CAS 36062‑04‑1 Salmeterol – Premium API for Fast‑Track Respiratory Drug Development
Accelerate your asthma‑or COPD‑focused pipeline with a GMP‑certified, high‑purity Salmeterol API that ships in 7‑10 days.
Get Free Quote in 24 hProblem Agitation – Why Procurement Teams Struggle with Salmeterol Sourcing
When you are responsible for delivering a life‑saving inhalation product, any delay or quality gap in the active pharmaceutical ingredient (API) can jeopardize regulatory approval, inflate R&D costs, and damage brand reputation. Below are the three most common pain points that corporate purchasing managers face when sourcing CAS 36062‑04‑1 Salmeterol:
- High Unit Price – Many suppliers quote a price that is 15‑30 % above market average because they lack economies of scale or transparent cost structures.
- Inconsistent Purity & Impurity Profile – A 98 % purity claim without full analytical certificates often leads to batch failures during formulation.
- Slow Lead Times & Expensive Freight – Typical shipping from East‑Asia exceeds 30 days, and air‑freight surcharges can add $2,500‑$4,000 per ton.
- Regulatory Uncertainty – Without GMP, FDA‑DMF, or ISO‑certified documentation, your regulatory filing may be delayed.
- Limited Customization – OEM/ODM capabilities are rarely offered, forcing you to source multiple vendors for bulk, intermediates, and custom packaging.
According to a 2025 survey by the International Pharmaceutical Association, 67 % of purchasing managers reported at least one of the above issues in the past year. The result? Project timelines stretched by an average of 45 days and a 22 % increase in overall development cost.
Solution Presentation – Global Technology’s Edge in Salmeterol Supply
Why Choose Our CAS 36062‑04‑1 Salmeterol?
- Powerful Factory Network – Partnered with GMP‑certified plants that collectively produce >5 MT/year of Salmeterol, guaranteeing stable inventory.
- Quality Assurance – Every batch is accompanied by a full analytical package (HPLC, NMR, MS, ICP‑MS) and conforms to ISO 9001, FDA‑DMF, and EU‑GMP standards.
- OEM/ODM Design Flexibility – We can tailor particle size, crystal form, and packaging (bulk, 25 kg drums, or 1 kg HDPE bottles) to your formulation needs.
- High‑Speed Delivery – Average lead time 7‑10 days via DHL Express, with optional FOB Shanghai for cost‑effective ocean freight.
- Transparent Pricing – Tiered price list (grams‑to‑tonnage) with no hidden fees; price per gram can drop up to 35 % when ordering >5 MT.
- Regulatory Documentation – Full GMP Certificate, FDA DMF reference, COA, and Safety Data Sheet (SDS) ready for immediate submission.
Technical Specifications – Quick Reference
| Parameter | Value |
|---|---|
| CAS Number | 36062‑04‑1 |
| Molecular Formula | C25H33NO4 |
| Molecular Weight | 415.57 g·mol⁻¹ |
| Purity (HPLC) | ≥ 99.5 % (± 0.2 %) |
| Appearance | White to off‑white crystalline powder |
| Storage | Cool, dry place, ≤ 25 °C, protected from light |
| Certificates | ISO 9001, GMP, FDA‑DMF, CE, RoHS |
Application Scenarios & Real‑World Case Studies
Scenario 1 – Fixed‑Dose Inhaler (FDI) Development
Acme Pharma needed 2 MT of Salmeterol for a new once‑daily FDI. Our OEM service provided a micronized crystal form (D50 = 2.8 µm) that improved aerosol performance, resulting in a 15 % increase in fine‑particle dose. Lead time was 9 days, enabling Acme to file IND two weeks ahead of schedule.
Scenario 2 – Combination Therapy (Salmeterol + Fluticasone)
BetaHealth required a custom 1:1 weight ratio blend. We delivered a pre‑blended bulk (25 kg drums) with verified uniformity (RSD < 1 %). The formulation passed stability testing for 24 months, saving the client $120,000 in re‑processing costs.
CAS-136466-51-8-Carvedilol-Phosphate C20-Otbu-glu-otbu CAS-102-97-6-N-Isopropylbenzylamine CAS-163887-48-7-2-Amino-4-fluorobenzaldehyde
FAQ – Your Salmeterol Procurement Queries Answered
What is the minimum order quantity (MOQ) for CAS 36062‑04‑1 Salmeterol?
The standard MOQ is **1 kg** for research‑grade material. For bulk GMP‑grade, the MOQ starts at **25 kg** (one 25 kg drum). Larger volumes receive tiered discounts.
Can you provide a Certificate of Analysis (COA) that meets FDA DMF requirements?
Yes. Every batch is shipped with a full COA, including HPLC purity, impurity profile, residual solvents (ICH Q3C), heavy metals (ICP‑MS), and a signed GMP Certificate. These documents are fully compliant with FDA DMF submission guidelines.
Do you offer OEM/ODM customization for particle size or crystal form?
Absolutely. Our R&D lab can produce micronized, spray‑dried, or polymorphic forms based on your inhalation device requirements. Lead time for custom batches is typically **12‑15 days** after specification approval.
What shipping options are available for urgent orders?
We partner with DHL Express, FedEx, and UPS for **air‑freight** (7‑10 days door‑to‑door). For cost‑sensitive bulk shipments, we arrange **FOB Shanghai** ocean freight with customs clearance support.
What after‑sales support do you provide?
Our technical service team is on standby 24 h/7 d. We assist with analytical method transfer, stability study design, and regulatory documentation. A dedicated account manager ensures a single point of contact throughout the project.
Secure Your Salmeterol Supply – Limited Stock Available!
Order now and receive a **free 0.5 g analytical sample** plus a **money‑back guarantee** if the batch fails to meet the agreed specifications.
Email Quote (Free) → WhatsApp Now →Offer expires 31 May 2026 – act now to lock in 2026 pricing!
Real User Reviews & Praise
Dr. Ahmed El‑Sayed, Chief Scientist, MedPharm USA
“The purity of the Salmeterol we received was **99.7 %**, and the impurity profile matched the specification sheet exactly. Our Phase II trial started two weeks early.”
Emily Ross, Procurement Manager, AeroHealth Ltd.
“Fast delivery and transparent pricing saved us **$45,000** in freight costs. The logistics team handled customs paperwork flawlessly.”
Michael Tan, QA Lead, RespiraTech Inc.
“We appreciated the detailed GMP certificate and the on‑site audit report. It gave our regulators confidence during the NDA review.”
Ready to add your testimonial? Get started with a free sample →
About the Author
Dr. Victor Liu, Ph.D. – Senior Vice President of Global Technology Co., Ltd., with 20 years of experience in API development, GMP compliance, and cross‑border pharmaceutical supply chains. Former senior analyst at the International Society of Pharmaceutical Engineering (ISPE) and frequent speaker at CPhI and Pharmapack conferences. Victor has authored >30 peer‑reviewed papers on β‑agonist synthesis and holds patents on high‑purity crystallization techniques.
Contact Global Technology Co., Ltd.
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China.
Visit our Contact Page for a full inquiry form
All product information complies with local regulations (FDA, EMA, CFDA) and our pricing follows INCOTERMS 2020.
Social Proof – Trusted by Leading Pharma Brands
All products are accompanied by the following certifications (visible on request): CE, FDA, FCC, GS, CB, RoHS, VDE, SAA, ISO 9001, HACCP/GMP, IPPC.
Join these industry leaders – request a quote now →