Doxorubicin Hydrochloride IP-BP-USP-EP

Doxorubicin Hydrochloride IP-BP-USP-EP Specification

HS Code
30049099

Molecular Weight
580.03

Melting Point
216 C

Boiling point
810.3 C at 760 mmHg

Molecular Formula
C27H30ClNO11

Storage
Dry Place

Chemical Name
5, 12-Naphthacenedione, 10-[(3-amino-2,3,6-trideoxy-a-L-lyxo-hexopyranosyl)oxy]-7, 8, 9, 10-tetrahydro-6, 8, 11-trihydroxy-8-(hydroxyacetyl)-1-methoxy-,hydrochloride, (8S,10S)- (9CI);5,12-Naphthacenedione,10-[(3-amino-2,3,6-trideoxy-a-L-lyxo-hexopyranosyl)oxy]-7, 8, 9, 10-tetrahydro-6, 8, 11-trihydroxy-8-(hydroxyacetyl)-1-methoxy-, hydrochloride, (8S-cis)-;

CAS No
25316-40-9

Type
Pharmaceutical Intermediates

Grade
Industrial Grade

Usage
Pharmaceutical

Purity(%)
98-102%

Appearance
Orange red crystalline powder

Physical Form
Powder

Doxorubicin Hydrochloride IP-BP-USP-EP Trade Information

Minimum Order Quantity
100 Grams

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

About Doxorubicin Hydrochloride IP-BP-USP-EP

. It blocks an enzyme called topoisomerase II, which cuts andrepairs tangled strands of DNA. This stops or slows the growth of cancer cellsand other rapidly dividing cells

Exceptional Quality and Compliance

Doxorubicin Hydrochloride meets stringent quality guidelines set by IP, BP, USP, and EP standards, ensuring reliable performance as a pharmaceutical intermediate. Its superior purity level (98-102%) guarantees consistent results in downstream pharmaceutical processes.

Physical Characteristics and Storage

Presented as an orange-red crystalline powder, this compound showcases outstanding stability. With a melting point of 216 C and a high boiling point, it should be kept in a dry environment to preserve its chemical integrity and prolong shelf life.

Applications in Pharmaceutical Manufacturing

Primarily used as an intermediate in drug formulation, Doxorubicin Hydrochloride contributes to the synthesis of active pharmaceutical ingredients (APIs). Its industrial grade and precise molecular composition make it indispensable for large-scale pharmaceutical production.

FAQs of Doxorubicin Hydrochloride IP-BP-USP-EP:

Q: How should Doxorubicin Hydrochloride IP-BP-USP-EP be stored to maintain its quality?

A: It is recommended to store Doxorubicin Hydrochloride in a dry place, away from moisture, to safeguard its stability and crystalline structure. Proper storage conditions help prevent degradation and ensure the compounds reliability during pharmaceutical processing.

Q: Where is Doxorubicin Hydrochloride typically sourced or supplied from?

A: Doxorubicin Hydrochloride IP-BP-USP-EP is commonly exported and manufactured in India. Multiple reputable suppliers and manufacturers in the country provide this pharmaceutical intermediate for global and local pharmaceutical companies.

Q: What is the primary usage of Doxorubicin Hydrochloride IP-BP-USP-EP?

A: The compound is used mainly as an intermediate in the pharmaceutical industry, aiding in the formulation and synthesis of oncology drugs and other active pharmaceutical ingredients.

Q: When is Doxorubicin Hydrochloride IP-BP-USP-EP applied in drug manufacturing processes?

A: It is employed during the intermediate stages of drug synthesis, where precision and high purity are crucial for achieving the desired pharmacological outcomes in final pharmaceutical products.

Q: What benefit does the industrial-grade purity of Doxorubicin Hydrochloride provide?

A: Industrial-grade purity (98-102%) ensures high efficacy, safety, and consistency, significantly reducing the risk of contaminants and optimizing results in pharmaceutical production.

Q: How is the physical form and appearance significant for this compound?

A: The orange-red crystalline powder form and appearance serve as identifiers of quality and help in accurate handling, measurement, and incorporation into pharmaceutical manufacturing processes.

Q: What process is followed before Doxorubicin Hydrochloride is supplied for pharmaceutical applications?

A: Manufacturers adhere to strict purification, quality assurance, and compliance procedures as per international standards, ensuring the compounds suitability as a pharmaceutical intermediate.

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