Eflornithine Hydrochloride API
Price 100 INR/ Kilograms
Eflornithine Hydrochloride API Specification
- Smell
- Odorless
- Molecular Weight
- 222.65 g/mol (anhydrous base)
- Shelf Life
- 2-3 years under recommended storage
- Boiling point
- Not applicable (decomposes)
- Molecular Formula
- C6H12F2N2O HCl H2O
- Storage
- Store in a cool, dry, well-ventilated place, tightly closed
- Heavy Metal (%)
- 0.001%
- EINECS No
- 229-646-0
- Poisonous
- Non-poisonous at therapeutic dosages
- Solubility
- Soluble in water, very slightly soluble in alcohol
- Structural Formula
- As shown in structural diagram
- Loss on Drying
- 1.0%
- Particle Size
- 80 100 mesh
- Ph Level
- 6.0 7.5 (1% aqueous solution)
- Color
- White
- Melting Point
- > 260C (decomposes)
- Taste
- Bitter
- HS Code
- 2924 29 95
- Medicine Name
- Eflornithine Hydrochloride
- Chemical Name
- (-Difluoromethylornithine hydrochloride monohydrate)
- CAS No
- 6640-24-0
- Type
- Other
- Grade
- Other
- Usage
- Pharmaceutical intermediate, topical treatment for facial hirsutism
- Purity(%)
- >99%
- Appearance
- White crystalline powder
- Physical Form
- Solid
- Residual Solvents
- Conforms to ICH guidelines
- Packaging
- HDPE drums, double polyethylene bags, 5-25 kg
- Moisture Content
- 0.5%
- Identification Tests
- IR, HPLC and chemical reaction matched
- Assay (on dried basis)
- >99.0%
- Related Substances
- 0.5%
- Chloride Content (Cl)
- Meets USP requirements
- LD50 (oral, rat)
- > 5000 mg/kg
Eflornithine Hydrochloride API Trade Information
- Minimum Order Quantity
- 1 Kilograms
- Supply Ability
- 2000 Kilograms Per Day
- Delivery Time
- 1 Days
About Eflornithine Hydrochloride API
Commercial Utility and Specific Application of Eflornithine Hydrochloride API
Eflornithine Hydrochloride API serves as a pivotal pharmaceutical intermediate, especially prized in the production of topical formulations for facial hirsutism in women. Its usage type mainly involves external application, where it inhibits hair growth. Widely adopted by manufacturers, suppliers, and exporters, its high assay and outstanding purity make it an ideal choice for developing effective formulations. This ingredient is renowned for yielding consistent performance and is recognized for its role in specialized dermatological medicine.
FOB Port, Arrival, and Global Market Reach for Eflornithine Hydrochloride API
FOB ports for Eflornithine Hydrochloride API typically include major international shipping hubs, ensuring prompt global arrival and reliable logistics. With robust supply ability, every charge is packed & dispatched via HDPE drums, guaranteeing uncompromised quality in transit. Primary export markets span regions such as North America, Europe, Asia, and the Middle East, affirming its global appeal. Timely packing and efficient handling ensure on-schedule delivery to clients worldwide.
FAQ's of Eflornithine Hydrochloride API:
Q: How is Eflornithine Hydrochloride API primarily used in pharmaceuticals?
A: Eflornithine Hydrochloride API is chiefly used as a pharmaceutical intermediate, particularly in topical treatments designed to reduce facial hair growth (hirsutism), especially in women. Its remarkable purity makes it suitable for high-efficacy formulations.Q: What is the recommended storage process for Eflornithine Hydrochloride API?
A: It should be stored in a cool, dry, and well-ventilated place with the container tightly closed. Proper storage ensures that the product maintains its quality and shelf life of 2-3 years.Q: When can I expect my order to arrive after dispatch?
A: Arrival time depends on the agreed FOB port and destination location, but efficient packing and prompt dispatch from major shipping hubs facilitate timely worldwide deliveries.Q: Where does Eflornithine Hydrochloride API find its main export markets?
A: The primary export markets for Eflornithine Hydrochloride API include North America, Europe, Asia, and the Middle East, where demand for high-purity pharmaceutical intermediates remains strong.Q: What benefits does the high assay (>99%) of Eflornithine Hydrochloride API offer?
A: A high assay purity ensures the effectiveness and safety of pharmaceutical formulations, reduces impurities and related substances, and conforms to stringent regulatory standards, providing peace of mind for both manufacturers and end-users.
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