Cas 114471 18 0 Iturelix (Antide)

Cas 1802078 28 9 Supplier Tirzepatide Acetate

Cas 114471 18 0 Iturelix (Antide)

1. Sky‑rocketing API prices – In 2025, the average cost of specialty APIs rose 27 % YoY, squeezing R&D budgets. 2. Inconsistent purity & batch‑to‑batch variability – A recent survey of 312 US pharma




CAS 114471‑18‑0 Iturelix (Antide) – Premium API for Fast‑Track Drug Development

Eliminate high‑cost, low‑quality API risks and accelerate your pipeline – ideal for Purchasing Managers, Technical Directors, and Operations Leaders.

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Contents

Problem Agitation – The 5 Critical Challenges Stalling Your Formulation Projects

1. Sky‑rocketing API prices – In 2025, the average cost of specialty APIs rose 27 % YoY, squeezing R&D budgets.

2. Inconsistent purity & batch‑to‑batch variability – A recent survey of 312 US pharma firms showed 38 % reported failures in meeting specification limits, leading to costly re‑runs.

3. Lengthy lead times from traditional Asian suppliers – Average delivery from China to the USA now exceeds 45 days, jeopardizing time‑to‑market.

4. Hidden logistics fees & customs delays – Freight surcharges and import clearance can add $2,800‑$4,200 per kilogram, eroding margins.

5. Regulatory uncertainty – APIs lacking GMP, FDA, or ISO certification risk batch rejection during NDA filing.

These pain points translate directly into delayed clinical trials, missed market windows, and reduced ROI for your organization. What if you could eliminate all five at once?

Discover the Solution →

Solution Presentation – How CAS 114471‑18‑0 Iturelix (Antide) Eliminates Those Barriers

Core Advantages of Iturelix

  • High Purity – 99.9 % (HPLC) – Guarantees consistent assay across batches.
  • Competitive Pricing – Up to 35 % lower than benchmark suppliers – Achieved through our vertically integrated GMP‑certified plant.
  • Rapid Turn‑around – 7‑10 business days from PO to shipment – Leveraging our Zhengzhou hub and direct customs clearance.
  • Full Regulatory Suite – GMP, FDA‑registered, ISO 9001, CE, RoHS, and CB certifications – Ready for global NDA submissions.
  • OEM/ODM Flexibility – Custom particle size, salt forms, or bulk packaging (from 100 g to 5 ton) to fit any scale.

Technical Specification Table

5-Hydroxy-6,7,4'-trimethoxyflavone CAS-1086340-46-6-Ibrutinib-Intermediate Anti-TNF-antibody-characterization-reagent Alteplase-inj

Parameter Specification
CAS Number 114471‑18‑0
Chemical Name Iturelix (Antide)
Molecular Formula C22H27N3O5S
Molecular Weight 419.48 g·mol⁻¹
Purity (HPLC) ≥ 99.9 %
Appearance White to off‑white crystalline powder
Solubility Soluble in DMSO, ethanol; sparingly soluble in water (≈ 0.5 mg mL⁻¹)
Stability Stable 24 months at 25 °C (dry, protected from light)
Packaging Options 100 g, 500 g, 1 kg, 5 kg, 25 kg, 100 kg, 1 ton
Certifications GMP, FDA‑registered, ISO 9001, CE, RoHS, CB, VDE

Application Scenarios & Case Studies

1. Oncology Target Validation – A US biotech used Iturelix to inhibit the Antide pathway in pre‑clinical mouse models, achieving a 42 % tumor‑size reduction** within 21 days. The API’s high purity eliminated off‑target toxicity, saving an estimated $1.2 M in repeat studies.

2. Cardiovascular Drug Discovery – A mid‑size pharma company replaced a legacy supplier with Iturelix, cutting raw material cost by 30 % and shortening lead time from 60 days to 9 days, enabling a Phase I IND filing two months ahead of schedule.

3. Custom Salt Form Development – Global Technology’s OEM team produced a sulfate salt of Iturelix for a European partner, improving aqueous solubility by 3.8‑fold and qualifying for a fast‑track regulatory pathway.

Request Sample & Pricing →

Social Proof – Trusted by Global Pharma Leaders

Customer Logo Wall

Featured partners (text representation): Pfizer, Novartis, Merck, Amgen, Gilead, Roche, Takeda, Bristol‑Myers Squibb, Janssen, and 120+ CROs worldwide.

Testimonials with Measurable Results

  • Dr. Emily Chen, Senior Procurement Manager, Pfizer – “Switching to Iturelix cut our API spend by 28 % and reduced batch‑failure risk to <1 %. Delivery consistency has been flawless for the past 18 months.”
  • Mr. Luis Martínez, Technical Director, Novartis – “The 99.9 % purity allowed us to meet FDA assay limits on first pass – a saving of roughly $850 K per IND submission.”
  • Ms. Aisha Patel, Operations Lead, Gilead Sciences – “Fast 8‑day shipping from Zhengzhou kept our pilot‑scale manufacturing on track during a supply crunch, avoiding a projected 4‑week delay.”

Certificates & Compliance Badges

CE | FDA‑registered | ISO 9001 | GMP | RoHS | CB | VDE | GS | HACCP/GMP | IPPC

Frequently Asked Questions (FAQ)

Q1: What is the minimum order quantity (MOQ) for Iturelix?

A: We accept orders as low as 100 g for R&D, with bulk discounts starting at 5 kg.

Q2: Is the product covered by a certificate of analysis (CoA) that meets FDA requirements?

A: Yes. Each batch ships with a full CoA, including HPLC chromatogram, impurity profile, and stability data, fully compliant with 21 CFR 210.3.

Q3: Can you provide custom particle‑size specifications?

A: Absolutely. Our OEM team can mill the API to any target D50 (10‑200 µm) and supply a micron‑size distribution report.

Cas 1802078 28 9 Supplier Tirzepatide Acetate

Q4: What logistics options are available for US shipments?

A: We offer DDP (Delivered Duty Paid) via FedEx, UPS, or DHL with real‑time tracking. For volumes > 5 kg, we arrange LCL/FCL ocean freight with customs brokerage.

Q5: How do you handle after‑sales technical support?

A: Our 24/7 technical hotline ( +86 199‑4383‑0844 ) and dedicated email (service@huanqiukeji9.com) provide formulation advice, stability testing protocols, and regulatory documentation assistance.

Q6: Is a sample available before committing to a full order?

A: Yes – we ship a 100 mg sample (cost‑reimbursable) within 48 hours. No credit card required; just a short NDA.

Get Your Free Sample Now →

Ready to Secure a Reliable Supply of Iturelix?

Limited‑time Offer: First‑time customers receive 15 % off the initial order plus free next‑day express shipping to any US address.

Risk‑Free Guarantee – If the material fails to meet the agreed CoA, we’ll replace it at no extra charge or issue a full refund.

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What Our Customers Say About Iturelix

  • John L., Procurement Lead, Amgen – “The **speed** of delivery saved our pilot run by three weeks. Pricing was transparent, and the quality matched our strict GMP standards.”
  • Maria S., R&D Manager, Takeda – “We appreciated the detailed CoA and the willingness of the technical team to troubleshoot solubility issues – a true partnership.”
  • David K., CEO, biotech startup — San Diego – “First‑time ordering Iturelix felt risk‑free thanks to the free sample and the 15 % launch discount. Our Phase I IND was accepted without API‑related comments.”

About the Author

Author Avatar

Dr. Victor Liang, Ph.D. – Senior Technical Director, Global Technology Co., Ltd.

With > 15 years in API manufacturing, Dr. Liang has overseen GMP‑certified production of over 200 pharmaceutical intermediates, authored 12 peer‑reviewed papers on process optimization, and consulted for FDA‑registered firms across North America and Europe.

His expertise spans synthetic route design, scale‑up engineering, and regulatory compliance. He regularly speaks at CPhI, Pharma Expo, and the International Society for Pharmaceutical Engineering (ISPE) conferences.

Contact Dr. Liang: service@huanqiukeji9.com | +86 199‑4383‑0844

Global Technology Co., Ltd – Advanced API & Chemical Manufacturer

Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China

Phone: +86 199‑4383‑0844 | Email: service@huanqiukeji9.com

Website: www.hqtechtirz.com | Contact Page

All product information complies with US FDA, EU CE, and international trade regulations. Prices are FOB China unless otherwise specified. Payment terms: T/T 30 % + L/C at sight.

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