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Levocetirizine DI HCL API

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MOQ : 100 Kilograms

Levocetirizine DI HCL API Specification

Heavy Metal (%)
Not more than 0.001%

Loss on Drying
Not more than 0.5%

Particle Size
95% passes through 60 mesh

Melting Point
213-221C

Structural Formula
C21H25ClN2O32HCl (structure as per IUPAC protein notation)

Shelf Life
3 Years

Molecular Weight
461.82 g/mol

HS Code
293339

Ph Level
4.0 - 5.0 (2% aqueous solution)

Solubility
Freely soluble in water, practically insoluble in acetone and in methylene chloride

Taste
Bitter

Molecular Formula
C21H25ClN2O32HCl

Smell
Odorless

Storage
Store in a well-closed container, protected from light and moisture

Color
White

Poisonous
NO

Medicine Name
Levocetirizine Dihydrochloride

Chemical Name
(R)-2-[2-(4-chlorophenyl)-2-phenylethyl]-1,3-dihydro-1,3,5-triazine-4,6-dione dihydrochloride

CAS No
130018-87-0

Type
Levocetirizine DI HCL API

Grade
Pharmaceutical Grade

Usage
Used in the manufacturing of antihistamine formulations for allergic rhinitis and urticaria

Purity(%)
>99%

Appearance
White to almost white powder

Physical Form
Solid

Assay
Not less than 99.0% and not more than 101.0%

Related Substances
Total impurities not more than 0.5%

Chloride Content
16.9% - 17.5%

Optical Rotation
-125 to -133

Identification
Conforms to standard (IR/UV/HPLC as applicable)

Residual Solvents
As per ICH guidelines

Water Content (by KF)
Not more than 1.0%

Levocetirizine DI HCL API Trade Information

Minimum Order Quantity
100 Kilograms

Supply Ability
1000 Kilograms Per Month

Delivery Time
7 Days

Main Export Market(s)
Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa

About Levocetirizine DI HCL API

Levocetirizine DI HCL API offers matchless purity and unrivaled value for pharmaceutical manufacturers. This fresh, white to almost white powder stands out in its class, featuring an assay between 99.0% and 101.0%, minimal impurities (total not more than 0.5%), and strictly regulated chloride content (16.9% - 17.5%). Identified via IR/UV/HPLC, it conforms to all applicable standards. Ravishing in its consistent quality, this solid, odorless, and bitter-tasting substance is the ephemeral yet essential base for antihistamine formulations, specifically for allergic rhinitis and urticaria. Store securely for a stable, 3-year shelf life.

Application, Type & Usage of Levocetirizine DI HCL API

Levocetirizine DI HCL API is predominantly applied in the manufacture of antihistamine medications for allergic rhinitis and urticaria. As a high-value pharmaceutical ingredient, it is suitable for processes requiring fresh, pure, and reliable materials. Its physical form as a fine powder allows seamless integration into various formulations. Its matchless performance and unrivaled quality have made it the preferred choice among pharmaceutical exporters, manufacturers, and suppliers in India.

Sample Policy, Packaging & Payment Terms for Levocetirizine DI HCL API

Our sample policy ensures potential partners can review product quality prior to order completion, minimizing initial expenditure. Secure packing in well-closed containers protects contents from light and moisture, preserving freshness throughout freight. Payment terms are tailored to streamline transactions and support long-term associations, with each consignment tracked from order to delivery. We are committed to seamless product acquisition for every pharmaceutical requirement.

FAQ's of Levocetirizine DI HCL API:

Q: How should Levocetirizine DI HCL API be stored to ensure its shelf life?

A: Levocetirizine DI HCL API should be stored in a well-closed container, protected from light and moisture, to preserve its matchless quality and maintain a shelf life of up to 3 years.

Q: What are the primary applications of Levocetirizine DI HCL API?

A: The primary applications include the manufacture of antihistamine formulations used for treating allergic rhinitis and urticaria, thanks to its fresh and high-purity pharmaceutical grade.

Q: When should sample requests for Levocetirizine DI HCL API be placed?

A: Sample requests can be made prior to bulk order completion, allowing for evaluation and minimizing initial expenditure on larger consignments.

Q: Where does Levocetirizine DI HCL API deliver unrivaled value in the pharmaceutical process?

A: It delivers unrivaled value as an API because of its extremely high purity, low impurity profile, and consistent performance in the preparation of antihistamine formulations.

Q: What benefits does using Levocetirizine DI HCL API provide to manufacturers?

A: Manufacturers benefit from its ravishing purity, minimal residual solvents, and superior solubility in water, ensuring efficiency and reliability in antihistamine drug production.

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