AH 7921
Formulation: A neat solid
| SIZE | PRICE | QUANTITY | SUBTOTAL |
|---|---|---|---|
| CART TOTAL | |||
| 1 mg | $65.00 | 0.00 | |
| 5 mg | $292.00 | 0.00 | |
Pricing updated 2018-08-16. Prices are subject to change without notice.
- This product has been manufactured and tested to meet ISO17025:2005 and Guide 34:2009 guidelines
- This product is intended to be used as an analytical reference standard
- Bulk material is available for academic research at qualified institutions; please contact our sales department for pricing
AH 7921 (Item No. 12036) is an analytical reference material categorized as an opioid.1 It is an analgesic with high addictive liability.2 AH 7921 is regulated as a Schedule I compound in the United States. This product is intended for research and forensic applications. This product is a qualified Reference Material (RM) that has been manufactured and tested to meet ISO17025 and Guide 34 guidelines. These materials are tested using validated analytical methods on qualified instrumentation to ensure traceability of measurements. All traceable RMs may be distinguished by their CofAs and can be downloaded below using the batch number located on the product label. For a representative CofA please contact our technical support.
Warning - this product is not for human or veterinary use.
Download Safety Data Sheet (SDS)
Download free InChI Key generation software
View our Base Peak Identification Tool
View our Flipbook Identification Tool
View the Cayman Structure Database for chemical structure definitions for many Cayman products
View the Cayman Spectral Library (CSL) for ChemStation-searchable GC-MS spectra of many of Cayman's emerging forensic drug standards
Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data pack, and GC-MS data.
1. Hayes, A.G., and Tyers, M.B. Determination of receptors that mediate opiate side effects in the mouse. Br.J.Pharmac. 79(3), 731-736 (1983).
2.
Brittain, R.T., Kellett, D.N., Neat, M.L., et al. Proceedings: Anti-
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