(Z)-7-(((S)-2-Amino-2-carboxyethyl)thio)-2-((S)-2,2-dimethylcyclopropane-1-carboxamido)hept-2-enoic acid
- CAS
- 107873-05-2
- Formula
- C16H26N2O5S
- MW
- 358.5 g/mol
ZX-027809
Impurity reference standards
Cilastatin impurity standards
Zemixal lists 5 reference materials related to Cilastatin, covering the drug substance itself, its process impurities and the products it forms on storage. Among them are 1 pharmacopoeial impurity.
5reference materials
1pharmacopoeial
Each lot ships with a certificate of analysis, and characterisation data such as 1H-NMR, mass spectrum and HPLC purity can be shared before you order. They are bought for system suitability, peak identification, quantitation against limits and the impurity justification sections of regulatory submissions.
By impurity type
Pharmacopoeial1EP, USP, BP or JP named impurities
Counts are based on product names. One compound can fall into more than one type.
All Cilastatin reference materials
1–5 of 5 standards
7-Chloro-2-(2,3-dimethylbut-3-enamido)hept-2-enoic Acid
- CAS
- 2519489-73-5
- Formula
- C13H20ClNO3
- MW
- 273.75 g/mol
ZX-028604
Questions
Cilastatin impurities, answered
How many Cilastatin impurity standards does Zemixal list?
The catalogue currently lists 5 compounds for Cilastatin, including 1 pharmacopoeial impurity. Each product page shows the CAS number where one is assigned, the structure, formula and molecular weight.
What documents come with a Cilastatin impurity standard?
A certificate of analysis travels with every lot. On request we share the characterisation set, usually 1H-NMR, mass spectrum, HPLC purity and IR, and for some materials TGA or water content. Ask for the data before ordering if your QA team needs to review it.
Can Zemixal make a Cilastatin impurity that is not listed?
Often yes. Send the structure, name or CAS number with the quantity you need and our sourcing team checks custom synthesis options, usually from 10 mg up to gram scale, with a quoted lead time.