Buy Sodium Lactate Injection IP 1.85% w/v 16 Molar Solution for Bulk Order
What is Sodium Lactate Injection IP 1.85% w/v 16 Molar Solution?
Sodium Lactate Injection IP 1.85% w/v 16 Molar Solution is a sterile, isotonic solution of sodium lactate, classified as an electrolyte solution used in various pharmaceutical applications. It serves as a buffering agent and is utilized in fluid and electrolyte therapy in clinical settings.
This compound is essential in the synthesis of other pharmaceuticals and is relevant in industries focusing on metabolic disorders treatment and hydration solutions. Regulatory bodies recognize its significance in clinical therapies, ensuring compliance with safety and efficacy standards.
What Are the Applications of Sodium Lactate Injection IP 1.85% w/v 16 Molar Solution?
- Fluid and electrolyte replenishment in clinical settings.
- Buffering agent in biochemical and pharmaceutical formulations.
- Used in research applications for metabolic studies.
- Therapeutic relevance in treating lactic acidosis.
- Potential application in surgical and intensive care environments.
Why Choose Pharmint as Your Sodium Lactate Injection IP 1.85% w/v 16 Molar Solution Supplier?
Pharmint offers a global sourcing capability, ensuring reliable access to high-quality Sodium Lactate Injection IP 1.85% w/v 16 Molar Solution. We provide essential documentation, including Certificates of Analysis (COA) and Material Safety Data Sheets (MSDS), along with bulk availability to meet your procurement needs.
Our commitment to regulatory compliance and superior customer service, including efficient lead times and export support, positions Pharmint as a preferred vendor for your pharmaceutical ingredient sourcing.
Storage & Handling Guidelines for Sodium Lactate Injection IP 1.85% w/v 16 Molar Solution
Store Sodium Lactate Injection IP 1.85% w/v 16 Molar Solution at controlled room temperature (20°C to 25°C). Protect from light and store in a tightly sealed container to prevent air exposure. This product is available in bulk packaging suitable for large-scale applications or in research-grade formats for laboratory use.
Regulatory, Documentation & Export Information
Sodium Lactate Injection IP 1.85% w/v 16 Molar Solution is not classified as a controlled precursor; however, end-use declaration may be required for specific applications. Available documentation includes Certificates of Analysis (COA), Material Safety Data Sheets (MSDS), and Drug Master Files (DMF) as applicable.
Sodium Lactate Injection IP 1.85% w/v 16 Molar Solution FAQs
What is the shelf life of Sodium Lactate Injection?
The shelf life of Sodium Lactate Injection is typically 24 months when stored under recommended conditions. Always refer to the specific COA for detailed information.
How should Sodium Lactate Injection be handled?
Handle Sodium Lactate Injection with care, using appropriate personal protective equipment (PPE). Ensure to follow standard laboratory safety protocols during handling and preparation.
Can Sodium Lactate Injection be used in research studies?
Yes, Sodium Lactate Injection IP 1.85% w/v 16 Molar Solution is widely used in research studies, particularly in metabolic and physiological investigations.
Is Sodium Lactate Injection suitable for intravenous administration?
Yes, Sodium Lactate Injection is suitable for intravenous administration as per clinical guidelines, provided it is used under medical supervision.
What documentation is required for procurement?
For procurement, a Certificate of Analysis (COA) and Material Safety Data Sheet (MSDS) are generally required. Additional regulatory documents may be necessary based on the end-use.
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