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Home > Pharmaceutical Intermediates > Antispasticity Agents > Levocetirizine dihydrochloride for Sale > 99% High Purity USP Pharmacy Grade Levocetirizine Dihydrochloride With Fast Delivery
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99% High Purity USP Pharmacy Grade Levocetirizine Dihydrochloride With Fast Delivery

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Unit Price: Get Latest Price
CAS No.:

130018-87-0

Grade:

Pharmaceutical Grade

Content:

99%

Port:

SHANGHAI

Brand:

HyperChem

Packaging:

1kg/Bag, 25kg/drum

Price valid (until):

2025-12-19

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

Pharmaceuticals,Peptide,Cosmetics,Nutritional Supplements

  • Product Description

  • Seller Information

  • Inquiry History

  • Description

    Name

    Levocetirizine dihydrochloride

    CAS number

    130018-87-0

    Description

    Levocetirizine dihydrochloride is a selective second-generation antihistamine and the active enantiomer of cetirizine, identified by the CAS Registry Number 130018-87-0.

    Structural formula

     Shop 99% High Purity USP Pharmacy Grade Levocetirizine Dihydrochloride With Fast Delivery-Detailed Image 1

    Molecular Formula

    C21H27Cl3N2O3

    Molecular Weight

    461.81 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

    Levocetirizine dihydrochloride More Info

    Levocetirizine dihydrochloride is a selective second-generation antihistamine and the active enantiomer of cetirizine, identified by the CAS Registry Number 130018-87-0. Its molecular structure is characterized by the R-enantiomer configuration, which is responsible for its potent pharmacological activity. The compound is formulated as a dihydrochloride salt to enhance its stability, crystallinity, and solubility for pharmaceutical development, typically appearing as a white to off-white powder.

     

    The mechanism of action for this pharmaceutical involves potent and selective antagonism of the peripheral H1 histamine receptors. By competitively blocking the binding of histamine to these receptors, it effectively inhibits the cascade of inflammatory and allergic responses triggered by this mediator. Its high specificity for peripheral receptors, coupled with a low affinity for central nervous system receptors, results in powerful anti-allergic effects with a minimal propensity for causing sedation, a common limitation of first-generation antihistamines.

     

    The primary clinical application of levocetirizine is the symptomatic relief of allergic conditions. It is extensively prescribed for the management of seasonal and perennial allergic rhinitis, providing relief from symptoms such as sneezing, rhinorrhea, and nasal itching. It is also highly effective in treating chronic idiopathic urticaria, reducing the occurrence and severity of hives and associated pruritus, thereby significantly improving patients' quality of life.

     

    This medication is administered orally and is available in various formulations, including immediate-release and orally disintegrating tablets, as well as oral solutions for pediatric use. It demonstrates rapid absorption and a high bioavailability, with its peak plasma concentration achieved within a short time after ingestion. A key pharmacokinetic advantage is its low metabolic turnover, being predominantly excreted unchanged by the renal system, which minimizes the potential for drug-drug interactions mediated by hepatic enzymes.

     

    The safety profile of levocetirizine is generally favorable and well-tolerated by most patients. The most commonly reported adverse effects are typically mild and may include headache, dry mouth, and occasional somnolence, though the incidence of sedation is notably lower than that associated with its racemic parent compound, cetirizine. Due to its renal pathway of elimination, dosage adjustment is recommended for patients with moderate to severe renal impairment to prevent potential accumulation and an increased risk of adverse effects.

     


    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.




    Certificates

    Basic Info
    Product Name:

    Levocetirizine dihydrochloride

    Other Name:

    Acetic acid,2-[2-[4-[(R)-(4-chlorophenyl)phenylmethyl]-1-piperazinyl]ethoxy]-,hydrochloride (1:2);Acetic acid,[2-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]ethoxy]-,dihydrochloride,(R)-;Acetic acid,[2-[4-[(R)-(4-chlorophenyl)phenylmethyl]-1-piperazinyl]ethoxy]-,dihydrochloride;Levocetirizine dihydrochloride;Xusal;Xyzal;Xyzall;UCB 28556;(R)-Cetirizine dihydrochloride;(R)-(-)-Cetirizine hydrochloride;Allercet;Lezyncet;Allear

    CAS No.:

    130018-87-0

    Molecular Formula:

    C21H25ClN2O3.2ClH

    InChIKeys:

    InChIKey=PGLIUCLTXOYQMV-GHVWMZMZSA-N

    Molecular Weight:

    461.81

    Exact Mass:

    460.108734

    EC Number:

    200-659-6

    UNII:

    W69HSF2416

    DSSTox ID:

    DTXSID60231691

    HScode:

    29335990

    Categories:

    Antispasticity Agents

    Characteristics
    PSA:

    53

    XLogP3:

    4.62800

    Appearance:

    white or off-white crystalline powder

    Melting Point:

    215-220°C

    Boiling Point:

    542.1°C at 760 mmHg

    Flash Point:

    281.6ºC

    Water Solubility:

    H2O: ≥23mg/mL

    Storage Conditions:

    room temp

    Specific rotation:

    D25 -12.79° (c = 1 in water)

    Hazard Identification

    Classification of the substance or mixture

    Acute toxicity - Category 4, Oral

    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)

    H302 Harmful if swallowed

    H400 Very toxic to aquatic life

    Precautionary statement(s)
    Prevention

    P264 Wash ... thoroughly after handling.

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

    P273 Avoid release to the environment.

    Response

    P301+P317 IF SWALLOWED: Get medical help.

    P330 Rinse mouth.

    P391 Collect spillage.

    Storage

    none

    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
    2 Inquiries
    Country Product Purchase Quantity Date Posted
    Norway

    Levocetirizine dihydrochloride

    50 KG Nov 18, 2025
    India

    Levocetrizine Hydrochloride

    100.00 G Mar 7, 2025
    Post an enquiry for this product
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