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Ciprofloxacin Hydrochloride Powder

Price 1000.0 INR/ Piece

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MOQ : 1000 Pieces

Ciprofloxacin Hydrochloride Powder Specification

Melting Point
>300C (decomposes)

HS Code
29419090

Heavy Metal (%)
0.001%

Particle Size
Typically 10-40 microns

Smell
Odorless

Molecular Formula
C17H18FN3O3HCl

EINECS No
610-613-2

Structural Formula
C17H18FN3O3HCl (as per structure shown)

Shelf Life
5 years

Solubility
Freely soluble in dilute acid, sparingly soluble in water

Loss on Drying
0.5%

Color
White to off-white

Boiling point
Not applicable / decomposes

Taste
Bitter

Molecular Weight
367.81 g/mol

Ph Level
4.0 - 5.5 (1% aqueous solution)

Storage
Store in a cool, dry place away from light

Poisonous
No (for pharmaceutical use under prescription)

Medicine Name
Ciprofloxacin Hydrochloride Powder

Chemical Name
Ciprofloxacin Hydrochloride

CAS No
86393-32-0

Type
Antibiotic API (Active Pharmaceutical Ingredient)

Grade
Pharmaceutical Grade

Usage
Used in the formulation of antibiotics for treatment of bacterial infections

Purity(%)
99% Min

Appearance
White to off-white crystalline powder

Physical Form
Powder

Related Substances
Total impurities 1.0%

Identification Method
HPLC/IR

Residual Moisture
Not more than 0.5%

Packing
Fiber drum with double polyethylene bags, 25kg net

Residual Solvents
Complies with ICH guidelines

Microbial Limits
Within pharmacopeial limits

Assay
>=99% (on dried basis)

Chloride Content
17.5% - 18.5%

Stability
Stable under recommended storage conditions

Bulk Density
0.280.46 g/cm

Ciprofloxacin Hydrochloride Powder Trade Information

Minimum Order Quantity
1000 Pieces

Supply Ability
1000 Pieces Per Day

Delivery Time
7 Days

Sample Available
No

Sample Policy
Contact us for information regarding our sample policy

About Ciprofloxacin Hydrochloride Powder

Grade Standard	BP
Purity	99%
Form	Powder
CAS Number	86393-32-0
Packaging Size	25Kg
Packaging Type	Bag
Grade	Pharma Grade
Shelf Life	24 Months

We are engaged in offeringiCiprfloxacin Powderito our clients. Our range of all products is widely appreciated by our clients.

Precision Quality and Purity

Ciprofloxacin Hydrochloride Powder is manufactured to stringent quality standards, featuring a minimum purity of 99%, low residual moisture (0.5%), and controlled heavy metal content (0.001%). Advanced identification methods like HPLC and IR guarantee product authenticity, while comprehensive testing ensures all pharmaceutical specifications, including microbial and related substances limits, are well within accepted norms.

Versatile Pharmaceutical Applications

This powder serves as an essential active ingredient in antibiotic formulations, trusted globally for the effective treatment of various bacterial infections. Its controlled particle size (10-40 microns) and excellent solubility profile facilitate smooth formulation processes, supporting manufacturers, importers, and suppliers in India and abroad in delivering safe, reliable antibiotics.

Safe Handling and Long-Term Stability

Packaged securely in fiber drums with double polyethylene bags, Ciprofloxacin Hydrochloride Powder is stable for up to 5 years when stored in cool, dry conditions away from light. Odorless and bitter-tasting, it remains non-poisonous under prescribed pharmaceutical use, ensuring both user and patient safety in all stages from production to administration.

FAQ's of Ciprofloxacin Hydrochloride Powder:

Q: How is the identity and purity of Ciprofloxacin Hydrochloride Powder verified?

A: Identity and purity are confirmed through HPLC and IR analysis, ensuring a minimum assay of 99% on a dried basis. Additional rigorous tests verify the product complies with pharmacopeial and ICH guidelines for residual solvents, related substances, and other critical parameters.

Q: What are the recommended storage conditions for Ciprofloxacin Hydrochloride Powder?

A: It should be stored in a cool, dry place away from direct light to ensure maximum stability and effectiveness throughout its 5-year shelf life.

Q: When should Ciprofloxacin Hydrochloride Powder be used in pharmaceutical manufacturing?

A: This API is incorporated during the active ingredient blending stage in the production of antibiotic medications formulated for bacterial infection treatment, as per prescribed pharmaceutical processes and standards.

Q: Where is Ciprofloxacin Hydrochloride Powder sourced from and how is it packed?

A: It is manufactured, exported, and supplied mainly from India and is typically packed in 25kg fiber drums with double polyethylene bags for protection during transport and storage.

Q: What are the main benefits of using this antibiotic API in pharmaceutical formulations?

A: Its high purity, low impurity profile, stability, and compliance with international quality standards make it an ideal choice for developing effective, reliable antibacterial medications.

Q: How should Ciprofloxacin Hydrochloride Powder be handled during processing?

A: Proper protective measures should be followed to avoid moisture and contamination, as well as adherence to pharmaceutical handling protocols to maintain product integrity and user safety.

Q: What applications is Ciprofloxacin Hydrochloride Powder intended for?

A: It is used by pharmaceutical companies in the manufacture of antibiotics designed to combat a wide range of bacterial infections, benefiting from its high purity and robust safety profile.

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