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Home > Pharmaceutical Intermediates > Antispasticity Agents > Prostaglandin E1 for Sale > Factory provided BP Prostaglandin E1 745-65-3
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Factory provided BP Prostaglandin E1 745-65-3

TDS 35 Inquiries

Unit Price: Get Latest Price
CAS No.:

745-65-3

Grade:

Pharmaceutical Grade

Content:

99%

Port:

SHANGHAI

Brand:

HyperChem

Packaging:

1kg/Bag, 25kg/drum

Price valid (until):

2025-09-12

Company Type:
Trader
Location:
China
Qualification:
Main Products:

Pharmaceuticals,Peptide,Cosmetics,Nutritional Supplements

  • Product Description

  • Seller Information

  • Inquiry History

  • Description

    Name

    Prostaglandin E1

    CAS number

    745-65-3

    Description

    Prostaglandin E1 is a naturally occurring eicosanoid derived from arachidonic acid metabolism, serving as a crucial autocrine and paracrine signaling molecule in human physiology.

    Structural formula

    Shop Factory provided BP Prostaglandin E1 745-65-3-Detailed Image 1

    Molecular Formula

    C20H34O5

    Molecular Weight

    354.48 g/mol

    Appearance

    White powder

    Quality Standard

    99%

    Storage Condition

    Cool dry place( away from the light)

    Shelf Life

    >2 years if stored properly

    Sample package

    Aluminium foil bag

    Commercial package

    Aluminium Tin, Fiber drum

    Origin

    China

    Prostaglandin E1 More Info

    Prostaglandin E1 (PGE1, CAS: 745-65-3) is a naturally occurring eicosanoid derived from arachidonic acid metabolism, serving as a crucial autocrine and paracrine signaling molecule in human physiology. This unsaturated fatty acid derivative exists as a viscous liquid at room temperature and demonstrates exceptional biological activity at extremely low concentrations. As the first prostaglandin to be isolated and characterized, it represents a benchmark compound in lipid mediator research. Modern production utilizes both biotechnological synthesis through enzymatic conversion and chemical synthesis routes to achieve pharmaceutical-grade material with stringent purity requirements (>98% by HPLC). Its inherent instability in aqueous solutions necessitates specialized formulation approaches for clinical applications.

     

    Key Applications

    PGE1 has established therapeutic roles across multiple medical specialties due to its vasodilatory, anti-inflammatory, and cytoprotective properties. In cardiovascular medicine, it serves as a critical treatment for peripheral arterial diseases and ductus arteriosus management in neonates. Urology applications include intracavernosal injections for erectile dysfunction therapy, while gastroenterology utilizes its mucosal protective effects. Emerging applications span tissue engineering (as a stem cell differentiation modulator) and dermatology (for wound healing acceleration). The compound's ability to regulate platelet aggregation also makes it valuable in hematological research and anticoagulation protocols.

     

    Market Dynamics

    The global PGE1 market is projected to maintain steady growth (CAGR 4.2% through 2030), driven by expanding geriatric populations requiring vascular therapies and increasing neonatal ICU admissions. Asia-Pacific dominates production capacity with China and India as key manufacturing hubs, while North America and Europe lead in therapeutic innovation and premium-priced formulations. Market segmentation shows injectable formulations commanding 68% revenue share, with growing interest in sustained-release delivery systems. The compound's inclusion in WHO Essential Medicines List ensures continued demand in emerging markets, though pricing pressures exist from generic competition. Recent patent expirations have stimulated development of novel analogs and combination therapies.

     

    Handling & Regulatory Considerations

    PGE1 requires strict cold chain maintenance (typically -20°C storage with desiccants) due to thermal and oxidative instability. Handling must follow potent compound protocols with appropriate PPE including nitrile gloves and eye protection. Regulatory frameworks classify it as a prescription drug substance requiring cGMP compliance for pharmaceutical use, with additional controls for controlled substance applications in certain jurisdictions. Documentation must include comprehensive stability data, chiral purity certification, and endotoxin testing reports. Special transport regulations apply for temperature-sensitive shipments, requiring validated packaging with temperature monitors. Clinical applications demand rigorous batch-to-batch consistency verification due to narrow therapeutic windows in critical care usage.


    Package Image

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    FAQ

    Q1. Can I get a free sample?

    We can send you a samll free sample, and you only need to pay for the shipping cost.


    Q2. What is the HyperChem payment term?

    T/T in advance
    LC at sight
    DP at sight

    Bank transfer

    PayPal

    Bitcoin...


    Q3. What is HyperChem shipment policy?

    Our policy is to strive for the quickest shipment time possible.

    For ready stock samples, they are usually shipped within 3 working days after payment received.
    For non-ready stock, please contact HyperChem sales team to negotiate.


    Q4. What is HyperChem shipment term?

    By Express  
    FedEx  UPS  DHL  EMS                               
    Fast: 3-7 days around, high cost, door to door service

    By Air                                        
    Suitable for more than 50kg 
    Fast: 3-7 days, hight cost, port to port, professional broker needed 

    By Sea
    Suitable for more than 500kg      
    Fast: 7-45 days, low cost, port to port, professional broker needed 


    We will always attempt to utilize the quickest and most affordable way for customers to receive orders. And follow -up with customers via email for all shipment details as well as updated track information until it arrives without damage.


    Q5. What HyperChem will provide after shipment?

    For sample orders: 
    After shipment is done, an timely email including:

    1. Track details (Fedex /TNT/DHL/EMS Track number)
    2. Packaging photo
    3. COA, MSDS, etc
    4. Dispatch date & Estimated arriving time
    5. Shipping invoice

    For commercial orders
    A full set of shipment documents as well as package photos can be provided in scan-copy and original, to help customers complete the customs clearance process.



    Company Profile

    Established in 2013, Hyper Chem has exclusive tie-ups with leading manufacturers, supplying raw materials produced in GMP and ISO 9002 certified facilities, and provides high-quality ingredients and raw materials to cater to the requirements of our diverse range of clients.


    Among them, our key client industrial sectors around the global are:

    Pharmaceuticals
    Nutrition Ingredients/ Dietary supplements
    Cosmetic Ingredients
    Food Ingredients
    Veterinary API
    Agriculture fertilizer
    Custom Synthesis lab supply


    HyperChem provides to its wonderful and honorable clients comprehensive purchasing and distribution services which ensure that we are delivering the right generic, raw, or customized product, make sure that we are delivering it at the right time, ensure that it is delivered in the specified amount, and in the right kind of packaging to clients and customers of all types of industries irrespective of their size of operation.




    ECHEMI Editorial Reference
    PG is a group of twenty-carbon straight-chain unsaturated fatty acid, arachidonic acid is usually the biosynthetic precursor, for prostate acid (prostanoic acid) is generated by enzymatic and non-enzymatic conversion , with an endogenous physiological skeleton active substance. In 1958 for the first time people obtained two pure PG crystallines from sheep seminal separation: PGE1 and PGF1α. Natural PG is classicified into three communities by structures (PG1, PG2, PG3), ten types (PGA, PGB, PGC, PGD, PGE, PGF, PGG, PGH, PGI, PGJ). E, F types in six natural PG, ie, PGE1, PGE2, PGE3 and PGF1α + PGF2α + PGF3α were earliest studied , the primary PG; A, B, C, D, G, H, I, J and other natural PG are called secondary PG. Various PG code names (such as E, F, etc.) are based on observations from the study during the early years. PG soluble in ether (ethyl) is represented by E, that is PGE, PG soluble in phosphate solution is represented by F (Swedish fosfate), namely PGF. PGA, PGB respectively are represented by PGE acid (acid) or base (base) processed end products.It is white or pale yellow needle-like crystal. Mp115-116 ℃, specific rotation-61.6 ° (c = 0.56, THF). Prostaglandin E1 is a physiologically active substance with the expansion of blood vessels and inhibit platelet aggregation, and can inhibit vascular smooth muscle cells free Ca2 +, inhibite vascular sympathetic nerve endings, release norepinephrine for vascular smooth muscle relaxation, to decrease peripheral resistance , lower blood pressure, increase coronary blood flow, reduce myocardial oxygen consumption, thereby to relieve angina and reduce the incidence of myocardial infarction and reduced infarct size. It can improve heart failure, myocardial contractility, increased cardiovascular output, improve the coronary circulation, protect the ischemic myocardium. It can effectively inhibit cholesterol formation of additional immune damage caused by atherosclerosis. It can inhibit smooth muscle cell growth and reduce plaque. Expansion of renal vessels and increase renal blood flow, regulate sodium and water balance, resulting in diuresis.
    Prostaglandin E1 is an endogenous prostaglandin with vasodilatory, anti-platelet, and anti-hypertensive activities. It is in clinical use for the treatment of erectile dysfunction and the emergency management of infants with patent ductus arteriosus. It has also been used in the treatment of peripheral arterial occlusive disease (PAD).
    Crystalline Solid
    ChEBI: Prostaglandin E1 is a prostaglandins E. It has a role as a platelet aggregation inhibitor, a vasodilator agent, an anticoagulant and a human metabolite. It is a conjugate acid of a prostaglandin E1(1-).
    PGE1, Alprostadil (Prostin VR Pediatric), is a naturally occurring prostaglandin that has found particular use in maintaining a patent (opened) ductus arteriosus in infants with congenital defects that restrict pulmonary or systemic blood flow.Alprostadil must be administered intravenously continually at a rate of approximately 0.1 μg/kg/min to maintain the patency of the ductus arteriosus until corrective surgery can be performed. Up to 80% of circulating alprostadil may be metabolized in a single pass through the lungs. Because apnea has been observed in 10% to 12% of neonates with congenital heart defects, this product should be administered only when ventilatory assistance is immediately available. Other commonly observed side effects include decreased arterial blood pressure, which should be monitored during infusion; inhibited platelet aggregation, which might aggravate bleeding tendencies; and diarrhea.

    Certificates

    Basic Info
    Product Name:

    Prostaglandin E1

    Other Name:

    Prost-13-en-1-oic acid, 11,15-dihydroxy-9-oxo-, (11a,13E,15S)-;(8S,11S,12S,13E,15R)-11,15-Dihydroxy-9-oxoprost-13-en-1-oic acid;ent-PGE1;Alprostadil (PGE1)/Prostaglandin E1;Alprostadil (PGE1);Prostaglandin E1 or AIPROSTADIL;l-3-hydroxy-2-(3-hydroxy-1-octenyl)-5-oxocyclopentaneheptanoicacid;l-cyclopentaneheptanoicaci

    CAS No.:

    745-65-3

    Molecular Formula:

    C20H34O5

    InChIKeys:

    GMVPRGQOIOIIMI-DWKJAMRDSA-N

    Molecular Weight:

    354.48

    BRN:

    5294062

    EC Number:

    212-017-2

    Color/Form:

    White to off-white

    HScode:

    29375000

    Categories:

    Antispasticity Agents

    Characteristics
    Density:

    1.0458 (rough estimate)

    Melting Point:

    115-116 °C

    Boiling Point:

    407.69°C (rough estimate)

    Refractive Index:

    1.6120 (estimate)

    Water Solubility:

    insoluble

    PKA:

    pKa 4.85± 0.07(H2O,t=25±0.1,I=0.1(NaCl)) (Uncertain)

    Critical Temperature & Pressure:

    -20°C

    Hazard Identification

    Classification of the substance or mixture

    Acute toxicity - Category 3, Oral

    Reproductive toxicity, Category 2

    GHS label elements, including precautionary statements

    Pictogram(s)
    Signal word

    Danger

    Hazard statement(s)

    H301 Toxic if swallowed

    H361 Suspected of damaging fertility or the unborn child

    Precautionary statement(s)
    Prevention

    P264 Wash ... thoroughly after handling.

    P270 Do not eat, drink or smoke when using this product.

    P203 Obtain, read and follow all safety instructions before use.

    P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...

    Response

    P301+P316 IF SWALLOWED: Get emergency medical help immediately.

    P321 Specific treatment (see ... on this label).

    P330 Rinse mouth.

    P318 IF exposed or concerned, get medical advice.

    Storage

    P405 Store locked up.

    Disposal

    P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.

    Other hazards which do not result in classification

    no data available

    Handling and Storage

    Precautions for safe handling

    Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.

    Conditions for safe storage, including any incompatibilities

    Store the container tightly closed in a dry, cool and well-ventilated place. Store apart from foodstuff containers or incompatible materials.

  • Seller Information
    Business Type:

    Trader

    Main Products:

    Pharmaceuticals,Peptide,Cosmetics,Nutritional Supplements

    Location:

    Rm. 803, Tower 4, LOFT49 Creative City Pioneer Zone, No.88 Jiru Rd. Gongshu Dist., Hangzhou, 310015 ZJ, China

    Payment Terms:

    TT against copy of documents,D/P,L/C,D/A,O/A,TT against B/L draft before shipment,100% TT in advance

    Average lead Time:

    10

    Total Annual Revenue:

    $5 million-$10 million

    Total Employees:

    11-50

    Year of Establishment:

    2013

    Certifications:

    Certification Report by Bureau Veritas

    About HyperChem

    Established in 2013, Hyper Chem has exclusive tie-ups with leading manufacturers, supplying raw materials produced in GMP and ISO 9002 certified facilities, and provides high-quality ingredients and raw materials to meet the needs of a diverse range of pharmaceutical cosmetics ingredients and nootropic supplements companies worldwide.

    Our Competitiveness

    One-stop supply

    Wide Range Of products including pharmaceutical, Cosmetic Ingredients and nootropic supplements

    Among all the pharmaceuticals,

    90% of them with GMP certificates,

    85% of them with DMF files and

    50% of them passed FDA approval,

    30% get CEP certificate

    20% are new R&D products.

    Custom Repackaging Service


    We can efficiently repackage your material into sample sizes, custom batch-specific sizes, or semi-bulk package sizes according to your specifications. And ensures the product is packaged in a quality-controlled environment and will maintain its integrity throughout every stage of the process.

    Quality Control/Quality Assurance


    HyperChem is committed to delivering on its promises of top-quality products with verified quality data.

    All materials are vigorously inspected by the factory and/or outsourced analytical laboratories to ensure each and every lot meets or exceeds our reference standards.

    Trade assurance service with 100% payment protection, It is best achieved by delivering products and services 100% right the first time, on time, every time.

    Professional

    Transparent Communication

    Fast Reaction,

    Professional Suggestion

    Beyond Expectation.

    We have exclusive partnerships with research and production facilities across the country and we offer varied pharmaceutical services in the most cost-efficient way. The production facilities are GMP, WHO-GMP, EU GMP and US FDA approved and are backed by strong regulatory support such as Dossier, DMF, Tech Pack and relevant Stability studies for regulatory filings.

  • Inquiry History
    35 Inquiries
    Country Product Purchase Quantity Date Posted
    United States

    Prostaglandin E1 CAS 745-65-3

    1 G Aug 7, 2026
    Spain

    Factory supply Pure Alprostadil powder CAS 745-65-3 Prostaglandin E1 pge1

    10 G Dec 20, 2024
    Egypt

    Pharmaceutical Raw Material Powder Prostaglandin E1 Alprostadil 745-65-3 99.9% powder

    10 KG Oct 7, 2023
    Turkey

    Pharmaceutical Raw Material Powder Prostaglandin E1 Alprostadil 745-65-3 99.9% powder

    1000 G Nov 13, 2023
    United States

    PGE1

    1 G Feb 11, 2025
    Philippines

    Alprostadil

    100 MG Aug 20, 2026
    United States

    Alprostadil

    1 MT May 12, 2026
    Philippines

    Alprostadil

    100 MG Apr 27, 2026
    United States

    alprostadil

    10 MG Apr 20, 2026
    United States

    Prostaglandin E1

    50 MG Mar 27, 2026
    United States

    Alprostadil

    1 G Mar 17, 2026
    Australia

    Alprostadil

    Jan 29, 2026
    United Kingdom

    Alprostadil

    10 MG Nov 21, 2025
    United Kingdom

    alprostadil

    100 MG Nov 17, 2025
    Philippines

    Alprostadil poedet

    100 MG Aug 6, 2025
    United States

    PGE1 powder

    1 G Jul 20, 2025
    South Korea

    (11α,​13E,​15S)​-11,15-Dihydroxy-9-oxoprost-13-en-1-oic acid

    10 G Aug 13, 2024
    South Africa

    prostaglandin e1

    1 MT Mar 21, 2024
    Brazil

    alprostadil

    21 G Apr 24, 2026
    Canada

    Alprostadil

    5 MT Mar 26, 2026
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