Drotaverin HCl
Drotaverin HCl

Drotaverin HCl

Drotaverin HCl Specification

  • Molecular Formula
  • C24H32ClNO4
  • Shelf Life
  • 2 Years
  • EINECS No
  • 213-573-2
  • Storage
  • Other
  • Ph Level
  • 5-7 (in aqueous solution)
  • Solubility
  • Freely soluble in water and ethanol
  • Heavy Metal (%)
  • 0.001%
  • Particle Size
  • Typically 5-20 microns
  • Color
  • White to Off-White
  • Taste
  • Bitter
  • Smell
  • Other
  • Boiling point
  • Not Applicable
  • Poisonous
  • NO
  • Melting Point
  • 210-216C
  • HS Code
  • 29332900
  • Structural Formula
  • C(O)=NC1=CC=C(C(OCH2CH(CH3)CH3)=O)C=C1N(CH3)CH2CH2Cl.CH3OH
  • Loss on Drying
  • 0.5%
  • Medicine Name
  • Drotaverin HCl
  • Chemical Name
  • Drotaverine Hydrochloride
  • CAS No
  • 985-12-6
  • Type
  • Pharmaceutical Intermediate
  • Grade
  • Pharmaceutical Grade
  • Usage
  • Used as an antispasmodic to treat smooth muscle spasms
  • Purity(%)
  • 99%
  • Appearance
  • White to Off-White Powder
  • Physical Form
  • Powder
 
 

About Drotaverin HCl

Drotaverine (INN, also known as drotaverin) is an antispasmodic drug, used to enhance cervical dilation during childbirth.


Packaging details:

Packaging details: 25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum.
Storage: Stored in a clean, cool, dry area; keep away from moisture and strong, direct light/heat
Shelf Life: 5 years if sealed and store away from direct sun light.


High-Quality Pharmaceutical Ingredient

Drotaverin HCl is synthesized and processed to meet exacting pharmaceutical grade specifications. The particle size, typically between 5-20 microns, ensures maximum solubility and uniform blending in formulations. Its remarkable purity and controlled heavy metal content make it a reliable substance for further pharmaceutical manufacturing.


Versatile Applications in Antispasmodic Treatment

Recognized for its potent antispasmodic action, Drotaverin HCl is extensively employed in the intervention of smooth muscle spasms. Its broad compatibility in water and ethanol facilitates easy dosing for development and production of various medicinal products.


Global Availability Through Trusted Channels

As a trusted distributor, exporter, manufacturer, supplier, trader, and wholesaler based in India, Drotaverin HCl is made readily accessible to global markets. With rigorous quality checks and compliance to international standards, customers can expect prompt and quality-assured delivery.

FAQ's of Drotaverin HCl:


Q: How is Drotaverin HCl used in pharmaceutical formulations?

A: Drotaverin HCl serves as a crucial antispasmodic agent in the formulation of medications that target smooth muscle spasms. It is typically blended into tablets, capsules, or injectable formulations due to its high solubility and purity.

Q: What are the main benefits of using Drotaverin HCl?

A: The primary benefit of Drotaverin HCl lies in its effective relief of smooth muscle spasms, making it valuable for treating gastrointestinal, urinary, and other muscular disorders. Its high purity and stability further enhance product efficacy and safety.

Q: When should Drotaverin HCl be considered for use in production?

A: This compound is best utilized during the development or mass production of pharmaceuticals intended to treat spasmodic conditions, particularly when a potent and safe antispasmodic intermediate is needed.

Q: Where is Drotaverin HCl manufactured and distributed from?

A: Drotaverin HCl is manufactured, distributed, and exported by leading pharmaceutical suppliers in India, ensuring global reach through an established distribution network.

Q: What makes Drotaverin HCl a preferred choice among pharmaceutical manufacturers?

A: Its high solubility, remarkable purity of 99%, stable shelf life, and adherence to pharmaceutical grade specifications make it the preferred intermediate for pharmaceutical manufacturers around the world.

Q: How is the quality of Drotaverin HCl ensured?

A: Quality is assured through controlled production processes, rigorous testing for heavy metals (0.001%), strict purity parameters (99%), and compliance with regulatory standards for pharmaceutical grade chemicals.

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