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ATORVASTATIN CALCIUM

Name: ATORVASTATIN CALCIUM
Brand: Shiv Enterprises

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MOQ : 25 Kilograms

ATORVASTATIN CALCIUM Specification

Heavy Metal (%)
Not more than 0.001%

Ph Level
Neutral

Poisonous
NO

Particle Size
90% passes through 60 mesh

Melting Point
159-160C

Molecular Formula
C33H34FN2O5 Ca

Shelf Life
3 years

Storage
Store in a cool, dry place below 30C. Protect from light and moisture.

Color
White to off-white

Smell
Odorless

Solubility
Slightly soluble in water, soluble in methanol and ethanol

HS Code
29420090

Boiling point
Not applicable (decomposes before boiling)

Loss on Drying
Not more than 0.5%

Structural Formula
C33H34FN2O5Ca

Molecular Weight
1209.42 g/mol (calcium salt)

Medicine Name
ATORVASTATIN CALCIUM

Chemical Name
Atorvastatin Calcium

CAS No
134523-03-8

Type
Active Pharmaceutical Ingredient (API)

Grade
Pharmaceutical

Usage
Used to lower cholesterol and triglyceride levels in the blood

Purity(%)
>99%

Appearance
White to off-white powder

Physical Form
Solid

End Use
Formulation of lipid-lowering pharmaceuticals

Storage Temperature
Below 30C

Residue on Ignition
Not more than 0.1%

Risk Phrase
R36/37/38 - Irritating to eyes, respiratory system and skin

Stability
Stable under recommended storage conditions

Microbial Limit
Total bacterial count not more than 1000 CFU/g

Identification
Complies with standard UV/IR spectrum

Specific Rotation
-39.0 to -45.0 (in methanol)

Packing
Packed in airtight, light-resistant containers

Related Substances
Each impurity not more than 0.1%, total impurities not more than 0.5%

ATORVASTATIN CALCIUM Trade Information

Minimum Order Quantity
25 Kilograms

Supply Ability
5000 Kilograms Per Month

Delivery Time
7 Days

About ATORVASTATIN CALCIUM

Experience monumental effectiveness with ATORVASTATIN CALCIUM, a cost-effective and highly customizable API, engineered for the formulation of polished, lipid-lowering pharmaceuticals. With an immaculate purity above 99% and rigorous microbial, impurity, and heavy metal limits, this product ensures consistent, reliable quality. Each batch is identified via UV/IR spectrum and delivers a white to off-white solid powder, stable for up to 3 years when stored below 30C. Pick yours today, backed by superior packing in airtight, light-resistant containers for lasting efficacy and safety.

Application Areas and Usage of ATORVASTATIN CALCIUM

ATORVASTATIN CALCIUM is tailored for the pharmaceutical industry, primarily in the development of formulations designed to reduce cholesterol and triglyceride levels. A key active ingredient, it is recommended for inclusion in oral dosage formulations. The usage and application process is straightforward-simply use as specified in validated manufacturing protocols under GMP conditions. For best results, follow precise direction of use for blending, ensuring correct dosage and stability throughout the formulation process.

Domestic Market, Certifications, and Payment Terms

ATORVASTATIN CALCIUM dominates the main domestic market in India and is supplied nationwide with quick dispatch and reliable transport services. Certified for pharmaceutical application, this API meets stringent quality regulations and industry certifications. Flexible payment terms facilitate seamless transactions, while supplier exchange programs are available upon request. Clients benefit from streamlined order processing and comprehensive after-sales support, underscoring commitment to quality and rapid delivery in a competitive market environment.

FAQ's of ATORVASTATIN CALCIUM:

Q: How should ATORVASTATIN CALCIUM be stored to ensure maximum stability?

A: Store ATORVASTATIN CALCIUM in a cool, dry place below 30C, protected from light and moisture in airtight, light-resistant containers to preserve its efficacy and stability for up to 3 years.

Q: What are the application areas of ATORVASTATIN CALCIUM in pharmaceuticals?

A: ATORVASTATIN CALCIUM is widely used for formulating lipid-lowering medications aimed at reducing cholesterol and triglyceride levels, supporting cardiovascular health.

Q: When should impurities and microbial limits be evaluated in ATORVASTATIN CALCIUM?

A: Impurities and microbial limits are evaluated during quality assurance before each distribution batch, ensuring total and individual impurities remain below established thresholds and compliance with regulatory standards.

Q: Where is ATORVASTATIN CALCIUM mainly available and supplied?

A: This product is primarily available throughout the Indian domestic market, with established supply networks ensuring rapid delivery and reliable transport to pharmaceutical manufacturers.

Q: What benefits do customers receive from the supplier's service model?

A: Customers enjoy quick dispatch, adaptable payment options, and support services, ensuring an efficient procurement process and satisfaction with every exchange.

Q: How is the quality and safety of ATORVASTATIN CALCIUM assured?

A: Quality and safety are maintained through rigorous testing for purity, impurity levels, microbial contamination, and compliance with UV/IR identification and industry certifications.

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