Product Introduction
Medroxyprogesterone Acetate (MPA) is a synthetic progestin derived from progesterone, widely used in pharmaceutical formulations for reproductive health regulation and hormonal therapy applications.
It is an important active pharmaceutical ingredient (API) used in:
- Contraceptive formulations
- Hormone Replacement Therapy (HRT)
- Gynecological disorder treatments
- Hormone-related research and formulation development
Product Specifications
|
Item |
Specification |
|
Product Name |
Medroxyprogesterone Acetate |
|
Appearance |
White Powder |
|
CAS Number |
71-58-9 |
|
Molecular Formula |
C24H34O4 |
|
Molecular Weight |
386.53 g/mol |
|
Purity |
99% |
|
Shelf Life |
2 Years (Proper Storage) |
|
Storage Condition |
Cool, dry, sealed, away from light |
|
Intended Use |
Research use only |
Key Functions
Strong Progestational Activity
MPA acts as a potent synthetic progestin, mimicking natural progesterone to regulate endocrine and reproductive functions.
Hormonal Regulation Support
It is widely used in formulations that regulate menstrual cycles, ovulation suppression, and hormone balance therapies.
Applications
Medroxyprogesterone Acetate Powder is commonly applied in:
- Injectable contraceptive formulations (depot long-acting systems)
- Oral hormone therapy tablets
- Hormone Replacement Therapy (HRT) products
- Treatment of endometriosis and abnormal uterine bleeding
- Oncology-related hormone research (breast/endometrial cancer supportive studies)
- Pharmaceutical R&D and formulation development
Quality Control System
Each batch undergoes a multi-stage pharmaceutical QC process:
Raw Material Verification
Identity confirmation via spectroscopy
Supplier qualification screening
In-Process Control
Reaction monitoring during synthesis
Intermediate purity tracking
Final Product Testing
HPLC purity analysis (99% requirement)
Moisture content testing
Residual solvent screening (ICH Q3C compliant)
Heavy metal control (ICH Q3D standard)
Batch Release Criteria
Only batches meeting full specification range are released with COA documentation
Packaging & Delivery
To ensure pharmaceutical stability and export safety:
- Inner packaging: Vacuum-sealed aluminum foil bag
- Secondary packaging: Double-layer PE protective liner
- Outer packaging: Pharmaceutical-grade sealed drum
- Optional customization: 1kg / 5kg / 10kg / bulk packaging
Customization Options
We support flexible OEM / B2B customization including:
Purity adjustment (98%–99.5%)
Particle size control (micronization available)
Packaging specification (bulk / retail / lab scale)
COA format customization (EU / US format)
Regulatory documentation support (DMF-ready format if required)
Regulatory & Documentation Support
Available upon request:
Certificate of Analysis (COA)
Safety Data Sheet (SDS)
HPLC chromatogram report
Stability data (long-term / accelerated)
GMP compliance statement
fAQ
Q: What is Medroxyprogesterone Acetate used for?
A: It is used as a synthetic progestin in contraceptive drugs, hormone therapy, and gynecological pharmaceutical formulations.
Q: Is this product suitable for pharmaceutical manufacturing?
A: Yes, it is produced under controlled GMP systems with 99% purity suitable for API-level formulation development.
Q: Do you provide regulatory documents for import registration?
A: Yes, we can provide COA, SDS, and regulatory support documents required for customs and registration.
Q: Can you support bulk or custom production orders?
A: Yes, we support lab scale to industrial bulk supply with flexible packaging and specification customization.
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