Buparvaquone Active Pharmaceutical Ingredients

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Buparvaquone Active Pharmaceutical Ingredients

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MOQ : 25 Kilograms

Buparvaquone Active Pharmaceutical Ingredients Specification

Melting Point
124-128 C

Molecular Formula
C18H18O3

Particle Size
98% passes through 30 mesh

Heavy Metal (%)
NMT 0.002%

Poisonous
Non-poisonous

Molecular Weight
282.34 g/mol

HS Code
29420090

Smell
Odorless

EINECS No
616-889-7

Loss on Drying
Not more than 0.5%

Color
Light Yellow

Storage
Store in a tightly closed container in a cool, dry place

Solubility
Practically insoluble in water, freely soluble in dichloromethane, sparingly soluble in methanol

Shelf Life
2 Years

Structural Formula
Available on request

Medicine Name
Buparvaquone API

Chemical Name
Buparvaquone

CAS No
88426-33-9

Type
Active Pharmaceutical Ingredient

Grade
Pharmaceutical Grade

Usage
Veterinary; treatment of theileriosis

Purity(%)
>98% (HPLC)

Appearance
Fine Powder

Physical Form
Solid

Residue on Ignition
NMT 0.1%

Assay
>98% (on dried basis)

ISO Certification
ISO 9001:2015 Certified Facility

Identification
Complies with standard by IR & HPLC

Transport Condition
Ambient temperature

Standards
In-house or as per client specification

Microbial Limit
Complies with standards

Related Substances
NMT 1.0%

Residual Solvent
As per ICH Q3C Guidelines

Packaging
HDPE drum with double polythene bags, 1kg/5kg/10kg/25kg or as required

Buparvaquone Active Pharmaceutical Ingredients Trade Information

Minimum Order Quantity
25 Kilograms

Payment Terms
Cash on Delivery (COD), Cash Against Delivery (CAD), Cash in Advance (CID)

Supply Ability
500 Kilograms Per Month

Delivery Time
5-7 Days

Main Export Market(s)
Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa

Main Domestic Market
All India

Buparvaquone Active Pharmaceutical Ingredients About

Discover the top-quality Buparvaquone Active Pharmaceutical Ingredient, a radiant solution trusted by veterinary professionals for the treatment of theileriosis. Manufactured in an ISO 9001:2015 certified facility, this gorgeous, light yellow fine powder boasts over 98% purity, as validated by both IR and HPLC methods. Shipped in secure HDPE drums with double polythene lining, this product is admired for its uncommon standards, competitive reduced price, and favorable customer reviews. Non-poisonous, odorless, and easy to handle, it maintains stable performance even under ambient conditions.

Distinct Features and Application of Buparvaquone API

Buparvaquone API stands out for its exceptional purity, uncommon stability, and compliance with strict industry standards. Best suited for veterinary usage, particularly in the effective treatment of theileriosis, it is ideal for veterinarians, research institutions, and animal health facilities. This pharmaceutical-grade ingredient comes as a fine, light yellow powder, suitable for formulating injectable or oral veterinary products. Its radiant efficacy and low residual impurities make it a preferred choice in the animal health sector.

Sample Availability, Supply Capacity, and Trusted Certifications

Take advantage of sample availability for Buparvaquone API at the lowest price to assess quality. With express shipping options and robust supply ability to meet large or custom orders, customers can expect shipped goods to arrive promptly and safely. Produced exclusively in an ISO 9001:2015 certified environment and conforming to ICH Q3C solvent guidelines, you receive a product that fulfills both regulatory requirements and market expectations efficiently.

FAQ's of Buparvaquone Active Pharmaceutical Ingredients:

Q: How should Buparvaquone API be stored for optimal stability?

A: Buparvaquone API should be stored in a tightly closed container in a cool, dry place away from direct sunlight to maintain its quality and efficacy over its 2-year shelf life.

Q: What is the primary veterinary application of Buparvaquone API?

A: This API is primarily used for the treatment of theileriosis in veterinary medicine, providing an effective solution to safeguard animal health.

Q: Where is Buparvaquone API manufactured and packaged?

A: The product is manufactured and securely packaged in India, in an ISO 9001:2015 certified facility, using HDPE drums with double polythene bags for optimal safety.

Q: What certifications and standards does Buparvaquone API comply with?

A: Buparvaquone API meets ISO 9001:2015 certification, conforming to ICH Q3C solvent guidelines and in-house or client-specified standards for high quality and regulatory compliance.