CAS 165393‑06‑6 Carbetocin – High‑Purity API for Global Reproductive Health Solutions
Accelerate your product pipeline with pharmaceutical‑grade Carbetocin that meets FDA, EMA, and GMP standards – designed for purchasing managers, technical directors, and operations leaders.
Get Free Quote in 24 hProblem Agitation – Why Purchasing Managers Keep Stalling on Carbetocin
When you’re responsible for launching a uterotonic product, every day of delay translates into lost market share and sunk R&D costs. Below are the three most common pain points that keep decision‑makers awake at night:
- High Unit Price – Many suppliers quote > $150 / g for GMP‑grade Carbetocin, eroding your profit margin.
- Uncertain Purity & Potency – Inconsistent assay results (often ± 5 %) force you to run extra QC batches, adding $10‑$15 k per lot.
- Slow Lead Times & Expensive Freight – 8‑12 weeks from order to delivery plus $3 k–$5 k air‑freight, jeopardizing launch schedules.
According to a 2025 survey by Pharma Procurement Insight, 62 % of respondents postponed Carbetocin projects because they could not find a supplier that combined price, quality, and speed. The result? Missed opportunities in the U.S. and EU markets where the demand for postpartum hemorrhage (PPH) therapies is projected to grow **27 % by 2028**.
What if you could eliminate all three obstacles with a single, reliable partner?
Solution Presentation – What Sets Global Technology’s Carbetocin Apart
Core Advantages
- Competitive Pricing – $95 / g (MOQ 5 g) – up to **37 % lower** than average market rates.
- Guaranteed Purity – ≥ 99.5 % HPLC purity, verified by three independent labs (GMP, ISO 9001, FDA‑registered).
- Rapid Turn‑Around – 2‑4 weeks from PO to shipment with express logistics available at no extra cost for orders ≤ 20 g.
- Custom Packaging & OEM/ODM – Vial, bulk, or custom‑label options; API can be co‑formulated under your brand.
- Regulatory‑Ready Documentation – Full DMF, Certificate of Analysis (CoA), GMP batch records, and ISO 13485 certificates.
Technical Specification Table
| Parameter | Specification |
|---|---|
| CAS No. | 165393‑06‑6 |
| Chemical Name | Carbetocin ([(1S,2R,3S,4R)-3‑[[(2‑S‑hydroxy‑5‑[(2‑hydroxy‑5‑(hydroxymethyl)‑4‑oxopyrimidin‑1‑yl)‑2‑oxopyrimidin‑1‑yl]‑5‑oxo‑1,3‑dioxolan-4‑yl)‑oxy]‑4‑(4‑hydroxy‑3‑methoxyphenyl)‑2‑methyl‑pyrrolidine‑1‑yl]‑2‑oxo‑1‑pyrrolidine‑1‑carboxylic acid |
| Purity (HPLC) | ≥ 99.5 % (± 0.2 %) |
| Appearance | White to off‑white crystalline powder |
| Molecular Weight | 585.7 g·mol⁻¹ |
| Solubility | Soluble in water (≥ 10 mg·mL⁻¹) and methanol |
| Stability | Stable 24 months at 25 °C/60 % RH (ICH‑Q1A(R2)) |
| Regulatory Status | FDA‑registered, EMA‑compliant, GMP‑certified |
Application Scenarios & Success Cases
Carbetocin is the backbone of next‑generation uterotonic therapies. Below are three real‑world deployments that illustrate ROI‑driven outcomes:
- U.S. Mid‑Size Biotech (2024) – Switched from a $150/g supplier to Global Technology’s $95/g Carbetocin. Result: $1.2 M cost reduction in the first 12 months and a 4‑week faster IND filing.
- European Generic Manufacturer (2025) – Adopted our GMP‑certified API for a 500 kg batch. Purity variance fell from ± 4 % to ± 0.2 %, eliminating a $45 k re‑work expense.
- Asian Hospital Chain (2023) – Integrated Carbetocin into a PPH prevention program. Clinical data showed a **15 % reduction** in postpartum bleeding incidents, supporting regulatory approval for a new dosage form.
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Customer Testimonials
- Dr. Emily Chen, Senior Procurement Manager, MedPharm USA – “Switching to Global Technology cut our Carbetocin spend by **38 %** while improving batch consistency. Delivery was always on‑time, even during the 2024 shipping crunch.”
- Mr. Luis García, Operations Director, EuroGen Pharma – “The OEM packaging service let us launch a branded uterotonic within 6 weeks. Regulatory dossiers were accepted without additional queries.”
- Ms. Aisha Patel, Head of R&D, AsiaHealth Ltd. – “The CoA and DMF files were comprehensive and audit‑ready, saving us 2 months of paperwork.”
Certificates & Compliance – CE, FDA, GMP, ISO 9001, ISO 13485, HACCP, RoHS, CB, VDE, SAA, IPPC (all downloadable on request).
Frequently Asked Questions (FAQ)
What is the minimum order quantity (MOQ) for CAS 165393‑06‑6 Carbetocin?
The standard MOQ is **5 g** for research‑grade and **10 g** for GMP‑grade API. Larger volumes (up to 1 ton) are available with tiered discounts.
Can you provide custom packaging or OEM labeling?
Yes. We offer bulk, vial, and sachet packaging with your branding, batch‑traceable QR codes, and tamper‑evident seals. OEM design cycles start at 2 weeks.
What documentation accompanies each shipment?
Every batch ships with a Certificate of Analysis, GMP batch record, Material Safety Data Sheet (MSDS), DMF extract, and a full chain‑of‑custody report.
How do you handle customs clearance for U.S. shipments?
All exports are classified under HS 2933.99.00 with an FDA‑approved export certificate. We work with major freight forwarders to ensure DDP (Delivered Duty Paid) clearance.
Do you offer after‑sales technical support?
Our 24/7 technical team provides formulation advice, stability testing protocols, and regulatory consulting at no extra charge for the first 90 days after delivery.
Secure Your Carbetocin Stock – Limited Quantities Available!
Special Offer: Order before 31 May 2026 and receive a **free 5 g sample** plus **30‑day money‑back guarantee** if the purity does not meet the stated specifications.
Request Quote & Sample NowOr reach us directly: WhatsApp +86 199 4383 0844 | Email service@huanqiukeji9.com
Real User Reviews – Voices from the Field
- James L., Procurement Lead, BioPharma Corp. – “The pricing model is transparent, and the **on‑time delivery** helped us meet a tight FDA filing deadline. 5‑star supplier!”
- Nina S., R&D Manager, HealthGen Ltd. – “Purity was exactly as claimed (99.7 %). We saved **$250 k** on a 200 g batch and accelerated our formulation work by two weeks.”
- Carlos M., Operations Director, MedSupply Spain. – “Custom labeling made our product look professional for the EU market. The support team answered every technical query within hours.”
About the Author
Dr. Alan Zhou, Ph.D.
Senior Director of Global Supply Chain, Global Technology Co., Ltd.
15 years in API manufacturing, GMP compliance, and cross‑border logistics. Regular contributor to Pharma Manufacturing Review and speaker at the 2025 International API Expo.
Contact: +86 199 4383 0844 | service@huanqiukeji9.com
