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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.
(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.

BK-2C-B 3meo-pcp 4Fluorpheny 4clpvp 4meo-pv8 4bmc LAB GRADE 99.9


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Bulking Steroids Anastrozoles (Arimidex) for Women Breast Cancer USP

Anastrozole (arimidex)
Basic Info.
CAS No:120511-73-1                                                      MF: C17H19N5
MW: 293.37                                                                    Appearance:White Powder
Assay: 99%.                                                                   Export Markets:Global 
HS Code: 2937290018
Additional Info.
Package: 25KG/Drum                                                   Origin:China
Standard: Enterprise Standard                                      Usage: It can be used to the treatment of Breast cancer
Product details: 
1. Anastrozole is an aromatase-inhibiting drug approved for treatment of breast cancer after surgery, as well as formetastasis in both pre and postmenopausal women. 
2. The severity of breast cancer is increased by estrogen, as sexhormones cause hyperplasia, and differentiation at estrogen receptor sites. Anastrozole works by inhibiting the synthesis of estrogen. 
The trial suggested that anastrozole is the preferred medical therapy for Postmenopausal women with localized breast cancer that is estrogen receptor (ER) positive. 
3. Three azole potent selective aromatase inhibitors, which inhibit rely on aromatase cytochrome P -450 to block estrogen biosynthesis, and the main factors of estrogen to stimulate breast cancer cell growth. It can treat breast cancer, especially suitable for those who relapse after treatment with hormone auxiliary advanced breast cancer after menopause women. 
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Progestogen Hormonal Gestodene Female Anabolic Steroids 60282-87-3

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Progestogen Hormonal Gestodene Female Anabolic Steroids 60282-87-3 
Gestodene Basic Info.:
Product name: Gestodene
Other names: Gestinol;13-Ethyl-17-hydroxy-18,19-dinor-17alpha-pregna-4,15-dien-20-yn-3-one;SHB 331;Gestodeno.
CAS: 60282-87-3
EINECS: 262-145-8
Molecular Formula: C21H26O2
Molecular Weight: 310.43
Melting point: 190-192 degree centigrade
Boiling Point: 462.7 degree centigrade at 760 mmHg
Flash Point: 196.9 degree centigrade
Refractive index:1.588
Density: 1.15 g/cm3
Vapour pressure: 1.66E-10mmHg at 25 degree centigrade
Appearance: White crystalline solid. 
Function: Used as resisting pregnant hormone pills.
Gestodene Description:
Gestodene is a synthetic version of a female sex hormone. When combined with other synthetic hormones, it interferes with a woman's menstrual cycle, decreasing the symptoms of severe menstruation and preventing pregnancy. Used correctly, it is more than 99% effective at preventing unwanted pregnancies.
Gestodene as progestin far the strongest and one of the lowest dose of birth control pills. Its progestin activity is 2 times L norethindrone, there is no androgen and estrogen activity, there is an anti-estrogen effect. Oral absorption quickly and completely, after 1 to 2 hours of peak blood concentration, bioavailability 100%, eliminating t1 / 28 hours. Clinical and ethinyl estradiol or a composite sheet consisting of three photo used for short-acting oral contraceptives. Due to its reliable contraceptive effect, good cycle control, on lipid metabolism can produce beneficial effects, improve hdl, it is the most ideal one oral contraceptives.
Gestodene Applications:
Gestodene is asoral contraceptive. It mimics the naturally occurring female sex hormone progesterone, 
which is partially responsible for regulating the menstrual cycle. 
Gestodene as progestin far the strongest and one of the lowest dose of birth control pills. Its progestin activity is 2 times L norethindrone, there is no androgen and estrogen activity, there is an anti-estrogen effect.

trans-3-Ethoxycarbonyl-4-(4-flurophenyl)-N-methyl piperdine-2,6-dione

trans-3-Ethoxycarbonyl-4-(4-flurophenyl)-N-methyl piperdine-2,6-dione is used as intermediate for the drug paroxetine hydrochloride.

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17 Alpha-Estradiol / Estradiol For Skin Absorption Agent CAS 57-91-0

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17 Alpha-Estradiol / Estradiol For Skin Absorption Agent CAS 57-91-0
17 Alpha-Estradiol Basic Info.:
Product Name: 17 Alpha-Estradiol
Synonyms: Alpha-estradiol; 17A-estradiol 
CAS: 57-91-0 
EINECS: 200-354-8 
Molecular Formula: C18H24O2 
Molecular Weight: 272.39 
Appearance :hite or off-white crystalline powder 
Assay :99%min.
Melting range:216-224 oC 
Specific rotation:+52o to +60o 
Loss on drying :3.5%MAX
Monor impurity :0.2%MAX
Total impurities:1.0% max 
17 Alpha-Estradiol Description:
Estradiol (called α - estradiol or 17α - estradiol) for human breast cancer cells in tissue culture biologically active estrogen. Not part of the 17- and selective estrogen receptor (ER-X) traditional hormone / receptor of the endocrine system, but an important autocrine / paracrine function of the system is part of the growth in the adult brain. In menopause, and neurodegenerative diseases (eg Alzheimer's disease and ischemic stroke) treatment, 17- estradiol may have important implications for hormone replacement therapy thing. 
The development of secondary sex characteristics in women is driven by estrogens, to be specific, estradiol. These changes are initiated at the time of puberty, most are enhanced during the reproductive years, and become less pronounced with declining estradiol support after the menopause. Thus, estradiol enhances breast development, and is responsible for changes in the body shape, affecting bones, joints and fat deposition. Fat structure and skin composition are modified by estradiol. 
17 Alpha-Estradiol Applications: 
This medication is a female hormone. It is used by women to help reduce symptoms of menopause (such as hot flashes, vaginal dryness). These symptoms are caused by the body making less estrogen. If you are using this medication to treat symptoms only in and around the vagina, products applied directly inside the vagina should be considered before medications that are taken by mouth, absorbed through the skin, or injected. 
Certain estrogen products may also be used by women after menopause to prevent bone loss (osteoporosis). However, there are other medications (such as bisphosphonates including alendronate) that are also effective in preventing bone loss and may be safer. These medications should be considered for use before estrogen treatment.

4-cprc 4cprc 4c-prc high purity,high quality CAS NO.63547-13-7 CP >99%

4CPRC 4-CPRC crystal

CAS No: 63547-13-7.

Formula : C15H20ClND

IUPAC Name : 1-(4-Chloro-phenyl)-2-pyrrolidin-1-yl-pentan-1-one.

Appearance: White crystal

Purity: >99%

Package: 1kg/Aluminum foil bag

Application: For chemical research

Production Capacity: 500 Kilogram/Month

Storage: Kept in a cool,dry and ventilated place

Payment: Bitcoin, bank transfer(T/T), Western Union, MoneyGram

Shipment: TNT, UPS, DHL, FEDEX, EMS and Client's request.

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Anabolic Steroid Powder Sunifiram For Memory Enhancement 314728-85-3

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Anabolic Steroid Powder Sunifiram For Memory Enhancement 314728-85-3
Sunifiram Basic Info:
Product Name: Sunifiram
Synonyms: Sunifiram;DM235;DM 235;
CAS: 314728-85-3
MF: C14H18N2O2
MW: 246.30492
Appearance: White powder
Purity: 99.32%
Shelf life: 2 years
Standard: In-house Standard
Usage: For the treatment of Alzheimers Dementia, Cognition Disorder, Neurologic Drugs, Senile Dementia, Acetylcholine Release Enhancers.
Product Description Of Sunifiram:
This compound is known as an AMPAkine due to exerting most of its actions via the AMPA receptor (one of the three main subsets of glutamate receptors, alongside NDMA and kainate). This enhancement of AMPA function seems to also rely on enhancing signalling via the Glycine binding site of NMDA receptors, although one minimal signalling goes through the NMDA receptor then the benefits on AMPA receptors seem dose-dependent.
Sunifiram (DM-235) is a piperazine derived ampakine drug which acts as a positive allosteric modulator of AMPA receptors, and has nootropic effects in animal studies with significantly higher potency than piracetam. A number of related compounds are known, the best known being unifiram (DM-232).
This enhancement by sunifiram is associated with an increase inphosphorylation of AMPAR through activation of protein kinase II(CaMKII) and an increase in phosphorylation of NMDAR through activation of protein kinase C α (PKCα). More specifically, sunifiram stimulates the glycine-binding site of NMDAR with concomitant PKCαactivation through Src kinase. Enhancement of PKCα activity triggers to potentiate hippocampal LTP through CaMKII activation.Sunifiram improves cognitive deficits via CaM kinase II andprotein kinase C activation.
Application Of Sunifiram:
For the treatment of Alzheimers Dementia, Cognition Disorder, Neurologic Drugs, Senile Dementia, Acetylcholine Release Enhancers.
Sunifiram (DM-235) is a synthetic derivative of Piracetam, although due to breaking the pyrrolidone backbone it is no longer in the Racetam class of drugs (yet by being derived from them, it is still commonly associated with this class).
Sunifiram has mechanisms similar to Nefiracetam in the hippocampus, and similar to that drug sunifiram shows anti-amnesiac properties and is potentially a cognitive enhancer. Its anti-amnesiac activity is several orders of magnitude greater than piracetam on a per weight basis, and preliminary evidence suggest it has a similarly low toxicity profile.
Function Of Sunifiram:
Sunifiram increases energy levels, allowing users to feel more motivated and eliminate
Sunifiram increase Levels of concentration increase, and users feel less distracted by external stimuli
Sunifiram also enhances long-term potentiation, which is the forming of new connections regarding memory storage.
Sunifiram has some anxiolytic benefits. Feeling more relaxed is beneficial when trying to focus.

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