Levosulpiride
Price 100 INR/ Kilograms
Levosulpiride Specification
- Smell
- Odorless
- Boiling point
- Not applicable (decomposes before boiling)
- Solubility
- Freely soluble in methanol, slightly soluble in water and ethanol
- Heavy Metal (%)
- 0.002%
- Taste
- Bitter
- Loss on Drying
- 0.5%
- Shelf Life
- 3 years
- Particle Size
- Micronized
- Molecular Formula
- C15H23N3O4S
- EINECS No
- 245-659-7
- Melting Point
- ~135C
- Color
- White to off-white
- Ph Level
- 5.0 - 7.0 (1% solution)
- Poisonous
- Non-poisonous under therapeutic use
- Storage
- Store in cool, dry place; protected from light
- HS Code
- 29349000
- Molecular Weight
- 341.43 g/mol
- Structural Formula
- Available on request
- Medicine Name
- Levosulpiride
- Chemical Name
- Levosulpiride
- CAS No
- 23672-07-3
- Type
- Other
- Grade
- Other
- Usage
- Pharmaceutical Intermediate; Used as antipsychotic and prokinetic agent
- Purity(%)
- 99% min
- Appearance
- White to off-white crystalline powder
- Physical Form
- Solid
- Impurity Level
- NMT 0.1%
- Regulatory Compliance
- Complies with BP/EP/IP/USP standards
- Stability
- Stable under recommended storage conditions
- Identification
- IR, HPLC Complies
- Specific Rotation
- +123 to +129
- Assay (HPLC)
- >=99%
- Packing
- Fiber Drum / HDPE Drum / Double PE Bags
- Certificate of Analysis (COA)
- Available upon request
- Storage Temperature
- Below 25C
- Export Markets
- Global
- Manufacturing Process
- Synthetic
- Microbial Limit
- Within prescribed pharmacopoeial standards
Levosulpiride Trade Information
- Minimum Order Quantity
- 1 Kilograms
- Supply Ability
- 2000 Kilograms Per Day
- Delivery Time
- 1 Days
About Levosulpiride
Levosulpiride is a drug which belongs to the class of antipsychotic which is mainly used to treat psychosis like delusions, hallucinations, paranoia or disordered thought, and bipolar disorders. It can also be used for the treatment of gastroesophagal reflux disease caused due to increased acid level in stomach. Levosulpiride works by binding to dopamine receptors in the brain which results in an increased tone of muscles in the gastrointestinal tract. This drug is not suitable for patients with breast cancer, pregnant and breastfeeding women, prolactin imbalance, heart diseases, alcohol intoxication and severe kidney or liver disease. Its dosage can only be taken as per the doctor's prescribed method.
Trusted Quality and Specifications
Levosulpiride is produced through a precise synthetic process, ensuring consistent quality as evidenced by specific rotation and impurity thresholds. Its physical form is a solid, micronized powder, freely soluble in methanol, and uniquely stable under our recommended conditions. Each batch is thoroughly tested via IR and HPLC to comply with all regulatory standards. We offer custom packing, including Fiber Drum, HDPE Drum, or double PE bags, catering to diverse global logistic requirements.
Versatile Pharmaceutical Applications
This compound is widely utilized as a pharmaceutical intermediate, with established roles as an antipsychotic and prokinetic agent. Its exceptional purity and stability make it suitable for use in regulated markets worldwide. Users benefit from its well-documented efficacy, prolonged shelf life, and compliance with major pharmacopeial standards, presenting a reliable option for manufacturers, suppliers, and distributors seeking high-quality active ingredients.
FAQs of Levosulpiride:
Q: How should Levosulpiride be stored to maintain its stability and potency?
A: Levosulpiride should be stored in a cool, dry place at temperatures below 25C and protected from light to ensure maximum stability and a shelf life of up to three years. Proper storage preserves its crystalline quality and maintains assay and impurity standards.Q: What are the primary uses of Levosulpiride in the pharmaceutical industry?
A: Levosulpiride serves as an intermediate in pharmaceutical manufacturing and as an active ingredient due to its proven antipsychotic and prokinetic effects. Its high purity and established safety make it suitable for diverse therapeutic applications.Q: When is a Certificate of Analysis (COA) provided for Levosulpiride shipments?
A: A comprehensive Certificate of Analysis is available upon request with each batch, detailing all critical parameters, including assay, impurity levels, microbial limits, and compliance with BP/EP/IP/USP regulatory standards.Q: Where can Levosulpiride be exported, and what packing options are available?
A: Levosulpiride is exported globally and can be supplied in Fiber Drum, HDPE Drum, or double PE bags, allowing flexibility for different regulatory and logistical needs.Q: What is the manufacturing process of Levosulpiride and how is its quality verified?
A: Levosulpiride is manufactured synthetically under controlled conditions, with each batch subjected to IR and HPLC verification, ensuring it meets stringent pharmacopoeial impurities, assay, and microbial specifications.Q: How is the purity and identity of Levosulpiride ensured?
A: Purity is verified by HPLC (99%), while identity is confirmed using IR spectroscopy and further analytical protocols. Impurity levels are strictly maintained at not more than 0.1% in accordance with pharmacopoeial requirements.Q: What are the key benefits of using Levosulpiride as supplied by your company?
A: Users benefit from its consistent high purity, robust packaging, global regulatory compliance, reliable stability, and technical support, making it an optimal choice for pharmaceutical manufacturers seeking trusted ingredients.
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