
N-Nitroso Cyclophosphamide USP Related Compound A NEW
Price | Get Latest Price | ||
Package | 5mg | 20mg | 50mg |
Min. Order: | 1mg |
Supply Ability: | 100000 |
Update Time: | 2025-06-18 |
Product Details
Product Name: N-Nitroso Cyclophosphamide USP Related Compound A | CAS No.: 67856-68-2 |
Min. Order: 1mg | Purity: >95% HPLC |
Supply Ability: 100000 | Release date: 2025/06/18 |
Molecular Formula:: C4H8Cl2N2O | Molecular Weight:: 171.02 |
Appearance: Black liquid | Storage: 2-8°C Refrigerator |
Product Catalog: | C094039 |
CAS No.: | 67856-68-2 |
Product Name: | N-Nitroso Cyclophosphamide USP Related Compound A |
Purity: | >95% HPLC |
Synonyms: | N,N-bis(2-chloroethyl)nitrous amide |
Molecular Formula: | C4H8Cl2N2O |
Mol. Weight: | 171.02 |
Appearance: | Black liquid |
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: | N-Nitroso Cyclophosphamide USP Related Compound A is a nitrosated derivative associated with cyclophosphamide, a widely - used chemotherapy drug for treating various cancers. At present, the research on N-Nitroso Cyclophosphamide USP Related Compound A mainly focuses on the detection and control of impurities. Due to the potential carcinogenicity of nitrosamine impurities, global pharmaceutical regulatory authorities and the pharmaceutical industry have paid great attention to them. The United States Pharmacopeial Convention (USP) has issued and continuously updated relevant general chapters, and launched a variety of nitrosamine impurity reference standards and drug analysis impurities, including N-Nitroso Cyclophosphamide USP Related Compound A, to assist enterprises in detecting and controlling the levels of nitrosamine impurities in drugs. |
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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