Mifepristerone Active Pharmaceutical Ingredients
Mifepristerone Active Pharmaceutical Ingredients

Mifepristerone Active Pharmaceutical Ingredients

MOQ : 25 Kilograms

Mifepristerone Active Pharmaceutical Ingredients Specification

  • EINECS No
  • 282-303-3
  • Molecular Formula
  • C29H35NO2
  • Color
  • White
  • HS Code
  • 29372900
  • Poisonous
  • No (when used as prescribed)
  • Storage
  • Store in a cool, dry place, protected from light
  • Smell
  • Odorless
  • Molecular Weight
  • 429.594 g/mol
  • Melting Point
  • 194-196C
  • Solubility
  • Slightly soluble in water, freely soluble in methylene chloride, soluble in acetone and ethanol
  • Structural Formula
  • C29H35NO2
  • Heavy Metal (%)
  • 0.001%
  • Shelf Life
  • 3 years
  • Loss on Drying
  • 0.5%
  • Medicine Name
  • Mifepristerone
  • Chemical Name
  • 17-Hydroxy-11-(4-(dimethylamino)phenyl)-17-(1-propynyl)-estra-4,9-dien-3-one
  • CAS No
  • 84371-65-3
  • Type
  • Active Pharmaceutical Ingredient
  • Grade
  • Pharmaceutical Grade
  • Usage
  • Used for the medical termination of intrauterine pregnancy, emergency contraception, Cushings syndrome
  • Purity(%)
  • 98.5%
  • Appearance
  • White or almost white crystalline powder
  • Physical Form
  • Solid
  • Specific Optical Rotation
  • +160 to +170 (C=1, CHCl3)
  • Water Content
  • 0.3%
  • Packaging
  • Double polyethylene bags in fiber drum
  • Microbial Limit
  • Meets pharmaceutical norms
  • Assay (by HPLC)
  • >98.5%
  • Identification
  • Meets pharmacopoeia specifications
  • Residual Solvents
  • Complies with ICH guidelines
  • Impurity Profile
  • Complies with pharmacopoeia limits
 

Mifepristerone Active Pharmaceutical Ingredients Trade Information

  • Minimum Order Quantity
  • 25 Kilograms
  • Payment Terms
  • Cash Against Delivery (CAD), Cash in Advance (CID), Cash on Delivery (COD)
  • Supply Ability
  • 500 Kilograms Per Month
  • Delivery Time
  • 5-7 Days
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • Main Domestic Market
  • All India
 

Mifepristerone Active Pharmaceutical Ingredients About



Jump on this eminent opportunity to own Mifepristerone Active Pharmaceutical Ingredients featuring a pristine purity level of 98.5%. Our pharmaceutical grade API is renowned for its towering pharmacopoeia compliance, meticulous impurity profile, and residual solvents aligned with ICH guidelines. Each batch is customizable for your specific requirements and currently offered on sale for both exporters and domestic traders. Packaged securely in double polyethylene bags within a fiber drum, this product demonstrates unparalleled integrity and reliability in medical applications, including pregnancy termination and Cushing's syndrome.

Features and Versatile Applications of Mifepristerone API

Mifepristerone API boasts specific optical rotation values between +160 and +170, pristine appearance as a white crystalline powder, and an assay of over 98.5%. Specifically engineered for medical termination of intrauterine pregnancy, emergency contraception, and Cushing's syndrome, this eminent ingredient excels in both general and niche pharmaceutical uses. Its stable molecular formula (C29H35NO2), exceptional solubility profile, and compliant microbial limits make it a top-tier choice for pharmaceutical manufacturers and suppliers.


Sample Availability, Certifications, and Packaging Insights for Mifepristerone API

Samples of our Mifepristerone API are available for qualified clients. Each batch meets stringent certifications and pharmacopoeia standards that enhance its market value and domestic mar appeal. The product is securely packaged in double polyethylene bags within fiber drums, ensuring pristine condition upon delivery. With a list price reflective of its superior quality and shelf life of three years, our API is engineered to maintain stability and integrity, reinforcing its standing in the global pharmaceutical market.


FAQ's of Mifepristerone Active Pharmaceutical Ingredients:


Q: How does Mifepristerone API comply with pharmacopoeia specifications?

A: Mifepristerone API is manufactured to meet or exceed pharmacopoeia specifications, including verified identification, specific optical rotation, impurity profile, and residual solvents, ensuring its quality and safety for end use.

Q: What are the main uses of Mifepristerone Active Pharmaceutical Ingredients?

A: This API is chiefly utilized for medical termination of intrauterine pregnancy, emergency contraception, and treatment of Cushing's syndrome. Its eminent purity and compliance make it suitable for a range of pharmaceutical applications.

Q: When should Mifepristerone API be stored and for how long is its shelf life?

A: Mifepristerone API should be stored in a cool, dry place away from light. Its shelf life is three years when stored under optimal conditions, maintaining both potency and efficacy.

Q: Where does Mifepristerone API stand out in terms of quality and safety?

A: Our Mifepristerone API boasts a pristine impurity profile, meets heavy metals limits (0.001%) and maintains low water content (0.3%), ensuring a high standard of quality and patient safety.

Q: What is the packaging process for Mifepristerone API during trading or export?

A: The API is meticulously packaged in double polyethylene bags and then sealed within fiber drums. This process protects it from contamination, moisture, and light, ensuring the product remains in pristine condition through transit.

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