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Miconazole Nitrate BP
Miconazole Nitrate BP is a high-purity, pharmaceutical-grade antifungal agent conforming to British Pharmacopoeia (BP) specifications. It is widely used in the formulation of topical and oral pharmaceutical products for the treatment of fungal infections caused by dermatophytes and yeasts, including Candida species. Miconazole Nitrate functions by inhibiting the biosynthesis of ergosterol, a vital component of fungal cell membranes, leading to cell death.
This white to off-white crystalline powder is highly effective and exhibits broad-spectrum antifungal and some antibacterial activity. It is commonly utilized in creams, ointments, powders, and gel formulations.
Miconazole Nitrate BP
Primary Uses
- Antiprotozoal Therapy
- Treatment of amoebiasis (intestinal and hepatic).
- Management of giardiasis (Giardia lamblia infections).
- Used in trichomoniasis (vaginal and urethral infections).
- Antibacterial Therapy
- Active against anaerobic bacteria (e.g., Bacteroides, Clostridium).
- Used in bacterial vaginosis and pelvic inflammatory disease (PID).
- Prophylaxis in colorectal and gynecological surgeries.
- Helicobacter pylori Eradication
- Part of triple/quadruple therapy for peptic ulcers.
Secondary Uses
- Veterinary Medicine
- Treatment of anaerobic infections in dogs and cats.
- Used in fish farming to control protozoan parasites.
- Dermatology
- Topical formulations for rosacea and acneiform eruptions.
- Dental Infections
- Adjunct therapy for acute necrotizing ulcerative gingivitis (ANUG).
1. Basic Identification Attributes
- Chemical Name (IUPAC): 2-Methyl-5-nitro-1H-imidazole-1-ethanol benzoate
- Common/Trade Name: Metronidazole Benzoate BP
- CAS Number: 13182-89-3
- HS Code: 2933.29.90 (Other heterocyclic compounds)
- Synonyms: Metronidazole benzoate ester; Flagyl benzoate
2. Physical & Chemical Properties
- Physical State: White to pale yellow crystalline powder
- Color & Odor: Odorless or faint characteristic odor
- Melting Point: ~98–102°C
- Solubility:
- Slightly soluble in water
- Freely soluble in methanol, ethanol, chloroform
- pH: Neutral (~6.0–7.5 in suspension)
3. Safety & Hazard Attributes
- GHS Classification:
- H302 (Harmful if swallowed)
- H315 (Causes skin irritation)
- H319 (Causes serious eye irritation)
- H335 (May cause respiratory irritation)
- Toxicity: Low acute toxicity; avoid prolonged exposure
- Exposure Limits: No specific OEL; handle as pharmaceutical powder
4. Storage & Handling Attributes
- Storage Conditions:
- Store in tightly sealed containers at ≤25°C.
- Protect from light and moisture.
- Container Type: Amber glass or HDPE containers.
- Shelf Life: Typically 24–36 months if stored properly.
- Handling Precautions:
- Use gloves, mask, and goggles.
- Avoid dust formation.
5. Regulatory & Compliance Attributes
- Complies with:
- British Pharmacopoeia (BP) standards.
- USP/NF (if applicable for formulations).
- ICH Q7 (GMP for APIs).
- Regulatory Status:
- Prescription-only drug in most countries.
6. Environmental & Health Impact
- Biodegradability: Readily biodegradable.
- Ecotoxicity: Low risk; no significant bioaccumulation.
- Carcinogenicity/Mutagenicity:
- Not classified (metronidazole is a possible carcinogen with chronic exposure).
Safety Handling Precautions
- PPE Required:
- Nitrile gloves, dust mask, lab coat, safety goggles.
- Handling Guidelines:
- Use in well-ventilated areas.
- Avoid contact with skin/eyes.
- Storage Measures:
- Keep away from strong oxidizers.
First Aid Measures
- Inhalation: Move to fresh air; seek medical help if irritation persists.
- Skin Contact: Wash with soap and water; remove contaminated clothing.
- Eye Contact: Rinse with water for 15 mins; consult ophthalmologist.
- Ingestion: Rinse mouth; do NOT induce vomiting; seek medical attention.
Firefighting Measures
- Fire Hazards: Non-flammable but may decompose at high temperatures.
- Extinguishing Media: Use water spray, CO₂, or dry chemical.
- Hazardous Combustion Products: Nitrogen oxides (NOx), CO, CO₂.
Related products
Diclofenac Sodium BP
Diclofenac Sodium is a nonsteroidal anti-inflammatory drug (NSAID) widely used for its potent analgesic, anti-inflammatory, and antipyretic properties. It is the sodium salt form of diclofenac, providing enhanced solubility and rapid absorption. Diclofenac Sodium BP (British Pharmacopoeia standard) ensures pharmaceutical-grade purity and compliance with stringent quality standards. It is commonly formulated in oral tablets, topical gels, injections, and ophthalmic preparations.
Dicyclomine Hydrochloride
Dicyclomine Hydrochloride is an anticholinergic and antispasmodic agent used primarily to relieve smooth muscle spasms in the gastrointestinal tract. It works by blocking muscarinic receptors, thereby reducing muscle contractions and spasms, which helps alleviate symptoms of irritable bowel syndrome (IBS) and other functional bowel disorders. It is commonly available in oral tablets, capsules, and injectable formulations.
Diphenhydramine HCL BP
Diphenhydramine HCL BP is a first-generation antihistamine with potent anticholinergic, sedative, and antiemetic properties. It is commonly used to relieve symptoms associated with allergies, hay fever, the common cold, and motion sickness. Diphenhydramine HCL is a white crystalline powder, highly soluble in water, making it suitable for oral, topical, and injectable pharmaceutical formulations. Due to its ability to cross the blood-brain barrier, it causes sedation and is often used as a sleep aid and for managing Parkinson’s disease symptoms.
Enrofloxacin Hydrochloride
Enrofloxacin Hydrochloride is a broad-spectrum fluoroquinolone antibiotic used primarily in veterinary medicine. It is the hydrochloride salt of enrofloxacin, offering enhanced solubility and bioavailability. Enrofloxacin inhibits bacterial DNA gyrase and topoisomerase IV, disrupting DNA replication in Gram-negative and Gram-positive organisms as well as some Mycoplasma species. It is available as a white to off-white crystalline powder, used in injectable, oral, and topical formulations designed for livestock, companion animals, and aquatic species.
Mebendazole USP ( Micronized white)
Mebendazole USP (Micronized White) is a pharmaceutical-grade anthelmintic agent used for the treatment of parasitic worm infections. The micronized white powder form offers enhanced bioavailability and better dispersion in pharmaceutical formulations. It is effective against a broad spectrum of intestinal parasites including roundworms, whipworms, hookworms, and pinworms. Mebendazole is commonly used in oral tablet and suspension preparations, ensuring efficient parasite eradication with minimal side effects.
Mepyramine Maleate BP
Mepyramine Maleate BP is an antihistamine drug commonly used to relieve allergic symptoms such as hay fever, urticaria, and other allergic reactions. It works by blocking histamine H1 receptors, reducing allergic responses like itching, swelling, and redness. This compound is a white or off-white crystalline powder, soluble in water and alcohol, widely used in pharmaceutical formulations including tablets, creams, and injectables.
Methyl Salicylate BP
Methyl Salicylate BP is a clear, colorless to pale yellow oily liquid with a characteristic strong, sweet, and minty odor. It is an organic ester commonly used for its analgesic, anti-inflammatory, and flavoring properties. Methyl Salicylate is widely used in pharmaceutical preparations, topical pain relief products, cosmetics, and as a fragrance ingredient.
Metronidazole Benzoate BP
Metronidazole Benzoate BP is a benzoate ester derivative of metronidazole, used primarily as an antiprotozoal and antibacterial agent. It is a prodrug that hydrolyzes in the body to release metronidazole, making it more palatable for pediatric and geriatric oral suspensions. It complies with the British Pharmacopoeia (BP) standards for purity and efficacy.
