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High Quality Crizotinib CAS 877399-52-5 Powder Fast Shipping Best Price

2 Inquiries

Unit Price: Get Latest Price
CAS No.:

877399-52-5

Grade:

Pharmaceutical Grade

Content:

99.5%

Port:

Hangzhou

Brand:

HyperChem

Packaging:

1kg/Bag

Price valid (until):

2025-12-28

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

Pharmaceuticals,Peptide,Cosmetics,Nutritional Supplements

  • Product Description

  • Seller Information

  • Inquiry History

  • Description

    Name

    Crizotinib

    CAS number

    877399-52-5

    Synonym

    Carboprost Tromethamine; 58551-69-2

    Description

    Levothyroxine, also known as L-Thyroxine, is hormone derived from the thyroid gland. Levothyroxine therapy is used in case of deficiency of the thyroid hormones in the human organism. Thyroxine is synthesized via the iodination of tyrosines (monoiodotyrosine) and the coupling of iodotyrosines (diiodotyrosine) in the thyroglobulin. Thyroxine is released from thyroglobulin by proteolysis and secreted into the blood.

    Structure

    Shop High Quality Levothyroxine Sodium CAS 55-03-8 Powder Fast Shipping Good Price-Detailed Image 1

    Molecular Formula

    C22H24ClFN4O3

    Molecular Weight

    446.9 g/mol

    Appearance

    White Powder

    Quality Standard

    99%

    Shipping Condition

    Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

    Storage Condition

    Dry, dark and at 2~8 ℃ for short term (days to weeks) or -20 ℃ for long term (months to years).

    Shelf Life

    >2 years if stored properly

    Sample package

    Aluminium foil bag, Bottle

    Commercial package

    Aluminium Tin

    Origin

    China

    Crizotinib More Info

    Carboprost Tromethamine is a synthetic prostaglandin analog primarily used in obstetrics and gynecology. It is known for its uterotonic properties and is mainly employed to manage specific complications of pregnancy.

     

    Mechanism of Action

    Carboprost Tromethamine works by mimicking the action of prostaglandins, which are naturally occurring compounds in the body that have various roles, including:

     

    Uterine Contractility: It stimulates uterine contractions, helping to expel contents from the uterus.

    Cervical Ripening: Carboprost may assist in softening and dilating the cervix, facilitating labor and delivery.

    Hemostasis: By inducing contractions, it can help reduce postpartum hemorrhage by constricting blood vessels and promoting uterine involution.

    Indications

    Carboprost Tromethamine is indicated for:

     

    Postpartum Hemorrhage: It is used to treat severe bleeding after childbirth when conventional methods have failed to control the bleeding.

    Termination of Pregnancy: It is used for the elective termination of pregnancy in the second trimester and in cases of fetal demise.

    Induction of Labor: In specific situations, it may be employed to induce labor in patients who meet certain medical criteria.

    Dosage and Administration

    Carboprost is usually administered by a healthcare professional:

     

    Postpartum Hemorrhage: The recommended dosage is typically 250 micrograms (0.25 mg) given intramuscularly, which may be repeated every 15-90 minutes as needed, with a maximum cumulative dose of 2 mg.

    Termination of Pregnancy: For medical termination, the usual dose is 800 micrograms (0.8 mg), administered intramuscularly, preferably repeated at regular intervals according to clinical protocols.

    Induction of Labor: Dosing protocols may vary based on hospital guidelines and individual patient circumstances.

    Side Effects

    Common side effects associated with carboprost may include:

     

    Gastrointestinal Symptoms: Nausea, vomiting, diarrhea, and abdominal cramping are frequent adverse reactions.

    Uterine Hypertonicity: Excessive uterine contractions can occur, leading to potential complications.

    Fever and Chills: Some patients may experience transient fever or chills following administration.

    Allergic Reactions: Though rare, anaphylactic reactions are possible.

    Contraindications

    Carboprost Tromethamine should be avoided in certain conditions, including:

     

    Active Liver Disease: Patients with liver disease may experience adverse effects due to impaired metabolism.

    Asthma: Use in patients with a history of asthma or significant respiratory issues should be approached with caution, as prostaglandins can cause bronchospasm.

    Pelvic Inflammatory Disease: Patients with active pelvic infections should not receive this medication.

    Drug Interactions

    Carboprost may interact with other medications. Caution should be exercised when used with:

     

    Uterotonics: Concurrent use with other uterotonics may increase the risk of uterine hyperstimulation.

    Blood Pressure Medications: Since carboprost can affect vascular tone, its use with antihypertensive drugs requires careful monitoring.

    Safety and Precautions

    Key safety considerations include:

     

    Monitoring: Patients receiving carboprost should be monitored closely for signs of excessive uterine activity, bleeding, or adverse reactions.

    Emergency Preparedness: Healthcare providers should be prepared to manage potential complications, including severe hypotension or respiratory distress.

    Regulatory Status

    Carboprost Tromethamine is approved by various health regulatory authorities for use in obstetric practice, and it is included in treatment guidelines for managing postpartum hemorrhage and aspects of labor induction.

     

    Conclusion

    Carboprost Tromethamine is a valuable medication in managing postpartum hemorrhage and facilitating labor. Its ability to induce uterine contractions and promote cervical ripening makes it critical in obstetric care. Careful administration, monitoring, and awareness of contraindications and side effects are essential for ensuring patient safety and efficacy in treatment.


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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.

    ECHEMI Editorial Reference
    Crizotinib is a potent inhibitor of c-Met and ALK with an IC50 of 11 nM and 24 nM in cell-based assays, respectively.
    Crizotinib is a 3-[1-(2,6-dichloro-3-fluorophenyl)ethoxy]-5-[1-(piperidin-4-yl)pyrazol-4-yl]pyridin-2-amine that has R configuration at the chiral centre. The active enantiomer, it acts as a kinase inhibitor and is used for the treatment of patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) It has a role as an antineoplastic agent, a biomarker and an EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor. It is an enantiomer of an ent-crizotinib.|Crizotinib an inhibitor of receptor tyrosine kinase for the treatment of non-small cell lung cancer (NSCLC). Verification of the presence of ALK fusion gene is done by Abbott Molecular's Vysis ALK Break Apart FISH Probe Kit. This verification is used to select for patients suitable for treatment. FDA approved in August 26, 2011.|Crizotinib is a Kinase Inhibitor. The mechanism of action of crizotinib is as a Cytochrome P450 3A Inhibitor, and Receptor Tyrosine Kinase Inhibitor, and Cytochrome P450 2B6 Inhibitor, and P-Glycoprotein Inhibitor, and Organic Cation Transporter 1 Inhibitor, and Organic Cation Transporter 2 Inhibitor.|Crizotinib is a selective tyrosine kinase receptor inhibitor used in the therapy of selected cases of advanced non-small cell lung cancer. Crizotinib is associated with transient elevations in serum aminotransferase levels during treatment and rare instances of clinically apparent acute liver injury that can be severe and even fatal.|Crizotinib is an orally available aminopyridine-based inhibitor of the receptor tyrosine kinase anaplastic lymphoma kinase (ALK) and the c-Met/hepatocyte growth factor receptor (HGFR) with antineoplastic activity. Crizotinib, in an ATP-competitive manner, binds to and inhibits ALK kinase and ALK fusion proteins. In addition, crizotinib inhibits c-Met kinase, and disrupts the c-Met signaling pathway. Altogether, this agent inhibits tumor cell growth. ALK belongs to the insulin receptor superfamily and plays an important role in nervous system development. ALK dysregulation and gene rearrangements are associated with a series of tumors.|A piperidine and aminopyridine derivative that acts as an inhibitor of RECEPTOR PROTEIN-TYROSINE KINASES, including ANAPLASTIC LYMPHOMA KINASE (ALK) and HEPATOCYTE GROWTH FACTOR RECEPTOR (HGFR; c-Met). It is used in the treatment of NON-SMALL CELL LUNG CANCER.

    Basic Info
    Product Name:

    Crizotinib

    Other Name:

    2-Pyridinamine,3-[(1R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy]-5-[1-(4-piperidinyl)-1H-pyrazol-4-yl]-;3-[(1R)-1-(2,6-Dichloro-3-fluorophenyl)ethoxy]-5-[1-(4-piperidinyl)-1H-pyrazol-4-yl]-2-pyridinamine;[3-[[(R)-1-(2,6-Dichloro-3-fluorophenyl)ethyl]oxy]-5-[1-(piperidin-4-yl)-1H-pyrazol-4-yl]pyridin-2-yl]amine;PF 2341066;PF 02341066;Crizotinib;(R)-3-[1-(2,6-Dichloro-3-fluorophenyl)ethoxy]-5-(1-piperidin-4-yl-1H-pyrazol-4-yl)pyridin-2-ylamine;Xalkori;3-((R)-1-(2,6-Dichloro-3-fluorophenyl)ethoxy)-5-(1-(piperidin-4-yl)-1H-pyrazol-4-yl)pyridin-2-amine;912279-98-2

    CAS No.:

    877399-52-5

    Molecular Formula:

    C21H22Cl2FN5O

    InChIKeys:

    InChIKey=KTEIFNKAUNYNJU-GFCCVEGCSA-N

    Molecular Weight:

    450.343

    Exact Mass:

    450.34

    EC Number:

    1308068-626-2

    UNII:

    53AH36668S

    NSC Number:

    749005

    NCI Thesaurus Code:

    C74061

    ATC Code:

    L01XE16|L - Antineoplastic and immunomodulating agents

    HScode:

    29333990

    Categories:

    Other Chemical Drugs

    Characteristics
    PSA:

    78

    XLogP3:

    3.7

    Density:

    1.5±0.1 g/cm3

    Melting Point:

    192 °C

    Boiling Point:

    599.177°C at 760 mmHg

    Flash Point:

    316.2±30.1 °C

    Refractive Index:

    1.673

    Hazard Identification

    Classification of the substance or mixture

    Skin sensitization, Category 1

    Eye irritation, Category 2

    Germ cell mutagenicity, Category 2

    Hazardous to the aquatic environment, short-term (Acute) - Category Acute 1

    GHS label elements, including precautionary statements

    Pictogram(s)
    Signal word

    Warning

    Hazard statement(s)

    H317 May cause an allergic skin reaction

    H319 Causes serious eye irritation

    H341 Suspected of causing genetic defects

    H400 Very toxic to aquatic life

    Precautionary statement(s)
    Prevention

    P261 Avoid breathing dust/fume/gas/mist/vapours/spray.

    P272 Contaminated work clothing should not be allowed out of the workplace.

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

    P264 Wash ... thoroughly after handling.

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

    P273 Avoid release to the environment.

    Response

    P302+P352 IF ON SKIN: Wash with plenty of water/...

    P333+P317 If skin irritation or rash occurs: Get medical help.

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

    P362+P364 Take off contaminated clothing and wash it before reuse.

    P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.

    P318 IF exposed or concerned, get medical advice.

    P391 Collect spillage.

    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 days

    Total Annual Revenue:

    $5 million-$10 million

    Total Employees:

    11-50

    Year of Establishment:

    2013

    Company Certificates
    • Hangzhou Hyper Chemicals LimitedCertification Report by Bureau Veritas 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
    2 Inquiries
    Country Product Purchase Quantity Date Posted
    Russia

    Wholesale Crizotinib Raw Material Powder 99% White Powder CAS 877399-52-5 Crizotinib Powder

    50 KG Nov 19, 2023
    Pakistan

    Crizotinib

    1 KG Jun 20, 2025
    Post an enquiry for this product
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