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Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API
Atenolol IP third party API

Atenolol IP third party API

Price 1650 INR/ Kilograms

MOQ : 100 Kilograms

Atenolol IP third party API Specification

  • Poisonous
  • NO
  • Molecular Formula
  • C14H22N2O3
  • HS Code
  • 29420090
  • Heavy Metal (%)
  • Not more than 0.001%
  • Color
  • White
  • Loss on Drying
  • Not more than 0.5%
  • Storage
  • Store in a cool, dry and dark place, below 30C
  • EINECS No
  • 249-028-3
  • Structural Formula
  • (2RS)-4-(2-Hydroxy-3-isopropylaminopropoxy)phenylacetamide
  • Boiling point
  • Not applicable (decomposes before boiling)
  • Molecular Weight
  • 266.34 g/mol
  • Taste
  • Slightly bitter
  • Solubility
  • Freely soluble in water, sparingly soluble in chloroform, methanol
  • Ph Level
  • 5.5 - 7.5 (1% aqueous solution)
  • Smell
  • Odorless
  • Particle Size
  • 90% pass through 60 mesh
  • Shelf Life
  • 5 years
  • Melting Point
  • 152C - 154C
  • Medicine Name
  • Atenolol IP Third Party API
  • Chemical Name
  • Atenolol
  • CAS No
  • 29122-68-7
  • Type
  • API (Active Pharmaceutical Ingredient)
  • Grade
  • Pharmaceutical Grade
  • Usage
  • Used in the formulation of antihypertensive and cardiovascular drugs
  • Purity(%)
  • 99% min
  • Appearance
  • White crystalline powder
  • Physical Form
  • Solid
  • Packaging
  • 25 kg HDPE drum / customized packing
  • Specific Optical Rotation
  • -0.1 to +0.1 (1% in water)
  • Residual Solvents
  • Complies with ICH guidelines
  • Related Substances
  • Not more than 0.5%
  • Identification
  • By IR and HPLC
  • Total Microbial Count
  • Not more than 100 cfu/g
  • Bacterial Endotoxins
  • Less than 0.5 IU/mg
 

Atenolol IP third party API Trade Information

  • Minimum Order Quantity
  • 100 Kilograms
  • FOB Port
  • UDARA
  • Payment Terms
  • Cash in Advance (CID), Letter of Credit at Sight (Sight L/C)
  • 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
  • Main Domestic Market
  • , All India, South India, Central India, West India, North India, East India
 

About Atenolol IP third party API



Introducing the New and Trending Atenolol IP Third Party API, renowned for its ineffable purity and valorous performance in the pharmaceutical industry. Now on Sale, this famed Active Pharmaceutical Ingredient (API) highlights exceptional quality-99% minimum purity and stringent controls on related substances, residual solvents, and heavy metals. Identified by IR and HPLC, this white crystalline powder is ideal for antihypertensive and cardiovascular drug formulations. Safety assured with low endotoxin and microbial counts, Atenolol IP is available in 25 kg HDPE drums or custom packaging. Trust in this reliable solution, distributed by India's esteemed exporters, manufacturers, and suppliers.

Features and Usage Directions of Atenolol IP Third Party API

Atenolol IP Third Party API is a pharmaceutical grade, white crystalline powder used as a potent ingredient in antihypertensive and cardiovascular drug formulations. Users should handle with standard laboratory precautions, ensuring the product is stored below 30C, away from light and moisture. Type of usage includes formulation, blending, and processing as per authorized pharmacopoeial requirements. Its valorous stability and ineffable reliability make it a preferred choice for distributors, manufacturers, and researchers alike.


Sample Policy and Supply Ability: Price and Delivery Simplified

We offer a sample policy tailored to ease your evaluation process-samples are available at the lowest price with convenient transportation and drop-off options. Our supply ability ensures timely fulfillment, meeting large-scale requirements seamlessly. Whether you need a single drum or custom packaging, we are committed to fast, reliable delivery across India. Contact us directly to discuss your distribution or manufacturing needs, and experience our trusted service for Atenolol IP Third Party API.


FAQ's of Atenolol IP third party API:


Q: How is the quality of Atenolol IP Third Party API ensured?

A: The quality is assured through identification by IR and HPLC, compliance with strict impurity and microbial limits, adherence to ICH residual solvent guidelines, and production under pharmaceutical grade standards.

Q: What are the main uses of Atenolol IP Third Party API?

A: Atenolol IP is widely used in the formulation of antihypertensive and cardiovascular drugs, serving as a highly effective active pharmaceutical ingredient for manufacturers and researchers.

Q: When should Atenolol IP Third Party API be stored and handled?

A: It should be stored in a cool, dry, and dark place below 30C, handled with care according to pharmaceutical manufacturing or laboratory standards to maintain efficacy and safety.

Q: Where is Atenolol IP Third Party API typically supplied from?

A: Atenolol IP Third Party API is supplied from India by reputed distributors, exporters, manufacturers, and wholesalers, with reliable supply chains for domestic and international delivery.

Q: What is the process for obtaining a sample of Atenolol IP Third Party API?

A: You can request a sample at the lowest price; transportation and drop-off can be arranged directly through our distribution or sales team for convenient evaluation prior to large orders.

Q: How does using Atenolol IP Third Party API benefit pharmaceutical companies?

A: Its high purity, consistent quality, and compliance with global standards ensure safety and efficacy in finished drug products, offering confidence and regulatory assurance to pharmaceutical manufacturers.

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