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Fluocinolone powder

I have found results from50+products and20+suppliers aboutFluocinolone powder

Commonly Used:
US$
—
Customization Available
Sample Available
Manufacturer First
Product Attributes:
Synthesis Material Intermediates
Appearance: Powder
Quality: Refined
Colour: White
Powder: Yes
Customized: Customized
Certification: GMP
Suitable for: Elderly
State: Solid
Purity: >99%
Resource: Chemosynthesis
Packaging Material: Paper
Storage Method: Normal
Shelf Life: >12 Months
Nutrient Composition: Vitamin
The content of active substances: >90%
Assay Method: HPLC
Application Form: Tablet
Application: Food
Feature: Stocked
Organic Chemical Material
Status: Solid State
Customized: Non-Customized
Certification: HSE
Certification: ISO 9001
Certification: USP
Certification: BP
Certification: ISO
Certification: FDA
Certification: RoHS
Certification: BRC
Certification: HACCP
Suitable for: Adult
Suitable for: Children
State: Powder
Purity: >98%
Resource: Natural
Assay Method: HPLC-MS
Assay Method: GPC
Assay Method: UV
Application Form: Capsule
Health Care Products
Application: Medicine
Application: Cosmetics

Sourcing guidance for Fluocinolone Powder

What are the key technical specifications and purity standards for Fluocinolone Powder?

Fluocinolone acetonide powder must typically meet a purity level of ≥98% or ≥99% as per pharmacopeia standards. Buyers should verify the CAS number (67-73-2) and request a Certificate of Analysis (COA) that details the melting point, loss on drying (usually ≤1.0%), and residue on ignition (usually ≤0.1%). For topical formulations, micronized powder is often preferred to ensure uniform distribution and optimal absorption.

Which international compliance standards are mandatory for sourcing this API?

As an Active Pharmaceutical Ingredient (API), the supplier must adhere to Good Manufacturing Practices (GMP). Depending on the target market, the product should comply with USP (United States Pharmacopeia), BP (British Pharmacopeia), or EP (European Pharmacopeia) standards. Ensure the manufacturer holds a valid ISO 9001 certification and, if possible, a Drug Master File (DMF) number for regulatory filing support.

What are the primary usage scenarios and functional applications for this product?

Fluocinolone is a corticosteroid primarily used in the pharmaceutical industry to manufacture topical ointments, creams, and lotions. Its main functions are anti-inflammatory, anti-pruritic, and vasoconstrictive. It is highly effective for treating dermatological conditions such as eczema, psoriasis, and seborrheic dermatitis. It is not intended for direct consumer use and must be handled by professional laboratories or manufacturers.

How should the stability and storage of Fluocinolone Powder be managed?

The powder is sensitive to light and heat. It must be stored in light-resistant, airtight containers at controlled room temperatures (typically 15°C to 30°C). Suppliers should provide stability testing data to guarantee a shelf life of at least 24 to 36 months when stored under proper conditions.

Cross-Border Procurement & Risk Management for Chemical APIs

What are the specific shipping and customs requirements for Fluocinolone Powder?

Since this is a chemical substance, you must ensure the supplier provides a Material Safety Data Sheet (MSDS) and a Safe Transport of Chemical Goods Certificate. For international shipping, use reputable couriers experienced in sensitive chemicals. Be aware that customs may require an Import License for Drugs/APIs depending on your local regulations; always verify this before the goods depart.

How can I mitigate transaction risks when dealing with new chemical suppliers?

Utilize Made-in-China.com's Secured Trading services to protect your payment. Always request a pre-shipment sample for third-party lab testing (such as HPLC analysis) to verify purity. Avoid suppliers who refuse to provide factory audits or those who offer prices significantly below the market average, as this often indicates substandard purity or counterfeit material.

What strategies should be used for price negotiation in bulk API sourcing?

Negotiations should be based on volume tiers and long-term supply contracts. For orders exceeding 5kg-10kg, buyers can typically negotiate a 10-15% discount. Discussing incoterms (e.g., DAP vs. FOB) is crucial; for high-value powders, DAP (Delivered at Place) is often safer for the buyer as the supplier retains risk until arrival.

What are the common pitfalls in cross-border pharmaceutical chemical sourcing?

The biggest risks include mismatched specifications (e.g., receiving industrial grade instead of pharma grade) and seizure by customs due to improper labeling. Ensure all packaging is discreetly but accurately labeled with the correct HS Code and that the packaging integrity is vacuum-sealed to prevent moisture ingress during sea or air transit.

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