DMDM乙内酰脲

NA.24

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards..

These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.
DMDM Hydantoin may be used as a pharmaceutical reference standard for the determination of the analyte in cosmetics by thermal desorption electrospray ionization mass spectrometry (TD-ESI-MS).

These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available.

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

To see an example of a Certificate of Analysis for this material enter LRAA1411 in the slot below. This is an example certificate only and may not be the lot that you receive.

300

certified reference material
pharmaceutical secondary standard

current certificate can be downloaded

pharmaceutical (small molecule)

neat

2-30℃

GHS08

Danger

H319 - H334

P261 - P305 + P351 + P338 - P342 + P311

Eye Irrit. 2 - Resp. Sens. 1

12 - Non Combustible Liquids

WGK 1