Temozolomide Chemical

Temozolomide Chemical Specification

Melting Point
212 C

Boiling point
526.6 C at 760 mmHg

Molecular Weight
194.15

Molecular Formula
C6H6N6O2

Shelf Life
5 Years

Storage
Dry Place

Medicine Name
Temozolomide

Chemical Name
3, 4-Dihydro-3-methyl-4-oxoimidazo(5, 1-d)-as-tetrazine-8-carboxamide

CAS No
85622-93-1

Type
Pharmaceutical Intermediates

Grade
Industrial Grade

Usage
Pharmaceutical and Food grade

Purity(%)
99.7%

Appearance
Off-white to light-pink crystalline solid

Physical Form
Powder

Temozolomide Chemical Trade Information

Minimum Order Quantity
100 Kilograms

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

About Temozolomide Chemical

Temozolomide is used to treat specific types of brain cancer (eg, glioblastoma multiforme, anaplastic astrocytoma) in patients whose tumors have returned or whose tumors have just been diagnosed. It belongs to the group of medicines known as antineoplastics (cancer medicines).Temozolomide interferes with the growth of cancer cells, which are then destroyed by the body. Since the growth of normal body cells may also be affected by temozolomide, other side effects may occur. Some of these may be serious and must be reported to your doctor. Some side effects may not occur for months or years after the medicine is used.

Stability and Shelf Life

Temozolomide boasts a shelf life of five years, provided it is kept in a dry environment. Its excellent stability ensures long-lasting efficacy, making it suitable for large-scale production, storage, and global export. Reliable preservation is achievable due to its resilient crystalline structure.

High Purity and Pharmaceutical Standards

With a purity level of 99.7%, Temozolomide meets rigorous pharmaceutical and food-grade requirements. This impeccable quality renders it highly suitable for sensitive applications in pharmaceutical manufacturing and food industries, ensuring safety and performance.

Versatile Applications

The compound serves as an intermediate in pharmaceutical synthesis, particularly within oncology. Its robustness and fine powder form also make it adaptable for laboratory analysis and formulation development across diverse sectors, expanding its utility beyond primary medical use.

FAQs of Temozolomide Chemical:

Q: How is Temozolomide typically used in pharmaceutical and food industries?

A: Temozolomide is primarily used as an intermediate in the synthesis of medications, especially for cancer treatment. Due to its high purity (99.7%) and stability, it is also suitable for select food industry applications once processed according to regulatory standards.

Q: What are the storage requirements to maintain Temozolomides shelf life?

A: Temozolomide should be stored in a dry place at room temperature, protected from moisture and direct sunlight. Proper storage conditions help retain its off-white to light-pink crystalline appearance and ensure a shelf life of up to five years.

Q: When should Temozolomide be used during pharmaceutical manufacturing?

A: Temozolomide is introduced as an intermediate during the synthesis of active pharmaceutical ingredients, particularly in anticancer medication production. Its use ensures the formation of the desired active compounds with optimal purity and efficacy.

Q: Where is Temozolomide manufactured and exported from?

A: Temozolomide is manufactured, supplied, and exported from India by certified pharmaceutical exporters and manufacturers, ensuring adherence to global quality and safety regulations.

Q: What are the processing steps for Temozolomide in pharmaceutical production?

A: In pharmaceutical manufacturing, Temozolomide undergoes controlled synthesis, purification, and crystallization processes before being incorporated into final formulations or dosage forms, ensuring consistency and pharmacological safety.

Q: What benefits does Temozolomide provide over other chemical intermediates?

A: Due to its high purity and extended shelf life, Temozolomide offers superior stability and reliability during storage and handling, which reduces waste and ensures consistent pharmaceutical product quality.

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