A robust pharmaceutical supply chain is built on the foundation of reliable sourcing for Active Pharmaceutical Ingredients (APIs) and their essential intermediates. The quality and consistent availability of these precursors directly impact the production capacity and market readiness of vital medications. NINGBO INNO PHARMCHEM CO.,LTD. plays a crucial role in this ecosystem by providing high-purity Baricitinib intermediates, such as the compound 4-(1H-Pyrazol-4-yl)-7-((2-(Trimethylsilyl)Ethoxy)Methyl-7H-Pyrrolo[2,3-d]Pyrimidine (CAS 941685-27-4).
Baricitinib, a key therapeutic agent for conditions like rheumatoid arthritis and alopecia areata, requires meticulously synthesized intermediates to ensure the final API meets stringent pharmaceutical standards. Our Baricitinib intermediate is manufactured with a focus on purity and consistency, typically presented as a liquid with a purity level exceeding 98%. This adherence to quality in pharmaceutical intermediate synthesis is critical for our clients, allowing them to maintain production timelines and meet regulatory requirements for drugs targeting autoimmune diseases and other critical health issues.
NINGBO INNO PHARMCHEM CO.,LTD. recognizes that the pharmaceutical landscape is constantly evolving, with new research and development projects emerging regularly. To support this innovation, we offer comprehensive custom synthesis services. This allows pharmaceutical companies to procure bespoke chemical entities, including specialized Baricitinib intermediates or novel compounds, tailored to their specific R&D needs. Our custom synthesis capabilities are designed to accelerate the drug discovery and development process, providing researchers with the precisely engineered molecules they require.
By partnering with NINGBO INNO PHARMCHEM CO.,LTD., pharmaceutical companies gain a reliable ally in their supply chain management. We are committed to ensuring a stable and dependable source of critical intermediates, thereby facilitating the continuous production of essential medications. Our dedication to high-quality pharmaceutical intermediate synthesis, coupled with our responsive custom services, makes us an ideal partner for companies aiming to secure their API supply chains and bring innovative therapies to patients worldwide.
Manufacturing Facilities
Professional Export Experience
to Global Customers
1. 20 years of R&D, manufacturing and sales experience, serving customers in 60 countries and regions around the world;
2. Own R&D laboratory, pilot platform and large-scale production workshop, which can meet the audit requirements of global customers;
3. We can satisfy customers' perfect transition from small scale lab requirements (gram level) to commercialization requirements (hundred tons level).
A: We don't have Minimum Order Quantity, exact quantity should be provided before quotation for us to calculate the exact cost.
A: We don't provide free samples due to lots of request and expensive international courier's cost, we can deduct the sample charge after commercial order placed.
A: Our payment terms: Small or sample order: T/T IN ADVANCE. Commercial order: First order should be by T/T IN ADVANCE or L/C at sight, and following orders T/T 30~90days is acceptable subject to approval of credit application.