Linzagolix Choline Impurity 12: High-Purity Pharmaceutical Intermediate
Unlock advancements in reproductive health with our premium pharmaceutical intermediate.
Get a Quote & SampleProduct Core Value
2-(Chloromethyl)-3,4-Difluoro-1-Methoxybenzene
This high-quality pharmaceutical intermediate plays a critical role in the synthesis of Linzagolix, a groundbreaking GnRH receptor antagonist. Its precise chemical structure supports the development of novel treatments for estrogen-dependent conditions such as uterine fibroids and endometriosis. We provide reliable supply chains for this essential pharmaceutical intermediate Linzagolix Choline.
- Discover the critical role of Linzagolix Choline Impurity 12 CAS 1073435-67-2 in the research and development of advanced pharmaceutical compounds.
- Benefit from a reliable supply of CAS 1073435-67-2 buy options from a trusted manufacturer, ensuring continuity in your synthesis projects.
- Understand how this GnRH antagonist intermediate contributes to developing therapies for conditions like endometriosis treatment.
- Leverage our expertise for your Linzagolix synthesis intermediate needs, ensuring the highest purity and consistency.
Key Advantages
Uncompromised Quality and Purity
We ensure the highest standards for our high purity pharmaceutical intermediate, crucial for demanding research and production environments.
Facilitating Innovative Therapies
Our product supports the creation of treatments targeting women's reproductive health, contributing to advancements in uterine fibroids treatment intermediate development.
Expertise in Chemical Synthesis
Rely on Nanjing Xinbell Pharmaceutical intermediates for expert knowledge and reliable production of complex chemical compounds for your drug discovery needs.
Key Applications
Pharmaceutical Synthesis
Essential for the precise manufacturing of complex drug molecules, supporting the development of novel pharmaceuticals for various therapeutic areas.
Drug Discovery Research
A vital component in early-stage drug discovery, enabling researchers to explore new therapeutic targets and pathways, especially within oral bioavailability enhancing compounds.
Analytical Standards
Used as a reference standard in analytical chemistry for quality control and method development in pharmaceutical quality assurance.
API Intermediate Manufacturing
Crucial for the production of Active Pharmaceutical Ingredients (APIs), ensuring the consistent quality required for patient safety and drug efficacy.