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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
Cetirizine Dihydrochloride
Cetirizine Dihydrochloride is a second-generation antihistamine widely used to relieve allergy symptoms such as hay fever, urticaria (hives), and other allergic conditions. It is the dihydrochloride salt form of cetirizine, presenting as a white to off-white crystalline powder that is odorless or nearly odorless and slightly bitter in taste. Cetirizine Dihydrochloride acts as a selective antagonist of peripheral H1 histamine receptors, preventing the effects of histamine and thereby reducing allergic symptoms without causing significant sedation. It is a commonly prescribed active pharmaceutical ingredient (API) in oral tablets, syrups, and capsules.
Chloramphenicol Palmitate Micronised
Chloramphenicol Palmitate Micronised is a micronized, lipophilic ester derivative of chloramphenicol, designed for improved solubility and bioavailability compared to the parent drug. It appears as a fine, white to off-white powder with enhanced surface area due to micronization. This antibiotic is widely used for oral formulations, particularly pediatric suspensions, due to its palatability and controlled release properties. Chloramphenicol Palmitate exhibits broad-spectrum antibacterial activity against both Gram-positive and Gram-negative bacteria. Its ester form offers better stability and reduced bitterness, making it a preferred choice in pharmaceutical 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.
Diloxanide Furoate
Diloxanide Furoate is an orally administered antiprotozoal agent used primarily for the treatment of amoebiasis. It is a furan-based derivative that acts as a luminal amoebicide, effectively targeting Entamoeba histolytica cysts and trophozoites within the intestinal lumen. This compound is well-regarded for its efficacy in eradicating asymptomatic cyst carriers and as a follow-up treatment after systemic amoebicidal therapy. Diloxanide Furoate has good oral bioavailability and a favorable safety profile.
Doxycycline Hyclate BP
Doxycycline Hyclate BP is a broad-spectrum, semisynthetic tetracycline-class antibiotic available as the hemihydrate salt form of doxycycline. It is widely used in pharmaceutical formulations due to its high bioavailability, broad antibacterial activity, and favorable pharmacokinetic profile. The compound exhibits bacteriostatic action by inhibiting protein synthesis in susceptible bacteria, making it effective against a wide range of Gram-positive and Gram-negative organisms as well as atypical pathogens. It is typically supplied as a fine, white to off-white crystalline powder soluble in water and suitable for oral and parenteral dosage forms.
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.
Lidocaine HCL BP
Lidocaine HCL BP is a white crystalline powder or granules that are highly soluble in water. It is a local anesthetic and antiarrhythmic agent widely used in medical and dental fields. Lidocaine HCL BP acts by blocking nerve signal transmission, providing rapid and effective numbing of targeted areas. It conforms to British Pharmacopoeia (BP) standards, ensuring pharmaceutical-grade purity and consistency. It is commonly formulated into injections, topical gels, creams, and patches for pain relief and arrhythmia treatment.
Neomycin Sulphate BP Oral
Neomycin Sulphate BP Oral is an aminoglycoside antibiotic derived from Streptomyces fradiae. It is used primarily for treating infections caused by susceptible aerobic gram-negative and some gram-positive bacteria. The oral form is especially utilized for intestinal antisepsis, to reduce bacterial flora before gastrointestinal surgery, or to treat hepatic encephalopathy by decreasing ammonia-producing bacteria in the gut. It is available in powder or tablet form conforming to British Pharmacopoeia (BP) standards, ensuring high purity and efficacy.
