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CIPROFLOXACIN HCL IP/BP/EP/USP

Name: CIPROFLOXACIN HCL IP/BP/EP/USP
Brand: IPSUM LIFESCIENCES LLP
Price: 1800 INR
Availability: InStock

Price 1800 INR/ Kilograms

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MOQ : 25 Kilograms

CIPROFLOXACIN HCL IP/BP/EP/USP Specification

Molecular Formula
C17H18FN3O3HCl

Particle Size
D90 10 microns (on request)

Residue on Ignition
0.1%

Assay
99%

Storage
Keep container tightly closed in a dry and well-ventilated place. Store at room temperature.

EINECS No
425-860-6

Moisture (%)
0.5%

Ph Level
Not less than 3.0 and not more than 4.5 (1% solution)

Loss on Drying
0.5%

Heavy Metal (%)
0.001%

Melting Point
Circa 320C (decomposes)

Molecular Weight
385.8 g/mol

Place of Origin
India

Boiling point
Not applicable (decomposes)

HS Code
29419060

Other Names
Ciprofloxacin Hydrochloride, Ciprofloxacin HCl

CAS No
86393-32-0

Type
Antibiotic API

Grade
IP/BP/EP/USP Grade

Usage
Pharmaceutical raw material, Antibacterial

Purity
99%

Appearance
Crystalline powder

Application
Active Pharmaceutical Ingredient; Used to manufacture tablets, capsules, injections, and oral suspensions.

Raw Material
Yes

Smell
Odorless

Color
Almost White to Pale Yellow

Form
Powder

Related Substances
Total impurities 0.5%

Water Content (by KF)
0.5%

Endotoxins
Complies with pharmacopeial limits

Identification
By IR and UV-match with standard

Bacterial Endotoxins
NMT 0.5 IU/mg

Compatibility
Compatible with standard pharmaceutical excipients

Country of Export
India

Packaging
HDPE drums/cardboard fiber drums of 25 kg net or as per customer requirement

Solubility
Freely soluble in acetic acid and slightly soluble in water and ethanol

Microbial Purity
Meets pharmacopeia standards

Shelf Life
4 years if stored properly

Specific Optical Rotation
+30 to +35 (1% solution)

Chloride Content
Conforms to specifications as per pharmacopeia

About CIPROFLOXACIN HCL IP/BP/EP/USP

The chemical structure of ciprofloxacin hydrochloride is characterized by its molecular formula C17H18FN3O3 HCl and a molecular weight of approximately 385.82 g/mol. It appears as a white to slightly yellowish crystalline powder, freely soluble in water but only slightly soluble in ethanol, and practically insoluble in acetone and ether.

Product Quality and Compliance

Ciprofloxacin HCl is produced in compliance with leading pharmacopoeias (IP/BP/EP/USP) and conforms to strict quality standards. The product is assessed for purity (99%), related substances (0.5%), loss on drying (0.5%), and microbial content as per pharmacopeial requirements, ensuring safety and efficacy for pharmaceutical manufacturing.

Packaging and Storage

To maintain its stability and quality, Ciprofloxacin HCl is packaged in robust HDPE or cardboard fiber drums, each containing a net weight of 25kg, or as per customer requests. For optimum shelf life of up to four years, storage in tightly closed containers within a dry, well-ventilated environment at room temperature is recommended.

Pharmaceutical Application and Benefits

As a high-purity antibiotic API, Ciprofloxacin HCl is crucial for manufacturing various dosage forms, including tablets, oral suspensions, and injectables. Its broad-spectrum antibacterial activity and reliable compliance with international standards make it a preferred choice for pharmaceutical companies worldwide.

FAQ's of CIPROFLOXACIN HCL IP/BP/EP/USP:

Q: How should Ciprofloxacin HCl be stored to ensure maximum shelf life?

A: The product should be kept in a tightly closed container, stored in a dry, well-ventilated place at room temperature. Proper storage conditions help maintain its quality and extend its shelf life up to four years.

Q: What are the main pharmaceutical uses of Ciprofloxacin Hydrochloride?

A: Ciprofloxacin HCl is primarily used as an active ingredient in manufacturing antibiotics, including tablets, capsules, injections, and oral suspensions. Its broad-spectrum antibacterial activity makes it effective against a wide range of bacterial infections.

Q: What are the identifying features of Ciprofloxacin HCl IP/BP/EP/USP grade?

A: Identification is performed by infrared (IR) and ultraviolet (UV) spectroscopic methods, ensuring a precise match with the standard. Additional specifications such as specific optical rotation, solubility, and assay confirm its authenticity.

Q: When can Ciprofloxacin HCl be used in pharmaceutical formulations?

A: This API can be incorporated in pharmaceutical formulations at any stage where a high-purity antibiotic is required, given its compatibility with standard excipients and its stability under recommended storage conditions.

Q: Where is Ciprofloxacin HCl typically manufactured and exported from?

A: This product is manufactured and exported from India, with high quality standards supported by leading manufacturers, suppliers, and traders.

Q: What is the process for packaging Ciprofloxacin HCl for export?

A: Ciprofloxacin HCl is packed in HDPE drums or cardboard fiber drums with a net weight of 25 kg or according to customer requirements, ensuring product integrity during storage and transport.

Q: What benefits does Ciprofloxacin HCl offer to pharmaceutical manufacturers?

A: Ciprofloxacin HCl offers high purity, compliance with major pharmacopeias, reliable antibacterial efficacy, and ease of formulation, making it ideal for a variety of finished dosage forms.

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