Vonoprazan Fumarate powder TAK-438 CAS 881677-11-8

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MOQ : 1 Kilograms

Vonoprazan Fumarate powder TAK-438 CAS 881677-11-8 Specification

Loss on Drying
0.5

Color
White to off-white or tan

Heavy Metal (%)
10ppm

Molecular Weight
461.46

Shelf Life
24 months when properly stored Months

Particle Size
50ppm

Smell
Sweet

Storage
Other

Molecular Formula
C21H20FN3O6S

Ph Level
4.0

Medicine Name
Vonoprazan Fumarate

Chemical Name
Vonoprazan fumarate TAK-438

CAS No
881677-11-8

Type
Other

Grade
Other

Usage
API for acid-related diseases

Purity(%)
99%

Appearance
White to off-white or tan solid powder

Physical Form
Powder

Form in Image
Fine crystal powder

Inspection
COA available

CAS Synonyms
16133-25-8, 881674-56-2, 1240948-72-4, 1240948-77-9

Application
Acid suppressing agent

Active Ingredient
TAK-438

Packaging
Sealed HDPE/drum

Vonoprazan Fumarate powder TAK-438 CAS 881677-11-8 Trade Information

Minimum Order Quantity
1 Kilograms

Payment Terms
Cash Against Delivery (CAD), Telegraphic Transfer (T/T)

Supply Ability
100 Kilograms Per Month

Delivery Time
7 Days

Packaging Details
Aluminum foil bags or cardboard barrels

Main Export Market(s)
Asia, Central America, North America, South America, Eastern Europe, Western Europe

Main Domestic Market
All India

Certifications
ISO 9001:2015

About Vonoprazan Fumarate powder TAK-438 CAS 881677-11-8

Last Chance to secure Prime-quality Vonoprazan Fumarate Powder (TAK-438, CAS 881677-11-8) for your pharmaceutical needs at a Special Rate. This Gilt-edged API, boasting 99% purity and crafted to GMP standards, is available as a white to off-white fine crystal powder. Each order is supplied in sealed HDPE drums for optimal storage. Ace your production processes-ideal as an acid-suppressing agent for acid-related disorders. Immediate order for exporters, manufacturers, suppliers, and wholesalers in China. Inspection COA is available upon request.

Widespread Applications and Suitability

GMP Standard Vonoprazan Fumarate powder TAK-438 finds widespread use as an acid suppressing agent within the pharmaceutical sector. Suitable for incorporation into advanced medication formulations, it is tailored for research labs and pharmaceutical plants specializing in API manufacturing for acid-related diseases. Its excellent solubility and consistent quality make this product ideal for both small and large-scale plant application, ensuring reliable results across different research and production environments.

Dispatched with Excellence-Shipping, Terms, and Supply

Our GMP Standard Vonoprazan Fumarate powder TAK-438 can be speedily dispatched from major domestic maritime FOB ports across China. Flexible payment terms facilitate smooth handover for clients across the globe. With robust supply ability, we accommodate orders of various scales-ensuring that your requirements are met promptly. All shipments are securely packed for safe transit, and rigorous tracking accompanies each order for utmost confidence during the shipping process.

FAQ's of GMP Standard Vonoprazan Fumarate powder TAK-438 CAS 881677-11-8:

Q: How should Vonoprazan Fumarate TAK-438 powder be stored?

A: The powder should be kept in a cool, dry, and dark location. Properly following storage instructions ensures a shelf life of up to 24 months.

Q: What is the primary usage of Vonoprazan Fumarate TAK-438 in pharmaceuticals?

A: It acts as a potent acid-suppressing agent and is primarily used as an Active Pharmaceutical Ingredient (API) for treating acid-related diseases.

Q: Where is the product shipped from and who can order it?

A: Vonoprazan Fumarate powder is shipped from trusted FOB ports in China and can be ordered by exporters, manufacturers, suppliers, and wholesalers worldwide.

Q: When will I receive my COA and product documentation?

A: A Certificate of Analysis (COA) and relevant product documentation are provided alongside each shipment, ensuring you have regulatory support upon dispatch.

Q: What benefits does GMP certification offer for this product?

A: GMP certification guarantees prime quality, excellent purity, and manufacturing standards, which ensure safety, consistency, and compliance for pharmaceutical applications.