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Specifications
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Grade |
CP2015 |
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Appearance |
Light yellow crystal powder |
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Assay (HPLC, on the dried substance) |
98.5% min |
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Melting Point |
192°C to 196°C |
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Specific Optical Rotation |
+124° to +129° |
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Loss on Drying (105°C, 3h) |
0.5% max |
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Total Impurities (HPLC) |
2.0% max |
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Maximum Unspecified Impurity (HPLC) |
1.0% max |
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Identification (By IR/UV) |
The IR spectrum of sample complies with that of RS; maximum absorption at 304 nm and 260 nm |
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Granularity (D[90]) |
20μm max |
Transport Information
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Parameter |
Specification |
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UN Number |
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Class |
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Packing Group |
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H.S. Code |
2937239090 |
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Stability & Reactivity |
The product is chemically stable under standard ambient conditions. |
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Storage |
Tightly closed. Dry. Keep in a well-ventilated place. Keep locked up or in an area accessible only to qualified or authorized persons. Storage stability Recommended storage temperature2 - 8 °C |
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Condition to Avoid |
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Package |
1kg/bottle |
Manufacturing Information
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Parameter |
Specification |
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Capacity |
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Frequency |
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Main Export Countries |
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Capacity/Batch |
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Experience |
Production since 2015 |
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Stock |
Applications
1. Medical Termination of Pregnancy
● Primary clinical use: Mifepristone丨CAS 84371-65-3 is FDA-approved for medical abortion during the first trimester (up to 10 weeks gestation), in combination with misoprostol.
● Mechanism: Blocks progesterone receptors, preventing the hormone from maintaining the uterine lining, leading to detachment of the embryo.
● When followed by misoprostol (a prostaglandin analogue), it induces uterine contractions and expulsion of pregnancy tissue.
2. Cushing's Syndrome (Hyperglycemia Management)
● Mifepristone is approved under the trade name Korlym for managing hyperglycemia secondary to Cushing's syndrome in adults with type 2 diabetes or glucose intolerance who are not candidates for surgery.
● Mechanism: Acts as a glucocorticoid receptor antagonist, helping mitigate the effects of excessive cortisol.
3. Research in Endocrinology and Oncology
● Studied in experimental settings for:
o Breast cancer and endometrial cancer (as it inhibits progesterone signaling)
o Psychiatric disorders (e.g., major depression with psychotic features) due to its glucocorticoid receptor blockade
o Leiomyoma (fibroids) and endometriosis management
4. Emergency Contraception (Investigational Use)
● Although not its primary indication, low-dose mifepristone has been studied as a postcoital contraceptive, showing effectiveness in preventing ovulation and implantation when used within a specific timeframe.
Benefits
1. Non-Invasive Alternative to Surgery
● Mifepristone offers a safe, effective, and less invasive alternative to surgical abortion when used properly under medical guidance.
2. Receptor-Specific Activity
● High affinity for progesterone and glucocorticoid receptors, allowing targeted modulation with limited off-target hormonal effects at therapeutic doses.
3. Expanded Therapeutic Potential
● Its glucocorticoid antagonism opens avenues for treating metabolic disorders, psychiatric illness, and hormone-sensitive cancers.
4. Oral Bioavailability
● Mifepristone is well-absorbed orally and has a long half-life (~20–85 hours), which supports convenient dosing schedules.
Conclusion
Mifepristone丨CAS 84371-65-3 is a powerful and versatile pharmaceutical compound with well-established use in medical abortion and Cushing's syndrome, and promising investigational roles in oncology, reproductive health, and endocrinology. Its dual action as a progesterone and glucocorticoid receptor antagonist allows it to address complex hormone-dependent conditions while providing patients with non-invasive treatment options. Ongoing research continues to explore its broader therapeutic potential in various medical domains.
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