Product Overview
Temozolomide is the API that is mostly utilised to treat specific types of brain tumors.
It is a second-generation derivative of dacarbazine that belongs to the imidazotetrazine family.
It can get past the blood-brain barrier, which makes it good for treating brain tumors.
The chemical alters DNA methylation, which makes it cytotoxic.
This causes tumor cells to die by apoptosis.
Temozolomide is an important formulation in modern neuro-oncology protocols, and its pharmacokinetics are very predictable.
It is made under strict cGMP conditions, which guarantee its excellent quality, consistency, and purity.
We use cutting-edge technology to make our Temozolomide API.
It meets the requirements set by the IP, EP, and USP.
We ensure that the manufacturing is done with strict quality and safety measures.
Therapeutic Applications
Therapeutic class: Alkylating agent, antineoplastic, and DNA synthesis inhibitor
It is used in the treatment of the following:
Specification Parameters
-
Chemical Name is 3,4-Dihydro-3-methyl-4-oxoimidazo[5,1-d]-1,2,3,5-tetrazine-8-carboxamide
-
CAS number is 85622-93-1.
-
C6H6N6O2 is the molecular formula.
-
Molecular Weight is 194.15 grams per mole
-
Outlook is like a white to pale yellow crystalline powder
-
Assay is at least 98.0%
Packaging & Storage
Packaging for temozolomide keeps the product stable and safe while it is being moved and stored.
Put in an HDPE or fiber drum with a double PE bag and an aluminium foil pouch.
We can make custom packaging to meet your needs.
Follows all rules in labelling, such as including the batch number, the dates of manufacture and expiration, storage directions, and so forth.
Store it in a cool place (between 2°C and 8°C)
Protect from light, heat, and moisture.
Keep the container well closed and in a dry place with good air flow.
Why Choose Us
There are ample reasons why our industry is preferred for buying all these APIs. Here, the following are our highlights.
-
Manufacturing facilities that follow cGMP and have been approved by international regulatory bodies (EU-GMP, WHO-GMP, and ISO).
-
Assay and impurity control are guaranteed to be within pharmacopeial standards.
-
The packaging and paperwork can be changed to meet the needs of worldwide exports.
-
Regulations Guidance is available, and you can obtain a full DMF (Drug Master File) upon request.
-
Proven Supply Chain Efficiency that makes sure deliveries around the world are on time.
-
A dedicated QA/QC team makes sure that quality is always high.
-
A history of working with oncology APIs, with a focus on high-potency medicines
