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Labetalol HCL
Labetalol HCL

Labetalol HCL

MOQ : 100 Kilograms

Labetalol HCL Specification

  • Smell
  • Odorless
  • Shelf Life
  • 5 years
  • Storage
  • Store in a cool, dry place, protected from light
  • Heavy Metal (%)
  • 0.001%
  • Particle Size
  • D90 50 m
  • Poisonous
  • No (when used in prescribed dosages)
  • Structural Formula
  • Refer to product documentation
  • Loss on Drying
  • 0.5%
  • Boiling point
  • Not applicable (decomposes before boiling)
  • Melting Point
  • 166C to 170C
  • Solubility
  • Freely soluble in water, soluble in methanol
  • Molecular Formula
  • C19H24N2O3HCl
  • Taste
  • Bitter
  • Ph Level
  • 4.0 - 5.5 (1% solution)
  • HS Code
  • 29420090
  • Color
  • White to off-white
  • EINECS No
  • 253-275-0
  • Molecular Weight
  • 364.86 g/mol
  • Medicine Name
  • Labetalol HCL
  • Chemical Name
  • Labetalol Hydrochloride
  • CAS No
  • 36894-69-6
  • Type
  • Active Pharmaceutical Ingredient (API)
  • Grade
  • Pharmaceutical Grade
  • Usage
  • Used as antihypertensive agent for treating high blood pressure
  • Purity(%)
  • 99.0
  • Appearance
  • White to off-white powder
  • Physical Form
  • Solid
  • Related Substances
  • Total impurities 1.0%
  • Residual Solvents
  • Complies with ICH Q3C guidelines
  • Specific Optical Rotation
  • +120 to +126 (in water)
  • Assay
  • 98.5% to 101.0% (on anhydrous basis)
  • Packing
  • Packed in HDPE/LDPE containers with double polyethylene bags
  • Microbial Limit
  • Complies with pharmacopeial standards
  • Identification
  • By IR, HPLC and chemical tests
 

Labetalol HCL Trade Information

  • Minimum Order Quantity
  • 100 Kilograms
  • Supply Ability
  • 1000 Kilograms Per Week
  • Delivery Time
  • 7 Days
 

Labetalol HCL About



Explore the virtue of Labetalol HCL-a top-rated, must-have pharmaceutical API crafted for precision in antihypertensive therapies. This radiant, polished white to off-white powder exhibits a purity of 99.0% and is packed virtuoso-style in double-bagged HDPE/LDPE containers to ensure integrity and safety. Identified by IR, HPLC, and chemical tests, Labetalol Hydrochloride meets stringent ICH Q3C and pharmacopeial benchmarks for residual solvents, impurities, and microbial limits. Freely soluble in water, this API is an essential, globally trusted choice for pharmaceutical manufacturers and suppliers.

Advantages and Applications of Labetalol HCL

Labetalol HCL delivers a harmonious balance of exceptional efficacy and safety for managing high blood pressure. Its key advantages include consistent purity, reliable assay range, and excellent solubility. The application surface spans from pharmaceutical formulations and hospitals to clinical settings, making it an indispensable antihypertensive agent. Highlighted features comprise stringent impurity controls, optimal particle size, and extended shelf life, establishing this API as a trusted cornerstone for healthcare solutions.


Sample Policy, Certifications, and Export Markets for Labetalol HCL

We offer quotations for Labetalol HCL samples, allowing evaluation prior to confirming the sale price and expenditure. Each batch is supported by robust certifications and analytical documentation, affirming compliance with international standards. Our main export markets include Asia, Africa, Europe, and the Americas, with each consignment adhering to strict regulatory norms. Our sample policy fosters trust and transparency, encouraging partnerships with exporters, suppliers, and traders worldwide.


FAQ's of Labetalol HCL:


Q: How should Labetalol HCL be stored to ensure maximum shelf life?

A: Labetalol HCL should be stored in a cool, dry place, protected from light, and kept in its original HDPE/LDPE containers with double polyethylene bags to maintain its stability and efficacy for up to five years.

Q: What are the main benefits of using Labetalol HCL as an antihypertensive agent?

A: Labetalol HCL provides exceptional control over high blood pressure due to its high purity, compliance with international pharmaceutical standards, consistent assay results, and excellent solubility profile, ensuring effective dosage and patient safety.

Q: When does Labetalol HCL reach peak efficacy after administration?

A: Labetalol HCL usually begins to show therapeutic effects shortly after administration, with peak efficacy typically observed within a few hours, depending on the pharmaceutical formulation and patient-specific factors.

Q: Where can Labetalol HCL be sourced and is it available globally?

A: Labetalol HCL is available for sourcing from reputable exporters, suppliers, and traders in India and is widely exported to major pharmaceutical markets across Asia, Europe, Africa, and the Americas.

Q: What is the process of identifying and ensuring the purity of Labetalol HCL?

A: Identification of Labetalol HCL is performed by IR, HPLC, and chemical tests. Purity and quality are confirmed through assay (98.5%-101.0%), residual solvent checks compliant with ICH Q3C, impurity profiling, and microbial limit testing according to pharmacopeial standards.

Q: How is Labetalol HCL typically used in pharmaceutical preparations?

A: Labetalol HCL is commonly incorporated as the active ingredient in tablet or injectable formulations for treating high blood pressure, following precise calculations based on its purity and therapeutic dosage requirements.

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