TELMISARTAN

TELMISARTAN Specification

Impurity
Single impurity 0.1%

Solubility
Insoluble in water, soluble in DMSO and methanol

Molecular Weight
514.62 g/mol

Loss on Drying
0.5%

Product Name
TELMISARTAN

Shelf Life
2 years

Purity
99% min

Storage
Store in a cool, dry place

Identification
By IR and HPLC

Usage
Pharmaceutical, Used in treatment of hypertension

Stability
Stable under recommended storage conditions

Appearance
White to off-white powder

HS Code
29349900

CAS No
144701-48-4

Form
Powder

Packaging Type
Drum / HDPE Bag

Boiling Point
Not applicable (decomposes before boiling)

Melting Point
261263C

Odor
Odorless

Grade
Pharmaceutical Grade

Molecular Formula
C33H30N4O2

About TELMISARTAN

TELMISARTAN, a best-seller among antihypertensive pharmaceuticals, delivers monumental efficacy in managing hypertension. Manufactured in India to strict pharmaceutical grade, this odorless, white to off-white powder showcases marvelous purity of 99% minimum. Its stability under recommended storage and dominant performance in IR and HPLC identification make it an ephemeral yet essential addition for healthcare advancements. Soluble in DMSO and methanol but insoluble in water, it boasts a shelf life of 2 years. It is provided in sturdy Drum or HDPE Bag packaging per HS Code 29349900. TELMISARTAN is a marvel for global exporters, manufacturers, suppliers, and traders.

Exceptional Features and Competitive Advantages of TELMISARTAN

TELMISARTAN offers superior stability, with a shelf life of two years and remarkable purity (99% min). Use entails dissolving in suitable solvents like DMSO or methanol. The products identification and low impurity level ensure confident pharmaceutical formulation. Our competitive advantages include reliable export capacity, monumental quality control, and prompt delivery, making us the dominant supplier for hypertension treatment solutions worldwide.

TELMISARTAN Sample Policy and Supply Capability

We provide TELMISARTAN samples to support market value assessment and minimize expenditure prior to bulk purchase. Transparent sample policies facilitate easy handover and product evaluation, ensuring customers gain confidence in our monumental supply abilities. With consistent stock and capability to meet dynamic requirements, we assure timely delivery and robust inventory control, making us trusted market leaders for sample and bulk supply.

FAQs of TELMISARTAN:

Q: How should TELMISARTAN be stored to maintain its stability?

A: TELMISARTAN should be stored in a cool, dry place within the original packaging, such as a Drum or HDPE Bag, to maintain its stability over the recommended shelf life of two years.

Q: What competitive advantage does TELMISARTAN offer to pharmaceutical distributors?

A: TELMISARTAN provides pharmaceutical distributors with exceptional purity, minimal impurity levels, stability, and robust packaging options, reinforcing their position in the market with a reliable, high-quality product for treating hypertension.

Q: Where is TELMISARTAN manufactured and exported from?

A: TELMISARTAN is manufactured and supplied by exporters, manufacturers, and traders in India, adhering to stringent pharmaceutical grade standards for global distribution.

Q: What is the primary usage of TELMISARTAN in the medical field?

A: TELMISARTAN is primarily used in the treatment of hypertension, serving as a pivotal active pharmaceutical ingredient in various antihypertensive formulations.

Q: Can I request a sample of TELMISARTAN before making a bulk purchase?

A: Yes, sample policies are available, allowing customers to request a TELMISARTAN sample before finalizing bulk orders to evaluate quality and market suitability with minimal initial expenditure.

Q: Which analytical methods can verify the identity and purity of TELMISARTAN?

A: TELMISARTAN identity and purity can be verified using IR (Infrared Spectroscopy) and HPLC (High Performance Liquid Chromatography), ensuring compliance with strict pharmaceutical standards.

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