GMP factory High purity API powder Tacrolimus CAS 104987-11-3 Special price

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GMP factory High purity API powder Tacrolimus CAS 104987-11-3 Special price

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MOQ : 100 Grams

GMP factory High purity API powder Tacrolimus CAS 104987-11-3 Special price Specification

Smell
Odorless

Melting Point
128-132C

Poisonous
Yes (requires handling care)

Solubility
Slightly soluble in water

Color
White

Particle Size
Micronized

Boiling point
Not applicable (decomposes)

Loss on Drying
0.5%

Shelf Life
2 Years

Molecular Weight
804.02

Storage
Store In A Cool, Dry Place

Structural Formula
Not shown

Molecular Formula
C44H69NO12

Taste
Tasteless

Heavy Metal (%)
0.002%

Medicine Name
Tacrolimus

Chemical Name
Tacrolimus

CAS No
104987-11-3

Type
API Powder

Grade
GMP

Usage
Immunosuppressant

Purity(%)
High Purity (98%)

Appearance
White Powder

Physical Form
Powder

Manufacturing Origin
China GMP factory

Dosage Form
Depends on use

Moisture content
Low

USP Standard
Conforms

Sample
Available

Stability
Stable when dry

Application
Transplant therapy

Packing
PVC or foil bag

Offer
Special price

GMP certified
Yes

Pharmaceutical API
Yes

GMP factory High purity API powder Tacrolimus CAS 104987-11-3 Special price Trade Information

Minimum Order Quantity
100 Grams

Supply Ability
5000 Grams Per Month

Delivery Time
7 Days

Main Domestic Market
All India

About GMP factory High purity API powder Tacrolimus CAS 104987-11-3 Special price

Experience the laureate quality of GMP factory High Purity API Powder Tacrolimus CAS 104987-11-3, now offered at a reduced and kingly price. Sourced directly from a certified Chinese GMP manufacturer, this exquisite immunosuppressant is renowned for its high purity (98%) and low moisture content. Perfectly suited for transplant therapy, its stable, micronized white powder form ensures outstanding consistency and efficiency in every application. Benefit from access to GMP-certified excellence and seize this bargain opportunity for pharmaceutical production and distribution.

Exquisite GMP Tacrolimus: Usage, Application, and Type

Our GMP factory High Purity API powder Tacrolimus (CAS 104987-11-3) serves as a kingly solution for pharmaceutical manufacturers and research facilities specializing in transplant therapy. With its immunosuppressive application, this Active Pharmaceutical Ingredient supports reduced organ rejection rates and stable therapeutic outcomes. Suitable for diverse dosage forms, its high purity and stability render it indispensable for critical plant and clinical applications that demand uncompromising quality.

Sample Availability, Packaging, and Certifications: Special Offer

Avail the opportunity to access a sample at a minimal outlay before committing to a full order of Tacrolimus API powder. Supplied in PVC or protective foil bags, every batch is carefully handled to maintain product integrity during handover. Backed by GMP certification and conforming to USP standards, our API guarantees adherence to global pharmaceutical benchmarks-ensuring safety, reliability, and excellence for any professional application.

FAQ's of GMP factory High purity API powder Tacrolimus CAS 104987-11-3 Special price:

Q: How should Tacrolimus API powder be stored for optimal stability?

A: Tacrolimus API powder should be stored in a cool, dry place to maintain its stability, as it remains stable when kept dry and properly sealed.

Q: What is the main application of Tacrolimus from this GMP factory?

A: This high purity Tacrolimus is primarily used as an immunosuppressant in transplant therapy to help reduce the risk of organ rejection.

Q: When can customers request a sample of Tacrolimus, and is it included in the offer?

A: Customers can request a sample at any time prior to placing a full order. This valuable option is included in our current special offer, allowing product evaluation with minimal initial outlay.

Q: Where does the manufacturing and export of this Tacrolimus API originate?

A: The manufacturing and export of Tacrolimus API is carried out in a GMP-certified factory located in China, ensuring rigorous production quality and standards.

Q: What process ensures Tacrolimus meets GMP and USP certifications?

A: Every batch undergoes strict GMP protocol and is analyzed to meet USP standards, confirming high purity, controlled moisture, and heavy metal content for pharmaceutical compliance.

Q: What are the benefits of using this high purity, GMP-certified Tacrolimus?

A: Using this exquisite, GMP-certified Tacrolimus ensures a reduced risk of impurity-related complications, stable dosage forms, and confidence in its therapeutic efficacy for transplantation.

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