Losartan Chemical

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MOQ : 100 Kilograms

Losartan Chemical Specification

Melting Point
183-184C

Smell
Odorless

Structural Formula
Available on request

Molecular Weight
422.91 g/mol

Storage
Store in a cool, dry place, away from light

Poisonous
NO

Molecular Formula
C22H23ClN6O

Particle Size
40-80 Mesh

Solubility
Slightly soluble in water, soluble in methanol and DMSO

Loss on Drying
0.5%

Shelf Life
5 Years

Color
White

HS Code
29339900

Heavy Metal (%)
0.002%

Medicine Name
Losartan

Chemical Name
2-butyl-4-chloro-1-[[2-(1H-tetrazol-5-yl)[1,1-biphenyl]-4-yl]methyl]-1H-imidazole-5-methanol

CAS No
124750-99-8

Type
Pharmaceutical Chemical

Grade
Medicine Grade

Usage
Used in the treatment of high blood pressure and heart failure

Purity(%)
99.0%

Appearance
White to off-white powder

Physical Form
Solid

Packing
25 kg HDPE Drum

Standard
USP/EP/BP

Impurity Level
0.2%

Identification Method
HPLC, IR, NMR

Application
API (Active Pharmaceutical Ingredient) for formulation

Assay
>=99.0% (HPLC)

Losartan Chemical Trade Information

Minimum Order Quantity
100 Kilograms

Supply Ability
1000 Kilograms Per Week

Delivery Time
7 Days

Losartan Chemical About

Experience the rare and sizzling excellence of our Losartan Chemical, a trending choice among meritorious pharmaceutical solutions. With an inestimable purity of 99.0% (HPLC), this best-in-class API (Active Pharmaceutical Ingredient) boasts a low impurity level of just 0.2%, ensuring superior quality for hypertension and heart failure treatments. Adhering to USP/EP/BP standards, our Losartan is delivered in a secure 25 kg HDPE drum, white to off-white in appearance, and odorless. Trust this premium grade chemical-crafted to elevate formulation outcomes and pharmaceutical efficacy, with inestimable value for your applications.

Losartan Chemical: Methods and Applications

Losartan Chemical is most effective when used as an API for the formulation of medications targeting high blood pressure and heart failure. It is administered orally, making it versatile for both specific and general therapeutic applications. Beyond these, it may be applied in research contexts or studies exploring cardiovascular health. The chemical is compatible with a variety of pharmaceutical formulations owing to its stability, high purity, and adherence to globally recognized standards.

Sample, Delivery & Certificates: Your Smooth Outlay

Losartan Chemical samples are available upon request so you can evaluate its fit for your requirements. With prompt delivery and efficient drop-off services, your order arrives as scheduled-minimizing any business outlay or production downtime. Each batch comes with complete certifications, ensuring you receive only the most credible and compliant material for regulated pharmaceutical use. Choose us for seamless ordering, reliable transport, and documented quality assurance every time.

FAQ's of Losartan Chemical:

Q: How is the quality and purity of Losartan Chemical verified?

A: The identity and purity of Losartan Chemical are verified using HPLC, IR, and NMR methods. Each batch guarantees a purity of at least 99.0% (HPLC) with impurity levels restricted to just 0.2%, meeting USP, EP, and BP standards.

Q: What are the common uses of Losartan Chemical?

A: Losartan Chemical is primarily used as an API in the formulation of medications for the treatment of high blood pressure and heart failure, but it can also be used in pharmaceutical research and development.

Q: When can I expect the delivery of Losartan Chemical after placing an order?

A: Losartan Chemical is supplied swiftly with reliable delivery services. Lead times depend on order quantity and destination, but efficient drop-off minimizes wait and ensures timely supply.

Q: Where should Losartan Chemical be stored for optimal shelf life?

A: This chemical should be stored in a cool, dry place away from light to maintain its effectiveness and extend its shelf life up to 5 years.

Q: What certifications accompany Losartan Chemical upon delivery?

A: Each delivery is accompanied by complete quality certifications, including analytical and compliance documents in accordance with USP/EP/BP standards.