responsible for sexual excitement) and decreasing serotonin (responsible for sexual inhibition). In clinical studies, flibanserin was evaluated for its ability to increase the frequency of satisfying sexual events, increase the intensity of sexual desire and decrease the associated distress women feel from its loss.
 
Flibanserin Application:
 
Flibanserin is being hailed as "Viagra for women." The experimental drug - designed for post-menopausal women with low sex drives - has now won approval from an advisory panel for the Food and Drug Administration (FDA).
 
Flibanserin is an antidepressant that failed to help depression in clinical trials, but was noted to have improved sexual health outcomes. It's not uncommon for a drug to be developed for one purpose, then approved for another. Sildenafil (Viagra) was originally developed to lower blood pressure, but failed those trials. The benefit of both of these drugs was discovered by accident. However, flibanserin has now been studied for its effects on sexual health for nearly a decade.
 
Flibanserin doesn't have any interactions with hormonal medications, Thorp says. It does seem to interact with the original libido helper, though: some panelists recommended a warning against drinking alcohol while taking it, Reuters reported. (Interested in natural alternatives to hormone replacement therapy? The Natural Menopause Solution has everything you need to tame symptoms and trigger rapid, healthy weight loss in menopausal women.)
 
HSDD is the most commonly reported form of female sexual dysfunction. HSDD is defined as a persistent or recurrent deficiency or absence of sexual fantasies and desire for sexual activity that causes marked distress or interpersonal difficulty, and which is not better accounted for by a medical, substance-related, psychiatric (e.g., depression) or other sexual condition. The cause of HSDD is believed to involve a multitude of social, psychological and biological factors and may be attributed to
a complex interplay of these factors.
 
Flibanserin Function:
 
A new drug designed to boost sexual desire in women is controversial for some and eagerly awaited by others, but it's hit a potentially serious snag. The drug didn't boost women's desire any more than a placebo in two clinical trials. The Food and Drug Administration posted the clinical trial results on its website today in advance of a committee meeting on Friday, when a panel of experts will vote whether or not to recommend approval of the drug called flibanserin.(The FDA usually follows the recommendations of its expert panels.) Although there was a slight increase in the number of sexually satisfying events flibanserin users had each month, the FDA staff who reviewed the results said the so-called response rate isn't "particularly compelling."
 

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