Send Inquiry

Request To Call Back

TELMISARTAN IP/BP/EP/USP

Name: TELMISARTAN IP/BP/EP/USP
Brand: IPSUM LIFESCIENCES LLP
Price: 1800 INR
Availability: InStock

Price 1800 INR/ Kilograms

Get a Price/Quote

MOQ : 25 Kilograms

TELMISARTAN IP/BP/EP/USP Specification

Storage
Store in a cool, dry & dark place, below 25 C, protected from light and moisture

Loss on Drying
0.5%

HS Code
29339900

Particle Size
D90 < 20 m

Place of Origin
India

Melting Point
> 260 C (decomposes)

Assay
99.0% (by HPLC)

Molecular Weight
514.63 g/mol

Ph Level
Neutral

Moisture (%)
0.5%

Molecular Formula
C33H30N4O2

Heavy Metal (%)
0.001%

Residue on Ignition
0.1%

Other Names
Micardis

CAS No
144701-48-4

Type
Pharmaceutical Raw Material

Grade
Pharmaceutical Grade

Usage
Used in treatment of hypertension

Purity
99% min

Appearance
White to off-white powder

Application
Antihypertensive Agent

Raw Material
For pharmaceutical formulation

Smell
Odorless

Color
White to off-white

Form
Powder

Biological Source
Synthetic

Manufacturing Process
As per cGMP guidelines

Impurity Level
Single impurity 0.1% ; Total impurities 0.2%

Identification
Complies with standard IR and HPLC spectrum

Certificate of Analysis
Available with every batch

Pharmacopoeias Complied
IP/BP/EP/USP

Pack Size
1 kg, 5 kg, 25 kg or as required

Shelf Life
36 months from manufacturing date if stored as recommended

Solubility
Practically insoluble in water, soluble in strong acid or base

About TELMISARTAN IP/BP/EP/USP

Telmisartan is a medication classified as an angiotensin II receptor antagonist, commonly prescribed to manage hypertension (high blood pressure) and mitigate cardiovascular risks in patients with certain conditions. Its chemical composition includes a molecular formula of C33H30N4O2, indicative of its tetrazole derivative structure.

High Purity & Quality Assurance

Telmisartan ensures a minimum assay of 99.0% by HPLC and strict impurity limits (single impurity 0.1%, total impurities 0.2%). Each batch is backed by a comprehensive Certificate of Analysis, confirming its pharmaceutical-grade quality and compliance with international standards.

cGMP Manufacturing & Reliable Supply

Produced using cutting-edge synthetic methods in facilities conforming to cGMP protocols, Telmisartan is supplied directly from India's leading pharmaceutical manufacturer. Customizable pack sizes (1kg, 5kg, 25kg) are available to suit research, formulation, or production needs, ensuring consistent and timely delivery.

Optimal Stability & Storage Guidelines

With a shelf life of 36 months from manufacturing, Telmisartan retains its potency and integrity when stored in cool, dry, and dark conditions below 25C. Packaging is designed to protect from light and moisture, thus maintaining product quality throughout its shelf life.

FAQ's of TELMISARTAN IP/BP/EP/USP:

Q: How should Telmisartan IP/BP/EP/USP be stored for maximum shelf life?

A: Telmisartan should be stored in a cool, dry, and dark place, below 25C, and protected from light and moisture to preserve its stability and 36-month shelf life from the manufacturing date.

Q: What is the recommended use of Telmisartan as a pharmaceutical raw material?

A: Telmisartan is primarily used in the formulation of antihypertensive agents for the treatment of hypertension. Its high purity and compliance with international pharmacopoeias make it suitable for pharmaceutical manufacturing.

Q: What identification methods confirm the authenticity of Telmisartan?

A: Each batch of Telmisartan is identified and verified using standard IR (infrared spectroscopy) and HPLC (high-performance liquid chromatography) spectrum as required by IP/BP/EP/USP standards.

Q: Where is Telmisartan manufactured and supplied from?

A: Telmisartan is manufactured in India under current Good Manufacturing Practices (cGMP), ensuring quality and regulatory compliance throughout the production process.

Q: What are the benefits of selecting Telmisartan complying with IP/BP/EP/USP standards?

A: Choosing Telmisartan that meets IP/BP/EP/USP standards ensures high purity, precise quality control, and global regulatory acceptance, making it ideal for pharmaceutical applications targeting hypertension.

Q: How are impurities controlled in Telmisartan IP/BP/EP/USP?

A: Impurity levels are rigorously controlled and tested, with single impurity levels not exceeding 0.1% and total impurities limited to 0.2%, as presented in the accompanying Certificate of Analysis.

Tell us about your requirement