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Home > Pharmaceutical Intermediates > Anticonvulsants > N1-[(2E)-3,7-Dimethyl-2,6-octadien-1-yl]-N2-tricyclo[3.3.1.13,7]dec-2-yl-1,2-ethanediamine for Sale > Cenobamate API - High Purity Antiepileptic Drug for Partial-Onset Seizure Treatment.
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Cenobamate API - High Purity Antiepileptic Drug for Partial-Onset Seizure Treatment.

Unit Price: Get Latest Price
CAS No.:

502487-67-4

Grade:

Pharmaceutical Grade

Content:

98%

Port:

Hefei

Brand:

Lifang

Packaging:

2kg/drum (tentative)

Price valid (until):

2025-09-26

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

Felodipine,Nifedipine,Bempedoic Acid,Doxazosin mesylate,Ivabradine hydrochloride,Azilsartan KaMedoxomil

  • Product Description

  • Seller Information

  • Description


       Product Detail   


    Cenobamate (CAS: 913088-80-9) is a novel, high-purity Active Pharmaceutical Ingredient (API) used as a next-generation antiepileptic drug. It is specifically indicated for the treatment of partial-onset seizures in adults, offering a new therapeutic option for patients with uncontrolled epilepsy. Manufactured by Hefei Lifeon Pharmaceutical under strict cGMP guidelines, our Cenobamate API guarantees exceptional quality, consistency, and reliability for your formulation development and commercial production needs.

    Shop Cenobamate API - High Purity Antiepileptic Drug for Partial-Onset Seizure Treatment.-Detailed Image 1 Shop Cenobamate API - High Purity Antiepileptic Drug for Partial-Onset Seizure Treatment.-Detailed Image 2

    Items Specifications
    Product Name Cenobamate
    generic name YKP3089
    IUPAC Name (1R)-1-[(2S)-2-Hydroxybutanoyl]-2-methoxyethyl carbamate
    Molecular Weight 233.26 g/mol
    Solubility Slightly soluble in water, soluble in organic solvents
    Melting Point 98-102℃


      company profile


    Founded in 2002, Hefei Lifeon Pharmaceutical Co., Ltd. was successfully listed on the main board of Shenzhen Stock Exchange in December 2020 (stock code: 003020). Now it has six pharmaceutical industrial enterprises and one chain pharmacy. It is an innovative pharmaceutical enterprise integrating drug R&D, manufacturing and commercialization, and its products involve cardiovascular, central nervous system, digestive system, topical skin medicine and ophthalmology. It won the title of "China Pharmaceutical Industry's Most Valuable Enterprise" twice, and was selected as "China Chemical Pharmaceutical Industry's Top 100 Enterprises with Comprehensive Strength" for eight consecutive years.
    It has been committed to the development and industrialization of osmotic pump technology for a long history. Lifeon’s internationally pioneering formulation technology of insoluble single-layer core osmotic pump won the first prize of Anhui Science and Technology Award. Till now, Its listed products and the industrialization ability are in the leading position in China.
    At the same time, in order to build a differentiated competitive advantage, the company has laid out moat products with higher policies and regulations limitations:
    Psychotropic drugs.
    Lifeon Pharma is one of the few designated manufacturers of psychotropic drugs and narcotic drugs in China.
    Modern Chinese Tradition Medicine
    Lifeon Pharma inherits modern Chinese medicine with clear innovative components and clear mechanism in the field of Chinese medicine.
    High-end long-acting complex injections
    Lifeon Pharma actively explores the field of high-end long-acting complex injections.
    Hefei Lifeon Pharma has formed a product pipeline with distinctive characteristics and strong market competitiveness.
    Hefei Lifeon Pharma has five industrial bases, including its own factory, Chengzhi Bio, Dayu Pharmaceutical, Jiufang Pharmaceutical and Noratec Pharmaceutical. The company has established 33 GMP production lines, including tablets, granules, capsules, ointments, gels, APIs, oral solutions, and traditional Chinese medicine extraction. Among them, the osmotic pump workshop can achieve an annual output of 1.4 billion tablets.
    In the future, Hefei Lifeon Pharma will continue to give full play to the advantages of osmotic pump technology platform, refined anti-psychotic and modern Chinese medicine, intensively cultivate and create the differentiated advantage of "specialization and novelty", provide high-quality medical products and services, and make greater contributions to healthy China.Shop Cenobamate API - High Purity Antiepileptic Drug for Partial-Onset Seizure Treatment.-Detailed Image 3 Shop Cenobamate API - High Purity Antiepileptic Drug for Partial-Onset Seizure Treatment.-Detailed Image 4

    Shop Cenobamate API - High Purity Antiepileptic Drug for Partial-Onset Seizure Treatment.-Detailed Image 5 Shop Cenobamate API - High Purity Antiepileptic Drug for Partial-Onset Seizure Treatment.-Detailed Image 6 Shop Cenobamate API - High Purity Antiepileptic Drug for Partial-Onset Seizure Treatment.-Detailed Image 7

    Our innovation is driven by a strategic focus on attracting and nurturing top talent.

    • Introduction:  We recruit top-tier domestic and international experts in fields like drug delivery technology, monoclonal antibodies, and chemical synthesis.

    • Cultivation:  We implement structured mentorship and training programs to foster innovation and career growth within our R&D teams.

    • Collaboration:  We maintain long-term partnerships with external domain experts to integrate advanced intellectual resources directly into our projects.

    Frequently Asked Questions (FAQs)

    Q1: What is Lifeon Pharma’s core competitive advantage?

    A: Lifeon specializes in osmotic pump controlled-release technology, with internationally leading expertise in single-layer core formulations. We are one of China’s largest manufacturers of osmotic pump tablets, with an annual capacity of 1.4 billion tablets. Our product portfolio spans cardiovascular, CNS, diabetes, dermatology, and oncology, supported by 33 GMP production lines and two advanced API manufacturing sites.

    Q2: Are your manufacturing facilities compliant with international standards?

    A: Yes. Our facilities are fully cGMP-compliant, and we have passed multiple U.S. FDA audits (e.g., for DMSA in November 2024). We also hold certifications such as National High-Tech Enterprise and Anhui Province Pharmaceutical Quality Award, and we operate in accordance with ISO quality management systems.

    Q3: What product documentation can you provide?

    A: We provide comprehensive support documents including:

    Certificate of Analysis (CoA)

    GMP Compliance Certificate

    Stability Study Data

    Process Validation Reports

    Material Safety Data Sheet (MSDS)
    Customized documentation can be prepared upon request.

    Q4: Do you offer custom synthesis or contract manufacturing services?

    A: Yes. We offer custom synthesis of APIs and intermediates, and contract manufacturing for both APIs and finished dosage forms. Our strong R&D team and flexible production lines allow us to support projects from development to commercial scale.

    Q5: What is your minimum order quantity (MOQ)?

    A: MOQ is negotiable depending on the product and order frequency. We are flexible to accommodate both small-scale development batches and large commercial volumes.

    Q6: How do you ensure supply chain reliability?

    A: We have a robust dual-site production strategy with two dedicated API facilities. Our vertically integrated supply chain—from raw materials to finished products—ensures consistent supply. We also maintain long-term partnerships with reliable logistics providers to guarantee on-time delivery.

    Q7: What is your typical lead time?

    A: For commercial products in stock, lead time is generally 2–4 weeks. For custom projects or new synthesis, lead times will be confirmed based on project scope.

    Q8: Which markets do you currently serve?

    A: We supply APIs and finished products to domestic Chinese markets and have growing exports to Asia, Latin America, the Middle East, and Europe. Our products are well-positioned for both generic and branded drug markets.

    Q9: Can you supply products in accordance with USP/EP/ChP standards?

    A: Yes. Our products can be manufactured and released to meet USP, EP, ChP, or customer-specific standards. Quality and compliance are tailored to target market requirements.

    Q10: How does Lifeon support customers technically?

    A: We offer:

    Technical data packages

    Regulatory support for drug master files (DMFs)

    Formulation development assistance

    Ongoing process optimization support Our team includes PhD-level scientists and experienced engineers ready to collaborate.


    Business photos


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    Basic Info
    Product Name:

    N1-[(2E)-3,7-Dimethyl-2,6-octadien-1-yl]-N2-tricyclo[3.3.1.13,7]dec-2-yl-1,2-ethanediamine

    Other Name:

    1,2-Ethanediamine,N1-[(2E)-3,7-dimethyl-2,6-octadien-1-yl]-N2-tricyclo[3.3.1.13,7]dec-2-yl-;1,2-Ethanediamine,N-[(2E)-3,7-dimethyl-2,6-octadienyl]-N′-tricyclo[3.3.1.13,7]dec-2-yl-;N1-[(2E)-3,7-Dimethyl-2,6-octadien-1-yl]-N2-tricyclo[3.3.1.13,7]dec-2-yl-1,2-ethanediamine;SQ 109;NSC 722041

    CAS No.:

    502487-67-4

    Molecular Formula:

    C22H38N2

    InChIKeys:

    InChIKey=JFIBVDBTCDTBRH-REZTVBANSA-N

    Exact Mass:

    330.55

    Categories:

    Anticonvulsants

    Characteristics
  • Seller Information
    Business Type:

    Manufactory

    Main Products:

    Felodipine,Nifedipine,Bempedoic Acid,Doxazosin mesylate,Ivabradine hydrochloride,Azilsartan KaMedoxomil

    Location:

    LIFANG FACTORY ,NO.669,CHANGJIANG ROAD WEST, HEFEI CITY

    Payment Terms:

    TT against copy of documents,100% TT in advance

    Average lead Time:

    15

    Total Annual Revenue:

    Above $100 million

    Total Employees:

    501-1000

    Year of Establishment:

    2002

    Founded in 2002, Hefei Lifeon Pharmaceutical Co.,Ltd. is a joint-stock enterprise integrating drug R&D, manufacturing and sales. It owns 5 pharmaceutical industrial enterprises and 1 pharmaceutical retail chain enterprise. It covers the full range of production including APIs, traditional Chinese medicine extracts, Chinese patent medicines and chemical pharmaceutical preparations, etc. Moreover, Lifeon has the largest osmotic pump preparation production base in China.

    In 2013, the post-doctoral research workstation officially started operation.

    In 2018, Succimer API passed FDA inspection with zero deficiencies.

    In 2020, Lifeon listed on Shenzhen Stock Exchange.

    In 2023, a new API factory called Hefei Dayu Pharmaceutical Co.,Ltd obtained the DML and started production.

    In 2024, Doxazosin Mesylate, and Prilocaine APIs passed NMPA GMP inspection. Succimer API received renewed FDA certification. Completed registration applications for 6 API varieties within the same year.

    In the past 23 years, Lifeon has obtained numerous honors, including national high-tech enterprise, innovative enterprise in Anhui Province, enterprise technology center in Anhui Province, engineering technology research center for sustained and controlled release of drugs in Anhui Province, etc. For eight consecutive years, it has been selected as one of the “China's Top 100 Chemical and Pharmaceutical Industrial Enterprises with Comprehensive Strength”.


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