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Losartan Powder

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Losartan Powder Specification

Poisonous
No (when used as directed)

Shelf Life
2 years

Loss on Drying
0.5%

Particle Size
D90 100 m

Heavy Metal (%)
0.001%

Molecular Formula
C22H23ClN6O

Solubility
Slightly soluble in water, soluble in methanol and DMSO

Smell
Odorless

Molecular Weight
422.91 g/mol

Structural Formula
Available on request

Taste
Bitter

HS Code
29339900

Medicine Name
Losartan Powder

Type
Active Pharmaceutical Ingredient (API)

Grade
Pharmaceutical Grade

Usage
Used for the treatment of hypertension and cardiovascular diseases

Purity(%)
>=99%

Physical Form
Powder

Losartan Powder Trade Information

Payment Terms
Letter of Credit at Sight (Sight L/C), Telegraphic Transfer (T/T)

Supply Ability
5 Per Month

Delivery Time
3 Week

Sample Available
Yes

Sample Policy
Within a certain price range free samples are available

Packaging Details
Fiber drum ,Plastic, Carboys & Barrels.

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

About Losartan Powder

Owing to our wide knowledge in this domain, we have become a desirable exporter and supplier of superior quality Losartan Powder. This powder is basically used to treat high blood pressure. The offered powder is exactly processed under the most hygiene environment using top-notch quality basic chemicals and innovative techniques. Furthermore, the provided power can also be used in treatment of heart disease. To meet the exact demands of clients, we are offering this Losartan Powder in several packaging options at very reasonable price.

Features:

Accurate composition
Zero side effects
Precise pH value
Effectiveness

Details

Cas Number 124750-99-8
Mol.Formula C22h22clkn6o
Mol.Weight- 461.01
It Is A White To Off-white Free-flowing Crystalline Powder With A Melting Range Of 184 degree c. It Is Freely Soluble In Water, Soluble In Alcohols.
Standard Offered Of Pharmaceutical Grade BP/USP/EP
Packing Offered In Export Worthy Packing Of 25 Kilos Or As Per Our Customer Requirements.

Specifications

Type	Pharmaceutical Raw Material
Form	Powder
Solubility	Soluble In Water, Soluble In Alcohols
Packing	25 Kilos Or As Per Our Customer Requirements
Color	White
Standard Grade	Pharmaceutical Grade BP/USP/EP

Precision in Pharmaceutical Manufacturing

Losartan Powder is designed for exceptional performance in drug formulation processes. Its consistent particle size and high purity support reliable production of antihypertensive and cardiovascular medications. The ingredients slight solubility in water and higher affinity for methanol and DMSO enable versatile application across different pharmaceutical systems, allowing producers to meet diverse therapeutic requirements.

Reliable Quality Control

Every batch of Losartan Powder is thoroughly tested to ensure pharmaceutical-grade quality, including compliance with purity, shelf life, loss on drying, and heavy metal standards. These stringent checks guarantee product integrity and safety in medicinal applications, minimizing risks and enhancing patient outcomes. Traders and exporters benefit from dependable documentation and regulatory compliance.

FAQs of Losartan Powder:

Q: How is Losartan Powder used in the treatment of hypertension?

A: Losartan Powder serves as a key active ingredient in the formulation of medications prescribed for hypertension management. It acts by blocking angiotensin II receptors, thus aiding in the reduction of blood pressure and supporting cardiovascular health.

Q: What are the benefits of using pharmaceutical grade Losartan Powder?

A: Pharmaceutical grade Losartan Powder guarantees 99% purity, low heavy metal content, and consistent particle size. These attributes ensure that medicinal products are effective, safe, and meet regulatory standards for patient health.

Q: When should Losartan Powder be incorporated into drug manufacturing?

A: Losartan Powder should be added during the active ingredient blending phase of pharmaceutical production. Its fine powder form and stable molecular profile make it suitable for processes requiring precision and uniformity.

Q: Where is Losartan Powder typically sourced for export and trade?

A: Losartan Powder is primarily manufactured and exported from India, adhering to international pharmaceutical regulations and quality controls to ensure suitability for global markets.

Q: What is the process for ensuring the purity and quality of Losartan Powder?

A: Each batch undergoes rigorous analytical testing for purity (99%), loss on drying (0.5%), heavy metal content (0.001%), and particle size distribution, conforming to pharmaceutical standards before release.

Q: How should Losartan Powder be stored to maintain its shelf life?

A: Losartan Powder should be stored in well-sealed containers at controlled room temperature, protected from moisture and direct sunlight to preserve its efficacy and two-year shelf life.

Q: Is Losartan Powder suitable for all medicinal formulations?

A: Losartan Powder is suitable for various cardiovascular and antihypertensive formulations, given its chemistry and safety profile. Solubility considerations should be taken into account for specific drug delivery systems.

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