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Send InquiryLevomilnacipran .
Price 100 INR/ Kilograms
MOQ : 1 Kilograms
Levomilnacipran . Specification
- Molecular Weight
- 246.35 g/mol
- Melting Point
- 184-186C
- Color
- White to off-white
- Loss on Drying
- 0.5%
- Poisonous
- NO
- Particle Size
- Typically <10 microns
- Heavy Metal (%)
- 0.001%
- Structural Formula
- C[C@@]1(CNC(=O)N(CC)CC)CC1c2ccccc2
- Solubility
- Slightly soluble in water, soluble in methanol and ethanol
- HS Code
- 29349900
- Shelf Life
- 24 months
- Molecular Formula
- C15H22N2O
- Smell
- Odorless
- Taste
- Characteristic
- Storage
- Store at 28C, protected from light and moisture
- EINECS No
- 643-083-6
- Medicine Name
- Levomilnacipran
- Chemical Name
- (1S)-2-(aminomethyl)-N,N-diethyl-1-phenylcyclopropane-1-carboxamide
- CAS No
- 96847-46-8
- Type
- Other
- Grade
- Other
- Usage
- Pharmaceutical intermediate, treatment of major depressive disorder
- Purity(%)
- 99.0%
- Appearance
- White to off-white solid
- Physical Form
- Powder
- Delivery Form
- API raw material
- Residual Solvents
- Complies with ICH guidelines
- Packaging
- Available in double polyethylene bags placed in fiber drum
- Impurity Profile
- Total impurities 1.0%
- Manufacturing Standard
- cGMP certified
- Microbial Limit
- Complies with pharmacopeial standards
- Identification by HPLC
- Conforms
- Specific Optical Rotation
- +15 to +20 (c=1, H2O)
- Chiral Purity
- >=99% (enantiomeric purity)
Levomilnacipran . Trade Information
- Minimum Order Quantity
- 1 Kilograms
- Supply Ability
- 2000 Kilograms Per Day
- Delivery Time
- 1 Days
- Main Domestic Market
- All India
About Levomilnacipran .
Jump on the latest, affordable, and preeminent pharmaceutical solutionLevomilnacipran. Renowned for its resplendent purity (99% chiral and enantiomeric), this remarkable API is manufactured under cGMP certification and conforms to stringent HPLC identification standards. With total impurities 1.0% and compliance with ICH residual solvent guidelines, Levomilnacipran assures excellent quality for medicinal use, particularly in major depressive disorder treatment. Delivered as a white to off-white powder, it is odorless, has a melting point of 184-186C, and maintains long shelf-life. Secure packaging ensures optimal delivery worldwide from leading manufacturers, exporters, and suppliers in India.
Application Spectrum of Levomilnacipran
Levomilnacipran exhibits remarkable utility as a pharmaceutical intermediate, primarily serving the treatment of major depressive disorder. Its surface of application lies within drug formulation and research laboratories, making it an essential component for pharmaceutical plants and R&D establishments. Application places extend to manufacturing facilities, analytical labs, and pharmaceutical processing plants, where its high purity and precise characteristics support innovative drug development and clinical research.
Packaging, Certification, and Order Arrival of Levomilnacipran
Every expenditure for Levomilnacipran guarantees robust packagingsupplied in double polyethylene bags inside fiber drums for uncompromised integrity. The product is cGMP certified, further ensuring quality. Upon order processing, prompt delivery is prioritized, with typical arrival times depending on international shipping and logistical protocols. Comprehensive packaging details and certification documents accompany each shipment, supporting smooth import/export transactions for commercial buyers and distributors.
Application Spectrum of Levomilnacipran
Levomilnacipran exhibits remarkable utility as a pharmaceutical intermediate, primarily serving the treatment of major depressive disorder. Its surface of application lies within drug formulation and research laboratories, making it an essential component for pharmaceutical plants and R&D establishments. Application places extend to manufacturing facilities, analytical labs, and pharmaceutical processing plants, where its high purity and precise characteristics support innovative drug development and clinical research.
Packaging, Certification, and Order Arrival of Levomilnacipran
Every expenditure for Levomilnacipran guarantees robust packagingsupplied in double polyethylene bags inside fiber drums for uncompromised integrity. The product is cGMP certified, further ensuring quality. Upon order processing, prompt delivery is prioritized, with typical arrival times depending on international shipping and logistical protocols. Comprehensive packaging details and certification documents accompany each shipment, supporting smooth import/export transactions for commercial buyers and distributors.
FAQs of Levomilnacipran .:
Q: How is Levomilnacipran delivered, and what packaging is used for shipping?
A: Levomilnacipran is delivered as a raw powder API, securely packed in double polyethylene bags placed within fiber drums to ensure safety and stability during transit.Q: What are the primary applications and usage areas for Levomilnacipran?
A: The compound is primarily applied as an intermediate in pharmaceutical manufacturing, specifically for the treatment of major depressive disorder. It is widely used in drug formulation labs, R&D facilities, and manufacturing plants.Q: When can customers expect arrival after placing an order for Levomilnacipran?
A: After order processing, delivery timelines typically depend on the destination and shipping arrangements. Most orders are dispatched promptly, and arrival can be coordinated to meet the buyers schedule.Q: Where is Levomilnacipran manufactured and exported from?
A: Levomilnacipran is manufactured, distributed, and exported by leading pharmaceutical companies based in India, catering to global markets.Q: What certifications confirm the quality of Levomilnacipran?
A: Levomilnacipran is produced following cGMP standards, with conformity to pharmacopeial microbial limits, ICH residual solvent guidelines, and rigorous impurity controls. Certification documentation is provided with each shipment.Q: How does the remarkable chiral purity benefit pharmaceutical applications?
A: With an enantiomeric purity of 99%, Levomilnacipran ensures high efficacy and safety in pharmaceutical formulations, minimizing unwanted side effects and optimizing therapeutic outcomes.
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