Opioid Adulterants Test

DTADT

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Turnaround Time:

2-3 Days

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Opioid Adulterants Test

Method Description

The Qualitative Determination of Pain Management Adulterants in Botanical Products by Liquid Chromatography-Tandem Mass Spectrometry (LC-TQ) involves analyzing botanical samples for the presence of potential adulterants using chromatographic separation and mass spectrometric detection. LC-TQ provides high sensitivity and specificity, allowing for the identification of adulterants commonly found in pain management botanical products. This method is essential for quality control and consumer safety in the herbal and nutraceutical industries, ensuring that botanical products are free from unwanted substances and comply with regulatory standards. The qualitative results help to authenticate and guarantee the purity of botanical formulations used in pain management.

Analyte List

Analyte Name LOD LOQ
4-Fluoro-Isobutyryl Fentanyl 1.2 ug/g N/A
Acetyl Fentanyl 0.48 ug/g N/A
Benzoyl Fentanyl 1.2 ug/g N/A
Buprenorphine 4.8 ug/g N/A
Butyryl Fentanyl 1.2 ug/g N/A
Carfentanyl 1.2 ug/g N/A
Codeine 4.8 ug/g N/A
Cyclopropyl Fentanyl 0.48 ug/g N/A
Fentanyl 0.48 ug/g N/A
Furanyl Fentanyl 0.48 ug/g N/A
Heroin 4.8 ug/g N/A
Hydrocodone 4.8 ug/g N/A
Hydromorphone 4.8 ug/g N/A
Meperidine 4.8 ug/g N/A
Methadone 4.8 ug/g N/A
Morphine 4.8 ug/g N/A
Oxycodone 4.8 ug/g N/A
Oxymorphone 4.8 ug/g N/A
Tramadol 4.8 ug/g N/A

Technical Data Sheet

Test Name - Common
Opioid Adulterants Test
Method Name
Qualitative Determination of Pain Management Adulterants in Botanical Products
Method Code
LAB-TM-074
Equipment
Liquid Chromatography - Tandem Mass Spectrometry (LC-TQ)
Method Reference
Reportable Unit
Detect/Non-detect
Sample Size Requirements
Available for
Food Products, Dietary Supplements, Botanicals (Raw Materials, Extracts, Finished Products), API (Isolates, Active Ingredients)
Additional Information
*Prices and offerings are subject to change without notice.