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desogestrel

I have found results from10products and5suppliers aboutdesogestrel

Commonly used:
US$
Customization Available
Sample Available
Manufacturer First
Product attributes:
Type: Biological Products
Type: Chemical Reagent
Application: Internal Medicine
For oral administration
Suitable for: Adult
State: Solid
Shape: Tablet
Pharmaceutical Technology: Chemical Synthesis
Powder: Yes
Customized: Customized
Certification: GMP
Purity: >99%
Hormones and Regulation of Endocrine Function of Drug
Grade Standard: Medicine Grade
Volatile: Not Volatile
Appearance: Powder
Colour: White
Suitable for: Elderly
Suitable for: Children
State: Liquid
Customized: Non-Customized
Certification: ISO 9001
Certification: HSE
Certification: USP
Certification: BP
Purity: ≦96%
Urinary System Agents

Sourcing guidance for Desogestrel

What are the key technical specifications and purity standards for Desogestrel API?

As a potent synthetic progestin, Desogestrel must adhere to strict pharmacopeial standards such as USP (United States Pharmacopeia) or EP (European Pharmacopeia). Buyers should verify a purity level of ≥98% and check for specific impurity profiles. Key technical indicators include optical rotation, loss on drying (≤0.5%), and heavy metal content (≤20ppm). Always request a Certificate of Analysis (COA) from the manufacturer to confirm these parameters before shipment.

What regulatory compliance and certifications are required for international sourcing of Desogestrel?

Due to its nature as a pharmaceutical active ingredient, the supplier must possess a GMP (Good Manufacturing Practice) certificate. For entry into regulated markets, a DMF (Drug Master File) or CEP (Certificate of Suitability) is essential. Ensure the manufacturer is registered with the relevant local health authorities (e.g., NMPA in China) and can provide a Written Confirmation (WC) for export to the EU if required.

How should the stability and storage conditions of Desogestrel be evaluated?

Desogestrel is sensitive to light and heat. It must be stored in tight, light-resistant containers at controlled room temperatures, typically 20°C to 25°C. When sourcing, confirm that the supplier uses double-layer PE bags inside fiber drums and provides stability testing data (accelerated and long-term) to ensure the product maintains its potency throughout its shelf life, which is usually 24 to 36 months.

What are the common usage scenarios and formulation considerations for Desogestrel?

Desogestrel is primarily used in the production of oral contraceptives (both combined pills and progestogen-only 'mini-pills') and hormone replacement therapy (HRT). Because it is effective at very low dosages (microgram scale), buyers must ensure the supplier's material has excellent particle size distribution (micronization) to guarantee content uniformity during the tableting process.

Cross-Border Procurement Risks and Strategic Advice for Desogestrel

How can buyers mitigate transaction risks and ensure payment security?

For high-value pharmaceutical chemicals, use secure payment methods like Letter of Credit (L/C) or trade assurance services provided by reputable platforms like Made-in-China.com. Avoid direct wire transfers to unknown accounts. Conduct a third-party factory audit to verify the supplier's production capacity and legal existence before making a significant down payment.

What are the logistics and customs precautions for shipping Desogestrel internationally?

Desogestrel is classified as a non-hazardous chemical in most jurisdictions, but it requires a Material Safety Data Sheet (MSDS) and a Non-Hazardous Cargo Declaration for smooth customs clearance. Ensure the HS Code is correctly declared (typically 293723) to avoid delays. For shipping to specific countries, verify if an Import License for hormonal substances is required by the destination's Ministry of Health.

How to negotiate effectively with pharmaceutical chemical suppliers?

Focus on long-term supply stability rather than just the lowest price. Negotiate based on tiered pricing (e.g., 1kg vs 10kg vs 50kg) and request free pilot samples (1-5g) for lab testing. Discuss lead times clearly, as pharmaceutical synthesis cycles can be long; reputable suppliers on Made-in-China.com typically offer a lead time of 2-4 weeks for stocked API.

What should be included in the quality guarantee agreement?

The contract should explicitly state that the product must meet USP/EP specifications and that the buyer has the right to a full refund or replacement if third-party testing (e.g., by SGS or Intertek) shows the material is off-spec. Include a clause for retention samples to be kept by both parties for at least one year after the expiry date.

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