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Varde-nafil Powder API

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Varde-nafil Powder API Specification

Smell
Odorless

Particle Size
D90 150 m

Poisonous
No (use only as prescribed)

Melting Point
220222C

Molecular Formula
C23H32N6O4S

HS Code
29335990

Solubility
Soluble in DMSO and methanol, slightly soluble in water

Storage
Store in tightly closed containers at 2-8C, protected from light and moisture

Boiling point
Not applicable (decomposes before boiling)

Shelf Life
24 months

Molecular Weight
488.6 g/mol

Color
White or almost white

Structural Formula
C23H32N6O4S (structure available on request)

Taste
Characteristic

Loss on Drying
0.5%

Ph Level
5.0 - 7.0 (1% aqueous suspension)

Heavy Metal (%)
0.001%

Medicine Name
Varde-nafil Powder API

Chemical Name
Vardenafil

CAS No
224785-91-5

Type
Active Pharmaceutical Ingredient (API)

Grade
Pharmaceutical Grade

Usage
For the treatment of erectile dysfunction

Purity(%)
99%

Appearance
White to off-white powder

Physical Form
Powder

Related Substances
Total impurities 1.0%

Hazard Statement
For research and pharmaceutical manufacturing use only. Not for personal or veterinary use.

Residual Solvents
Complies with ICH guidelines

Stability
Stable under recommended storage conditions

Assay
>=99% (on anhydrous basis)

Identification Methods
HPLC, IR, UV

Microbial Limit
Complies with pharmacopeial standards

Packing Details
Available in 1kg, 5kg, 10kg double polyethylene bags in HDPE drum

Varde-nafil Powder API Trade Information

Minimum Order Quantity
100 Kilogram

Supply Ability
10000 Per Day

Delivery Time
7 Days

Sample Available
Yes

Sample Policy
Contact us for information regarding our sample policy

About Varde-nafil Powder API

CAS Number	224785-90-4
Molecular Weight	488.6 g/mol
Chemical Formula	C23H32N6O4S
Packaging Size 25 Kg Packaging Type Bag Minimum Order Quantity	25 KG
Grade	IP/BP/USP
Minimum Order Quantity	100 Kg

Vardenafil is usedto treat erectile dysfunction (impotence; inability to get or keep an erection) in men. Vardenafil is in a class of medications called phosphodiesterase (PDE) inhibitors. It works by increasing blood flow to the penis during sexual stimulation. This increased blood flow can cause an erection

Quality and Purity Assurance

This API offers exceptional purity, with 99% assay verified through robust identification methods such as HPLC, IR, and UV spectroscopy. Total impurities are maintained at 1.0%, and heavy metal content is 0.001%, supporting reliable pharmaceutical research and production.

Secure Packaging and Stability

Varde-nafil Powder API is packed in double polyethylene bags and HDPE drums, available in 1kg, 5kg, and 10kg sizes. With optimal stability for up to 24 months under recommended storage conditions, the product remains safe and effective for use in pharmaceutical environments.

Pharmaceutical Grade for Research and Manufacturing

Compliant with global standards, including ICH and pharmacopeia requirements, this ingredient is suitable exclusively for research and pharmaceutical manufacturing purposes. It is not intended for personal or veterinary use and should be handled by qualified professionals.

FAQ's of Varde-nafil Powder API:

Q: How is the identity and purity of Varde-nafil Powder API confirmed?

A: The identity and purity of Varde-nafil Powder API are confirmed using analytical methods such as High-Performance Liquid Chromatography (HPLC), Infrared (IR) spectroscopy, and Ultraviolet (UV) analysis. These procedures ensure an assay value of 99% and verify that total impurities are 1.0%.

Q: What are the recommended storage conditions for Varde-nafil Powder API?

A: Varde-nafil Powder API should be stored in tightly closed containers at 2-8C, protected from light and moisture. Adhering to these guidelines maintains stability and ensures product integrity throughout its 24-month shelf life.

Q: Where is Varde-nafil Powder API commonly used?

A: This API is utilized in pharmaceutical research and manufacturing, specifically for developing treatments for erectile dysfunction. It provides high assay purity and complies with pharmacopeial standards, making it suitable for formulation development and large-scale production.

Q: What packaging options are available for Varde-nafil Powder API?

A: The API is available in 1kg, 5kg, and 10kg packaging sizes, secured in double polyethylene bags inside HDPE drums. This packaging ensures product safety during transit and storage, protecting it from environmental contaminants.

Q: Who should handle Varde-nafil Powder API and for what purpose?

A: Varde-nafil Powder API is intended exclusively for use by professionals in research labs or pharmaceutical manufacturing facilities. It must not be used for personal or veterinary purposes due to its potency and regulatory restrictions.

Q: Does Varde-nafil Powder API meet regulatory requirements for impurities and solvents?

A: Yes, it complies with ICH guidelines for residual solvents and pharmacopeial standards for microbial limits. Total impurities are maintained below 1.0%, and heavy metal content does not exceed 0.001%, aligning with international pharmaceutical quality requirements.

Q: What benefits does Varde-nafil Powder API offer for pharmaceutical manufacturing?

A: With its high purity, stable physical properties, and compliance with stringent regulations, Varde-nafil Powder API ensures reliable performance in drug development and manufacturing, enhancing product quality and efficacy.

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