Remedy Labs

Chlorohexidine Gluconate 20% API.

Product Name: Chlorhexidine digluconate solution 20% / Chlorohexidine Gluconate 20% API.CAS No.: 18472‑51‑0Synonyms: Chlorhexidine digluconate 20% solution, CHG 20%, 1,1’‑hexamethylenebis[5‑(4‑chlorophenyl)biguanide] digluconate.Molecular Formula: C₂₂H₃₀Cl₂N₁₀·2C₆H₁₂O₇, (20% w/v).
Form: Clear liquid solution (colourless to pale yellow).Grade: IP / BP / USP / EP (as required).

Product Overview:
Chlorhexidine Gluconate 20% API is a pharmaceutical‑grade antiseptic and disinfectant active ingredient supplied as a high‑purity liquid solution. It is widely used in healthcare and pharmaceutical formulations for its broad‑spectrum antimicrobial properties, effective against a wide range of bacteria, fungi and some viruses. It serves as a key API in the production of antiseptic gels, surgical scrubs, wound care products and oral hygiene solutions.
Key Specifications:Appearance: Almost colourless to pale yellow, clear liquid. Assay / Purity: Typically 19–21 % w/v active chlorhexidine gluconate CAS No.: 18472‑51‑0. Solubility: Miscible with water; soluble in alcohols and other solvents. pH (typical): ~5.5 – 7.0. Packaging: Drums / IBCs / customized packaging available. Documentation: COA and MSDS provided on request.
Product Features:Pharmaceutical‑grade API: Manufactured to comply with major pharmacopeial standards (IP/BP/USP/EP). Broad‑spectrum antimicrobial activity: Effective against gram‑positive and gram‑negative bacteria, fungi and various pathogens. Stable, clear liquid: Consistent quality and easy formulation handling. Complete documentation: Supplied with COA, MSDS and batch traceability for compliance.
Applications:Chlorhexidine Gluconate 20% API is widely used across pharmaceuticals, healthcare and personal care Antiseptic Formulations: Used in surgical scrubs, hand washes and skin cleansers to control infection risk. Wound Care & Surgical Preparations: Key active ingredient in pre‑operative skin preparation and wound disinfectants. Oral Hygiene Products: Utilized in medicated mouthwashes, dental rinses and periodontal care solutions. Topical Antimicrobials: Ingredient in gels, creams and lotions for skin antisepsis. Medical Devices & Cleaners: Used in cleaning solutions for instruments and catheter disinfection. 
Handling & Storage:Store Chlorhexidine Gluconate 20% API in airtight containers in a cool, dry, well‑ventilated area, away from heat and direct sunlight. Follow standard pharmaceutical safety practices and handle with appropriate PPE.
Why Choose Our Chlorhexidine Gluconate 20% API:Reliable Quality: High‑grade antiseptic API with consistent performance. Regulatory Compliance: Meets global quality standards with full documentation. Versatile Use: Suitable for a range of pharmaceutical and healthcare applications. Bulk Supply & Support: Flexible packaging and supply solutions for exporters and manufacturers.

Microcrystalline Cellulose (API) Powder – Product Description
Product Name: Microcrystalline Cellulose PowderAlso Known As: MCC Powder, Pharmaceutical Grade Cellulose, API Grade MCC
Description:
Microcrystalline Cellulose (MCC) is a high-purity, white, odorless, and tasteless pharmaceutical excipient widely used as a tablet binder, filler, and disintegrant in solid dosage formulations. Derived from purified wood pulp through controlled hydrolysis, MCC offers excellent compressibility, flowability, and consistency, making it a preferred choice in the pharmaceutical industry.
Key Features & Benefits:Pharmaceutical Grade API: Manufactured to meet stringent pharmacopoeial standards (USP/EP/BP) for API and excipient applications.High Purity & Consistency: Low ash content and minimal impurities ensure formulation stability.Superior Compressibility: Provides excellent binding properties for uniform tablet formation.Optimal Flow Properties: Ensures smooth processing with reduced manufacturing variability.Good Disintegration: Aids in rapid tablet break-up and effective drug release.Inert & Non-Reactive: Chemically stable, non-toxic, and compatible with a wide range of drug actives.
Specifications (Typical):Chemical Name: Microcrystalline Cellulose.Appearance: White to off-white free-flowing powder.Assay / Purity: ≥99.0% (meets USP/EP standards).pH (1% Aqueous): 5.0 – 7.0.Loss on Drying: As per pharmacopoeial limits.Particle Size: Controlled distribution for optimal performance.
Packaging Options:25 Kg / 50 Kg Multi-Layer Paper Bag with Inner Liner.HDPE Bag with Inner PE Liner.Custom/Re-sealable Packaging as per client requirement.Bulk SUPPLY for OEM/Contract Manufacturing.
Why Choose Our Microcrystalline Cellulose Powder?We deliver premium quality API grade MCC with consistent performance backed by rigorous quality control. Our product is compliant with USP/EP/BP standards, offering reliable tablet integrity, enhanced manufacturability, and excellent batch-to-batch uniformity — making it ideal for pharmaceutical, nutraceutical, and contract manufacturing needs.

Divalproex Sodium BP
Product Name: Divalproex Sodium BP – Pharmaceutical Active Ingredient (API)CAS No.: 76584-70-8.Chemical Name: Valproate semisodium (sodium hydrogen bis(2-propylpentanoate)).Grade: Pharmaceutical API – British Pharmacopoeia (BP) compliant.Appearance: White to off-white crystalline powder.Molecular Formula: C₁₆H₃₁NaO₄.Molecular Weight: ≈ 310.4 g/mol.Packaging: 5 kg / 10 kg / 25 kg HDPE drums with inner liners (custom export packaging available).

Product Description:
Divalproex Sodium BP is a high-quality active pharmaceutical ingredient (API) widely used in the manufacture of anticonvulsant and mood-stabilizing medications. It is a stable coordination compound comprising sodium valproate and valproic acid in a 1:1 molar relationship. Supplied as a white to off-white crystalline powder, this BP-grade API meets regulatory standards for pharmaceutical use and is suitable for formulation into oral dosage forms such as tablets and capsules. 
Key Features & Benefits:BP-Grade Pharmacopoeial Quality: Manufactured and tested in compliance with British Pharmacopoeia (BP) standards for purity and quality. High Assay Purity: Typically ≥ 98 % API purity, ensuring consistent performance and reliability in formulations. Stable Powder Form: Easy to handle, store, and process in pharmaceutical production environments. Broad Therapeutic Use: Core ingredient for antiepileptic and mood-stabilizing drug products. Documentation Available: Supplied with Certificate of Analysis (CoA) and other compliance documents on request. 
Applications:Divalproex Sodium BP API is widely used in pharmaceutical formulation for:Anticonvulsant Medicines: API for drugs that help control epileptic seizures in adults and children. Mood Stabilizers: Used in formulations for bipolar disorder to manage manic and mixed episodes. Migraine Prophylaxis: API in extended-release products aimed at preventing migraine headaches. Pharmaceutical R&D: Suitable for research and development of new and generic antiepileptic products.
Storage & Handling:Store Divalproex Sodium BP API in a cool, dry, and well-ventilated area, protected from moisture, heat, and direct sunlight. Ensure containers are tightly sealed when not in use. Use appropriate PPE (gloves, mask, goggles) to minimize exposure to dust during handling.

Additional Information:

• Delivery Time: one week