Item no.
USP-1A00370
CAS Number
[1847568-87-9]
Unit
10 mg
Molecular formula
C8H16N2O3
Molecular weight
188.23
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Description
Note: Pharmaceutical Analytical Impurities are released using a process developed by USP's subject matter experts. The release process is based on internal policies, standard operating procedures, and requirements as defined by USP's Quality Management System. USP is an ISO 9001:2015 certified facility. PAI products are different from official USP Reference Standards. PAI products are not required for compendial compliance.
Structure formula
Contents
Miscellaneous
Certificate of Analysis (specimen)
Reference Material CoA specimen: for the current lot, please contact your customer service representative at info@labmix24.com
Product data sheet
View all available product details e.g. description, analytes/parameters, CAS Number, concentrations/values, sales unit/product format, method, source, transport information
Quality Solution Sheet (QSS)
A QSS is a resource for you integrating newly released reference standards and monographs with an overview of all relevant associated physical materials, PAIs, and soon: General Chapters, excipients, education, and other products and services. Get all the information you need at a glance.
US Pharmacopeia Standards set a global benchmark, enabling efficient, reliable, and cost-effective development and quality control of pharmaceuticals.
Official USP Reference Standards are highly characterized physical specimens intended for quality control use when conducting assays and tests for medicines as described in the USP-NF. When you conduct tests and assays required by the USP-NF using the USP reference standards specified, the results can be considered conclusive.
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- USP Reference Standards
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