
Mianserin Impurity 12(Hydrochloride) NEW
Price | Get Latest Price | ||
Package | 5mg | 20mg | 50mg |
Min. Order: | 1mg |
Supply Ability: | 100000 |
Update Time: | 2025-05-27 |
Product Details
Product Name: Mianserin Impurity 12(Hydrochloride) | Min. Order: 1mg |
Purity: >95% HPLC | Supply Ability: 100000 |
Release date: 2025/05/27 | |
Molecular Formula:: C11H16ClNO·HCl | Molecular Weight:: 213.70 36.46 |
Appearance: White soild | Storage: 2-8°C Refrigerator |
Product Catalog: | M048012A |
CAS No.: | |
Product Name: | Mianserin Impurity 12(Hydrochloride) |
Purity: | >95% HPLC |
Synonyms: | 2-((2-chloro-2-phenylethyl)(methyl)amino)ethanol hydrochloride |
Molecular Formula: | C11H16ClNO·HCl |
Mol. Weight: | 213.70 36.46 |
Appearance: | White soild |
Storage: | 2-8°C Refrigerator |
Contact: | WhatsAPP: +86 17320513646 E-mail: anna@molcoo.com |
Note: | We can also customize related analogues and modified peptides including HPLC, MS, 1H-NMR, MS, HPLC, IR, UV, COA, MSDS. This product is intended for laboratory use only! |
Background: | 2 - ((2 - Chloro - 2 - phenylethyl)(methyl)amino)ethanol hydrochloride is an organic compound with a complex structure. It combines aromatic, chloro - substituted, and amine - containing functional groups. Mianserin Impurity 12 is an impurity associated with mianserin, a tetracyclic antidepressant used to treat various depressive disorders.Mianserin is a tetracyclic antidepressant that was first synthesized in the 1970s. It works by blocking the reuptake of serotonin and noradrenaline in the brain, thereby increasing their levels and improving mood. Scientists focus on developing accurate detection and quantification methods for Mianserin Impurity 12 to ensure that the drug meets regulatory standards. |
Company Profile Introduction
1. Drug standards and drug impurity reference substances: provide more than 20,000 kinds of spot impurity reference substances, with sufficient supply and same-day delivery. We have a professional R&D team and comprehensive quality control testing to ensure product quality and reliability.
2. Customized synthesis of impurities and new molecules: Quickly respond to the customized needs of CDE impurities, stably supply impurities that have established quality standards, and provide customized synthesis services for new compounds in the research and development of innovative drugs.
3. Preparation and separation of unknown impurities: With a professional impurity preparation and separation technical team and SFC preparation and separation instruments, we can solve the problems of impurity preparation in complex projects.
4. Process development of new drug intermediates: provide the supply of new drugs and new molecular impurities, process optimization services, as well as the screening and impurity analysis of commercialization routes.
5. Peptide synthesis: Provide customized peptide synthesis services, and cover all kinds of degradation impurities and process impurities generated in the research and development of peptide drugs. At the same time, it provides comprehensive structural confirmation data and customized testing services.
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